random Flashcards

0
Q

Heberden and Bouchard nodes

A
  • can be cause by severe osteoarthritis

- hard, bony nodules over the distal (Heberden) and proximal (Bouchard) interphalangeal joints, respectively

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1
Q

rheumatoid nodules

A
  • firm, flesh-colored and NONTENDER
  • typically occur over pressure points such as the elbow and extensor surface of the proximal ulna
  • almost all these pts will have positive rheumatoid factor levels
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2
Q

“sausage digit”

A

-severe PSORIATIC arthritis typically first affects the distal interphalangeal joints and clinically manifests as a “sausage digit”, where the digit takes on a swollen fusiform shape w/ significant hyperemia

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3
Q

Chronic tophaceous gout

A
  • urate crystals can be deposited in the skin resulting in the formation of tumors (tophi) w/ a chalky white appearance
  • be on the lookout for the great toe being affected (podagra) w/ monosodium urate crystals
  • Uric acid crystals form in the renal tubules and collecting system resulting in NEPHROLITHIASIS
  • Ddx includes rheumatoid nodules and calcinosis cutis when suspected tophi are seen
  • Note that diuretics in general have a hyperuricemic effect resulting from hypovolemia-associated enhancement of uric acid reabsorption in the proximal tubule
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4
Q

myocardial contusion

A
  • tachycardia, new bundle branch blocks or arrhythmia

- sternal fracture is commonly associated injury

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5
Q

myocardial rupture

A
  • cardiac tamponade (muffled heart sounds, hypotension, distended neck veins)
  • diagnosis is made rapidly w/ US
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6
Q

esophageal rupture

A
  • rare following blunt trauma
  • Iatrogenic (ie w/ endoscopy) and esophagitis-related etiologies are more common
  • may have pneumomediastinum and PLEURAL EFFUSIONS
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7
Q

Diaphragmatic rupture

A
  • abdominal pain, pain referred to the shoulder, shortness of breath, and/or vomiting
  • CXR may show abdominal viscera above the diaphragm, and/or loss of the diaphragmatic contour
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8
Q

Hemothorax

A
  • may result from injuries to the aorta, myocardium, hilar blood vessels or lung parenchyma
  • symptoms depend on degree of blood loss and can range from SOB to shock
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9
Q

Pts sustaining rapid deceleration injuries to the chest require radiographic evaluation for aortic injury w/ x-ray, CT scan and possibly TEE as well

A

.

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10
Q

Persistent pneumothorax and significant air leak following chest tube placement in a patient who has sustained blunt chest trauma suggests what?

A
  • Tracheobronchial rupture

- other findings include pneumomediastinum and subcutaneous emphysema

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11
Q

rash associated w/ secondary syphilis

A
  • generalized maculopapular lesions involving the trunk and extremities w/ associated lymphadenopathy
  • rash typically does NOT spare the palms and soles
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12
Q

Disseminated gonococcal infection

A
  • causes high fever, chills, tenosynovitis, polyarthralgia, and pustular lesions on the trunk and extremities
  • should be considered when risk factors for gonococcal infection are present
  • routine blood and pustule cultures can be negative due to the fastidious nature of Neisseria gonorrhoeae
  • may also have migratory asymmetric polyarthralgia without purulent arthritis (wrists, ankles, fingers, and knees)
  • recurrent DGI: check terminal complement activity
  • treat for chlamydia empirically w/ azithromycin or doxycycline
  • treat gonorrhea w/ IV ceftriaxone
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13
Q

Osteoarthritis

A
  • non-inflammatory arthritis presenting with pain that is worse w/ activity and improved w/ rest
  • x-ray findings include joint space narrowing and osteophytes, and subchondral sclerosis/cysts.
  • synovial fluid analysis will reveal fewer than 2000 WBC/ml, no organisms, and no crystals
  • most commonly affects hands and weight-bearing joints
  • increasing age is leading risk factor
  • typically have mild morning stiffness (
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14
Q

Punched out erosions w/ a rim of cortical bone

A
  • characteristic x-ray findings in gouty arthritis
  • acute joint pain and synovial fluid shows WBC count 2000-50,000/mL and NEEDLE-SHAPED, NEGATIVELY birefringent crystals (yellow when parallel)
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15
Q

periarticular osteopenia and joint margin erosions

A
  • classic for rheumatoid arthritis (RA)
  • inflammatory arthritis presenting w/ morning stiffness ( >30 minutes) and systemic symptoms of fever, malaise, and weight loss
  • WBC count of synovial fluid is 2,000-50,000/mL
  • wrists, MCP and PIP joints are commonly involved
  • the joints will be warm to the touch
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16
Q

normal joint space w/ soft tissue swelling

A
  • infectious arthritis

- cell count of > 50,000/mL is typical on synovial fluid and gram stain is often positive

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17
Q

calcification of cartilaginous structures

A
  • CHONDROCALCINOSIS
  • typical of pseudogout, or calcium pyrophosphate dihydrate (CPPD) deposition
  • acute swelling, stiffness, and pain of the knee after surgery or medical illness
  • synovial fluid = 2,000 - 50,000mL w/ RHOMBOID, POSITIVELY birefringent crystals (blue when parallel)
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18
Q

Ankylosing spondylitis

A
  • pts can develop restrictive lung disease due to diminished chest wall and spinal mobility
  • PFTs show a mildly restrictive pattern w/ reduced vital capacity and total lung capacity but normal FEV1/FVC
  • low back pain (age of onset
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19
Q

obstructive lung disease patten on PFTs

A

-FEV1:

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20
Q

Restrictive lung disease (including obesity) pattern on PFTs

A
  • FEV1: 70%

- FVC:

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21
Q

Rotator cuff tear

A
  • may result from trauma (eg falling on an outstretched arm) or as the end result of chronic impingement and tendonitis
  • similar to pts w/ rotator cuff tendinitis, pts often complain of pain upon reaching and lifting the arm over head. However, weakness of the shoulder is more common in rotator cuff tears, and symptoms do not improve w/ lidocaine injection
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22
Q

Adhesive capsulitis

A
  • aka “frozen shoulder”
  • idiopathic condition characterized by pain and contracture
  • inability to lift the arm above the head due to fibrosis of the shoulder capsule
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23
Q

Cervical radiculopathy

A
  • typically presents w/ pain of the neck and arm
  • paresthesias of the arm are present in 80% of pts
  • weakness may affect the shoulder, elbow, or wrist
  • movement at the neck exacerbates symptoms
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24
thoracic outlet syndrome
- combination of numbness, weakness and swelling due to compression of the subclavian vessels and lower trunk of the brachial plexus - a weakened radial pulse and reproduction of symptoms w/ specific arm movements supports the diagnosis
25
Rotator cuff tendonitis
- usually caused by impingement and is most common in middle-aged and older pts who perform repetitive arm movements above the head - presents w/ pain when lifting the arm - may be differentiated from rotator cuff tear and frozen shoulder by injection of the joint w/ lidocaine - in the case of isolated rotator cuff tendonitis, any pain and limitation of motion is resolved by the injection
26
who may be rheumatoid factor positive?
-pts w/ rheumatoid arthritis, SLE, Sjogren syndrome, dermatomyositis, HCV infection and others
27
Antimitochondrial antibodies is associated w/ what?
Primary biliary cirrhosis
28
Anti-neutrophil cytoplasmic antibodies
-granulomatosis w/ polyangiitis (Wegener's)
29
Anti-smooth muscle antibodies
-autoimmune hepatitis
30
anti-topoisomerase-1 antibodies
systemic sclerosis
31
Systemic sclerosis
- form of scleroderma w/ widespread organ involvement - GERD, right heart failure, and hypertension result from involvement of the esophagus, pulmonary arteries and kidneys, respectively. - antinuclear autoantibodies and anti-topoisomerase-1 antibodies would most likely be present
32
Pseudogout
- cannot be reliably distinguished from gout and septic arthritis based on history and physical alone - diagnosed by the presence of RHOMBOID, POSITIVELY birefringent crystals on synovial fluid analysis, and radiographic evidence of CHONDROCALCINOSIS - acute form of calcium pyrophosphate dihydrate (CPPD) crystal disease - frequently precipitated by trauma, surgery, or medical illness - knee is most commonly affected joint
33
gout
- monosodium urate crystals | - needle-shaped and NEGATIVELY birefringent on synovial fluid analysis
34
most common crystal found in renal calculi?
calcium oxalate
35
type of renal calculi found in pts w/ UTI caused by urease-producing organisms (Klebsiella, Proteus)?
Struvite (magnesium ammonium phosphate)
36
Initial disease-modifying antirheumatic drug of choice in pts w/ rheumatoid arthritis? side effects?
- Methotrexate - side effects: GI symptoms, oral ulcers or stomatitis, rash, alopecia, hepatotoxicity, pulmonary toxicity, and bone marrow suppression - FOLIC ACID supplementation has been shown to reduce the incidence of adverse effects of MTX therapy w/o loss of efficacy
37
Anti-cytokine agents used for treatment of rheumatoid arthritis?
- TNF-a inhibitors (etanercept, infliximab, adalimumab), IL-1 receptor antagonists (anakinra, canakinumab), and IL-6 receptor antagonists (tocilizumab) - these agents are generally reserved for use in pts resistant to intitial DMARD therapy - TNF-a inhibitors can cause neutropenia, infections (reactivation of latent TB, opportunists), exacerbations of heart failure, demyelinating illness, and increased risk of malignancy
38
Side effects of chronic glucocorticoid use?
-weight gain, HTN, peptic ulcer disease, glucose intolerance, myopathy, osteoporosis, increased risk of infections
39
Felty syndrome
-clinical disorder seen in pts w/ severe, long-standing (>10 yrs) RA that is characterized by neutropenia and splenomegaly.
40
Pts w/ RA have an approx. 2-fold increase risk of lymphoma, which may present w/ low-grade fever, fatigue, and a palpable spleen
.
41
Polymyalgia rheumatica (PMR)
- age > 50 - subacute to chronic (>1 month) pain in the shoulder and hip girdles - morning STIFFNESS lasting > 1 hour - constitutional symptoms - elevated ESR (> 40) - no other apparent explanation of symptoms - Tx: low-dose prednisone (if uncomplicated), which should result in rapid relief of symptoms
42
Fibromyalgia
- most commonly presents in young to middle-aged women w/ widespread pain, fatigue, and cognitive/mood disturbances - pts have point muscle tenderness in areas such as the mid trapezius, lateral epicondyle, costochondral junction in the chest, and greater trochanter - regular aerobic exercise and good sleep hygiene are recommended
43
NSAIDS are occasionally useful in polymyalgia rheumatica for mild breakthrough discomfort or minor relapse of symptoms while tapering glucocorticoids. However, they are much less effective than glucocorticoids for initial management and are not recommended.
.
44
what are you concerned about in a chronically wounded, scarred or inflamed skin over time? what is the eponym?
- Squamous cell carcinoma - malignancy should be suspected in all non-healing wounds - SCC arising within burn wounds is known as a MARJOLIN ULCER - SCC has also been described arising in the skin overlying a focus of osteomyelitis, radiotherapy scars and venous ulcers; these types tend to be more aggressive - a biopsy should be obtained in all chronic wounds failing to heal in order to rule out malignancy
45
When a wound fails to heal after a prolonged period, biopsies should be obtained to ensure the ulcer has not degenerated into a squamous cell carcinoma. When SCC arises within a burn wound, these ulcers are known as what?
Marjolin ulcers
46
Melanoma
-typically occurs in pts w/ a nevus that has increased in size, changed color, become palpable or become symptomatic (painful, pruritic, or bleeding)
47
Basal cell carcinoma
- classically presents on chronically sun-exposed skin | - lesions are usually pearly telangiectatic papules w/ a central "rodent" ulceration
48
Dysplastic nevi
- melonocytic nevi exhibiting characteristics not seen in standard nevomelanocytic nevi - size greater than 6 mm, irregular borders, irregular pigmentation - varying degrees of architectural disorders and cytologic atypia
49
precursor lesion to squamous cell carcinoma?
Actinic keratosis (common on chronically sun-exposed skin)
50
Polymyositis
- idiopathic inflammatory muscle disease - slowly progressive PAINLESS, PROXIMAL WEAKNESS of the LOWER EXTREMITIES characterized by difficulty ascending and descending stairs or rising from a seated position; proximal arm weakness usually follows, leading to difficulty combing hair or working w/ the hands overhead - pts may develop dysphagia due to involvement of the striated muscles of the upper pharynx - there are NO skin findings in PM, distinguishing it from dermatomyositis - a MUSCLE BIOPSY is the best diagnostic test and typically shows a mononuclear infiltrate surrounding necrotic and regenerating muscle fibers
51
Myasthenia gravis
- muscle weakness and fatigability - cranial nerve and proximal limb weakness that worsens w/ repeated activity and resolves w/ rest - symptoms resolve rapidly w/ administration of edrophonium (anticholinesterase test)
52
Electroencephalography (EEG)
-used primarily in the evaluation of pts w/ seizure or sleep disorders
53
Lumbar puncture
-useful to evaluate weakness in cases of suspected Guillain-Barre syndrome (ascending weakness w/ paresthesias and autonomic disturbances) or multiple sclerosis (episodic optic neuritis or transverse myelitis)
54
Hyperkalemia is a possible complication of ACE inhibitor (eg lisinopril) therapy and may present w/ flaccid paralysis. However, uncommon in pts w/o underlying renal insufficiency or additional meds that cause hyperkalemia
.
55
Giant cell arteritis
- a temporal artery biopsy is necessary to make the diagnosis - usually presents w/ headache, jaw claudication, and systemic symptoms - commonly associated w/ polymyalgia rheumatica, which causes diffuse PAIN in the shoulders and hips but NOT WEAKNESS
56
Tension pneumothorax
- emergency situation and needs immediate needle thoracostomy based on clinical diagnosis (no imaging needed!) - placement of subclavian central venous catheters accounts for approx. 1/4 of iatrogenic pneumothorax - clinically characterized by rapid onset severe SOB, tachycardia, tachypnea, hypotension, and distention of the neck veins due to SVC compression - tx: immediate needle thoracostomy to decompress pleural cavity, followed by an emergency tube thoracostomy w/ underwater seal
57
Cardiac tamponade
- hypotension, tachycardia, elevated systemic venous pressure and pulsus paradoxus - pericardiocentesis is indicated
58
Mild traumatic brain injury (TBI) management
- pts w/ mild TBI w/ repeated vomiting, headache, or LOC should undergo head CT scan without contrast or observation for 4-6 hours - if head CT scan is normal or the observation period is uneventful, pt can be discharged home w/ a reliable guardian; detailed return precautions should also be provided - Mild TBI: GCS 13-15, LOC
59
serious TBI
- GCS 5 min, neuro deficit, signs of basilar skull fracture - require neuroimaging w/ non-contrast head CT, close inpatient monitoring w/ neuro checks q2 hrs, and a neurosurgery consult
60
Minor head trauma
- GCS of 15, normal mental status, no abnormal neuro or funduscopic findings, and no evidence of skull fracture - do NOT require neuroimaging or hospitalization
61
why order non-contrast head CT in trauma?
because contrast looks like an acute bleed, thus distinguishing them more difficult
62
Sjogren syndrome
- diagnosed when subjective or objective evidence of dry eyes and mouth exists in the presence of either histologic evidence of lymphocytic infiltration of the salivary glands or serum autoantibodies against SSA (Ro) and / or SSB (La). - autoimmune condition that most commonly affects women in their fifth and sixth decade - keratoconjunctivitis sicca (xerophthalmia, dry eyes) and xerostomia (dry mouth); increased incidence of dental caries; difficulty swallowing
63
Antimitochondrial antibodies
-associated w/ Primary Biliary Cirrhosis (PBC), an autoimmune disease characterized by progressive jaundice, varices, and other signs of cirrhosis
64
Barium swallow test
-used to assess disease of esophageal motility such as achalasia or presence of esophageal diverticulum
65
test to diagnose Barrett esophagus
- esophageal endoscopy w/ biopsy | - Barrett's: metaplasia of squamous epithelium to columnar epithelium and is a precursor of esophageal adenocarcinoma
66
what is the most common cause of lower extremity edema?
- Venous insufficiency (valvular incompetence) | - classically worsens throughout the day and resolves overnight when the patient is recumbent
67
how does edema caused by lymphatic obstruction present?
- uncommon cause of edema - may result from malignant obstruction of lymph nodes, lymph node resection, trauma, and filariasis - classically affects the DORSA OF THE FEET and causes MARKED THICKENING and RIGIDITY of the skin
68
signs of arterial occlusion in extremity?
pain, pallor, paresthesias, pulselessness, and coolness to the touch
69
Rotator cuff tears
- result from chronic rotator cuff tendonitis and shoulder trauma - shoulder pain and weakness when lifting the arm above the head (or mid arc abduction, external rotation) is suggestive of rotator cuff pathology - a lidocaine injection ameliorates the pain and weakness of rotator cuff TENDONITIS, while it does not improve symptoms of rotator cuff TEAR - MRI is excellent at visualizing soft tissue structures and is the study of choice for diagnosing rotator cuff tears
70
what can shoulder x-ray diagnose?
-fractures, dislocations, and calcific tendonitis
71
Multiple myeloma presentation
- pain in the spine, ribs, or back | - may be accompanied by hypercalcemia and anemia
72
Fat embolism
- presents w/ dyspnea, confusion and petechiae in the upper part of the body and occurs after multiple fractures of long bones - severe respiratory distress, petechial rash, subconjunctival hemorrhage, tachycardia, tachypnea, and fever - diagnosis can be confirmed by FAT DROPLETS IN URINE or presence of intra-arterial fat globules on fundoscopy; may occur 12 to 72 hrs after the injury - serial x-rays shows increasing diffuse bilateral pulmonary infiltrates within 24-48 hrs of onset of clinical findings - tx: prompt respiratory support (use of heparin, steroids, LMW dextran is controversial)
73
air embolism
- can occur in a trauma patient who is on a respirator, or with subclavian vein access - can result in sudden collapse and cardiac arrest
74
amniotic fluid embolism
-occurs immediately after the rupture of membranes
75
Thromboembolism
-can cause pulmonary embolism in bed-ridden patient
76
what does morning stiffness indicate?
INFLAMMATORY arthritides
77
Psoriatic arthritis
- occurs in 5-30% of pts w/ psoriasis - classic presentation involves the DIP joints - morning stiffness, deformity, dactylitis (sausage digit), and nail involvement are common - current tx options for psoriatic arthritis include NSAIDs, methotrexate, and anti-TNF alpha agents
78
tophi
cutaneous deposits of monosodium urate crystals in chronic gout -commonly occur over joints and the helix of the ear, and may ulcerate
79
Gottron's papules
- violaceous plaques, slightly scaly - can present with dermatomyositis - usually over the MCP joints, which at times can look similar to psoriasis
80
Enteropathic arthritis
- occurs in 10-20% of pts w/ Chron disease and UC - most often affects the lower extremities and sacroiliac joints and tends to wax and wane w/ the symptoms of bowel disease - these pts have prominent GI symptoms and other extraintestinal manifestations of inflammatory bowel disease
81
Neuropathic arthropathy (Charcot joint)
- most commonly affects the lower limbs - most cases occur w/ diabetes, but syphilis and alcoholism are other causes - peripheral neuropathy is believed to result in decreased proprioception, which leads to frequent trauma and eventual destruction of the joint
82
Rheumatoid arthritis often presents w/ morning stiffness (indicating inflammatory etiology). The MCP and PIP joints are prominently involved, whereas the DIP joints classically are not. Dactylitis and nail involvement are also not expected in RA
.
83
joint and skin involvement in sarcoidosis?
- polyarthritis affecting the ankles and knees - causes protean cutaneous manifestations, the most common of which is ERYTHEMA NODOSUM - also often have cough, chest pain, and dyspnea
84
Bowel ischemia (colonic ischemia)
- may complicate up to 7% of procedures on the aortoiliac vessels and most commonly affects the distal left colon - pts report dull pain over the ischemic bowel as well as hematochezia - colonoscopy shows a discrete segment of cyanotic and ulcerated bowel
85
Acute diverticulitis typically does not present with rectal bleeding, while diverticulosis does
.
86
radiation proctitis
- diarrhea, rectal bleeding, tenesmus and incontinence | - later, strictures and fistulae may form
87
C. diff colitis (pseudomembranous colitis)
- abdominal pain, fever, and watery diarrhea | - diagnose by detecting toxin in the stool w/ ELISA
88
IBD can be differentiated from colonic ischemia both by the acute onset of the latter as well as differences in appearance on colonoscopy. Namely, ischemia typically spares the rectum and involves only a segment of the colon while IBD does not.
.
89
Glasgow coma scale (GCS)
- all trauma pts should be triaged using the GCS, which can predict the severity and prognosis of coma, during the primary survey. - the GCS assesses the patient's ability to open his/her eyes, motor response, and verbal response
90
All pts w/ smoke inhalation should be suspected to have what?
- acute carbon monoxide poisoning - tx w/ 100% oxygen via a nonrebreather facemask - early symptoms of carbon monoxide poisoning are typically neurological and include agitation, confusion, and somnolence - diagnosis confirmed clinically and documenting an elevated carboxyhemoglobin level (> 3% in nonsmokers and > 15% in smokers) - pulse ox is unreliable!
91
a bolus of 50% dextrose and IV thiamine is indicated in any unconscious patient as an emergency measure to assess for hypoglycemia.
.
92
Volkmann's ischemic contracture
-the final sequel of compartment syndrome in which the dead muscle has been replaced w/ fibrous tissue
93
Reflex sympathetic dystrophy
- vague painful condition seen as a sequel of infection on trauma which may be minor - characterized by pain, hyperesthesia and tenderness, which are out of proportion to the physical findings - Sudeck's atrophy is a radiographic term for spotty rarefaction seen in pts w/ RSD
94
manifestations of SLE
- constitutional: fever, fatigue and weight loss - symmetric, migratory arthritis - butterfly rash and photosensitivity - serositis: pleurisy, pericarditis, and peritonitis - thromboembolic events (due to vasculitis and antiphospholipid antibodies) - cognitive dysfunction and seizures - hemolytic anemia, thrombocytopenia, and leukopenia - HYPOCOMPLEMENTEMIA (c3 and c4) - ANA (sensitive) and ANTI-dsDNA and ANTI-SM (specific) - renal involvement: proteinuria and elevated creatinine
95
Systemic Lupus Erythematosus (SLE)
- autoimmune disease that is most commonly diagnosed in young women - more than 90% of patients w/ SLE have joint involvement, most often affecting the hands - Joint pain may be severe but SLE induced arthritis is usually NON-DEFORMING (unlike RA)
96
Tx of joint symptoms in SLE
- most pts will respond to conservative treatment w/ NSAIDs | - low dose glucocorticoids or antimalarials (eg hydroxychloroquine) can be added for more severe joint symptoms
97
"pencil-in-cup" deformities
-distal phalangeal resorption is characteristic of the ARTHRITIS MUTILANS variant of psoriatic arthritis
98
Cartilage degradation is the underlying pathologic mechanism of osteoarthritis (OA). Pts w/ OA may develop muscle atrophy from limitations of joint movement.
.
99
Subluxation of the cervical vertebrae and tendon damage in the hands may occur in RA
.
100
SLE
- autoimmune disease most commonly diagnosed in young women - 90% of pts have joint involvement, most often affecting the hands - joint pain may be severe but SLE induced arthritis is usually NON-DEFORMING (ie no bone resorption or subluxation or permanent deformity)
101
Inflammatory breast cancer
- uncommon - presents w/ an erythematous and brawny edematous cutaneous plaque overlying a mass on the breast commonly with axillary lymphadenopathy - 25% of pts w/ this condition will have metastatic disease at time of presentation
102
Nipple discharge in a NON-lactating women should ALWAYS raise suspicion for breast cancer, especially if spontaneous, unilateral, localized to a single duct, occurs in a patient over 40 years old, is bloody, or is associated with a mass! Biopsy with histology must be done
.
103
mastitis
- typically in younger lactating women - tx w/ an antibiotic that covers Staph and Strep, and encourage continued breast feeding or breast pumping of the affected breast
104
cellulitis of breast that fails to respond to empiric antibiotic therapy
- biopsy for culture | - acid-fast organisms and fungi may rarely cause mastitis and breast abscess
105
Rheumatic fever
- preventable complication of streptococcal group A pharyngitis - usually precedes the onset of rheumatic fever by 2-4 weeks - diagnosed clinically using Jones criteria (2 major, or 1 major and 2 minor) - Criteria includes, major: Carditis, migratory polyarthritis, sydenham chorea, subcutaneous nodules, and erythema marginatum; minor: fever, arthralgias, elevated ESR/CRP, prolonged PR interval - supportive lab findings: positive strep antigen test or elevated ASO titer - prevented w/ treatment w/ penicillin of strep pharyngitis
106
ALL
-malignancy of WBC's that causes lymphocytosis or lymphopenia along w/ anemia or thrombocytopenia
107
Juvenile idiopathic arthritis
- diagnosed when arthritis is present > 6 weeks | - systemic symptoms including rash, can be seen in children with JIA, but the arthritis is usually NOT migratory
108
Henoch-Schonlein purpura
-small vessel vasculitis that can cause a transient, migratory arthritis and rash that is purpuric (arthritis typically involves lower joints)
109
Acute rheumatic fever
- peak incidence age 5-15; twice as common in girls - Major: Joints (migratory arthritis), Carditis, Nodules (subcutaneous), Erythema marginatum, Sydenham chorea - Minor: fever, arthralgias, elevated ESR/CRP, Prolonged PR interval - late sequelae: mitral regurgitation/stenosis - prevention: penicillin for GROUP A STREP (strep pyogenes) pharyngitis - diagnosis based on evidence of preceding group A strep infection along w/ 2 major criteria, or 1 major plus 2 minor criteria
110
SLE
- autoimmune disease that affects multiple organ systems - arthritis and elevated CRP/ESR can be seen, but the rash is usually present across the cheeks (malar rash). - Multiple organ system involvement (eg, hematologic, neurologic, renal) is needed for the diagnosis
111
diagnostic criteria for SLE?
SOAP BRAIN MD -Serositis (pleuritis/pericarditis) -Oral ulcers -Antinuclear antibody (ANA)- very SENSITIVE -Photosensitivity (skin rash to sunlight) -Blood (hemolytic anemia, leukopenia, thrombocytopenia) -Renal (proteinuria and cell casts) -Arthritis (symmetric, involving 2+ small or large peripheral joints) -Immunologic (anti-dsDNA) -Neurological (seizures, psychosis) Note that anti-smith antibodies are the most SPECIFIC for SLE! -Need 4 out of 11 to diagnose SLE
112
Acute appendicitis
- CLINICAL diagnosis - classic presentation of migratory RLQ pain, nausea, vomiting, fever, leukocytosis, McBurney point tenderness, and Rovsing sign should have IMMEDIATE appendectomy to prevent appendiceal rupture. - imaging studies such as CT and US are useful for pts with NONCLASSIC symptoms, equivocal findings on initial assessment, or delayed presentation
113
Role of antibiotics in appendicitis?
- Abx should be given PREoperatively to all pts and should be continued POSToperatively for those w/ appendiceal rupture - pts w/ appendicitis who have had symptoms > 5 days usually have a PHLEGMON with an abscess that has walled off; they can be managed conservatively w/ IV abx, bowel rest, and delayed appendectomy weeks later
114
Presentation of cardiac tamponade
hypotension, tachycardia, distant heart sounds, neck vein distension, ELECTRICAL ALTERNANS (varying amplitude of the QRS complexes from beat to beat) on ECG
115
Blunt abdominal trauma
- often causes splenic injury which can present w/ delayed onset hypotension, LUQ pain, and left shoulder pain (Kehr sign) - pts should have an abdominal CT scan w/ IV contrast for diagnosis - those w/ persistent hemodynamic instability require urgent laparotomy
116
Patellofemoral syndrome
- very common cause of anterior knee pain - symptoms are chronic and associated w/ activities such as CLIMBING STAIRS w/ extension at the knee - women are affected much more often than men - diagnosis is based on history and physical exam; tx involves stretching and strengthening the thigh muscles in addition to avoiding activities that worsen the pain - risk factors include overuse, malalignment, and trauma - diagnostic test includes the PATELLAR GRIND TEST (patellofemoral compression test) and reproduction of pain w/ squatting - subacute to chronic pain, increased w/ squatting, running, prolonged sitting, using stairs
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patellar tendonitis
- primarily athletes ("jumper's knee") | - episodic pain and tenderness at inferior patella
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Osgood-Schlatter disease
- preadolescent/adolescent athletes; recent growth spurt | - increased pain w/ sports, relieved by rest; tenderness and swelling at tibial tubercle
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Penile fracture
- surgical EMERGENCY that requires emergent urethral imaging (retrograde urethrogram) and surgical repair - the most common cause is a crush injury of the erect penis, most commonly during intercourse where the female is on top of the male - often accompanied by snapping sensation or sound, followed by severe pain and swelling; due to tearing of the tunica albuginea, which invests the corpus cavernosum
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Circumsision
- treatment of choice for phimosis, paraphimosis, and Zoon's balanitis - also associated w/ lower risk of squamous cell carcinoma of the penis
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Acute mediastinitis
- can occur following cardiac surgery that is usually due to intra-op wound contamination and presents w/ fever, chest pain, leukocytosis, and mediastinal widening on chest x-ray - its a serious condition that requires drainage, surgical debridement, and prolonged antibiotic therapy - typically presents within 14 days post-op - clinical diagnosis and confirmed during surgery when pus is seen in mediastinum - high mortality rate even with appropriate treatment
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Atrial fibrillation commonly (up to 15-40%) occurs within a few days after CABG and is usually self-limited, w/ resolution in 24 hours after CABG.
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treatment for pericarditis
NSAIDS
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Postpericardiotomy syndrome
- fever, leukocytosis, tachycardia, and chest pain - usually autoimmune and occurs a few weeks following a procedure with a pericardium incision - NSAIDS or steroids treat the inflammation, and pericardial puncture is indicated if tamponade occurs
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what to do with amputated part in traumatic amputations?
- amputate parts should be wrapped in saline-moistened sterile gauze, sealed in a plastic bag, placed on a bed of ice and brought to the ED with the patient - younger pts w/ sharp amputations w/ no crush injury or avulsion are the best candidates for amputation reimplantation
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Baker cysts
- develop as a result of excessive fluid production by an inflamed synovium, as occurs in cases of RA, osteoarthritis, and cartilage tears - the excess fluid accumulates in the popliteal bursa which expands, creating a tender mass in the popliteal fossa - baker cysts occasionally burst and release their contents into the calf, resulting in an appearance similar to a DVT
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MCL tears
- MCL is most commonly injured ligament of the knee - surgery is rarely necessary for MCL tears; bracing and early ambulation is the preferred treatment - MRI is the investigation of choice for defining soft tissue injuries of the knee
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If a patient develops a whistling noise during respiration following rhinoplasty, what should you suspect?
- Nasal septal perforation likely resulting from a septal hematoma - up to 25% of rhinoplasties need to be revised - common complications include patient dissatisfaction, nasal obstructions and epistaxis; those that involve the nasal septum are less common but more serious - additional conditions that can cause septal perforation are self-inflicted trauma (nose picking), syphilis, TB, intranasal cocaine use, sarcoidosis, and granulomatosis w/ polyantiitis (Wegener's)
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nasal polyps
- usually seen in pts w/ asthma and allergic disorders but may also occur in pts w/ other inflammatory conditions of the nasal mucosa - they may cause chronic nasal obstruction and should be surgically removed in symptomatic pts
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foreign bodies in nose
- common in children - pts will have nasal obstruction and may have a foul odor, halitosis, and nasal bleeding - following surgery, a retained foreign body such as nasal packing most classically would cause toxic shock syndrome
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allergic rhinitis
- presents w/ rhinorrhea, nasal pruritis, cough and occasionally dyspnea - on exam, the nasal mucosa is edematous and pale, and polyps may be present
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nasal furunculosis
- results from staphylococcal folliculitis following nose picking or nasal hair plucking - potentially life threatening as it can spread to the cavernous sinus - pts may complain of pain, tenderness, and erythema in the nasal vestibule
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management of a suspected urethral injury?
- Retrograde urethrogram should be first step! - foley catheterization in the presence of a urethral injury will predispose the patient to abscess formation and worsening of the urethral damage - classic signs of posterior urethral injury include blood at the urethral meatus, inability to void and a high-riding prostate on digital rectal exam. Perineal or scrotal hematomas are also frequently seen and such an injury is most classically associated w/ pelvic fracture
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how are urethral injuries managed?
- Retrograde urethrogram is almost always the first step - immediate surgical repair is occasionally done in cases of ANTERIOR urethral injury - most cases of urethral injury are treated w/ urinary diversion via a suprapubic catheter while the primary injury and associated hematomas are allowed to heal. After healing is complete, residual damage, such as urethral stricture, is assessed and repaired
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Retrograde cystogram with post void films
- used for diagnosis of BLADDER INJURY - may occur following major trauma, especially pelvic fracture - pts typically complain of gross hematuria
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Ileus can occur as a result of a vagal reaction caused by ureteral colic from kidney stones. Needle-shaped crystals on urinalysis indicate uric acid stones! Uric acid stones are radiolucent, and must be evaluated by abdominal CT, US, or IV pyelography. Ileus will resolve when the ureterolithiasis is treated. Stones
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Colonoscopy is NOT indicated for right-sided pathology and should NOT be performed in ACUTE pathology of the bowel wall due to the risk of perforation.
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Enteroclysis
-used to diagnose small bowel tumors and other pathology, which can cause intestinal obstruction
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What should ALWAYS be obtained following placement of central venous catheter?
Chest x-ray to confirm proper placement of the catheter tip and absence of complications before administering drugs or other agents through the catheter - complications: arterial puncture, pneumothorax, hemothorax, thrombosis, air embolism, sepsis, vascular perforation, myocardial perforation leading to tamponade - catheter tip should be located proximal to either the cardiac silhouette or the angle between the trachea and the right mainstem bronchus; ideally in the superior vena cava
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Esophageal rupture (Boerhaave syndrome)
- most commonly occurs following instrumentation of the esophagus - less commonly, it may occur in pts w/ protracted vomiting who have been resisting the urge to vomit; rupture in these cases typically occurs into the mediastinum resulting in pneumomediastinum; rupture typically occurs a few centimeters above the gastroesophageal junction - retrosternal chest pain and crepitus in the suprasternal notch are common following rupture of esophagus within the mediastinum
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True or false: acute pancreatitis can cause a left sided pleural effusion?
True
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perforated duodenal ulcer
-epigastric pain and air would be visualized under the diaphragm on upright abdominal x-ray, but pneumomediastinum is NOT associated w/ duodenal perforation
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Mallory-Weiss tear
- an INCOMPLETE mucosal tear at the gastroesophageal junction usually resulting from protracted vomiting - the common presentation is self-limited hematemesis - pneumomediastinum does NOT occur in such tears because the rupture is incomplete
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Serum sickness-like reaction
- most commonly caused by antibiotics (B-lactams and sulfa drugs) - symptoms arise 1-2 weeks after exposure and include fever, urticarial rash, arthralgia, and lymphadenopathy. the abnormalities should resolve within 48 hours w/ withdrawal of the offending agent. some cases may need steroid treatment - type III hypersensitivity reaction - lab findings: nonspecific hypocomplementemia and elevated ESR/CRP, which are consistent with any type III hypersensitivity reaction
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acute rheumatic fever
- can follow untreated strep pharyngitis and may present w/ frank arthritis, erythema marginatum, and fever - ARF after appropriate antibiotic therapy is extremely rare and highly unlikely
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Anaphylaxis
- presents acutely w/ skin changes plus hypotension, respiratory distress, or GI symptoms - type 1 hypersensitivity reaction
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Henoch-Schonlein purpura
- systemic IgA-mediated vasculitis occurring after an upper respiratory infection - presents w/ fever, arthralgia, and a palpable purpuric rash of the lower extremities
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Mononucleosis
- presents as fever, cervical lymphadenopathy, pharyngitis, and malaise - those treated w/ an aminopenicillin can develop a MORBILLIFORM (measles-like) rash on the trunk; however, the rash typically spares the extremities and arthralgia does not occur
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Scarlet fever
-presents w/ fever, and scarlatiniform "sandpaper" rash following strep pharyngitis
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Stevens-Johnson syndrome
- severe mucocutaneous reaction most commonly triggered by medications (eg sulfa drugs, anticonvulsants). - affected pts develop acute high fever, vesicular or bullous lesions, and painful hemorrhagic oral erosions
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Palpable breast abnormalities
- pts 30 are evaluated w/ mammogram and US - palpable breast masses should generally have an imaging evaluation even if the findings are relatively benign on physical exam - imaging evaluation is helpful both in characterizing the lesion as benign or malignant, and for guiding biopsy if needed
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physical exam findings of a rubbery, firm, freely mobile mass are suggestive of a fibroadenoma or other benign mass. findings of a hard, irregular, and fixed mass are typically palpated in patients w/ breast malignancies.
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Anterior spinal cord syndrome
- can be due to spinal cord infarction as a potential complication of thoracic aortic aneurysm surgery - typically presents w/ spinal shock (abrupt onset of bilateral flaccid paralysis and loss of pain/temp sensation below the level of spinal injury) - upper motor neuron signs (spasticity and hyperreflexia) subsequently develop over days to weeks - vibration and proprioception are usually preserved - the anterior spinal artery (ASA) supplies the anterior 2/3 of the spinal cord, including motor tracts (eg anterior corticospinal tract) and sensory tracts involved in pain/temp sensation (eg spinothalamic tract); the ASA is particularly dependent on blood supply for the radicular arteries that originate from the thoracic aorta, such as the artery of Adamkiewicz
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lumbar plexopathy
-peripheral neuropathy characterized by asymmetrical focal weakness, numbness, and paresthesias due to involvement of multiple adjacent nerve roots
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Medial meniscus tears
- typically injured during forceful torsion of the knee with the foot planted - pts complain of a popping sound and severe pain at the time of injury; McMurray's sign is commonly positive on physical exam - a bucket handle tear of the medial meniscus leads to locking of the knee joint during terminal extension
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ACL tear
- hx of forceful hyperextension injury to knee or a noncontact torsional injury of the knee during deceleration - effusion is seen rapidly following injury due to the ACL being well-perfused - Lachman's test, anterior drawer test and pivot shift test are used for clinical diagnosis
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PCL tear
- classically seen in the "dashboard injury", which refers to forceful posterior-directed force on the tibia with the knee flexed at 90 degrees - the posterior drawer, reverse pivot shift and posterior sag tests will help w/ clinical diagnosis
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Main mechanism responsible for pain relief in pts w/ anginal pain treated w/ nitroglycerin?
- dilation of veins (capacitance vessels) and decrease in ventricular preload - it is unclear whether nitro significantly increases coronary blood flow in pts w/ obstructive coronary heart disease
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Positive predictive value
- proportion of subjects with a positive test who actually have the disease out of all subjects who test positive for the disease - PPV = TP/TP+FP
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Negative predictive value
- proportion of subjects with a negative test, and who actually do NOT have the disease out of the total number of people who test negative for the disease - NPV = TN/TN+FN
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Sensitivity and specificity are useful for assessing the VALIDITY of a test. Predictive values are not true indices of the validity of a test, but are still important because pts present with positive or negative test results, and their true disease state is frequently unknown.
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Hyperparathyroidism predisposes to what?
- Pseudogout - pseudogout tends to present as an acute onset, painful monoarthritis affecting the knee; rhomboid shaped, positively birefringent crystals are diagnostic of pseudogout - hyperparathyroidism causes elevated calcium levels and low phosphorus concentrations. Subsequently hypercalcemia can cause constipation, fatigue, excessive urination, abdominal pain, urinary stones, mental status changes, and osteoporosis
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Gout
- needle shaped crystals w/ NEGATIVE birefringence | - presents as acute onset, painful monoarthropathy
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Struvite crystals
-have the shape of coffin lids and are seen in nephrolithiasis caused by chronic UTI with urease-producing organisms
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otitis externa vs malignant (necrotizing) otitis externa
- topical antibiotics and corticosteroids are appropriate for otitis externa, but not for malignant otitis externa, which requires IV abx and possible debridement if no response to abx - the severity of pain, presence of granulation tissue, and elevated ESR are all clues that distinguish OE from MOE
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antibiotics effective against Pseudomonas aeruginosa
- Anti-pseudomonal penicillins: Ticarcillin, Piperacillin - Cephalosporins: Ceftazidime (3rd gen), Cefepime (4th gen) - Aminoglycosides: Amikacin, Gentamicin, Tobramycin - Fluoroquinolones: Ciprofloxacin, Levofloxacin - Monobactams: Aztreonam - Carbapenems: Imipenem, Meropenem
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Malignant (necrotizing) otitis externa
- severe infection of the external auditory canal and skull base usually caused by Pseudomonas aeruginosa - its seen most frequently in elderly pts w/ diabetes or immunosuppression - presents as severe, unrelenting ear pain (especially prominent at night), purulent drainage w/ a sense of fullness, and conductive hearing loss on the affected side. Otoscopy shows granulation tissue and an edematous external auditory canal - as the infection spreads beyond the external auditory canal, osteomyelitis of the skull base or TMJ can develop and present w/ pain exacerbated by chewing - EMPIRIC TREATMENT WITH IV CIPROFLOXACIN
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Hazard ratios
- proportions that indicate the chance of an event occurring in the treatment group compared to the chance of the event occurring in the control goup - when reviewing a drug advertisement, it is important to critically read all presented info - hazard ratios 1 signifies that an event is more likely to occur in the treatment group. A ratio close to 1 implies little difference between the two groups. In addition, if the 95% confidence interval contains the null value of 1, this indicates that there is no significant difference between the two groups.
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Successful randomization in a clinical trial
- allows a study to eliminate bias in treatment assignments - an ideal randomization process minimizes selection bias, results in near-equal treatment and control group sizes, and achieves a low probability of confounding variables
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The null hypothesis
- is always the statement of NO RELATIONSHIP between the exposure and the outcome - to state the null hypothesis correctly, you should recognize the study design first
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what is the key pathogenic factor in the development of type 2 DM and associated abnormalities (hypertension, dyslipidemia)?
-Insulin resistance typical for pts w/ central-type obesity!
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Metabolic syndrome
- hypertension, impaired fasting glucose, and dyslipidemia - pts are also characteristically overweight w/ predominantly central (abdominal) fat distribution - Insulin resistance plays a central role in the pathogenesis of the metabolic syndrome - Diagnosis of the metabolic syndrome is based on at least 3 of the 5 following criteria: 1. abdominal obesity (men: waist circuference > 40 in; women: waist circumference > 35 in) 2. fasting glucose > 100 - 110 mg/dL 3. BP > 130/80 4. Triglycerides > 150 mg/dL 5. HDL (men:
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Insulin resistance is associated w/ several other systemic effects such as?
-dyslipidemia, endothelial dysfunction, procoagulable state, increased sympathetic activity, increased markers of inflammation, decreased uric acid excretion, increased sodium absorption, disordered breathing and increased testosterone production from the ovaries
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In clinical trials, randomization is said to be successful when a similarity of baseline characteristics of the patients in the treatment and placebo groups is seen
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Tx of uncomplicated cystitis
- Nitrofurantoin for 5 days (avoid in suspected pyelonephritis or creatinine clearance 20%) - Fosfomycin single dose - Fluoroquinolones only if above options cannot be used - Urine culture needed only if initial treatment fails
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Tx of complicated cystitis
- Fluoroquinolones for 5-14 days (do NOT use in pregnancy; consider nitorfurantoin, amoxicillin, and cephalexin instead), extended spectrum abx (ampicillin/gentamicin) for more severe cases - obtain sample for urine culture prior to initiating therapy and adjust abx as needed - associated w/ diabetes, pregnancy, renal failure, urinary tract obstruction, indwelling catheter, urinary procedure (eg cystoscopy), immunosuppression and hospital-aquired
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Tx of pyelonephritis
- Outpatient: fluoroquinolones (eg ciprofloxacin, levofloxacin) - Inpatient: IV abx (fluoroquinolone, aminoglycoside +/- ampicillin) - obtain sample for urine culture prior to initiating therapy and adjust abx as needed
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Uncomplicated cystitis
- commonly occurs in otherwise healthy pts and has a low risk of tx failure - UA confirms diagnosis - Pts can be tx without a urine culture, which may be done later in those who fail initial therapy - oral TMP/SMX, nitrofurantoin, and fosfomycin are effective first-line tx options - presents w/ dysuria, urinary frequency, and suprapubic tenderness
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Recommended vaccines for chronic liver disease
- Tdap/Td: Tdap once as substitute for Td booster, then Td every 10 years - Influenza: annually - Pneumococcal vaccines: PPSV23 once, then revaccination w/ sequential PCV13 and PPSV23 at age 65 - Hepatitis A: 2 doses 6 months apart with initial negative serologies - Hepatitis B: 3 doses at 0 months, 1 month and at least 4 months w/ initial negative serologies
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Pneumococcal vaccines
- the 13-valent pneumococcal conjugate vaccine (PCV13) is recommended initially for all adults age > 65 followed by the 23-valent pneumococcal polysaccharide vaccine (PPSV23) after at least 6-12 months - for adults age
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Following splenectomy, pts are at increased risk for sepsis due to encapsulated organisms including Streptococcus pneumoniae, Neisseria meningitidis, and Haemophilus influenzae. Vaccinations against each of these organisms should be administered either > 14 days before scheduled splenectomy or > 14 days after splenectomy.
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most common cause of sepsis in post-splenectomy pts?
-Strep pneumoniae
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Strep pneumo vaccination in asplenic pts
- following splenectomy, the 13-valent pneumococcal conjugate vaccine (PCV13) should be given first, followed by the 23-valent pneumococcal polysaccharide vaccine (PPSV23) at least 8 weeks later. Pts need revaccination w/ PPSV23 fiver years later and again at age 65 - all pts should receive vaccines either >14 days before scheduled splenectomy or > 14 days after splenectomy
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hepatorenal syndrome
- seen in pts w/ severe liver cirrhosis secondary to systemic and renal hypoperfusion - pts have acute renal failure (creatinine > 1.5 mg/dL) w/ a very low urine sodium level, typically
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Pathophysiology of hepatorenal syndrome
- pts w/ severe liver cirrhosis have increased nitric oxide generation in the splanchnic circulation secondary to portal hypertension. This is thought to cause systemic vasodilation, which reduces peripheral vascular resistance and BP, causing renal hypoperfusion. Reduced renal perfusion would then activate compensatory pathways (the renin-angiotensin-aldosterone system, sympathetic nervous system, and antidiuretic hormone) that increase water and sodium retention and worsen volume overload. Any factor that may further reduce glomerular capillary pressure (such as hypotension from GI bleeding) causes an acute decline in glomerular filtration and can precipitate hepatorenal syndrome. - lab results are similar to those of prerenal azotemia: elevated serum creatinine (> 1.5 mg/dL) and a very low urine sodium level, typically
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common glomerular disease associated with Hepatitis C infection?
Membranoproliferative glomerulonephritis
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Interstitial nephritis
-usually presents w/ eosinophils or leukocytes in the urine
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Remember that acute kidney injury is NOT seen in obstructive uropathy unless BOTH URETERS ARE OBSTRUCTED!!!!
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Renal vein thrombosis
- usually occurs in pts w/ a predisposing condition, such as hypercoagulability, trauma, nephrotic syndrome, or severe dehydration - acute renal vein thrombosis presents w/ abdominal pain and hematuria
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Nonalcoholic fatty liver disease (NAFLD)
- resembles alcohol-induced liver injury on histology but occurs in pts w/ minimal or no alcohol hx - most likely mechanism is insulin resistance leading to increased peripheral lipolysis, triglyceride synthesis, and hepatic uptake of fatty acids - definition: hepatic steatosis on imaging or biopsy; exclusion of significant alcohol use; exclusion of other causes of fatty liver - features: mostly asymptomatic; metabolic syndrome; +/- steatohepatitis (AST/ALT ratio 35 - macrovesicular fat deposition and peripheral displacement of the nucleus
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Approximately 10-20% of pts on isoniazid will develop mild aminotransferase elevation within the first few weeks of treatment. This hepatic injury is typically self-limited and resolve without intervention. Liver enzymes should be
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Diabetic nephropathy
- begins w/ HYPERfiltration (increased GFR) and microalbuminuria (incipient nephropathy); if not treated adequately, microalbuminuria may progress to macroproteinuria, defined as urine protein excretion > 300 mg/24 hrs; this increase in urinary protein is accompanied by a progressive decline in GFR - the most beneficial therapy to reduce progression of diabetic nephropathy is STRICT BLOOD PRESSURE CONTROL; pts w/ diabetic nephropathy should be treated toward a target BP of 130/80 mmHg - ACE inhibitors or ARBs are first-line tx for pts w/ diabetes mellitus, but must be initiated carefully as they may induce an acute decline in GFR and hyperkalemia
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daily protein recommendations for pts w/ diabetic nephropathy and azotemia?
-0.8g/kg/day protein
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Intensive glycemic control (HbA1c
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Pts w/ mild primary hyperaldosteronism may not have spontaneous hypokalemia, but they are prone to developing diuretic-induced hypokalemia. Other findings include metabolic alkalosis and mild hypernatremia (143-147 mEq/L). The best screening test is early-morning plasma aldosterone concentration (PAC) to plasma renin activity (PAC) ratio. A PAC/PRA ratio > 20 w/ plasma aldosterone > 15 ng/dL suggests primary hyperaldosteronism.
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Secondary hyperaldosteronism
- causes: diuretic use, cirrhosis or CHF, renovascular HTN (renal artery stenosis or fibromuscular dysplasia), renin-secreting tumor, malignant HTN, coarctation of aorta - Increased plasma renin activity and plasma aldosterone concentration, but with a PAC/PRA ratio
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Dexamethasone suppression test
- can diagnose Cushing's syndrome | - central obesity, purple striae, proximal muscle wasting, glucose intolerance, and HTN
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what is the preferred initial screening test for primary hyperaldosteronism?
- the ratio of plasma aldosterone concentration to plasma renin activity via early morning sampling; a PAC/PRA ratio > 20 with plasma aldosterone > 15 ng/dL suggests primary hyperaldosteronism - adrenal suppression testing is then used to confirm diagnosis, and positive tests requires adrenal imaging by CT. Adrenal vein sampling is the most SENSITIVE test for differentiating adrenal adenoma and bilateral adrenal hyperplasia in pts w/o discrete unilateral adrenal mass on imaging, can then be done to differentiate between hyperplasia and adenoma. Surgery for adenoma, medical therapy for hyperplasia.
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pheochromocytoma
- plasma free metanephrines would be elevated | - HTN and the classic triad of episodic headache, sweating, and palpitations w/ tachycardia
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management of pts w/ hyperkalemia and significant EKG changes (QRS prolongation and peaked T waves)?
-therapy includes emergent administration of IV calcium gluconate to stabilize the cardiac membrane, then lowering serum potassium by driving potassium intracellularly with insulin and glucose, sodium bicarb, or beta-2 agonists such as albuterol; the final step would be to excrete excess potassium by elimination from the body.
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example of an alpha 1 agonist
-phenylephrine
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beta 1 agonists have chronotropic and inotropic effects
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alpha 1 antagonists
-cause peripheral vasodilation, and are used in the tx of HTN and BPH
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beta 1 blockers
-commonly used in tx of HTN, heart failure, and atrial fibrillation
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most health care providers believe that insulin resistance is the first event in the development of type 2 DM; however, type 2 DM does NOT develop without a beta cell secretory defect. Increased insulin secretion from the beta cells is required to cope with increased insulin resistance. If beta cells are able to compensate for the increased insulin resistance, subjects generally remain normoglycemic at the expense of very high insulin levels; however, if beta cells are unable to compensate fully, glucose intolerance and type 2 DM results.
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Tempromandibular joint (TMJ) dysfunction
- can result in referred pain to the ear that is worsened with chewing - pts typically report a hx of nocturnal teeth grinding - pain is worsened w/ chewing; some hear audible clicks or crepitus w/ jaw movement, but not always - initial tx consists of conservate measure such as nighttime bite guard, but surgical intervention is sometimes necessary
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Ramsay Hunt syndrome
- form of herpes zoster infection that causes Bell's palsy | - vesicles are typically seen on the outer ear
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Glossopharyngeal neuralgia
-pts experience intermittent, severe, stabbing pain in areas innervated by CN IX and X, which includes the ear.
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Otitis media
-can result in ear pain, but it will usually cause erythema and/or limited mobility of the TM
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Otitis externa
-usually results in ear discharge and pain w/ pulling on the pinna
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Cerumen impaction
-usually causes conductive hearing loss as opposed to pain
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Diabetic ketoacidosis (DKA)
- presents w/ metabolic acidosis, polyuria, dehydration, decreased level of consciousness, and diffuse abdominal pain, and is often precipitated by acute infection - DKA is characterized by an osmotic diuresis that reduces total body potassium stores even though serum potassium level may be elevated - occurs in type 1 DM - infection can precipitate DKA in type 1 DM due to systemic release of insulin couterregulatory horomes such as catecholamines and cortisol; the resultant excess of glucagon causes hyperglycemia, ketonemia, and an osmotic diuresis; this diuresis is accompanied by a net renal loss of potassium w/ depletion of total body potassium stores; despite reduction in TOTAL body potassium, the SERUM potassium concentration may be elevated due to acidemia and decreased insulin activity, causing redistribuation of potassium to ECF compartment - mild leukocytosis may also be seen - reduction in effective circulating blood volume, which activates the RAAS and accelerates renal potassium losses - increase in circulating free fatty acids due to underlying relative excess of glucagon to insulin and consequent increase in lipolysis - hyperglycemia in DKA contributes not only to osmotic diuresis and hypovolemia but also to serum HYPERosmolality, which will most likely promote pituitary vasopressin release - hepatic gluconeogenesis would be increased due to both the increased ratio of circulating glucagon to insulin and the increased circulating levels of catecholamines and cortisol - hyperglycemia and hyperketonemia in DKA cause an osmotic diuresis and increased urinary excretion of glucose, ketones, sodium, potassium, Mg, and phosphate
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Calcium oxalate crystals (rectangular, envelope-shaped crystals) are seen in what?
- pts w/ ETHYLENE GLYCOL (anti-freeze) poisoning | - Ethylene glycol, methanol and ethanol intoxication causes metabolic acidosis w/ both an anion gap and an osmolar gap
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normal pH
7.35 - 7.45
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normal anion gap
6-12
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normal osmolar gap
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must always calculate anion gap when you have a metabolic acidosis! When the anion gap is markedly elevated and frank uremia is NOT present, the osmolar gap should be calculated to assess for ethanol, methanol, or ethylene glycol intoxication!
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how do you calculate serum osmolality?
serum osmolality = [2Na + Glu/18 + BUN/2.8]
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how do you calculate the osmolar gap?
osmolar gap = observed osmolarity - calculated osmolarity normal is
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sequelae following ethylene glycol ingestion
-ARDS, heart failure, renal failure
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Aspirin (salicylate) toxicity
-causes a MIXED anion gap metabolic acidosis and respiratory alkalosis with NO osmolar gap
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Methyl alcohol poisoning
-can cause visual changes ("snowfield vision") and acute pancreatitis
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Uremia (renal failure) causes an anion gap metabolic acidosis due to failure to excrete acids as NH4+
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McCune-Albright syndrome
- rare condition characterized by the 3 P's: Precocious puberty, Pigmentation (cafe au lait spots), and Polyostotic fibrous dysplasia - responsible for 5% of cases of female precocious puberty and may be associated with other endocrine disorders - sporadic and has been attributed to defect in the G-protein cAMP-kinase function in affected tissue
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Peutz-Jeghers syndrome
- GI tract polyposis and mucocutaneous pigmentation | - may also involve the development of an estrogen-secreting tumor, leading to precocious puberty
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Sturge-Weber disease
-sporadic phakomatosis characterized by mental retardation, seizures, visual impairment and a characteristic port-wine stain over the territory of the trigeminal nerve
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Edema, stasis dermatitis, and venous ulcerations result from lower extremity venous insufficiency due to valve incompetence. Such disease classically occurs on the medial leg superior to the medial malleolus. Increased pressure in postcapillary venules causes extravastion of RBCs, leading to hemosiderin deposition in skin causing the characterstic color changes. Venous congestion causes microvascular disease and ultimately ulcerations. Xerosis (dry skin) is the most common early finding; lipodermatosclerosis and ulcerations characterize late disease.
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arterial thrombosis
- classically presents w/ a pt complaining of severe pain in a single extremity - onset of pain is less acute than that seen in arterial occlusion due to EMBOLUS - the extremity typically exhibits coolness to touch, pallor, pulselessness, and paralysis on exam
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Raynaud disease
- arterial spasm in response to cold or emotional stress causing discoloration and discomfort of the distal digits - may ultimately result in distal digital gangrene if severe
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Neurosyphilis
may cause tabes dorsalis, a lesion of the posterior spinal cord characterized by loss of proprioceptive sensation from the legs, ataxia, and paresthesias
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Syringomyelia
-classically presents w/ central cord syndrome; weakness of upper extremities and loss of pain and temp sensation in a "cape-like" distribution over the neck, shoulders, upper arms and hands
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Cystic fibrosis
- clinical features: chronic sinopulmonary disease (eg bronchiectasis), GI and nutritional abnormalities (eg pancreatic insufficiency, meconium ileus, failure to thrive), salt loss syndromes (eg acute salt depletion, chronic metabolic alkalosis), male urogenital abnormalities (eg obstructive azoospermia) - diagnosis: one or more clinical features OR hx of cystic fibrosis in a sibling OR positive newborn screening test PLUS increased sweat chloride concentration > 60 mmol/L on 2 or more occasions OR identification of 2 CF mutations OR abnormal nasal epithelial ion transport (potential difference) - recurrent respiratory infections, steatorrhea, and failure to thrive are hallmark features. Sweat chloride testing by QUANTITATIVE PILOCARPINE IONTOPHORESIS is the gold standard for diagnosis. Pilocarpine is a cholinergic drug that is applied to the patient's extremity to induce sweating. A chloride level of > 60 mmol/L on 2 separate occasions confirms the diagnosis. Abnormal or intermediate results should be followed by DNA analysis. Nasal potential difference measurement can be performed if sweat testing and DNA analysis are equivocal.
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Pts w/ X-linked agammaglobulinemia suffer from recurrent sinopulmonary infections and failure to thrive. However, only boys are affected by the Bruton tyrosine kinase gene mutation!
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what is the screening test for primary ciliary dyskinesia?
-Exhaled nasal nitric oxide test
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Severe combined immunodeficiency syndrome (SCID)
- X-linked or autosomal recessive disorder characterized by recurrent respiratory infections and chronic diarrhea - affected pts have an absolute lymphocyte count
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The diagnosis of celiac disease is confirmed by the appearance of duodenal villous atrophy on small bowel biopsy
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Congenital toxoplasmosis
- classic triad: chorioretinitis, hydrocephalus, and intracranial calcifications - maternal infection is acquired by exposure to feces from infected cats, or ingestion of infected raw meat or unpasteurized goat's milk - risk of transmission during pregnancy increases as pregnancy progresses, but severity of disease decreases - other complications include: hydrocephalus, microcephaly, hepatosplenomegaly, microphthalmia, microcephaly, diffuse lymphadenopathy, jaundice, diffuse petechiae - lab results show hyperbilirubinemia and thrombocytopenia
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Congenital syphilis
-intermittent fever, osteitis and osteochondritis, mucocutaneous lesions, lymphadenopathy, hepatomegaly, and persistent rhinitis
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Congenital rubella syndrome
- microcephaly, microphthalmia, and meningoencephalitis; sensorineural deafness, cardiac anomalies (eg persistent ductus arteriosus, atrial septal defects), congenital glaucoma and cataract - classic triad: deafness, cataracts, and cardiac defects
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Herpes simplex infection in birth
-encephalitis, chorioretinitis, and disseminated disease
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Developmental milestones of a 1 year old
- fine motor: two-finger pincer grasp, turns several pages of a book at a time - gross motor: walks w/o assistance, waves bye, climbs up on furniture - language: says 2-3 words, says "mama" and "dada" - social: imitates actions, plays reciprocal games (peek-a-boo), indicates wants
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developmental milestones of a 2 year old
- fine motor: builds tower of 6 cubes, turns individual pages of a book - gross motor: walks up and down stairs, jumps, throws a ball overhead - language: 200 word vocabulary, uses 2-word phrases, 2-quarters (50%) of speech intelligible - social: follows 2-step commands, remove clothes
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developmental milestones of a 3 year old
- fine motor: copies a circle, uses utensils to feed self, stacks 9 blocks - gross motor: climbs stairs w/ alternative feet, rides a TRIcycle, kicks a ball - language: uses 3 word sentences, states first name, 3-quarters (75%) of speech intelligible - social: washes/dries hands, helps w/ simple household tasks, group play
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developmental milestones of a 4 year old
- fine motor: copies a cross, draws a person, begins to use scissors, holds crayon w/ tripod grasp - gross motor: hops on one foot w/o losing balance, jumps over objects - language: counts to 10, tells stories, uses plurals and prepositions - social: cooperative play, has imaginary friends, imitates adult roles
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Cerebral palsy
- group of syndromes characterized by nonprogressive motor dysfunction; 3 primary subtypes- spastic, dyskinetic, and ataxic - the etiology is often multifactorial, with PREMATURITY as the leading risk factor - affected pts have uncoordinated and limited voluntary movements - risk factors: prematurity, IUG restriction, IU infection, antepartum hemorrhage, placental pathology, multiple gestation, maternal alcohol consumption, maternal tobacco use - managment: physical, occupational and speech therapies; Baclofen and botulinum toxin for spasticity - comorbidities: intellectual disability, epilepsy, strabismus, scoliosis
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what is the primary medications tx for preeclampsia?
Magnesium sulfate
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what is the treatment of choice for pregnant pts w/ syphilis? what if they have an allergy to that drug?
- Penicillin is treatment of choice - if patient is allergic to penicillin, the allergy should be confirmed w/ skin testing and the patient should then undergo desensitization using incremental doses of oral penicillin V so that she can safely take the medication
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adverse effects of Tetracycline during pregnancy?
-harmful effect on teeth and bones of the fetus
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why can't fluoroquinolones be used during pregnancy?
-musculoskeletal system risks to fetus
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what is the most common cause (80%) of postpartum hemorrhage within 24 hours of delivery?
- UTERINE ATONY - its important to make a quick diagnosis by checking the firmness and location of the uterus fundus; if bleeding persists despite treatment, other causes should be ruled out - a soft, "boggy", poorly contracted uterus is characteristic - risk factors: uterine overdistention (eg multiple gestation, polyhydramnios, macrosomia) and uterine fatigue (prolonged labor)
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most common cause of excess postpartum blood loss? Treatment?
- Uterine atony - Initial tx includes bimanual uterine massage (resolves hemorrhage in most cases), fluid resuscitation (SBP > 90), uterotonic agents (eg oxytocin, methylergonovine, carboprost), and blood transfusion as needed
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when is hysterectomy indicated in postpartum bleeding?
-abnormally adherent placenta (eg placenta accreta), or when all other attempts to control bleeding are unsuccessful or a rupture uterus cannot be repaired
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when is curettage indicated in postpartum hemorrhage?
-when suspected retained placental tissue; this can be determined by an echogenic mass on US, absence of the normal endometrial stripe on US, or a nonintact placenta on exam
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Uterine artery embolization or ligation of the uterine or internal iliac arteries can be used for a patient w/ stable vital signs and persistent bleeding if the rate of loss is not excessive. It can also be used as an alternate to hysterectomy in a stable patient who wishes to preserve fertility.
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Postictal lactic acidosis
- commonly occurs following a tonic-clonic seizure - its a transient anion gap metabolic acidosis that resolves without treatment within 60 to 90 minutes following resolution of seizure activity
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Dopamine is a positive inotrope and a vasoconstrictor used in pts w/ hypotension who do not respond to less aggressive measures such as IV fluids
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Squamous cell carcinoma
- 2nd most common form of non-melanoma skin cancer (after basal cell carcinoma) - the single most important risk factor for the development of squamous cell carcinoma is exposure to sunlight - polygonal cells with atypical nuclei at all levels of the epidermis with zones of keratinization - SCC is more aggressive than basal cell carcinoma because it metastasizes frequently
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what imaging study would you use to evaluate increasing head circumference and signs of increased intracranial pressure in children?
CT scan of the brain - note that you could also perform a sedate MRI if stable and asymptomatic to spare child from radiation exposure - US is most useful in infants under 6 months of age - Tx of hydrocephalus consists of a shunt that is placed from the ventricle to the peritoneum, pleura, or right atrium
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when caring for an unemancipated minor, informed consent from one parent or guardian is considered legally sufficient to justify proceeding with therapy. Physicians should also provide care in urgent situations without waiting for parental consent.
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Parents cannot deny their children life-saving treatment unless the benefits are minimal or would not alter the prognosis.
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Circumstances in which minors do not require consent
- medical: emergency care, STIs, substance abuse, prenatal care - emancipated minor: homeless, parent, married, military, financially independent, high school graduate
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agents used to shift potassium intracellulary
- insulin and glucose - sodium bicarb - beta 2 agonists
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Medical tx for patients with rheumatoid arthritis?
- ALL pts should receive DMARDs as early as possible in the disease course - Methotrexate is the initial DMARD of choice in most pts w/ active RA - NSAIDS and glucocorticoids should be used for initial temporary symptomatic relief while awaiting response to DMARD therapy; they do NOT alter disease progression however - nonbiologics: methotrexate, hydroxychloroquine, sulfasalazine, leflunomide, azathioprine - biologics: etanercept, infliximab, adalimumab, tocilizumab, rituximab - pts should be tested for hep B and C and TB before starting therapy! - if pts do not respond after 6 months, they may require biologic DMARDs such as TNF-a inhibitors (etanercept, infliximab) as step-up therapy
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Eczema herpeticum
- form of primary herpes simplex virus infection associated w/ atopic dermatitis - numerous vesicles over the area of atopic dermatitis are typical - the infection can be life-threatening in infants; thus, prompt tx with acyclovir should be initiated
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Varicella
-vesicular eruption that is not localized, but tends to spread over the head and to the trunk
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Impetigo contagiosa
-manifests as thick-crusted facial lesions that are frequently honey-colored
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The 13-valent pneumococcal conjugate vaccine (PCV13) is recommended for all adults age > 65 followed by the 23-valent pneumococcal polysaccharide vaccine (PPSV23) 6-12 months later. Sequential PCV13 and PPSV23 are also recommended for adults age
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Histoplasma
- usually causes an asymptomatic or minor respiratory illness in healthy pts, but immunocompromised pts can develop severe pulmonary or disseminated disease - the most rapid and sensitive test to diagnose disseminated histoplasmosis in immunocompromised pts is urine or serum assay for Histoplasma antigen - disseminated disease typically presents w/ systemic symptoms and involves the reticuloendothelial system, resutling in cytopenias, lymphadenopathy, and hepatosplenomegaly.
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treatment for histoplasmosis?
- mild to moderate: no treatment or oral itraconazole | - severe: amphotericin B (switche to oral itraconazole once initial response is documented
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Flucytosine
-anti-fungal effective against Cryptococcus and Candida
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Metronidazole
-effective against amebiasis and other anaerobic bacterial infections
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what is the preferred antifungal tx for histoplasmosis?
Itraconazole
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Diagnostic criteria for ADHD
- 6 or more inattentive and/or 6 or more hyperactive/impulsive symptoms for 6 or more months - several symptoms present before age 12 - symptoms occur in at least 2 settings - functional impairment (social, academic) - subtypes: predominantly inattentive, predominantly hyperactive/impulsive, combined type
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By age 12 months, a child's weight and height should...?
- weight should triple; height should increase by 50% - developmental milestones include walking independently, using a 2-finger pincer grasp, saying a few words other than "mama" and "dada", and imitating the actions of others.
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UTI antibiotics in pregnancy
- recommended: nitrofurantoin, amoxicillin, amoxicillin-clavulanate, cephalexin - contraindicated: tetracylines (interfere with fetal bone and tooth development), fluoroquinolones (bone deformities and arthropathy), TMP-SMX (contraindicated in first trimester as it interferes w/ folic acid metabolism, should be avoided during third trimester as it increases the risk of kernicterus in the newborn) - pregnant women w/ asymptomatic bacteriuria should be treated w/ antibiotics to decrease the risk of pyelonephritis, preterm birth, low birth weight, and perinatal mortality.
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Cardiac output/index, SVR, and LVEDV in CHF?
-CHF due to left ventricular systolic dysfunction is characterized by decreased cardiac output/index, increased systemic vascular resistance (SVR), and an increase in left ventricular end-diastolic volume (LVEDV)
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cardiac index/output, SVR, and LVEDV after acute or recent myocardial infarction?
-Cardiac index is reduced due to myocardial dysfunction, while SVR is increased to maintain vital organ perfusion; LVEDV remains relatively normal in the early phase before LV remodeling and/or dilatation occurs over the following several weeks
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Cardiac index/output, SVR, and LVEDV in high-output CHF (severe anemia, thyrotoxicosis, aortic regurgitation)
-increased LVEDV, decreased SVR, normal/increased CI
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Placental abruption
- laboring pts w/ placental abruption at term may be allowed to deliver vaginally if the woman and fetus are stable - Cesarean delivery is indicated if the mother is hypotensive w/ severe bleeding or if the condition of the fetus deteriorates - presents as vaginal bleeding and hyperactive and tender uterus - bleeding between the decidua and placenta interface causes placental detachment, which can compromise the fetus - US should be performed to rule out placenta previa (contraindication to vaginal delivery), but it detects only 25% of cases of abruption - laboring patients > 34 WEEKS GESTATION CAN PROCEED TOWARD VAGINAL DELIVERY
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Placental abruption overview
- risk factors: maternal HTN or preeclampsia/eclampsia, abdominal trauma, prior placental abruption, cocaine and tobacco use - presenation: sudden-onset vaginal bleeding, abdominal or back pain, high-frequency and low-intensity contractions, hypertonic tender uterus - diagnosis: clinical presentation, US (not required for diagnosis) to rule out placenta previa - Tx: unstable maternal VS or nonreassuring fetal heart tracing at any gestational age means emergent C-section; stable maternal VS, reassuring fetal heart tracing, no placenta previa and >34 wks gestation means a trial of vaginal delivery
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full term
> 37 weeks
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Kleihauer-Betke test
- used to measure the amount of fetal hemoglobin transferred into the maternal bloodstream - it should be performed on an Rh-negative woman w/ an Rh-positive fetus to determine the dose of Rh immune globulin to prevent Rh sensitization
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management of suspected bacterial meningitis in adult
- empiric abx must NOT be delayed while awaiting results of CT scan or performing LP to diagnose bacterial meningitis - VANCOMYCIN plus AMPICILLIN plus CEFEPIME is the drug regimen of choice for immunocompromised pts w/ suspected bacterial meningitis - Corticosteroids must be started at the same time as abx and should be discontinued if cultures show an organism other than Strep pneumoniae
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evaluation of bacterial meningitis
- head CT, blood cultures, LP - indications for head CT: immunocompromised, previous CNS disease, new onset seizure, papilledema, altered mental status, focal neuro deficits
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bacterial meningitis in 2-50 year olds
- most commonly N. meningitidis, S. pneumoniae | - give Vancomycin plus a 3rd generation cephalosporin
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bacterial meningitis in age > 50
- S. pneumoniae, N. meningitidis, Listeria | - Vancomycin plus ampicillin plus a 3rd gen cephalosporin
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bacterial meningitis in neurosurgery/shunt patient
- gram negative rods, S. aureus, and coagulase-negative Staph - Vancomycin plus cefepime
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Bacterial meningitis in immunocompromised state
- Pneumococcus, N. meningitidis, Listeria, gram negative rods - Vancomycin plus ampicillin plus cefepime
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Bacterial meningitis in penetrating trauma to skull
- S. aureus, coagulase-negative Staph, and gram negative rods - Vancomycin plus cefepime
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what leads on ECG do you look at for axis deviation evaluation?
lead 1 lead aVF -if up in 1 and up in aVF, then its a normal axis -axis deviation can be a sign of ventricular hypertrophy or bundle branch block
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how to evaluate ECG?
-rate, rhythm, axis, intervals, ischemia, and hypertrophy
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normal intervals on ECG?
- PR interval: 120-200 msec; in AV block PR interval > 200 msec or there will be no QRS after a P wave - QRS interval: 120msec; LBBB has deep S wave and no R wave in V1, and a wide/tall R waves in 1, V5, V6; RBBB has RSR' ("rabbit ears") complex w/ wide R wave in V1 and wide S wave in V5, V6. - QT interval: 440 msec, and predispose to ventricular tachyarrhythmias
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what leads do you look at on ECG for bundle branch blocks?
V1 and V5/V6 | -WiLLiaM MaRRoW
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signs of ischemia/infarction on ECG?
- T wave inversion --> ST segment changes (elevation or depression) -- Q waves (> 40 msec or more than 1/3 the QRS amplitude; note that Q waves signify either an acute or prior ischemic event and do NOT give info on when the event occurred - poor R wave progression; on normal ECG, R waves increase in size from V1 through V5
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signs of hypertrophy on ECG?
- Right atrial hypertrophy: tall P wave in lead II (>2.5 mm) - Left atrial hypertrophy: wide P wave in lead II (>120 msec); notched P waves are frequently seen (cameL has Left atrial enlargement) - LVH: S wave amplitude in V1 + R wave amplitude in V5/V6 = > 35 mm; alternatively, amplitude of R in aVL + S in V3 is > 28 mm in men or > 20 mm in women - RVH: Right axis deviation and an R wave in V1 > 7 mm
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what conditions is Kussmaul sign seen?
- Cardiac tamponade and constrictive pericarditis | - Increase in JVP w/ inspiration is Kussmaul sign
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harsh systolic ejection murmur that radiates to the carotids?
aortic stenosis
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holosystolic murmur that radiates to the axilla
mitral regurgitation
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a midsystolic click or late systolic murmur with a preceding click
mitral valve prolapse
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Diastolic murmurs are ALWAYS ABNORMAL!
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an early decrescendo murmur
-aortic regurgitation
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a mid to late, low-pitched murmur
-mitral stenosis
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S3 gallop
- sign of fluid overload | - often normal in younger pts and in high-output states (eg pregnancy)
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S4 gallop
- sign of decreased compliance (ie HTN, diastolic dysfunction) - usually pathologic but can be normal in younger pts and athletes
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things that can cause peripheral edema
-right heart failure, biventricular failure, nephrotic syndrome, hepatic disease, lymphedema, hypoalbuminemia, and drugs
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pulsus paradoxus
- decreased SBP w/ inspiration - possible sign of Pericardial tamponade; also seen in obstructive lung disease, tension pneumothorax, and foreign body in airway
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increased peripheral pulses
-compensated aortic regurgitation (bounding pulses), coaractation (greater in arms than legs), PDA
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pulsus alternans
- alternating weak and strong pulses | - cardiac tamponade, impaired left ventricular systolic function; poor prognosis
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pulsus parvus et tardus
- weak and delayed pulse | - aortic stenosis!
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management options for atrial fibrillation
ABCD - anticoagulate - B blockers for rate control!! - cardiovert/calcium channel blockers - Digoxin (in refractory cases)
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opening snap followed by a mid diastolic murmur
mitral stenosis
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machine-like murmur
PDA
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CHA2DS2-VASc score
- used to estimate stroke risk in pt w/ atrial fibrillation; anticoagulate if score is > 2 - CHF (1 point) - HTN (1 point) - Age > 75 (2 points) - Diabetes (1 point) - Stroke or TIA hx (2 points) - Vascular disease (1 point) - Age 65-74 (1 point) - Sex category (female; 1 point)
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first degree AV block
- can occur in normal individuals; associated w/ increased vagal tone and w/ B-blocker or CCB use - asymptomatic - PR interval > 200 msec - no treatment necessary
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Second degree AV block (Mobitz type 1/Wenckebach)
- drug effects (digoxin, B-blockers, CCBs) or increased vagal tone; right coronary ischemia or infarction - usually asymptomatic - progressive PR lengthening until a dropped beat occurs; the PR interval then resets - Tx: stop offending drug; Atropine as indicated
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Second degree AV block (Mobitz type II)
- results from fibrotic disease of the conduction system or from acute, subacute, or prior MI - occasonally syncope; frequent progression to third-degree AV block!!!! - unexpected dropped beat(s) without a change in PR interval - Tx is PACEMAKER PLACEMENT
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Third degree AV block (complete)
- no electrical communication between the atria and ventricles - syncope, dizziness, acute heart failure, hypotension, cannon A waves - no relationship between P waves and QRS complexes - Tx is PACEMAKER PLACEMENT
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Sick sinus syndrome/ tachycardia-bradycardia syndrome
- a heterogeneous disorder that leads to intermittent supraventricular tachyarrhythmias and bradyarrhythmias - secondary to tachycardia or bradycardia; may include syncope, palpitations, dyspnea, chest pain, TIA, and stroke - this is the MOST COMMON INDICATION FOR PACEMAKER PLACEMENT
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drug used to treat Wolff-Parkinson-White syndrome?
Procainamide
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Atrial fibrillation
- acute AF: PIRATES: Pulmonary disease, Ischemia, Rheumatic heart disease, Anemia/Atrial myxoma, Thyrotoxicosis, Ethanol, Sepsis. - chronic AF: HTN, CHF - often asymptomatic but may present w/ SOB, chest pain, or palpitations; physical exam shows an IRREGULARLY IRREGULAR pulse - no discernable P waves w/ variable and irregular QRS response - for chronic AF, initial therapy: RATE CONTROL WITH B-BLOCKERS, CCB, or Digoxin; Anticoagulate w/ warfarin for pts w/ CHADS-VASc > 2; for unstable AF, or new-onset AF ( 2 days or unclear duration, must get TEE to rule out atrial clot!!!!
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atrial flutter
- circular movement of electrical activity around the atrium at a rate of approx. 300 times per minute - usually asymptomatic but can present w/ palpitations, syncope, and lightheadedness - regular rhythm; "SAWTOOTH" APPEARANCE OF P WAVES; atrial rate is usually between 240-320 bpm and ventricular rate is about 150 bpm. - Tx: anticoagulation, rate control, and cardioversion as in atrial fibrillation
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multifocal atrial tachycardia
- multiple atrial pacemakers or reentrant pathways; COPD, hypoxemia - may be asymptomatic; at least 3 DIFFERENT P WAVE MORPHOLOGIES - three or more unique P waves, rate > 100 bpm - treat the underlying disorder; verapamil or B-blockers for rate control and suppression of atrial pacemakers (not very effective)
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AVNRT
- a reentry circuit in the AV node depolarizes the atrium and ventricle nearly simultaneously - occurs at AV junction - rate 150-250 bpm; P WAVE IS OFTEN BURIED in QRS or shortly after - Tx: cardiovert if hemodynamically unstable; carotid massage, valsalva, or adenosine can stop the arrhythmia
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AVRT
- occurs at AV junction - an ectopic connection between the atrium and ventricle that causes a reentry circuit; seen in WPW - a retrograde P wave is often seen after a normal QRS; PREEXCITATION DELTA WAVE IS CHARACTERISTICALLY SEEN IN WPW - cardiovert, valgal maneuvers, adenosine
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Paroxysmal atrial tachycardia
- rapid ectopic pacemaker in the atrium (not sinus node) - rate > 100 bpm; P wve w/ an unusual axis BEFORE each normal QRS - Tx: adenosine can be used to unmask underlying atrial activity by slowing down the rate
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PVCs
- ectopic beats arise from ventricular foci; associated w/ hypoxia, electrolyte abnormalities, and hyperthyroidism - early, wide QRS not preceded by a P wave; PVCs are usually followed by a compensatory pause - Treat the underlying cause; if symptomatic, give B-blockers
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Wolff-Parkinson-White syndrome
- abnormal fast accessory pathway from atria to ventricle - characteristic DELTA WAVE w/ widened QRS complex and shortened PR interval - tx is observation for asymptomatic pts
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Ventricular tachycardia
- can be associated w/ CAD, MI, and structural heart disease - can progress to VF and death - 3 or more consecutive PVCs; wide QRS complexes in a regular rapid rhythm; may see AV dissociation - cardioversion if unstable; antiarrhythmics (amiodarone, lidocaine, procainamide)
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Ventricular fibrillation
- totally erratic wide-complex tracing | - immediate electrical defibrillation and ACLS protocol!
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Torsades de pointes
- associated w/ long QT syndrome, proarrhythmic response to meds, hypokalemia, congenital deafness, and alcoholism - polymorphous QRS; VT w/ rates between 150 - 250 bpm - give MAGNESIUM initially and cardiovert if unstable; correct underlying disorder
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use of diuretic and digoxin in CHF?
-used for symptomatic relief only and confer NO mortality benefit
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most common presenting symptoms of systolic dysfunction?
-exertional dyspnea
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lab abnormality in CHF?
- brain natriuretic peptide (BNP) > 500 pg/mL | - decreased EF
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Acute treatment of CHF?
- Loop diuretics (most commonly; Lasix)for aggressive diuresis - Morphine - Nitrates - Oxygen - Position (upright) - LMNOP - AVOID B-BLOCKERS IN DECOMPENSATED CHF, but resume once euvolemic
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chronic treatment of CHF?
- lifestlye: limit dietary sodium and fluid intake - meds: b-blockers and ACEIs/ARBs (help prevent remodeling of the heart and decrease mortality; avoid CCBs!). Diuretics prevent volume overload. Low-dose spironolactone has been shown to decrease mortality w/ advanced heart failure. Daily aspirin and a statin if underlying cause was prior MI - advanced tx: implantable cardiac defibrillator if EF
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Loop diuretics Lose calcium; thiazides take it in
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Diastolic dysfunction/ nonsystolic dysfunction
- decreased ventricular compliance w/ normal systolic function - ventricle either has IMPAIRED ACTIVE RELAXATION or IMPAIRED PASSIVE FILLING - LVEDP is increased, cardiac output remain normal, and EF IS NORMAL OR INCREASED
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Loop diuretics
- Furosemide (Lasix), ethacrynic acid, bumetanide, torsemide | - side effects: ototoxicity, HYPOKALEMIA, HYPOCALCEMIA, dehydration, gout
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Thiazide diuretics
- HYDROCHLOROTHIAZIDE, chlorothiazide, chlorthalidone - side effects: hypokalemic metabolic alkalosis, hyponatremia, and hyperGLUC (hyperGlycemia, hyperLipidemia, hyperUricemia, hyperCalcemia)
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potassium sparing diuretics
- SPIRONOLACTONE, triamterene, amiloride | - side effects: hyperkalemia, gynecomastia, sexual dysfunction
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Carbonic anhydrase inhibitors as diuretics
- Acetazolamide | - side effects: hyperchloremic metabolic acidosis, neuropathy, NH3 toxicity, sulfa allergy
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Osmotic agents as diuretics
- Mannitol | - side effects: pulmonary edema, dehydration; contraindicated in anuria and CHF
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dilated cardiomyopathy
- left ventricular dilation and decreased EF must be present - most cases are idiopathic; most common secondary causes are ischemia and long-standing HTN; also coxsackievirus, Chagas disease are rare - ECHO is diagnostic - an S3 gallop signifies rapid ventricular filling in the setting of fluid overload and is associated with dilated cardiomyopathy
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Differentiate between dilated, hypertrophic, and restrictive cardiomyopathies
- Dilated: impaired contractility, increase LVEDV, increased LVESV, decreased EF, and usually decreased wall thickness - Hypertrophic: impaired relaxation, decreased LVEDV, decreased LVESV, increased or normal EF, markedly increased wall thickness - Restrictive: impaired elasticity, increased LVEDV, increased LVESV, decreased or normal EF, usually increased wall thickness
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most common cause of sudden death in young athletes?
hypertrophic obstructive cardiomyopathy - inherited as an autosomal dominant trait - key finding is a systolic ejection crescendo-decrescendo murmur that increases with decreased preload - Echo is diagnostic and shows an asymmetrically thickened septum and dynamic obstruction of blood flow - Tx: B-blockers are initial therapy; CCB are second-line; avoid intense athletic competition and training
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Restrictive cardiomyopathy
- decreased elasticity of myocardium leading to impaired diastolic filling w/o significant systolic dysfunction; caused by INFILTRATIVE DISEASE (amyloidosis, sarcoidosis, hemochromatosis) or by scarring and fibrosis - right sided heart failure symptoms often predominate - echo is diagnostic, w/ rapid early filling and a near-normal EF - ECG frequently shows LBBB; low voltages are seen in amyloidosis - Tx: generally palliative only; cautious use of diuretics for fluid overload and vasodilators to decrease filling pressure
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Prinzmetal (variant) angina
-mimics angina pectoris but is caused by vasospasm of coronary vessels; classically affects young women at rest in the early morning and is associated w/ ST segment elevation in the absence of cardiac enzyme elevation
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angina pectoris
- substernal chest pain secondary to myocardial ischemia - classic triad: substernal chest pain, precipitated by stress, relieved by rest - pain can radiate to neck or arm or associated with SOB, N/V, diaphoresis, or lightheadedness; pain is usually dull and pressure-like - ECG is best initial test for any type of chest pain (ECG stress test is contraindicated for pts w/ abnormal baseline ECGs)
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Differential diagnosis of chest pain
- cardiac origin - GERD (hx of hoarseness and worse after meals; relief w/ PPIs) - MSK/costochondritis (pain is tender to palpation and movement) - Pneumonia/pleuritis (worsening w/ breathing (pleuritic)) - Anxiety (hx of panic disorder or anxiety attacks)
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Tx for chronic stable angina
- aspirin, b-blockers, and nitroglycerin | - risk factor reduction (smoking, cholesterol, HTN)
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unstable angina vs NSTEMI
- unstable angina: new onset, accelerating, or occurring at rest; signals impending infarction based on plaque instability - NSTEMI: myocardial necrosis marked by elevations in troponin I and CKMB - Unstable angina is NOT associated w/ elevated cardiac enzymes; NSTEMI is diagnosed by serial cardiac enzymes (elevated) and ECG - Tx: aspirin, oxygen, IV nitro, IV morphine, B-blockers - admit to hospital and monitor until acute MI has been ruled out by serial cardiac enzymes - Pts w/ refractory chest pain, a TIMI score of > 3, a troponin elevation, or ST changes > 1 mm should be given IV heparin and scheduled for angiography and possible PCI or CABG
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TIMI risk score for unstable angina/NSTEMI
- age > 65 (1 point) - 3 or more CAD risk factors (premature family hx, DM, smoking, HTN, increased cholesterol) (1 point) - known CAD (stenosis > 50 %) (1 point) - ASA use in past 7 days (1 point) - severe angina (2 or more episodes within 24 hours) (1 point) - ST deviation > 0.5 mm (1 point) - + cardiac marker (1 point) - scale from 0-7; pts at higher risk 3 or more points benefit from enoxaparin, glycoprotein IIb/IIIa inhibitors, and early angiography
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best predictor of survival in STEMI?
LV ejection fraction
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Treatment of MI
- MOAN - Morphine - Oxygen - ASA - Nitro
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Remember that women, diabetics, the elderly, and post-transplant heart pts may have atypical or clinically silent MIs
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most sensitive and specific cardiac enzyme
- Troponin I | - stays elevated longer than CK-MB
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ST-segment abnormalities on ECG with Inferior, Anterior, Lateral, and Posterior MIs
- Inferior MI: involving RCA/PDA, ST elevation in leads II, III, and aVF; obtain a right-sided ECG to look for ST elevation in right ventricle! - Anterior MI: involving LAD and diagonal branches; ST elevation in leads V1-V4 - Lateral MI: involving LCA; ST elevation in leads I, aVL, and V5-V6 - Posterior MI: ST depression in V1-V2 (anterior leads); obtain posterior ECG leads V7-V9
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initial tx of STEMI
- ASA, b-blockers (unless in heart failure or cardiogenic shock; instead give ACEIs if not hypotensive), clopidogrel, morphine, nitrates, and oxygen - in inferior wall MI, avoid nitrates due to risk of severe hypotension
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Emergent angiography and PCI vs thrombolysis
-If PCI cannot be performed within 90 minutes, AND there are no contraindications to thrombolysis (eg a hx of hemorrhagic stroke, or recent ischemic stroke, severe heart failure, or cardiogenic shock), AND the pt presents within 3 hrs of chest pain onset, thrombolysis w/ tPA, reteplase, or streptokinase should be performed instead of PCI
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common post-MI complications
- first day: heart failure - 2-4 days: arrhythmia, pericarditis - 5-10 days: left ventricular wall rupture (acute pericardial tamponade causing electrical alternans, pulseless electrical activity), papillary muscle rupture (severe mitral regurgitation) - weeks to months: ventricular aneurysm (CHF, arrhythmia, persistent ST segment elevation, mitral regurgitation, thrombus formation) - Dressler syndrome: an autoimmune process occurring 2-10 wks post-MI, presents w/ fever, pericarditis, pleural effusion, leukocytosis, and elevated ESR
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dyslipidemia
- total cholesterol > 200 mg/dL - LDL > 130 mg/dL - Triglycerides > 150 mg/dL - HDL 35 years of age or > 20 w/ CAD risk factors, then every 5 yrs. - Tx: hx of CAD, CVA, or PAD --> high intensity statin; LDL between 70-189 WITHOUT diabetes (>7.5% 10 yr risk--> high intensity statin; between 5-7.5% 10 yr risk--> moderate intensity statin; no statin); LDL between 70-189 WITH diabetes (>7.5% 10 yr risk--> high intensity statin; moderate intensity statin); for pts w/ LDL > 190--> high intensity statin - high intensity therapy is a goal reduction of > 50% LDL; moderate intensity is reduction of 30-50% LDL - first intervention should be a 12 week trial of diet and exercise
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Statins
- decrease LDL | - decrease triglycerides
363
Fibrates (gemfibrozil)
- decrease triglycerides | - increase HDL
364
cholesterol absorption inhibitors (ezetimibe)
-decrease LDL
365
Niacin
- increase HDL - decrease LDL - causes skin flushing which can be prevented with aspirin ingestion
366
bile acid resins (cholestyramine)
- decrease LDL | - can decrease absorption of other drugs in GI tract
367
HTN definition
- SBP > 140, and/or DBP > 90 on 3 measurements separated in time in pts 60, SBP > 150 and/or DBP > 90 (if no hx of CKD, DM) - pts > 18 yrs w/ CKD or DM, SBP > 140 and/or DBP > 90 - you will initiate treatment above any of these variables for these populations
368
Treatment of HTN
ABCD - ACEIs/ARBs - B-blockers - CCBs - Diuretics (typically thiazides)
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treatment of HTN in pregnancy
-b-blockers (typically labetalol), hydralazine
370
tx of HTN in CKD
ACEIs, ARBs
371
Hypertensive urgency
-elevated BP with MILD TO MODERATE SYMPTOMS (headache, chest pain) WITHOUT end-organ damage
372
Hypertensive Emergency
- elevated BP w/ signs or symptoms of impending end-organ damage such as acute kidney injury, intracranial hemorrhage, papilledema, or ECG changes suggestive of ischemia or pulmonary edema - tx w/ IV meds (labetalol, nitroprusside, nicardipine) w/ goal of lowering MAP by no more than 25% over the fist 2 hours to prevent cerebral hypoperfusion or coronary insufficiency
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Tx of pheochromocytoma
- Diagnose w/ urinary metanephrines and catecholamine levels or plasma metanephrine - surgical removal of tumor after treatment with BOTH A-BLOCKERS AND B-BLOCKERS
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Conn syndrome (hyperaldosteronism)
- most often secondary to an aldosterone-producing adrenal adenoma - causes the triad of HTN, unexplained hypokalemia, and metabolic alkalosis - metabolic workup w/ plasma aldosterone and renin levels; increase aldosterone and decreased renin levels suggest primary hyperaldosteronism; surgical removal of tumor
375
Cushing syndrome
- due to ACTH producing pituitary tumor, an ectopic ACTH secreting tumor, or cortisol secretion by an adrenal adenoma or carcinoma; also due to exogenous steroid exposure - tx is surgical removal of tumor; removal of exogenous steroids
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Causes of pericarditis
CARDIAC RIND - Collagen vascular disease - Aortic dissection - Radiation - Drugs - Infections - Acute renal failure - Cardiac (MI) - Rheumatic fever - Injury - Neoplasma - Dressler syndrome - viral infection, TB, SLE, uremia, drugs, radiation, neoplasms, post-MI or Dressler's
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classic presentation of pericarditis
- pleuritic chest pain, dyspnea, cough, fever - chest pain tends to WORSEN IN THE SUPINE POSITION, and with inspiration; classic patient is SEEN SITTING UP AND BENDING FORWARD - may hear pericardial friction rub on exam, elevated JVP, pulsus paradoxus (a decrease in SBP > 10mmHg on inspiration) if tamponade present - ECG will show DIFFUSE ST-SEGMENT ELEVATION AND PR-SEGMENT DEPRESSIONS, followed by T wave inversions
378
B-blockers
- decrease cardiac contractility and renin release | - side effects: bronchospasm (in severe active asthma), bradycardia, CHF exacerbation, impotence, fatigue, depression
379
ACEIs
- block aldosterone formation, reducing peripheral resistance and salt/water retention - side effects: cough, angioedema, rahes, leukopenia, hyperkalemia
380
ARBs
- sartan - block aldosterone EFFECTS, reducing peripheral resistance and salt/water retention - side effects: rashes, leukopenia, and hyperkalemia but NO COUGH
381
Caclium channel blockers
- Dihydropyridines (nifedipine, felodipine, amlodipine), and Nondihydropyridines (diltiazem, verapamil) - decrease smooth muscle tone and cause vasodilation; may also decrease cardiac output - Dihydropyridines: headache, flushing, peripheral edema - Nondihydropyridines: decreased contractility
382
Vasodilators
- Hydralazine: headache, lupus-like syndrome - Minoxidil: orthostasis, hirsutism - decrease peripheral resistance by dilating arteries/arterioles
383
a1-adrenergic blockers
- prazosin, terazosin, phenoxybenzamine - cause vasodilation by blocking actions of norepinephrine on vascular smooth muscle - side effects: orthostatic hypotension
384
centrally acting adrenergic agonists
- methyldopa, clonidine - inhibit the sympathetic nervous system via central a2 adrenergic receptors - side effects: somnolence, orthostatic hypotension, impotence, rebound HTN
385
exam of a patient w/ acute tamponade
- Beck triad (hypotension, distant heart sounds, JVD), a narrow pulse pressure, pulsus paradoxus, and Kussmaul sign (increased JVD on inspiration) - CXR will show enlarged, globular, water-bottle shaped heart - ECG could show ELECTRICAL ALTERNANS, which is diagnostic
386
S1Q3T3 on ECG?
Pulmonary embolism
387
size of AAA determines treatment
> 5 cm--> surgical repair | monitoring
388
Screening for AAA?
-screen all men 65-75 years of age w/ a hx of smoking once by US
389
classic exam finding for aortic stenosis?
Pulsus parvus et tardus (weak, delayed carotid upstroke) | -also, systolic murmur radiating to the carotids
390
exam findings with aortic regurgitation
- blowing diastolic murmur at left sternal border, mid-diastolic rumble (Austin Flint murmur), and midsystolic apical murmur - WIDENED PULSE PRESSURE causes de Musset sign (head bob w/ heartbeat), Corrigan sign (water-hammer pulse), and Duroziez sign (femoral bruit)
391
Dissections involving the ASCENDING aorta are surgical emergencies! Those involving the DESCENDING aorta can often be managed w/ BP and heart rate control
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392
Virchow triad
- hemostasis - trauma (endothelial damage) - hypercoagulability
393
Treatment for DVT?
anticoagulate w/ IV unfractionated heparin or subcutaneous LMWH followed by PO warfarin for a total of 3-6 months
394
Diagnosis of PAD
-get and ABI; if
395
Orthostatic hypotension
-drop in SBP > 20 mmHg when moving from lying down to standing and is typically preceded by a lightheaded or presyncopal sensation
396
All pts w/ hypotension/shock after a MVA should be presumed to have hypovolemic shock from hemorrhage. An elevated pulmonary capillary wedge pressure at baseline should raise the suspicion of myocardial dysfunction due to cardiac contusion and prompt an urgent echocardiogram.
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397
High-energy, blunt, rapid deceleration trauma to the chest commonly causes aortic injury. In most cases of aortic rupture, death is the immediate result. In pts w/ a contained rupture, the diagnosis must be made quickly. Widened mediastinum and left-sided hemothorax are classic chest x-ray abnormalities pointing to this diagnosis.
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esophageal rupture
- causes pneumomediastinum and pleural effusion | - diagnosis confirmed w/ water-soluble contrast esophagography
399
bronchial rupture
-pneumothorax that does not resolve w/ chest tube placement, pneumomediastinum and subcutaneous emphysema
400
Wolff-Parkinson-White syndrome
- pts w/ WPW who develop atrial fibrillation w/ a rapid ventricular rate should be treated w/ cardioversion if hemodynamically unstable, or antiarrhythmics such as PROCAINAMIDE or ibutilide if stable. AV nodal blockers such as beta blockers, calcium channel blockers, digoxin, and adenosine should be avoided as they can cause increased conduction through the accessory pathway!! - accessory pathway conducts depolarization directly from atria to ventricles w/o traversing the AV node
401
Acute type A aortic dissection
- type A involves the ascending aorta and is a SURGICAL EMERGENCY; all other locations are type B - type A can extend into the pericardial space, causing hemopericardium and rapidly progressing to cardiac tamponade and cardiogenic shock - bedside TEE is typically performed in the ED for rapid diagnosis and early treatment!!
402
aortic dissection
- risk factors: HTN (most common), Marfan syndrome, cocaine use - features: severe, sharp, tearing chest or back pain; > 20 mmHg variation in SBP between arms - complications (involved structure): Stroke (carotids), acute aortic regurgitation (aortic valves), Horner's syndrome (superior cervical sympathetic ganglion), acute MI (coronary artery), pericardial effusion/tamponade (pericardial cavity), hemothorax (pleural cavity), lower extremity weakness (spinal or common iliac arteries), abdominal pain (mesenteric artery)
403
all pts who have had a MI should receive secondary prevention. Which meds have been shown to have a mortality benefit when given as secondary prevention?
- aspirin (75-325 mg/day) - beta-blockers - ACE inhibitors - lipid lowering statin drugs -in addition, CLOPIDOGREL should be given to all pts w/ unstable angina/NSTEMI, as well as pts who are post percutaneous coronary intervention (PCI)
404
Clopidogrel
- should be given to all pts w/ unstable angina/NSTEMI, as well as those having had a PCI - belongs to drug class called Thienopyridines, and has an anti-platelet effect by antagonizing ADP - for pts who need to be on aspirin but cannot tolerate it, clopidogrel is an appropriate alternative because it is as effective - for pts who are post UA/NSTEMI, clopidogrel + aspirin has been shown to be more effective in terms of mortality than aspirin alone. Clopidogrel should be taken for 12 months, aspirin indefinitely. - clopidogrel + aspirin is more effective than aspirin alone for the first 30 days following PCI as it helps prevent subacute stent thrombosis - basically, clopidogrel should be prescribed for at least 12 months following UA/NSTEMI, 30 days for bare metal stents, and up to 1 year for drug eluting stents following PCI
405
Amiodarone
- class III antiarrhythmic agent, well known for causing pulmonary fibrosis - thyroid dysfunction (hypo and hyper), hepatotoxicity, corneal deposits and skin discoloration (blue-gray) are other potential side effects - excellent drug for BOTH atrial and ventricular arrhythmias
406
Procainamide
- used to treat atrial AND ventricular arrhythmias | - side effects: nausea, drug-induced lupus, agranulocytosis, and QT prolongation
407
Lidocaine
- class IB anti-arrhythmic agent use to treat VENTRICULAR arrhythmias - high doses can cause confusion, seizures and respiratory depression
408
Quinidine
- class IA anti-arrhythmic used to treat ATRIAL arrhythmias | - side effects: diarrhea, tinnitus, QT prolongation, torsades de pointes, hemolytic anemia and thrombocytopenia
409
Digoxin
- inotrope used to treat ATRIAL arrhythmias | - can cause nausea, anorexia, AV block, and ventricular and supraventricular arrhythmias
410
Chagas disease
- chronic disease that can cause megaesophagus, megacolon, and/or cardiac dysfunction - the PROTOZOAN Trypanosoma cruzi, endemic to Latin America, is responsible
411
Don't give beta blockers to cocaine-using individuals, as this allows unopposed alpha agonist activity that can worsen vasospasm. Instead use calcium channel blockers and alpha blockers like phentolamine to help reduce vasospasm.
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412
Right ventricular myocardial infarction (RVMI)
- presents w/ hypotension, elevated JVP, and clear lung fields in the setting of acute inferior MI - pts require increased RV preload to maintain cardiac output and may need IV fluid support - Nitrates, diuretics, and opioids can reduce RV preload and should be avoided!
413
Situational syncope
- should be considered in differential of syncopal episodes - the typical scenario would be a middle age or older male, who loses his consciousness immediately after urination, or a man who loses his consciousness during coughing fits
414
pulmonary capillary wedge pressure (PCWP)
- estimation of left ventricular end diastolic pressure - elevated in pts w/ left ventricular systolic and/or diastolic dysfunction - elevation typically causes signs of pulmonary edema
415
Cor pulmonale
- impaired function of the right ventricle due to PULMONARY HYPERTENSION that usually occurs due to chronic lung disease - signs of right ventricular failure: elevated JVP, right ventricular 3rd heart sound, tricuspid regurgitation murmur, hepatomegaly w/ pulsatile liver, lower-extremity edema, ascites, and/or pleural effusions - echo will shows signs of increased right heart pressures, and right heart catheterization will show pulmonary systolic pressure > 25 mmHg
416
calcium channel blockers
- dihydropyridine: amlodipine, nimodipine, nifedipine - non-dihydropyridine: diltiazem, verapamil - mechanism: block voltage dependent L-type calcium channels of cardiac and smooth muscle, thereby reduce muscle contractility; - Verapamil is most effective in cardiac muscle (Verapamil = Ventricle) - DHPs (except nimodipine) are used for HTN, angina, Raynaud's - Non-DHPs are used for HTN, angina, ATRIAL FIBRILLATION/FLUTTER - Nimodipine: subarachnoid hemorrhage (prevents cerebral vasospasm) - side effects: cardiac depression, AV block, peripheral edema, flushing, dizziness, hyperprolactinemia, and constipation
417
Digoxin
- cardiac glycoside - mechanism: direct inhibition of Na/K ATPase leads to indirect inhibition of Na/Ca exchanger/antiport. Increased Ca conduction leads to positive inotropy. Stimulates vagus nerve which decreases HR. - used to increase contractility in CHF, and to slow conduction at AV node and SA node in ATRIAL fibrillation - can cause change in color vision, hyperkalema, AV block - antidote is to slowly normalize potassium, cardiac pacer, anti-digoxin Fab fragments, Mg
418
Antiarrhythmics
- Na channel blockers (class 1) - B-blockers (class 2) - potassium channel blockers (class 3) - Calcium channel blockers (class 4) "Some Blokes Possess Cardio"
419
Class 1 anti-arrhythmics (sodium channel blockers)
- slow or block conduction (esp in depolarized cells); decrease slope of phase 0 depolarization and increase threshold for firing in abnormal pacemaker cells; they are state dependent (selectively depress tissue that's frequently depolarized; hyperkalemia causes increased toxicity for all class 1 drugs - Class 1A: Quinidine, Procainamide, Disopyramide ("the Queen Proclaims Diso's Pyramid"); increase AP duration, increase refractory period, increase QT interval; used for BOTH ATRIAL AND VENTRICULAR ARRHYTHMIAS, esp re-entrant and ectopic SVT and VT BOTH ATRIA AND VENTRICLES - Class 1B: Lidocaine, Mexiletine; decrease AP duration; preferentially affect ischemic or depolarized Purkinje and ventricular tissue; used for ACUTE VENTRICULAR ARRHYTHMIAS (esp post-MI), digitalis induced arrhythmias (1B is Best post-MI) VENTRICLES - Class 1C: Flecainide, Propafenone ("Can I have Fries, Please"); significantly prolongs refractory period in AV NODE; minimal effect on AP duration; used for SVTs, INCLUDING ATRIAL FIBRILLATION; contraindicated post-MI!!!!! ATRIA
420
Class 2 anti-arrhythmics (B-blockers)
- Metoprolol, propranolol, esmolol, atenolol, timolol, carvedilol - decrease SA and AV nodal activity by decreasing cAMP, decreasing Ca currents; suppress abnormal pacemakers by decreasing slope of phase 4 - used for SVT, slowing VENTRICULAR rate during a. fib and a. flutter - treat overdose with glucagon
421
Class 3 anti-arrhythmics (Potassium channel blockers)
- Amiodarone, Ibutilide, Dofetilide, Sotalol ("AIDS") - increase AP duration, increase effective refractory period, increase QT interval (all the same as class 1 anti-arrhythmics) - used for ATRIAL FIBRILLATION, ATRIAL FLUTTER, VENTRICULAR TACHYCARDIA (amiodarone, sotalol) - know that amiodarone can cause PULMONARY FIBROSIS, hepatotoxicity, hypo/hyperthyroidism, corneal deposits, skin deposits, etc.; must check PFTs, LFTs, and TFTs when using amiodarone; it also has class I,II,III, and IV effects and alters the LIPID MEMBRANE
422
Class 4 anti-arrhythmics (calcium channel blockers)
- Verapamil, diltiazem - decrease conduction velocity, increase effective refractory period, increase PR interval - used for prevent NODAL ARRHYTHMIAS (eg SVT), rate control in ATRIAL FIBRILLATION - can cause flushing, constipation, edema, AV block, CHF
423
Adenosine
- increase potassium out of cells leads to hyperpolarizing the cell and decrease Ca conductance - drug of choice in DIAGNOSING/ABOLISHING SUPRAVENTRICULAR TACHYCARDIA; very short acting (~15 sec) - may cause flushing, hypotension, chest pain; effects blocked by theophylline and caffeine
424
Mg
-effective in torsades de pointes and DIGOXIN toxicity
425
Anti-arrhythmics used for VENTRICULAR arrhythmias?
Class 1a, 1b (sodium blockers), and class 3 (potassium blockers)
426
anti-arrhythmics for atrial arrhythmias?
-class 1a, 1c (sodium blockers), class 2, class 3
427
Adenosine
-inhibits L-type calcium channels, decreasing conduction velocity in the AV node; this can lead to a transient AN nodal block and is used in the tx of AV node-dependent reentrant tachycardia
428
Complete heart block
- type 3 AV block - temporal dissociation of P waves and QRS complexes (AV dissociation) - pts w/ symptomatic 3rd degree AV block should be managed w/ temporary pacemaker insertion while undergoing further evaluation to identify and correct reversible causes - a permanent pacemaker is indicated if no reversible causes of heart block are found.
429
Antibiotic therapy in pts w/ infective endocarditis
- should be tailored to the specific organism as soon as they are identified (start empiric IV vancomycin first) - most viridans group strep are highly susceptible to penicillin and should be treated w/ IV aqueous penicillin G or IV ceftriaxone for 4 weeks
430
Dihydropyridine Ca-channel blockers most common side effect
-peripheral edema
431
what is the most frequent cause of isolated aortic stenosis in elderly patients?
age-dependent idiopathic sclerocalcific changes | -these changes are common and usually have minimal hemodynamic significance, but sometimes may be severe
432
ECG in pts w/ Wolff-Parkinson-White syndrome
-shortened PR interval, delta waves, and widening of the QRS complex
433
Mitral regurgitation
- holosystolic murmur heard best at the apex w/ radiation to the axilla - exertional dyspnea, fatigue, atrial fibrillation, and signs of heart failure
434
Pts w/ persistent tachyarrhythmia (narrow or wide complex) causing hemodynamic instability should be managed w/ IMMEDIATE SYNCHRONIZED DC CARDIOVERSION. Pts who have minimal symptoms and remain hemodynamically stable during an episode of regular, narrow-complex SVT can be managed initially w/ a trial of vagal maneuvers and/or IV adenosine.
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435
murmur of atrial septal defect?
-fixed, split S2 in addition to systolic ejection murmur at the left upper sternal border
436
Coarctation of aorta
- associated w/ Turner syndrome | - diminished or absent lower extremity pulses and upper extremity HTN
437
PDA
- continuous machine-like murmur | - strongly associated w/ congenital rubella syndrome
438
Tetralogy of Fallot
-cyanosis, a single second heart sound, and a harsh crescendo-decrescendo murmur caused by right ventricular outflow tract obstruction
439
Truncus arteriosus
-strongly associated w/ DiGeorge syndrome
440
Half of pts w/ Down syndrome have congenital cardiac defects. What are the most common ones?
- failure of endocardial cushion fusion results in AV septal defects - Complete AV septal defects causes heart failure in early infancy (~6 wks) and require surgical repair - Complete AV septal defects > Ventricular septal defect > Atrial septal defect
441
Diastolic and continuous murmurs as well as loud systolic murmurs revealed on cardiac auscultation should always be investigated using TTE. Midsystolic soft murmurs (grade I-II/VI) in an asymptomatic young patient are usually benign and need no further work-up
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442
Constrictive pericarditis
-important cause of right heart failure and is characterized by progressive peripheral edema, ascites, elevated JVP, pericardial knock (middiastolic sound), and pericardial calcifications on chest x-ray
443
Cardiac amyloidosis
- echo will show increased ventricular wall thickness w/ a normal or nondilated left ventricular cavity - pts w/ amyloidosis may also have heavy proteinuria, periorbital purpura, and hepatomegaly
444
Mitral stenosis
- classically presents during pregnancy | - its most often due to rheumatic fever and occurs much more often in countries w/ limited access to abx
445
Pericardial effusion
- can occur within days or months after cardiac surgery and is referred to as postpericardiotomy syndrome - life-threatening fluid accumulation is characterized by distant heart sounds, hypotension, and distended jugular veins (Beck's triad) and requires drainage
446
Bacterial endocarditis
-fever, new murmur, petechiae, splinter hemorrhages, Osler nodes, Janeway lesions, Roth spots
447
high dose niacin
- used to treat lipid abnormalities, but frequently produces cutaneous flushing and pruritis - prostaglandin-induced peripheral vasodilatation and can be reduced by low-dose aspirin
448
Paroxysmal supraventricular tachycardia (PSVT)
- sudden onset, regular, and narrow-complex tachycardia | - Adenosine and vagal maneuvers can terminate PSVT by transiently slowing SA and AV node conduction
449
In atrial fibrillation (AF) w/ rapid ventricular response (RVR), rate control should be attempted initially w/ beta blockers or calcium channel blockers. Immediate synchronized electrical cardioversion is indicated in hemodynamically unstable pts w/ rapid AF.
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450
Pts presenting the the ED w/ chest pain and suspected acute coronary syndrome should be administered aspirin as soon as possible! Early antiplatelet therapy w/ aspirin reduces the rate of MI and overall mortality in pts w/ ACS
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451
PVCs
- common in pts post-MI and can be recognized by their widened QRS (> 120msec), bizarre morphology, and compensatory pause - even though they may indicate a worse prognosis, tx is NOT indicated unless the patient is symptomatic (then give beta blockers)
452
Digoxin can be used to treat atrial arrhythmias like atrial flutter and atrial fibrillation, but it HAS NO ROLE IN THE TREATMENT OF VENTRICULAR ARRHYTHMIAS!!!
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453
4 anomalies in tetralogy of fallot?
- VSD - RVH - pulmonary stenosis - overriding aorta
454
Tetralogy of Fallot
- presents w/ varying degrees of cyanosis depending on the severity of right ventricular outflow tract obstruction - "Tet" spells result from sudden spasm of the right ventricular outflow tract during exertion - the murmur is typically a harsh crescendo-decrescendo systolic murmur over the left upper sternal border, reflecting turbulence at the stenotic pulmonary artery
455
Infective endocarditis
- can present w/ several nonspecific symptoms and physical exam findings due to immunologic and/or vascular phenomena - early recognition is important to avoid a missed or late diagnosis in such pts - definitive diagnosis is based on Duke Criteria and requires a more comprehensive evaluation
456
Adult Still's disease
- inflammatory disorder characterized by recurrent high fevers (>39C), rash, and arthritis - the rash is often maculopapular and nonpruritic, affecting the trunk and extremities during febrile episodes
457
Variant angina (Prinzmetal's angina)
- vasospastic disorder that typically occurs in young female smokers - chest pain usually occurs in the middle of the night, and episodes are associated w/ transient ST elevations on ECG - treatment is with CCB or nitrates
458
up to 70% of pts w/ mitral stenosis will develop atrial fibrillation because of the significant LEFT atrial dilatation.
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aortic dissection
- causes chest pain that is classically described as sudden, tearing, and radiating to the back - HTN is the most common predisposing factor
460
Marfan's syndrome
- mutation of the FIBRILLIN gene, which results in "weakened" connective tissue - pts are at increased risk for aortic dissection
461
Ehlers-Danlos syndrome
-connective tissue disease involving collagen that can predispose to aortic dissection
462
the fourth heart sound (S4)
-low frequency sound heard at the end of diastole just before S1 that is commonly associated w/ LVH from prolonged HTN
463
Dilated cardiomyopathy
- can be seen following viral myocarditis, particularly after a Coxsackievirus B infection - diagnosis made by Echo, which typically shows dilated ventricles and diffuse hypokinesia resulting in systolic dysfunction (low ejection fraction) - tx is largely supportive, involving mainly the management of CHF symptoms
464
Asymmetric septal hypertrophy
- hypertrophic cardiomyopathy | - young pts; athletes; sudden cardiac death
465
concentric hypertrophy
- follows chronic pressure overload, such as w/ valvular aortic stenosis or untreated HTN - only develops in CHRONIC conditions
466
eccentric hypertrophy
- follows chronic volume overload, as seen in valvular regurgitation - develops slowly over time in response to ventricular volume overload
467
Mitral stenosis
-mid-diastolic murmur and an opening snap, ECG can show left atrial hypertrophy (camel hump, wide P wave in lead II)
468
Exertional heat stroke
- defined as a body temp > 40C (104F) WITH CNS dysfunction or end-organ damage - most commonly induced by strenuous exercise during hot and humid weather - dehydration, hypotension, and tachycardia are common - systemic effects such as seizures, ARDS, DIC, and hepatic/renal failure may also occur - Tx consists of rapid cooling by ice-water immersion and supportive managment
469
Nonexertional (classic) heat stroke
- occurs in absence of strenuous activity and typically affects elderly pts w/ significant underlying comorbidities that limit their ability to escape or cope w/ excessive heat - management involves EVAPORATIVE COOLING, rather than ice-water immersion which is used in exertional heat stroke; this is due to increased mortality with that method in this population
470
Serotonin syndrome vs malignant hyperthermia
- serotonin syndrome: typically seen in pts taking SSRI - malignant hyperthermia: usually triggered by certain anesthetic agents - both conditions cause MUSCULAR RIGIDITY, serotonin syndrome has significant HTN
471
sustained monomorphic ventricular tachycardia (SMVT)
- electrical cardioversion is indicated for SMVT pts who are hemodynamically unstable, pulseless, or severely symptomatic - hemodynamically stable pts can first be given anti-arrhythmics (IV amiodarone) as these may lead to sinus rhythm and avoidance of the need for cardioversion
472
Carotid sinus massage
-useful vagal maneuver to terminate paroxysmal supraventricular tachycardia (PSVT), a regular, narrow-complex tachycardia
473
Digoxin
- used for rate control in SUPRAVENTRICULAR ARRHYTHMIAS (a. flutter, fibrillation, atrial tachycardia), esp in pts w/ hypotension and/or heart failure who are unable to tolerate beta blockers or calcium channel blockers!!!! - can potentially worsen ventricular arrhythmias!
474
Beta blocker overdose
- presents w/ bradycardia, hypotension, wheezing, hypoglycemia, delirium, seizures, and cardiogenic shock - IV fluids and atropine are the first-line treatment options - IV glucagon should be administered in pts w/ profound or refractory hypotension
475
aminophylline
-methylxanthine which acts by blocking phosphodiesterase, thereby increasing levels of cAMP; causes bronchodilation and has positve inotropic/chronotropic effects
476
Digoxin-specific antibody (Fab)
-antidote to digoxin toxicity, which usually presents w/ fatigue, anorexia, nausea, blurred vision, disturbed COLOR PERCEPTION, and cardiac arrhythmias
477
Dobutamine
-inotropic agent that can cause significant vasodilation and worsen hypotension
478
Digitalis toxicity
- causes increased ectopy and increased vagal tone - atrial tachycardia w/ AV block occurs from the combination of these two digitalis effects, and is relatively specific for digitalis toxicity
479
Digitalis can be used to increase vagal tone and is sometimes used to treat atrial fibrillation if beta-blockers or calcium channel blockers have NOT been completely effective
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480
Multifocal atrial tachycardia is associated with what?
Pulmonary disease
481
Warfarin or target-specific oral anticoagulants (eg rivaroxaban, apixaban, dabigatran) should be used to reduce the risk of systemic thromboembolism in pts w/ atrial fibrillation and moderate to high risk of thromboembolic events (CHA2DS2-VASc score 2 or greater). Pts w/ lone AF (score 0) are at low risk of systemic embolization and anticoagulant therapy is not indicated.
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murmur of aortic regurgitation
- best heard along the left sternal border at the 3rd and 4th interspaces - may be heard in some pts only by applying firm pressure w/ the diaphragm of the stethoscope while the patient is sitting up, leaning forward, and holding breath in full expiration - congenital bicuspid aortic valve is the most common cause of AR in young adults in developed countries - Rheumatic heart disease is the most common cause in developing countries
483
Innocent cardiac murmurs
- result from normal blood flow from a structurally normal heart - the intensity is typically grade 1 or 2 and DECREASES with maneuvers that decrease venous blood return, such as standing. - benign murmurs are also early or mid-systolic in timing - management consists of observation and reassurance
484
which meds to hold prior to cardiac stress test?
- Beta blockers, calcium channel blockers, and nitrates are anti-anginal agents and should be withheld for at least 48 hrs prior to cardiac stress testing - however, these meds should be continued in pts w/ known CAD undergoing stress testing to assess the efficacy of antianginal therapy
485
Mobitz type 1 second degree AV block
- progressive prolongation of PR interval leading to a non-conduction P wave and a dropped QRS complex - the PR interval prolongation is best appreciated by measuring the PR intervals just before and after the dropped QRS complex - constant PP interval, decreasing RR interval
486
PACs
- indicate depolarization of the atria originating in a focus outside the SA node - they are seen on ECG as a P wave w/ abnormal morphology, often occurring earlier in the cardiac cycle than a normal P wave
487
Impaired SA node automaticity
- leads to sick sinus syndrome, which is often due to degeneration and/or fibrosis of the SA node and surrounding atrial myocardium - pts may present w/ fatigue, lightheadedness, palpitations, presyncope, or syncope - ECG often shows bradycardia, sinus pauses/arrest, SA exit block, or alternating bradycardia and atrial tachyarrhythmias (tachy-brady syndrome)
488
Wolff-Parkinson-White syndrome
- ventricular preexcitation that is due to an accessory conduction pathway that directly connects the atria and ventricle, bypassing the AV node - the ECG shows a characteristic pattern of short PR interval (
489
Gastroesophageal reflux in infants
- extremely common due to their shorter esophagus, incomplete closure of the lower esophageal sphincter, and greater time spent in the supine position - parents should be reassured about adequate weight gain and advised to hold the infant upright after feeds
490
Indicators of a severe asthma attack
-include normal to increased PCO2 values, speech difficulties, diaphoresis, altered sensorium, cyanosis, and "silent" lungs
491
Immobilization of an individual w/ high bone turnover results in increased osteoclastic activation that can lead to hypercalcemia. Bisphosphonate therapy and hydration in immobilized pts is helpful in reducing hypercalcemia and preventing osteopenia
.
492
approx. 40% of circulating serum calcium is bound to proteins, mostly albumin. Changes in the albumin level will affect the total serum calcium without affecting the ionized fraction.
.
493
causes of hypercalcemia in malignancy
-local osteolytic metastasis, secretion of parathyroid hormone-related protein (PTHrP), and increased formation of 1,25-dihydroxyvitamin D
494
Malaria
- should be suspected in any ill pts, esp. those w/ a hx of febrile paroxysms, who have traveled to an endemic-tropical region - thick and thin blood smears should be ordered for parasite detection and quantification - nonimmune children are at highest risk of death, but the sickle cell trait confers some protection from severe complications - Plasmodium falciparum, P. vivax, P. ovale, or P. malariae transmitted by bite of infected Anopheles mosquito - antimalarial drugs: atovaquone-proguanil, doxycycline, mefloquine, chloroquine, hydroxychloroquine
495
Monosymptomatic (isolated) enuresis
- urinary incontinence in children age >5 - urinalysis, urologic imaging for children w/ significant daytime sx and hx of recurrent UTI - avoid sugary/caffeinated beverages, void regularly during the day and immediately before bed, drink ample fluids in the morning and early afternoon; minimize fluid intake before bed, reward system - ENURESIS ALARM: 1st line intervention when behavior modifications fail; best long-term outcome - meds: DESMOPRESSION (1st line), TCAs (2nd line)
496
anterior MI on ECG
- blocked vessel is LAD | - some or all of leads V1-V6 involved
497
inferior MI on ECG
- RCA or L circumflex artery | - ST elevation in leads II, III, and aVF
498
posterior MI on ECG
- L circumflex or RCA - ST depression in leads V1-V3 - ST elevation in leads I and aVL (LCX) - ST depression in leads I and aVL (RCA)
499
Lateral MI on ECG
- L circumflex, or diagonal artery - ST elevation in leads I, aVL, V5 and V6 - ST depression in leads II, III, and aVF
500
Right ventricle MI (occurs in 1/2 of inferior MI) on ECG
- RCA | - ST elevation in leads V4-V6R
501
The right coronary artery supplies blood to the AV node through the AV nodal artery in 90% of pts; and RCA occlusion can cause AV block. Inferior MI is most commonly associated w/ sinus bradycardai due to increased vagal tone in the first 24 hrs after infarction and decreased RCA blood supply to the SA node
.
502
Right coronary artery occulsion
- can cause acute inferior and posterior wall MIs - inferior wall MI presents w/ ST segment elevations in the inferior leads (II, III, and aVF) - ST segment depression in leads V1 and V2 in this setting usually suggests a posterior wall MI - Inferior MI is also associated w/ hypotension, bradycardia, and AV block
503
Acute pericarditis on ECG
-diffuse PR segment depression and diffuse ST segment elevation across multiple limb and precordial leads
504
Left anterior descending coronary artery occlusion
- LAD usually supplies the anterior walls of the left ventricle as well as the anterior 2/3rds of the septum - occlusion of this vessel can cause ST segment elevation in all precordial leads, but most commonly in V1-V4 - second degree AV block can be seen
505
Left circumflex coronary artery
- supplies the posterolateral wall of the left ventricle | - occlusion can cause ST segment elevation in leads I, II, III, and aVL
506
Occlusion of the left main coronary artery
- usually a catastrophic event and presents as sudden cardiac death in the majority of pts - occlusion of both LCX and LAD causes ST segment elevations in anterior and lateral leads (I aVL, V1-V6)
507
In pts w/ sickle cell disease, acute severe anemia w/ low or absent reticulocytes
- APLASTIC CRISIS - this is an acute drop in Hgb and is known complication of sickle cell disease - alternative things that can cause an acute drop in Hgb: hyperhemolytic crisis, splenic sequestration, or an aplastic crisis - aplastic crisis is a transient arrest of erythropoiesis that results in a severe drop in Hgb and virtual absence of reticulocytes on peripheral smear (reticulocytes
508
hyperhemolytic crisis
- rare complication of sickle cell disease that is characterized by a sudden, severe anemia accompanied by an APPROPRIATE RETICULOCYTOSIS (in contrast to aplastic crisis) - etiology unknown
509
Splenic sequestration
- occurs in sickle cell pts who have not yet developed auto-splenectomy - caused by vasoocclusion and pooling of red cells within the spleen, which may lead to severe hypotensive shock - characterized by a dramatic drop in Hgb concentration that is accompanied by persistent reticulocytosis - physical exam shows a rapidly enlarging spleen - mortality rate of 10-15% and 50% chance of recurrence, so splenectomy is usually recommended after the first episode
510
Acute chest syndrome
- characterized by the presence of fever, chest pain, and an infiltrate on chest x-ray - multifactorial and related to pulmonary infarction and infection
511
vasoocclusive crisis
- acute onset of pain and caused by vasoocclusion secondary to the sickling of RBCs - these crises may be precipitated by changes in weather, dehydration, or infection
512
Oliguria, azotemia and an elevated BUN/creatinine ratio of >20:1 in the post-op state
- pre-renal failure from hypovolemia most likely, though urinary catheter obstruction should first be ruled out - the next step in diagnosis/management of acute renal failure manifesting as oliguria or anuria is an IV fluid challenge
513
pre-renal vs intrinsic renal disease
-elevated BUN/Cr ratio > 10:1 and FENa 1 is intrinsic renal
514
finding of atypical squamous cells of undetermined significance on cytology
- women age 21-24 yrs: repeat cytology in 1 year - women age >25 yrs: HPV DNA test; those who test positive for HPV require colposcopy; pts w/ a negative HPV test can be followed w/ repeat Pap smear and HPV test in 3 yrs
515
routine cervical cancer screening guidelines
- cytology every 3 yrs or a combo of cytology and HPV DNA test every 5 yrs in women age >30 yrs - for women age 21-29 yrs, cytology every 3 yrs is recommended
516
Central retinal artery occlusion syndrome
- ophthalmologic emergency! - treated w/ an ocular massage and high-flow oxygen! - painless loss of monocular vision - risk factors: carotid artery disease, endocarditis, cardiac valvular disease, long bone fx, hypercoagulable states, vasculitis, atrial myxoma - amaurosis fugax
517
management of acute angle closure glaucoma
- topical pilocarpine and beta-blockers | - sudden, painful loss of vision w/ red eye
518
oropharyngeal dysphagia
-difficulty w/ initiating swallowing associated w/ coughing, choking, or nasal regurgitation
519
esophageal dysphagia
- can initiate swallowing but have difficulty passing the food down the esophagus - dysphagia which is initially w/ solids but eventually liquids favors a mechanical obstruction - progressive dysphagia suggests esophageal stricture or cancer - nonprogressive dysphagia favors esophageal rings - upper GI endoscopy is initially recommended except in pts w/ hx of prior radiation, caustic injury, complex stricture, or surgery for esophageal/laryngeal cancer; these pts have increased risk of perforation w/ endoscopy and can benefit from having a barium swallow first; pts w/ negative endoscopy should then have barium swallow for further evaluation - pts w/ dysphagia to liquids and solids at onset favor a motility disorder; intermittent dysphagia suggest a primary esophageal motility disorder; progressive dysphagia indicates secondary causes such as achalasia or systemic sclerosis (scleroderma); barium swallow is recommended initially for these pts as its more effective than endoscopy in evaluating motlity disorders; pts who have a barium swallow suggesting a motility disorder then undergo esophageal motility studies (manometry) to confirm the diagnosis
520
24 hr pH monitoring
-might be helpful to confirm diagnosis of gatroesophageal reflux
521
Bee stings are a common cause of anaphylaxis. Anaphylaxis requires emergency administration of IM epinephrine to prevent and treat respiratory distress and circulatory collapse.
.
522
what is the treatment of all nondisplaces scaphoid fractures (fractures w/
- wrist immobilization for 6-10 wks - if x-rays are negative but suspicion is high, immobilize wrist and re-image in 7-10 days or proceed immediately w/ CT scan
523
Orthotopic liver transplantation remains the only effective mode of treatment of fulminant hepatic failure and should be considered in any patient presenting w/ this condition, regardless of etiology. Contraindications include: irreversible cardiopulmonary disease, incurable or recent (
.
524
Diagnostic peritoneal lavage
-done on hemodynamically UNSTABLE pts w/ BLUNT abdominal trauma and INCONCLUSIVE FAST exam
525
any penetrating wound below the 4th intercostal space (ie level of the nipples) is considered to involve the abdomen and requires an exploratory laparotomy in unstable pts
.
526
CURB-65
- Pneumonia hospitalization criteria, 2-3 = consider inpatient tx; > 4 = admission - Confusion - Uremia (BUN > 19) - Respiratory rate ( > 30 breaths/min) - Blood pressure (SBP 65 yrs
527
common causes of pneumonia by age
- neonates: GBS, E. coli, Listeria - children: Viruses, S. pneumo, Mycoplasma, Chlamydia pneumoniae, S. aureus - adults (18-40): Mycoplasma, S. pneumo, Viruses, C. pneumoniae - adults (40-65): S. pneumo, H. influenza, Mycoplasma, Viruses, Anaerobes - elderly: S. pneumo, H. influenza, Viruses, S. aureus, gram - rods, anaerobes
528
atypical pneumonia
-MCL (mycoplasma, chlamydophila, legionella)
529
nosocomial pneumonia
-GNRs, Staph, anaerobes, Pseudomonas (intubated pts)
530
Immunocompromised pneumonia
-Staph, gram + rods, fungi, viruses, Pneumocystis jirovecii (w/ HIV), mycobacteria
531
Alcoholics/IV drug users pneumonia
-S. pneumo, Klebsiella, Staph
532
Cystic fibrosis pneumonia
-staph, Pseudomonas, Burkholderia, mycobacteria
533
COPD pneumonia
-H. influenza, Moraxella catarrhalis, S. pneumo
534
Postviral pneumonia
-Staph, S. pneumo, H. influenza
535
recurrent pneumonia
-obstruction, bronchogenic carcinoma, lymphoma, Wegener granulomatosis, immunodeficiency, unusual organisms (Nocardia, Coxiella burnetii, Aspergillus, Pseudomonas)
536
Tx for suspected community acquired pneumonia
macrolide or doxycycline
537
Tx for pneumonia in > 65 or w/ comorbidities
Fluoroquinolone or B-lactam + macrolide
538
tx of pneumonia requiring ICU care
antipneumococcal B-lactam + either azithromycin or fluoroquinolone
539
Tx of hospital acquired pneumonia
- extended spectrum cephalosporin or carbapenem w/ antipseudomonal activity - add an aminoglycoside or a fluoroquinolone for coverage of resistant organisms (Pseudomonas) until lab sensitivities are back
540
common side effects of TB meds
- Rifampin turns body fluids red/orange - Ethambutol can cause optic neuritis - INH causes peripheral neuropathy and hepatitis
541
how to diagnose active and latent TB?
- active: sputum culture or gram stain for acid-fast bacilli; chest x-ray - latent: PPD and chest x-ray
542
Tx of TB
active disease: directly observe tx w/ 4 drug regimen (INH, pyrazinamide, rifampin, ethambutol) x 2 months followed by INH and rifampin for 4 months; must give vitamin B6 w/ INH! latent disease: + PPD w/o symptoms needs INH x 9 months or INH x 6 months or rifampin x 4 months
543
PPD readings as positive
>5 mm: HIV or risk factors, close TB contacts, CXR evidence of TB >10 mm: indigent/homeless, residents of developing nations, IV drug use, chronic illness, prisoners, healthcare workers > 15 mm: everyone else, including those w/ no known risk factors -note that a negative test w/ negative controls implies anergy from immunosuppression, old age, or malnutritions and does NOT rule out TB
544
Lemierre syndrome
-thrombophlebitis of the jugular vein due to Fusobacterium, an oral anaerobe
545
Modified Centor criteria
- used to determine tx plan for acute pharyngitis - Fever 1 point - tonsillar exudate 1 point - tender anterior cervical lymphadenopathy 1 point - lack of cough 1 point - 3-14 yrs of age 1 point - 15-45 yrs of age 0 point - > 45 yrs of age -1 point - if 4-5 points, treat empirically; if 2-3 points, perform rapid antigen test. if + test, treat w/ abx. if - test, perform throat culture; if 0-1 point, no testing or abx required, symptomatic tx only
546
tx of acute bacterial sinusitis
-amoxicillin/clavulanate for 10 days or clarithromycin, azithromycin, TMP-SMP, a fluoroquinolone, or a second-generation cephalosporin for 10 days
547
meningitis in newborn
- GBS - E. coli/GNRs - Listeria
548
meningitis in children
- S. pneumo - N. meningitidis - H. influenza serotype b - Enteroviruses
549
meningitis in adults
- N. meningitidis (#1 in teens) - S. pneumo - Enteroviruses - HSV
550
meningitis in elderly
- S. pneumo - GNRs - Listeria - N. meningitidis
551
meningococcal meningitis
- petechial or purpuric rash - waterhouse-friderichsen syndrome (adrenal insufficiency due to bleeding into the adrenal gland) is characterized by profound hypotension and has high mortality
552
how to differentiate Guillain-Barre from MS on LP?
GB has high protein levels in CSF; MS has high gamma globulin in CSF
553
Tx of bacterial meningitis
Give abx as soon as possible! - close contacts w/ meningococcal meningitis should receive Rifampin, Ciprofloxacin, or ceftriaxone - Dexamethasone decreases complications in S. pneumo meningitis only! - if immunocompromised, elderly, or neonate, add ampicillin for Listeria - 60 yrs/alcoholism/chronic illness: Ampicillin + vancomycin + cefotaxime or ceftriaxone
554
The presence of RBCs in CSF without a hx of trauma is highly suggestive of what?
- HSV encephalitis | - subarachnoid hemorrhage
555
most common causes of encephalitis
-HSV and arboviruses
556
Giemsa stain
trypanosomes
557
Tx for common encephalitis conditions
- HSV encephalitis: IV acyclovir - CMV encephalitis: IV ganciclovir +/- foscarnet - Doxycycline for Ricketsia such as Rocky Mountain spotted fever or ehrlichiosis - Lyme encephalitis: Ceftriaxone
558
classic triad in brain abscess
headache, fever, and a focal neurologic deficit
559
Treatment of brain abscess
-broad spectrum IV antibiotics and surgical drainage; lesions
560
AIDS defining illnesses
- Esophageal candidiasis - CMV retinitis - Kaposi sarcoma (HHV-8) - CNS lymphoma, toxoplasmosis, PML - P. jirovecii pneumonia or recurrent bacterial pneumonia - HIV encephalopathy - Disseminated mycobacterial or fungal infection - invasive cervical cancer
561
If a pregnant HIV + patient is not on ART at the time of delivery, she should be treated w/ Zidovudine (AZT) intrapartum. Infants should receive AZT for 6 wks after birth
.
562
initial tx regimen for HIV?
-combo of 2 nucleoside/nucleotide reverse transcriptase inhibitors (RTIs), plus either one non-nucleoside RTI or one protease inhibitor or one integrase inhibitor
563
common side effects of HIV meds
- Protease inhibitors: hyperglycemia, hyperlipidemia, lipodystrophy - Nucleoside RTIs: bone marrow suppression, neuropathy - Indinavir: crystal induced nephropathy, nephrolithiasis - Didanosine: pancreatitis - Abacavir: hypersensitivity rxn - Nevirapine: liver failure - Efavirenz: vivid dreams, hallucinations
564
what are the only live vaccines that should be given to HIV pts (if CD4 > 200)?
MMR and varicella
565
Prophylaxis for HIV related opportunistic infections
P. jirovecii: CD4 5mm or high risk; INH x 9mo (+pyridoxine) or rifampin x 4 mo Candida: fluconazole or fluconazole or nystatin mouth wash HSV: daily suppressive acyclovir, famciclovir, or valacyclovir S. pneumo: Pneumovax every 5 yrs if CD4 > 200 Influenza: annual vaccine
566
Aspergillus appearance
- 45 degree angle branching septate hyphae (think of the capital letter "A" and how it's angle is 45 degrees) - rare fruiting bodies
567
cryptococcus appearance
- yeasts w/ wide capsular halo | - narrow-based buds
568
Mucor appearance
-irregular broad nonseptate hyphae, wide-angle branching
569
the CSF antigen test for cryptococcal meningitis is highly sensitive and specific. Can also use india ink stain
.
570
how to differentiate thrush from hairy leukoplakia?
thrush can be easily rubbed off, hairy leukoplakia cannot
571
tx of cryptococcal meningitis
-IV amphotericin B + flucytosine x 2 wks; then fluconazole x 8 wks
572
diagnosis of histoplasmosis
CXR: diffuse nodular densities, focal infiltrate, cavity, or hilar lymphadenopathy Urine and serum polysaccharide antigen test is most sensitive.
573
Tx of histoplasmosis
- mild: supportive or itraconazole - moderate: itraconazole for > 1 year - severe: liposomal amphotericin B followed by itraconazole for 1 yr or greater
574
appearance of histoplasmosis
-histiocyte macrophage containing numerous yeast cells
575
Nocardia
- partially acid-fast, gram +, branching rod found in soil that is a common cause of lung and CNS infection in immunocompromised - TMP-SMX is treatment
576
Hypercalcemia of malignancy
- most commonly (80%) due to parathyroid hormone-related peptide (PTHrP) production - other mechanisms include excess vitamin D production, bone metastasis w/ local cytokine release to induce bone resorption, and ectopic PTH production - breast cancer most commonly causes hyper calcemia by producing PTHrP, either systemically or locally by bone metastases
577
cytokines produce in osteoclastic bone resorption in malignancies (multiple myeloma, lymphomas, leukemia)?
- IL-6 - IL-3 - RANK-L - TNF-a - macrophage inflammatory factor 1-a
578
Ectopic PTH production is an extremely rare cause of hypercalcemia of malignancy. PTH-independent hypercalcemia usually has serum PTH levels 40 pg/mL. PTH levels of 20-40 pg/mL are considered indeterminant. When both calcium and PTH levels are elevated in malignancy pts, its imperative to rule out coexistent primary hyperparathyroidism before diagnosing ectopic PTH production by the tumor.
.
579
Peripheral artery aneurysm
- manifests as a pulsatile mass that can compress adjacent structures (nerves, veins) and can result in thrombosis and ischemia - popliteal and femoral artery aneurysms are the most common peripheral artery aneurysms - they are frequently associated w/ AAA
580
Inguinal hernias are located above the inguinal ligament; an indirect hernia may descend into the scrotum
.
581
when choosing between meds for depression, consider tx guidelines as well as the safety and side effect profiles. Also, consider a med that may be effective for more than one condition. Buproprion is an example of a med w/ 2 uses, as it is an antidepressant and a smoking cessation aid
.
582
uses for amitriptyline other than depression?
diabetic neuropathy and prevention of migraine headaches
583
mirtazapine
effective antidepressant; however, weight gain is fairly common
584
Phenelzine
MAOI
585
Cushing's syndrome
- if due to ectopic ACTH production, it causes rapid onset of HTN, metabolic alkalosis, hyperglycemia, hypokalemia, and proximal muscle weakness - in contrast to Cushing's DISEASE (ACTH-producing pituitary adenoma), administration of high-dose dexamethasone does NOT suppress plasma cortisol levels in most pts w/ ectopic ACTH syndrome - ACTH independent: usually due to exogenous steroids, adrenal adenoma, or primary pigmented nodular adrenocortical hyperplasia; get an adrenal CT to exlude adrenal adenoma - ACTH dependent: most commonly due to Cushing's disease (ACTH-producing pituitary adenoma), ectopic ACTH production, or ectopic CRD production; due a high-dose dexamethasone suppression test; failure to suppress serum cortisol levels by 50% makes ectopic ACTH most likely
586
first step in management of a suspected urethral injury
-retrograde urethrogram (helps determine urethral injury and location for repair)
587
Sporotrichosis
- gardener's disease - the initial lesion, a reddish nodule that later ulcerates, appears at the site of the thorn prick or other skin injury - from the site of inoculation, the fungus spreads along the lymphatics forming subcutaenous nodules and ulcers
588
Metoclopramide
- prokinetic agent used to treat nausea, vomiting, and gastroparesis - pts taking this med should be monitored closely for the development of drug-induced extrapyramidal symptoms (dystonic rxn most commonly; tx involves stopping the drug and giving benztropine or diphenhydramine)
589
4 questions to ask when evaluating case of arthritis?
1. Is it an inflammatory process? 2. Is it monarticular or polyarticular? 3. Is it symmetric or asymmetric? 4. What is the duration of symptoms?
590
Viral arthritis
- can preset w/ symmetric small joint inflammatory arthritis - distinguished from other causes of symmetric inflammatory arthritis by the fact that it tends to resolve within two months - positive inflammatory markers such as ANA and rheumatoid factor may occur - tx involves NSAIDs for resolution of symptoms - antiviral therapy is unnecessary as the symptoms are self-limited - causative agents include: parvovirus, hepatitis, HIV, mumps, and rubella among many others
591
seronegative spondyloarthropathies
- include ankylosing spondylitis, reactive arthritis, and psoriatic arthritis - asymmetric arthritis and inflammatory back pain w/ a negative rheumatoid factor
592
Polymyalgia rheumatica
- occurs most commonly in pts over 50 - inflammatory condition which presents w/ sore and stiff muscles, particularly in the neck and shoulders - ESR typically > 40, while the ANA is normal
593
missed abortion
- variable presentation from no symptoms to light vaginal bleeding - pregnancy symptoms may decrease - CLOSED cervix - Nonviable fetus on US
594
Inevitable abortion
- vaginal bleeding, uterine cramps - possible intrauterine fetus w/ heartbeat - OPEN cervix; fetus w/ possible heartbeat on US
595
Incomplete abortion
- vaginal bleeding w/ passage of large clots or tissue - uterine cramps - products of conception often visualized in dilated cervical os - OPEN cervix; products of conception often in cervix
596
Threatened abortion
- variable amount of vaginal bleeding - pregnancy can proceed to viable birth - CLOSED cervix; viable pregnancy on US
597
Septic abortion
- fever, malaise, signs of sepsis - foul smelling vaginal discharge, cervical motion and uterine tenderness - rarely occurs after spontaneous abortion - usually w/ induced abortions, can be life-threatening - USUALLY OPEN cervix; usually retained products of conception on US
598
missed abortion
- form of spontaneous abortion (defined as intrauterine fetal death before 20 wks gestational age) w/ complete retained products of conception and a closed cervix - pts often develop loss of pregnancy symptoms and scant to light vaginal discharge - pelvic US is necessary for diagnosis
599
Inevitable, missed, and incomplete abortions can be managed surgically, medically, or expectantly. Although all 3 methods can be effective, surgery achieves more complete evacuation than medical or expectant management. In the case of medical and expectant management, US is generally performed to confirm that there are no retained POC.
.
600
Complete androgen insensitivity syndrome
- x linked mutation of androgen receptor - breast development present - absent uterus and upper 1/3 of vagina; cryptorchid testes - minimal to absent pubic and axillary hair - 46 XY
601
Mullerian agenesis (Mayer-Rokitansky-Kuster-Hauser syndrome)
- Hypoplastic or absent mullerian ductal system - breast development present - absent or rudimentary uterus and upper 1/3 of vagina; normal ovaries - normal pubic and axillary hair - 46 XX
602
Transverse vaginal septum
- malformation of urogenital sinus and Mullerian ducts - breast development present - normal uterus, abnormal vagina; normal ovaries - normal pubic and axillary hair - 46 XX
603
Turner syndrome
- complete/partial absence of 1 X chromosome - variable breast development depending on ovarian function - normal uterus and vagina; streak ovaries - normal axillary and pubic hair - 45 X
604
Primary amenorrhea
-absence of menses by age 15 in someone who has normal growth and secondary sexual characteristics
605
Androgen insensitivity syndrome
- caused by mutated androgen receptor that results in end-organ resistance to androgens - 46 XY pts have testicular secretion of anti-Mullerian hormone, resulting in primary amenorrhea - in addition, testosterone secreted from the testes is converted to estrogen, resulting in breast development
606
46 XY individuals w/ 5a-reductase deficiency
- cannot convert testosterone to DHT | - ambiguous genitalia at birth (undervirilization) and a male internal urogenital tract (due to AMH)
607
Epiglottitis
- presents w/ abrupt onset of fever, sore throat, dysphagia, and drooling - airway obstruction is the most concerning potential complication, and often requires nasotracheal intubation - in unimmunized children, H. influenza type b is a likely cause
608
Peritonsillar abscess
- fever, sore throat, muffled voice, and occasionally drooling - unilateral tonsillar swelling w/ uvular deviation
609
vascular rings
-rare congenital anomaly where aortic arch remnants encircle and compress the trachea or esophagus
610
croup
- most commonly caused by parainfluenza virus type 1 - fever, TRIDOR, and barking cough - drooling is UNCOMMON - Corticosteroids or nebulized epinephrine may be used in tx
611
foreing body aspiration
- common cause of respiratory distress in children - pts w/ a laryngeal foreign body present w/ wheezing and in severe cases, cyanosis - diagnosis typically confirmed radiographically - rigid bronchoscopy is used to remove foreign body
612
Duodenal ulcer disease
- typically presents w/ epigastric pain that improves w/ eating (alkali solution is injected into duodenum w/ food ingestion; this is in contrast to GASTRIC ulcers, which get worse w/ food ingestion due to acid increase in stomach) - over 90% of pts w/ duodenal ulcer disease are infected w/ H. pylori - tx is acid suppression w/ PPI and amoxicillin plus clarithromycin
613
Tourette syndrome
- multiple motor and one or more vocal tics that present before the age of 18; grimacing, eye blinking, nose twitching, head jerking, and shoulder shrugging, barking, grunting, squeaking, coughing, throat clearing, coprolalia - sx exacerbated by stress and tend to subside during sleep - comorbid conditions: ADHD, OCD
614
Apgar scores
- helpful in assessing the STATUS of a neonate and RESPONSE to neonatal resuscitation - routinely measured at 1 and 5 minutes; most infants score 7-9/10 - scores
615
APGAR score
- Appearance/color: completely blue/pale 0 points, body pink and extremities blue 1 point, completely pink 2 points - Pulse: absent 0 points, 100/min 2 points - Grimace/reaction: absent 0 points, grimace/whimper 1 point, cough/sneeze/cry 2 points - Activity/muscle tone: limp 0 points, some flexion 1 point, active/spontaneous 2 points - Respiratory effort: absent 0 points, slow/weak cry 1 point, regular good cry 2 points
616
Sleep apnea syndrome
-typical presentation is a moderately obese middle-aged man complaining of daytime somnolence, morning headaches, increased fatigability, and who is noted to snore loudly. Try weight reduction, avoidance of sedatives and alcohol, and avoidance of supine posture during sleep as a first step
617
Cystic fibrosis
- common AUTOSOMAL RECESSIVE disease characterized by recurrent sinopulmonary infections - bilateral nasal polyps exacerbate nasal obstruction and chronic rhinosinusitis - Quantitative pilocarpine iontophoresis is the gold standard for diagnosis!
618
ALL
- most common cause of childhood cancer - numerous infections and weight loss - Hepatosplenomegaly, lymphadenopathy, and petechiae are often seen
619
Primary ciliary dyskinesia (immotile-cilia syndrome)
- autosomal recessive disorder of mucociliary clearance | - recurrent sinopulmonary infections, nasal polyposis, and digital clubbing
620
Tachycardia-mediated cardiomyopathy
- can develop in pts who have persistent or recurrent tachyarrhythmia w/ prolonged periods of rapid ventricular rate - initial tx is aimed at restoration of sinus rhythm or aggressive control of ventricular rate and can lead to significant improvement in left ventricular function
621
The most common renal vascular lesions seen in HTN are arteriosclerotic lesions of afferent and efferent renal arterioles and glomerular capillary tufts. DM nephropathy is characterized by increased extracellular matrix, basement membrane thickening, mesangial expansion, and fibrosis
.
622
Diabetic nephropathy
- leading cause of end stage renal disease in US - increased extracellular matrix, BM thickening, mesangial expansion, and fibrosis - within the first year: glomerular HYPERFUSION and renal HYPERTROPHY w/ INCREASED GFR - first five years: glomerular BM thickening, glomerular hypertrophy, and mesangial volume expansion w/ GFR returning to normal - within 5-10 yrs: microalbuminuria, which later progresses to overt nephropathy
623
Analgesic abuse nephropathy is primarily a tubulointerstitial disease characterized by focal glomerulosclerosis
.
624
what is the major cause of delayed morbidity and mortality in subarachnoid hemorrhage?
Vasospasm | -vasospasm can best be prevented w/ initiation of NIMODIPINE
625
REBLEEDING is the major cause of death within the FIRST 24 HRS of subarrachnoid hemorrhage, especially within the first 6 hrs of untreated SAH. VASOSPASM can occur in up to 30% of SAH pts from day 3-10 after presentation and is the major cause of DELAYED MORBIDITIY AND DEATH.
.
626
Whipple disease
- multisystem disorder w/ a varied presentation caused by infection w/ the gram-positive bacillus Tropheryma whippelii - chronic malabsorptive diarrhea, weight loss, migratory non-deforming arthritis, lymphadenopathy and a low-grade fever are the most common presenting symptoms - diagnosis made by small intestinal biopsy and PCR; shows PAS-positive macrophages in the lamina propria containing non-acid fast gram positive bacilli
627
Reactive arthritis
- occurs following an infection - HLA-B27 associated reactive arthropathy characterized by conjunctivitis, urethritis, and arthritis - typically follows infections by Chlamydia, Shigella, Salmonella, Yersinia, Campylobacter, and C. diff
628
Non-caseating granulomas
Sarcoidosis
629
UC shows acute and chronic inflammation of the mucosa leading to CRYPT ABSCESS FORMATION. Crohn disease shows full-thickness inflammation w/ granuloma and lymphoid aggregate formation and skin lesions.
.
630
Celiac disease (celiac sprue, gluten-sensitive enteropathy)
- autoimmune disease causing malabsorptive diarrhea | - anti-endomysial and anti-transglutaminase antibodies and histopath shows effacement of small intestinal villi
631
Intestinal lymphoma
- abdominal pain, weight loss, N/V, distention, and occult blood in stool - diffuse infiltrate by atypical lymphocytes
632
The first step in the care of pts w/ acute suicidality is to ensure their safety by admitting them to a psych unit (against their will if necessary). A major depressive episode can occur in response to loss of a loved one, but it differs from normal grief and must be treated appropriately. The most significant suicide risk factors are a PREVIOUS ATTEMPT and a CLEAR PLAN. Having a clear plan is what differentiates the need for immediate hospitalization vs outpatient management.
.
633
Consider CMV infection in a patient w/ mononucleosis-like symptoms, atypical lymphocytes on the blood smear, and a negative monospot test. Unlike EBV-associated mononucleosis, sore throat and lymphadenopathy are UNCOMMON in CMV infection
.
634
CLL
-affects pts over 60; mature-appearing small lymphocytes and "smudge" cells are seen
635
Inflammatory bowel disease
- may occur in association w/ an inflammatory arthritis - ankylosing spondylitis and IBD are both associated w/ HLA-B27 and may occur in association w/ one another - Both conditions may also be associated w/ a positive p-ANCA despite the absence of vasculitis in both conditions.
636
Reactive arthritis
- may follow infectious diarrhea caused by Shigella, Salmonella, Yersinia, Campylobacter, or C. diff - urethritis, conjunctivitis/uveitis, arthritis, malaise and skin findings (keratoderma blennorrhagica and balanitis circinata)
637
Characteristic cutaneous finding of Celiac disease
Dermatitis herpetiformis
638
common cutaneous finding in UC
erythema nodosum, pyoderma gangrenosum
639
Infection by the protozoan Giardia lamblia typically causes a frothy, foul-smelling steatorrhea due to malabsorption caused by the infecting organism. Bloody diarrhea is uncommon.
.
640
Blood in the chest, if it is not evacuated by surgery, can get infected. The majority of pts will present w/ a low-grade fever, dyspnea, and chest pain. Surgery is required to remove the clotted blood and fibrinous peel.
.
641
Rubella (german measles)
- presents w/ fever and occipital or posterior cervical lymphadenopathy followed by a blanching, erythematous maculopapular rash that spreads in a cranial-caudal pattern (starts on face and spreads to trunk) and SPARES THE PALMS AND SOLES - affected adult women also suffer from arthritis that can last up to a month after resolution of other symptoms - can be contagious for up to 3 wks during incubation period prior to symptomatic manifestation - postinfectious encephalitis is a rare complication that can occur within a week of the exanthem - congenital disease: sensorineural hearing loss, intellectual disability, cardiac anomalies (PDA), cataracts/glaucoma - children: low grade fever, conjunctivitis, coryza, cervical lymphadenopathy, Forschheimer spots, maculopapular rash - diagnosis: PCR, acute and convalescent serology for anti-rubella IgM and IgG - prevention: live attenuated rubella vaccine - tx: supportive
642
measles
- same rash as rubella - high fever (> 104F) and cranial-caudal spread of rash takes days vs less than 24 hrs in rubella - arthritis does not occur
643
Disseminated gonococcal infection
- triad of tenosynovitis, dermatitis, and migratory asymmetric polyarthralgias - vesiculopustular, few in number, and rarely involves the face
644
Rocky Mountain spotted fever
-febrile prodrome followed by an erythematous macular rash that starts over the wrists and ankles, involves the palms and soles, and spreads centrally
645
Secondary syphilis
- fever and maculopapular rash involving the entire trunk and extremities - INCLUDES the palms and soles
646
first-line tx for noninflammatory (comedonal) acne
-Topical retinoids
647
Inflammatory acne
- tx w/ topical retinoids and benzoyl peroxide - moderate to severe inflammatory acne benefits from the addition of topical antibiotics - oral antibiotics and isotretinoin are usually reserved for severe or recalcitrant acne (nodular/cystic acne; severe inflammatory)
648
Idiopathic intracranial HTN (pseudotumor cerebri)
- presents w/ headache, vision changes (blurry or double vision), papilledema, and/or cranial nerve palsies (usually CN VI) - CSF shows increased opening pressure >250 mmHg! and normal studies - most common in young obese women - GH, tetracyclines, and excessive vitamin A and its derivatives can cause it - withdrawal of these meds is tx; also weight loss and acetazolamide for idiopathic causes
649
MS
- usually presents w/ 2 or more distinctive episodes of CNS dysfunction w/ at least some resolution - optic neuritis, Lhermitte's sign, Uhthoff's phenomenon (worse symptoms w/ increased body temp), motor and sensory deficits, and bowel or bladder dysfunction
650
usually cause of NPH?
impaired absorption of CSF
651
Human milk is the ideal form of nutrition for term infants. The major protein source is whey, which is more easily digested than casein and helps to improve gastric emptying. Newborns should be exclusively breastfed (w/ vitamin D supplementation) until 6 months, then slow introduction to solid foods and continued breastfeeding until 1 yr.
.
652
Familial colonic polyposis
- autosomal dominant; mutation in adenomatous polyposis coli (APC) gene - affects both sexes equally - pts have hundreds of adenomas in the colon and have a 100% risk of cancer, if not treated appropriately w/ elective proctocolectomy at time of diagnosis
653
Schistocytes (helmet cells)
- fragmented erythrocytes - occur in microangiopathic hemolytic anemias (DIC, HUS, TTP) and due to RBC destruction by prosthetic cardiac valves - Hemolytic anemias are characterized by a decreased serum haptoglobin level, increased LDH and indirect bilirubin, increased urinary urobilinogen
654
Differential diagnosis of menorrhagia
- Endometriosis: pain w/ menses, dyspareunia, infertility - Fibroids: heavy menses w/ clots, constipation and pelvic pain/heaviness, enlarged uterus - Adenomyosis: dysmenorrhea and pelvic pain, menorrhagia, bulky/globular/tender uterus - Endometrial cancer/hyperplpasia: hx of obesity, nulliparity, or chronic anovulation; irregular, intermenstrual, or postmenopausal bleeding, small, nontender uterus - endometritis: recent instrumentation of the uterus, foul smelling discharge, fever
655
Adenomyosis
- occurs most frequently in parous women age > 40 and typically presents w/ dysmenorrhea, menorrhagia, and pelvic pain - uterus is symmetrically enlarged, globular, and boggy (due to retained blood in uterine musculature) but is usually
656
Endometrial carcinoma and hyperplasia
- often present w/ irregular menstrual bleeding or postmenopausal bleeding - women age > 45 w/ irregular bleeding require an endometrial biopsy to exclude malignancy
657
Endometriosis
- infertility, pain w/ intercourse, and dysmenorrhea - symptoms begin in 20's/30's - does NOT cause uterine enlargement as foci of endometrial glands are outside the uterus
658
Leiomyomas (uterine fibroids)
- benign smooth muscle tumors of the uterus - dysmenorrhea, menorrhagia, and an enlarged uterus, frequently coexist w/ adenomyosis - firm, irregularly enlarged uterus that can vary in size from normal to the size of a full-term gestation - symptoms of mass effect
659
von Willebrand disease (vWD)
- inherited bleeding disorder that causes easy bruising, bleeding, heavy menses, nosebleeds, and excessive bleeding after surgery or delivery - platelet count is normal
660
Bacterial vaginosis
- Gardnerella vaginalis - thin, off-white discharge w/ fishy odor, no inflammation - pH > 4.5, CLUE CELLS, positive whiff test (amine odor w/ KOH) - Metronidazole is tx
661
Trichomoniasis
- Trichomonas vaginalis - thin, yellow-green, malodorous, frothy discharge; VAGINAL INFLAMMATION - pH > 4.5, motile trichomonads - Tx: Metronidazole, treat sexual partner also
662
Candida vaginitis
- Candida albicans - thick "cottage cheese" discharge, vaginal inflammation - normal pH (3.8-4.2), pseudohyphae - Tx: fluconazole
663
Trichomonas infection
- causes vaginal discharge, pruritis, dysuria, and dyspareunia, although it is sometimes asymptomatic - Pts and their sexual partners should be treated w/ oral metronidazole and abstain from sex until tx has been completed to prevent recurrence
664
most effective abx against Trichomonas
-Metronidazole and tinidazole
665
Emphysematous cholecystitis
- common form of acute cholecystitis in elderly diabetic males - arises due to infection of the gallbladder wall w/ gas-forming bacteria - pts typically males 50-70 - predisposing factors: vascular compromise, immunosuppression, gallstones, infection w/ gas-forming bacteria - crepitus in the abdominal wall adjacent to gallbladder is occasionally detectable - abdominal radiograph will show air fluid levels in gallbladder or US shows curvilinear gas shadowing in gallbladder - Tx: immediate fluid and electrolyte resuscitation, early cholecystectomy, and IV abx against gram-positive Clostridium sp (ampicillin-sulbactam, piperacillin-tazobactam, or combo of aminoglycoside or quinolone w/ clindamycin or metronidazole)
666
Acute cholangitis
- infection of the biliary tree; high fever, jaundice, and RUQ pain (Charcot's triad) - arises due to biliary tract obstruction and a resultant bacterial contamination of the bile - causes: choledocholithiasis, biliary tract manipulations/stenting, and hepatobiliary malignancies - alk phos and WBC are often markedly elevated
667
Studies have shown that the risk for sepsis is present up to 30 yrs and probably longer after splenectomy. Current recommendations state the pt should receive anti-pneumococcal, Haemophilus, and meningococcal vaccines several weeks before the operation, and daily oral penicillin prophylaxis for 3-5 yrs following splenectomy
.
668
6 interventions shown to be useful in management of diabetic foot ulcers
1. off-loading 2. debridement 3. wound dressings 4. Abx 5. Revascularization 6. Amputation
669
Always suspect lacunar stroke if a patient presents w/ a limited neurologic deficit. The typical lacunar stroke scenarios are pure motor stroke (posterior limb of internal capsule), pure sensory stroke (thalamus), ataxic-hemiparesis (anterior limp of internal capsule), and dysarthria-clumsy hand syndrome (basis pontis). The principle cause of lacunar stroke is HTN, leading to lipohyalinosis of small vessels.
.
670
CSF analysis in common conditions
- normal: 0-5 WBC, 40-70 glucose, 1000 WBC, 250 protein - Tuberculosis meningitis: 5-1000 WBC, 250 protein - Viral meningitis: 100-1000 WBC, 40-70 glucose,
671
Cryptococcal meningoencephalitis
- IV amphotericin (plus flucytosine) is induction therapy - subacute meningitis, that presents after weeks of symptoms - usually immunocompromised - increased ICP w/ ELEVATED OPENING PRESSURE on spinal tap
672
Chlordiazepoxide
-used to treat alcohol withdrawal in hospitalized pts
673
Viral encephalitis
- CSF findings of elevated WBC counts w/ lymphocytic predominance, normal glucose, and elevated protein concentration - start IV acyclovir
674
Measles (rubeola)
- extremely contagious; spread by droplets from repiratory secretions; virus can remain airborne for several hours - fever, cough, coryza, non-purulent conjunctivitis, and Koplik spots (pathognomonic for measles!; bluish-white lesions) which appear on buccal mucosa and sometimes in conjunctivae and vaginal mucosa - on days 3-5 of ilness, the erythematous, macular exanthem is sometimes pruritic; begins on the face; and spreads in a cephalocaudal and centrifugal pattern to the rest of the body; the rash persists for a week, coalesces, and darkens to a reddish-brown color - diagnosis: 4-fold rise in antibody titers and confirmed by PCR - Tx: symptomatic relief w/ antipyretics and hydration; VITAMIN A can be given to pts who are deficient in this vitamin or hospitalized children at high risk of complications - complications: otitis media, pneumonia, neruologic (encephalitis, acute disseminated encephalomyelitis, subacute sclerosing panencephalitis), gastroenteritis
675
Erythema infectiosum (fifth disease)
- caused by human parvovirus B19 | - children develop fever and an erythematous malar rash ("slapped cheeks")
676
Kawasaki disease
-fever for 5 or more days, mucous membrane changes, extremity changes, nonexudative conjunctivitis, cervical lymph node > 1.5cm, and a polymorphous rash
677
Roseola (exanthema subitum, sixth disease)
- caused by human herpes virus 6 | - maculopapular rash appears as the fever resolves
678
Difference between rubella and measles
- rubella is similar to measles but is relatively mild and shorter in duration - the rubella rash spreads cephalocaudally but does not darken as does measles - the fever is also lower and no Koplik spots are seen
679
The initial step in the management of children w/ speech delay is an audiology evaluation
.
680
the incidence of vertical transmission of HCV infection is ~ 2-5%. All pts w/ chronic hepatitis C infection, including pregnant women, should be immunized against hepatitis A and B if they are not already immune.
.
681
When hemorrhage occurs, tachycardia and peripheral vascular constriction are the first physiological changes! These responses act to maintain the blood pressure within normal limits until severe blood loss has occurred.
.
682
The SBP in hemorrhagic shock begins to decrease in Class II but does not significantly decrease until at least 30% of the intravascular volume has been lost (Class III and IV)
.
683
The immediate management of splenic trauma caused by blunt abdominal injury depends on the pts hemodynamic status and response to fluids (SBP > 100). If pt is initially hemodynamically unstable but improves w/ fluid administration, the best next step is to obtain an abdominal CT scan. If pt is initially hemodynamically unstable and is unresponsive to fluid administration, then emergent exploratory laparotomy is required.
.
684
Positive pressure mechanical ventilation increases intrathoracic pressure, which decreases venous return to the heart and thereby decreases the ventricular preload. In pts w/ hypovolemic shock, this effect may cause circulatory collapse if the pts intravascular volume is not replaced before mechanical ventilation is attempted.
.
685
Lyme disease
- results from the transmission of the spirochete Borrelia burgdorferi from Ixodes tick bites to humans - Pts traveling to tick-infested areas should be advised to wear permethrin-treated pants and long-sleeved shirts, to apply insect repellents to the skin, and to check the entire body for ticks
686
The antidepressant of choice for depressed pts who do not respond to first-line tx w/ a SSRI is another medication in the same class. If still no response or side effects after 2 trials, then switch to different class of antidepressant.
.
687
brief psychotic disorder
-positive psychotic symptoms lasting at least 1 day but less than 1 month
688
The duration of schizophreniform disorder is more than 1 month and less than 6 months; schizophrenia requires duration of at least 6 months
.
689
Delusional disorder
- involves one or more delusions and the absence of other psychotic symptoms in an otherwise high-functioning individual - > 1 month duration
690
Breech presentation
- palpation of the vertex at the fundus indicates fetus is breech - a breech diagnosed before the 37th week of gestation does NOT require any intervention, as they often convert to vertex before the 37th week - external cephalic version is indicated if breech presentation is persistent after 37 weeks, and if this fails, then planned C-section is indicated
691
Patients w/ Turner syndrome have ovarian dysgenesis and poor ovarian function; FSH should be high due to lack of negative feedback
.
692
Acute exacerbations of MS are treated with what?
- corticosteroids - beta-interferon or glatiramer acetate is used to decrease the frequency of exacerbations in pts w/ relapsing-remitting or secondary progressive form of MS; however, they have no proven role in the tx of acute exacerbations
693
Vitamin B12 deficiency is common after a total or partial gastrectomy. Vitamin B12 is a necessary cofactor in purine synthesis, and its deficiency causes defective DNA synthesis. This results in ineffective erythropoiesis, presenting as megaloblastic anemia
.
694
gold standard for diagnosis of OSA?
Nocturnal polysomnography
695
Congenital hypothyroidism
- associated w/ neurodevelopmental injury if not recognized and treated early - decreased activity, hoarse cry, and jaundice are commonly associated w/ congenital hypothyroidism, but the majority of infants w/ congenital hypothyroidsim are asymptomatic - thyroid dysgenesis is the most common cause worldwise - tx: levothyroxine immediately to prevent neurodevelopmental injury
696
what screening STI tests are recommended for all pregnant women regardless of their risk factors for STIs?
Syphylis, HIV, and hepatitis B
697
Viral infections may present w/ symmetric arthritis. Viral arthritis is distinguished from rheumatoid arthritis and other causes of symmetric arthritis by its acute onset, lack of elevated inflammatory markers, and resolution within 2 months. Parvovirus is most common cause.
.
698
Polymyalgia rheumatica
- pain and stiffness of pelvis and shoulders | - markedly elevated ESR
699
Fibromyalgia
- chronic, diffuse MSK pain syndrome most common in females - often accompanied by fatigue, mood disorders, insomnia, abdominal pain, and IBS - diagnosis depends on tenderness in at least 11 of 18 defined trigger sites
700
Amebiasis
- should be considered in pts w/ a liver abscess who have lived or traveled in an endemic area for Entamoeba histolytica - initial evaluation includes imaging, serologic testing, and empiric tx w/ metronidazole (to treat the abscess) and a luminal agent (to eradicate intestinal colonization). - cyst drainage is not recommended routinely
701
Simple renal cysts
- almost always benign and do not require further evaluation - features concerning for malignant renal mass: multilocular mass, irregular walls, thickened septae, and contrast enhancement
702
Bacillus cereus
- causes nausea and vomiting after eating rice | - symptom onset is within one to six hours
703
Staphylococcus aureus toxin
- present in foods such as dairy, salad, meat, and eggs - N/V/D and abdominal pain - rapid onset of symptoms due to preformed toxin
704
Clostridium perfringens
- spore forming organism - spores germinate in foods such as meats, poultry, or gravy - watery diarrhea due to production of toxin in gut - symptom onset is later than with preformed toxin (8-14 hrs after ingestion)
705
common complication of pts w/ sickle cell trait?
painless hematuria is most common; may also develop isosthenuria (impairment in concentrating ability); increased risk of UTI in pregnancy; splenic infarct possible at high altitudes
706
Hemi-sensory loss w/ severe dysesthesia (thalamic pain phenomenon) of the affected are is typical for a THALAMIC stroke in the VPL nucleus
.
707
Carcinoid syndrome
- presents w/ episodic flushing, secretory diarrhea, wheezing, and murmur of tricuspid regurgitation - elevated 24 hr urinary 5-HIAA can confirm the diagnosis in most pts
708
facial nerve (CN VII)
- responsible for facial movement, taste in the anterior 2/3 of the tongue, lacrimation (via the greater petrosal/vidian nerves), salivation (via chorda tympani), and eyelid closure - also carries sensory fibers supplying sensation to parts of the external ear and the nasopharynx
709
Oculomotor nerve (CN III)
-responsible for the majority of eye movement (adduction via the medial rectus, elevation via the superior rectus and inferior oblique, and depression via the inferior rectus), eyelid opening, and pupillary constriction
710
Optic nerve (CN II)
-carries visual info to the brain as well as mediates the afferent limb of the pupillary light reflex pathway
711
vagus nerve (CN X)
- swallowing, palate elevation, phonation, and parasympathetic outflow to the thoracoabdominal viscera, including monitoring the aortic arch baro- and chemoreceptors - also responsible for taste in the epiglottis and sensation from parts of the external ear; also mediates the afferent limb of the cough reflex and efferent limb of gag reflex
712
Isolated systolic hypertension
- important cause of HTN in elderly pts, and its caused by decreased elasticity of the arterial wall - should always be treated due to its association w/ an increased risk for cardiovascular events - initial tx involves monotherapy w/ a low-dose thiazide, an ACE inhibitor, or a long-acting calcium channel blocker
713
ARDS
- form of non-cardiogenic pulmonary edema caused by leaky alveolar capillaries - causes include: sepsis, severe infection, severe bleeding, toxic ingestions and burns - mechanical ventilation w/ low tidal volumes (6 ml/kg) and PEEP can improve oxygenation - potential complications of PEEP include barotrauma and tension pneumothorax
714
Based on urinary chloride levels and ECF volume status, metabolic alkalosis can be classified as saline-responsive and saline-unresponsive. Saline-responsive metabolic alkalosis is associated w/ low urinary chloride excretion and volume contraction, and corrects w/ saline infusion alone. Saline-unresponsive metabolic alkalosis typically presents w/ urinary chloride > 20 mEq/L. Name some causes of each.
- Saline unresponsive (> 20 mEq/L): can have expanded ECF w/ hypervolemia (primary hyperaldosteronism, Cushing syndrome, excessive black licorice ingestion, ectopic ACTH production) or appear hypo/euvolemic (Bartter syndrome, Gitelman syndrome) - Saline responsive (
715
All forms of renal tubular acidosis cause a non-anion gap metabolic acidosis.
.
716
Primary hyperaldosteronism
-increases urinary H+ and K+ excretion to cause metabolic alkalosis. Pts also typically develop HTN, expanded ECF volume, and hypokalemia. Urine Cl- is usually > 20 mEq/L as there is no stimulus for renal NaCl retention.
717
Most antidepressants must be taken for 4-6 weeks before they provide symptomatic relief.
.
718
Breastfed infants
- decreased risk of developing otitis media, respiratory, GI, and UTIs; and necrotizing enterocolitis - lower rates of type 1 DM and childhood cancer - the only absolute infant contraindication to breastfeeding is galactosemia
719
Management of hepatic encephalopathy
- supportive care, tx the precipitating cause (volume depletion, electrolyte abnormalities), and lowering serum ammonia - Disaccharides (lactulose, lactitol) are initially preferred for lowering serum ammonia - Rifaximin can be added to lactulose in pts w/o improvement after 48 hrs or used as monotherapy in those unable to take lactulose
720
most common causes of brain metastases
- Lung, breast, unknown primary, melanoma, colon, and renal cell carcinoma - Lung cancer is most common cause of brain metastasis in pts w/ a hx of smoking and no prior incidence of cancer - tumors that RARELY metastasize to the brain include prostate cancer, esophageal cancer, oropharyngeal carcinoma, hepatocellular carcinoma, and non-melanoma skin cancers - Brain mets from breast, colon, and renal cell usually have SOLITARY brain mets - Lung cancer and malignant melanoma can present w/ multiple brain mets
721
Glioblastoma multiforme
- primary CNS tumor arising within the brain parenchyma | - usually presents as solitary mass w/ central necrosis and extensive vasogenic edema
722
Ankylosing spondylitis (AS)
- occurs most often in adults aged 20-30 years - Pts suffer from limited spine mobility and progressive back pain of greater than 3 months duration - the pain and stiffness are worse in the morning and improve w/ exercise - Bilateral sacroiliitis on plain film of a pt w/ suspected symptoms is diagnostic - the most prominent extraarticular manifestation of AS is ANTERIOR UVEITIS
723
Thoracic aortic aneurysm
-associated w/ Marfan syndrome, Ehlers-Danlos syndrome, and syphilis; also inflammatory arthritides
724
Episcleritis is most strongly associated w/ what?
Rheumatoid arthritis and inflammatory bowel disease
725
Oral ulcers are associated w/ what?
SLE, Crohn's, Behcet's
726
SIADH
- common complication of small cell lung cancer | - initial tx is fluid restriction to
727
Pneumococcal vaccination plus penicillin prophylaxis can prevent almost all cases of pneumococcal sepsis in pts w/ sickle cell disease. 2x daily administration of prophylactic penicilline should be given to kids w/ sickle cell disease until the age of 5.
.
728
Acute liver failure
- most often due to acute viral hepatitis, acetaminophen toxicity, and ischemic hepatopathy - acute onset of markedly elevated transaminases (often in the thousands), reduced hepatic synthetic function, and encephalopathy
729
Acute alcoholic hepatitis and nonalcoholic steatohepatitis usually cause mild to moderate AST and ALT elevations that rarely exceed 500 U/L. In additions, alcoholic hepatitis typically occurs in pts who drink heavily (> 100g/day) and classically produces an AST/ALT ratio > 2:1.
.
730
Liver metastasis
most often due to breast cancer, small cell lung cancer, and lymphoma
731
Infectious mononucleosis
- most commonly caused by the Epstein-Barr virus and presents w/ fever, fatigue, exudative pharyngitis, and diffuse cervical lymphadenopathy - a polymorphous, maculopapular rash frequently develops after administration of amoxicillin - pts should avoid sports for >3 wks due to risk of splenic rupture
732
Adenoviruses
- frequent causes of upper respiratory infections and typically present w/ coryza, pharyngitis, tonsillitis, and conjunctivitis - other manifestations: fever, malaise, headache, and abdominal pain
733
Coxsackie virus
-can cause hand-foot-mouth disease and herpangina (vesicles on the hard palate)
734
Group A beta-hemolytic strep
- responsible for 15-30% of cases of pharyngitis in children | - fever, exudative pharyngitis, and enlarged anterior cervical lymph nodes
735
Chikungunya fever
- mosqutio-borne viral illness (Aedes mosquito) that typically presents w/ flulike illness, symmetric polyarthralgias, macular or maculopapular rash on the limbs and trunk, peripheral edema, and cervical lymphadenopathy - tx is supportive, lasts 7-10 days - lymphopenia and thrombocytopenia
736
Reactive arthritis
-usually presents 1-4 wks after a GI or GU infection w/ asymmetric oligoarthritis, conjunctivits, and oral lesions
737
Postoperative cholestasis
- can develop after a prolonged surgery characterized by hypotension, extensive blood loss into tissues, and massive blood replacement - bilirubin and alk phos are elevated
738
Recurrent chalazion
- requires histopathologic exam because there is a risk for an underlying sebaceous (meibomian gland) carcinoma - additionally, basal cell carcinoma is the most common malignancy of the lid margin, and may appear clinically similar to a chalazion
739
management of myasthenia crisis w/ respiratory failure consists initially of endotracheal intubation followe by tx w/ corticosteroids as well as IVIG or plasma exchange (preferred)
.
740
The lupus anticoagulant, an anti-phospholipid antibody, is a pro-thrombotic immunoglobulin that causes a spuriosly prolonged partial thromboplastin time in vitro.
.
741
Antiphospholipid syndrome
1. Venous thromboembolism or recurrent early miscarriages 2. presence of an antiphospholipid antibody such as the lupus anticoagulant, anticardiolipin antibody, or beta 2 glycoprotein 1 antibody
742
Always suspect multiple sclerosis (MS) in a female w/ multiple neurologic presentations that are interspaced between time periods. Optic neuritis can result in blurring of vision, and is often associated w/ retrobulbar pain.
.
743
Trousseau's syndrome (migratory superficial thrombophlebitis)
- hypercoagulability disorder presenting w/ recurrent and migratory superficial thrombophlebitis at unusual sites (eg arm, chest area) - usually associated w/ an occult VISCERAL malignancy such as pancreatic (most common), stomach, lung, or prostate carcinoma
744
Arterial occlusion of an extremity will cause pain, pulselessness, pallor, paresthesias, and paralysis in the affected limb. Embolic occlusion classically causes sudden-onset severe pain and asymmetric pulselessness.
.
745
coarctation of the aorta
- HTN in the upper part of the body and relative hypoperfusion in the lower part of the body - a mild, continuous murmur heard all over the chest is due to the development of collaterals between the hypertensive and hypoperfused vessels - RIB NOTCHING, caused by the dilatation of the collateral chest wall vessels, is specific for coarctation
746
Penile fracture
-surgical emergency that requires emergent urethral imaging and surgical repair
747
Pts w/ upper GI bleeding who have a depressed level of consciousness and ongoing hematemesis should be intubated to protect the airway as a part of initial stabilization and resuscitation. Prompt enoscopic tx w/ band ligation or sclerotherapy should then be performed to stop the bleeding.
.
748
Torsades de pointes (TdP)
- refers to polymorphic ventricular tachycardia that occurs in the setting of a congenital or acquired prolonged QT interval - immediate defibrillation is indicated in hemodynamically unstable pts w/ TdP, while IV magnesium is first-line for stable pts w/ recurrent episodes of TdP
749
Adenosine
- acute termination of paroxysmal SUPRAventricular tachycardia (PSVT) - NOT recommended for tx of ventricular tachycardia
750
Amiodarone
- class III anti-arrhythmic (K+ blocker) - used for BOTH atrial and ventricular tachycardia - used occasionally in pts w/ polymorphic VT (and normal baseline QT interval) due to myocardial ischemia or infarction
751
Atropine
-used in tx of symptomatic SINUS BRADYCARDIA or AV NODAL BLOCK
752
Calcium gluconate
- useful for pts w/ cardiotoxicity due to hyperkalemia - occasionally used in pts w/ beta-blocker and/or calcium channel blocker overdose - ECG of pts w/ hyperkalemia shows peaked T waves, followed by lengthening of the PR and QRS intervals, eventually resulting in a sine wave
753
Sodium bicarb
useful in management of pts w/ TdP due to quinidine use; also those in cardiac arrest from metabolic acidosis, hyperkalemia, or TCA overdose
754
Sotalol
- class III antiarrhythmic | - causes QT prolongation and TdP
755
signs and symptoms of PE
- nonspecific and highly variable - suspect in any pt who presents w/ some comb of sudden-onset SOB, pleuritic chest pain, low-grade fever, and hemoptysis - tachypnea, tachycardia, and hypoxemia are common exam findings - calf swelling and Virchow's triad (stasis, endothelial injury, and hypercoagulable state) are not always present in PE - ECG: S1Q3T3 - CXR: Hampton's hump, Westermark's sign)
756
Genital ulcers
- Painful: Herpes simplex virus (MULTIPLE small, grouped ulcers w/ erythematous base; shallow; tender lymph nodes; most common in US; recurrence is common) and Haemophilus ducreyi (chancroid)(single or multiple deep ulcers, often w/ irregular/ragged border; base may be friable and have gray/yellow exudate; matted lymph nodes which can suppurate/rupture) - Painless: Treponema pallidum (syphilis)(single, indurated, well-circumscribed painless ulcer known as CHANCRE; clean base; nontender lymph nodes), Chlamydia trachomatis serovars L1-3 (LGV)(small and shallow ulcers often absent; matted lymph nodes; large, painful, fluctuant BUBOES; sinus tracts), and Klebsiella granulomatis (granuloma inguinale)(extensive and progressive nodules--> ulcers/beefy-appearing lesions w/ bleeding; base may have granulation like tissue)
757
Anti-D immune globulin
- should be administered to any Rh D-negative mother who delivers an Rh D-positive baby - the standard dose is usually adequate at 28 wks gestation - after delivery or procedures, the Kleihauer-Betke test is used to determine whether a higher dose is needed due to the increased risk of fetal blood cells entering the maternal circulation
758
Bite cells and Heinz bodies
-Glucose-6-phosphate dehydrogenase deficiency
759
type of RBC in autoimmune hemolysis
Spherocytes
760
First step in managing caustic ingestions
- assessing ABCs - contaminated clothing should be removed promptly - upper GI endoscopy is the diagnostic study of choice to evaluate the extent of injury and should be done within 24 hrs - attempting to neutralize the alkali w/ vinegar or lavage is dangerous as these interventions may trigger vomiting, which may cause further mucosal damage - all pts w/ persistent dysphagia or significant esophageal burns on endoscopy should undergo barium contrast studies 2-3 weeks after ingestion to assess for ESOPHAGEAL STRICTURES or PYLORIC STENOSIS
761
Ewing's sarcoma
-often confused w/ osteomyelitis; however, x-ray findings of lamellated appearance or "onion-skin" periosteal rxn; lytic, central lesion accompanied by endosteal scalloping; often followed w/ a "moth-eaten" or mottled appearance and extension into soft tissue
762
Osteomyelitis
- fever, malaise, local joint pain, and swelling | - chronic osteomyelitis: central lytic bone defect w/ surrounding sclerosis termed as Brodie's abscess
763
Precision
- measure of random error - the tighter the confidence interval, the more precise the result - increasing the sample size increases precision
764
Validity and accuracy
- measures of systematic error (bias) - accuracy is reduced if the result does not reflect the true value of the paramater measured - increasing the sample size increases the precision of the study, but does not affect accuracy
765
Physiologic jaundice of the newborn
- common and usually benign; resolve on its own by age 1-2 weeks - the indirect hyperbilirubinemia is due to increased bilirubin production, decreased bilirubin clearance, and increased enterohepatic recycling - phototherapy is the gold standard tx for rapidly rising hyperbilirubinemia to prevent kernicterus
766
biliary atresia
- jaundice is usually the first sign - the neonatal liver can conjugate bilirubin, but the obstructed biliary tract cannot transport bile to the intestine, resulting in hepatic bile retention (cholestasis), direct hyperbilirubinemia, and jaundice - direct hyperbilirubinemia is defined as conjugated bilirubin > 2mg/dL or > 20% of total bilirubin
767
The most common cause of CNS mass lesions in AIDS pts?
- Toxoplasmosis - TMP-SMX is used for PROPHYLAXIS - Sulfadiazine and pyrimethamine are used for TREATMENT purposes
768
Uncomplicated cystitis tx
- TMP-SMP - Nitrofurantoin - Fosfomycin
769
Complicated cystitis tx (diabetes, CKD, pregnancy, immunocompromised, obstruction, hospital-acquired, procedural associated, indwelling foreign body)
-oral fluoroquinolones, IV ceftriaxone if more severe
770
Pyelonephritis tx
- stable: oral fluoroquinolones | - severe: IV ceftriaxone
771
Bupropion
contraindicated in pts w eating disorders as it can provoke seizures
772
most widely used antipsychotic for anorexia nervosa tx?
Olanzapine | -can be considered in pts who fail to gain weight despite initial nutritional rehab and CBT
773
Raloxifene
- mixed agonist/antagonist of estrogen receptors - in breast and vaginal tissue, its an ANTAGONIST; whereas in bone, its an AGONIST - first line agent for prevention of osteoporosis, and it DECREASES breast cancer risk - INCREASES risk of thromboemolism
774
Tamoxifen increases risk for what type of cancer?
Endometrial cancer
775
All depressed pts (at least 5 of SIGECAPS for 2 wks) should be screened for suicidal ideation. Then ask if they have a specific plan, if so, hospitalize.
.
776
IgA nephropathy
- most common cause of glomerulonephritis in adults - pts have recurrent episodes of gross hematuria, usually within 5 days after a URI (SYNPHARYNGITIC) - differentiated from postinfectious glomerulonephritis based on earlier onset of URI-related GN and normal serum complement levels - kidney biopys can also help differentiate (IgA deposits in mesangial cells vs subepithelial humps of C3 complement)
777
Acute interstitial nephritis
- acute inflammatory process involving the renal tubules and interstitium following exposure to a drug (abx, NSAIDs, PPIs). - other findings: fever, skin rash, eosinophilia, eosinophiluria, or WBC casts
778
Alport syndrome
- X-linked defect in collagen-IV (basement membranes) formation and present w/ hearing loss, ocular abnormalities, hematuria, and progressive renal insufficiency - thinning of glomerular BMs
779
Anti-GBM disease
- anti-GBM antibodies against collagen IV (alpha-5 chain) damaging the glomeruli and alveolar lining - can be renal limited process (rapidly progressive GN) or alveolar hemorrhage (pulmonary renal syndrome) - Goodpasture's syndrome refers to pulmonary-renal syndrome that is a manifestation of anti-GBM disease
780
Benign recurrent hematuria
- thin BM nephropathy | - benign familial condition that presents as isolated microscopic hematuria
781
Henoch-Schonlein purpura
- systemic form of IgA involvement of the glomeruli, skin, joints, and intestines - more common in children and presents as erythematous and papular skin rash invovling the dorsal aspect of lower extremities, abdominal pain, arthralgia/arthritis, and microscopic hematuria/proteinuria
782
Lupus nephritis
- nephritis syndrome, nephrotic syndrome, RPGN, or pulmonary-renal syndrome - low complement levels (C3 and C4) and positive lupus antibodies (ANA, anti-dsDNA, anti-Smith)
783
Dementia w/ Lewy bodies
- usually associated w/ Parkinsonian symptoms - gradually progressive dementia w/ fluctuations in cognitive function, persistent and well-formed visual hallucinations, and EPS
784
Huntington's disease
- autosomal dominant; affects caudate and putamen - mean onset age 35-44 - choreoathetoid movements, behavioral disturbances, and dementia
785
Sudden onset of abdominal pain, fetal heart rate abnormalities, and recession of the presenting part during active labor indicated what?
probable uterine rupture | -risk factors include a pre-existing uterine scar or abdominal trauma
786
small cervical lymph nodes are a common observation in children and young adults. Pts w/ asymptomatic, soft lymph nodes can be observed for node growth or the development of symptoms.
- small, rubbery lymph nodes are rarely pathologic; nodes les than 1 cm are almost always benign - nodes > 2 cm are associated w/ greater likelihood of malignancy or granulomatous disease
787
Inhaled anti-muscarinic agents such as ipratropium are the mainstay of symptom management in COPD. These anti-cholinergic meds may be combined w/ short acting beta agonists for greater symptom relief
.
788
the most common causes of hyperkalemia include acute or chronic kidney disease, meds, or disorders impairing the renin-angiotensin axis. Common offending meds include nonselective beta blockers, potassium sparing diuretics (triamterene), ACE inhibitors, ARBs, and NSAIDS
.
789
Modified Wells criteria can assess pretest probability of acute P, as it can have variable presentaitons. Pts w/ likely PE based on these criteria should be further evaluated w/ CTA.
.
790
Aortic regurgitation
-produces an early diastolic murmur and can be associated w/ several physical signs caused by a hyperdynamic pulse, including bounding or "water hammer" peripheral pulses
791
PID
- may lead to tubo-ovarian abscess, abscess rupture, pelvic peritonitis, and sepsis if left untreated - inability to take oral meds due to nausea and vomiting is an indication for inpatient tx of PID
792
Tx of hepatic encephalopathy
lactulose, rifaximin, and laxatives
793
Prolonged gastric acid suppression w/ PPIs or Histamine 2 receptor blockers is a risk factor for C. diff infection. The diagnosis of C. difficile colitis can be confirmed w/ a stool assay for toxins A and B
.
794
Serum gastrin levels
-may be measured in pts w/ suspected gastrinoma and Zollinger-Ellison syndrome (recurrent duodenal ulcers, gastroesophageal reflux, diarrhea)
795
The presence of a systolic-diastolic abdominal bruit in a patient w/ HTN and atherosclerosis is strongly suggestive of what?
Renal artery stenosis
796
DKA
- main precipitating factor is omission of insulin w/ or w/o infections or other stressors - affects type 1 diabetics - diagnosis: blood glucose > 250 mg/dL, pH
797
Succinylcholine
- depolarizing neuromuscular blocker that can cause life-threatening hyperkalemia! - it should NOT be used in pts w/ or at high risk for hyperkalemia, such as burn and crush injury pts and pts w/ prolonged demyelination!
798
Hypersensitivity pneumonitis (HP)
- inflammation of the lung parenchyma caused by antigen exposure - acute episodes present w/ cough, breathlessness, fever, and malaise that occur within 4-6 hours of antigenic exposure - chronic exposure may cause weight loss, clubbing, and honeycombing of the lung - cornerstone of management is avoidance of the responsible antigen - may develop to pulmonary fibrosis and a RESTRICTIVE pattern on lung spirometry - eg "bird fancier's lung" and "farmer's lung"
799
Diaphragmatic rupture
- more common on the left side because of the right side tends to be protected by the liver - pts have respiratory distress and can have deviation of the mediastinal contents to the opposite side - elevation of the hemidiaphragm on the CXR might be the only abnormal finding - CXR showing NG tube in pulmonary cavity is diagnostic
800
Causes of hyponatremia include SIADH and primary polydipsia. Primary polydipsia?
- more common in pts w/ psych conditions, possible due to a central defect in thirst regulation - pts typically develop hyponatremia and dilute urine w/ urine osmolality
801
Hydrocele
- fluid collection within the processus or tunica vaginalis (the peritoneal projection that accompanies the testis during its descent into the scrotum) - when processus vaginalis fails to obliterate, peritoneal fluid may accumulate within the processus causing a COMMUNICATING hydrocele - a collection of fluid within the tunica vaginalis that has properly obliterated its communication w/ the peritoneum is a NON-COMMUNICATING hydrocele - hydroceles will transilluminate, while other masses will note - most will resolve spontaneously by age of 12 months and can be safely observed during that period - hydroceles that do not resolve spontaneously should be removed surgically due to risk of inguinal hernia
802
Diagnostic testing for coronary artery disease (CAD)
- should NOT be performed in low-risk pts as they frequently have false-positive test results - Pts w/ intermediate probability of CAD should receive appropriate stress testing based on ECG findings and their ability to exercise - high-risk pts should be started on appropriate medical therapy, w/ expert evaluation to consider coronary angiography
803
Lithium should NOT be administered to pts w/ renal dysfunction. Valproic acid, w/ or w/o an antipsychotic, is suitable alternate therapy for the initial tx of bipolar disorder, manic or mixed-phase.
.
804
Laboring pts w/ placental abruption > 34 wks may be allowed to deliver vaginally if the woman and fetus are stable. Cesarean delivery is indicated if mother is hypotensive w/ severe bleeding or if the condition of the fetus deteriorates.
.
805
Pts w/ decreased fetal movement should undergo antenatal fetal testing starting w/ a nonstress test (NST) followed by a contraction stress test (CST) or biophysical profile (BPP) if the NST is nonreactive. a CST can be performed if there is no contraindication to labor. Fetal heart decelerations during spontaneous or induced contractions are concerning for fetal compromise.
.
806
A normal contraction stress test indicates that fetal compromise is unlikely. The chance of fetal death within 1 week of a normal test is rare; antepartum fetal testing may be repeated 1 week later.
.
807
Iron deficiency anemia
- most common nutritional deficiency in children, often caused by excessive intake of cow's milk (> 24 oz a day) and results in a microcytic anemia - can be differenitiated from thalassemia by an elevated RDW, which is typically > 20% in iron deficiency
808
Tx of choice for early localized Lyme disease in children
- Oral amoxicillin - Oral doxycycline, amoxicillin, and cefuroxime have equivalent efficacy. Doxy is usually used because it can also treat possible co-infection w/ Anaplasma phagocytophilum in Ixodes tick bites, but should not be used in children
809
Lyme meningitis and heart block tx
-IV ceftriaxone
810
most common predisposing factor for acute bacterial sinusitis?
a preceding viral upper respiratory infection | -tx: amoxicillin plus clavulanic acid
811
somatic symptom disorder
-excessive anxiety and preoccupation w/ 1 or more unexplained symptoms
812
illness anxiety disorder
-fear of having a serious illness despite few or no symptoms and consistently negative evaluations
813
conversion disorder (functional neurologic symptom disorder)
- neurologic symptom incompatible w/ any known neurologic disease; often acute onset associated w/ stress - symptoms NOT PRODUCED INTENTIONALLY - severe enough to cause social and functional impairment, although pts may appear indifferent ("la belle indifference")
814
factitious disorder
-intentional falsification or inducement of symptoms w/ goal to assume SICK ROLE
815
Malingering
-falsification or exaggeration of symptoms to obtain external incentives (SECONDARY GAIN)
816
Somatic symptom disorder
- inovles one or more somatic complaints (including pain) that are distressing or result in significant disruption of daily life, w/ excessive thoughts, feelings, or behaviors related to these symptoms and lasting 6 or more months - pts may have concurrent medical illness, or the symptoms may represent normal bodily function
817
Pregnant women w/ HGSIL on Pap testing should be evaluated w/ colposcopy. If the initial colposcopy is negative, repeat cytology and colposcopy are recommended after delivery. Cervical biopsy and loop electrosurgical excision procedure are NOT performed during pregnancy unless there is a lesion suggestive of invasive cancer.
.
818
Lewy body dementia
-fluctuating cognitive impairment, recurrent visual hallucinations and motor features of Parkinsonism
819
Acute aortic dissection
- high mortality rate and requires rapid diagnosis - effective and less invasive modalities for rapid diagnosis include TEE, and CT; TEE is preferred over CT scan in pts w/ kidney disease due to risk of contrast-induced nephropathy
820
Contrast-induced nephropathy
- transient spike in Cr within 24 hrs of contrast administration, w/ a return to normal renal function within 5-7 days - Pts w/ diabetes and elevated baseline Cr are at especially high risk - adequate IV hydration w/ isotonic bicarb or normal saline and administration of N-acetylcysteine help to minimize the risk of contrast-induced nephropathy
821
Viridans group streptococci (most commonly S. mutans) are the most common causes of endocarditis following dental procedures. Other viridans group: S. mitis, S. sanguis, S. salivarius
,
822
Strep bovis
- normal inhabitant of the GI tract, and S. bovis bacteremia is associated w/ colon cancer - colonoscopy should be performed when this organism is isolated from blood cultures
823
risk factors for Group B strep endocarditis
-DM, carcinoma, alcoholism, hepatic failure, elective abortion, and IV drug use
824
Oliguria, azotemia, and an elevated BUN/Cr ratio > 20:1 in post-op state most likely indicate acute pre-renal failure from hypovolemia, though urinary catheter obstruction should first be ruled out. The next step in the diagnosis/management of acute renal failure manifesting as oliguria or anuria is an IV fluid challenge.
.
825
Strongest predictors of abdominal aortic aneurysm expansion and rupture
- Large aneurysm diameter, rapid rate of expansion, and current cigarette smoking - current indiations for operative or endovascular repair include aneurysm size > 5.5 cm, rapid rate of aneurysm expansion (> 0.5cm in 6 months or > 1 cm per year), and presence of symptoms (abdominal, back, or flank pain; lim ischemia) regardless of aneurysm size
826
Buproprion is FDA-approved for smoking cessation. It should be used in conjunction w/ counseling and nicotine replacement.
.
827
Anabolic steroid use by a man
-can produce infertility by suppressing the production of GnRH, LH, and FSH
828
Klinefelter syndrome
- XXY (seminiferous tubule dysgenesis) - inherited disorder characterized by testicular fibrosis (primary hypogonadism), azoospermia, gynecomastia, decreased intelligence, increased axial skeletal growth, and high FSH and LH levels
829
Myotonic dystrophy
-testicular atrophy as well as widespread muscular atrophy, weakness, lower-than-normal testosterone levels, and high FSH and LH levels
830
Varicocele
-"bag of worms" sensation on palpation
831
P-value
-probability of observing a given (or more extreme) result due to chance alone, assuming the null hypothesis is true
832
A 95% confidence interval that contains 1.0 would mean that the results are NOT statistically significant
.
833
Graft-versus-host-disease
- caused by recognition of host major and minor HLA-antigens by donor T-cells and consequent cell-mediated immune response - organs typically affected include the skin, intestine, and liver
834
In acute appendicitis, the initial peri-umbilical pain is referred pain and visceral in nature; however, pain shifts to the right lower quadrant w/ involvement of the parietal peritoneum and becomes somatic in nature.
.
835
Multiple endocrine neoplasia (MEN)
- type 1: primary hyperParathyroidism, enteroPancreatic tumors, Pituitary tumors (PPP); due to mutations in then MEN 1 tumor suppressor gene - type 2A: Medullary thyroid cancer, Pheochromocytoma, Parathyroid hyperplasia (MPP) - type 2B: Medullary thyroid cancer, Pheochromocytoma, Marfanoid habitus/Mucosal and intestinal neuromas (MMMP) - MEN 2A/2B: autosomal dominant; germline mutations involving RET proto-oncogene on chromosome 10
836
Renal angiomyolipomas
Tuberous sclerosis
837
Trimethoprim
- can cause hyperkalemia due to blockade of the epithelial sodium channel in the collecting tubule - TMP also competitevely inhibits renal tubular creatinine secretion and may cause an artificial increased in serum creatinine w/o affecting the GFR
838
Single photon emission CT scan (SPECT)
- useful tool to evaluate for CAD and indicates inducible ischemia when a reversible defect is noted on stress and rest images - antiplatelet therapy is the preferred tx to prevent CAD in these pts
839
Pleural effusion
-decrease in movement of ipsilateral chest wall, dullness to percussion, and DECREASED breath sounds
840
consolidation of lung on auscultation
dullness to percussion, bronchial breath sounds (assuming patent airways), and egophony
841
Clinical manifestations of infectious mononucleosis
- extreme fatigue, malaise, sore throat, fever, and generalized maculopapular rash - posterior cervical lymphadenopathy and palatal petechiae can be present - Splenomegaly is common - Heterophile antibodies are very sensitive and specific, but may be negative early in the illness; repeat testing may be helpful
842
Pts w/ typical GERD symptoms require an upper GI endoscopy if they have alarm symptoms (dysphagia, odynophagia, weight loss, anemia, GI bleeding, or recurrent vomiting) or are men age > 50 w/ chronic (> 5 yrs) symptoms and cancer risk factors (eg tobacco use). All other pts can receive an empiric trial of PPI therapy and further evaluation if refractory to therapy
.
843
Fresh frozen plasma is the therapeutic agent of choice for the coagulopathy in pts w/ liver failure
.
844
Light's criteria
- used to classify pleural fluid as an exudate or transudate - must have at least one of the following to be conisdered an exudate: 1. pleural fluid protein/serum protein ratio > 0.5 2. pleural fluid LDH/serum LDH ratio > 0.6 3. pleural fluid LDH > 2/3 of the upper limit of normal for serum LDH - exudative pleural effusion, along w/ pleural fluid acidosis (pH
845
Peptic ulcer disease (PUD)
- may present w/ epigastric pain, nausea, and/or early satiety in associated w/ food - symptoms of duodenal ulcer classically occur in the absence of a food buffer (eg 2-5 hrs after meals, on an empty stomach, or at night). - melena is a manifestation of upper GI bleeding, w/ PUD being one of the most common causes
846
Vision development is critical during the first few years of life, and screening should occur at every well-child exam. Infants should be evaluated by observing fixation and tracking. The cover-uncover test should be performed in older infants and children to assess for strabismus. Visual acuity should begin at age 3 w/ the tumbling E or Snellen chart
.
847
quadrivalent meningococcal vaccine
-should be give at age 11-12 followed by a booster dose at age 16 due to the risk of college outbreaks
848
rotavirus vaccine
-given at age 2-8 months
849
Abdominal US is the study of choice for diagnosis and follow-up of AAAs, as it has nearly 100% sensitivity and specificity for this condition
.
850
Aminoglycosides
- abx used to treat serious gram-negative infections | - potentially nephrotoxic and drug levels and renal function must be monitored closely during therapy
851
Most likely cause of UTI in pts w/ alkaline urine?
Proteus species - P. mirabilis secretes urease to alkalinize the urine (pH >7), leading to formation of struvite stones; the stone becomes a permanent source of bacteria to perpetuate the cycle; staghorn calculi - other urease producing bacteria: Morganella morganii, Pseudomonas species, Providencia species, Staph species, and Ureaplasma urealyticum
852
pathogens most likely in acute onset prosthetic joint infection (
- Staph aureus - gram negative rods - anaerobes
853
pathogens most likely responsible for prosthetic joint infection subacutely (> 3 months)?
- Coagulase negative staph - Propionibacterium species - Enterococci
854
Parents cannot deny their children life-saving tx unless the benefits are minimal or would not alter the prognosis.
.
855
Malaria
- should be suspected in any ill pt, especially those w/ a hx of FEBRILE PAROXYSMS, who have traveled to an endemic-tropical region. - THICK AND THIN BLOOD SMEARS should be ordered for parasite detection and quantification - Nonimmune children are at highest risk of death, but the sickle cell trait confers some protection from severe complications like cerebral malaria
856
HIV infection should be suspected when an infant has failure to thrive, lymphadenopathy, and thrush in the setting of maternal IV drug abuse. Pregnant pts w/ risky behavior should undergo HIV antibody testing in the 1st AND 3rd trimesters (all women get HIV test in 1st trimester), as it can take up to 3 months to develop detectable antibody. Diagnosis is confirmed in infants up to 18 months by PCR TESTING
.
857
Consider CMV as a late complication in post bone marrow transplant recipients who present w/ pneumonitis and colitis.
- typically develops in 45 days | - multifocal diffuse patchy infiltrates, upper and lower GI ulcers, arthralgias, myalgias, esophagitis
858
Most common organ involved in graft-versus-host disease?
THE SKIN - skin rash is almost always seen - other organs commonly involved include the intestine, liver, and lung (bronchiolitis obliterans)
859
Encapsulated bacteria, especially Strep pneumo, are the most common cause of pneumonia in HIV pts due to impaired humoral immunity
.
860
Pneumocystis pneumonia
- dry cough and dyspnea | - CXR usually demonstrates bilateral diffuse infiltrates
861
most common pathogen causing pneumonia in nursing home residents?
- Streptococcus pneumoniae | - also the most common cause of community-acquired pneumonia in adults
862
Pts w/ cystic fibrosis suffer from life-threatening, recurrent sinopulmonary infections due to accumulation of viscous airway secretions. what are the most common organisms?
- Staph aureus is the most common cause of bacterial pneumonia in young children w/ CF!, esp. those w/ coexisting influenza infection - Pseudomonas is most common above the age of 20
863
Pertussis
- should be suspected in an inadequately vaccinated pt w/ severe, paroxysmal cough, inspiratory whoop, or posttussive emesis - during the first month of illness, the diagnosis is confirmed by cultures and/or PCR of nasopharyngeal secretions - MACROLIDE ABX are the preferred tx of prevent spread of infection - will have LYMPHOCYTE-PREDOMINANT LEUKOCYTOSIS
864
Right-sided endocarditis
- should be considered in pts w/ presumed hx of IV drug use - empiric abx tx of native-valve endocarditis should be geared toward methicillin-resistant Staph aureus, streptococci, and enterococci - Vancomycin is the most appropriate empiric abx
865
Maternal combination antiretroviral therapy during pregnancy and neonatal zidovudine therapy can reduce perinatal HIV transmission to
- Zidovudine should be administered to the neonate for >6 wks - 3 drug regimine should be used for mother
866
Elective C-section is beneficial if maternal HIV viral load is > 1,000 copies/mL, as it can reduce trasmission by 50%. Zidovudine plus C-section reduces the risk of transmission more than either intervention alone. However, combination antiviral therapy is more effective than any of these strategies in preventing neontal HIV infection.
.
867
most common causes of acute bacterial rhinosinusitis?
- Strep pneumo - nontypeable H. flu - Moraxella catarrhalis - Due to increasing beta-lactamase resistance, the tx of choice is amoxicillin-clavulanic acid
868
Entamoeba histolytica
- causative agent of amebiasis - found mostly in Southeast Asia, Africa, and central and south america - abdominal pain and bloody diarrhea
869
Shigella
- common bacterial cause of acute diarrhea | - fever, abdominal pain, and bloody diarrhea
870
Strongyloides stercoralis
- parasite found primarily in tropical and subtropical regions and can cause skin, GI, and pulmonary manifestations - N/V/ abdominal pain
871
Cryptosporidium
- emerging and important cause of traveler's diarrhea | - consider in pts w/ persistent, nonbloody, watery diarrhea for > 2 wks
872
in diabetic pts, the pathogenic mechanism of osteomyelitis adjacent to a foot ulcer is CONTIGUOUS SPREAD of infection
.
873
C-section should be performed on women w/ active genital herpes lesions (primary or secondary) at the time of delivery to reduce the risk for neonatal HSV.
.
874
HIV pts are at high risk for TB. A positive PPD test (skin induration of > 5 mm in HIV pts) requires prophylaxis w/ isoniazid (and pyridoxine) for 9 months.
.
875
Alternatives to use of isoniazid and pyridoxine for 9 months as chemoprophylaxis in PPD positive individuals w/o active infection
- Pyrazinamide w/ Rifampin or Rifabutin for 2 months | - Rifampin alone for 4 months
876
Sporotrichosis
- Gardener's disease - the initial lesion, a reddish nodule that later ulcerates, appears at the site of the thorn prick or other skin injury - from the site of inoculation, the fungus spreads along the lymphatics forming subcutaneous nodules and ulcers - adenopathy and systemic signs of infection are usually absent
877
Meningococcal meningitis
- most common cause of bacterial meningitis in children and young adults - typically presents w/ fever, headache, neck stiffness, AMS, and a PETECHIAL OR PURPURIC RASH - prompt diagnosis and tx are critical given that it has a high morbidity and mortality rate even w/ appropriate tx
878
Borrelia burgdorferi
- causes Lyme disease - usually acquired in late summer months after and Ixodes tick bite - rash (erythema chronicum migrans), headaches, fever, chills, and malaise
879
Cytomegalovirus
-can cause infectious mononucleosis like illness, which presents w/ high fevers, fatigue, malaise, splenomegaly, and pharyngitis
880
Haemophilus influenzae
-may cause meningitis, rhinorrhea, fever, epiglottitis, and ear infections
881
Herpes simplex virus
-causes temporal lobe encephalitis in neonates and infants and typically presents w/ seizures
882
Listeria monocytogenes
- transmitted vaginally, is 1 of the 3 most common causes of meningitis in newborns - also transmitted through unpasteurized milk or cheese from infected cows
883
Erysipelas
- sudden onset of a sharply-demarcated, erythematous, edematous, tender skin lesion w/ raised borders in a febrile patient suggests erysipelas - most frequently implicated organism is group A beta-hemolytic streptococcus - specific type of cellulitis; inflammation of the superficial dermis - abrupt onset, and usually systemic signs, including fever and chills
884
Clostridium perfringens
causative organism of gas gangrene
885
All pts who are started on anti-tubercular therapy should also be started on vitamin supplements, especially pyridoxine (10 mg/day), to avoid peripheral neuropathy and other neurological complications. If the peripheral neuropathy has already developed, the dose of pyridoxine is increased to 100 mg/day. Hepatitis is another known side effect of isoniazid.
.
886
Indications for transfusion of fresh frozen plasma?
- INR > 1.6: inherited deficiency of single clotting factors; prevent active bleeding in pt on anticoagulant therapy before a procedure; active bleeding - emergent reversal of warfarin: major or intracranial hemorrhage; prophylactic transfusion in a surgical procedure that cannot be delayed - acute DIC: w/ active bleeding and correction of underlying condition - microvascular bleeding during massive transfusion: > 1 blood volume (5L in adults) - replacement fluid for apheresis in thrombotic microangiopathies: TTP; HUS
887
Indications for transfusion of platelets in adults
- 100,000 (rarely): surgery w/ active bleeding | - 100.4 or undergoing invasive procedure
888
indications for transfusion of platelets in neonates
- 20,000: always transfuse - 20-30,000: consider transfusion; transfuse for clinical reasons (active bleeding, LP) - 30-50,000: transfuse if any of the following exist: - first week of life w/ birth weight
889
Indications for transfusion of packed RBCs?
- acute sickle cell crisis to prevent stroke - acute blood loss > 1500mL (30% of blood volume) - symptomatic anemia (fatigue, weakness, dizziness, reduced exercise tolerance, SOB, changes in mental status, muscle cramps, angina, severe CHF) if they cannot function w/o treating the anemia - Hgb
890
new onset pancytopenia almost always needs a bone marrow aspirate evaluation to help determine cause!
.
891
name some CYP450 inducers
-carbamazepine, phenobarbital, phenytoin, rifampin
892
name some CYP450 inhibitors
-phenothiazines, TCAs, cimetidine
893
pain management in cancer pts
-follow WHO algorithm. Basically, start w/ non-opiods such as acetaminophen, NSAIDs, aspirin, COX inhibitors. If that doesn't work, then progress to weak opiods like vicodin, and possibly add non-opiods to regimen. Finally, progress to pure opioid regimen for sever pain. You can titrate pure opioids until pain relief, and you are only limited by patient side effects. From here you can switch to a different opiod due to low cross-tolerance between meds of this class.
894
Central retinal VEIN occlusion
- blocks retinal vein, causing walls of vein to leak blood and excess fluid into retina. When fluid collects in the macula (area of retina responsible for central vision), vision becomes blurry. - "floaters" in your vision are another symptom from clotted blood in vitreous - in severe cases, the blocked vein causes painful pressure in the eye - commonly occurs w/ glaucoma, diabetes, age-related vascular disease, HTN, and blood disorders - no cure - look for DILATED TORTUOUS RETINAL VEINS ON EXAM
895
Central retinal ARTERY occlusion
- ages 50-70 usually - most common medical problem associated with it is ARTERIOSCLEROSIS (carotid disease is found in 50%) - most common cause is THROMBOSIS, and less likely, embolus - first sign is SUDDEN and PAINLESS loss of vision that leaves you barely able to count fingers or determine light from dark - irreversible damage occurs after 90 minutes--> EMERGENCY - AFFERENT pupillary defect will be present - affected portion of retina (ischemic) will appear white and the foveal center (center of macula) appears red (cherry red spot)
896
connection between pancreatitis and a blood lipid?
TRIGLYCERIDES - this is the 3rd most common cause of pancreatitis behind alcohol and gallstones - Tg >1000 (normal is
897
Top causes of small bowel obstruction
- adhesions - malignancy - Crohn disease - hernias
898
signs and symptoms of small bowel obstruction
- nausea - vomiting (associated w/ more proximal obstructions) - diarrhea (early finding) - constipation (late finding, as evidenced by the absence of flatus or bowel movements) - fever and tachycardia (occur late and may be associated w/ strangulation) - previous abdominal or pelvic surgery, inflammatory bowel disease, previous radiation therapy, may be part of the patient's medical hx - hx of malignancy (particularly ovarian and colonic)
899
Remember that even if some children are not walking by age 12, it is usually OK, some may take until age 16-17 months.
.
900
mechanism of action of ACE-inhibitors
- inhibit conversion of angiotensin-I to angiotensin-II - angiotensin-II is a potent vasoconstrictor and promotes production of aldosterone. Aldosterone promotes sodium and water retention. By inhibiting angiotensin-II production, ACE-i cause vasodilation and indirectly inhibit fluid volume increases that result from the actions of aldosterone
901
most appropriate pharmacotherapy for pts w/ PCOS who want to conceive?
- Clomiphene citrate | - lifestyle modification such as diet and exercise also help
902
Management of post-exposure prophylaxis to hepatitis B (HBsAg positive source)
- unvaccinated person who got exposed: hepatitis B vaccine series and hepatits B immune globulin - vaccinated person who got exposed: Only the hepatitis B vaccine booster! No need for HBIG if you already have circulating antibodies - if the source has an unknown HBsAg status, then administer hep B vaccine in unvaccinated person; no treatment for those already vaccinated
903
at what gestational age are steroids (Betamethasone) indicated in preterm birth?
23 - 34 weeks | -before 23 weeks the fetus is unable to benefit, and after 34 weeks the lungs are already developed
904
name some tocolytics
- terbutaline - magnesium sulfate - nifedipine - indomethacin
905
definition of preterm labor
occurring before 37 weeks
906
normal pregnancy length
37 - 42 weeks | -measured from first day of last menstrual period
907
cervical cerclage
- placement of stitches in cervix to hold it closed | - used to keep a weak cervix from opening early
908
most common causes of pneumonia from birth to 3 wks?
viral: CMV, rubella, HSV bacterial: GBS, Listeria, E. coli
909
most common causes of pneumonia from 3 wks to 3 months?
- viral: RSV, Parainfluenza virus, Influenza virus, Adenovirus - bacterial: S. pneumo, Chlamydia trachomatic, Bordetella pertussis
910
most common causes of pneumonia from 4 months to 5 years?
- viral: RSV, parainfluenza virus, adenovirus, human metapnuemovirus, influenza type A - bacterial: S. pneumo, Chlamydia pneumoniae, Mycoplasma pneumoniae
911
most common causes of pneumonia from 5 years to 18 years
- viral: adenovirus, EBV, parainfluenza, influenza, rhinovirus - bacterial: S. pneumo, S. aureus, Atypical pneumonia (Mycoplasma, Chlamydia)
912
most common causes of pneumonia from 18 years to 65 years (no comorbidity)?
- viral: parainfluenza virus, adenovirus, influenza virus | - bacterial: S. pneumo, atypical pneumonia (Mycoplasma, Chlamydia)
913
most common causes of pneumonia over 65 years (no comorbidity)
- viral - bacterial: S. pneumo, respiratory viruses, Haemophilus influenzae, gram negative bacilli, S. aureus (moraxella and Legionella are less common)
914
most common causes of pneumonia in smokers?
- S. pneumo - Haemophilus influenzae - Moraxella catarrhalis - Legionella pneumonia
915
most common causes of pneumonia in alcoholics?
- S. pneumo - Anaerobes - Klebsiella
916
most common cause of pneumonia in IV drug users?
S. aureus
917
most common causes of pneumonia in CF?
- early disease: S. aureus | - late disease: Pseudomonas aeruginosa
918
most common causes of pneumonia from animal exposure?
- birds: Psittacosis - rabbits: tularemia - livestock or cats: Coxiella burnetii
919
number one cause of kidney stones?
Hyperparathyroidism! | -everyone must be tested for parathyroid gland malignancy or problem
920
Type of transfusion reaction in pts w/ IgA deficiency if given blood with IgA in it?
ANAPHYLACTIC
921
Acute hemolytic transfusion reaction
- type 2 hypersensitivity reaction - Intravascular hemolysis (ABO blood group incompatibility) or extravascular hemolysis (host antibody reaction against foreign antigen on donor RBCs) - fever, hypotension, tachypnea, tachycardia, flank pain, hemoglobinemia (intravascular), jaundice (extravascular)
922
allergic nonhemolytic transfusion reaction
- type 1 hypersensitivity reaction against plasma proteins in transfused blood - urticaria, pruritis, wheezing, fever - treat with antihistamines
923
Anaphylactic transfusion reaction
- severe allergic reaction - IgA deficient individuals must receive blood products that lack IgA - Dyspnea, bronchospasm, hypotension, respiratory arrest, shock
924
Febrile nonhemolytic transfusion reaction
- type 2 hypersensitivity raction - host antibodies against donor HLA antigens and leukocytes - fever, headaches, chills, flushing
925
delayed hemolytic transfusion reaction
- can occur 1-4 wks after transfusion - usually extravascular hemolysis - mild symptoms; unexplained fatigue, jaundice, fever - direct coombs positive
926
initial management of acute aortic dissection?
Beta blockers! Then possible nitroprusside, followed by surgical correction if indicated
927
which 3 disorders have a common presentation in the elderly
-hypothyroidism, depression, anemia
928
what lab value is frequently increased in non-hodgkin's lymphoma?
serum LDH
929
antihypertensives during pregnancy
- methyldopa - labetalol - nifedipine
930
antihypertensive for severe preeclampsia
Hydralazine
931
erysipelas
- sudden onset of a sharply-demarcated, erythematous, edematous, tender skin lesion w/ raised borders in a febrile patient - group A beta-hemolytic strep most frequent
932
All pts started on isoniazid should also be started on pyridoxine (vitamin B6) 10 mg/day. If peripheral neuropathy has already developed, increase dose to 100 mg/day.
.
933
Neurocysticercosis
- most common parasitic infection of the brain | - most prevalent in rural areas w/ poorer sanitary conditions and where pigs are raised
934
prion diseases
- Creutzfeldt-Jacob disease and Kuru - spongiform encephalopathy - intracytoplasmic vacuoles diffusely throughout gray matter on microscopy
935
Hydatid cysts
- caused by Echinococcus species - usually seen in the liver and lungs - more common in SHEEP BREEDERS
936
Bacillary angiomatosis
- bright red, firm, friable, exophytic nodules in an HIV infected patient usually - caused by Bartonella, a gram negative bacillus - oral erythromycin is tx
937
Molluscum contagiosum
- caused by poxvirus | - centrally-umbilicated, dome-shaped papules that are non-pruritic
938
Kaposi sarcoma
- usually on trunk, face, and extremities - papules that become plaques or nodules - color changes from light brown, to pink, to dark violet
939
HIV infected individuals w/ CD4 count > 200/uL should receive all routine vaccinations for adults, as well as serial pneumococcal boosters. Men who have sex w/ men should also get hepatitis A vaccine. Pts w/ CD4 count
.
940
Acute HIV infection
- can present w/ a mononucleosis-like syndrome consisting of fever, night sweats, lymphadenopathy, arthralgias, and diarrhea - making the diagnosis at an early stage can be beneficial both to the individual patient and from a public health standpoint
941
In HIV infected pts, diarrhea can be due to a variety of organisms (Salmonella, shigella, campylobacter, C. diff, Giardia, Cryptosporidium, Mycobacterium avium, CMV). Therefore, an attempt should be made to identify the causal organism prior to instituting therapy so that an appropriate antibiotic may be chosen (stool culture, exam for ova and parasites, etc.)
.
942
Echinococcus granulosus
- in humans, hepatic hydatid cysts are due to infection by this organism - dogs are the definitive host - a cystic hepatic lesion w/ eggshell calcification is highly suggestive of infection w/ this organism - may or may not be a hx of sheep breeding - surgical resection under cover of albendazole
943
Pneumocystis jirovecii pneumonia
-common opportunistic infection in AIDS pts w/ CD4 35 to minimize pulmonary complications!
944
Risk factors for C. diff
- recent hospitalization, advanced age, or antibiotic use (most commonly fluoroquinolones, penicillins, cephalosporins, and clindamycin) - C. diff colitis can range from mild colitis (watery diarrhea, low-grade fever, abdominal pain, and leukocytosis) to fulminant colitis w/ toxic megacolon - diagnosis is usually confirmed w/ stool studies for C. diff toxin (PCR or enzyme immunoassay)
945
tx for C. diff colitis
Metronidazole or ORAL vancomycin
946
Unexplained leukocytosis in hospitalized pts should raise suspicion for C. difficile, even without diarrhea
.
947
Coccidiodomycosis
- endemic in southwestern U.S., as well as Central and South America - primary pulmonary infection: fever, fatigue, dry cough, weight loss, pleuritic chest pain - cutaneous findings: erythema multiforme, erythema nodosum, arthralgias
948
Histoplasmosis
- southeastern, mid-atlantic, and central U.S. | - acute pneumonia; cough, fever, and malaise
949
Blastomycosis
- south-central and north-central U.S. - affects lungs, skin, bones, joints, and prostate - infection in immunocompetent hosts is uncommon - primary pulmonary infection is asymptomatic or presents w/ flu-like symptoms
950
Invasive aspergillosis
- immunocompromised pts (those w/ neutropenia, taking cytotoxic drugs such as cyclosporine, high doses of steroids) - fever, cough, dyspnea, or hemoptysis - CXR may show cavitary lesions - CT: pulmonary nodules w/ THE HALO SIGN or lesions w/ an AIR CRESCENT
951
Cryptococcus
-meningoencephalitis in HIV pts whose CD4 count is
952
Tx for cryptococcus
initial: Amphotericin B w/ flucytosine maintenance: fluconazole
953
Pts w/ HIV who have subacute-onset of low-grade fever, headache, and signs of increased ICP should be evaluated for cryptococcal meningitis. Diagnosis is established by detection of the cryptococcal antigen or isolation of the organism in CSF.
.
954
Malignant otitis externa
- ear discharge and severe ear pain that worsens despite the use of topical antibiotics - pain often radiates to TMJ - presence of granulation tissue in the external auditory meatus - DM and immunosuppressive conditions are important risk factors - Pseudomonas aeruginosa most frequently!
955
Acute bacterial parotitis
- presents w/ painful swelling of the parotid gland that is aggravated by chewing - high fever and a tender, swollen, and erythematous parotid gland are common - this post-op complications can be prevented w/ adequate fluid hydration and oral hygiene - most common infectious agent is Staph aureus!
956
Fluoroquinolone use is associated w/ what complication?
- Tendinopathy and tendon rupture (Achilles most common) - Pts can develop tendon pain within 24 hrs w/ a median of 8 days after starting the drug - Pts should stop the drug at onset of symptoms, avoid exercise and/or use of the affected area, and seek medical care for symptom evaluation and changing to a non-fluoroquinolone antibiotic
957
Causes of diarrhea in HIV pts
- non-opportunistic infections: Salmonella, campylobacter, entamoeba, chlamydia, shigella, giardia - opportunistic infections: CMV, cryptosporidium, isopora belli, blastocystis, MAC, Herpes simplex virus, adenovirus, HIV itself - non-infectious: Kaposi sarcoma, lymphoma of GI tract - Hematochezia and lower abdominal cramps are usually due to colonic infection w/ CMV, C. diff, Shigella, Entamoeba, or campylobacter
958
CMV colitis
- suspect in HIV positive pt w/ bloody diarrhea and a normal stool exam; they should have a colonoscopy w/ biopsy - bloody diarrhea w/ abdominal pain - colonoscopy shows multiple ulcers and mucosal erosions - biopsy demonstrates large cells w/ eosinophilic intranuclear and basophilic intracytoplasmic inclusions (owl's eye effect) - tx is GANCICLOVIR; Foscarnet is used in cases of ganciclovir failure
959
Entamoeba histolytica
- parasite that cause bloody diarrhea, but can usually be diagnosed by visualization of trophozoites on stool exam - colonoscopy shows presence of "flask-shaped" colonic ulcers
960
TMP/SMX is used in HIV pts to prevent what?
- Pneumocystis jirovecii | - Toxoplasma gondii
961
Azithromycin is recommended for prophylaxis of Mycobacterium Avium complex in HIV + pts w/ CD4
.
962
Fluconazole is used for prophylaxis against Cryptococcus and Coccidioides in HIV + pts who have had these diseases in the past. Also used w/ frequent Candida infections.
.
963
Infectious mononucleosis
- most commonly caused by EBV - presents w/ fever, fatigue, exudative pharyngitis, and diffuse cervical lymphadenopathy - a polymorphous, maculopapular rash frequently develops after administration of amoxicillin! - pts should avoid sports for 3 or more wks due to risk of splenic rupture
964
Adenoviruses
- frequent causes of URI; coryza, pharyngitis, tonsillitis, conjunctivitis - fever, malaise, headache, and abdominal pain
965
Coxsackie virus
-cause hand-foot-mouth disease and herpangina (vesicles on hard palate)
966
CMV is a less common cause of infectious mononucleosis and tends to have a milder presentation
.
967
Hepatitis A vaccine
- chronic liver disease (including HBV and HCV) - men who have sex with men - IV drug users
968
Hepatitis B vaccine
-all pts w/o documented immunity to HBV
969
HPV vaccine
-men and women age 9-26
970
Influenza vaccine
-annually for all pts
971
Meningococcus vaccine
- all pts age 11-18 - large groups living in close proximity (college students, military recruits, incarcerated pts) - asplenia or complement deficiency
972
Pneumococcus vaccine
- PCV13 once | - PPSV23 8 weeks later, then every 5 years
973
Tetanus, diptheria & pertussis vaccine
- Tdap once - repeat Tdap for women during each pregnancy - Td every 10 years following Tdap
974
In addition to the vaccines recommended for the general population, pts w/ HIV infection should receive pneumococcal vaccination. Most pts w/ HIV should also receive vaccination for hepatits A and B if they do not have documented evidence of immunity to these viruses. Live vaccines are generally contraindicated.
.
975
Invasive aspergillosis
- occurs in immunocompromised pts, who may present w/ fever, cough, dyspnea, or hemoptysis - CXR may show a cavitary lesion, and CT scan shows pulmonary nodules w/ a halo sign or lesions w/ an air crescent
976
Postexposure HIV prophylaxis w/ 3 drug antiretroviral therapy for 4 weeks is recommended following high-risk occupational exposure to blood or body fluids from an HIV infected individual. Therapy should be started as soon as possible, preferably in the first few hours. Try Tenofovir-Emtricitabine with raltegravir.
.
977
Mumps
- can cause parotitis and orchitis - most common in postpubertal young men, ages 15-29 - infertility is a rare complication - tx is supportive w/ application of cold compresses to parotid area or testes - most common complications are aseptic meningitis and encephalitis
978
Pneumocystis pneumonia (PCP)
-likely in pts w/ HIV who have a nonproductive cough, exertional dyspnea, fever, severe hypoxia, bilateral interstitial infiltrates on CXR, and a normal white count, especially if their CD4 35 on room air
979
Retropharyngeal abscess
-should be suspected in children who present w/ fever, dysphagia, inability to extend the neck, muffled voice, and lateral x-ray showing a widened prevertebral space
980
common complications of supracondylar fracture of humerus
- brachial artery injury (most common) - median nerve injury (most common) - cubitus varus deformity - compartment syndrome/Volkmann ischemic contracture
981
supracondylar fractures of humerus
- associated w/ a high risk of neurovascular injury - radial and brachial pulses must be assessed before and after reduction as the brachial artery can be impinged - motor and sensory function should also be assessed due to risk of median nerve injury
982
neonatal chlamydial conjunctivitis
- typically occurs at 5-14 days of life and presents w/ eyelid swelling, chemosis, and watery or mucopurulent discharge - blood-stained eye discharge is highly characteristic of chlamydial conjunctivitis - first line tx is oral erythromycin
983
tx of choice for infants w/ gonococcal conjunctivitis (aka ophthalmia neonatorum)
- IV or IM ceftriaxone or cefotaxime - ceftriaxone should be avoided in infants w/ hyperbilirubinemia as it results in displacement of bilirubin from albumin-binding sites, increasing the risk of kernicterus
984
prophylaxis against gonococcoal conjunctivitis in neonate?
-topical erythromycin (note that once it has occured, it is treated w/ IM or IV ceftriaxone/cefotaxime)
985
Application of topical silver nitrate is used for routine neonatal ophthalmic prophylaxis in some countries, and unlike topical erythromycin ointment, is effective prophylaxis against penicillinase-producing strains of Neisseria gonorrhoeae. Topical silver nitrate is not available in US given an increased risk of chemical conjunctivitis w/ its use.
.
986
Legg-Calve-Perthes disease (idiopathic avascular necrosis of the femoral capital epiphysis)
-unilateral subacute hip pain in a male child coupled w/ a progressive antalgic gait, thigh muscle atrophy, decreased hip range of motion, and collapse of the ipsilateral femoral head on plain pelvic x-rays
987
Slipped capital femoral epiphysis (SCFE)
- the metaphysis and proximal femur slip relative to the epiphysis at the epiphyseal plate - the capital femoral epiphysis remains structurally intact within the acetabulum - classic presentation is obese adolescent w/ complainst of pain
988
Most common etiology of osteomyelitis in pediatrics?
-S. aureus due to hematogenous seeding to the metaphysis
989
Duchenne muscular dystrophy
- most common childhood myopathy | - causes proximal muscle weakness and calf pseudohypertrophy
990
Osteosarcoma
- primary bone cancer that produces Codman's triangle in the metaphysis of long bones - note that Ewing sarcoma tends to affect the diaphysis of long bones
991
false labor
- progressive cervical changes are absent! - contractions are usually irregular and discomfort is readily relieved by sedation! - all such pts need reassurance only
992
true labor
- contractions that occur at regular intervals w/ a progressively shortening interval and increasing intensity - pain is in the back and upper abdomen and is NOT relieved by sedation - cervical changes are typically observed
993
Retinoblastoma
- every case of leukocoria is considered retinoblastoma, until proven otherwise!!! such cases should be promptly referred to an ophthalmologist - inactivation of the Rb suppressor gene, may be familial or sporadic - highly malignant - other manifestations: strabismus, decreased vision, ocular inflammation, eye pain, glaucoma, orbital cellulits - mass w/ calcifications on US or CT is highly suggestive
994
initial tx of strabismus in children
-covering the normal eye
995
Hereditary spherocytosis
- autosomal dominant - should be suspected in a patient w/ persistent jaundice, hemolytic anemia, splenomegaly, positive family hx, and spherocytes on peripheral blood smear - RBC fragility on acidified glycerol lysis and eosin-5-maleimide binding tests confirm the diagnosis - mutation in ankyrin gene causes deficiency in SPECTRIN - increased mean corpuscular hemoglobin concentration
996
hereditary spherocytosis
- autosomal dominant, northern european - hemolytic anemia, jaundice, splenomegaly - increased MCH concentration, spherocytes, negative coombs test, increased osmotic fragility on acidified glycerol lysis test, abnormal eosin-5-maleimide binding test - tx: folic acid, blood transfusions, splenomegaly - complications: pigment gallstones, aplastic crises from parvovirus B19 infection
997
pharmacologic tx for Alzheimer's dementia
- cholinesterase inhibitors (donepezil, galantamine, rivastigmine) effective in mild to moderate dementia; may improve quality of life, cognitive functions, memory, language, thought, and reasoning; they slow the cognitive decline - Donepezil is approved for all stages of Alzheimer's dementia - Memantine, an N-methyl-D-aspartate receptor antagonist, is approved for moderate to severe dementia
998
moving from supine to sitting can increase the functional residual capacity (FRC) by 20-35%. In normal adults, this can amount to several hundred cubic centimeters of lung volume. Increasing FRC can help prevent post-op atelectasis.
.
999
Laparoscopy w/ visualization and biopsy of implants is the only definitive way to diagnose endometriosis. It is indicated when NSAIDs and hormonal contraceptives have failed.
.
1000
Pts w/ endometriosis
- increased risk of impaired fertility or infertility due to chronic inflammation and adhesion formation - endometriosis is diagnosed in 25-50% of women being evaluated for infertility, and almost half of women w/ endometriosis have impaired fertility
1001
risk factors for abruptio placenta
-advanced age, HTN, preeclampsia, renal disease, cocaine or tobacco use
1002
risk factors for breast cancer
-positive family hx, genetic mutations (BRCA1, BRCA2, p53), early menarche, late menopause, prolonged hormone replacement therapy, and nulliparity
1003
risk factors for endometrial carcinoma
-advancing age, unopposed estrogen or prolonged use of TAMOXIFEN, obesity, nulliparity, and anovulatory conditions (PCOS)
1004
Higher rates of ovarian cancer in pts w/ endometriosis
.
1005
Pts who have experienced 2 episodes of acute mania should be considered for long-term (years), if not lifetime, maintenance tx w/ lithium, esp. if the episodes were severe or there is a family hx. Pts w/ a hx of 3 or more relapses are recommended to have lifetime maintenance therapy.
.
1006
Enterobius vermicularis
- aka pinworms - highly contagious and manifests as nocturnal perianal pruritus - albendazole and pyrantel pamoate (for pregnant pts!) are first-line tx options - diagnosed by scotch tape test
1007
Trypanosoma cruzi
- aka Chagas disease - primarily affects the heart (cardiomyopathy, right bundle branch block) and GI tract (megacolon, megaesophagus) - Benznidazole is first-line anti-trypanosomal tx!
1008
Strongyloidiasis
- urticaria, abdominal pain, respiratory symptoms (eg dry cough, dyspnea, wheezing) - tx w/ IVERMECTIN
1009
Onchocerciasis
- aka river blindness - causes ocular lesions and dermatitis - tx w/ ivermectin
1010
Metronidazole
-used for protozoan infections such as amebiasis (acute dysentery, liver abscess) and trichomonas vaginitis (green-yellow, frothy, malodorous discharge) as well as anaerobic intra-abdominal infections (diverticulitis, peritonitis, cholangitis, abscess)
1011
Ankylosing spondylitis
- seronegative spondyloarthropathy that presents w/ progressive inflammatory back pain and stiffness - in the setting of suggestive findings on history and physical, AS is confirmed by plain film x-ray demonstrating fused sacroiliac joints and/or bamboo spine - presents in second or third decade of life usually; male:female ratio 2:1 - progressive low back pain and spinal stiffness of > 3 months duration usually - morning stiffness > 30 min and back pain improves w/ exercise - decreased lumbar spinal mobility and tenderness over SI joints is common - AP x-ray of SI joints; fusion of SI joints and/or bamboo spine is diagnostic
1012
Serum BUN and creatinine are usually DECREASED in pregnant pts due to an INCREASE in renal plasma flow and GFR.
.
1013
Teenagers w/ serious suicidal ideation must be hospitalized and their parents informed of the situation.
.
1014
Long-term supplemental oxygen therapy has been proven to prolong survival in pts w/ COPD and hypoxemia. Criteria for therapy?
- PaO2 55%) | - evidence of cor pulmonale
1015
opioid withdrawl
- symptoms: nausea, vomiting, cramps, diarrhea, dysphoria, restlessness, rhinorrhea, lacrimation, myalgias, arthralgias - physical exam: mydriasis, piloerection, hyperactive bowel sounds - oral or IM methadone is the tx of choice
1016
Guillain-Barre Syndrome
- 2/3 have an antecedent respiratory or GI infection - Campylobacter jejuni is most common precipitant; others include human herpes virus, Mycoplasma, H. influenza - more common in pts w/ lymphoma, sarcoidosis, and SLE - Recent HIV infection and immunization have also been associated
1017
Screening for secondary causes of HTN should be done when?
-in pts who have resistant HTN (requiring > 3 meds from different classes) and in young (
1018
Counseling for nonpharmacologic therapy (lifestyle modification) should be part of the overall management of HTN at every office visit. All pts should be encouraged to restrict dietary salt intake; have a diet rich in fruit, vegetables, and low-fat dairy products; engage in regular aerobic exercise; lose weight; and limit alcohol intake.
.
1019
Pts w/ Huntington's chorea
- usually present in 40s or 50s w/ chorea and/or behavioral disturbance - atrophy of the CAUDATE nucleus is a characteristic feature.
1020
diffuse atrophy of the cerebral cortex
Alzheimer's disease
1021
atrophy of the lenticular nucleus
Wilson's disease
1022
atrophy of the frontal and/or temporal lobes
Pick's disease
1023
carbon monoxide poisoning
- most important factor is the history, because physical symptoms can be vauge - suspect in cases of smoke inhalation and when multiple people from the same confined quarters present w/ headache, nausea, and abdominal discomfort - pinkish-red skin hue is noted on exam and diagnosis is confirmed by carboxyhemoglobin levels
1024
characteristic of inhaled cyanide
-bitter almond breath
1025
sudden-onset respiratory distress in a toddler w/ focal findings on physical exam
- foreign body aspiration - CXR is of limited help as most objects are radiolucent - a hx of choking, if witnessed, is very helpful in diagnosis - immediate bronchoscopy is indicated to remove the foreign body
1026
tx for croup?
-nebulized racemic epinephrine
1027
interstitial nephritis
- 70% of cases are caused by drugs such as cephalosporins, penicillins, sulfonamides, sulfonamide containing diuretics, NSAIDs, rifampin, phenytoin, and allopurinol - discontinuing the offending agent is the tx of drug-induced interstitial nephritis - clinical features include fever, rash, and arthralgias - peripheral eosinophilia, hematuria, sterile pyuria, eosinophiluria, and WBC casts
1028
Diabetic nephropathy
- characterized by proteinuria and a progressive decline in GFR - hallmark is nodular glomerulosclerosis (w/ Kimmelstiel-Wilson nodules) but diffuse glomerulosclerosis is more common - progression can be slowed w/ strict glycemic control, tx of HTN, and angiotensin axis blockade
1029
most common adverse effect of inhaled corticosteroid therapy?
-oropharyngeal thrush (oral candidiasis)
1030
PCOS
- diagnostic: 2 of 3 of the following: androgen excess, oligo- or anovulation, polycystic ovaries on US; AND exculsion of other hyperandrogenic conditions - tx: weight loss; combined hormonal contraceptives for hyperandrogenism and menstrual dysfunction; Clomiphene citrate for ovulation induction; metformin for coexisting type 2 DM - comorbidities: overweight/obesity,glucose intolerance/DM, dyslipidemia, OSA, endometrial hyperplasia/cancer
1031
first-line tx for ovulation induction in PCOS
clomiphene citrate
1032
absolute contraindications to combined hormonal contraceptives
-migraine w/ aura -> 15 cigarettes/day and age > 35 -stage 2 HTN (> 160/100) -Hx of venous thromboembolic disease -Hx of stroke or ischemic heart disease -breast cancer -cirrhosis and liver cancer -major surgery w/ prolonged immobilization -
1033
Always suspect MS in a female w/ multiple neurologic presentations that are interspaced between time periods. Optic neuritis can result in blurring of vision, and is often associated w/ retrobulbar pain.
.
1034
Myasthenia gravis
- weakness in the proximal limb and torso muscles; ocular muscles may or may not be involved - diplopia, ptosis, facial weakness, and dysphagia - 10-15% also have a thymoma - ocular involvement is painless - antibodies against post-synaptic Ach receptor
1035
most common primary tumors that metastasize to liver?
-GI tract, lung, breast
1036
alpha-fetoprotein
-can be used in diagnosis of hepatocellular carcinoma
1037
Drug induced interstitial nephritis
- usually caused by cephalosporins, penicillins, sulfonamides, NSAIDs, rifampin, phenytoin, and allopurinol - pts present w/ arthralgias, rash, renal failure and the UA will show WBC casts and eosinophiluria
1038
Vitiligo
- autoimmune condition characterized by areas of depigmentation completely lacking melanocytes - sometimes associated w/ other autoimmune conditions such as pernicious anemia, autoimmune thyroid disease, type 1 DM, primary adrenal insufficiency, hypopituitarism, and alopecia areata
1039
Alveolar hypoventilation w/ CO2 retention can lead to respiratory acidosis along w/ CO2 narcosis. Acute kidney injury can cause a non-anion gap metabolic acidosis due to impaired acid excretion or an anion gap acidosis due to retention of unmeasured uremic toxins.
.
1040
TCAs are the drugs of choice for diabetic neuropathy. They can worsen urinary symptoms (due to cystopathy) and orthostatic hypotension (due to CV autonomic neuropathy). Gabapentin is an alternative for these pts.
.
1041
HIV associated Kaposi sarcoma
- AIDS defining malignancy due to human herpesvirus 8 - cutaneous KS develops most commonly on the lower extremities, face, oral mucosa, and genitalia - the lesions usually appear as multiple violaceous papules - diagnosis is made clinically, but may require biopsy
1042
Condyloma acuminata (anogenital warts)
- due to human papillomavirus - pts develop skin-colored, whitish, or grayish verrucous and filiform papules in the anal/perianal area (more often in men), penile shaft, or vulvovaginal and cervical areas
1043
Leukocytoclastic vasculitis
- can be due to infections, medications, inflammatory conditions, or malignancy - typically presents as non-blanching, 1-3 mm violaceous papules that can cluster/coalesce into plaques - older lesions appear brownish-red; newer ones are more violaceous
1044
Neurofibromatosis type 1 typically presents w/ widespread subcutaneous nodules associated w/ multiple cafe-au lait spots. Neurofibromatosis type 2 can present w/ a vestibular schwannoma and raised plaque-like lesions or subcutaneous nodules (from nerve swelling)
.
1045
Necrotizing enterocolitis
- should be suspected in a newborn w/ feeding intolerance, abdominal distension, and bloody stools - risk factors: prematurity, hypotension, congenital heart disease - hallmark x-ray finding is PNEUMATOSIS INTESTINALIS - can result in strictures, short bowel syndrome, or death
1046
Craniopharyngiomas
-benign suprasellar tumors that present w/ visual defects, headache, and symptoms of pituitary hormonal deficiency
1047
Open-angle glaucoma
-causes GRADUAL loss of peripheral vision in both eyes, leading to tunnel vision
1048
optic neuritis
- inflammatory demyelinating disease usually associated with MS - pts typically develop acute or subacute PAINFUL vision loss w/ ABNORMAL PUPILLARY RESPONSE to light in the affected eye
1049
Pseudotumor cerebri
-most common in obese women age
1050
alpha-1 antitrypsin deficiency
-suspect in non-smoking adults
1051
pulmonary function testing in emphysema
- decreased FEV1/FVC ratio - increased TLC - Decreased DLCO
1052
most important causes of thyrotoxicosis with low radioactive iodine uptake?
1. subacute painless thyroiditis 2. subacute granulomatous (De Quervain's; painful) thyroiditis 3. iodine-induced thyroid toxicosis 4. levothyroxine overdose 5. struma ovarii
1053
Struma ovarii
-ovarian teratoma which produces thyroid hormones, thereby causing thyrotoxicosis
1054
Pseudotumor cerebri
- suspect in young obese female w/ a headache that is suggestive of a brain tumor, but w/ normal neuroimaging and elevated CSF pressure - papilledema, visual field defects, 6th nerve palsy - glucocorticoids, vitamin A, and OCPs can provoke - impaired absorption of CSF by arachnoid villi - tx: weight reduction and acetazolamide; possibly shunting or optic nerve sheath fenestration to prevent blindness
1055
Creutzfeldt-Jakob disease
- should be suspected in an older adult patient (between 50-70) w/ rapidly progressive dementia, myoclonus, sharp wave complexes on EEG, and/or elevated 14-3-3 proteins in CSF - a rapidly progressive course and prominent myoclonus differentiate CJD from other causes of dementia - can also test for PRNP gene
1056
most prevalent antibodies in pts w/ Hashimoto's thyroiditis?
-anti-TPO
1057
anti-mitochondrial antibodies
-primary biliary cirrhosis (bear holding a mitochondria)
1058
Ventricular aneurysm
- occurs as a late complication of acute ST segment elevation or transmural myocardial infarction - ECG shows persistent ST segment elevation along w/ deep Q waves in the same leads - progressive left ventricular enlargement causing heart failure may occur in addition to refractory angina, ventricular arrhythmias, or mural thrombus - echo is diagnostic
1059
extension of aortic dissection frequently involves the right coronary artery and results in acute inferior MI w/ ST-segment elevation in leads II, III, and aVF
.
1060
papillary muscle rupture
- complication of acute MI that typically occurs 2-7 days after infarct - acute severe mitral regurgitation leading to hypotension and pulmonary edema
1061
Tamoxifen
- mixed agonist and antagonist activity on estrogen receptors - estrogenic effects of tamoxifen increase the risk of endometrial cancer and venous thrombosis
1062
pulmonary contusion
- not uncommon after high-speed car accidents | - symptoms usually develop in the first 24 hrs and a patchy alveolar infiltrate on CXR is typical
1063
Note that although IV ceftriaxone is effective in treating early localized Lyme disease, it is reserved for early disseminated and late disease as oral doxycycline is very effective in resolving early localized disease.
.
1064
tx for lyme disease in children
amoxicillin (doxycycline can cause tooth discoloration and skeletal problems in children and fetusus)
1065
The hallmark erythema migrans rash in a pt w/ a tick bite hx is pathognomonic for early localized Lyme disease. Doxycycline is the tx of choice in pts who are not pregnant and > 8 years old.
.
1066
Contraindications to rotavirus vaccine
- anaphylaxis to vaccine ingredients - hx of intussusception - hx of uncontrolled congenital malformation of the GI tract (eg Meckel's diverticulum) - SCID
1067
what are the only treatments that have been shown to decrease mortality in pts w/ COPD?
- smoking cessation | - home oxygen therapy
1068
when should an echo be obtained?
-in all pts w/ syncope due to suspected STRUCTURAL HEART DISEASE
1069
Preeclampsia
HTN, proteinuria, edema
1070
arm position in anterior shoulder dislocation
abducted and externally rotated
1071
arm position in posterior shoulder dislocation
-adducted and internally rotated
1072
Magnesium toxicity
-N/V/D, muscle weakness, and DECREASED or ABSENT DTRs@
1073
Indications for GBS prophylaxis when GBS status is unknown
- delivery at 18 hours - GBS bacteriuria in any concentration during the current pregnancy - prior hx of delivery of an infant w/ GBS sepsis
1074
antenatal corticosteroids
- should be administered in pregnant females w/ PPROM before 32 wks gestation to reduce risks of respiratory distress syndrome, necrotizing enterocolitis, neonatal intraventricular hemorrhage, and neonatal death - beyond 32 wks, its unclear if steroids are efficacious w/ rupture of membranes, though many places continue to administer betamethasone between 32-34 wks for pts w/ PPROM; - steroids are typically not given after 34 wks gestation
1075
Pts w/ PPROM whose GBS status is unknown should receive antibiotics. If a woman is admitted to the hospital after 34 wks gestation w/ PPROM, delivery is usually recommended.
.
1076
Pts w/ severe BPH can eventually progress to urinary obstruction and renal failure. A renal US is advised for assessment of hydronephrosis and worsening kidney function.
.
1077
emergency contraceptive options
- copper IUD (most effective; 99%; can be used up to 5 days after) - Levonorgestrel pill (85%; used up to 3 days after) - Ulipristal pill (> 85%; used up to 5 days after) - OCPs (75%; used up to 3 days after)
1078
congenital CMV
- can cause developmental delay - sensorineural deafness - blindness - jaundice - hepatosplenomegaly - petechiae
1079
Fetal hydantoin syndrome
- due to pregnant women on phenytoin | - hypoplastic fingers/nails and cleft lip/palate
1080
congenital rubella syndrome
- developmental delay - sensorineural deafness - cataracts - hepatosplenomegaly - purpura
1081
Measles
- cough, coryza, conjunctivitis, and Koplik spots followed by a maculopapular rash that spreads in a cranial-caudal pattern - prevention is best through live attenuated measles vaccine
1082
Specific phobia
- fear of a specific object or situation | - behavioral therapy using exposure techniques is the preferred treatment
1083
Cerebral palsy
- group of syndromes characterized by nonprogressive motor dysfunction - etiology is multifactorial, w/ prematurity as the leading risk factor - affected pts have uncoordinated and limited voluntary movements
1084
biggest risk factor for cerebral palsy
prematurity
1085
For women w/ average risk for cervical cancer, a Pap test is recommended every 3 yrs from age 21-29. Between ages 30-65, pts w/ initial negative testing may have either a Pap test alone every 3 yrs or a combination of Pap test and HPV testing every 5 years (preferred).
.
1086
Screening for diabetes
- recommended in pts w/ sustained BP > 135/80 mmHg and may be considered in all pts over age 45, as well as those w/ additional risk factors for diabetes - screening options include fasting plasma glucose, 2 hr oral glucose tolerance test and hemoglobin A1c
1087
Trachoma
- caused by Chlamydia trachomatis serotype A-C - major cause of blindness worldwide - presents w/ follicular conjunctivitis and pannus (neovascularization) formation in the cornea - diagnosed by Giemsa stain exam of conjunctival scrapings - topical tetracycline or oral azithromycin should be started immediately
1088
Herpes simplex karatitis
- pain, photophobia, and decreased vision | - dendritic ulcer is most common presentation, may also have minute clear vesicles on corneal epithelium
1089
Gonococcal conjunctivitis
- acquired through contact w/ infected genital secretions, and occurs 2-3 days after birth - presents as copious, purulent eye discharge w/ swollen eyelids and chemosis
1090
viral conjunctivitis
- conjunctiva is red w/ copious, watery discharge - children more commonly infected through contaminated swimming pools - mostly caused by adenovirus type 3
1091
acid-base relationship w/ calcium
- increased extracellular pH (eg respiratory alkalosis) causes dissociation of hydrogen ions from albumin, allowing increased binding of calcium and a drop in unbound (ionized) calcium - ionized calcium is the physiologically active form, and decreased levels can result in clinical manifestations of hypocalcemia (crampy pain, paresthesias, carpopedal spasm)
1092
Edward's syndrome
-commonly present w/ microcephaly, prominent occiput, micrognathia, closed fists w/ index finger overlapping the 3rd digit and the 5th digit overlapping the 4th, and rocker bottom feet
1093
Patau's syndrome (trisomy 13)
-cleft lip, flexed fingers w/ polydactyly, ocular hypotelorism, bulbous nose, low-set malformed ears, small abnormal skull, cerebral malformation, microphthalmia, cardiac malformations, scalp defects, etc.
1094
Toxic shock syndrome
- due to Staph aureus; associated w/ menstruation (tampons), nasal packing, and post-surgery infections - pts usually develop fever, myalgias, marked hypotension, and diffuse erythematous macular rash (erythroderma) that can progress to multiorgan involvement
1095
Scarlet fever
- primarily seen in children - group A strep infection occurs earlier at another site (tonsillitis, pharyngitis) - skin findings are preceded by prodrome of fever, headache, vomiting, and sore throat - 12-48 hrs later, fine pink blanching papules appear on the neck and upper trunk and quickly generalize w/ flexural accentuation (rough, sandpaper-like texture)
1096
Daughters of women who received diethylstilbestrol during pregnancy are at increased risk of developing clear cell adenocarcinoma of the vagina and cervix. In addition, daughters and sons w/ in-utero exposure are at risk for genital tract anomalies.
.
1097
risk factors for squamous cell carcinoma of the cervix and vagina
-HPV and tobacco
1098
Multiple myeloma
- plasma cell disorder | - presents w/ lytic lesions, hypercalcemia, and renal failure
1099
Autosomal dominant polycystic kidney disease
- usually present w/ HTN, hematuria, proteinuria, palpable renal masses, or progressive renal insufficiency - may also have flank pain due to renal calculi, cyst rupture or hemorrhage, or upper UTI - HTN is a common early finding in pts w/ ADPKD and usually precedes the decline in renal function
1100
HIV and hep C infection should be suspected in pts w/ weight loss and hx of IV drug abuse. Pts w/ HIV are at risk of developing depression and dementia.
.
1101
Inhaled anti-muscarinic agents such as ipratropium are the mainstay of symptom management in COPD. These anti-cholinergic meds may be combined w/ short acting beta agonists for greater symptom relief.
.
1102
Epidermal inclusion cyst
- benign nodule containing normal epidermis that produces keratin - pts usually develop a dome-shaped, firm, freely movable cyst or nodule w/ a small central punctum - the lesion can remain stable or gradual increase in size but usually resolves spontaneously
1103
Gastrinoma (Zollinger-Ellison syndrome)
- suspect in pts w/ multiple stomach ulcers and thickened gastric folds on endoscopy - diagnosis is strongly suggested by a fasting serum gastrin level > 1000 pg/mL - pts w/ non-diagnostic serum gastrin levels should be evaluated w/ a secretin stimulation test
1104
triple therapy for H. pylori
PPI, amoxicillin, clarithromycin
1105
Bowel ischemia and infarction are possible early complications of operation on the abdominal aorta, such as AAA repair.
.
1106
Pronator drift
- relatively sensitive and specific physical exam finding for upper motor neuron damage affecting the upper extremities - some stroke pts will demonstrate pronator drift in the absence of other significant findings
1107
Dressler's syndrome
- presents weeks after a MI w/ chest pain that is improved by leaning forward - NSAIDs are the treatment of choice - anticoagulation should be avoided to prevent development of a hemorrhagic pericardial effusion
1108
Pts w/ esophageal dysphagia can initiate swallowing but have difficulty passing food down the esophagus. Dysphagia initially with solids and eventually liquids is likely due to a mechanical obstruction; dysphagia which affects solids and liquids from the onset is more likely due to a motility disorder. Barium swallow is recommended initially for suspected motility disorders, followed by motility studies (manometry) to confirm the diagnosis
.
1109
tx of acute limb ischemia
-start IV heparin immediately upon suspicion; definitive tx is surgical embolectomy or intra-arterial fibrinolysis/mechanical embolectomy via interventional radiology
1110
Cilostazol
- inhibits platelet aggregation and causes vasodilation | - sometimes used to treat chronic claudication
1111
Sickle cell is usually a chronic normocytic, hemolytic anemia w/ appropriate reticulocytosis response. Folate deficiency can occur due to increased RBC turnover and increased consumption of folate in the bone marrow. Daily folic acid supplementation is recommended in all SCD pts.
.
1112
Diastolic and continuous murmurs as well as loud systolic murmurs should always be investigated using TTE. Midsystolic soft murmurs in an asymptomatic young patient are usually benign and need no further work-up.
.
1113
Contrast administration has the potential to cause contrast-induced nephropathy, particularly in pts w/ renal insufficiency (Cr > 1.5) and/or diabetes. Non-ionic contrast agents are associated w/ lower incidence of nephropathy than the older ionic hyperosmolar agents. In addition, adequate IV hydration and acetylcysteine can decrease the incidence of nephropathy.
.
1114
Granulomatosis w/ polyangiitis (Wegener's)
- triad of systemic vasculitis, upper and lower airway granulomatous inflammation, and glomerulonephritis - nasal cartilage destruction and vasculitic cutaneous lesions (tender nodules, palpable purpura, ulcerations) are common external manifestations
1115
Primary Raynaud phenomenon
- increased vascular response to cold temperature or emotional stress - usually found in women age
1116
Uremic pericarditis (UP)
- occurs in 6-10% of renal failure pts, typically those w/ BUN levels > 60 mg/dL - most UP pts do not present w/ the classic ECG changes of pericarditis (eg diffuse ST segment elevation) - hemodialysis leads to rapid resolution of chest pain and reduces the size of any associated pericardial effusion
1117
Hypertrophic cardiomyopathy (HCM)
- autosomal dominant genetic disorder caused by mutation in one of several genes encoding the myocardial contractile proteins of the cardiac sarcomere - mutations in the cardiac myosin binding protein C gene and cardiac beta-myosin heavy chain gene are responsible for about 70% of identifiable mutations in pts w/ HCM
1118
Howell-Jolly bodies
- nuclear remnants within RBCs typically removed by the spleen - their presence strongly suggests physical or functional hyposplenism
1119
Heinz bodies
- hemoglobin precipitation seen in G6PD deficiency - hemoglobin becomes oxidized and forms insoluble precipitants - appear after staining w/ crystal violet dye
1120
Rectal bleeding does NOT usually occur in the setting of ACUTE diverticulitis
.
1121
Bowel ischemia may complicate up to 7% of procedures on the aortoiliac vessels and most commonly affects the distal left colon. Pts report dull pain over the ischemic bowel as well as hematochezia. Colonoscopy shows a discrete segment of cyanotic and ulcerated bowel.
.
1122
hydrocele
- most cases will disappear spontaneously by the age of 12 months and can be safely observed during that period - those that do NOT resolve spontaneously should be removed surgicallly due to risk of inguinal hernia
1123
Performance-related anxiety
- classified as social anxiety disorder, performance-only type - PRN beta-blockers or benzo's in pts w/o hx of substance abuse - CBT
1124
Lyme arthritis
- most common late manifestation of untreated Lyme disease | - synovial fluid typically about 25,000 WBC
1125
Threatened abortion
-any hemorrhage occurring before the 20th wk of gestation w/ a live fetus and closed cervix
1126
most common organisms responsible for epiglottitis, especially in adult population
H. influenza and Strep pyogenes
1127
Chronic HTN w/ superimposed preeclampsia
-HTN that occurs before pregnancy or before 20 weeks gestation w/ subsequent development of proteinuria
1128
Alpha-1 antitrypsin deficiency
-associated w/ panacinar emphysema and cirrhosis
1129
most common cause of nephrotic syndrome in children
minimal change disease - light microscopy shows normal architecture - EM shows effacement of foot processes - no biopsy if under 10 - tx w/ steroids
1130
most common cause of nephrotic syndrome in adults
FSGS
1131
second most common cause of nephrotic syndrome in adults
membranous glomerulonephritis (thickened BM, subepithelial spikes)
1132
Histoplasma capsulatum
- common and usually asymptomatic infection in endemic areas like Mississippi and Ohio River valleys and Central America - usually found in soil w/ a high concentration of bird or bat guano droppings
1133
Folic acid and cobalamin deficiencies both cause a macrocytic anemia w/ hypersegmented neutrophils. Deficiencies in either nutrient will result in increased homocysteine levels because both are involved in converting homocysteine to methionine. Only cobalamin deficiency, however, will cause an increase in methylmalonic acid (converts methylmalonyl-CoA to succinyl-CoA)
.
1134
normal osmolar gap
1135
rectangular, envelope-shaped crystals
- calcium oxalate crystals | - ethylene glycol poisoning
1136
Newborns of mothers w/ active hepatitis B infection should be passively immunized at birth w/ hepatitis B immune globulin followed by active immunization w/ recombinant HBV vaccine.
.
1137
Pemphigus vulgaris
- mucocutaneous blistering disease that is characterized by flaccid bullae and intercellular IgG deposits in the epidermis - autoantibodies are formed against desmoglein, an adhesion molecule
1138
Bullous pemphigoid
- benign pruritic disease characterized by tense blisters | - immunofluorescence shows IgG and C3 deposits in the dermal-epidermal junction
1139
Inflammatory acne
- tx w/ topical retinoids and benzoyl peroxide - moderate and moderate to severe cases will benefit from the addition of topical antibiotics - oral abx and isotretinoin are usually reserved for severe or recalcitrant acne
1140
Diabetic autonomic neuropathy
- can affect the GU tract to cause a neurogenic bladder w/ urinary retention and distended bladder - pts can then develop overflow incontinence (eg dribbling, poor urinary stream) w/ a high post-void residual volume
1141
Hemophilia A and B
- X-linked recessive bleeding disorders from factor VIII (A) and IX (B) deficiency - recurrent hemarthrosis and skeletal muscle hemorrhage after mild trauma are the most common manifestations of this disorder - hematuria is also seen, but renal function is usually normal
1142
what should you suspect in a young female w/ bilateral trigeminal neuralgia?
Multiple sclerosis
1143
what is atrophied in Huntington's disease?
Caudate nucleus
1144
what is a well-known complication of giant cell or temporal arteritis?
- Aortic aneurysms (due to involvement of the branches of the aorta) - pts should be followed w/ serial chest x-rays
1145
causes of membranous glomerulonephritis
-hepatitis B and C, syphilis, gold, penicillamine, SLE, and rheumatoid arthritis
1146
frostbite injuries
- best tx is rapid re-warming w/ warm water - NO ATTEMPT SHOULD BE MADE TO DEBRIDE ANY TISSUE INITIALLY; true demarcation between dead and viable tissue may take weeks
1147
Give the appropriate pain medications to cancer pts. Do NOT be afraid to use a narcotic drug if it is the most appropriate.
.
1148
Inactivation of pancreatic enzymes by increased production of stomach acid may lead to malabsorption in pts w/ Zollinger-Ellison syndrome
.
1149
Warfarin-induced skin necrosis
- typically occurs within the first few days of warfarin therapy - caused by a rapid decline in protein C levels, usually in pts w/ underlying hereditary protein C deficiency - tx involves immediate warfarin cessation and administration of protein C concentrate
1150
Heparin-induced thrombocytopenia
-caused by autoantibodies to platelet factor 4 (PF4) complexed w/ heparin, and is characterized by thrombocytopenia, arterial or venous thrombosis, and necrotic skin lesions at heparin injection sites within 5-10 days of therapy
1151
antithrombin III
- vitamin K-independent inhibitor of the clotting cascade | - antithrombin III deficiency predisposes to thrombus formation
1152
Factor V Leiden mutation
-increases the risk of venous thromboembolism -also increase risk of cerebral, mesenteric, and portal vein thrombosis -
1153
alcohol withdrawal
- develop signs between 12-48 hrs after last drink - acute stage: sweating, hyperreflexia, tremors, and seizures - next is acute hallucinosis in the absence of autonomic symptoms - final stage is delirium tremens: altered sensorium, hallucinations, autonomic instability (tachycardia, fever, sweating)
1154
Beta blocker overdose
- presents w/ bradycardia, hypotension, wheezing, hypoglycemia, delirium, seizures, and cardiogenic shock - IV fluids and atropine are first-line tx - IV glucagon should be administered in pts w/ profound or refractory hypotension
1155
Aminophylline
- methylxanthine which acts by blocking phosphodiestease, thereby increasing levels of cAMP - causes bronchodilation and has positive inotropic/chronotropic effects
1156
symptoms of digoxin toxicity
- life threatening arrhythmias - anorexia, N/V, abdominal pain - fatigue, confusion, weakness, CHANGES IN COLOR VISION
1157
Congenital hypothyroidism
- associated w/ neurodevelopmental injury if not recognized and treated early - decreased activity, hoarse cry, jaundice; majority of infants are asymptomatic though - thyroid dysgenesis is the most common cause worldwide
1158
what is the opening pressure in idiopathic intracranial HTN?
> 250 mm H2O
1159
The classic VSD murmur is harsh, holosystolic murmur best heard at the left lower sternal border. Echo should be performed to determine the location and size of the defect and to rule out other defects. Most small VSD close spontaneously and require no treatment.
.
1160
Best diagnostic test for diverticulitis in the acute setting?
Abdominal CT -look for inflammation in pericolic fat, presence of diverticula, bowel wall thickening, soft tissue masses (eg phlegmons), and pericolic fluid collections suggesting abscess
1161
Ruptured ovarian cyst
- presents w/ acute onset of unilateral pelvic pain immediately after strenuous activity or sexual intercourse - pelvic US can show free fluid in the pelvis - supportive care (eg analgesics) is recommended for uncomplicated cyst rupture; complicated rupture may require surgical intervention
1162
Respiratory distress syndrome
- caused by surfactant deficiency - important risk factors include prematurity and maternal diabetes mellitus - fetal hyperglycemia causes hyperinsulinemia, which antagonize cortisol and block the maturation of sphingomyelin
1163
Choanal atresia
- should be suspected in an otherwise well-appearing infant w/ intermittent cyanosis and distress during feeding that is relieved by crying - failure to pass a catheter through the nose into the oropharynx is suggestive of the diagnosis - a CT scan shows narrowing at the level of the pterygoid plate in the posterior nasal cavity
1164
First-line tx for OCD
SSRI or clomipramine
1165
acetaminophen toxicity
-causes centrilobular or diffuse hepatocyte necrosis
1166
alcoholic hepatitis on histopathology
-hepatocyte swelling and necrosis, Mallory bodies, and neutrophilic infiltration
1167
Primary sclerosing cholangitis
-periductal portal tract fibrosis and segmental stenosis of extrahepatic and intrahepatic bile ducts
1168
Severe pain in a patient w/ a mild urinary obstruction, such as BPH, may cause urinary retention due to inability to Valsalva.
.
1169
Amiodarone
-class 3 antiarrhythmic agent frequently used for conversion and maintenance of sinus rhythm in pts w/ AF
1170
Antithrombotic therapy w/ warfarin (or other anticoagulants such as dabigatran, rivaroxaban, and apixaban) is the most effective way to reduce the risk of systemic embolization in pts w/ nonvalvular AF. Risk stratification w/ the CHADS2 scoring system should be used in all AF pts to assess the need for long-term anticoagulation.
.
1171
Hypothyroidism should always be considered in pts w/ an unexplained elevation of serum creatine kinase concentration and myopathy. ANA may be positive in pts w/ Hashimoto's thyroiditis. Serum TSH is the most sensitive test to diagnose hypothyroidism
.
1172
Secondary amyloidosis
- complication of a chronic inflammatory condition (eg chronic infections, IBD, rheumatoid arthritis) resulting in extracellular tissue deposition of fibrils into tissues and organs. - pts can develop multi organ dysfunction (eg kidneys, liver, GI) - tx involves treating the underlying condition and Colchicine
1173
differentiate preseptal vs orbital cellulitis
- preseptal cellulitis is a mild infection of the eyelid anterior to the orbital septum - orbital cellulitis is a serious infection posterior to the orbital septum - orbital cellulitis causes pain w/ extraocular movements, diplopia, and ophthalmoplegia - dangerous complications include blindness and intracranial infection from orbital cellulitis
1174
surgery is rarely needed for MCL tears; bracing and early ambulation is the preferred treatment.
.
1175
Antiphospholipid antibody syndrome
- associated w/ false positive VDRL, prolonged PTT, and thrombocytopenia - can promote arterial and venous thromboses and a resultant tendency toward spontaneous abortions - prophylaxis w/ low dose aspirin and LMWH are recommended to avoid pregnancy loss
1176
Meningococcal vaccination
- should be provided to all adolescents at age 11-12 - a booster is recommended at age 16 - esp. important for military recruits, college students living in dorms, and travelers to sub-Saharan africa
1177
most common cause of viral meningitis
the non-polio enteroviruses, such as echoviruses and coxsackieviruses
1178
Erythema toxicum neonatorum
- benign neonatal rash characterized by blanching erythematous papules and/or pustules - resolves spontaneously within 2 wks after birth
1179
Maternal comorbidities such as chronic HTN require antepartum fetal surveillance to diagnose fetal compromise and prevent death. Nonstress tests should be performed at least weekly in the third trimester until delivery. A normal result consists of 2 heart rate accelerations and is reassuring.
.
1180
most common predisposing factor for acute bacterial sinusitis
viral URI
1181
Ludwig's angina
- infection of the submandibular and sublingual glands - the source of infection is most commonly an infected tooth, usually the second or third mandibular molar - asphyxiation is the most common cause of death in this disease - pts present w/ fever, dysphagia, odynophagia, and drooling
1182
first-line pharmacotherapy for enuresis
- Desmopressin - it can provide immediate improvement for frustrated families when behavior modifications and alarm therapy have failed but has a high rate of relapse if used alone
1183
Loss of consciousness is seen w/ complex partial seizures and partial seizures w/ secondary generalization, but not simple partial seizures. Pts w/ complex partial seizures typically have AUTOMATISMS during their loss of consciousness; these activities include chewing, picking movements of the hands, and lip smacking. In contrast, pts w/ a partial seizure with secondary generalization usually have tonic-clonic manifestations (diffuse muscle aches, elevated CPK).
.
1184
Noninvasive evaluation w/ compression US is recommended as an initial test in pts w/ moderate or high probability of DVT. In pts w/ low probability, a D-dimer assay can further assess risk, w/ an US performed only in pts w/ a positive D-dimer.
.
1185
A young woman who presents w/ a breast lump can be asked to return after her menstrual period for reexamination (which may reveal regression of the mass) if no obvious signs of malignancy are present.
.
1186
tx option for psoriatic arthritis
NSAIDS, methotrexate, anti-TNF agents
1187
VIPoma
- rare tumor affecting the pancreatic cells that produce VIP - most pts develop VIPoma syndrome (pancreatic cholera) w/ watery diarrhea, muscle weakness/cramps (due to hypokalemia), and hypo- or achlorhydria (due to decreased gastric acid secretion) - stool studies are consistent w/ secretory diarrhea; a VIP level > 75 pg/mL confimrs the diagnosis - most are located in the tail of the pancreas
1188
Carcinoid syndrome
- flushing, diarrhea, bronchospasm | - 70-80% arise in small intestine
1189
Hypocalcemia
- can occur during or immediately after surgery in pts undergoing major surgery and requiring extensive transfusions - HYPERactive deep tendon reflexes may be the initial manifestation
1190
any pt who returns from a developing country and has symptoms suggestive of malabsorption should be considered for empirical tx w/ metronidazole for giardiasis. Remember the pathophysiology (adhesive disks and malabsorption)
.
1191
what is the most common complication of peptic ulcer disease?
hemorrhage!
1192
Paget's disease of bone
- abnormal bone remodeling in "mosaic" pattern - many pts are asymptomatic and are diagnosed after an isolated elevation in alkaline phosphatase is noted on lab testing - headaches, increased head size, hearing loss, and compression of cranial nerves, spinal cord, or spinal nerve roots
1193
in the absence of identifiable bacteria on culture or Gram stain, a mucopurulent urethral discharge in a pt who is sexually active suggests chlamydial urethritis. Nucleic acid amplification testing confirms the diagnosis.
.
1194
Asymptomatic diverticulosis needs only dietary modifications in the form of HIGH FIBER INTAKE.
.
1195
Burr cells
- aka echinocytes | - spiculated RBCs seen in liver disease and end-stage renal disease
1196
Howell-Jolly bodies
- basophilic nuclear remnants that appear as small, black pellets in RBCs - seen in pts w/ hx of splenectomy or functional asplenia
1197
Spur cells
- aka acanthocytes | - RBCs w/ irregularly sized and spaced projections that are most commonly seen in liver disease
1198
Scleroderma renal crisis
- typically presents w/ acute renal failure (w/o previous kidney disease) and malignant HTN (eg headache, blurry vision, nausea). - UA may show mild proteinuria - peripheral blood smear can show microangiopathic hemolytic anemia w/ schistocytes and thrombocytopenia
1199
Initial hematuria suggests urethral damage. Terminal hematuria indicates bladder or prostatic damage, and total hematuria reflects damage in the kidney or ureters. Clots are NOT usually seen w/ renal causes of hematuria.
.
1200
Histoplasma
- usually causes an asymptomatic or minor respiratory illness in healthy pts, but immunocompromised pts can develop severe pulmonary or disseminated disease - the most rapid and sensitive test to diagnose disseminated histoplasmosis in immunocompromised pts is URINE or SERUM assay for Histoplasma antigen
1201
preferred antifungal tx for histoplasmosis?
Itraconazole for mild to moderate disease. Amphotericin B for severe disease
1202
COPD is characterized by progressive expiratory airflow limitation which causes air trapping, decreased VC and increased TLC. FEV1 is disproportionately decreased as compared to VC.
.
1203
Germ cell tumors typically affect young pts and display aggressive biologic behavior. Nonseminomatous germ cell tumors typically produce BOTH alpha fetoprotein and b-HCG! Also often present with anterior mediastinal mass.
.
1204
Congenital syphilis
- presents early on w/ hepatosplenomegaly, cutaneous lesions, jaundice, anemia, and rhinorhea - metaphyseal dystrophy and periostitis may be seen on radiography
1205
blueberry muffin rash
congenital rubella
1206
congenital CMV
-intrauterine growth restriction, hepatosplenomegaly, petechiae or purpura, microcephaly, chorioretinitis, sensorineural hearing loss, and periventricular calcifications
1207
mesna
-used to prevent hemorrhagic cystitis caused by cyclophosphamide
1208
n-acetylcysteine
-antidote for acetaminophen overdose and nephroprotective agent to prevent radiocontrast-induced nephropathy
1209
Gout
- can result from overproduction or underexcretion of uric acid - induction chemo results in rapid tumor cell lysis and releases uric acid into the circulation - distinguish between prevention and tx of gout: for prevention, allopurinol and probenecid are use; for tx during acute attacks, NSAIDs, colchicine, and steroids are used
1210
Allopurinol inhibits xanthine oxidase, which results in decrease PRODUCTION of uric acid. Probenecid increases uric acid excretion and has a slight increased risk of uric acid kidney stones with use.
.
1211
Lactose intolerance
- diagnosis: improvement after abstaining from dairy; acid pH of stool; presence of positive reducing sugars - confirmed by HYDROGEN BREATH TEST
1212
HUS
- suspect in child w/ sudden-onset abdominal pain, bloody diarrhea, and triad of anemia, thrombocytopenia, and renal failure - tx is supportive; possibly plasmapheresis
1213
pericardial effusion
- appears as an enlarged, "water bottle" shaped cardiac silhouette on CXR - physical exam findings of effusion w/o cardiac tamponade include diminished heart sounds on auscultation and a difficult to palpate PMI
1214
conditions w/ an S4 heart sound
-hypertensive heart disease, aortic stenosis, hypertrophic cardiomyopathy, acute phase of MI
1215
all children w/ recurrent episodes of nocturnal vulvar itching should be examined for pinworms and tx empirically w/ MEBENDAZOLE.
.
1216
Pts w/ severe aortic stenosis can have anginal chest pain due to increased myocardial oxygen demand
.
1217
Bedwetting is normal before age 5. Mastery of nighttime continence can take months to years, and boys generally achieve this milestone later than girls.
.
1218
SABAs administered 10-20 minutes before exercise are the first-line tx for exercise-induced bronchoconstriction if required only a few times a week (less than daily). Inhaled corticosteroids or anti-leukotriene agents can be used in pts who exercise daily.
.
1219
Riedel's (fibrous) thyroiditis
- inflammatory disorder characterized by fibrosclerosis of the thyroid, surrounding tissues, and often remote nonthyroidal structures (eg retroperitoneum) - subclinical or overt hypothyroidism may be seen, but most pts have a hard goiter
1220
any patient w/ an acute, severe illness may have abnormal thyroid function tests. Euthyroid sick syndrome ("low T3 syndrome") is characterized by a fall in total and free T3 levels w/ normal T4 and TSH levels.
.
1221
Platelet dysfunction is the most common cause of abnormal hemostasis in pts w/ chronic renal failure. PT, PTT, and platelet count are normal. Bleeding time is prolonged. DDAVP is usually the tx of choice, if needed. DDAVP increases the release of factor VIII: von Willebrand factor multimers from endothelial storage sites. Platelet transfusion is not indicated because the transfused platelets quickly become inactive
.
1222
Angiodysplasia
- common cause of recurrent or occult painless lower GI bleeding in pts age > 60 years - they have been reported to cause lower GI bleeding in pts w/ aortic stenosis (Heyde's syndrome) and end-stage renal disease due to increased bleeding risk in these pts unmasking sites prone to bleeding
1223
Nephrotic syndrome
- defined by: Proteinuria (> 3.5 g/day), hypoalbuminemia, edema, hyperlipidemia and lipiduria - HYPERCOAGULABLE condition which manifests as venous or arterial thrombosis, and even PE - renal vein thrombosis is the most frequent manifestation - complications include: protein malnutrition, iron-resistant microcytic hypochromic anemia, increased susceptibility to infection, and vitamin D deficiency
1224
obstructive vs restrictive lung disease
-obstructive: FEV1 70%, FVC
1225
Asthma diagnosis
- can be diagnosed in late adulthood - confirmed by PFTs - reversible airway obstruction (>12% increase in FEV1) w/ normal diffusion capacity for carbon monoxide suggest asthma regardless of age
1226
organism responsible for Kaposi sarcoma?
-human herpesvirus-8 (HHV-8)
1227
Dermatofibromas
-nontender, firm, hyperpigmented nodules that are usually
1228
Febrile nonhemolytic transfusion reaction
- most common adverse reaction that occurs within 1-6 hrs of transfusion - pts usually develop fever, chills, and malaise w/o hemolysis - leukoreduction of donor blood can prevent febrile nonhemolytic reaction and reduce the risk of HLA alloimmunization and CMV transmission
1229
a reciprocal translocation of chromosomes 9 and 22 can form the Philadelphia chromosome containing the BCR/ABL fusion gene, which is characteristic of CML. Tyrosine kinase inhibitors, which function by inhibiting the abnormal BCR/ABL gene, are a key component of tx for CML.
.
1230
Adhesive capsulitis
- results from chronic inflammation, fibrosis, and contracture of the joint capsule - pts experience shoulder stiffness out of proportion to pain, and exam shows reduction of both passive and active ROM
1231
Hepatojugular reflux
- clinically useful to differentiate between cardiac and liver disease-related causes of lower extremity edema - pts w/ peripheral edema due to heart failure have elevated JVP and positive hepatojugular reflux - those w/ peripheral edema from primary hepatic disease and cirrhosis have reduced or normal JVP and negative hepatojugular reflux
1232
The proximal deep leg veins are the most common source of symptomatic pulmonary embolism. Other less common sources of emboli include the calf veins, renal veins, pelvic veins, upper extremity veins, and right heart.
.
1233
Copious purulent ocular drainage and eyelid swelling in a 2 to 5 day old newborn are most consistent w/ what?
- Gonococcal conjunctivitis - can be prevented w/ application of topical erythromycin ointment within 1 hr of birth - conjunctivitis caused by Chlamydia trachomatis is usually milder and presents 5-14 days after birth
1234
Pts w/ Turner syndrome have a higher risk of osteoporosis due to lower estrogen levels and only having one copy of X chromosome genes involved in bone metabolism.
.
1235
the most common and feared complication associated w/ TPN?
catheter tip infection
1236
Nonstress test (NST)
- administered in high risk pregnancies to assess for fetal hypoxemia - considered reactive if there are 2 or more heart rate acclerations of 15 bpm above baseline that last for 15 seconds over 20 minutes of observation
1237
Ecthyma gangrenosum
- associated w/ Pseudomonas aeruginosa bacteremia that is characterized by rapidly progressive skin lesions that develop into nontender nodules w/ central necrosis - can be seen in pts who are immunocompromised, and tx should consist of anti-pseudomonal antibiotics
1238
Pts w/ chest pain, signs of decreased cardiac output, and pulsus paradoxus following a viral infection most likely have cardiac tamponade resulting from acute pericarditis. In this setting, right atrial filling is impaired, which results in an increase in the systemic venous pressure. However, the lungs remain clear to auscultation because there is no backup of blood into the pulmonary circulation.
.
1239
Pulmonary fibrosis
- causes decreased compliance of the lungs, and spirometry typically reveals decreased TLC, decreased FVC, decreased FEV1, and a normal FEV1/FVC ratio - bibasilar fine, dry crackles are typically heard on auscultation - note that normal values for FEV1 and the FEV1/FVC ratio are between 80% - 120% of predicted values!!!!
1240
spirometry findings in COPD
-decreased FEV1, normal FVC, decreased FEV1/FVC ratio
1241
Paraneoplastic Cushing syndrome
- most commonly caused by ectopic ACTH production by SMALL CELL LUNG CARCINOMA - hyperpigmentation is frequently present and is due to coproduction of melanocyte-stimulating hormone w/ ACTH
1242
overproduction of amino acid-derived hormomes
-typically seen in neuroendocrine tumors, such as carcinoid (serotonin) or pheochromocytoma (norepinephrine, epinephrine)
1243
Protraction of labor
- refers to a slow progression of cervical dilatation, whereas arrest disorders are diagnosed when the cervix ceases to dilate after reaching at least 4 cm - if the membranes are still intact, an amniotomy is usually the first step to promote the progression of labor
1244
Tuberculosis
- common cause of pleural effusions - the effusion is exudative w/ protein concentrations often greater than 4 g/dL - the fluid also consists of a lymphocytic leukocytosis w/ no gross purulence and a glucose concentration typically mildly below the serum glucose level
1245
causes of exudative pleural effusions
-empyema, malignancy, RA, esophageal rupture, pancreatitis, pulmonary infarction, TB
1246
drug used to protect against infection w/ Mycobacterium avium complex in pts w/ a CD4 count
Azithromycin
1247
Once the HIV diagnosis is made, pts should be given the pneumococcal vaccine as soon as possible. They should receive it again in subsequent 5 year intervals. Tx w/ prophylactic abx is not usually indicated until the CD4 count is
.
1248
SVC syndrome
- potential complication of lung malignancy, and is manifested by headache, facial swelling, and jugular venous engorgement without peripheral edema - the primary tx is radiation therapy as a palliative measure
1249
conditions that predispose pts to the development of aspiration pneumonia
- impaired consciousness (such as alcoholics, epileptics, or pts w/ a recent stroke) - the presence of tracheal or NG tubes - impaired gag reflex
1250
Spontaneous bacterial peritonitis
- common complication of ascites in which the peritoneal fluid becomes infected by an enteric organism that translocates across the intestinal wall - the finding on paracentesis of greater than 250 neutrophils/uL in the ascitic fluid is diagnostic
1251
Bullous pemphigoid
- autoimmune blistering disease that typically causes the formation of bullae in the flexural surfaces, groin, and axilla - biopsy of the lesion characteristically shows a subepidermal blister under light microscopy and linear Ig of basement membrane under immunofluorescence
1252
Pemphigus vulgaris
- autoimmune disease that causes INTRAepidermal blistering - usually have involvement of the oral cavity, and intact blisters are rare - tombstone appearance under light microscope
1253
classic MRI findings of MS
-ovoid plaques in the periventricular region, corpus collosum, and deep white matter
1254
most common primary CNS tumor in adults
glioma
1255
Brain metastases
- most common intracranial tumor in adults - most often due to melanoma, lung, breast, or renal cancer - appear as peripheral, circumscribed, enhancing lesions surrounded by vasogenic edema on MRI
1256
Polymyalgia rheumatica
-characterized by proximal muscle tenderness as opposed to weakness, and elevations of AST, ALT, and CPK are NOT typically seen
1257
Polymyositis
- symmetric, proximal muscle weakness along w/ the elevation of muscle enzymes, such as LDH and CPK - diagnosis can be confirmed using combination of autoantibody tests, EMG, and muscle biopsy
1258
The presence of both UMN signs (hyperreflexia, Babinski sign) and LMN signs (fasciculations, atrophy) is typical of ALS. Nerve conduction studies, EMG, and neuroimaging can be obtained to exclude alternative diagnoses.
.
1259
Pts w/ complex partial seizures often stare blankly for several minutes and may engage in automatisms such as lip smacking or chewing. The presence of postictal confusion or paralysis (Todd's paralysis) helps distinguish complex partial seizures from other neurological disorders. Complex seizures involve a loss of consciousness (in contrast to simple seizures), and partial seizures involve seizure activity w/ a focal origin within the brain (in contrast to generalized seizures where seizure activity occurs globally throughout the cortex).
.
1260
does post-ictal confusion occur in Absence seizures?
NO!
1261
Both preterm labor and fetal lung immaturity have a higher incidence in diabetic mothers. Antenatal betamehasone can be given to promote fetal lung maturity, but the maternal blood glucose must be carefully followed.
.
1262
SLE
- can cause an inflammatory arthritis that is usually migratory, polyarticular, and symmetric - the knees and hands are most commonly involved - the presence of other signs of SLE, such as renal disease and photosensitivity, can help to establish the diagnosis of lupus
1263
Adenosine
-used in the treatment of SUPRAventricular tachycardia (think of the den above the ventricles)
1264
Digoxin
-used in tx of SUPRAventricular tachyarrhythmias such as atrial fibrillation (think of digging oxygen to prevent atrial fibrillation, which is a common effect of hypoxemia)
1265
Verapamil
- used to treat SUPRAventricular tachycardia if adenosine is not effective in terminating the rhythm - NOT EFFECTIVE FOR VENTRICULAR TACHYCARDIA!!!!!
1266
Wide-complex tachycardia
- should be considered to be ventricular in origin unless its definitively interpreted as supraventricular tachycardia w/ aberrancy - in stable pts, tx consists of a loading dose of AMIODARONE ("aims at the down one" (ventricle))
1267
brain metastases
- most common intracranial tumor in adults - most often due to melanoma, lung, breast, or renal cancer, and appear as peripheral, circumscribed, enhancing lesions surrounded by vasogenic edema on MRI
1268
Esophageal rupture usually leads to mediastinitis, which in turn can cause severe sepsis and death.
.
1269
Pancreatic calcifications and atrophy are frequently seen on abdominal CT in pts w/ chronic pancreatitis. Common clinical features include steatorrhea, abdominal pain, and diabetes mellitus. The most common cause of chronic pancreatitis is alcoholism.
.
1270
Tx for Wilson's disease
Penicillamine (copper binder)
1271
ABI
- ratio of SYSTOLIC BP of ankle to SBP of brachial artery | - a normal ABI is 1.0-1.3; values between 0.4-0.9 suggest peripheral artery disease, and values
1272
Tx for Guillain-Barre syndrome
-IVIG
1273
Primary hyperaldosteronism
- most often due to bilateral adrenal hyperplasia or an aldosterone-producing adrenal adenoma - adrenalectomy is recommended for an adenoma, whereas aldosterone antagonists are recommended for bilateral hyperplasia - best test is early morning plasma aldosterone to renin ratio; elevated aldosterone (> 15 ng/dL) w/ a PAC/PRA ratio > 20 suggests PH - pts w/ PH should undergo CT of adrenal glands
1274
Hypercalcemia of malignancy (HoM)
- usually due to increased tumor production of parathyroid hormone-related peptide (PTHrP) - PTH levels are suppressed in pts w/ HoM - serum calcium levels are generally much higher in HoM than in primary hyperparathyroidism!
1275
Pts who have had gastric bypass surgery have a higher incidence of developing gallstones due to an increase in bile concentration. Prophylactic tx w/ what is recommended to decrease this risk?
Ursodeoxycholic acid
1276
Hematuria can be due to glomerular or extraglomerular pathologies. Proteinuria suggests a glomerular cause. IgA nephropathy and post-strep glomerulonephritis are the 2 most common causes of glomerular hematuria in pts following a URI.
.
1277
an elevated phosphate level and a low calcium level in the setting of chronic kidney disease are characteristic of secondary hyperparathyroidism. The resulting elevation in parathyroid hormone can cause renal osteodystrophy w/ associated bone pain.
.
1278
ANCA antibodies
-most frequently associated w/ small vessel vasculitides such as granulomatosis w/ polyangiitis (Wegener's)
1279
anti-smooth muscle antibodies
autoimmune hepatitis
1280
anti-mitochondrial antibodies
-primary biliary cirrhosis (PBC)
1281
anti-centromere antibodies
CREST syndrome
1282
specific antibodies for SLE
-anti-dsDNA and anti-smith antibodies
1283
Visceral pain
-usually more difficult to localize (eg generalized, crampy abdominal pain that pts experience w/ small bowel obstruction)
1284
neuropathic pain
pain secondary to destruction of nerve tissue itself, as in peripheral neuropathy -burning and tingling are common symptoms
1285
causalgia
-complex regional pain syndrome of the extremities characterized by swelling, pain, and bone demineralization often following minor trauma
1286
somatic abdominal pain
- well-localized, and is usually secondary to peritoneal irritation - in contrast, visceral pain is more vague in localization, and is usually the result of mechanical stretching of the abdominal viscera
1287
SIADH
- characterized by the inability of the kidneys to excrete water due to an abnormal amount of ADH - clinically, SIADH is suspected in a pt w/ hyponatremia, low serum osmolality, elevated urine osmolality, and elevated urine sodium
1288
Muscarinic antagonists are used to treat urge incontinence (detrusor instability), the most common cause of urinary incontinence. Pts w/ detrusor instability experience intense urges to urinate that cannot be delayed.
.
1289
overflow incontinence
- may result from a neurogenic bladder, and is treated w/ augmented voiding techniques and cholinergic agonists - more severe cases are treated w/ intermittent or indwelling bladder catheterization
1290
Spontaneous bacterial peritonitis (SBP)
- should be suspected in any patient w/ ascites and altered mental status - a diagnostic paracentesis that reveals more than 250 neutrophils/mm3 is diagnostic of SBP!!!! - initial tx consists of broad-spectrum antibiotics
1291
Non-selective beta blockers such as propranolol or nadolol are often used to reduce the risk of esophageal variceal hemorrhage. Nitrates, endoscopic band ligation, and TIPS are other options that may be used to prevent variceal hemorrhage if B-blockers alone are ineffective.
.
1292
Myocarditis should be suspected in young pts w/ a recent viral illness who present w/ heart failure, chest pain, or arrhythmias. Most pts will have at least partial recovery of myocardial function, but some will develop dilated cardiomyopathy.
.
1293
Atopic dermatitis (eczema)
- in adults, typically presents w/ an erythematous, scaly, pruritic rash - usually located on the flexural surfaces of the arms and knees as opposed to the extensor surfaces in psoriasis
1294
nummular eczema
-coin shaped, very pruritic patches of eczema that tend to involve the back and lower extremities
1295
dyshidrotic eczema
- form of dermatitis that involves the palms and soles | - tiny fluid filled blisters on palms and fingers
1296
Pityriasis versicolor
- skin infection caused by the YEAST, Malassezia furfur | - results in abnormally colored macules that are most commonly seen on the trunk and upper extremities
1297
Painless jaundice
- should be considered to be pancreatic cancer until proven otherwise - elevation of bilirubin and alk phos implies a cholestatic cause of jaundice, which can be caused by blockage of the common bile duct by a pancreatic mass
1298
iron poisoning
- causes GI hemorrhage, which is made evident by bloody diarrhea and hematemesis - severe poisoning may result in metabolic acidosis, hepatotoxicity, bowel obstruction, or death
1299
CXR in pts w/ active TB
-upper lobe infiltrate w/ cavitation and hilar lymphadenopathy
1300
carotid sinus massage
-can be both diagnostic and therapeutic for pts w/ SUPRAventricular tachycardia (SVT)
1301
Hyperthyroidism should ALWAYS be considered in the evaluation of pts w/ atrial fibrillation, particularly if other signs or symptoms are present. TSH and free T4 are the appropriate initial diagnostic tests.
.
1302
new-onset seizures are a common presentation of brain tumors, the most common of which in adults are astrocytomas. The prognosis of astrocytomas is most affected by TUMOR GRADE, with increased atypia, mitoses, neovascularity, or necrosis conveying a worse prognosis.
.
1303
monoclonal antibodies directed against TNF-a
-used to treat certain inflammatory diseases, such as RA or Crohn's disease
1304
IL-1
-cytokine that can be used to treat pts w/ RA
1305
monoclonal antibodies directed against epidermal growth factor receptor (EGFR) (eg. cetuximab)
-used in tx of various cancers including colorectal cancer
1306
imatinib
-inhibits BCR-ABL tyrosine kinase that is present in WBC of pts w/ CML!!!
1307
CLL
- occurs in elderly individuals - can be asymptomatic or have nonspecific symptoms such as fatigue, weight loss, or night sweats - may pts have a good prognosis even w/o tx, but treatment w/ a monoclonal antibody directed against the CD20 antigen on B lymphocytes may be used in symptomatic pts.
1308
Infective endocarditis may be complicated by brain abscess through hematogenous seeding of bacteria or systemic embolization of vegetations. Pts may develop focal neuro deficits, evidence of elevated ICP, and fever. Diagnosis can be confirmed w/ gadolinium-enhanced brain MRI.
.
1309
Extrarenal fluid losses can result in hypovolemic hyponatremia due to secretion of ADH and retiention of free water. Pts have a decreased serum osmolality (normal is 285-295), decreased urine sodium concentration (
.
1310
Children w/ sickle cell disease are susceptible to splenic infarction, which predisposes them to infection w/ encapsulated organisms, particularly Strep pneumo. These pts should receive the pneumococcal vaccine and penicillin prophylaxis to lower the risk of serious pneumococcal infections.
.
1311
Pts w/ mitral valve prolapse (systolic murmur that prolongs w/ Valsalva due to decreased LV volume) have a slightly higher risk of developing infective endocarditis after certain invasive procedures than those w/ normal mitral valves. However, the 2007 AHA guidelines for the prevention of infective endocarditis do not recommend antimicrobial prophylaxis for pts w/ MVP, including those w/ mitral regurgitation!
.
1312
Dantrolene
-muscle relaxant used in the tx of nueroleptic malignant syndrome, which refers to an idiosyncratic reaction to D2 antagonists characterized by fever, diffuse rigidity, mental status changes, and autonomic instability
1313
Acute dystonia
- type of extrapyramidal symptom and a common side effect of antipsychotic meds, particularly high-potency 1st generation antipsychotics (haloperidol) - tx consists of anticholinergic meds or diphenhydramine
1314
ovarian cancer
- should be in the differential diagnosis in any middle-aged woman w/ vague pelvic complaints, particularly if an adnexal mass is palpated - intraperitoneal spread is common in advanced cases
1315
Small bowel obstruction
- seen on plain radiography as dilatation of the small bowel greater than 3 cm w/ absence of air within the colon - most common cause of SBO in developed nations is adhesions from prior abdominal surgeries; next most common causes are indirect hernias or obstructing lesions
1316
in aortic stenosis, there is increased blood velocity through the stenotic segment in order to keep blood flow relatively unchanged. This increased velocity may result in turbulence, which can be appreciated as a murmur on cardiac auscultation.
.
1317
recurrent attacks of epigastric or RUQ pain after eating w/ radiation to the right should or back is characteristic of gallstone disease. Risk factors for gallstone disease include obesity, female gender, age greater than 40, and pregnancy.
.
1318
bromocriptine
-used to tx hyperprolactinemia caused by pituitary adenomas
1319
pts w/ irregular menstrual periods, infertility, obesity, and hirsutism likely have PCOS. The best initial tx for resuming ovulation is weight loss, but clomiphene and/or metformin can be used if weight loss alone is ineffective.
.
1320
Episodic dizziness that occurs while rolling over in bed is a classic hx for benign paroxysmal positional vertigo (BPPV). The most effective tx for BPPV is repositioning the displaced otoliths w/ techniques such as the Epley maneuver.
.
1321
median nerve injury may occur w/ fractures that involve the supracondylar region of the humerus.
.
1322
frequent complication of humeral midshaft fractures
- radial nerve injury | - results in weakness of the wrist and finger extensors as well as loss of sensation in the dorsum of the hand
1323
If a metastatic pancreatic head carcinoma causes extrahepatic cholestasis due to common bile duct obstruction, then immediate tx should include endoscopic placement of a common bile duct stent.
.
1324
sickle cell vasoocclusive crisises
- generally cause diffuse MSK pain - management involves pain control, hydration, and supplemental oxygen - sickle cell disease in general is more common in african americans and affected pts are usually chronically anemic
1325
Quinidine
-class 1 antiarrhythmic med that blocks sodium channels
1326
clonidine
-alpha-2-adrenergic agonist that functions as an anti-hypertensive agent by decreasing sympathetic outflow from the CNS
1327
amlodipine
-dihydropyridine calcium channel blocker that produces vasodilatation, thereby reducing BP
1328
anticoagulation in addition to rate and/or rhythm control are the accepted tx's for atrial fibrillation. In the presence of tachycardia, beta-adrenergic antagonists (metoprolol or esmolol) or non-diphydropyridine (diltiazem, verapamil) CCBs can be used to rapidly control the heart rate.
.
1329
Mobitz type 1 (Wenckebach) second degree AV block
-characterized by normal P waves and a PR interval that gradually increases w/ successive beats until a P wave fails to conduct to the ventricles, resulting in the absence of a QRS complex
1330
atrial septal defect
- characterized by wide, fixed splitting of the second heart sound on physical exam - a systolic murmur sometimes heard at the left upper sternal border from increased flow across the pulmonary valve, but there is usually not a murmur from the ASD itself
1331
C. diff
- most common cause of antibiotic-associated colitis - pts present w/ low grade fever, diarrhea, abdominal pain, and leukocytes in the stool - the most appropriate tx is oral metronidazole or oral vancomycin
1332
Dementia w/ Lewy bodies
- round, eosinophilic, and intracytoplasmic inclusions within the neurons of the substantia nigra - episodic fluctuating cognitive function (eg daytime drowsiness, daytime naps lasting > 2 hours, prolonged staring spells, episodes of disorganized speech), visual hallucinations, and parkinsonism
1333
Septic shock should be suspected in pts w/ hemodynamic instability and evidence of an infection. The initial tx consists of IV fluids, followed by vasopressors such as dopamine or norepinephrine if the patient does not respond to fluid resuscitation.
.
1334
Urinary 5-HIAA excretion
- measured as part of the work-up for possible carcinoid syndrome - affected pts present w/ diarrhea, abdominal cramping, flushing and telangiectasias
1335
Parasitic infections present w/ diarrhea, abdominal pain, bloating, and eosinophilia. They are most common in pts living or traveling outside the US. The diagnosis is made through serial stool exams for ova and parasites.
.
1336
A patient w/ a combo of renal failure, hypercalcemia, and anemia?
- evaluate for multiple myeloma - renal failure can occur in multiple myeloma from a variety of causes, but the most common is a toxic effect of light chain casts on the renal tubules - diagnosis is confirmed w/ serum protein electrophoresis (SPEP), urine protein electrophoresis (UPEP), bone marrow biopsy, and skeletal survey w/ plain radiographs to assess for lytic lesions.
1337
self-destructive behavior
Lesch-Nyhan syndrome
1338
The presence of a fragile site in a segment of the X chromosome after cell culture in folate-deficient media is diagnostic of Fragile X syndrome. typical clinical features of this condition include autism spectrum behaviors, mental retardation, an elongated face, and large testes. Can also do molecular analysis of the number of CGG repeats in the FMR-1 gene on the X chromosome.
.
1339
Pts w/ chronic dementia are predisposed to delirium, which can be precipitated by acute infections or other medical stressors. If a patient becomes agitated to the point that they are endangering themselves, antipsychotic meds such as haloperidol are used as first-line therapy.
.
1340
Cervical cancer can potentially be prevented by Pap smear screening at age >21. Premenopausal women age >30 should undergo Pap smear and HPV testing. Those w/ a low-grade squamous intraepithelial lesion on Pap smear plus HPV 16 and 18 or unknown HPV status require further evaluation w/ colposcopy and biopsy.
.
1341
vulvovaginal candidiasis
- causes inflammation of the vulva and vagina, resulting in erythema and pruritis - it can be distinguished from other causes of vaginitis by a normal vaginal pH of 3.8 - 4.2
1342
Pts w/ 3 alpha globin chain mutations
- (a,-)(-,-) - hemoglobin H disease (composed of 4 beta chains) - severe microcytic, hypochromic anemia w/ target cells and Heinz bodies as well as hepatosplenomegaly
1343
alpha thalassemia minima
- characterized by one alpha globin gene mutation (a,a)(a,-) | - pts typically have no clinical or lab abnormalities
1344
mutations in all 4 alpha globin genes (-,-)(-,-)
- hydrops fetalis - most severe form of alpha thalassemia - not compatible with life
1345
heterozygous alpha thalassemia minor
- typically asymptomatic although pts may complain of mild fatigability - affected pts will have mild hypochromic anemia, severe microcytosis, and target cells - may be cis (a,a)(-,-) or trans (a,-)(a,-)
1346
Hemiparalysis w/ abnormal function of a contralateral cranial nerve is sometimes referred to as crossed paralysis, and localizes a particular lesion to the brainstem. In the case of hemiparalysis w/ contralateral facial weakness, the lesion is most likely located in the facial nerve nucleus in the pons.
.
1347
The initial medical work-up of new-onset psychiatric symptoms often includes head CT scan, CBC, thyroid function tests, syphilis screen, metabolic panel, and urine toxicology
.
1348
Ventricular septum rupture is a complication that can occur 3-5 days after an MI. Pts present w/ acute hemodynamic compromise and a holosystolic murmur at the left sternal border. Cardiac catheterization may show an influx of oxygenated blood from the left ventricle into the right ventricle, as well as an increase in right-sided heart pressures from increased flow.
.
1349
cardiac tamponade classically causes equilibration of diastolic pressures on cardiac catheterization.
.
1350
PE should be considered in pts w/ hypoxia, tachypnea, and tachycardia. On cardiac catheterization, right heart pressures are elevated, as is the gradient between the pulmonary artery and the PCWP.
.
1351
normal pulmonary capillary wedge pressure?
6-12 mmHg | -provides indirect estimate of left atrial pressure
1352
Mitral stenosis
- characterized by a low-pitched diastolic murmur heard best at the apex - occurs earlier in diastole w/ worsening stenosis, and can become holodiastolic in pts w/ severe stenosis
1353
cervical cancer screening
- immunocompromised: onset of sexual intercourse; every 6 months x 2 then annually - age 65: no screening if negative prior screens and not high risk for cervical cancer - hysterectomy (w/ cervix removed): no screening if no hx of high-grade precancerous lesion, cervical cancer, or exposure to diethylstilbestrol
1354
sreening mammography is recommended every 2 years for women age > 50 as it can diagnose early asymptomatic breast cancer and improve mortality among screened pts. Other recommendations include monitoring lipid profile every 5 years and colon cancer screening (eg colonoscopy every 10 yrs). Cervical cancer screening can be discontinued in women > age 65 w/ previously normal results and low cervical cancer risk.
.
1355
a systolic murmur heard best at the left sternal border that decreases in intensity w/ increased preload
- characteristic of hypertrophic cardiomyopathy | - common in young pts who present w/ syncope, and is important to diagnose because it can lead to sudden cardiac death
1356
Pain relief w/ elevation of the testicle?
Epididymitis
1357
the acute onset of testicular pain in a teenage male should be considered testicular torsion until proven otherwise, and is a potential surgical emergency. The cremasteric reflex is almost always absent in testicular torsion and Prehn's sign (pain relief w/ evelation of the testicle) will be NEGATIVE, differentiating it from epididymitis.
.
1358
common adverse effects associated w/ cisplatin?
-nephrotoxicity, tinnitus and hearing loss, electrolyte abnormalities, severe nausea and vomiting, and neurotoxicity
1359
Findings for nephrotic syndrome
- urine protein excretion of > 3.5g/day, edema, and hypoalbuminemia - FSGS is the most common cause of NS in adults, particularly african americans
1360
pulmonary contusions
-common consequence of thoracic trauma that generally manifest over the course of the first day w/ an airspace opacity on CXR and findings consistent w/ alveolar fluid on physical exam
1361
Lennox-Gastaut syndrome
-typically diagnosed in children under the age of 7 who have a wide array of seizure types accompanied by mental retardation
1362
Juvenile myoclonic epilepsy
- usually present in their teenage years w/ a progression from absence to myoclonic to generalized tonic-clonic seizures - the seizures typically occur upon awakening - JME is genetic, and symptoms can be worsened w/ sleep deprivation
1363
Cushing's syndrome
- presents w/ central obesity, proximal muscle weakness, androgen excess, menstrual irregularities, HTN, and easy bruising - in the absence of exogenous glucocorticoid administration, the most common etiologies of Cushing's syndrome include increased pituitary secretion of ACTH (Cushing's disease), an adrenal tumor, and ectopic ACTH production
1364
Venodilation decreases the pain associated w/ acute MI by reducing preload, which leads to a reduction in myocardial oxygen demand. This effect is most commonly caused by the use of organic nitrates in the setting of acute MI
.
1365
Intestinal malrotation and midgut volvulus
- should be suspected in any neonate w/ bilious vomiting - rapid evaluation and surgical tx is required as bowel necrosis can develop quickly - the classic finding on upper GI series is a corkscrew-shaped duodenum that is abnormally located in the right abdomen
1366
tx for cryptococcal meningitis
combination of amphotericin B and flucytosine | -subacute presentation
1367
TREATMENT of toxoplasmosis
-pyrimethamine and sulfadiazine (NOT TMP-SMX!!!! This is for prophylaxis!!)
1368
Listeria monocytogenes
- important cause of meningitis in adults over the age of 60 and in immunocompromised pts - AMPICILLIN should be added to the empiric abx regimen of ceftriaxone and vancomycin in these pts
1369
oral colchicine
treats ACUTE gouty arthritis
1370
Febuxostat, allopurinol, probenecid
- febuxostat and allopurinol are xanthine oxidase inhibitors that decrease uric acid production - allopurinol is usually preferred, and febuxostat is reserved for pts who cannot tolerate allopurinol - probenecid is a uricosuric med that increases uric acid excretion in the kidneys
1371
lifestyle modifications, including alcohol cessation and weight loss, are considered first-line interventions following an initial gout attack. Meds for lowering serum urate are indicated for pts w/ repeated and disabling attacks of gouty arthritis, tophi, x-ray evidence of chronic gouty joint disease, uric acid kidney stones, or renal insufficiency
.
1372
an apical lung tumor in the thoracic inlet can compress the cervical and thoracic nerve roots that contribute to the ulnar nerve, resulting in pain, numbness and weakness in the ipsilateral arm.
.
1373
a diastolic decrescend murmur heard best at the left sternal border
- aortic regurgitation | - most common cause in an elderly patient w/ atherosclerotic risk factors is aortic root dilation
1374
Guillain-Barre syndrome
- typically presents w/ symmetric, ascending weakness and loss of reflexes w/ relative preservation of sensory function - it is often associated w/ a preceding respiratory or GI infection - the classic finding on LP in pts w/ GBS is an elevated protein content w/ a normal WBC count, referred to as ALBUMINOCYTOLOGIC DISSOCIATION
1375
somatic symptom disorder
-excessive anxiety and preoccupation with 1 or more unexplained symptoms
1376
illness anxiety disorder
-fear of having a serious illness despite few or no symptoms and consistently negative evaluations
1377
conversion disorder (functional neruologic symptom disorder)
-neurologic symptom incompatible w/ any known neurologic diseas; often acute onset associated w/ stress
1378
factitious disorder
-intentional falsification or inducement of symptoms w/ goal to assume SICK ROLE
1379
malingering
-falsification or exaggeration of symptoms to obtain external incentives (SECONDARY GAIN)
1380
most cases of pediatric pharyngitis are the result of self-limiting viral infections. No treatment or further workup is required when cough, runny nose, and oral vesicles are present.
.
1381
Churg-Strauss syndrome
- eosinophilic vasculitis | - may present w/ renal and upper airway symptoms, but asthma and eosinophillia are present in nearly all pts
1382
Granulomatosis w/ polyangiitis (Wegener's)
- form of granulomatous vasculitis that typically presents w/ involvement of the upper airways, lungs, and kidneys - diagnosis can be confirmed w/ serum ANCA testing or by finding granulomatous inflammation on biopsy of upper airway lesions
1383
Myelodysplastic syndrome (MDS)
- hematologic disorder that is more common in pts over 65 yrs old and usually presents w/ macrocytic anemia, leukopenia, and thrombocytopenia - ovalo-macrocytes are commonly seen on a peripheral smear along w/ neutrophils w/ decreased segmentation, as opposed to the megaloblastic, hypersegmented neutrophils seen in pts w/ B12 or folate deficiency
1384
atropine
-used in the treatment of severe bradycardia
1385
initial tx of pheochromocytoma
-first, a-blockade w/ a med such as phenoxybenzamine followed by the use of b-blockers, after which surgery should be performed
1386
impetigo
- presents as an erythematous skin lesion covered w/ a golden crust, and is typically seen on the face or upper extremities - S. aureus and group A strep are the most common etiologies - pts who have group A strep impetigo are at risk of developing post-strep glomerulonephritis
1387
COPD exacerbations
- should be diagnosed when a patient w/ underlying COPD presents w/ increased SOB, cough, or sputum production - systemic glucocorticoids should be given to pts w a COPD exacerbation because they have been shown to improve lung function and promote a shorter hospital stay
1388
tumor lysis syndrome
-marked by hypocalcemia, hyperphosphatemia, hyperkalemia, and elevated uric acid levels causing nausea and vomiting, bowel disturbances, low urine output, acute renal insufficiency, seizures, tetany, and/or arrhythmias
1389
Chemotherapy can cause neutropenia, putting pts at increased risk for systemic infections and sepsis. Neutropenic pts do not mount a normal immune response to infection, thus, signs and symptoms of sepsis may be subtler than in an immunocompetent patient.
.
1390
do NOT use topical abx on infected diabetic ulcers, debride instead and use oral or IV abx
.
1391
foot ulcers
- very common in diabetic pts due to a combination of peripheral neuropathy and peripheral vascular disease - important factors in evaluating foot ulcers include the depth of involvement and the presence of infection - if there is no infection and the ulcer does not involve the bone, debridement of the necrotic tissue is usually sufficient tx
1392
mood stabilizers, including lithium, lamotrigine, and valproic acid, are first-line maintenance treatments for bipolar disorder, w/ efficacy in bipolar depression w/ mixed features.
.
1393
Irregular menstrual periods, infertility, and galactorrhea are typical findings in hyperprolactinemia. It's commonly caused by a prolactin secreting pituitary adenoma, which can be treated w/ dopamine agonists to decrease the secretion of prolactin as well as to decrease the size of the tumor.
.
1394
observer bias
-type of measurement bias in which the investigator unconsciously influences the outcome of the study by knowing the exposure status of each participant
1395
The Hawthorne effect
-refers to a change in behavior that occurs if the participants know they are being studied
1396
ascertainment bias
-occurs when the results from an atypical population are extrapolated into the entire population
1397
if a patient's treatment regimen is selected based upon the severity of their condition, they may have a worse outcome because of selection bias and not necessarily due to the treatment itself.
.
1398
brief psychotic disorder
-characterized by sudden onset of psychotic symptoms (delusions, hallucinations, disorganized speech/behavior) lasting at least 1 day and less than 1 month
1399
schizoid personality disorder
-characterized by a lifelong pattern of detachment from social relationships and restricted range of emotions
1400
schizophreniform disorder
-characterized by psychotic symptoms that last 1-6 months
1401
schizotypal personality disorder
-pts are typically "odd", holding magical beliefs and strange (but not overtly psychotic) though processes
1402
borderline personality disorder
- involves a pervasive pattern of impulsivity, mood instability, and an unstable sense of self - associated characteristics include fear of abandonment and unstable chaotic relationships - transient paranoia and psychosis may occur and last minutes to hours; these have been termed "micropsychotic episodes"
1403
new-onset psychosis in a patient w/ active medical problems requires a workup to determine the medical cause. Pts w/ hypothyroidism are commonly diagnosed w/ depression and can also experience psychotic symptoms in severe cases.
.
1404
type 2 renal tubular acidosis
-impaired bicarb reabsorption in the proximal renal tubules, which causes a non-anion gap metabolic acidosis
1405
impaired urine acidification in the distal renal tubules
type 1 renal tubular acidosis, which causes a non-anion gap metabolic acidosis
1406
DKA
- presents w/ polyuria, polydipsia, abdominal pain, vomiting, and metabolic acidosis - low serum bicarb, elevated anion gap, and hyperglycemia are diagnostic of the condition - lack of insulin causes breakdown of fatty acids to ketones in the liver, which leads to acidosis and the clinical manifestations of DKA
1407
Tx of DKA
- consists of gradual fluid resuscitation w/ a 10 mL/kg bolus of normal saline over 1 hour; this should be followed by an IV insulin drip w/ isotonic fluids containing potassium - the patient can be transitioned to a subcutaneous insulin regimen when the anion gap closes and the metabolic acidosis resolves
1408
An elderly patient with lymphadenopathy and lymphocytosis likely has chronic lymphocytic leukemia (CLL). Smudge cells, which represent fragile but mature lymphocytes, may be seen on peripheral blood smear.
.
1409
Atelectasis is often seen in pts w/ post-op fever, but it has been shown that atelectasis by itself is not the cause of fever. This is a common misconception, and post-op fever should not be ascribed to atelectasis.
.
1410
Spherocytes are small, hyperchromic red cells without central pallor. Spherocytosis can be inherited or acquired. Affected pts are prone to bilirubin gallstones as a complication of chronic hemolysis.
.
1411
side effects of abacavir
-lactic acidosis, hepatitis, hypersensitivity reaction
1412
side effect of didanosine
pancreatitis
1413
side effects of Efavirenz?
non-nucleoside reverse transcriptase inhibitor known to cause insomnia with vivid, bizarre dreams
1414
urge incontinence
- refers to an involuntary leakage of urine accompanied by a sensation of urgency - initial tx are conservative, consisting of bladder training and establishing a voiding schedule
1415
Kawasaki disease
-childhood vasculitis that typically consists of fever, conjunctival injection, oral mucous membrane changes, erythema or edema of the palms and soles, polymorphous rash, and cervical lymphadenopathy
1416
Henoch-Schonlein Purpura
- childhood illness w/ pathologic findings of leukocytoclastic vasculitis w/ IgA deposition - clinical findings include palpable purpura, abdominal pain, renal failure, and arthralgia
1417
the most important conditions to consider in pts w/ third trimester bleeding are placenta previa and placental abruption. Placenta previa typically causes PAINLESS vaginal bleeding, while abruption is usually PAINFUL. Diagnosis can be made w/ TRANSABDOMINAL US, and vaginal exam should be WITHHELD until placenta previa has been excluded by US.
.
1418
Patients may have blunt chest trauma-related injury to the great vessels while remaining hemodynamically stable w/ few chest-related complaints. The finding of a widened mediastinum on chest x-ray requires further work-up w/ TEE or CT scanning.
.
1419
Bartholin's gland abscess
- can cause pain w/ walking, sitting, and sexual intercourse - exam reveals a tender mass in the medial aspect of the labia majora at either the 4 or 8 o'clock position - as with any abscess, incision and drainage is the most appropriate therapy
1420
The inability to extend the knee more than 135 degrees while the hip is flexed is known as Kernig's sign, and it is suggestive of meningeal irritation from meningitis.
.
1421
migraine therapies
- abortives: triptans, NSAIDs, acetaminophen, antiemetics, ergots - preventatives: topiramate, divalproex sodium, TCAs, beta-blockers
1422
Coadministration of a triptan and ergotamine may result in prolonged vasospasm due to overactivation of serotonin (5-HT) receptors. Therefore, triptans should not be given for at least 24 hrs after ergotamine is given and vice-versa.
.
1423
Kawasaki disease
- associated w/ the development of coronary artery aneurysms - tx w/ IVIG and aspirin helps decrease the risk of coronary complicaitons - diganosis: fever for 5 or more days, along w/ 4 or more of the following: oral mucous membranes changes (strawberry tongue, cracked lips), bilateral nonexudative conjunctivitis w/ limbal sparing, cervical lymphadenopathy (> 1.5 cm), polymorphous rash, erythema or edema of the hands and feet
1424
tx for rocky mountain spotted fever?
doxycycline
1425
Koplik spots
-small white spots on buccal mucosa seen in measles
1426
Forschheimer spots
-petechiae on soft palate seen in rubella
1427
Primary open angle glaucoma
- increased IOP | - presents w/ progressive loss of vision in the peripheral visual fields followed by central visual loss
1428
macular degeneration
-caused by pigment accumulation in the retina, which typically presents w/ central visual loss
1429
cataracts
- characterized by painless loss of vision that is worse at night; classically described as "glare" while driving at night - surgical tx is required
1430
most pts who have had a splenectomy will have thrombocytosis because one of the spleen's functions is to remove old platelets from the circulation.
.
1431
Infection w/ Chlamydia trachomatis
- should be suspected in any young pt w/ dysuria, cervical friability, or vaginal discharge, esp. if the Gram stain of the discharge shows numerous neutrophils w/o any organisms - chlamydial infection can lead to the development of PID if untreated, which can eventually cause infertility
1432
amiodarone
-antiarrhythmic used to manage VENTRICULAR arrhythmias in pts w/ heart failure and/or systolic LV dysfunction
1433
Digoxin
- adjunctive therapy for symptom control in pts w/ heart failure and LV systolic dysfunction - reduces the rate of hospitalization for heart failure but has not been shown to improve overall survival
1434
Medications that improve long-term SURVIVAL in pts w/ LV systolic dysfunction (EF
- ACE-I - ARBs - beta-blockers (metoprolol, carvedilol, bisoprolol) - aldosterone angatgonists - combo of hydralazine and nitrates in blacks
1435
Hypothyroidism can cause a variety of menstrual abnormalities, including amenorrhea, irregular menses, and menorrhagia. It can also cause hyperprolactinemia w/ associated galactorrhea due to TRH stimulation of lactotrophs.
.
1436
mechanism of carpal tunnel syndrome in pregnancy vs. hypothyroidism
- in pregnancy: fluid accumulation within the carpal tunnel - in hypothyroidism: accumulation of matrix substances (mucin, mucopolysaccharide) within both the perineurium as well as tendons
1437
tocolytics
-calcium channel blockers (eg nifedipine), b-agonists (terbutaline, ritodrine), and cyclooxygenase inhibitors (eg indomethacin; only between 24-32 wks though)
1438
magnesium sulfate in pregnancy
-used for fetal neuroprotection in preterm births
1439
Pulmonary edema should be considered in any patient with rapid-onset hypoxia, tachypnea, and bibasilar crackles. B-agonists are first-line tocolytics that can cause pulmonary edema.
.
1440
Cyanosis in highly vascularized tissues such as the lips and mucous membranes is consistent w/ CENTRAL CYANOSIS, as opposed to PERIPHERAL CYANOSIS which usually only involves the distal extremities. Central cyanosis is caused by low arterial oxygen saturation, whereas peripheral cyanosis is due to increased oxygen extraction secondary to sluggish blood flow.
.
1441
Pts w/ familial dysbetalipoproteinema (Frederickson Type III Hyperlipidemia)
- develop hypertriglyceridemia - a classic clinical finding is striate palmar xanthomas - the most appropriate initial tx is w/ a fibric acid derivative (eg fenofibrate)
1442
preterm labor
-regular contractions occurring before 37 wks gestation associated w/ cervical changes
1443
women w/ advanced cervical dilation in the absence of labor and abruption are candidates for cervical cerclage. If a woman is in labor, cervical cerclage is contraindicated.
.
1444
All women who are at risk for preterm delivery between 24 and 34 weeks of gestation are candidates for corticosteroid therapy to enhance fetal lung maturity and decrease neonatal morbidity.
.
1445
Sulfonylureas
-act on pancreas to increase endogenous insulin production
1446
metformin and the thiazolidinediones (TZDs)
-both increase the insulin sensitivity of peripheral tissues
1447
the most effective tx in slowing the progression of diabetic nephropathy?
-maintaining a BP of less than 130/80, particularly w/ ACE-I or ARBs
1448
Ulnar nerve compression
- usually occurs at the elbow, either in the epicondylar groove or the cubital tunnel - repetitive flexion and extension of the elbow, often secondary to occupational stress, may lead to compression in the cubital canal - typical symptoms include paresthesias in the 4th and 5th fingers as well as the medial forearm in addition to weakness of the intrinsic hand muscles
1449
hand-foot-mouth disease and herpangina organism?
Coxsackie virus
1450
common skin infections caused by Strep pyogenes?
- non-purulent cellulitis - impetigo (nonbullous) - scarlet fever (confluent erythematous rash preceded by strep pharyngitis) - erysipelas (raised, demarcated dermal inflammation/tenderness/warmth)
1451
Roseola infantum
- viral infection caused by human herpesvirus 6 | - characterized by 3-5 days of a very high fever followed by a rose-colored maculopapular exanthem
1452
Raynaud phenomenon
- cold induced vasospasm typically seen in the fingers, and is more common in pts w/ connective tissue disorders such as scleroderma - tx consists of CCBs such as nifedipine
1453
long-term use of combination oral contraceptives increases the risk of which cancers, and decreases the risk of which cancers?
- increases risk: breast and cervical (returns to normal within 10 yrs of dc) - decreases risk: endometrial and ovarian
1454
pts w/ TTP usually have changes in their mental status as well as renal insufficiency!
.
1455
Heparin-induced thrombocytopenia (HIT)
- should be suspected in pts w/ thrombocytopenia after a recent hx of heparin exposure - despite the low platelet count, most of the complications of HIT occur from thrombosis - therefore, tx w/ alternative anticoagulants is required after stopping all heparin containing therapies - do NOT give platelet transfusions!! may worsen hypercoagulability
1456
Severe hypercalcemia
- can lead to an altered mental status, and is sometimes seen in pts w/ squamous cell carcinoma of the lung due to the secretion of parathyroid hormone-related peptide (PTHrP) - pts w/ severe hypercalcemia are typically volume depleted, and as a result, initial therapy should consist primarily of fluid resuscitation w/ isotonic saline
1457
endometriosis
- common cause of infertility and cyclic pelvic pain in young females - possible findings on exam include pain or nodularity of the rectovaginal septum as well as fixation of the uterus in a retroverted position - diagnosis usually requires laparoscopy, but a pelvic US can sometimes be helpful in localizing a large endometrioma
1458
Pts w/ a subarachnoid hemorrhage typically complain of a severe headache of abrupt onset. A non-contrast CT scan of the head should be obtained in any patient in whom SAH is suspected.
.
1459
Arrhythmia should be suspected as the cause of a patient's syncope if there is a hx of rapid-onset loss of consciousness w/o a preceding prodrome. Usage of anti-arrhythmic drugs, structural heart disease, and hypokalemia and/or hypomagnesemia are all potential predisposing factors for torsades de pointes.
.
1460
Lidocaine
-may be used in the tx of ventricular arrhythmias, other than torsades de pointes
1461
adenosine
-may be used in tx of SUPRAventricular tachycardia
1462
digoxin
-may be used for the tx of heart failure or as a rate control agent in atrial fibrillation
1463
verapamil
-CCB used for rate control in SUPRAventricular tachycardias
1464
Amiodarone
-used in tx of ventricular and atrial arrhythmias
1465
Certain antiarrhythmic meds, structural heart disease, and hypokalemia and hypomagnesemia can predispose to QT interval prolongation and possible development of torsades de pointes. The initial tx of torsades in pts who are hemodynamically STABLE is magnesium sulfate, even if the pts magnesium level is normal.
.
1466
Amaurosis fugax
-sudden, painless, transient monocular vision loss that most commonly results from retinal artery emboli originating from a carotid artery atherosclerotic plaque
1467
Optic neuritis in MS can cause transient monocular visual disturbances or blindness, typically associated w/ other neurologic symptoms characteristic of MS
.
1468
fibroadenomas
- seen in young women as a firm, rubbery mass that moves easily w/ palpation - either FNA or sonogram can establish diagnosis - removal is optional
1469
giant juvenile fibroadenomas
- seen in very young adolescents, where they have very rapid growth - removal is needed to avoid deformity and distortion of the breast
1470
cystosarcoma phyllodes
- senn in late 20s - breast mass that grow over many years, becoming very large, replacing and distorting the entire breast, yet no invading or becoming fixed - most are benign, but they have malignant potential - core or incisional biopsy is needed (FNA is NOT sufficient), and removal is MANDATORY
1471
mammary dysplasia (fibrocystic disease)
- seen in 30s and 40s, w/ bilateral tenderness related to menstrual cycles (worse in last 2 weeks) and multiple lumps that seem to come and go (they are cysts) - persistent mass requires aspiration, if clear fluid and mass goes away, that's it; if mass persists, formal biopsy required
1472
intraductal papilloma
- seen in young women (20s to 40s) w/ BLOODY NIPPLE DISCHARGE - mammogram is needed to identify other potential lesions, but will not show papilloma - galactogram may be diagnostic and guides surgical resection
1473
breast abscess
- seen only in lactating women | - I&D is needed, but biopsy of the abscess wall should be done also
1474
breast cancer
- should be suspected in any woman w/ a palpable breast mass - other indicators: ill-defined fixed mass, retraction of overlying skin, "orange peel" skin, recent retraction of nipple, eczematoid lesion of the areola, reddish orange peel skin over mass (INFLAMMATORY breast cancer), and palpable axillary nodes - note that a hx of trauma does NOT rule out cancer!!
1475
breast cancer during pregnancy
- diagnosed exactly as if pregnancy did not exist and is treated the same way except for: no radiotherapy during ENTIRE pregnancy, and no chemo during the FIRST TRIMESTER - termination of the pregnancy is not necessary
1476
infiltrating ductal carcinoma
- standard form of breast cancer - INFLAMMATORY cancer is the only variant w/ much worse prognosis (and the need for pre-op chemo) - other variants (lobular, medullary, mucinous) have slightly better prognosis and are treated the same way as the standard infiltrating ductal - lobular has higher incidence of bilaterality
1477
ductal carcinoma in situ
- cannot metastasize (thus no axillary sampling is needed), but has very high incidence of recurrence if only local excision is done - total simple mastectomy is recommended for multicentric lesions throughout the breast - lumpectomy followed by radiation is used if the lesion is confined to 1/4 of the breast
1478
inoperability of breast cancer is based on LOCAL EXTENT (not metastases)
.
1479
abx that treat pseudomonas
- cefTAZidime (3rd gen) - cefePIME (4th gen) - aminoglycosides (gentamicin, amikacin, streptomycin, tobramycin, etc.) - ticarcillin - aztreonam - carbapenems - ciprofloxacin
1480
conductive vs sensorineural hearing loss
Rinne test results: -Normal hearing will show an air-conduction time that is twice as long as the bone conduction -If a patient has conductive hearing loss, the bone conduction sound is longer than or equal to the air conduction sound. -If a patient has sensorineural hearing loss, air conduction is heard longer than bone conduction, but it is not heard to be twice as long. Weber Test Results: -Normal hearing will indicate sound in both ears. -Conductive loss will indicate the sound travels towards the poor ear. -Sensorineural loss will indicate the sound travels towards the good ear