UWorld 1 Flashcards
Physical exam findings of pulmonary embolism
Tachycardia, tachypnea
Hypoxemia (VQ mismatch)
Signs of DVT
Elevated brain natriuretic peptide
(a) Where is BNP released from?
(b) What does it indicate
(c) Correlated physical exam finding
Elevated BNP
(a) BNP released from ventricular myocytes in response to high ventricular filling pressures and wall stress, seen in CHF pts
(b) Elevated levels of BNP correlate w/ the severity of LV systolic dysfunction
- normal BNP vales practically rule out CHF as a cause of dyspnea => prompts search for noncardiac cause of dyspnea
(c) Third heart sound = passive ventricular filling during diastole
- highly specific for CHF due to LV systolic dysfunction
22 yo M w/ hematuria 5 days after a UTI
- no skin findings
- normal complement levels
Ddx and dx?
Hematuria following URI: IgA nephropathy vs. post-infectious glomerulonephritis
Dx = IgA neprhopathy- more common in young adult males, normal complement levels, seen sooner after URI (average of 5 days)
Post-infectious glomerulonephritis: more common in kids, seen 10-21 days after URI
-low complement
Lupus: more common in females, would have low complement levels
Common cause of abrupt onset of mild eye pain and redness (redness of the white of the eye)
Episcleritis = inflammation of the episclera
- tx: symptom relief, lubricating eye drops
- rather benign condition
What type of arrhythmias are most common in post-MI state?
Ventricular arrhythmias (PVVs, VT, VFib) more common post-Mi than atrial arrhythmias
-specifically reentrant ventricular arrythmia (V. fib)
Describe why severe hypernatremia must be corrected very gradually
Must correct hypernatremia very slowly/gradually to prevent cerebral edema
Quickly making serum comparatively hypotonic will draw water into the CNS => cerebral edema
Describe why severe hyponatremia must be corrected very gradually
Correct hyponatremia w/ 3% NS, but at very slow rate under .5 mEq/L/hr to prevent osmotic demyelination or central pontine myelinosis
Rapid correction of serum sodium draws water out of the intracellular (neuron and glia) into the extracellular compartment => cell damage
19 yo w/ fever, myalgia, and rash that started on face and spread to rest of body
+lymphadenopathy
Rubella = German measles
Large mediastinal mass w/ elevated AFP and beta-hCG
Nonseminomatous germ cell tumor
Primary germ cell tumor
See increased AFP and beta-hCG
-just elevated AFP could be HCC
-just elevated beta-hCG could be seminoma
3 findings of severe uremia
Symptomatic uremia (ex: from acute kidney failure)
- encephalopathy: significant alteration in consciousness in uremic pts w/o any other notable cause
- pericarditis: results from inflammation of the visceral and parietal membranes of the pericardial sac
- bleeding
What is pronator drift?
(a) What does it indicate
Pronator drift = weakness in supination that results in dominance of pronator muscles
-when pt closes eyes and stretched arms outward w/ hands up: affected side palm turns inward and downward (not just downward as seen in feigned upper-extremity weakness)
(a) Sensitive and specific for upper motor neuron disease
What is albumino-cytogenic dissociation on LP?
(a) What does it suggest?
Albumino-cytogenic dissociation = high protein but normal cell count on spinal tap
(a) Suggestive of Guillain-Barre syndrome
Subdural vs. epidural hematoma
(a) Which vessel is ruptured
(b) Location of the bleed
(c) Presenting symptoms
(d) CT appearance
Subdural hematoma
(a) Rupture of bridging veins (those that drain into dural sinuses)
(b) Bleed is btwn the dura and arachnoid layers- aka subdural space
(c) Present w/ gradually increasing HA and confusion
(d) Crosses suture lines on CT:semi-lenticular hematoma
Epidural hematoma
(a) Rupture of middle meningeal artery
(b) Bleed is btwn the skull and the dura mater
(c) Presents w/ lucid interval followed by unconsciousness
(d) Lens-shape, does not cross suture lines
Name two medications that can trigger bronchoconstriction in an asthmatic/atopic pt
Aspirin and beta-blockers
Most common cause of AR in young adults in
(a) developed countries
(b) undeveloped countries
Aortic regurgitation, most common etiology in
(a) Developed countries = bicuspid aortic valve
(b) Undeveloped countries = rheumatic heart disease
First step tx for pts presenting in acute decompensated heart failure and dyspnea
IV diuretics (furosemide): tx the pulmonary edema and relieve SOB
+supplemental O2, possible vasodilator herapy (nitroglycerine, nitroprusside)
Diagnostic test of choice for acute aortic dissection, explain why or why not for each
(a) CT
(b) MRI
(c) TEE
(d) TTE
Acute aortic dissection diagnosis
(a) CT- requires normal kidney fxn b/c requires contrast
- so not possible if elevated creatinine
(b) MRI- too slow, time consuming and requires pts to remain motionless for several minutes => not used to dx in acute setting
(c) TEE- bing bing bing, gold standard- gives great visualization of the abdominal aorta and doesn’t require contrast/kidney fxn
(d) Wouldn’t do transthroacic echo b/c doesnt give good visualization of the abdominal aorta
Meniere’s disease
(a) Phsyiology
(b) Lifestyle modifications
(c) Medication tx
Meniere’s disease
(a) distention of the endolymphatic compartment of the inner ear
(b) Low salt diet, avoid cafffeine EtOH and nicotine- basically all things that increase endolymphatic retention
(c) Meds: diuretics, antihistamines and anticholinergics
Tension pneumothorax
(a) Presenting symptoms
(b) Presenting signs
Tension pneumothorax-
(a) CP, SOB, hypotension.
(b) Absent breath sounds in one hemithorax and deviated trachea on physical exam
What is cardiac tamponade?
Cardiac tamponade = pericardial tamponade- when a large pericardial effusion compresses/puts pressure on the heart
-when substance (pus, blood, clots, gas, fluid) accumulates in the pericardium at a rate faster than the pericardium can expand => pressure put on the heart
WPW findings on EKG
WPW = ventricular preexcitation
- short PR intervals
- widened QRS (more time of ventricles depolarizing since one part starts early)
- delta waves = slurred upstroke of the QRS due to ventricular preexcitation
Common bacteria responsible for
(a) sinusitis extension to brain abscess
(b) endocarditis extension to brain abscess
(a) Viridans streptococci = most common bug causing sinusitis that may spread to brain abscess
(b) Endocarditis- thinking gram negatives and staph aureus
Physical exam findings of pleural effusion
Diminished breath sounds and dullness to percussion on exam
Classic presentation of aortic dissection
Sudden onset tearing chest and back pain in pt w/ chronic HTN
2 presentations of anti-basement membrane antibodies
Can be renally limited => hematuria and elevated creatinine/BUN
Or renal + lungs (alveolar hemorrhage) = Goodpasture’s
What conditions can give a false positive VDRL
False positive syphilis test
- pregnancy
- lymes disease
- lupus
- antiphospholipid antibody syndrome
- possibly some pneumonia, malaria, and Tb
What type of anemia is seen in ESRD?
(a) Tx
(b) Main side effect of the tx
Normochromic normocytic anemia = anemia commonly seen in end stage renal disease
(a) Tx = recombinant EPO (well this is after you r/o iron deficiency as a possible cause of the anemia and try iron supplementation)
- decrease risk of worsening HTN if give SC instead of IV
(b) 30% of pts will have worsening htn- mechanism not known
Indications fo urgent dialysis: AEIOU
Indications for urgent dialysis:
Acidemia: metabolic acidosis w/ pH under 7.1 not responsive to medical tx
Electrolyte abnormality: symptomatic hyperkalemia (EKG changes of ventricular arrhythmia) or severe hyperkalemia (K over 6.6)
Ingestion: toxic alcoholcs, salicylate, lithium, sodium valproate, carbamazepine
Overload- volume overload refractory to diuresis
Uremia- symptomatic: encephalopathy, pericarditis, bleeding (ex: pericarditis from ARF secondary to post-strep GN)
Hypokalemia
(a) Presenting features
(b) Late findings
(c) EKG findings
Hypokalemia
(a) Presents w/ fatigue, weakness, and muscle cramps
(b) Late/severe findings- paralysis and arrhythmia
(c) EKG findings: flat broad T waves, U waves, ST depression, premature ventricular beats
What kind of anemia (high normal low MCV, retic count in normal MCV) is caused by the following
(a) Lead intoxication
(b) Medication side effect
(c) Hereditary spherocytosis
(d) Autoimmune
(e) Leukemia
(f) Aplastic anemia
(g) Sideroblastic anemia
(h) Infection
(i) Thalassemia
(j) Folate deficiency
Etiology of anemia
(a) Lead intoxication => microcytic
(b) Medication side effect => normocytic w/ low reticulocyte count
(c) HS => normocytic w/ high retic count
(d) Autoimmune => normocytic w/ high retic count
- high liver enzymes and positive Coombs test
(e) Leukemia => normocytic w/ low retic count
(f) Aplastic anemia => normocytic w/ low retic count
(g) Sideroblastic anemia => microcytic
(h) Infection => normocytic w/ low retic count
(i) Thalassema => microcytic
(j) Folate deficiency => macrocytic
What is antiphospholipid antibody syndrome?
(a) Presentation
(b) Associated test findings
Antiphospholipid antibody syndrome = acquired hypercoagulable state
-many types of causative antibodies
(a) Presentation: recurrent fetal loss (lots of miscarriages), thrombocytopenia, prolonged PTT, arterial or venous thrombosis
(b) Can commonly cause false (+) VDLR (syphilis test)
G3P0 F w/ (+) VDRL, (-) FTA-ABS
-thrombocytopenia, prolonged PTT
(a) Dx
(b) Tx
Lots of pregnancies w/o babies => lots of miscarriages
- false positive VDRL
- hypercoagulable state w/ thrombocytopenia
(a) Acquired hypercoagulable state + recurrent fetal loss + thrombocytopenia + false positive VDRL = Antiphospholipid antibody syndrome
(b) Tx = LMWH (low molecular weight heparin) and aspirin to avoid pregnancy loss
What kind of syncope occurs w/ heavy activity?
(a) Associated features
Valvular heart disease caused syncope can occur during activity
(a) SOB, CP, fatigue
56 yo M w/ fullness of the face, splenomegaly, and BP 160/94
-elevated hematocrit and RBC count
Polycythemia vera = clonal myeloproliferative disease of the pluripotent hematopoietic stem cell
=> presents w/ high red count => increased viscosity causes reversible moderate HTN
-also have mild leukocytosis and high platelet count
Differentiate the liver biopsy findings of
primary biliary cirrhosis and primary sclerosing cholangitis
Liver biopsy findings of
Primary biliary cirrhosis = destruction of intrahepatic bile ducts
Primary sclerosing cholangitis = inflammation and fibrosis of intra and extra hepatic bile ducts
-segmental stenosis of intra andextra-hepatic bile ducts
Ankle-branchial index
Ankle BP: upper arm BP
Lower in ankle indicates blocked arteries due to peripheral artery disease
Under .8 = some arterial disease
Under .5 = severe arterial disease
What drugs treat the following types of esophagitis in an HIV pt
(a) Candida
(b) CMV
(c) HSV
Esophagitis in HIV pt- as presented by dysphagia and odynophagia
(a) Candida => treat w/ fluconazole
(b) CMV- tx w/ ganncyclovir
(c) HSV- tx w/ acyclovir
More likely to be acute or chronic bacterial prostatitis
(a) Young age
(b) E. coli
(c) dull, poorly localized pain
(d) fevers, chills
(e) extremely tender prostate
(f) dysuria, frequency
Acute vs. chronic bacterial prostatitis
(a) Young age- more likely to be acute
(b) E. coli and other GNR- cause both acute and chronic
(c) Dull, poorly localized pain = chronic
- acute presents w/ perineal and lower back pain
(d) Fevers and chills- acute
(e) Extremely tender prostate = acute
- enlarged and nontender prostate seen in chronic
(f) Dysuria and frequency (irritative voiding) seen in both
Beta-blocker use in acute and chronic heart failure
Cardioselective beta-blockers (carvedilol) are beneficial for long-term management of pts w/ stable HF due to LV dysfunction
- should be avoided in acute decompensated heart failure b/c they can acutely worsen HF symptoms
- can be initiated after adequate diuresis
Most reliable and predictable sign of opioid intoxication
Decreased respiratory rate (ex: RR of 6)
-would also expect pinpoint pupils but not always! pupils can be dilated or even normal, pupils not as reliable of a sign as RR
Pt w/ DM, HTN, HLD who presents w/ myalgia
On a statin for their HLD? Test their CPK- if elevated then stop the statin
-can progress to rhabdomyolysis w/ renal failure
Hallmark feature of cat scratch disease
Self-limited lymphadenopathy
-and usually hx of exposure to cats…
Describe signs/symptoms of hypercalcemia
Body systems effected by hypercalcemia
Kidneys- trying to filter more out => increased thirst and urination
GI tract => upset stomach, diarrhea, nausea, vom
Bone pain
Brain => altered mental status, confusion, fatigue
29 yo w/ paraplegia, urinary incontinence, and urgency
-h/o trigeminal neuralgia
+spasiticity, LE hyperreflexia
Multiple sclerosis
Physical exam findings indicating
(a) Cerebellar dysfunction
(b) Impaired proprioception
(a) Cerebellar dysfunction: ataxic gait, dysdiadokinesis (rapid alternating movements), dysmetria (impaired finger to nose)
- upward drift on pronator drift test
(b) Impaired proprioception: Romberg test: can’t maintain balance w/ feet together when they close their eyes
Effect of aldosterone activity
Aldo promotes Na+ and water retention, lowers plasma K+
- Upregulates and activates Na/K pumps on DCT and collecting duct
- upregulates ENaC
Increases: Na reabsorption
Increases H+ secretion and K+ secretion
Presentation of Alport’s disease
Alport’s = X-linked collagen IV mutation, presents w/ hearing loss, ocular abnormalities, hematuria, and gradual kidney dysfunction
Mechanism of renin activity- final effect
Renin = released by JGA cells (kidney) when hypoperfusion sense, function is to increase BP by
- activating RAAS system => more angiotensin II to cause vasoconstriction
- increase ADH and aldo secretion
- stimulate hypothalamus to stimulate thirst reflex
Pt is acutely post-MI, had episode of syncope
Most common cause of the syncopal episode
Reentrant ventricular arrhythmia = common cause of sudden cardiac arrest (and therefore syncope) in immediate post-MI period
ADAMTS13
von Willebrand factor-cleaving protease whose activity is severely reduced in TTP (thrombotic thrombocytopenic purpura)
Differentiate the following:
(a) Biliary colic
(b) Cholecystitits
(c) Choledocholithiasis
(d) Cholangitis
Spectrum of gall bladder/stone d/o
-many gall stones are passed asymptomatically, when they do produce pain it is called biliary colic
(a) Biliary colic = due to pressure of gallstones against the walls of the cystic or common bile duct
-intermittent RUQ pain
(b) Cholecystitis- occurs in about 20% of pts that have biliary colic
= when prolonged cystic duct obstruction causes inflammation of the gall bladder wall (gall bladder inflammation)
(c) Choledocholithiasis = bile stone gets lodged in the common bile duct
(d) Cholangitis = infection of the biliary duct
-high morbidity/mortality
-can be life threatening
Most common location of hypertensive cranial hemorrhage
Putamen and thalamus
Lambert-Eaton syndrome
(a) Mechanism
(b) Etiology
(c) Presentation
(d) Tx
Lambert-Eaton syndrome
(a) Rareautoimmune disorder
(b) 60% due to lung cancer, most typically small cell lung cancer
(c) Presents w/ muscle weakness of the limbs
(d) Tx- to treat the underlying lung cancer
Polycythemia vera
(a) Common presentation
(b) Two associated features
(c) Tx
Polycythemia vera
(a) Itching/pruritis
(b) Associated w/ gouty arthritis and PUD
(c) Phlebotomy- remove some of the excess volume of blood