UWorld Step3 Flashcards

1
Q

What is subclinical Hypothyroidism?

A

Mild elevation in TSH levels (5-10) w/normal free T4 levels.

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2
Q

When are considered “convincing hypothyroid sxs” hypothyroidism?

A
When there is presence of:
1-	Antithyroid antibodies
2-	Abnormal lipid profile
3-	Sxs of hypothyroidism
4-	Ovulatory and menstrual dysfunction

should obtain anti-TPO abs in all pts. before treating

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3
Q

Common signs of hypothyroidism overtreatment:

A

Bone Loss

aFib

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4
Q

Features of cough-variant asthma:

A

Chronic non-productive cough is predominant sx instead of wheezing and SoB.
Allergens are common triggers as well as exercise and forced expiration.
Commonly occurs at night.

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5
Q

Features of Radiation Proctitis:

A

Often presents w/diarrhea, mucus discharge and tenesmus during or w/in 6wks of pelvic radiation.
Chronic cases occur >9wks to yrs after radiation.
Chronic radiation proctitis commonly a/w strictures, fistula formation and rectal bleeding.

Colonoscopy findings: continuous lesions w/pallor, friability, telangiectasias, and mucosal hemorrhage

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6
Q

Tx of chronic radiation proctitis:

A

Sucralfate or Glucocorticoid enemas

Acute cases often tx’d w/supportive measures

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7
Q

Characteristics of tracheomalacia:

A

Weakness of tracheal walls leading to expiratory airway collapse.
Sxs: coughing, SoB and stridor on PE

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8
Q

Features of Upper Airway Cough Syndrome (UACS):

A

Aka Post-Nasal Drip

Chronic non-productive cough, rhinorrhea, and often oropharyngeal cobblestoning on PE

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9
Q

Tx of Generalized convulsive status epilepticus:

A
  1. Stabilize circulation, airway/breathing; Evaluate for cause; Give IV BENZOS (lorazepam, diazepam or Midazolam)
  2. Give adjunctive IV agent: fosphenytoin, phenytoin, valproate
  3. If seizure still not terminated: EEG + continuous infusion of barbituate, midazolam or propofol
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10
Q

When should a skeletal survey be done in a patient with multiple myeloma?

A

At time of diagnosis – can assess extent of skeletal involvement and identify impending pathologic fractures.
Typically reveal punched-out lytic lesions and diffuse osteopenia

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11
Q

What kind of lesions do Technetium-99m bone scans primarily detect?

A

Blastic bony lesions

Much less sensitive than conventional xray for lytic lesions

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12
Q

Features of Hyperviscosity Syndrome:

A

Nasal or oral bleeding (d/t impaired platelet fxn)
Blurry vision
Neurologic sxs (confusion, HA)
Heart Failure
should obtain plsamapheresis for symptomatic pts

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13
Q

Cxs of Multiple Myeloma (6):

A
Hypercalcemia
Renal Insufficiency
Infections (pneumonia, UTIs)
Skeletal lesions
Hyperviscosity syndrome
Thrombosis (arterial and venous)
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14
Q

Common signs/sxs of renal failure:

A
Dyspnea
Nausea
Peripheral edema
Mental status changes
Eventual anemia
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15
Q

Common sxs of hypercalcemia:

A
Anorexia
Nausea
Polyuria
Constipation
Weakness
Confusion
Pleuritis
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16
Q

Uterine effects of Tamoxifen in pre- v. post- menopausal women:

A

Post-menopausal: have increased risk of endometrial hyperplasia/cancer and uterine sarcoma
Pre-menopausal: increased risk of endometrial polyp development

Tamoxifen will increase endometrial thickness in both groups

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17
Q

When should pts taking Tamoxifen be screened for adverse effects on the uterus?

A

Only if they develop sxs: AUB, postmenopausal bleeding, etc.

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18
Q

What is a meta-analysis?

biostats

A

When data is pooled from several studies
It is used to increase the power of a study (ability to detect difference in outcomes if one exists) by increasing the sample size.

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19
Q

What is stratified analysis?

biostats

A

Analyzing pts based on the presence or absence of a certain variable.
Used to control confounding factors and distinguish b/w confounding and effect modification.

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20
Q

What is quarternary prevention?

biostats

A

Set of health activities that mitigate and/or limit the consequences of unnecessary or excessive intervention by the health system.

Ex: use of shared EMR to limit unnecessary, repeat procedures in a pt who has already had a specific procedure done

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21
Q

What is the preferred choice of meningococcal post-exposure prophylaxis?

A

Rifampin – prescribed 2x/d for 2 days.

Ciprofloxacin (single 500mg oral dose) and Ceftriaxone (250mg single dose) are acceptable alternatives for those who cannot take Rifampin

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22
Q

When should Rifampin not be prescribed as meningococcal pphx?

A

In women taking oral contraceptives or anyone taking a CYP450 metabolized drug
(it’s a CYP450 inducer and increases hepatic clearance)

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23
Q

What type of HS is caused by the scabies mite?

A

Delayed type IV HS rxn to the mite and its feces and ova

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24
Q

How is Scabies diagnosed?

A

Clinically plus confirmation by skin scrapings from lesions that reveal mites, ova and feces under LM.

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25
Q

CYP 450 Inducers (7):

A
*These will decrease drug effects*
Carbamezapine, phenytoin
Ginseng, St. John’s Wort
Oral Contraceptives
Phenobarbital
Rifampin
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26
Q

CYP450 Inhibitors (11):

A
*These will increase drug effects*
Acetaminophen, NSAIDs
Abx/Antifungals (metronidazole)
Amiodarone
Cimetidine
Omeprazole/PPIs
Cranberry Juice, Ginko, Vit.E
Thyroid hormone
SSRIs (fluoxetine)
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27
Q

Laboratory abnormalities in hypothermic patients (9):

A
anion-gap Metabolic acidosis
Respiratory acidosis
Azotemia
Hyperkalemia
Hypergylcemia
Elevated lipase
Elevated Hct/Hemoconcentration
Coagulopathy w/increased coagulation markers (INR and aPTT)
Leukopenia/Thrombocytopenia
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28
Q

Medical contraindications to pregnancy (6):

A
LVEF <40%
NYHA class III-IV heart failure
Prior peripartum cardiomyopathy
Severe obstructive cardiac lesions
Severe pHTN (Eisenmenger syndrome)
Unstable aortic dilation >40mm
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29
Q

First line contraceptive option for pts w/Eisenmenger syndrome:

A

Hysteroscopic sterilization or subdermal progestin implant

Estrogen-containing methods are contraindicated d/t increased risk of thromboembolism

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30
Q

Risk factors for spontaneous abortion:

A

Previous spontaneous abortion
Advanced maternal age
Substance abuse
Extremes in BMI

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31
Q

What is the Wells criteria?

A

Calculates pretest probability for PE
+3 points for: Clinical signs of DVT; Alternate dx less likely than PE
+1.5 points for: previous PE or DVT; Heart rate >100; Recent surgery or immobilization
+1 point for: Hemoptysis; Cancer

Total Score = 4 is low pretest probability (PE unlikely); >4 is high pretest probability (PE likely)

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32
Q

What are the 2 distinctive features of acute HIV/retroviral syndrome?

A

Painful mucocutaneous ulcer (shallow, discrete, white base)

Generalized maculopapular rash that may include the palms and soles

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33
Q

What is a Type II error?

A

A false negative
The failure to detect a difference bw groups when one exists.
The smaller a study the less power and higher likelihood of type II error

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34
Q

When should balloon valvuloplasty be performed in pts w/bicuspid aortic valves?

A

Done in symptomatic or asx (pts who plan to become pregnant or participate in competitive sports) young adults if the following criteria are met:
Aortic Stenosis
No significant AV calcification or AR
Peak gradient >50mmHg

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35
Q

Contraindications to fibrinolysis w/tPA (6):

A

Presence of active internal bleeding
Bleeding diathesis (platelets <100k)
Hypodensity in >33% of an arterial territory on CT
Presence of intracranial hemorrhage on CT
Intracranial surgery in last 3mos
BP > 185/110mmHg

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36
Q

What must be present to diagnose ankylosing spondylitis?

A

Evidence of sacroiliitis

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37
Q

What are the extraarticular manifestations of ankylosing spondylitis?

A

Apical pulmonary fibrosis/Restrictive lung disease
Ocular: acute anterior uveitis, cataracts, cystoid macular edema
Cardiac: aortic regurg, MVP
Varicocele
GI: ileal and colonic mucosal ulcerations
Atlanto-axial subluxation –> spinal cord compression
Cauda equina syndrome
Nephrotic syndrome caused by IgA nephropathy and secondary amyloidosis

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38
Q

What are risk factors for disability/poor px in ankylosing spondylitits?

A

Smoking is a/w very bad px

Prolonged standing and exposure to cold conditions increase risk of disability

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39
Q

1st line therapy for prevention of cluster headaches:

A

Verapamil – usually initiated at 240mg
Should not be taken repeatedly, and should only be used as a preventive treatment started at the onset of a cluster period.
Occasionally topiramate may be added to verapamil therapy.

Sumatriptan may be used in the acute setting but is not preventative

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40
Q

What is onychomycosis and how is it tx’d?

A

Fungal infection of finger or toenails most commonly caused by dermatophyte Trichophyton rubrum
1st line: Terbinafine, Itraconazole
2nd line: Griseofulvin, Fluconazole, Ciclopirox

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41
Q

How to distinguish a-thalassemia from B-thal minor:

A

Both will have same lab values (decreased MCV, normal RDW, norm/high RBCs, norm/high Iron and ferritin) and same peripheral smear (target cells).

Must distinguish w/Hb electrophoresis – will show increased HbA2 for B-minor and normal for a-thal

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42
Q

What is the major threat to internal validity?

biostats

A

Confounding

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43
Q

What is hungry bone syndrome?

A

A complication that can be seen following parathyroidectomy
Caused by sudden withdrawal of PTH in pts w/severe hyperparathyroidism, causing an increased influx of Ca2+ from the circulation into the bone.
Typically see signs/sxs of hungry bone syndrome 2-4 days post-op
Pre-op risk factors: severe hyperparathyroidism, severe bone disease and VitD def.
(all these conditions have v high bone turnover)

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44
Q

What are the likely causes of hypocalcemia following a parathyroidectomy?

A

Relative hypoparathyroidism – suppression of normal parathyroid glands by high Ca2+ levels pre-op fail to respond to low Ca2+ levels post-op

Hungry bone syndrome – when PTH levels fall post-op the dynamics of bone turnover shift from net efflux of Ca2+ from bone to net influx of Ca2+ into bone.

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45
Q

What is the diagnostic criteria of Acute Chest Syndrome?

A

New pulmonary infiltrate on CXR plus one or more of the following:
Increased work of breathing, cough, tachypnea, wheezing
Temp >38.5C/101.3F
Hypoxemia
Chest pain

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46
Q

What is the initial tx of Acute Chest Syndrome?

A

Ceftriaxone/Cefotaxime + Azithromycin
IVF
Pain control

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47
Q

When should a blood transfusion be given in acute chest syndrome?

A

If O2 sat is <92%
Significant anemia
Worsening sxs despite initial tx

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48
Q

How does VitB12 def cause hyperbilirubinemia?

A

Ineffective erythropoiesis causes hemolytic anemia and indirect hyperbilirubinemia

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49
Q

What is the classic pattern of pain seen in pts w/rotator cuff injuries?

A

Lateral shoulder or deltoid pain aggravated by reaching or lifting the arms up.
Seen in rotator tears and tendonitis, impingement syndrome and frozen shoulder

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50
Q

What are the 5 steps of a root cause analysis in order?

biostats

A
  1. Collect Data
  2. Create causal factor flow chart
  3. Identify root causes
  4. Generate recommendations and implement changes
  5. Measure success of changes
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51
Q

What medications can cause digoxin toxicity?

A

Verapamil
Quinidine
Amiodarone
Spironolactone

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52
Q

How is spontaneous bacterial peritonitis diagnosed?

A

Diagnostic paracentesis w/either positive cultures or 250+ neutrophils in the ascitic fluid

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53
Q

How is a patient’s 90-day survival calculated in the setting of End-Stage liver disease?

A

With the MELD score
Values used to calculate are serum BR, INR, and serum Creatinine.
Na+ is sometimes added to the calculation

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54
Q

How to tell between an obstructive stone v. sloughed renal papilla:

A

If there is no evidence of stone on CT then check BUN/Cr
Only renal papillary injury will cause increases in BUN/Cr
Stones will only lead to kidney injury if it is a solitary kidney or they are bilaterally obstructing.

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55
Q

What are some of the side effects of licorice?

A

May cause HTN and hypokalemia

Will likely see as a result a suppression of the RAAS system with low renin and aldosterone

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56
Q

What is a side effect of black cohosh?

A

Hepatic injury

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57
Q

When is Indomethacin indicated for tocolysis?

A

When <32 weeks gestation

32+ weeks it is contraindicated d/t risk of oligohydramnios and premature closure of ductus arteriosus.

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58
Q

When should tocolytics be given?

A
To pts <34 weeks gestation
Give CCBs (Nifedipine) when 32-34 weeks
Indomethacin when <32 weeks
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59
Q

What is the tx for V. vulnificus infection?

A

Doxycycline + Ceftriaxone

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60
Q

What should be done in pts w/cryptococcal meningitis w/recurrent sxs of elevated ICP?

A

These pts need serial lumbar punctures until the sxs stop – often the yeast and capsular polysaccharides can clog the arachnoid vili and lead to markedly increased ICP which if not managed can cause herniation/death.

In rare cases VP shunts need to be placed

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61
Q

What are the 3 tx-stages for HIV pts w/cryptococcal meningitis?

A
  1. Induction – amphotericin B + flucytosine for 2+ weeks (until sxs stop and CSF is sterile)
  2. Consolidation – high dose oral fluconazole for 8wks
  3. Maintenance – low dose oral fluconazole for 1+yr to prevent recurrence

This is the same tx strategy for disseminated/cutaneous cryptococcus

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62
Q

What is the definition of a non-preventable adverse event?

biostats

A

Harm/injury caused by medical management, not by disease/condition

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63
Q

What lab testing should be ordered in a patient found to have an adrenal mass?

A
ALL adrenal masses should be worked up.
Serum electrolytes
Dexamethasone suppression testing
24-hr urine catecholamine
Metanephrine
VMA
17-ketosteroid measurement
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64
Q

When should surgical excision be recommended for an adrenal tumor?

A
All functional tumors (hormone secreting, etc.)
All malignancies (which demonstrate characteristic heterogenous appearance on imaging)
All tumors >4cm
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65
Q

Features of lateral Medullary Syndrome:

A

aka Wallenberg syndrome – most sxs ipsilateral
Vertigo, falling to side of lesion, diplopia, nystagmus, difficult sitting upright, limb ataxia
Abnormal facial sensation or pain
Dysphagia, aspiration, hoarseness
Horner’s syndrome, hiccups, lack of autonomic respiration

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66
Q

Where would a lesion be expected to cause sensory loss in the contralateral face and body?

A

The thalamus or cortex – loss in face and body on the same side, contralateral to the lesion

Contrast to lesions in the brainstem (medulla) involving the CNs, these will cause losses in ipsilateral face and contralateral body

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67
Q

What type of contraception is ideal for pts w/PCOS?

A

1st line are combined OCPs, but they should all receive progestins – these confer endometrial protection and help thin and reverse the hyperplasia thereby reducing the risk of cancer

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68
Q

What exam findings are consistent w/severe aortic stenosis?

A
  1. Soft, single second heart sound (S2) – d/t delayed closure of the aortic valve
  2. Pulsus parvus et tardus – delayed and diminished carotid pulse
  3. Loud and late-peaking systolic murmur
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69
Q

What is most likely to cause multi-nutrient malabsorption in a young patient?

A

Celiac disease

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70
Q

What are some of the extraintestinal manifestations of celiac disease?

A
General: fatigue, weight loss
Skin: dermatitis herpetiformis, vitiligo
MSK: osteopenia/porosis, osteomalacia – high alk phos levels, low Ca2+, low PO4-, low Vit. D
Heme: anemia (esp. Fe-deficient)
Neuro: peripheral neuropathy, HAs
Endocrine: AI thyroiditis, Type I DM
Psych: depression, psychosis
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71
Q

What are the characteristics and causes of subclinical hyperthyroidism?

A

Characteristics: Suppressed TSH, normal thyroid hormone levels, +/- hyperthyroid sxs

Causes: Exogenous thyroid hormone, graves disease, nodular thyroid disease, inflammatory thyroiditis

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72
Q

When is tx indicated in the setting of subclinical hyperthyroidism?

A
If TSH is persistently <0.1
If TSH is 0.1-0.5 PLUS additional risk factor:
   Age 65+
   Heart disease
   Osteoporosis
   Nodular thyroid disease
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73
Q

What is the tx of symptomatic bacterial vaginosis?

A

Oral or vaginal Metronidazole or Clindamycin

during pregnancy only symptomatic pts are tx’d; tx does not decrease cxs in asx pts

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74
Q

When should a carotid endarterectomy be performed?

A

In patients w/symptomatic carotid artery disease who have high grade stenosis (70-99%) and a life expectancy of 5+ years

Risks outweigh benefits in pts who are poor surgical candidates or have shorter life expectancies.

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75
Q

What are the 3 CHD risk equivalents/most significant predictors of adverse cardiovascular outcomes?

A
  1. Noncoronary atherosclerotic disease (carotid, PAD, AAA)
  2. Diabetes
  3. CKD
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76
Q

How is Juvenile myoclonic epilepsy diagnosed?

A

EEG showing bilateral polyspike and slow wave activity/discharges

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77
Q

What are the characteristics and tx of infantile spasms?

A

Epileptic disorder of infancy characterized by symmetric spasms, developmental delay and hypsarrhythmia on EEG.
Gold-standard tx: Corticotropin (ACTH) and Vigabatrin

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78
Q

What are common secondary causes of restless leg syndrome?

A
Fe-deficiency anemia
Uremia/ESRD/CKD
DM
MS or Parkinson
Pregnancy
Drugs – antidepressants, metoclopramide
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79
Q

How would cholecystitis and cholangitis be differentiated on US?

A

Cholecystitis will show gallbladder wall thickening and edema/pericholecystic fluid (no obstruction, just inflammation)

Cholangitis will show dilation of the intrahepatic ducts and common bile duct (obstruction leading to infection)

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80
Q

What is a common complication of gallstone pancreatitis?

A

Acute cholangitis – should be suspected in anyone w/gallstone pancreatitis who has fevers, RUQ pain, jaundice, AMS, and HoTN.
Must do ERCP stat to relieve obstruction to prevent development of sepsis and death

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81
Q

What Rxs are contraindicated or should be avoided in pts w/RVMI?

A

Nitrates – decrease RV preload and cause profound HoTN and cardiogenic shock
Diuretics – volume depletion and HoTN
Opiates – venous dilation and decreased RV preload
BBs – sometimes appropriate, but contraindicated in pts w/bradycardia or cardiogenic shock

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82
Q

How can a large PE be differentiated from RV MI?

A

PE is more likely to cause tachycardia, dyspnea, and syncope
RVMI is more likely to cause bradycardia and arrhythmias
Both can cause RV dysfxn, increased CVP and decreased LV preload and CO

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83
Q

What are signs of RV MI?

A

Often in patients w/acute inferior wall MI d/t occlusion of the RCA proximal to the RV brs.

Signs/Sxs: chest pain, HoTN, autonomic signs (diaphoresis, V), and EKG findings of ST elevation in leads II, III, and aVF.
May also have JVD, +Kussmaul’s sign, and clear lung fields suggestive of RVF
Possible bradycardia or AV block bc enhanced AV tone.

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84
Q

EKG leads involved in RV MI:

A

Blocked RCA
ST elevation in V4-V6
Occurs in 1/2 of Inferior MIs

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85
Q

EKG leads involves in lateral MI:

A

LCX, diagonal vessel blocked
ST elevation in I, aVL, V5 and V6
ST depression in II, III, and aVF

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86
Q

EKG leads involved in posterior MI:

A

LCX or RCA blocked
ST depression in V1-V3
ST elevation in I and aVL (LCX)
ST depression in I and aVL (RCA)

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87
Q

EKG leads involved in inferior MI:

A

RCA or LCX blocked
ST elevation in leads II, III, and aVF
Inferior MIs are a/w HoTN, bradycardia and AV block.

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88
Q

EKG leads involved in anterior MI:

A

LAD blocked

Some or all of V1-V6

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89
Q

Anticholinergic effects of TCAs:

A
Dry mouth
Blurred vision
Dilated pupils
Flushing
Hyperthermia
Urinary retention
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90
Q

How is Dementia w/Lewy bodies treated?

A
Cholinesterase inhibitors (donepezil) for cognitive impairment
Carbidopa-levodopa for parkinsonism
Melatonin for REM sleep behavior disorder

antipsychotics may be used to tx functionally impairing visual hallucinations/delusions, but pts w/DLB are vv sensitive to antipsychotics and they can cause significant worsening of confusion, parkinsonism and autonomic dysfunction

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91
Q

If antipsychotics need to be prescribed in DLB which should be used?

A

Low-potency 2nd gens like Quetiapine

High-potency 2nd gens (Risperidone) and 1st gens are a/w significant exacerbations of sxs

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92
Q

What is the MoA of Organophosphates?

A

They inhibit acetylcholinesterase at the NMJ – causes CHOLINERGIC toxicity

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93
Q

What is the MoA of Atropine?

A

Competitive inhibition of acetylcholine at muscarinic receptors – causes anticholinergic toxicity.

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94
Q

What are the signs/sxs of Cholinergic toxicity?

A
Muscarinic effects: “DUMBELS”
   Defecation/diarrhea
   Urination
   Miosis
   Bronchospasm/bradycardia
   Emesis
   Lacrimation
   Salivation
Nicotinic effects: mm. weakness, paralysis, fasciculation
CNS: respiratory failure, seizure, coma

often caused by organophosphate poisoning

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95
Q

Mgmt of organophosphate poisoning:

A
Emergent resuscitation – O2, IVF, intubation
Atropine &amp; Pralidoxime
Activated charcoal (if w/in 1hr of exposure)
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96
Q

Common sxs seen in anticholinergic toxicity:

A
Dry mucous membranes
Flushing
Mydriasis
Urinary retention
Decreased bowel motility
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97
Q

1 risk factor for PID:

A

Multiple sexual partners

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98
Q

Common signs/sxs of salicylate toxicity:

A

Brain: Tinnitus, dizziness, AMS, cerebral edema, seizures
Lungs: tachypnea, pulmonary edema
Heart: arrhythmia
Liver: hepatitis
Stomach: nausea, vomiting
Systemic: fever/hyperthermia, metabolic acidosis/lactic acidosis

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99
Q

Tx of salicylate toxicity:

A

Alkalinization of serum and urine w/sodium bicarb

Other options: supplemental glucose (dextrose 5% H2O), activated charcoal (if w/in 2hrs of ingestion), dialysis (if pt has pulm edema, fluid overload, AMS, renal failure, cerebral edema, severe acidosis or v high salicylate levels)

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100
Q

What are the typical lab findings in RMSF?

A

Thrombocytopenia
Hyponatremia
Increased AST and ALT

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101
Q

What is the tx of RMSF?

A

Doxycycline – even for children and pregnant women

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102
Q

What is the tx of Lyme disease?

A

Doxycycline for all late stages and early stage in everyone >8yo
Amoxicillin for early lyme in children <8

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103
Q

When should inotropic agents be used in pts w/RVMI?

A

When a pt. has persistent HoTN despite aggressive fluid resuscitation.
Dopamine is the initial Rx of choice

Dobutamine should be avoided as it can decrease PVR and worsen HoTN.

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104
Q

When would hypertrophic osteoarthropathy be seen?

A

It is a paraneoplastic syndrome a/w intrathoracic malignancy + other pulm diseases (CF)
Polyarthropathy a/w digital clubbing and periostosis (xs bone formation)

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105
Q

Dx of Polymyositis:

A

Elevated m. enzymes – CK, aldolase, AST
Auto-Abs – ANA, anti-Jo-1
Bx – Endomysial infiltrate and patchy necrosis

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106
Q

DTR in polymyositis:

A

NORMAL! Differentiates it between other causes of muscle weakness – Hypothyroidism (delayed), and Lambert Eaton (absent)

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107
Q

What is mixed connective tissue disease and what are the lab findings?

A

AI disorder w/variable features of: SLE, Systemic Sclerosis and Polymyositis

Lab findings: Anti-U1 ribonucleoprotein, ANA, RF, anti-CCP, elevated CK, anemia/cytpoenias

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108
Q

What is the difference b/w PMR and Polymyositis?

A

PMR has pain and stiffness in muscles, but NO weakness. Have increased ESR and CRP, but CK, aldolase, etc are all normal

Polymyositis has severe weakness, but pain is mild/absent and no stiffness. Will have increased CK, aldolase, AST and ANA/Anti-Jo-1 Abs. Need muscle bx to dx this but not PMR

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109
Q

What are the side effects of SGLT2 inhibitors?

A

Sodium-glucose cotransporter-2 inhibitors (canagliflozin) can cause:
Genitourinary infections – vulvovaginal candidiasis, UTIs
Fluid loss – symptomatic HoTN, AKI
Metabolic abnormalities: Hyperkalemia, hyperglycemia, euglycemic ketoacidosis
Misc – low trauma fractures, amputation

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110
Q

What is the approximate chance of a patient with acute HBV infection progressing to chronic HBV infection?

A

The chance decreases with age:
Perinatally acquired infections have 90% chance of progressing to chronic HBV
Children age 1-5 have a 20-50% progression rate
Adults have <5% progression rate

In contrast, HAV has an almost 0% progression rate, and HCV has a 75-85% progression rate

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111
Q

What should be suspected in an alcoholic who develops weakness after feeding/fluids are started?

A

Rhabdomyolysis 2/2 hypophosphatemia that is exacerbated/unmasked by refeeding

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112
Q

What electrolyte disturbances are seen in refeeding syndrome?

A

Increased insulin occurs d/t carbohydrate ingestion (IV or enteral)
This causes increased cellular uptake and decreased serum levels of: K+, PO4, Mg2+, and Thiamine

Phosphate is the primary deficient electrolyte bc its needed to make ATP

Deficiencies in Mg2+ and K+ cause cardiac arrhythmias

Thiamine deficiency causes Wernicke

Aggressive nutrition w/o adequate electrolyte replacement – cardiopulmonary failure

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113
Q

DoC for folate-def anemia induced by MTX therapy:

A

Folinic acid (Leucovorin) – more potent than folic acid, and can rescue RBCs by bypassing the block on DHFR

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114
Q

What are the features of Tuberous sclerosis complex?

A

Neurocutaneous disorder w/benign tumors in multiple organs – intracardiac rhabdomyomas, renal angiomyolipomas
Angiofibromas, ash-leaf spots and shagreen patches (thick leathery skin, dimpled like an orange peel)

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115
Q

What are the features of Sturge-Weber syndrome?

A

Triad of port-wine stain on the face, ocular disease (visual deficits or glaucoma), and leptomeningeal capillary-venous malformations.
Often have seizures from the malformations

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116
Q

When does renal biopsy need to be performed in the pediatric population?

A

Kids >10 w/nephrotic syndrome
Kids of all age w/nephritic syndrome
Patients <10 w/minimal change that don’t respond to steroids

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117
Q

What imaging should be part of the initial evaluation in a pt. suspected to have Tuberous Sclerosis Complex?

A

Brain MRI/EEG – determine if there are any tumors or baseline seizure activity
Abdominal US or MRI – evaluate for renal involvement (obstructive renal angiomyolipomas)

Neurologic impairment/epilepsy is the #1 cause of death in TSC and renal involvement is the 2nd

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118
Q

How is Cerebral palsy diagnosed?

A

Clinically (usually by 1-2yrs) + Brain MRI (shows periventricular leukomalacia, brain malformation, ischemia, BG lesions, etc.)
EEG should only be done in pts who have seizure-like activity

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119
Q

Sxs of Scombroid poisoning:

A

Flushing, throbbing HA, palpitations, abdominal cramps, diarrhea, oral burning, skin erythema, wheezing, tachycardia, and HoTN
Occurs when fish is stored improperly and histidine undergoes decarboxylation to form histamine

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120
Q

Sxs of pufferfish poisoning:

A

Primarily neurologic: perioral tingling, incoordination, weakness, etc.

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121
Q

What are the common features of subphrenic abscess and how is it diagnosed?

A

Commonly seen 14-21 days after abdominal surgery
Often have hx of abdominal surgery, swinging fever, leukocytosis, and cough and shoulder-tip pain may be the presenting sxs.
Abdominal US is best diagnostic test

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122
Q

What is the role of Lamotrigine in bipolar patients?

A

An anticonvulsant, it is used in the depressed phase and for maintenance therapy
It is not effective for treating mania.

Quetiapine and Lurasidone are alternatives for bipolar depression

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123
Q

When should antibiotics be added to the mgmt. of a pt. w/COPD exacerbation?

A
If they have any 2 of the following:
   Increased sputum purulence
   Increased sputum volume
   Increased dyspnea
Or if they require any type of mechanical ventilation (invasive or non)
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124
Q

What is the definition of macrocephaly and when should neuroimaging be sought?

A

Macrocephaly is head circumference >97th percentile for age
Neuroimaging should be done to evaluate for pathologic processes when:
Rapidly expanding HC (>2cm/mo in an infant <6mo)
Neuro abnormalities (seizures etc)
Developmental delay

Head US is best study in infants w/open anterior fontanelle

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125
Q

What measure of association should be used in case control studies, and how is it calculated?
biostats

A

Odds ratio should be used. It is the odds of an event occurring in exposed patients divided by the odds of an event in unexposed pts. (null value is 1)

OR = (a/c) / (b/d) = (ad)/(bc)

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126
Q

What measure of association should be used in cohort studies and how is it calculated?
biostats

A

Relative risk (null value is 1.0)

RR = (a (a+b)) / (c (c+d))
= (risk of developing disease in the exposed group) / (risk in the unexposed)

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127
Q

What does the kappa statistic measure?

biostats

A

Inter-rater reliability

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128
Q

What is the null value when assessing OR?

biostats

A

1.0

Ho = 1.0 for RR and HR as well.

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129
Q

What is the most specific finding to suggest cardiac tamponade?

A

Early diastolic collapse of the RV and RA – seen on echo
Electrical alternans on EKG is also fairly specific for tamponade

In contrast, low-voltage QRS on EKG, kussmaul sign, and pulsus paradoxus are all non-specific and can be seen in multiple other disease states.

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130
Q

What are the signs/sxs of Ethylene glycol (antifreeze) toxicity?

A

Early signs: nausea, vomiting, slurred speech, ataxia, nystagmus, lethargy, kussmaul’s breathing/rapid and deep (d/t severe anion-gap metab acidosis)

Later signs/further toxicity: tachypnea, agitation, confusion, flank pain, renal failure, pulmonary edema, AMS, eventual coma

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131
Q

When do oral glucocorticoids need tapering?

A

If they have been taken for 3+ weeks, especially if they were taken at high doses or at night. Need a roughly 3 week tapering period

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132
Q

What antibiotic has increased risk for tendon ruptures/tears?

A

FLUOROQUINOLONES

Hydroxychloroquine also increases risk

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133
Q

What medication is approved for photoaged skin?

A

Tretinoins

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134
Q

What is the main complication of anal abscesses?

A

Fistula formation – up to 50% of pts w/anal abscesses develop chronic fistula

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135
Q

What diseases are WSW at higher risk for?

A

HPV infection and therefore cervical cancer
Ovarian and breast cancers – d/t higher rates of smoking and obesity, less freq screening, lower parity and less OCP use
Bacterial vaginosis
DM-II
CVD

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136
Q

What is net clinical benefit?

biostats

A

The clinical usefulness of a medication – it’s a measure of its possible benefit minus its harm

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137
Q

What is the primary purpose of using an “intention-to-treat” approach?
biostats

A

To preserve randomization

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138
Q

Causes of acute, painless vision loss:

A
  1. Central retinal a. occlusion – have pale fundus w/”cherry red spot”
  2. Central retinal v. occlusion – fundus w/retinal hemorrhages and optic disc edema
  3. Retinal detachment – fundus w/vitreous hemorrhages and marked elevation of retina
  4. Vitreous hemorrhage – decreased red reflex, visible hemorrhage on fundoscopy
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139
Q

What is length-time bias?

biostats

A

When pts w/rapidly progressive form of a disease are less likely to be detected by screening when compared to those w/slowly progressive disease
Slowly progressive pts remain asx for longer and increase their chances of being diagnosed by screening measures.

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140
Q

What are the calculations for Sensitivity and Specificity?

biostats

A
Sensitivity = True Positives / (TP + FN) or A / (A + C)
Specificity = True Negatives / (TN + FP) or D / (B + D)
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141
Q

What are the calculations for PPV and NPV?

biostats

A
PPV = TP/ all(+) or A/(A + B)
NPV= TN/ all(–) or D/(D + C)
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142
Q

What is the only azole that should not be used in Aspergillus infection?

A

Fluconazole – has limited activity against aspergillus and shouldn’t be used

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143
Q

What is the treatment of Allergic Bronchopulmonary Aspergillosis?

A

Systemic glucocorticoids
Antifungal therapy – itraconazole or voriconazole are DoCs
Omalizumab may occasionally be used

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144
Q

What findings should raise suspicion for TB meningitis?

A

Brain imaging showing basilar meningeal enhancement
CSF showing: increased protein, low glucose, lymphocytic pleocytosis, elevated adenosine deaminase
May also see choroidal tubercles (yellow-white nodules near optic disc) on fundoscopy

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145
Q

When should colchicine NOT be used in an acute gouty attack?

A

In patients taking other medications that cause leukopenia as that is also a risk of colchicine, and in patients w/renal failure

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146
Q

When do hepatic adenomas require treatment?

A

If they are symptomatic or >5cm – surgical resection

If asx and <5 then stop offending meds (OCPs)

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147
Q

What are some of the common features to suggest Cervical Myelopathy?

A

LMN signs at the level of the lesion – weakness and atrophy in the arms
UMN signs below the lesion – gait dysfxn, and hyperreflexia in the legs

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148
Q

How would paraneoplastic myelopathy present?

A

It is lesion against the spinal cord and will present w/flaccid or spastic paraplegia or quadriplegia, sensory deficits +/- urinary or fecal retention/incontinence

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149
Q

Common findings in invasive aspergillosis:

A

Triad of fever, chest pain and hemoptysis
Pulmonary nodules (yes plural) with halo sign (surrounding ground-glass opacities)
Positive cell wall biomarkers (galactomannan, beta-D-glucan)

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150
Q

Tx of Invasive Aspergillosis:

A

1-2wks of IV Voriconazole + an Echinocandin (Capsofungin)

Then can be transitioned to prolonged oral tx of Voriconazole alone

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151
Q

Tx of ITP:

A

glucocorticoids

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152
Q

What should all patients with presumed ITP be tested for?

A

HIV and HCV

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153
Q

What kind of infection is ringworm?

A

It is a Dermatophyte infection – Tinea Corporis
Aka this is a fungal, NOT parasitic infection and needs to be tx’d 1st line w/topical anti-fungals (Clotrimazole, terbinafine)

Dermatophyte infection involving the scalp (tinea capitis), diffuse or refractory cases are tx’d w/oral anti-fungals (griseofulvin, terbinafine)

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154
Q

What are the main organisms that cause central line-associated bloodstream infections?

A
#1: Coagulase negative staph.
Others: S. aureus, gram negs. (Klebsiella, pseudomonas), and Candida
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155
Q

When should Cefepime be part of the tx regimen for meningitis?

A

If the person is IMCP’d or it occurs after neurosurgery/penetrating skull trauma
It’s a 4th gen-ceph and covers: S. pneumo, N. meningitidis, GBS, H. influenzae, MSSA and Pseudomonas

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156
Q

Common causes of adrenal hemorrhage:

A

Pts on anticoagulants w/acute stress (sepsis)

Hemorrhagic necrosis w/systemic infections: meningococcemia or pseudomonas sepsis

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157
Q

What characteristic of CF bronchiectasis helps differentiate it from other causes?

A

Upper lung lobe involvement – CF is the main cause of bronchiectasis involving the upper lobes
Infection w/Pseudomonas is also characteristic

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158
Q

Febrile Neutropenia common causes and treatment:

A

G-negs (P. aeruginosa especially) are most common infection in febrile neutropenia.
Once blood cultures are taken monotherapy w/an anti-pseudomonal B-lactam should be started – cefepime, meropenem, pip-tazo.

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159
Q

Presentation of Langerhans cell histiocytosis:

A

Lytic bone lesions (skull, jaw, femur) seen in diaphysis of long bones
Skin lesions (purplish papules, eczematous rash)
Lymphadenopathy, hepatosplenomegaly
Pulmonary cysts/nodules
Central DI

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160
Q

What is the most common cause of Pneumonia in CF children v. adults?

A

In children, S. aureus is the most common and Pseudomonas is in adults.
S. aureus starts to decline around age 20 whereas pseudomonas begins to peak.
Both pathogens should be covered in tx of pneumonia in CF children.

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161
Q

What renal disease are HBV+ people most at risk of getting?

A

Membranous nephropathy.

Normally uncommon in children, but can occur in those w/HBV

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162
Q

What cyanotic heart diseases of the newborn present with a single S2?

A

Transposition – Single S2 +/- VSD murmur
Tricuspid atresia – Single S2 + VSD murmur
Truncus arteriosus – Single S2 + systolic ejection murmur

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163
Q

Most common congenital cyanotic heart disease in the neonatal period:

A

Transposition of the great vessels.

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164
Q

What kind of bacteria is Bartonella henselae and what is the tx?

A

Fastidious gram neg bacilli
Tx: Azithromycin; However, many cases are self-limiting and don’t require tx
*may also add clindamycin if lymphadenopathy is present but dx is unclear

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165
Q

Tx of Sporotrichosis:

A

3-6mo of oral Itraconazole

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166
Q

Most common cause of secondary amenorrhea:

A

Pregnancy

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167
Q

What is the single-item screening question used for alcohol abuse?

A

How many times in the past year have you had 5 (4 for women) or more drinks in a day?

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168
Q

When is metformin contraindicated?

A

In pts w an estimated GFR <30

Should be used w caution in those w/eGFR 30-45

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169
Q

Mgmt of pancreatogenic diabetes:

A

Occurs d/t chronic pancreatitis destroying islet cells (alpha and beta)
Tx: Metformin for mild hyperglycemia, Insulin for more severe or symptomatic hyperglycemia

these pts are prone to developing hypoglycemia d/t loss of glucagon-producing a-cells, but ketoacidosis is rare bc of this glucagon loss

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170
Q

What is the typical difference in differentiating Upper GI Bleed (UGIB) v. LGIB?

A

UGIB mostly presents as hematemesis or melena

LGIB is more commonly hematochezia or bright red blood from the rectum

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171
Q

How does CHF cause hyponatremia?

A

Low CO and decreased perfusion P at baroreceptors and renal afferent aa. –> increased release of renin and NE + secretion of ADH.
ADH binds to V2 receptors in collecting ducts and increases H2O reabsorption
Renin and NE increase proximal Na+ and H2O reabsorption and limit water delivery to distal tubules
This all leads to water retention and dilutional hyponatremia

Hyponatremia in CHF parallels the severity of HF and is a predictor of adverse outcomes

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172
Q

When should hyponatremia be corrected in the setting of CHF?

A

If the patient develops sxs of hyponatremia or if they are asx in severe hyponatremia (Na+ <120)
Initial tx is water intake restriction

Correction of hyponatremia doesn’t improve clinical outcomes a/w HF

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173
Q

What abx pose increased risk of infantile hypertrophic pyloric stenosis?

A

Macrolides: Azithromycin and Erythromycin

- often given as post-exposure pphx for pertussis to infants w/a sick contact

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174
Q

What is the main cause of otitis-conjunctivitis syndrome?

A

Nontypeable H. Influenzae

Causes concurrent otitis media and purulent conjunctivitis

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175
Q

Tx of acute otitis media:

A

Initial: Amoxicillin
2nd Line: Amoxicillin-clavulanate (given for recurrent AOM if pt already received amoxicillin w/in the same month)
Penicillin-allergic: clindamycin or azithromycin

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176
Q

When is a cerclage typically placed?

A

at 12-14 weeks gestation

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177
Q

What is the tx of scleroderma renal crisis?

A

ACEIs are the DoC (captopril esp.) bc they reverse the angiotensin-induced vasoconstriction
If the pt. has malignant HTN w/CNS manifestations a 2nd agent may be added, like IV nitroprusside

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178
Q

What tests should be ordered when adrenal insufficiency is suspected and how are they interpreted?

A

Need morning plasma cortisol w/concurrent ACTH

  1. Low cortisol + high ACTH – diagnostic for primary adrenal insufficiency
  2. Low cortisol + low ACTH – secondary or tertiary adrenal insufficiency
  3. If testing is indeterminate get further tests to assess pituitary fxn
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179
Q

How will hypoaldosteronsim present?

A

Often asx w/hyperkalemia and mild metabolic acidosis

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180
Q

How will Chronic adrenal insufficiency present?

A

Fatigue, weight loss, myalgias, increased pigmentation, decreased axillary and pubic hair

Labs: hyponatremia, hyperkalemia, hyperchloremic metabolic acidosis

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181
Q

How long can lymphadenopathy be observed for following a viral illness?

A

Lymphadenopathy is common in mono especially and can be observed for 3-4 weeks or less if the pt. presents w/ signs of malignancy.
After this time period they should be referred for biopsy

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182
Q

What are the key differences b/w Aplastic crisis and splenic sequestration crisis in sickle cell pts?

A

Aplastic crisis – reticulocytes go down (<1%); transient arrest of erythropoiesis, secondary to infection
Splenic sequestration – reticulocytes increase; vaso-occlusion causes rapidly enlarging spleen, only occurs prior to autosplenectomy

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183
Q

When should a long-term tunneled catheter be removed in the setting of suspected catheter-related bloodstream infection?

A

If any of the following are present:
1. Severe sepsis
2. Hemodynamic instability
3. Evidence of metastatic infection (endocarditis)
4. Pus at the exit site of the catheter
5. Continued sxs >72 hrs after abx
6. Blood culture confirmation of: S. aureus, P. aeruginosa, or fungi (candida)
All other pts should just have catheter changed over a guidewire once afebrile and stable

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184
Q

1st line treatment of HTN in Gout pts:

A

ARBs and ACEIs
*Especially Losartan: has a mild uricosuric effect
Most diuretics (thiazides, furosemide) decrease urate excretion and should be avoided

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185
Q

When is a CT urogram safe during pregnancy?

A

Only in the 2nd and 3rd trimesters

It should never be the 1st imaging test ordered in pregnancy – start w/renal and pelvic US, if negative do transvaginal US, if negative either treat empirically for stone or can do MRU or low-dose CTU

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186
Q

What abx have activity against Pseudomonas?

A

Cefepime and Ceftazidime (cephalosporins)
Amikacin and tobramycin (aminoglycosides)
Carbapenems
Levofloxacin, gemofloxacin (respiratory fluoroquinolones)
Aztreonam
Colistin (aka polymyxin E)
Pip-tazo
Ticarcillin-clavulanate

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187
Q

What is the leading cause of death in patients with parkinson’s disease?

A

Aspiration pneumonia

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188
Q

How should all patients w/unexplained new-onset HF be evaluated?

A

Echo, EKG, and Stress testing or coronary angiography to assess for CAD

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189
Q

What adjunctive therapy can be used to tx PCP?

A

In addition to TMP-SMX corticosteroids may be used and have been shown to reduce mortality in severe cases.
Indications: PaO2 <70 or A-a gradient >35 on room air.

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190
Q

Difference b/w diagnostic tests of choice for Diverticulitis v. Diverticulosis:

A

Diverticulosis – barium enema is test of choice, may do colonoscopy
Diverticulitis – Contrast CT is test of choice (barium enema and colonoscopy are contraindicated until rupture is r/o)

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191
Q

Scleroderma renal crisis:

A

Sudden onset of renal failure (w/o previous kidney disease), malignant HTN (HA, blurry vision, N).
UA may show mild proteinuria
PBS may show microangiopathic hemolytic anemia or DIC w/schistocytes and thrombocytopenia.

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192
Q

Auto-Abs in Scleroderma:

A

Antinuclear-Ab (most sensitive, but not specific)
Anti-topoisomerase I (anti-Scl-70) Ab & anti-RNA pol III (most specific)
Anticentromere-Ab (mostly in limited disease/CREST)

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193
Q

What kind of shock can be seen in mineralocorticoid deficiency?

A

Distributive shock – norm from primary adrenal insufficiency.
Will have HoTN from low aldosterone levels and low SVR a/w hyperkalemia and hyponatremia.

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194
Q

How to differentiate between primary and secondary adrenal insufficiency:

A

Primary – d/t AI destruction of adrenal gland will see hyperpigmentation and mineralocorticoid deficiency, HoTN etc. Eosinophilia and hyperplasia of lymphoid tissues (tonsils) are also common findings.

Secondary – d/t destruction of the pituitary gland will not have these effects and will only present w/signs of glucocorticoid and androgen deficiency.

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195
Q

What anesthetic can lead to adrenal insufficiency?

A

Etomidate – it inhibits 11B-hydroxylase

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196
Q

Tx of tinea versicolor:

A

Topical anti-fungals (azoles are DoC)

If topical tx is ineffective or there is extensive disease, switch to oral azole

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197
Q

What is a 24-hr holter monitoring used for?

A

To diagnose suspected paroxysmal cardiac arrhythmias

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198
Q

What are the 5 diagnostic criteria for Kawasaki disease?

A
  1. Rash – inguinal folds, perineum, trunk
  2. Nonexudative conjunctivitis
  3. Swelling +/- erythema of palms/soles
  4. Mucositis – erythema of lips, tongue, oral mucosa
  5. Cervical lymph node >1.5cm
    All these must be present w/fever for 5+ days
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199
Q

How should a child w/suspected Kawasaki disease be managed when they don’t meet all 5 diagnostic criteria?

A

If 3 or less criteria are met in a child w/5+ days of fever then CRP, or ESR should be measured, ibuprofen should be given and daily follow up should occur to monitor for more sxs

If 4 criteria are met then you can diagnose KD and give aspirin + IVIG (only given until response is seen)

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200
Q

What challenge does the mgmt. of Kawasaki pose in children?

A

It is tx’d w/IVIG which interferes w/the body’s normal immune response to live vaccines and therefore live vaccines should be deferred for 11 months after receiving IVIG

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201
Q

What type of dysphagia is seen in Barrett’s esophagus?

A

None – it doesn’t cause dysphagia

If it transitions into malignancy the associated malignancy can cause obstructive dysphagia

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202
Q

What are the antipsychotic induced extrapyramidal effects and how are they treated?

A

Acute Dystonia – benztropine, diphenhydramine
Akathisia – BB (propranolol), benzodiazepine (lorazepam), benztropine
Parkinsonism – Benztropine, amantadine
Tardive dyskinesia – valbenazine, deutetrabenazine

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203
Q

How is spontaneous splenic rupture managed?

A

Initially non-operatively w/volume resuscitation and gaining hemodynamic stability
If pts remain hemodynamically unstable despite adequate resuscitation cut em open

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204
Q

Analgesics a/w Rx-induced pancreatitis:

A

Acetaminophen
NSAIDs
Mesalamine, Sulfasalazine
Opiates

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205
Q

Antibiotics a/w Rx-induced pancreatitis:

A

Isoniazid
Tetracyclines
Metronidazole
TMP-SMX

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206
Q

Antiepileptics a/w Rx-induced pancreatitis:

A

Valproate

Carbamazepine

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207
Q

Anti-hypertensives a/w Rx-induced pancreatitis:

A

Thiazides, furosemide

Enalapril, losartan

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208
Q

Antivirals a/w Rx-induced pancreatitis:

A

Lamivudine

Didanosine

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209
Q

Immunosuppressants a/w Rx-induced pancreatitis:

A

Azathioprine, mercaptopurine

Corticosteroids

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210
Q

What is the most likely outcome of chronic urticaria?

A

Spontaneous resolution w/in 2-5 years

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211
Q

What EKG findings are the diagnostic criteria of STEMI?

A

New ST elevation at the J-point in 2+ anatomically contiguous leads w/the following threshold:
- >1mm in all leads except V2 and V3
- 1.5+ mm in women, 2+mm in men 40+, and 2.5+mm in men <40 in leads V2 and V3
New LBBB w/clinical presentation consistent w/ACS

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212
Q

When are cleft lip/palate reconstruction surgeries typically performed?

A

By 3mos/10wks of age

Rule of 10s: 10lbs of weight, 10wks of age, 10g of hemoglobin

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213
Q

What are the 2main causes of acute mitral regurgitation?

A

Papillary muscle rupture – occurs d/t MI or trauma

Chordae tendineae rupture – can be 2/2 MVP, Infective endocarditis, Rheumatic heart disease, trauma

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214
Q

Main differences b/w bacterial otitis externa and bacterial otitis media:

A

Both caused by bacteria and typically have purulent ear drainage (if tympanic membrane is ruptured in AOM)

  • Otitis externa almost always has pain on manipulation of the ear, and fever is generally absent
  • Otitis media almost always has fever, but pain is often absent once the tympanic membrane is ruptured
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215
Q

Characteristics of late decels on FHR tracing:

A

Onset w/contraction and 30+ seconds to the nadir

Often seen in setting of fetal hypoxia

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216
Q

Characteristics of variable decels on FHR tracing:

A

<30 sec to nadir with variable depths, can have more than one between contractions
Often caused by umbilical cord compression

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217
Q

What cancers cause primarily osteoblastic lesions when they have bone mets?

A

Prostate
Small cell lung
Hodgkin lymphoma
evaluate w/radionuclide bone scan

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218
Q

What cancers primarily have osteolytic lesions when they have bone mets?

A

Myeloma
Non-small cell lung
Non-hodgkin lymphoma
evaluate w/XR, PET or PET/CT

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219
Q

What abx can be used to treat UTI in pregnancy?

A
Nitrofurantoin is DoC (5-7d)
Amoxicillin (3-7d)
Amoxicillin-clavulanate (3-7d)
Fosfomycin (single dose)
Cephalexin (3-7d)
**Tetracyclines, flouroquinolones and TMP-SMX are contraindicated**
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220
Q

When should chelation therapy be used to tx lead poisoning?

A

When venous lead levels are >45 ug/dL
Dimercaptosuccinic acid (succimer) is used when levels are 45-69
Dimercaprol (British anti-Lewisite) + EDTA is used in emergency when levels are >70 or there are signs of acute encephalopathy.

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221
Q

What are some of the features unique to Ehlers-Danlos syndrome?

A

Skin manifestations – transparent/hyperextensible skin, easy bruising, poor healing, velvety w/atrophy and scarring
Abdominal and inguinal hernias
Uterine prolapse
High arched palate

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222
Q

What are some of the features unique to Marfan syndrome?

A
Tall w/long extremities
Pectus carinatum
Progressive aortic root dilation
Lens and retinal detachment
Spontaneous pneumothorax
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223
Q

Genetics a/w Ehlers-Danlos and Marfan syndromes:

A

Both AD inheritance
ED – COL5A1 and COL5A2 mutations
Marfan – FBN1 mutation

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224
Q

Calculation for NNT:

biostats

A

NNT = 1/ARR
ARR = (% affected in control group) – (% affected in treatment group)
= (c/(c+d)) – (a/(a+b))

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225
Q

How is PPV influenced by other factors?

biostats

A

PPV increases with increasing prevalence and increases with increased specificity
NPV increases with increasing sensitivity

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226
Q

What is attributable risk and how is it calculated?

biostats

A

AR is the difference in risk b/w exposed and unexposed

AR = (a/(a+b)) - (c/(c+d))

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227
Q

Risk factors of cerebral palsy:

A

Prematurity
Low birth weight

Smoking and EtOH use are NOT risk factors

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228
Q

Why does prematurity increase the risk of Cerebral Palsy?

A

Premature infants are more likely to have periventricular leukomalacia (white matter necrosis from ischemia/infarction) and intraventricular hemorrhage
Both of these are a/w CP

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229
Q

Diagnostic study for suspected aortic dissection:

A

TEE or CTA – but can’t use CTA in renal disease.

TTE should not be used

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230
Q

What complications can be prevented by lowering HbA1c/achieving glycemic control in DM?

A

The microvascular complications – nephropathy and retinopathy – will be reduced.
It will have no change on the macrovascular complications – MI, stroke.

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231
Q

Most common AE w/in 1-6hrs of transfusion:

A

Febrile nonhemolytic transfusion rxn. – can be prevented with leukoreduction.

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232
Q

When should cells be washed prior to transfusion?

A

If the pt. has IgA deficiency or had a prior allergic transfusion rxn.

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233
Q

Difference in lung region affected by Silicosis v. Asbestosis:

A

Asbestosis is one of the only pneumoconiosis that affects the LOWER lobes of the lungs

Pneumoconioses that affect the upper lobes:
Silicosis (a/w sandblasting and foundries, increases risk of TB)
Berylliosis (a/w aerospace engineering, vv. high risk of lung ca.)
Coal worker’s pneumoconiosis (aka black lung disease)

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234
Q

Evaluation of hypergastrinemia in patients on a PPI:

A

Nearly all pts on long-term PPIs will have hypergastrinemia (typically <400)

1st step to evaluate is withdrawal PPI and repeat gastrin levels; most pts will have normal gastrin levels after withdrawal
If gastrin levels are still high after PPI d/c then evaluate for other causes: H. pylori, ZES, gastrinoma, etc.

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235
Q

What are cannon waves and when are they seen?

A

Cannon waves are large a-waves seen on JVP tracings – d/t the RA contracting against a closed tricuspid valve

Seen in heart block and ventricular tachycardia/AV dissociation

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236
Q

What Rxs are used for rate control in aFIb?

A

CCBs – diltiazem, verapamil

BBs – metoprolol, propranolol, esmolol, atenolol, timolol, carvedilol

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237
Q

What supplement can cause a false-negative occult blood stool test?

A

Vitamin C

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238
Q

What should be given as long-term tx in anxiety attacks/panic attacks?

A

SSRI is 1st line

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239
Q

In children with viral GE what can exacerbate sxs and should be avoided?

A

Fruit juice – juice high in fructose or sorbitol increases the osmotic load and causes fructose malabsorption in the SI. Juices should be avoided until sxs of GE resolve.

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240
Q

What diagnostic tests should be done at the time of diagnosis of Scleroderma?

A

PFT +/- TTE
Should evaluate for pulmonary involvement as it is common in systemic sclerosis
ILD is common in diffuse cutaneous systemic disease, and pHTN is common in CREST syndrome

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241
Q

How long is the washout period from discontinuing one serotonergic Rx before beginning another?

A

Most antidepressants require a 14-day washout period before beginning another serotonergic med, but Fluoxetine has a long t1/2 and requires at least 5 weeks.

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242
Q

Mgmt of acute colonic ischemia:

A

IVF and bowel rest
Abx w/enteric coverage
Colonic resection if necrosis develops

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243
Q

Drugs that decrease levothyroxine absorption:

A

Bile acid-binding agents (cholestyramine)
Iron
Calcium
Aluminum hydroxide
PPIs
Sucralfate
can try taking these at a different time of day than levothyroxine to avoid malabsorption

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244
Q

Drugs that increase TBG concentration:

A
Estrogen (oral not IUDs)
Pregnancy
Tamoxifen, raloxifene, HRT
Heroin, methadone
Acute hepatitis
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245
Q

Drugs that decrease TBG concentration:

A
Androgens
Glucocoticoids/hypercortisolism
Anabolic steroids
Slow-release nicotinic acid
Chronic liver disease
Hypoproteinemia: nephrotic syndrome, starvation
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246
Q

Drugs that increase thyroid hormone metabolism:

A

Rifampin
Phenytoin
Carbamazepine

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247
Q

What imaging should be done to assess for suspected osteonecrosis of the femoral head?

A

MRI – much more sensitive than XR

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248
Q

What are the indications for parathyroidectomy?

A

Age <50
Symptomatic hypercalcemia
Cxs: Osteoporosis, nephrolithiasis/calcinosis, CKD (GFR <60)
Elevated risk of cxs: Ca2+ 1+ above normal, urinary Ca2+ excretion >400mg/day

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249
Q

What complications of lead toxicity occur at the lowest levels?

A

Cognitive impairment and behavioral problems can occur at levels as low as 10-20
Encephalopathy and hemolytic anemia only occur with severe toxicity (70+)

Decreases in nerve conduction can also occur at low lead levels but peripheral neuropathy is uncommon.

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250
Q

Contraindications to breastfeeding:

A
Active, untreated TB
HIV infection
Herpetic breast lesions
Active varicella infection
Chemo or radiation therapy
Active substance use disorder
Galactosemia in the infant
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251
Q

When should external cephalic version be performed?

A

37+ weeks gestation

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252
Q

What is the definitive mgmt. of a tension pneumothorax?

A

Chest tube placement – needle decompression is appropriate in the emergency setting where tension physiology is present and they are at risk of cardiac arrest, but then should always be replaced with a chest tube.
Needle decompression should not be done in a patient who is stable and has not yet developed tension physiology (tachycardia, JVD, tachypnea, hypoxemia, decreased/absent breath sounds)

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253
Q

Tx of urinary schistosomiasis:

A

Praziquantel

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254
Q

Tx of Keloid scars:

A

Intralesional glucocorticoids

Surgical excision can be considered if steroids fail

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255
Q

Tx of Cyanide toxicity

A

Sodium thiosulfate

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256
Q

What are common causes of SIADH?

A
CNS disturbance – stroke, hemorrhage, trauma
Drugs – carbamazepine, SSRIs, NSAIDs
Lung disease – pneumonia
Ectopic ADH secretion – SCLC
Pain and nausea
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257
Q

How to differentiate SIADH v. XS water ingestion:

A

SIADH will have serum hypotonicity (<275 mOsm), inappropriately high urine osmolality (>100mOsm), high urine sodium (>40), and clinical euvolemia
Excessive water ingestion will have low urine osmolality (<100mOsm) and euvolemic hyponatremia

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258
Q

Tx of Tourette syndrome:

A

2nd generation antipsychotics: Risperidone, aripiprazole, are preferred tx
1st generation antipsychotics: fluphenazine, pimozide, haloperidol, can also be used
Other 2nd line options: a2-agonists (clonidine, guanfacine), and tetrabenazine (DA depleter)

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259
Q

What is the most likely outcome of Sarcoidosis?

A

Resolution of sxs without recurrence (~75%)

Many need no tx, but those who do typically are treated for 1-2 years with steroids and then they are discontinued

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260
Q

Mgmt of Heparin-induced thrombocytopenia:

A

1st stop all heparin products
2nd start a direct thrombin inhibitor (argatroban) or fondaparinux (these are not oral)
3rd transition to warfarin (bc it is oral) after platelet count has recovered to >150k

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261
Q

Preferred tx of hyperthyroidism:

A

Methimazole is preferred over PTU bc of the severe hepatotoxicity a/w PTU
PTU is only preferred for women in the first trimester of pregnancy

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262
Q

What is raloxifene?

A

A SERM – used for breast ca prevention and tx of osteoporosis

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263
Q

What is sensitivity analysis?

biostats

A

Repeating a primary analysis calculations after modifying certain criteria or variable ranges
Used to determine if such modifications significantly affect the results initially obtained

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264
Q

What are the main complications of HOCM?

A

Sudden cardiac death
Arrhythmias – Vtach, aFib, etc.
Strong a/w WPW which increases risks of SCD

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265
Q

Drugs that are contraindicated in pts. w/WPW:

A
BBs
CCBs
Digoxin
Adenosine
**AVN conduction should NOT be slowed in these pts. which all these Rxs do**
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266
Q

Diseases associated with HOCM:

A

Wolf-Parkinson White

Friedreich ataxia

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267
Q

What is saw palmetto often used to tx and what are its side effects?

A

BPH

Side effects include mild GI sxs and increased bleeding risk

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268
Q

What are Likelihood ratios and how are they calculated?

biostats

A

LR is the probability of a given test result occurring in a pt. w/a disorder compared to the probability of the same result occurring in a pt. w/o the disorder.
Provides clinically useful information for individual patients and is not effected by prevalence

+LR = sensitivity / (1- specificity) ; -LR = (1-sensitivity)/specificity
LR>2 rules in the disease; LR<0.5 rules out the disease; LR 0.5-2 is equivocal

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269
Q

What does aFib w/rapid ventricular response look like on EKG and what is used to tx?

A

Narrow QRS-complex tachycardia
Absence of organized P waves
Irregularly irregular rhythm w/varying R-R intervals

Tx w/an AVN blocking agent like a BB or CCB (diltiazem, verapamil); unstable pts need cardioversion
Although adenosine is used to tx narrow-complex tachycardia it has no role in tx of aFib

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270
Q

What should be the initial test in determining the cause of polycythemia?

A

Serum EPO level

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271
Q

Rxs that increase lithium levels:

A
Thiazides
ACEIs/ARBs
NSAIDs (but not aspirin)
Abx: tetracycline and Metronidazole
Also, volume depletion (often d/t the above stated Rxs)

acetaminophen does not

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272
Q

When should pts w/Lithium toxicity be treated w/hemodialysis?

A

If levels are >4mEq/L
>2.5 w/sxs or renal failure
Increasing level despite tx w/IVF

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273
Q

What are common signs/sxs of Cushing’s syndrome?

A
HTN
Hyperglycemia – newly diagnosed DM
Osteoporosis
Mood Swings
Hypokalemia
Metabolic Alkalosis

Evaluate with overnight dexamethasone suppression test or 24hr urinary free cortisol

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274
Q

Common causes of constrictive pericarditis:

A

Idiopathic or viral
Cardiac surgery
Radiation therapy
TB pericarditis in endemic areas

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275
Q

What is cardiac cirrhosis?

A

Hepatic congestion that occurs 2/2 RHF that eventually leads to cirrhosis
Often seen as a result of constrictive pericarditis

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276
Q

Treatment of alopecia areata:

A

Topical or intralesional corticosteroids

side note: fingernail pitting is commonly a/w this condition

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277
Q

What is the initial mgmt. of DKA?

A

IV insulin + aggressive IVF (NS) + Potassium supplementation if <5.2

Once serum glucose falls <200 the rate of insulin infusion should be halved and dextrose should be added to IVF to prevent hypoglycemia

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278
Q

When should IV insulin be switched to subQ in DKA?

A

SubQ insulin can be started for the following: pt is able to eat, glucose is <200, anion gap <12 and serum HCO3 is 15+

IV insulin and SubQ insulin should be overlapped by 1-2hrs

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279
Q

When should mammography begin?

A

Between 40-50; 50 is recommended for general population but can start as early as 40 depending on individual and patient’s preferences

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280
Q

When should genetic testing for inherited breast cancer disorders be recommended?

A

2 1st-degree relatives w/breast ca (1 before age 50)
3 first or second degree relatives w/breast ca (at any age)
1st or 2nd degree relative w/breast and ovarian ca
1st degree relative w/ bilateral breast ca
Breast ca in a male relative
Ashkenazi jews w/any 1st or 2nd degree relative w/breast or ovarian ca

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281
Q

Tx for shingles:

A

7d of oral valacyclovir if they present <72hrs after rash onset
If >72hrs after rash onset typically just get analgesia and topical rash care (zinc oxide cream)
If IMCP’d or widespread disease – get IV acyclovir for 7+ days

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282
Q

How does splenic vein thrombosis often present?

A

May be asx, but can present w/variceal bleeding d/t isolated gastric varices – this is the hallmark of the disease
May also see portal HTN, ascites and congestive splenomegaly
Often a/w pancreatitis

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283
Q

How should infants of +HBV mothers be managed?

A

At birth HBV vaccine and HBV-Ig should be administered
Then HBV vax series should be completed at 2 and 6 months
Serology should be taken at 9months – if no HBsAg at that time, infant is uninfected

liver function tests are not used in detection of infantile HBV

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284
Q

Causes of central retinal a. occlusion:

A
Carotid a. atherosclerosis (most common)
Cardiogenic embolism
Sm. a. disease d/t DM +/- HTN
Carotid a. dissection
Hematologic disease (SCD, hypercoagulability)
Vasculitis (giant cell arteritis)

central retinal v. occlusion in contrast is usually not d/t embolic disease

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285
Q

What skin manifestation is highly concerning for Neurofibromatosis1?

A

Axillary and inguinal freckling

They also have numerous, widespread café-au-lait macules (more numerous than the gen population)

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286
Q

What should take precedence in evaluation of a patient suspected to have NF1?

A

Ophthalmologic evaluation – asses for bilateral optic pathway gliomas
These are pathognomonic for NF1, but often initially asx

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287
Q

When is egg allergy a contraindication to vaccine?

A

It’s not – personal or FHx is not a contraindication bc anaphylaxis is so rare
Can be given in an inpatient setting though if they want

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288
Q

What do overlapping confidence intervals imply?

biostats

A

Overlapping areas may or may not imply a statistically significant difference
Non-overlapping areas do imply a statistically significant difference.

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289
Q

What are the features of Pemphigoid gestationis?

A

Aka herpes gestationis
It’s an autoimmune disease typically presenting in the 2nd or 3rd trimester w/pruritis that precedes a truncal rash
Characteristic rash: begins periumbilical as urticarial papules and plaques – develop into vesicles and bullae
Rash spreads over entire body but spares mucous membranes

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290
Q

Tx of Pemphigoid gestationis:

A

High-potency topical steroids (triamcinolone)
Antihistamines
Typically resolves after delivery

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291
Q

When should IV-potassium be given in Diuretic-induced hypokalemia?

A

If the patient has dysfunctional bowel/paralytic ileus, cardiac or neurologic complications

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292
Q

What is penetrance?

A

The probability of a gene or trait being expressed
Aka will someone with a gene show any presence at all that they have the gene or will they be a silent carrier with no phenotypic expression

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293
Q

What is expressivity?

A

The variation in phenotypic expression

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294
Q

How to differentiate Sm Bowel Obstruction v. Ileus:

Causes, PE findings and Imaging findings

A

Small Bowel Obstruction:
Causes – prior surgery (wks to years)
PE – distended abdomen, increased bowel sounds
Imaging – small bowel dilation present; Large bowel distention ABSENT; air-fluid levels

Ileus:
Causes – recent surgery (hrs to days), metabolic (hypokalemia), medication induced
PE – possible distention, reduced/absent bowel sounds
Imaging – small bowel AND large bowel dilation; gas in colon and rectum, no air-fluid levels

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295
Q

Risk factors for testicular cancer:

A

Cryptorchidism – #1 risk
FHx
HIV infection

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296
Q

Workup in suspected testicular cancer:

A

Scrotal US
PE – firm ovoid mass or unilateral swelling, absence of transillumination
Tumor markers – AFP, B-hCG
Staging imaging – CT scan, Chest XR

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297
Q

Locations with highest prevalence of tick paralysis:

A

Australia
Western North America
most cases caused by Rocky Mtn. Wood tick and American Dog Tick

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298
Q

Features of tick paralysis:

A

Neurotoxins in tick saliva are transmitted over 4-7days and then sxs start:
Brief prodrome of fatigue and paresthesias
Gait ataxia and ascending paralysis develop over hrs
Absent DTRs
Fever and sensation abnormalities are usually absent and Lab and imaging are typically normal

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299
Q

Tx of Tick paralysis:

A

Meticulous skin examination to find and remove offending agent (tick)
Most patients recover completely after this and have dramatic improvement in sxs w/in few hrs after removal of tick

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300
Q

What features on head CT in an infant would suggest abuse over accident?

A

A mixed-density pattern showing both acute (hyperdense) subdural bleeds on chronic (hypodense) subdural bleeds

Accidental trauma is more likely to only show acute, hyperdense, bleeding

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301
Q

Mgmt of Shoulder Dystocia:

A

BE CALM: should be performed in this order
B – breathe, do not push
E – Elevate legs/flex hips (McRoberts)
C – call for help
A – apply suprapubic pressure
L – enlarge vaginal opening w/episiotomy
M – Maneuvers: deliver post. arm; rotate post. shoulder; adduct post. fetal shoulder; mother on hands and knees; all else fails replace fetal head and go for cesarean

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302
Q

When should endoscopic screening be performed to evaluate for Barrett esophagus?

A

Hx of chronic GERD (>5yrs) or frequent reflux sxs and 2+ of the following risk factors:
Age >50
Male sex
White
Hiatal hernia
Obesity/increased waist circumference (>102cm)
Current or former tobacco use
1st-degree relative w/Barrett esophagus or esophageal adenocarcinoma

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303
Q

What is the standard caloric intake recommended for enteral feeding?

A

30 kcal/kg/d with 1g/kg of protein

lower amounts are used for pts w/severe malnutrition to prevent refeeding syndrome

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304
Q

What are the tx options and durations of tx for Strep pharyngitis?

A

Penicillin is preffered tx – should be given orally for 10d minimum

Single dose IM Penicillin can be given to those who can’t tolerate oral abx

Azithromycin or Clindamycin may be given for 5d to those w/anaphylactic Pen allergies
Cefazolin is given for mild pen allergies

abx are continued for this length of time to reduce risk of ARF and suppurative cxs

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305
Q

What is the tx of papulopustular rosacea?

A

Topical metronidazole – most commonly prescribed

Others:
Azelaic acid
Topical clindamycin
Benzoyl peroxide

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306
Q

Common manifestations of ocular rosacea:

A
Burning or foreign body sensation
Blepharitis
Keratitis
Conjunctivitis
Corneal ulcers
Recurrent chalazion
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307
Q

What patients have a higher association of angiodysplasia?

A

Those with advanced renal disease, Von Willebrand, and Aortic stenosis (d/t acquired vWF deficiency).

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308
Q

What is likely to cause jejunal atresia and how will it present?

A

Jejunal and ileal atresia likely d/t vascular insults in utero that cause necrosis and resorption of fetal intestine
Common causes: maternal vasoconstrictive meds, tobacco or cocaine abuse
Presents w/bilious emesis, abdominal distension and “triple bubble” sign on xray and gasless colon typically w/in first 24hrs

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309
Q

What is the mgmt. and contraindications for chest pain in cocaine use?

A

Managed with benzos for BP and anxiety
Aspirin, Nitroglycerin, and CCBs for pain
BBs are contraindicated and Fibrinolytics should be avoided d/t risk of ICH.
Cardiac catheterization w/reperfusion done when indicated aka if there are signs of STEMI on EKG.

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310
Q

What kind of arrhythmia is Carotid massage used for?

A

Helps to terminate PSVT – a regular, narrow-complex tachycardia. It increases PSNS activity which helps directly slow AVN conductivity
Not used in the tx of aFib
Contraindications: recent TIA/stroke, carotid bruit

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311
Q

What is a desmoid tumor?

A

Locally aggressive benign tm arising from fibroplastic elements w/in the muscle or fascial planes
It has v. low potential for mets or differentiation
Thought to be d/t abnormal wound healing or clonal chromosomal abnormalities causing neoplastic behavior
Increased risk in patients w/familial adenomatosis polyposis (Gardner syndrome)

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312
Q

How do desmoid tms often present?

A

As deep seated painless, sometimes painful, masses in the trunk/extremity, intraabdominal bowel and mesentery, and abdominal wall.
They have high rate of recurrence even after aggressive surgery removal

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313
Q

What does exertional lightheadedness/exertional syncope raise suspicion for?

A

Cardiogenic syncope – d/t an underlying structural heart defect

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314
Q

What sided heart failure causes pulmonary edema?

A

LEFT – back up in the pulmonary a. leading into the LA will cause pulm edema

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315
Q

What findings on PFT suggest an obstructive lung disease?

A

Reduced FEV1
Reduced FEV1/FVC ratio – bc FVC is typically normal

TLC, and DLCO are typically normal but may be slightly elevated in asthma and DLCO is decreased in COPD.

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316
Q

What findings of PFT suggest a restrictive lung disease?

A

FEV1 and FVC both decreased
FEV1/FVC ratio normal or increased
TLC and DLCO are also decreased

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317
Q

What size lesions should be considered suspicious for melanoma?

A

6+ mm in diameter – these need excisional/punch biopsies with 1-3mm margins

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318
Q

Rxs that can either cause increase or decrease in Lithium levels:

A

Loop diuretics – furosemide

CCBs – verapamil; but these Rxs are usually considered safe and Amlodipine is routinely used

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319
Q

Rxs that decrease Lithium levels:

A

K+ sparing diuretics (Spironolactone)

Theophylline

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320
Q

What conditions has Bullous Pemphigoid often been a/w?

A

Many neurologic conditions such as dementia, Bipolar and MS

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321
Q

What is one of the major complications seen in Sjogren’s Syndrome?

A

polycloncal B-cell activation and infiltration of the salivary glands leading to B-cell NH lymphoma
Often detected as a submandibular mass

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322
Q

What range of proteinuria is seen in Nephrotic Syndromes?

A

> 3-3.5 g/d

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323
Q

What is hypoglycemia defined as?

A

<60mg/dL

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324
Q

What are common EKG findings for Brugada syndrome and long QT syndrome?

A

Brugada – right bundle branch block and ST elevation in V1-V3
Long QT syndrome – QTc >450 msec in men and >470 in women

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325
Q

What are features of anomalous aortic origin of a coronary artery?

A

Common cause of SCD in young athletes
May have premonitory sxs of exertional angina, lightheadedness or syncope; SCD may also occur without any prior sxs
EKG and TTE are often nondiagnostic and appear normal
CTA or coronary MRA are diagnostic tests of choice

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326
Q

What is the problem created by anomalous aortic origins of a coronary artery?

A

By having both L and R coronary artery originate from only one aortic sinus the defect creates a sharp curvature for the anomalous artery and makes it less amenable to high-volume flow.
The anomalous artery also passes between the aorta and pulmonary a. and makes it susceptible to external compression during exercise

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327
Q

Differences b/w Pseudoaneurysm and AV fistula:

A

Pseudoaneurysm – bulging, pulsatile mass with audible systolic bruit
AVF – no mass, continuous bruit
Both may present with localized pain to the area and can typically be diagnosed w/US

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328
Q

What is the standardized incidence ratio?

biostats

A

A measure used to determine if the occurrence of a disease in a small population is high or low relative to an expected value derived from a larger comparison population
It is calculated by dividing the observed cases in that population by the expected number of cases

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329
Q

Preferred tx for Guillain-Barre:

A

Pooled human immune globulin (IVIG) or therapeutic plasma exchange

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330
Q

What is the mgmt. of severe malnutrition (marasmus/kwashiorkor)?

A

Rewarming for hypothermia
Abx for presumed systemic infection
Rehydration – oral fluids preferred; IVF if in shock
Refeed cautiously

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331
Q

What should pts w/alcohol use disorder and progressive cognitive decline be tested for?

A

Folate deficiency

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332
Q

What is used to assess the respiratory mm. weakness and monitor respiratory status in pts w/GBS?

A

Frequent measurement of Vital Capacity and negative inspiratory force

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333
Q

What is a/w broad-notched P-waves on EKG?

A

Mitral stenosis

EKG shows “P mitrale” (broad, notched P waves), atrial tachyarrhythmias, RVH (tall R waves in V1 and V2)

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334
Q

When is skeletal maturity typically reached?

A

By the end of puberty with Tanner stage 5

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335
Q

What is the main cause of spreading for viral conjunctivitis?

A

Eye discharge – pts. are infective and should stay home from school/limit contacts until eye discharge has resolved.
Eye redness and morning crusting may occur after discharge has stopped but these are not considered signs of contagiousness

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336
Q

What is a factorial design?

A

A study that involves the randomization to different interventions w/additional study of 2+ variables.

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337
Q

Therapy for hyperkalemia and when it should be instituted:

A

Acute tx: Calcium gluconate or chloride, insulin w/glucose

Should be given to pts. w/ ECG changes, K+ > 7 w/out ECG changes, or rapid K+ d/t tissue breakdown.

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338
Q

Manifestations of hyperkalemia:

A

Chronic may be asx until K+ > 7mEq/L
Acute causes sxs at lower levels –> ascending m. weakness, flaccid paralysis, ECG changes (peaked Twaves, short QT interval, loss of P wave, QRS widening, sine wave w/vFIb).

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339
Q

What pediatric patients are at risk for Wilm’s tm. and hepatoblastoma?

A

Patients with Beckwith-Wiedemann syndrome, as well as those with isolated Hemi-hyperplasia
(WAGR complex and Denys-Drash are also at risk for Wilm’s tm.)
Both need to undergo frequent screening w/US and AFP measurements

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340
Q

Features of Neuroblastoma:

A

Neural crest origin, involves adrenal medulla and sympathetic chain.

Often presents <2yrs, w/abdominal mass. Can get Horner syndrome if in SNS chain
Other features: periorbital ecchymoses (orbital mets), spinal cord compression from epidural invasion, opsoclonus-myoclonus syndrome (rapid vertical and horizontal nystagmus w/myoclonus), HTN, flushing and diaphoresis

Dx: elevated CAs (VMA, HVA), n-myc amplification, small round blue cells on histo.

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341
Q

What is the attributable risk percent (ARP)?

biostats

A

It’s a measure of excess risk
Estimates the proportion of the disease in the exposed subjects that is attributable to exposure status
ARP = (risk in exposed – risk in unexposed) / (risk in exposed)
= (RR-1)/RR

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342
Q

What is Population attributable risk percent (PARP)?

biostats

A

It is a measure of excess risk in the total population, not only in exposed subjects
PARP = (Risk in total population – Risk in unexposed) / (Risk in total population)
= [(Prevalence)(RR-1)] / [(Prevalence)(RR-1) +1]

Risk in total population = (risk in exposed)(proportion of exposed) + (risk in unexposed)(proportion of unexposed)

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343
Q

What is the best PE maneuver to assess for complete rupture of the Achilles tendon?

A

The Thompson test – squeeze the calf to see if there is plantar flexion; no plantar flexion is basically pathognomonic of complete rupture of Achilles tendon.

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344
Q

What signs/sxs would be seen if there were a tibial nerve defect?

A

Loss of gastrocnemius-soleus motor function

Loss of plantar sensory function

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345
Q

What makes S. pneumoniae more invasive in pts. w/HIV infection?

A

Its encapsulated and they have deficits in opsonization, humoral immunity and macrophage/neutrophil fxn

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346
Q

When is UDS needed to evaluate incontinence?

A

If the patient has mixed incontinence or complicated incontinence.

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347
Q

How to differentiate constitutional delay of growth and puberty from familial short stature:

A

Familial short stature – short stature will be seen with normal growth velocity and a normal bone age

Constitutional delay of puberty – delayed bone age on xray with height and pubertal development correlated more closely with the bone age rather than chronological age

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348
Q

At what age is puberty considered delayed?

A

If no secondary sexual characteristics (testicular enlargement/breast development) are present by age 14 in boys and 12 in girls

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349
Q

What diet should be recommended in pts w/viral GE?

A

A normal age-appropriate diet

A bland diet is no longer recommended and diets high in sugar and fats should be avoided until sxs resolve

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350
Q

When should steroids be used in the setting of Infectious Mononucleosis?

A

If airway obstruction appears imminent – tonsillar enlargement is so large it will cut off the airway
Or if pts are IMCP’d/experiencing other serious cxs: aplastic anemia, overwhelming infection, thrombocytopenia

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351
Q

What is the mgmt. of pediatric patients w/Meningoencephalitis?

A

Most common causes are viral; enteroviruses (coxsackie) are #1 and HSV is #2
However, empiric tx should be started
Get LP right away and then start IV Acyclovir and abx (Vancomycin + 3rd gen Cephalosporin)
Once HSV and bacterial infections are excluded can stop abx and acyclovir and tx supportively

Steroids are NOT useful in viral meningoencaphalitis

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352
Q

What is Metolazone?

A

A thiazide diuretic

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353
Q

What are the Kocher Criteria to differentiate septic arthritis v post-viral inflammatory arthritis?

A
  1. Non-weight bearing
  2. Fever >101.3
  3. ESR >40 or CRP >2
  4. Leukocytosis

If peds patients have 3 or more than its most likely septic and joint aspiration needs to be done ASAP

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354
Q

What are the most common organisms in pediatric septic arthritis?

A

S. aureus > S. pneumoniae > S. pyogenes
These should be covered w/IV Vancomycin

Can add a 3rd gen cephalosporin when there is suspicion for unusual pathogens (Kingella in a kid<3 w/oral ulcers; H influenzae in unimmunized kids; Neisseria in sexually active adolescents)

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355
Q

What are common signs of Acute Decompensated HF?

A

Pulmonary edema
JVD
Presence of an S3

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356
Q

When are BBs contraindicated in the mgmt. of NSTEMI and unstable angina?

A

If the patient has bradycardia or heart failure (may worsen pulmonary edema in ADHF)

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357
Q

What medications can be used for bipolar mania during pregnancy?

A

Haloperidol

Lithium – should be continued if already started and can be initiated for severe mania

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358
Q

What is late-life depression a significant risk factor for?

A

Major neurocognitive disorder (dementia) both vascular and Alzheimer types
It is not a/w development of comorbid anxiety as is earlier development of depression

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359
Q

What DM medications pose the biggest risk for hypoglycemic events?

A

Insulin

Oral agents that increase insulin secretion even when blood glucose levels are normal:
Sulfonylureas – glyburide, glipizide, glimepride
Meglitinides – nateglinide, repaglinide

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360
Q

What is idiopathic premature pubarche?

A

Isolated pubic hair development

Patients will have normal bone age and no additional signs of adrenarche (acne, etc.)

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361
Q

What causes central v. peripheral precocious puberty?

A

Central is d/t early maturation of the hypothalamic-pituitary-gonadal axis

Peripheral is d/t excess sex hormone production from the gonads, adrenal glands, or an exogenous source

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362
Q

What is the tx of nonclassical Congenital Adrenal Hyperplasia?

A

Hydrocortisone

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363
Q

What is the pathophysiology seen in nonclassic congenital adrenal hyperplasia?

A

It is AR inheritance
Decreased 21-hydroxlase activity leads to increased 17-hydroxyprogesterone levels and increased androgens
Patients will have normal glucocorticoids and mineralocorticoids (aka no salt wasting like seen in classic CAH)

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364
Q

Clinical features of nonclassic Congenital Adrenal Hyperplasia:

A

Early pubic/axillary hair growth
Severe acne
Hirsutism and oligomenorrhea in girls
Increased growth velocity and bone age (makes tall children, but short adults)
Typically no evidence of precocious pubertal testicular or breast development

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365
Q

What is the mgmt. and EKG findings of Mobitz Type II AV Block?

A

On EKG will see intermittent non-conducted P waves (dropped beats not preceded by a change in the length of the PR interval) and regular PR intervals
Often have significant bradycardia

Need placement of permanent pacemaker as this commonly progresses to complete block

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366
Q

What is the role of Atropine in treating patients with Mobitz type II?

A

If patients become unstable and have Mobitz type II AV block or any other bradycardia they should receive IV Atropine.
However, if a patient is stable then it should not be given in Mobitz bc it may worsen the bradycardia

367
Q

What kind of skin manifestations can be seen in NF-2?

A

Some bullshit reverse “café-au-lait” spots
Basically hypopigmented spots, described like ash-leaf spots seen in TSC, but FHx will be significant for bilateral deafness which is not a feature of TSC

368
Q

Characteristics of NF2:

A
Bilateral acoustic schwannomas
Juvenile cataracts
Meningiomas
Ependymomas
Hypopgimented café-au-lait spots (reverse of whats seen in NF1)
369
Q

What are the clinical features of Neurofibromatosis 1?

A

Café-au-lait macules (1st cutaneous finding-often in infancy), axillary and inguinal freckling, Lisch nodules and neurofibromas
Pseudoarthrosis
Pheochromocytoma

These pts are at increased risk for neurologic disorders: cognitive deficits, learning disabilities, seizures, intracranial neoplasms (astrocytomas, brainstem gliomas), and optic pathway gliomas

370
Q

What are the common inherited forms of Pheochromocytoma?

A

VHL gene w/Von hippel-Lindau
RET gene – MEN type 2
NF1 gene – Neurofibromatosis Type I
Sturge-Weber Syndrome

371
Q

What condition do you see facial port-wine stain?

A

Sturge-Weber

372
Q

Features of Sturge-Weber syndrome:

A

Congenital NON-inherited anomaly of neural crest derivatives d/t activating mutation of GNAQ
Port wine stain in V1/V2 distribution (nevus flammeus)
Leptomeningeal capillary-venous malformation
Seizures +/- hemiparesis
Intellectual disability
Visual field defects
Glaucoma

373
Q

What condition is characterized by multiple telangiectasias?

A

Osler-Rendu-Weber

374
Q

Characteristics of Osler-Rendu-Weber:

A

Aka Hereditary hemorrhagic telangiectasia
AD disease w/diffuse telangiectasis (ruby-colored papules that blanch w/pressure), recurrent epistaxis, and widespread AVMs.

Pulmonary AVMs – can cause blood to shunt from R to L heart which causes chronic hypoxemia, clubbing, and reactive polycythemia

Vascular lesions of the CNS

375
Q

Why might pts w/Osler-Weber-Rendu have increased Hct?

A

If a pulmonary AVM is present.
Will shunt blood from the R – L heart causing chronic hypoxemia, digital clubbing, and reactive polycythemia.
Pulmonary AVMs can lead to massive, sometimes fatal hemoptysis.

376
Q

What would cause “beaked” midbrain on imaging?

A

Chiari II malformation aka Arnold Chiari malformation

377
Q

Exercises not recommended/contraindicated in pregnancy:

A
Scuba diving
Contact sports
Exercise w/falling risk (horse-back riding, gymnastics)
Skydiving
Hot yoga (regular is fine)
378
Q

What are the common characteristics of congenital toxoplasmosis:

A

Eye abnormalities – chorioretinitis
Neuro findings – diffuse intracranial calcifications, hydrocephalus/macrocephaly
Hearing impairment

Infection in mother often goes undetected and is common after eating undercooked meat, or fruits/veggies from contaminated soil; infection is highest in S America

379
Q

Features of congenital Rubella syndrome:

A
Congenital heart defects (PDA)
Eye abnormalities (cataracts)
Hearing impairment (sensorineural hearing loss)
Infants are typically normocephalic and do not have intracranial calcifications

Typically see at least mild symptoms in the mother during pregnancy (fever, rash)

380
Q

Most common bacteria to cause necrotizing fasciitis:

A

GAS (S. pyogenes) is #1 in healthy patients

Others:
S. aureus
C. perfringens (almost always a/w crepitus and gas formation)
Polymicrobial (mostly seen in pts w/underlying DM and PVD)
Pseudomonas (in IMCP’d)

381
Q

What is the most common cause of necrotizing fasciitis in a patient with DM?

A

DM and PVD patients are more likely to have polymicrobial infections
Common organisms: S. aureus, Bacteroides fragilis, E. coli, Group A Strep, Prevotella spp.

382
Q

What bacteria are most likely to cause crepitus and gas formation in Necrotizing fasciitis?

A

Anaerobic bacteria, most common are C. perfringens and B. fragilis

383
Q

What is the mgmt. of necrotizing fasciitis?

A

Urgent, aggressive surgical exploration (even if the patients are hemodynamically unstable)
Broad spectrum abx:
Pip-tazo or a Carbapenem – covers Group A Strep and Anaerobes
Vancomycin – covers S. aureus (including MRSA)
Clindamycin – added to inhibit toxin formation by streptococci/staphylococci

once culture confirms offending organism abx can be narrowed

384
Q

First line treatment of insomnia:

A

CBT

385
Q

What effects do antihistamines have on the prostate?

A

Bc of their anticholinergic effects they can worsen BPH

Diphenhydramine and others should be avoided in men w/BPH

386
Q

What is the effect of glucocorticoids on calcium?

A

Glucocorticoids decrease the intestinal absorption of Ca2+ and increase Ca2+ excretion in the urine
They also accelerate bone resorption
Patients taking chronic steroids should also be given supplemental Ca2+ and Vit. D

Bisphosphonates can be added if osteoporosis risk is v high (esp. in post-menopausal women)

387
Q

What is the role of bone densitometry in the mgmt. of patients taking steroids?

A

Patients who will be treated w/steroids for more than 3 months (or 6 if low doses) require a baseline densitometry and then it should be repeated each year for as long as the therapy continues to monitor for adverse skeletal effects

388
Q

What imaging is safe in pregnancy?

A

US > MRI&raquo_space; CT

389
Q

What is Pylephlebitis and what are common causes of it?

A

It is an infective (often polymicrobial), suppurative portal vein thrombosis
Although rare, it is most commonly a complication of untreated appendicitis or other intraabdominal or pelvic infections (diverticulitis)

390
Q

Clinical features of Pylephlebitis:

A
Acute or chronic onset of fever
RUQ pain
Jaundice
Hepatomegaly
Labs: elevations in alk phos, and GGT
391
Q

What are complications of pylephlebitis?

A

Bowel ischemia
Portal HTN
Hepatic abscess
Need prolonged, broad spectrum abx to prevent these

392
Q

When should steroids be given to pregnant women with DM at risk of preterm delivery?

A

<34 weeks gestation (as opposed to <37 weeks in general population)
Steroids can cause hyperglycemia in pts w/DM

393
Q

When should an amnioinfusion be given?

A

To alleviate the compression of the umbilical cord that causes variable decels
It is not given in the mgmt. of oligohydramnios as it cannot correct chronic placental insufficiency

394
Q

Tx of acute epididymitis:

A

If gonorrhea is suspected/cannot be ruled out – ceftriaxone + doxycycline
Low risk of gonoccal infection – Fluoroquinolones (levofloxacin)

395
Q

Common causes of viral orchitis:

A

Mumps, Rubella, Parvo
These are most commonly seen in children/adolescents and often involve extraurinary manifestations (parotitis, meningitis)

396
Q

Risk factors for AAA:

A
Smoking is #1
Male sex
Older (>65)
White 
FHx of AAA
Atherosclerotic disease
397
Q

Mgmt of AAA:

A
Smoking cessation is most important
Aspirin and statin therapy
Elective repair for:
   Large (5.5+ cm)
   Rapidly enlarging (>0.5cm in 6 months)
   AAA a/w PAD or aneurysm
398
Q

What is the follow-up imaging schedule recommended for AAAs?

A

Medium (4-5.4cm): US every 6-12mos

Smaller (<4cm): US every 2-3 years

399
Q

Most common location for a AAA:

A

Infrarenal aorta

400
Q

What are indications for getting XRays in low back pain?

A

Osteoporosis/compression fracture
Suspected malignancy
Ankylosing spondylitis

If XR is abnormal then should proceed to MRI

401
Q

What are indications for getting an MRI in the setting of low back pain?

A

Sensory/motor deficits
Lumbosacral radiculopathy/sciatica lasting >1month
Cauda equina syndrome (urine retention, saddle anesthesia)
Suspected epidural abscess/infection (fever, IVDU, concurrent infection, hemodialysis)
Known malignancy

402
Q

What are the indications for getting a CT or Radionuclide bone scan in the setting of low back pain?

A

If the patient has indications for an MRI but they are not able to have an MRI

403
Q

What are red flag features for low back pain?

A
Constitutional sxs (fever, wt. loss)
Age >50
IVDU
Immune suppression
Recent bacterial infection
Nocturnal pain
Hx of Malignancy
404
Q

Clinical features of prolactinoma:

A

Premenopausal women – oligo/amenorrhea, infertility, galactorrhea, hot flashes, decreased bone density
Postmenopausal women – mass effect sxs (HA, visual field defects/bitemporal hemianopsia)
Men – infertility, decreased libido, impotence, gynecomastia

405
Q

Tx of Prolactinomas:

A

DA-agonists – Cabergoline, Bromocriptine

Surgery for those who don’t respond to meds

406
Q

What are the guidelines for managing BP in an acute ischemic stroke patient?

A

In patients who did not receive thrombolytic therapy BP up to 220/120 is acceptable as this allows appropriate perfusion to borderline ischemic areas in the brain.

Patients who did receive thrombolytic therapy should be maintained at BPs <185/105 for at least 24hrs to minimize the risk of hemorrhage

407
Q

What is the most common cause of early death in acute stroke patients?

A

Subsequent PE – therefore pts should be managed on SQ low-dose Heparin or LMWH as DVT pphx
Pts who suffered hemorrhagic stroke should initially be managed w/mechanical DVT pphx (SCDs)

408
Q

Features and tx of benign essential tremor:

A

Aka familial tremor (AD inheritance)
Intention tremor that is both present at rest and then worsens when reaching for something or completing an activity.
Often effects both hands but is not a/w other neurologic sxs

Tx: BB propranolol

409
Q

What test should be used to assess TB status in a person who received the BCG vaccine?

A

Interferon-gamma release assay (IGRA)
They often have a false positive to the PPD test
Patients who have latent TB will have positive result to PPD and IGRA and should be assessed w/CXR

410
Q

Tx options for latent TB infection:

A

Isoniazid + Rifapentine weekly for 3 mo under direct observation (not recommended for HIV+)
Isoniazid monotherapy for 6-9months
Rifampin monotherapy for 4mos

healthcare workers recommended to receive Isoniazid for 9mo

411
Q

What is the role of anti-dsDNA antibodies in SLE?

A

Renal involvement in SLE is d/t immune complex-mediated glomerular injury, and the immune complexes are composed primarily of anti-dsDNA antibodies
These antibody complexes are deposited in the mesangial, subendothelial, or subepithelial space and cause inflammation and destruction of the kidney

412
Q

What should be used to monitor renal disease activity in Lupus nephritis?

A

anti-dsDNA antibody levels and complement levels

anti-Smith Abs also become elevated in SLE renal disease, but they remain elevated even after the disease is no longer active and therefore are not useful in monitoring but may identify pts at risk of developing renal disease.

413
Q

What antibodies are sensitive for Drug-Induced SLE?

A

Anti-histone Abs

414
Q

What Rxs can cause Rx-induced SLE?

A
Isoniazid
Hydralazine
Procainamide
D-penicillamine
Minocycline
anti-TNFa (etanercept, infliximab)
415
Q

What are the complications of Infantile Hemangiomas?

A

Ulceration/scarring
Vision impairment if near eye
Life-threatening if near airway

Most regress and don’t need tx but can use topical BBs (propranolol) for ulcerated or cosmetically sensitive areas

416
Q

What is the common presentation of systemic-onset juvenile arthritis?

A

Chronic oligoarthritis (worse in the morning)
Daily fever (quotidian fever >2wks)
Rash (pink, macular, worsens during fever)
Possible lymphadenopathy and hepatosplenomegaly

417
Q

How would SLE likely present in childhood?

A

With neuropsychiatric sxs, immune-mediated anemia (Coombs +), thrombocytopenia, arthritis, and nephritis

418
Q

What bug is most commonly a/w pediatric seizures in the setting of acute bacterial gastroenteritis?

A

Shigella spp.
The seizures are typically self-limited with a quick return to baseline
(unlike seizures a/w Reye syndrome or hyponatremia)
If the seizure occurs a week after the diarrhea has resolved, likely HUS

419
Q

Features and tx of TTP:

A

Decreased ADAMTS13 – uncleaved vWF multimers – platelet trapping and activation.
Causes hemolytic anemia w/schistocytes, renal failure, neuro sxs and fever
Tx w/plasma exchange, glucocorticoids, and rituximab

420
Q

What is the light criteria to define an exudative pleural effusion?

A

Must have at least one of the following (pleural/serum):
Pleural fluid protein/serum protein ratio >0.5
Pleural fluid LDH/serum LDH >0.6
Pleural fluid LDH >2/3 of the upper limit of normal for serum LDH.

421
Q

How do the two different types of Lichen Planus present?

A

Erosive variant (most common): Erosive, glazed lesions w/white border, vaginal involvement +/- stenosis, associated oral ulcers

Papulosquamous variant: Small pruritic papules w/purple hue often seen near wrists, vulva or penis

Both present in women age 50-60 w/vulvar pain or pruritus, and dyspareunia
Associated with HCV when seen outside of GU region

422
Q

What are the poor prognostic factors of CLL?

A

Multiple chain LAD
Hepatosplenomegaly
Anemia and thrombocytopenia

423
Q

Most common causes of death in patients w/CLL:

A

Infection and Secondary malignancy (Richter transformation)

But typically have 10+ year survival rate

424
Q

What fetal risks are common in poorly controlled gDM?

A
Macrosomia
Hypocalcemia
Hypoglycemia
Hyperviscosity d/t polycythemia
Respiratory difficulties
Transient HCMP
425
Q

What type of heart disease is common in newborns of gDM mothers?

A

Hypertrophic cardiomyopathy (typically transient and doesn’t require tx) – occurs d/t hyperinsulinemia that triggers glycogen synthesis and XS glycogen and fat are deposited w/in the myocardium (esp. the IV septum)

This occurs d/t poorly controlled DM in the 2nd and 3rd trimesters (so more common among gDM pts and not pre-pregnancy DM).
Congenital heart diseases (hypoplastic LH syndrome, etc) occur d/t hyperglycemia in the 1st trimester and therefore are only seen in pregestational DM mothers

426
Q

What is congenital pulmonary valve stenosis typically associated with?

A

Noonan syndrome – RV outflow obstruction may result in R to L shunting and cyanosis
also a/w facial structure abnormalities, bleeding disorders and bone and rib cage malformations

427
Q

What is characterized by atrialization of the RV?

A

Ebstein anomaly d/t malformed tricuspid valve

428
Q

What is standardized mortality ratio?

biostats

A

It quantifies mortality in a specific group compared to the general population
SMR = observed # of deaths / expected # of deaths
SMR < 1 means deaths are lower than expected; >1 deaths are higher than expected

429
Q

Locations of auscultation for heart valves:

A

Aortic – 2nd ICS to the R sternal border
Pulmonic – 2nd ICS to the L sternal border
Erb’s point – 3rd ICS to the L sternal border
Tricuspid – 5th ICS to the lower L sternal border
Mitral – apex, PMI and 5th ICS at Midclavicular line

430
Q

What should patients with megaloblastic anemia be monitored for immediately after tx?

A

Hypokalemia
Treatment w/B12 causes newly forming RBCs to rapidly uptake K+ and can cause significant hypokalemia
Patients should be monitored during the first 48hrs of tx
Can lessen the risk by giving packed RBC transfusion prior to initiating B12 treatment

431
Q

How are thyroglossal duct cysts commonly detected?

A

After they become secondarily infected after a URI which causes erythema and tenderness

432
Q

What should be done once a thyroglossal duct cyst is discovered?

A

Thyroid imaging – TDCs are commonly associated with ectopic thyroid tissue and the TDC may be the only site of functioning thyroid tissue. Therefore thyroid imaging needs to be done before definitive tx (resection is the only curative therapy and should be done to prevent recurrent infections)

433
Q

What are the current guidelines for biventricular pacing devices?

A

Patients in sinus rhythm who meet ALL of the following should receive one:

  1. LV ejection fraction <35%
  2. NYHA class II, III, or IV HF sxs (essentially presence of any sxs)
  3. LBBB with QRS duration >150msec
434
Q

What is one of the major morbidities following gastric bypass surgery and how is it treated?

A

Malabsorption
For prevention all patients should take lifelong supplementation of vitamins: B1, B12. Folic acid and Vitamin D; and minerals: iron, calcium, trace minerals
Vitamin D should be supplemented in high levels 2000-3000+ U/d

435
Q

What is likely to be seen on lab studies in a nonfunctioning pituitary adenoma?

A

Suppressed/absent LH and FSH with increased levels of the a-subunit
These tumors are composed of gonadotropin-secreting cells and mainly just secrete the a-subunit of the gonadotrophs

Large tumors can compress the pituitary stalk and block the normal inhibition of prolactin secretion causing mild prolactinemia (<200), but not high levels like prolactinomas (>200)

436
Q

What is the standard tx for patients with Splenic v. thrombosis and GI hemorrhage?

A

Splenectomy

437
Q

After what gestational age do tocolytics become contraindicated?

A

> 34 weeks

Risks of perinatal morbidity and mortality no longer outweigh risks of maternal tocolytic exposure after this point

438
Q

When can a partial nephrectomy be offered to a patient?

A

Only if the renal mass is still confined within the renal capsule aka Stage I disease

439
Q

When is multifocal atrial tachycardia most commonly seen?

A

In elderly patients with an acute exacerbation of underlying pulmonary disease
First step is to correct underlying disturbance – ie give O2 or ventilation

Other common causes are electrolyte disturbances: hypokalemia, hypomagnesemia – should replace electrolytes before initiating pharmacotherapy

440
Q

What is pseudohypoparathyroidism?

A

End-organ resistance to PTH
Will have elevated PTH which distinguishes it from hypoparathyroidism
Chronic hypocalcemia (leading to cataracts and basal ganglia calcifications), elevated phosphorous and low vitamin D can be seen in both disorders

441
Q

What is Albright hereditary osteodystrophy?

A

A subtype of psuedohypoparathyroidism
Will have dysmorphic features – round facies, short stature, short 4th/5th metacarpals as well as the other features of psueohypoPTH (high PTH, high phosphorus, low Ca2+ and Vit. D)

442
Q

What is meningovascular syphilis?

A

Low-grade syphilis infection in the subarachnoid space – can affect the intracranial vessels and potentially result in stroke
CSF is likely to show similar results to viral encephalopathies: Elevated WBCs with lymphocyte predominance, elevated protein, normal glucose +/- xanthochromia
Tx with IV Penicillin

443
Q

What is the most common complication of diverticulitis?

A

Colonic abscess – can occur in 15-50% of patients
Need IV abx, bowel rest and most need urgent percutaneous drainage + partial colectomy several weeks later
If pts w/diverticulitis don’t have improvement in sxs after 2-3 days they should have repeat CT to assess for abscess and other cxs (obstruction, fistula, perforation)

444
Q

What is the tx for seborrheic dermatitis?

A

TOPICAL agents:
Antifungals – selenium sulfide shampoo, ketoconazole
Glucocorticoids
Calcineurin inhibitors – pimecrolimus
Salicylic acid
May need treatment as often as every 1-2 weeks in order to prevent recurrence

445
Q

What antifungal should be strongly avoided in seborrheic dermatitis?

A

Griseofulvin – it has no activity against malassezia spp. and can worsen SD

446
Q

What is the mgmt. of sudden sensorineural hearing loss?

A

Urgent ENT evaluation – they need to do full audiologic testing + imaging, etc
Steroids should also be given (orally and/or injected into middle ear)

447
Q

What is effect modification?

A

Aka interaction bias
It occurs when a variable/effect modifier changes the direction or strength of the effect that the independent variable (exposure or treatment) has on the dependent variable (outcome)

Ex: age is an effect modifier on aspirin usage and reye syndrome development

448
Q

What is the mgmt. of symptomatic patients w/HOCM?

A

Negative inotropic agents – BBs (metoprolol), Verapamil or Disopyramide

Patients w/persistent sxs refractory to medical therapy can have alcohol septal ablation

449
Q

What drugs should be avoided in HOCM?

A

Vasodilators – dihydropyridine CCBs (amlodipine, nifedipine)
ACEIs and ARBs
Nitrates
these can all decrease SVR which may worsen the LVOT gradient and sxs

450
Q

Best initial approach to sicca syndrome?

A

Schirmer test – confirms secretory deficiency

autoantibody screen – anti-Ro, anti-La, RF and ANA

451
Q

What strategy should be used to reduce risk of exposure from patients with disseminated herpes zoster infection?

A

Patients should be placed on contact and airborne precautions until all lesions have crusted over
Hospitalized patients with localized infection can be held on standard precautions with lesion covering

452
Q

What are common risk factors for Dupuytren contracture?

A
Male sex
Age >50
FHx
Diabetes
Tobacco and alcohol use
453
Q

What is the treatment of acute pericarditis/peri-infarction pericarditis?

A

NSAIDS – in the setting of peri-infarction only Aspirin should be used, in the setting of viral or idiopathic Naproxen is best choice
+ Colchicine (aspirin should be tried as monotx in peri-infarction pericarditis, but colchicine can be added later if sxs persist. Colchicine should be used in combo w/Naproxen for viral/idiopathic)

454
Q

In measures of central tendency, which point is most valid for the central location?

A

In normally distributed (bell curves) the mean is most valid

In skewed or asymmetrical distributions, the median is most valid

455
Q

How to differentiate CML from CLL:

A

CML has marked leukocytosis of predominately neutrophil origin
CLL has marked leukocytosis of predominately lymphocyte origin

456
Q

How to differentiate Hairy cell leukemia from the chronic leukemias:

A

All may cause massive splenomegaly
Hairy cell – pancytopenia (d/t fibrosis of bone marrow: dry tap)
CLL – lymphocytosis
CML – leukocytosis

Myelofibrosis may also cause massive splenomegaly w/pancytopenia

457
Q

Which benzo is most likely to result in seizures following abrupt dc?

A

Alprazolam – short t1/2

458
Q

What are features suggestive of bronchiectasis?

A

Recurrent infections and daily cough w/mucopurulent sputum production (often green-yellow and foul smelling)
Can get hemoptysis from repeated mucosal inflammation leading to rupture of small blood vessels

459
Q

How is carbon monoxide poisoning diagnosed?

A

ABG showing elevated levels of Carboxyhemoglobin
Tx w/High flow O2; intubation/HBO for severe cases

Often seen after smoke inhalation

460
Q

When would methemoglobin levels be elevated?

A

When Fe-molecules in Hb are oxidized to form methemoglobinemia – prevents O2 binding and has increased affinity for cyanide
May present w/cyanosis and chocolate colored blood
Most common causes: Rxs (dapsone, benzocaine), and toxins (aniline dyes)
Tx: methylene blue and vitamin C

461
Q

What should be assessed before initiating therapy with EPO?

A

Correctable causes of anemia – evaluate Fe stores, folate and B12 levels, reticulocyte count and FOBT; even if MCV is normal
Fe-stores also should be checked at regular intervals while on EPO bc they can quickly become depleted from new RBC production.

462
Q

What is the mgmt. of poison ivy contact dermatitis?

A

Immediate removal of contaminated clothing, and gentle cleansing of exposed area (minimizes spread)
Tx is then supportive – cool compresses, topical steroids; Oral steroids can be given in severe dermatitis or dermatitis that involves the face or genitals
Antihistamines have NO ROLE as poison ivy dermatitis is not histamine-mediated (its Type IV HS)

463
Q

What is the proper mgmt. of anticoagulation in pregnancy?

A

Warfarin should only be used in the preconception and postpartum periods (breastfeeding)
LMWH should replace warfarin in the 1st trimester and be continued throughout pregnancy
UFH should replace LMWH in the last few weeks of pregnancy before delivery (it is quicker to reverse)

All anticoagulation should be discontinued at the onset of labor and before epidural anesthesia is started

464
Q

What are the indications for intrapartum pphx of GBS infection?

A

GBS + in current pregnancy
Prior infant w/early-onset neonatal GBS infection
Unknown GBS status in current pregnancy + any of the following:
1. <37 weeks
2. Intrapartum fever
3. Rupture of membranes for 18+ hours

465
Q

Which gender correlates with a higher risk of malignant probability in solitary pulmonary nodules?

A

Female

466
Q

What size solitary pulmonary nodules require workup?

A

Nodules >0.8cm need further workup or surveillance; those <0.6cm require no follow up
Nodules >2cm have >50% chance of being malignant

467
Q

What is the workup for dyspepsia?

A

If age 60+ they need upper endoscopy

Age <60 should be tested/treated for H. pylori, and upper endoscopy only for high risk patients

468
Q

What are the alarm sxs in dyspepsia?

A
Progressive dysphagia
Fe-def anemia
Odynophagia
Palpable mass/LAD
Persistent vomiting
FHx of GI malignancy
**Patients with 1 or more of these should get upper endoscopy to evaluate for malignancy**
469
Q

What is the treatment for narcolepsy associated cataplexy?

A

SNRIs (Venlafaxine), SSRIs, TCAs

Sodium oxybate can be considered but it is rarely used d/t abuse potential

470
Q

What should be the first steps in evaluating suspected lead poisoning?

A

CBC + serum Fe and ferritin levels + reticulocyte count

If chelation therapy is required need BMP + UA

471
Q

What should be suspected in a young patient with fever and sxs of Subarachnoid hemorrhage?

A

Mycotic aneurysm rupture 2/2 infective endocarditis
Most commonly seen in those w/IVDU
Likely to present w/sxs of SAH (HA, lethargy, neck stiffness) + fever, petechiae, and a heart murmur

472
Q

What are the renal-associated cxs of infective endocarditis?

A

Renal infarction
Glomerulonephritis
Drug-induced AIN from IE therapy

473
Q

How are intracerebral mycotic aneurysms likely to present?

A

As an expanding mass w/focal neurologic findings

May also remain asx until rupture w/stroke or SAH

474
Q

What are the cardiac cxs of IE?

A

Valvular insufficiency – common CoD
Perivalvular abscess
Conduction abnormalities
Mycotic aneurysm – can occur in systemic circulation or cerebral

475
Q

Characteristics of HSV encephalitis:

A
Acute-onset (<1week) fever
HA
Seizures
AMS
Focal neurologic findings – hemiparesis or CN deficits
476
Q

Who are considered high-risk patients and need to have CT after minor head trauma?

A
Age 65+
Coagulopathy
Drug or EtOH intoxication
High-risk injury mechanism:
   Pedestrian struck by vehicle
   Ejection from vehicle
   Fall from height
477
Q

What are considered high-risk sxs and indications for CT after minor head trauma?

A

Retrograde amnesia (30+ min before injury)
Vomiting 2+ times
Seizure
Severe HA

478
Q

What are signs of basilar skull fracture and indications for head CT?

A

Battle sign – mastoid/postauricular ecchymoses
Rcacoon eyes – orbital ecchymoses
CSF rhinorrhea or otorrhea
Hemotympanum

479
Q

Mgmt of Hemophilic pts post-head trauma:

A

Even after minor head trauma patients should immediately receive non-con CT and Factor 8 or 9 should be replaced asap

480
Q

Mgmt of HPV in pregnancy:

A

HPV can be vertically transmitted and c-section does not prevent this transmission, therefore expectant mgmt. and vaginal delivery should be planned.

481
Q

What nerves are injured in Erb-Duchenne palsy?

A

C5-C7

Have pronated forearm, flexed wrist and fingers

482
Q

What effect will intense glycemic control in DM-2 patients have on overall mortality?

A

It has no change or may increase mortality

483
Q

What are the antithrombotic therapy recommendations in pts w/mechanical valves?

A

All should receive aspirin + warfarin:
Aspirin 75-100mg/d + warfarin in all pts w/aortic or mitral valve replacement
Patients who cannot take warfarin should have increased doses of aspirin: 75-325
Warfarin w/goal INR 2.0-3.0: for AV replacement w/no risk factors
Warfarin w/goal INR 2.5-3.5: MV replacement, AV replacement +risk factors, in the first 3mo post-AV replacement

risk factors: aFIb, severe LV dysfxn (EF<30), prior TE, presence of hypercoagulability

484
Q

What is Idarucizumab and what is it used for?

A

It is a monoclonal Ab – used to reverse anticoagulation from Dabigatran (direct thrombin inhibitor)

485
Q

What are pts. w/alopecia areata at risk for?

A

Other AI diseases: AI thyroid disease, vitiligo, pernicious anemia
They often also have associated nail pitting

486
Q

When should a renal US be done in children?

A

All children <24 months w/a febrile UTI needs a renal/bladder US to evaluate for hydro and ureteral dilation. Children >2 don’t need US if UTI sxs resolve w/treatment
US should be performed after the acute illness has been tx’d to prevent false-+ results
If US is abnormal – VCUG to look for VUR (also done if recurrent, febrile UTIs in a child)

487
Q

What are females with subclinical hypothyroidism at risk for?

A
Recurrent spontaneous miscarriages (even euthyroid women w/anti-TPO abs are at risk)
Severe preeclampsia
Preterm birth
Low birth weight
Placental abruption
488
Q

What anticonvulsant increases the risk of kidney stones?

A

Topiramate – inhibits renal carbonic anhydrase

489
Q

Causes of tongue enlargement:

A
Longstanding hypothyroidism
Amyloidosis
Acromegaly
Mucopolysaccharidosis (Hurler and Hunter syndromes)
MEN 2B
490
Q

What is a funnel plot used for?

biostats

A

To assess publication bias
Funnel plots should be symmetric in the absence of study heterogeneity and publication bias – aka there should be the same number of dots on both sides of the triangle at similar spots
Asymmetry (all points on one side of the triangle, etc.) suggest publication bias

491
Q

How would sample size effect a funnel plot?

A

A small sample size/low power would lead to more studies/dots at the base of the triangle
Studies with large sample sizes/high power would be at the top of the triangle

492
Q

How should evaluation of suspected renovascular HTN be done?

A

Renal duplex Doppler US, CT or MR angiography w/contrast can all be done, but v. important not to do contrast studies in those w/renal insufficiency, therefore US should be done 1st in these patients

493
Q

Classic EKG findings in PE:

A

Sinus tachycardia is most common finding.
Others: all occur d/t RV strain
New RBBB
Atrial arrhythmias
Q-waves or ST-segment changes in the inferior leads

494
Q

What are common Echo findings to support diagnosis of acute PE?

A

RV dysfunction
Decreased RV contractility
Presence of RV thrombus
Moderate/functional tricuspid regurg – d/t pHTN causing dilation of the TV annulus

495
Q

What are the high-risk features for TBI/intracranial injury in children <2 years?

A

AMS (fussy behavior)
LoC
Severe mechanism of injury (fall >3ft, high impact, MVC)
Non-frontal scalp hematoma (aka occipital, parietal hematomas)
Palpable skull fracture

496
Q

What type of scalp hematomas have the highest risk of skull fracture in pediatric pts (<2)?

A

Large (>3cm) parietal and temporal hematomas – highest risk of TBI/intracranial injury

497
Q

Most common bacteria causing cellulitis and skin & soft tissue abscesses:

A

Cellulitis – S. pyogenes (also main cause of Erysipelas)

Abscess – S. aureus

498
Q

What are the gestational cxs in female kidney donors?

A

Fetal loss
Preeclampsia
gDM
gHTN

499
Q

What allergen has the strongest association w/asthma?

A

House dust mites (responsible for 60-90% of asthma cases)

Other allergens: cat, dog, and cockroach
Air pollution doesn’t have an association with asthma

500
Q

What are the adverse effects of amiodarone therapy?

A

Pulmonary toxicity is the most serious and is responsible for the most deaths a/w amiodarone

Photosensitivity 
Skin discoloration
Bone marrow suppression
Thyroid dysfunction
Abnormal liver fxn tests
501
Q

When should calcineurin inhibitors be used for atopic dermatitis?

A

Topical Tacrolimus
If it is significantly effecting the face, eyelids, or flexural areas
Otherwise topical corticosteroids should be used (hydrocortisone, triamcinolone, etc.)

502
Q

What are the common signs/sxs of Primary Biliary Cholangitis?

A
Fatigue and pruritus are most common
Inflammatory arthritis
Hyperpigmented skin
RUQ discomfort
Xanthelasmata and xanthomata

increased risk if there is FHx

503
Q

How to diagnose and tx Primary Biliary Cholangitis:

A

Dx – elevated ALP, positive anti-mitochondrial Abs, liver biopsy if AMA is negative
Tx – Ursodeoxycholic acid; Liver transplant in advanced cirrhosis

AST, ALT and BR levels may all be normal or mildly elevated

504
Q

What are anti-smooth-muscle antibodies associated with?

A

Autoimmune Hepatitis

505
Q

What is a frequent complication of Primary Biliary Cholangitis?

A

Metabolic bone disease – osteopenia/porosis

Vitamin D levels are typically normal though

506
Q

What are the common surgical cxs of adrenalectomy for pheochromocytoma?

A

HTN crisis – give IV nitroprusside, phentolamine or nicardipine

HoTN (d/t decreased CAs after tm removal) – give NS bolus + pressors if unresponsive

Hypoglycemia (increased insulin secretion after tm removal) – give IV dextrose

Tachyarrhythmias (from increased CA release from adrenal gland handling) – IV lidocaine or esmolol

507
Q

What are the indications for treatment in subclinical hypothyroidism?

A

TSH 10+ uU/mL: treat all patients
TSH 7-9.9:
Age <70 – treat
Age 70+ – tx if convincing hypothyroid sxs
TSH upper limit of normal (6.9):
Age <70 – tx if convincing hypothyroid sxs, enlarging goiter, or elevated anti-TPO titer
Age 70+ – do not treat, may cause harm

508
Q

How should warfarin anticoagulation be reversed prior to urgent surgery?

A

1 – Immediately dc warfarin
2 – administer Prothrombin complex concentrate (contains vitK-dependent cofactors + normalizes INR <10 min)
3 – Give IV vitamin K
If PCC is unavailable can give FFP (IV colloid) but it is less effective

509
Q

What would the results of cardiac catheterization in a patient w/a PE show?

A
Cardiac output: decreased
RA pressure: increased
RV pressure: increased
Pulmonary a. pressure: increased
PCWP: normal
510
Q

Lung cancer screening:

A

Can be done w/annual low-dose CT for patients 55-80 with >30 pack year smoking history + current smoker or quit w/in last 15 years
CXR has not been shown to reduce mortality as a screening method.

511
Q

What is the cause of myasthenia gravis?

A

Autoantibodies attacking the acetylcholine receptors at the NMJ

512
Q

What is the most important single risk factor for osteoporosis and osteoporotic bone fractures?

A

Age

513
Q

Initial treatment for stool impaction?

A

Manual disimpaction followed by enema or suppository to empty the colon
Increased dietary fiber + stool softeners should then be started after disimpaction

514
Q

What are the characteristics of mycosis fungoides?

A

Cutaneous T-cell lymphoma
Has highly variable appearance – may present as papules, plaques or hyper-/hypo-pigment patches
May have subQ tumors
Extradermal spread can cause regional LAD, infiltration of the lung, liver or spleen and occasionally can cause bone marrow and CNS involvement

515
Q

Strongest predictor of coronary artery stent thrombosis:

A

Premature discontinuation of dual antiplatelet therapy: aspirin and P2T12 Receptor blocker (clopidogrel, prasugrel, ticagrelor)

516
Q

What does a negative exercise stress test indicate?

A

That the patient has a low risk (<1%) for cardiac events in the near future (w/in the next year)
It does not exclude the possibility that the patient has CAD as it could be nonobstructive or microvascular

517
Q

First line treatment of heat stroke:

A

Augmentation of evaporative cooling – naked patient sprayed w/water mist or covered w/a wet sheet while large fans circulate air

518
Q

Cxs of Diphtheria:

A

Toxin-mediated myocarditis, neuritis, and kidney disease

519
Q

What anti-hyperglycemic agents can be used in gDM?

A

Insulin, metformin and glyburide can all be used if diet doesn’t control gDM
Glyburide has higher risk of neonatal hypoglycemia than insulin though

520
Q

What are common manifestations and characteristics of autoimmune hepatitis?

A

Most common in young/middle-age women
Often have other autoimmune manifestations: arthritis, erythema nodosum, thyroiditis, pleurisy pericarditis, anemia and sicca syndrome
Labs: increased AST, and ALT; typically have normal/near-normal ALP and BR
Common auto-Abs: ANA, and anti-smooth muscle Abs (against actin)

521
Q

What is the usual cause of high GGT?

A

Cholestasis

Can also help differentiate if ALP elevations are from liver pathology or bone

522
Q

What are contraindications to VZV vaccine?

A

Anaphylaxis to neomycin
Anaphylaxis to gelatin
Immunodeficient state – congenital immunodefs., long-term immunosuppressive tx, heme or solid tms, severe HIV infection

523
Q

What should be done to prevent cxs post-VZV vaccine in pts. w/IMCP’d contacts?

A

Close monitoring for a vaccine-associated VZV rash – this is contagious to immunocompromised individuals
If a rash develops then the IMCP’d individual needs VZV-Ig asap (w/in 10d of initial exposure), but otherwise they do not require Ig if they previously were vaccinated for VZV

524
Q

Tx of Bacterial conjunctivitis:

A

Erythromycin ointment
Polymyxin-TMP drops
Azithromycin drops
Fluoroquinolone drops – preferred in contact wearers bc higher risk of Pseudomonas

525
Q

What is a complication of bacterial conjunctivitis?

A

Bacterial keratitis – more common in contact wearers

526
Q

How does keratitis present?

A

With photophobia, blurred or impaired vision, foreign body sensation w/difficulty opening the eye
Needs urgent Ophtho evaluation

527
Q

What should be suspected in a patient with chest pain + new neurologic findings of R sided weakness?

A

Acute dissection of the ascending aorta w/carotid a. involvement – causes cerebral ischemia
Need CTA, MRA or TEE asap

528
Q

How should pts be followed while on cardiotoxic chemotherapy agents?

A

With a baseline Radionuclide ventriculography (aka MUGA) and then repeat before each subsequent chemo dose
A decrease in EF by 10+ % may warrant discontinuation of therapy, and those w/baseline EF <30% cardiotoxic agents are contraindicated

529
Q

When should therapy be considered for serous otitis media?

A

SOM is a middle ear effusion – commonly occurs after an episode of AOM
Watchful waiting can be done for up to 3mos in a unilateral effusion
If SOM persists >3mos or is bilateral then further therapy should be considered

530
Q

When should a patient’s 10-yr ASCVD risk be calculated?

A

When considering if statin therapy should be started

531
Q

What do overlapping SEM (standard errors of measurement) bars on a graph represent?
biostats

A

There’s a non-statistically significant difference between the two

532
Q

What are the 2 main groups normocytic/normochromic anemia can be divided into?

A

1 – diseases w/decreased RBC production
2 – hemolytic disorders w/increased RBC destruction

Need reticulocyte count to differentiate – elevated retics mean hemolysis, low means decreased production

533
Q

What is most likely to be injured in digital injuries?

A

Tendons – bc they run on the anterior surface of the phalanges
Veins, arteries and nerves run along the sides

534
Q

Most common causes of dysentery:

A

Aka bloody diarrhea
Most commonly caused by bacterial enteritis
Most common pathogens: Salmonella, Shigella, E. coli (enterohemorrhagic or enteroinvasive), Campylobacter, Yersinia
Tx: fluid repletion (abx only needed for IMCP’d pts, or invasive disease/sepsis)

STEC must be excluded before giving abx bc they can predispose to HUS

535
Q

Calculation to correct serum Ca2+ for serum albumin:

A

Corrected calcium = (measured serum Ca2+) + 0.8(4.0 – measured serum albumin)

536
Q

Tx of Syphilis in pregnancy:

A

Penicillin – if the patient is allergic they need to become desensitized and then get penicillin

537
Q

How should pregnant women be screened for syphilis?

A

Universally at first prenatal visit
If positive then they must get repeat screening in 3rd trimester (28-32wks) – a 4-fold or greater decrease in serologic titer indicates treatment success; Anything less needs re-treatment

538
Q

What should be done in patients who have PPI-refractory GERD associated cough?

A

They need a 24hr esophageal pH monitoring to reevaluate the diagnosis

539
Q

When should Bisphosphonates be used to prevent fractures?

A

In all postmenopausal women w/a DEXA T-score -2.5 or less, or those w/a hx of low-trauma hip or vertebral fractures regardless of T-score
Other recommendations are when 10-yr FRAX is >20% for major osteoporotic fractures or >3% for a hip fracture

540
Q

Tx of Lyme Disease in a pregnant woman:

A

14-21 days of Amoxicillin or Cefuroxime

541
Q

What causes diverticular bleeding?

A

Small artery erosion d/t colonic mucosal outcropping

542
Q

When can TMP-SMX be used in pregnancy?

A

Only second trimester and early third
First trimester – increased risk of neural tube defects
Late third – increased risk of neonatal kernicterus
Should avoid altogether

543
Q

What does Clindamycin cover?

A

G+ and anaerobes

Has no gram negative coverage – v. little role in GU infections

544
Q

Tx of Pyelonephritis during pregnancy:

A

Need hospitalization w/IVF hydration
IV abx w/broad-spectrum B-lactams – ceftriaxone, cefepime
Once afebrile for 48hrs can switch to oral abx for 10-14d and then daily suppressive tx w/low-dose Nitrofurantoin or Cephalexin until 6wks post-partum

545
Q

Tx of acute aortic dissection:

A

Pain control – morphine
IV BBs – esmolol
+/- Sodium Nitroprusside (if SBP >120mmHg; but monotx is contraindicated)
Emergent surgical repair for ascending dissection

546
Q

Mgmt of symptomatic ureteral stones:

A

Stone 10+mm need Uro consult for removal
Stone <10mm should be managed w/hydration, pain control, a-blockers and strain urine
If pts have uncontrolled pain or no stone passage w/in 4-6 weeks consult Uro
Patient w/any stone size that have urosepsis, ARF or complete obstruction – uro for surgery

547
Q

Mgmt of C. diff recurrence:

A

1st recurrence – Vancomycin PO (even if used in the initial episode) or Fidaxomicin if Vanc was used in initial episode
2nd recurrence – Same as first recurrence, or Vanc PO followed by rifaximin, or fecal transplant

548
Q

When is Metronidazole used to treat C. diff?

A

Only in fulminant disease (HoTN/shock, ileus, megacolon) – IV metronidazole + high-dose IV Vanc and surgical eval

549
Q

What are common causes of serum sickness-like reaction?

A

Immune complex formation (Type III HS)
Antibiotics – B-lactams, sulfa
Acute HBV infection

550
Q

What are common extrahepatic manifestations of circulating HBV immune-complexes?

A

Serum-sickness like reaction
Polyarteritis nodosa
Glomerulonephritis – normally membrane nephropathy, less commonly membranoproliferative glomerulonephritis

551
Q

When is diabetic retinopathy screening required in DM patients?

A

DM-2 – at the time of diagnosis

DM-1 – beginning 5 years after initial diagnosis (no matter the age at diagnosis)

552
Q

What medication should be started in all patients w/DM 40+years old?

A

Statin – for both Type I and II DM
Should also calculate their 10-yr ASCVD risk to determine intensity of statin (moderate or high), but all DM patients 40+ need a statin regardless of their ASCVD risk

553
Q

What are common CSF findings in traumatic LP and how is it differentiated from SAH?

A

Traumatic LP – RBC count >6,000, elevated WBC count (typically 1 WBC per 750-1000 RBCs), elevated protein and glucose
Xanthochromia will be absent in traumatic LP and will be present in >90% of SAH w/in 12hrs and starts to show up w/in 2-4hrs

A WBC/RBC ratio <0.01 has an almost 100% NPV for meningitis (viral or bacterial)

554
Q

What causes Chagas disease and what are the cardiac manifestations?

A

Caused by protozoan Trypanosoma cruzi (most common in Mexico, Central and S. America)

Cardiac Manifestations – can have any or all of the following:

 1. Biventricular HF (R>L) w/cardiomegaly
 2. Ventricular apical aneurysm (LV apical aneurysm is pathognomonic for chagas CMP)
 3. Mural thrombosis w/embolic complications
 4. Fibrosis leading to conduction abnormalities (heart block, VTach)
555
Q

What are the GI manifestations of Chagas disease?

A

Progressive dilation of esophagus and colon – megacolon

Caused by T. cruzi

556
Q

What is Borreliosis?

A

Lyme disease

557
Q

What is giant cell myocarditis?

A

Rare form of idiopathic myocarditis – thought to be AI-mediated
Echo can show LV dilation w/segmental and/or global LV systolic dysfunction

558
Q

What are cardiac manifestations of HIV?

A

Dilated cardiomyopathy

559
Q

Findings and tx of Measles:

A

Prodromal sxs – fever, fatigue, cough, coryza (stuffy nose), and conjunctivitis
Koplik spots often appear after the onset of prodromal sxs and resolve when rash appears
After 2-4d of prodromal sxs the patient typically looks very ill and a maculopapular rash starts on the face and spreads cephalocaudally sparing the palms and soles
Often have cervical LAD as well

Tx: supportive (IVF, antipyretics); hospitalized patients/severe cases get Vitamin A

560
Q

Features of Roseola:

A

HHV-6
Often does not have a prodrome of sxs and presents w/high fevers (possible to provoke seizures) for several days and then followed by a diffuse macular (often described as lacy) rash once the fevers resolve

will not have fever and rash at same time`

561
Q

Features of Erythema Infectiosum:

A

Parvovirus

Have nonspecific prodrome (fever, cough) followed by rash “slapped cheeks” with spread to trunk

562
Q

What is apathetic thyrotoxicosis?

A

An atypical presentation of hyperthyroidism seen in older patients – characterized by lethargy, confusion and depression. May coincide with dementia which makes diagnosis more difficult.
Other sxs that may be present: tachycardia, tremor, decreased appetite, constipation, etc.

563
Q

What is ANOVA used for?

biostats

A

When the mean values of a continuous variable in several groups (categorical variable) are being compared

564
Q

What would cause Hyperthyroidism w/low RAI uptake + high serum thyroglobulin?

A

Thyroiditis
Iodide exposure

  • *if both were low it would be d/t exogenous hormone**
  • *high/high would be d/t toxic adenoma, goiter or Graves**
565
Q

What is the first line therapy for mild-to-moderate plaque psoriasis?

A

High-potency topical corticosteroids – fluocinonide, augmented betamethasone dipropionate 0.05%
Low-potency (1% hydrocortisone) can be used on the face or intertriginous areas

566
Q

What is Nelson’s syndrome?

A

Pituitary enlargement and hyperpigmentation following bilateral adrenalectomy for Cushing’s disease.
Pituitary enlargement is d/t loss of feedback by adrenal glucocorticoids – the tm development is aggressive and needs surgery or pituitary radiation

567
Q

What are some modifiable risk factors a/w colorectal cancer?

A

Alcohol intake (even modest 2-3/d) – possibly d/t its effect on folate absorption
Cigarette smoking – typically in current, long term smokers (30+ years)
Obesity
Low-fibre diet

Regular NSAID use, hormone replacement tx and high-fiber offer protection against CRC

568
Q

What is the typical outcome of Rabies infection?

A

Coma, respiratory failure and death w/in weeks
Once sxs manifest tx is primarily palliative
Post-exposure Pphx w/rabies Ig and vaccine can help prevent the disease if there are no clinical manifestations but it has no use once clinical manifestations occur

569
Q

What is the general blood transfusion threshold in the general population?

A

Don’t transfuse unless Hb is <7
In pts w/CVD Hb should be maintained above 8
In unstable patients transfusion may need to occur at higher levels d/t an inaccurate reflection of the Hb at time of lab tests

570
Q

What will be seen on CSF analysis in patients w/MS?

A

Oligoclonal IgG bands

571
Q

What should be used to tx an acute exacerbation of MS?

A

IV or oral corticosteroids can be used, unless optic neuritis is present, then IV need to be used
Oral steroids have an increased risk of recurrent optic neuritis
Plasmapheresis can be considered in glucocorticoid-refractory patients

572
Q

What should be used for chronic maintenance therapy for relapsing-remitting MS?

A

Disease-modifying agents – B-interferon and glatiramer acetate
Long-term steroids are typically not recommended

573
Q

What should be used to tx fatigue and neuropathic pain in MS patients?

A

Fatigue – amantadine or stimulants If sleep hygiene and regular exercise fail
Neuropathic pain – gabapentin or duloxetine

574
Q

What are indications for an endometrial bx for women >35yrs?

A

Atypical glandular cells on pap test

575
Q

What are indications for endometrial bx in women <45?

A

AUB plus:
Unopposed estrogen (obesity, anovulation)
Failed medical mgmt.
Lynch syndrome (HNPCC)

576
Q

What are indications for endometrial bx in women >45?

A

AUB or postmenopausal bleeding

577
Q

What should be done to investigate ACG on pap?

A

Aka atypical glandular cells.
May be d/t either cervical or endometrial adenocarcinoma.
Investigated w/colposcopy, endocervical curettage and endometrial bx – allows evaluation of ecto- and endo cervix and endometrium

578
Q

What are the 3 first line tx options for smoking cessation and what are their contraindications?

A

1 – Transdermal patch and gum or lozenge (no contra’s)
2 – Varenicline (an a-4 B-2 nicotinic Ach-R partial agonist).
Contra’s: recent suicidality and unstable psych disorders; relative – preexisting CVD. It increases risk of CVS events in these pts.
3 – Buproprion (NE-DA reuptake inhibitor)
Contra’s: seizure disorders, active bulimia or anorexia

579
Q

What further hx needs to be obtained from a patient prior to initiating Rxs for smoking cessation?

A

Seizure hx – bc buproprion lowers seizure threshold
Psych hx – varenicline is a/w increased risk of suicide and neuropsych side effects (can’t use in unstable psych pts or those w/recent suicidal ideation)

580
Q

What is sinus bradycardia w/o a pulse considered?

A

Pulseless electrical activity – different than normal symptomatic bradycardia
Need to tx based on ACLS – continuous CPR + Epi every 3-5min; atropine not used in bradycardia a/w PEA

581
Q

How should pulseless VTach be managed?

A

Defibrillation + CPR and Epi

Unlike pulseless bradycardia this is a shockable rhythm

582
Q

What is keratosis pilaris and how is it treated?

A

Aka “chicken skin” looks like goosebumps
Benign condition of retained keratin plugs in the hair follicles, most commonly presents w/small painless papules, and a roughened skin texture; Can become pruritic in cold, dry weather
Posterior upper arm is most common location
Often a/w eczema and asthma
Tx: topical keratolytics – salicylic acid or urea cream (help soften papules)

583
Q

Tx of OCD:

A

1st line – SSRIs +/- CBT

2nd line – Clomipramine +/- CBT

584
Q

When can ocular melanomas be observed?

A

if the patient is asx w/a tumor <10mm in diameter and <3mm depth/thickness
Should reexamine in 3mos and then every 6mos

If the tm becomes larger than that or the patient has associated sxs then radiotherapy is the preferred tx (brachytx or EBRT)

585
Q

What should be done to manage dumping syndrome?

A

common after a gastrectomy
Change in diet to high protein, and fractionated, smaller but more frequent food portions usually relieves the sxs
Metoclopramide should be avoided as it increases gastric emptying

586
Q

What is a common condition that can precipitate TTP?

A

Pregnancy – it causes an ADAMTS13 deficiency that becomes more pronounced w/increasing gestational age

587
Q

What are the antibiotic recommendations in pediatric sepsis?

A

28d or less – Ampicillin + Gentamicin or Cefotaxime (E. coli and GBS most common)

> 28d – Ceftriaxone or Cefotaxime +/- Vanc if meningeal involvement is suspected (S. pneumo and N. meningitidis most common)

588
Q

When can ceftriaxone be used in infants?

A

> 28 days – before this it can displace albumin-bound BR and increase risk of kernicterus

589
Q

What would be used to tx a sulfonylurea overdose?

A

Dextrose is 1st line, but Octreotide (a SST analog) can also be used in pts w/persistent hypoglycemia, as it decreases insulin secretion

590
Q

What initial antibodies should be tested when SLE is suspected?

A

anti-dsDNA these are the most sensitive (about 70%) and specific

ANA are very sensitive but not specific
Anti-Smith are very specific but not very sensitive (only about 25%)

591
Q

What are the main benefits to using Hydroxychloroquine in SLE?

A

It is particularly effective at improving arthralgias, serositis, pleurisy, and cutaneous sxs

592
Q

When is cyclophosphamide typically initiated in a patient w/SLE?

A

If they have serious manifestations such as nephritis, CNS involvement or vasculitis

593
Q

When should Syphilis patients be treated w/benzathine v. aqueous penicillin?

A

IM Benzathine penicillin G for: Primary and secondary stages, latent infections, unknown durations of infection and gummatous/CV syphilis

IV aqueous crystalline penicillin G for: Neurosyphilis and congenital infections

594
Q

What are the non-surgical options for SCC of skin?

A

Cryotherapy, electrosurgery and radiation therapy

595
Q

What is the amniotic fluid index?

A

Measures amniotic fluid volume surrounding the fetus. Normal AFI is 5-23cm
AFI <5cm – oligohydramnios
AFI 24+ cm – polyhydramnios

596
Q

How should pulseless electrical activity be managed?

A

This is a rhythm on the monitor w/o a palpable pulse or measurable BP
Mgmt: CPR x 2min, IV access, Epi every 3-5min, possible advanced airway. Continue this until there is a shockable electrical rhythm or the underlying causes have been reversed

597
Q

What type of injury to the knee would cause hemarthrosis?

A

ACL or possibly PCL injury

V unlikely meniscal injuries would cause this

598
Q

What is the goal of hyperthyroid tx during pregnancy?

A

To maintain a mild hyperthyroid state (up to 1.5x normal serum values)
Overtreatment can result in fetal hypothyroidism and goiter

599
Q

How is cutaneous cryptococcosis diagnosed?

A

Biopsy of the lesion for histopath exam and staining

600
Q

Tx of Porhpyria Cutanea Tarda:

A

Phlebotomy or Hydroxychloroquine

IFa can be used in those w/HCV

601
Q

What should be the first steps to improve sxs in ADHF?

A

Reduce cardiac preload w/diuretics and IV vasodilators (in pts w/o HoTN) – will reduce pulmonary edema and dyspnea

602
Q

What are high risk factors for preeclampsia and what can be done to prevent it?

A

High Risk:

  1. Prior preeclampsia
  2. CKD
  3. Chronic HTN
  4. DM
  5. Multiple gestation
  6. AI disease

Patients at high-risk for preeclampsia should take daily low-dose aspirin starting at 12 weeks

603
Q

What should be given to tx postpartum endometritis?

A

BSA w/penicillin-resistant anaerobic coverage
Most common: Clindamycin + Gentamicin
Clindamycin – aerobic G+ cocci and pen-resistant anaerobes (can use amp-sulbactam too)
Gentamicin – G- and some G+ (staph)

604
Q

What is commonly used to tx Chorioamnionitis?

A

Ampicillin + Gentamicin

No anaerobic coverage in this combo

605
Q

What is commonly used to tx PID?

A

Cefoxitin + Doxycycline

606
Q

What can be used for GBS pphx in pen-allergic women?

A

Vancomycin

607
Q

What is commonly used to tx breast abscesses?

A

Vancomycin

608
Q

What are common risk factors for postpartum endometritis?

A

C-section (biggest risk factor, esp if started after onset of labor)
Chorioamnionitis
GBS colonization
Prolonged rupture of membranes
Operative vaginal delivery
BV during pregnancy (but not candidiasis)
Preterm (<37wks) and Post-term (42+wks) gestations

609
Q

Clinical features of postpartum endometritis:

A

Fever >24hr postpartum
Uterine fundal tenderness
Purulent lochia

610
Q

What is pulseless electrical activity?

A

An organized cardiac rhythm (sinus bradycardia, aFIb) unable to generate sufficient CO to create a measurable BP or palpable pulse
Aka bradycardia w/o pulse or aFIb w/o pulse
These are NON-SHOCKABLE rhythms and need immediate, continuous, CPR w/Epi

611
Q

Reversible causes of asystole/PEA:

A

5 Hs and 5Ts

H’s: 1. Hypovolemia, 2. Hypoxia, 3. H+ ions (acidosis), 4. Hypo or hyperkalemia, 5. Hypothermia

T’s: 1. Tension pneumo, 2. Tamponade, 3. Toxins (narcotics, benzos), 4. Thrombosis (PE/coronary), 5. Trauma

612
Q

When is synchronized cardioversion used?

A

For supraventricular tachycardia (aFib w/RVR) in a hemodynamically unstable patient w/a pulse
(if they lose the pulse it becomes PEA and need CPR)

613
Q

What ligaments are involved in ovarian torsion?

A

Infundibulopelvic/suspensory ligament of the ovary (houses ovarian blood supply)
Utero-ovarian ligaments

614
Q

What are common associated disorders of Turner Syndrome?

A

Hypothyroidism
Celiac disease
Learning disabilities (although normal intelligence is expected)
Should be screened for every few years in childhood and neuropsych testing prior to school entry

615
Q

What do Turner syndrome patients require screening for at birth?

A

Echo and 4-extremity BP measurements for coarctation – can cause neonatal cardiogenic shock
May also identify bicuspid aorta although this is not threatening for the newborn
Renal US to identify horseshoe kidney – can predispose to UTIs

Turner is caused by sporadic event and is not considered an inherited syndrome – risk is same as general population in subsequent pregnancies and regardless of maternal age

616
Q

Common anatomic features seen in Turner syndrome:

A
Narrow, high-arched palate
Low hairline
Posteriorly rotated ears
Small maxilla
Short, webbed neck
Cubitus valgus (elbows bent outward)
Short stature
Congenital lymphedema (hands and feet swollen at birth)
617
Q

Common features of Rett syndrome:

A
Developmental regression
Microcephaly
Epilepsy
Stereotypic hand movements
**Girls w/Rett appear normal at birth and have no dysmorphic features**
618
Q

What is the risk of having a child w/Down Syndrome in a mother carrier of Chromosome 21 Robertsonian translocation?

A

About 10%

619
Q

What is the Mentzer index?

A

The ratio of MCV to total RBC count
In Fe-def anemia the Mentzer index is typically high >13
In thalassemias mentzer index is typically <13 as they have high numbers of RBCs

620
Q

What conditions are a/w Basophilic stipling?

A
Lead poisoning
Sideroblastic anemia
Myelodysplastic syndromes
Alcoholism
Thalassemias
621
Q

In fe-def anemia what measures will be the first to increase/normalize after tx w/ferrous sulfate?

A

Reticulocyte count will first increase w/in 1-2wks and then Hb and Hct will begin to normalize within about a month.
Ferritin will not rise until after the Hb has normalized

622
Q

When should Demeclocycline be used to tx Hyponatremia?

A

Only if a patient has persistent severe hyponatremia after water restriction, salt intake and loop diuretics have all failed

623
Q

What are hospitalized pts w/recent variceal bleeding at risk for?

A

Cxs include: Infections, hepatic encephalopathy and renal failure

Infections are most important though and occur in up to 50% of pts.; Can develop – UTIs, SBP, resp. infections, aspiration pneumonia or primary bacteremia
Can help to prevent infections w/pphx abx – preferred regimen is fluoroquinolone for 7-10d

624
Q

What should be given to patients hospitalized for acute variceal bleeding?

A

Prophylactic antibiotics to prevent infectious cxs (SBP, UTI, pneumonia, bacteremia)
Fluoroquinolone (Cipro, ofloxacin or norfloxacin) for 7-10d

625
Q

What are the maternal cxs a/w adolescent pregnancy (age 19 or younger)?

A
Hydatidiform mole
Preeclampsia
Anemia
Operative vaginal delivery
Postpartum depression
626
Q

What are the fetal cxs a/w adolescent pregnancy?

A
Gastroschisis
Omphalocele
Preterm birth (risk does not continue w/ subsequent pregnancies after the teenage years)
Low birth weight
Perinatal death
627
Q

How to differentiate Gastroschisis from Omphalocele:

A

Gastroschisis has no membrane covering intestines and the umbilical cord is found to the L of the defect
Omphalocele has membrane covering defect and umbilical cord is attached to that membrane at the apex

628
Q

What are the single-item predictors that correlate with severity of acute pancreatitis?

A

All of the following are associated with more severe disease or increased risk of death:
Older age
Obesity
Hematocrit (>44%)
CRP – >150 and rising slower than other acute markers (Hct, BUN) a/w severe AP 24-48hrs after admission
BUN – 20+ on admission increases risk of death

629
Q

What is the recommended tx for a DVT or PE?

A

Oral factor Xa inhibitors (Rivaroxaban) for 3+ months for those who do not have cancer
In patients w/underlying malignancy LMWH is considered superior (then must bridge to warfarin)

630
Q

What is the best alternative to reduce hot flashes in patients who cannot use HRT?

A

SSRIs or SNRIs

631
Q

What are the features of MEN1?

A

AD mutation of MEN1 (menin – tm suppressor gene)
3 Ps:
Parathyroid adenomas/hyperplasia (most need parathyroidectomy)
Pituitary adenomas (prolactin or GH)
Pancreatic endocrine tms (ZES, Insulinomas, VIPomas, Glucagonomas)

May also have multiple cutaneous lipomas

632
Q

Features of MEN2:

A

AD mutations in RET gene (TK receptor gene)

MEN2a: Parathyroid hyperplasia, MTC, Pheochromocytomas

MEN2b: MTC, pheochromocytomas and Marfan habitus/Mucosal neuromas (oral/intestinal ganglioneuromatosis)

633
Q

What are the exercise recommendations for a patient after cerclage placement?

A

Exercise is contraindicated in pts w/cerclage placement as well as those w/cervical insufficiency, preterm labor during current pregnancy, PPROM, placenta previa or persistent 2nd or 3rd trimester bleeding

634
Q

What type of infection is commonly caused by Corynebacterium minutissimum?

A

Erythrasma

635
Q

What diseases are patients post-renal transplant at risk of developing?

A

DM – has highest risk of developing and is typically the quickest to occur (w/in months)
Subclinical Hypothyroidism
Osteoporosis
RCC in the native kidney

636
Q

What effect will deranged magnesium levels have on the DTRs?

A

Mild hypermagnesemia may have decreased DTRs and severe hyperMg causes loss of DTRs
Hypomagnesemia can cause increased DTRs (most commonly d/t alcoholism)

637
Q

What is the most common post-op electrolyte disturbance to effect the DTRs?

A

Hypocalcemia – occurs d/t volume expansion and hypoalbuminemia or bc of citrate in pts w/massive blood transfusions

Causes increased DTRs

638
Q

What is SAAG and how does it differentiate causes of ascites?

A

SAAG = Serum albumin – Ascitic fluid albumin; >1.1 indicates presence of portal HTN

SAAG 1.1+ – CHF, Cirrhosis, EtOH Hepatitis, Budd-Chiari
SAAG <1.1 – peritoneal carcinomatosis (ovarian cas), peritoneal TB, nephrotic syndrome, pancreatitis, and serositis

639
Q

What are the side effects of Kava Kava?

A

Herbal supplement to tx Anxiety and Insomnia

Can cause severe liver damage

640
Q

What commonly used herbal supplements can cause increased bleeding risk?

A

Ginkgo biloba
Saw palmetto
Ginseng

Besides mild GI upset from saw palmetto this is the only main AE of these supplements

641
Q

What conditions are a/w eruption of multiple skin tags?

A

Insulin resistance, obesity, overt diabetes, metabolic syndrome
Pregnancy
Crohn disease – seen perianally

642
Q

When should ACEIs be started in patients with HF?

A

Anyone w/asx LVSD (EF 40% or less)
Can delay onset of symptomatic HF and improve long-term morbidity and mortality

Once suitable ACEI dose has been achieved a BB should be added

643
Q

Precipitating factors of Hepatic Encephalopathy:

A
Drugs (sedatives, narcotics)
Hypovolemia (diarrhea)
Electrolyte changes (hypokalemia)
Increased Nitrogen load (GI bleed)
Infection (pneumonia, UTI, SBP)
Portosystemic shunting/TIPS
644
Q

How will changes in K+ affect patients w/cirrhosis?

A

Hypokalemia is a common precipitant to hepatic encephalopathy and even slight decreases require prompt repletion. This commonly occurs after the initiation of diuretics which deplete K+ and cause low intravascular volume despite total volume overload

Metabolic alkalosis (increased HCO3-) is often a/w hypokalemia which also exacerbates HE by increasing conversion of NH4+ to NH3

645
Q

What are the definitions of sensitivity and specificity?

A

Sensitivity – the probability of a diseased person testing positive
Specificity – the probability of a nondiseased person testing negative

646
Q

What is iritis?

A

Anterior uveitis – characterized by pain, redness, variable visual loss and a constricted and irregular pupil
Will see leukocytes in the anterior segment which contains the aqueous humor
May also see hazy “flare” which is indicative of protein accumulation secondary to damaged blood-aqueous barrier

Tx: antimicrobials for bacterial and viral causes, topical steroids for noninfectious causes

647
Q

What is the uvea and how is uveitis differentiated?

A

Uvea = Iris, pars planus, choroid and ciliary body

Anterior uveitis – iritis; see leukocytes in the anterior segment which contains aqueous humor
Intermediate uveitis – pars planitis
Posterior uveitis – choroiditis and/or retinitis

May also have hypopyon (pus in anterior chamber) and conjunctival redness

648
Q

How will infectious keratitis present?

A

With severe photophobia and difficulty keeping the eye open

Penlight exam will show corneal opacity or infiltrate

649
Q

What are risk factors for Stress Hyperglycemia?

A
ICU admission
Fevers >102.2
Severe illness
Sepsis
CNS infection – meningitis
650
Q

How to differentiate Stress Hyperglycemia from DM-I in a patient presenting w/ketoacidosis?

A

If a patient does not have known diabetes and does not meet diagnostic criteria for DM then it is most likely stress hyperglycemia w/ketoacidosis
DM-I patients who present w/DKA as their first sign will still have signs of chronic hyperglycemia – HbA1c 6.5% or greater

DM criteria: Random plasma glucose 200+ w/classic sxs of hyperglycemia OR HbA1c 6.5% or more OR Fasting glucose 126+ OR 2hr glucose 200+ during oral glucose tolerance test

651
Q

How should Hypothyroidism in pregnancy be managed?

A

Increase Levothyroxine dose 30% at time of positive pregnancy test
Measure TSH every 4 weeks after that and adjust dose to trimester-specific TSH norms

652
Q

What is the best diagnostic test to detect pneumothorax in the acute setting?

A

Bedside US – much higher sensitivity and specificity (>90%) than portable CXR (50%)
Will visualize the parietal and visceral pleuras and the inability to detect lung sliding, the 2 pleural layers moving against each other during respiration, is diagnostic of pnx

In patients w/high suspicion of tension pnx, diagnostic confirmation isn’t needed and treatment (decompression/tube placement) shouldn’t be delayed for it

653
Q

What are patients w/identified Trichomonas infection at risk for?

A

HIV – presence of trichomonas increases rates of HIV transmission
So both patient and partner need to be treated regardless if they have sxs or are asx

654
Q

What is ascertainment bias?

biostats

A

When results from an atypical population are extrapolated into the entire population

655
Q

How does anaphylaxis present?

A

Presentation is extremely variable. If it is at all suspected just give IM Epi
Any or all of the following sxs may be present:
HoTN (often the only symptom)
GI distress – N/V, diarrhea, crampy abdominal pain
Swelling of lips and tongue
Rash, itching, hives
Respiratory distress

656
Q

What medications can be secondary causes of Osteoporosis?

A

Glucocorticoids
Phenytoin, Carbamazepine
PPIs

657
Q

What initial tests should be done to assess a chronic cough?

A

If there is absence of specific historical or examination findings suggesting an underlying cause initial evaluation should begin with:
Spirometry and CXR

658
Q

How to differentiate aFIb v. aFlutter v. SVT on EKG:

A

aFib – RR intervals will be regular and equal, the baseline b/w RR will be irregular and no discernible P-waves will be identified

aFlutter – RR intervals will be regular and equal, baseline will show sawtooth pattern w/back-to-back atrial depolarizations and typically a 4:1 sawtooth to QRS pattern

SVT – RR intervals will be regular and equal, mostly see narrow QRS-complexes, have retrograde P waves seen as pseudo S and pseudo R waves. Baseline b/w RR will be regular.

659
Q

Mgmt of Supra-ventricular tachycardia:

A

Different types of SVT – sinus tach, AVNRT, AVRT, aFIb and aFlutter
In hemodynamically stable pts first identify type of SVT by giving IV Adenosine or w/vagal maneuvers – these will slow AVN conduction and help differentiate the cause of the SVT

In unstable patients they need immediate synchronized direct-current cardioversion

660
Q

When should XR be done in patients w/suspected scoliosis?

A

If there is an obvious deformity on exam or an abnormal scoliometry – spinal rotation 7+ degrees (or 5+ in overweight children)

661
Q

When does Scoliosis require treatment?

A

Cobb angle <10 – considered normal variant, f/u only if new findings (pain, neuro sxs) develop
Cobb angle 10+ degrees – observation or back brace
Cobb angle 40+ degrees – severe scoliosis, need surgical evaluation

Once puberty/skeletal maturity are complete no tx is needed unless severe deformity is present

662
Q

When is tx indicated in Paget disease?

A

Give Bisphosphonates or Calcitonin in those who can’t tolerate bisphosphonates
Symptomatic disease – intolerable pain, etc.
Involvement of weight-bearing bones (femur)
Neurological involvement

Rare indications:
Hypercalcemia
Hypercalciuria
CHF

663
Q

What is the inheritance pattern of Hemophilia?

A

X-linked recessive for both A and B

664
Q

What should be done in a patient w/epigastric fullness and nausea?

A

This is considered dyspepsia even if there is no associated pain – H. pylori testing first if <60y/o

665
Q

What should be the first step in managing a cystic lesion in the pancreas?

A

Endoscopic US and aspiration – will differentiate cyst v. malignancy and guide tx

666
Q

What is bile salt-induced diarrhea?

A

Secondary bile acids cause colonic stimulation and diarrhea
Common post-cholecystectomy, post-ileal resection and in short bowel syndrome
Tx w/Cholestyramine (bile salt-binding resin)

667
Q

What is the preferred antiarrhythmic therapy in patients w/aFib?

A

No CAD or structural heart disease – Flecainide or Propafenone
CAD w/o HF – Dronedarone or Sotalol
LV Hypertrophy – Dronedarone or Amiodarone
HF – Amiodarone or Dofetilide
aFib refractory to meds – radiofrequency ablation

668
Q

What is the tx of Croup?

A

Aka Laryngotracheitis
Mild (no stridor at rest) – humidified air (softens secretions) +/- corticosteroids (oral or IM)
Moderate/Severe (stridor at rest) – Corticosteroids + Nebulized Epi

Nebulized SABAs (albuterol) have no role in management

669
Q

What virus causes Croup?

A

Parainfluenza

Bronchiolitis is caused by RSV

670
Q

What causes unilateral headache and partial, unilateral Horner Syndrome?

A

Always carotid a. dissection until proven otherwise
Occurs in younger patients (~45)
Tx: Thrombolysis if w/in 4.5hr of onset; Antiplatelet tx +/- anticoagulation
Should get CT or MR angiography right away

671
Q

What is the timeline required to diagnose preeclampsia?

A

Occurs at 20+ weeks gestation, but can occur up to 12 weeks postpartum
Tx is the same for postpartum preeclampsia – Mag sulfate + BP control

672
Q

What is the schedule for DTaP vaccines?

A

Series should be completed at 2, 4 and 6 months with an additional dose at 15-18mos and again at 4-6 years
Boosters should then be given every 10 years and w/every pregnancy at 28wks

Only contraindications are encephalopathy after previous dose or anaphylaxis to a vaccine component; Immunosuppression of any kind is not a contraindication

673
Q

What is a common cause of endobronchial obstruction in younger patients?

A

Carcinoid tumor – obstruction can lead to recurrent pneumonia and infection + scarring
Can occur at any age but is especially seen in younger non-smokers

674
Q

What is the best test to diagnose endobronchial obstructive lesions?

A

Flexible bronchoscopy

CT should be obtained first, but CT cannot diagnose, only a tissue biopsy can

675
Q

What nerve adducts the leg?

A

Obturator

676
Q

What nerve is responsible for ankle jerk?

A

Sciatic

677
Q

When should PCI be done over CABG?

A

PCI – for refractory angina in patients w/severe single or two-vessel CAD not involving the proximal LAD

CABG – superior in pts w/multivessel CAD (especially involving the LAD) and LV dysfunction

678
Q

What is the mgmt. of symptomatic PAD?

A

Step 1A: Risk factor mgmt. – smoking cessation, BP and DM control, antiplatelet (aspirin) + Statin therapy
Step 1B: Supervised exercise therapy
Step 2: Cilostazol (PDE3 inhibitor)
Step 3: Revascularization for persistent sxs

679
Q

How would a uterine sarcoma present on US?

A

Almost identical to a leiomyoma – enlarged and irregular uterus w/a mass seen
May often also see ascites as free fluid in posterior cul-de-sac
Commonly met to the lungs and cause pleural effusions
Need hysterectomy urgently to diagnose, stage and treat
Should be suspected in postmenopausal patients w/pelvic radiation or tamoxifen use

680
Q

How to differentiate acute cholecystitis v. choledocholithiasis:

A

Often present the same: abdominal pain, fever, leukocytosis

Choledocholithiasis usually also has common bile duct dilation on US, elevated BR and ALP

681
Q

What is the initial workup for delayed puberty in boys?

A

FSH, LH, testosterone, TSH and prolactin levels

Bone age radiograph

682
Q

Causes of delayed puberty in boys:

A

Primary hypogonadism – will have elevated FSH/LH
Klinefelter syndrome
Secondary hypogonadism – will have low/normal FSH/LH
constitutional, chronic illness, malnutrition
Hypothyroidism
Hyperprolactinemia
Kallmann syndrome
Craniopharyngioma

683
Q

What is used to tx Neuroleptic Malignant Syndrome?

A

Dantrolene

684
Q

How should confirmation of H. pylori eradication be done?

A

Either fecal antigen testing or urea breath test, but neither should be done until 4 weeks after completion of therapy.

685
Q

What orbital structures are likely to be injured in eyelid lacerations?

A

Horizontal lacerations of upper lateral eyelid – may involve the orbital septum and levator palpebrae muscle as well as the lacrimal gland

Medial lacerations of the eyelid likely to injure canaliculi as well as the punctum, nasolacrimal duct and lacrimal sac

686
Q

What test should be done in a child w/suspected Hirschprung?

A

Rectal mucosal suction biopsy – will show absence of ganglion cells
Commonly a/w Down syndrome

687
Q

What is the most likely outcome of trastuzumab-associated cardiotoxicity?

A

Causes decline of LVEF and although usually asx may lead to overt clinical HF
However, there is typically complete recovery of cardiac fxn after trastuzumab is dc’d

It is not dose-related as is the irreversible cardiotoxicity a/w anthracyclines (doxorubicin)

688
Q

When should a pregnancy be able to be visualized on US?

A

At B-hCG levels >1500

689
Q

What should be the initial evaluation in a patient w/dysentery?

A

Stool culture
Immunoassay for Shiga toxin
Fecal leukocyte count

690
Q

Mgmt of uncomplicated pediatric pneumonia:

A

Preschool age or focal lung findings – most common cause S. pneumo; tx w/high-dose amoxicillin

Older child or well-appearing w/bilateral lung findings – most common cause M. pneumo; tx w/Azithromycin

691
Q

What are 1st line therapies for patients w/alcohol use disorder?

A

Naltrexone – can be initiated while still drinking, but is contraindicated in those taking opioids, or who have acute hepatitis or liver failure
Acamprosate can also be used as 1st line therapy

692
Q

How should the efficacy of anti-thyroid therapy be assessed?

A

With total T3 and free T4 – TSH may remain suppressed for several mos after initial therapy and therefore does not accurately reflect thyroid functional status

693
Q

What is the most reliable method for verification of proper endotracheal tube placement?

A

Capnography w/persistent waveform w/ventilation

694
Q

Pathogenesis and common causes of phototoxic drug rxns:

A

D/t production of ROS that then directly damage cell membranes and DNA.
Sxs can be seen in both sun-exposed areas as well as non-exposed areas.
Common causes: Abx (tetracyclines), Antipsychs (chlorpromazine), Diuretics (furosemide, thiazides), Amiodarone, promethazine, piroxicam.

695
Q

What metabolic/lab abnormalities can hypothyroidism cause?

A

Hyperlipidemia (decreased LDL-Rs or decreased LDL-R activity)
Hyponatremia (d/t decreased free H2O clearance)
Asx elevation in creatinine kinase
Elevated serum transaminases
Macrocytic anemia

696
Q

Clinical features of HELLP:

A

Preeclampsia (increased BP + urine proteins after 20 wks)
Nausea/vomiting
RUQ abdominal pain

697
Q

Definition of preeclampsia:

A

New-onset HTN (SBP 140+ and/or DBP 90+) at 20+ weeks gestation PLUS proteinuria &/or end-organ damage

698
Q

Severe features of preeclampsia (6):

A
SBP >160 or DBP 110 (2x 4hrs apart)
Thrombocytopenia
Increased Creatinine
Increased Transaminases
Pulmonary edema
Visual or cerebral sxs (hyperreflexia/clonus)
699
Q

Mgmt of preeclampsia:

A

W/out severe features – delivery at 37+ weeks
W/severe features – delivery at 34+ weeks
Mag sulfate for seizure pphx + Anti-HTNs should be started first in regardless of gestation

C-section is not indicated unless there is a contraindication to labor, or there’s a non-reassuring FHR

700
Q

What should be given to patients with HELLP syndrome? When should this be given, and for how long?

A

Mag sulfate – given immediately on diagnosis and continued for 24hrs after delivery.

701
Q

What clue on PE often suggests diaphragmatic paralysis?

A

Paradoxical abdominal wall retraction during inspiration while lying supine
Patients often have SoB worse while supine that can be mistaken for a cardiac origin of dyspnea

702
Q

What is the most common adverse event that occurs in hospitalized non-operative/procedural patients?

A

Adverse drug events; Second is hospital acquired infection

In patients undergoing an operation/procedure then operative/post-procedure adverse events become the most common; These include wound infections, bleeding and DVTs

703
Q

How should epistaxis be managed?

A

First apply direct compression w/nostril pinching, if this fails add topical vasoconstrictor (Oxymetazoline) via squirt bottle or cotton pledget.
If this fails next step is chemical (silver nitrate) or electrical cautery, then anterior nasal packing w/bacitracin covered sponge if there is continued bleeding.

If bleeding appears to be posterior then nasal packing needs to be done, but this is much less common

704
Q

How are vesicovaginal fistulas commonly diagnosed?

A

With methylene blue instillation into the bladder – positive test will turn tampon in the vagina blue d/t leakage through the fistula

705
Q

What does the “Q-tip test” diagnose?

A

Urethral hypermobility – >30-degree angle of movement during Valsalva is diagnostic

706
Q

When should an ear wick be placed?

A

If the patient has otitis w/a completely occluded ear canal

707
Q

What are the TSH goals of levothyroxine in patients w/differentiated epithelial thyroid cancer?

A

Differentiated epithelial thyroid cancer = Papillary and Follicular

Small, low-risk tms: Target TSH 0.1-0.5 for 6-12mo and then kept at low normal range (0.5-1ish)
Intermediate risk: Target TSH 0.1-0.5
Large, aggressive tms: Target TSH <0.1 and should be continued at this level for several years

Suppressing TSH will decrease risk of recurrent disease

708
Q

How should actinic keratosis be managed?

A

Lesions should be removed/destroyed at time of detection
Individual lesions – liquid nitrogen cryosurgery, surgical excision or curettage
Numerous lesions – field therapy w/5-FU cream (best), imiquimod cream, topical diclofenac or photodynamic therapy

709
Q

What are the two most important predictors of survival in COPD patients?

A

Age and FEV1 (<40% indicates severe disease)

After adjusting for age, FEV1 is the single most important factor to determine prognosis

710
Q

What is the recommended Cervical cancer screening in Immunosuppressed women?

A

aka those w/SLE, organ transplant, etc.

Screening should start at onset of sexual intercourse and should occur annually w/pap and HPV cotesting

711
Q

Most common congenital heart disease in children w/Down’s syndrome:

A

Enodcardial cushion defect

712
Q

What are common conditions that patients w/Down Syndrome are at increased risk for?

A
Acute leukemia
Alzheimer-like dementia
Autism
ADHD
Atlanto-axial instability
Depressive disorder
Duodenal atresia
Seizure disorder
Hypothyroidism
713
Q

Complications of chlamydia infection in pregnancy:

A

Maternal – PPROM, preterm labor, postpartum endometritis

Fetal – neonatal conjunctivitis and neonatal pneumonia

714
Q

What is construction apraxia?

A

Difficulty in copying simple line drawings, most commonly seen in patients who have damage to their nondominant parietal lobe

May also have confusion and dressing apraxia (difficulty in wearing cloths, and getting dressed) as these are also common in parietal lobe lesions

715
Q

What would likely be seen in a patient with a nondominant temporal lobe lesion?

A

Visual disorders – homonymous upper quadrantanopia

Auditory agnosia – impaired perception of complex sounds

716
Q

What is Gerstmann syndrome?

A

Often occurs w/damage to the dominant parietal lobe
Patients can have acalculia (difficulty performing simple math), finger agnosia (inability to name individual fingers), agraphia, and R/L confusion (difficulty identifying the R from L side of the body)

717
Q

How should gDM be managed postpartum?

A

Anti-hyperglycemic therapy should be stopped after delivery of placenta
Obtain fasting glucose at 24-72hr and then do 2hr 75g GTT at the 6-12 week postpartum visit
These patients should also undergo DM screening every 3 years as they are at increased risk

718
Q

Who should receive Iron supplementation in ESRD?

A

All patients w transferrin saturation 30% or less and ferritin 500 or less
These patients may have normal iron stores but can’t mobilize them, also ferritin is an acute phase reactant and can be increased d/t the inflammation a/w ESRD therefore it is a poor indicator of Fe-status in patients w/ESRD

719
Q

How does G6PD present?

A

Often in childhood after an oxidative stress w/jaundice, pallor, dark urine + abd/back pain
May also occur in neonatal period w/jaundice and anemia on day 2-3 of life and rapid increase in unconjugated BR (differentiated from ABO incompatibility based on timing, ABO <24hrs, and other physiologic jaundice by the presence of anemia which is not seen in physio jaundice)
X-linked disease

720
Q

How are cat bites managed?

A

Cat bites are considered high risk for infection and always require abx regardless of the cleanliness or benign appearance of the wound
Tx: amoxicillin-clavulanate

721
Q

What is labor protraction and how is it managed?

A

Labor protraction: cervical dilation 1cm or less/2hr during the active phase of labor (6cm-10cm cervical dilation)
Tx: Oxytocin + amniotomy (artificial rupture of membranes) are first line therapies

722
Q

Most common AE w/in 1-6hrs of transfusion:

A

Febrile nonhemolytic transfusion rxn. – can be prevented with leukoreduction.

723
Q

When should cells be washed prior to transfusion?

A

If the pt. has IgA deficiency or had a prior allergic transfusion rxn.

724
Q

What should be given to transplant pts. to prevent opportunistic infections?

A

TMP-SMX.
This prevents PCP, some Listeria and toxoplasma infections.
Can be discontinued 6-12 months post-transplant.
Some pts. may also receive Ganciclovir for pphx against CMV

725
Q

What is the prognosis of children with a single febrile seizure?

A

No long-term sequelae but they are at increased risk for subsequent febrile seizures and have slight increased risk of epilepsy (~1%)

726
Q

What are the endoscopy recommendations for patient’s w/Barrett’s esophagus?

A

Metaplasia but no dysplasia: PPI + surveillance endoscopy in 3-5 years
Low-grade dysplasia: PPI + surveillance endoscopy 6-12mo OR endoscopic eradication
High-grade dysplasia: Endoscopic eradication therapy (ablation, mucosal resection)

727
Q

What is the major problem that leads to difficulty finding cross-matched blood for patients?

A

Alloantibodies – most commonly seen in pts w/multiple transfusions (SCD, myelodysplasia)

Side note: RBCs do not express HLA antigens

728
Q

What are the clinical features and mgmt. of primary ovarian insufficiency?

A

Features:
Amenorrhea at age <40
Hypoestrogenic sxs (hot flashes)
Increased FSH (increased/normal LH), decreased Estrogen
Tx: Estrogen therapy + progestin if patient has an intact uterus (reduces risk of endometrial ca)
Continue therapy until around normal age of menopause (50) and then dc

729
Q

What are the major causes of Primary ovarian insufficiency?

A
Turner syndrome (45,XO)
Fragile X
Autoimmune oophoritis
Anticancer drugs
Pelvic radiation
Galactosemia
730
Q

What is oculoglandular syndrome?

A

aka Parinaud syndrome – specific manifestation of cat-scratch disease
Presents w/lymphadenitis (often chronic, >2wk) of the preauricular or cervical nodes with involvement of the conjunctivae – conjunctivitis w/clear drainage
Typically self-resolving but sometimes the LNs can suppurate and drain onto the skin (needle-aspiration can prevent rupture and relieve sxs)
Tx not always indicated but Azithromycin can accelerate recovery

731
Q

What is the tx of Psoriasis?

A

Limited plaque psoriasis – topical glucocorticoids or Vit. D derivatives (calipotriene)
Extensive plaques or joint involvement/arthritis – methotrexate or other biologics

732
Q

What is the tx of Ecthyma Gangrenosum?

A

IV abx that cover Pseudomonas – anti pseudomonal B-lactam (pip-tazo) + aminoglycoside
Others that can be used: select cephalosporins, monobactams, fluoroquinolones and carbapenems
Usually does not require surgery/debridement like nec fasc which it commonly resembles – can differentiate based on pain – ecthyma gangrenosum is typically painless

733
Q

What are the features of glucocorticoid-induced Diabetes?

A

Typically resemble Type II DM and is characterized by insulin resistance rather than insulin deficiency like seen in type I.
DKA is very uncommon in these patients

734
Q

What conditions are commonly associated with Ketoacidosis?

A

Stress-induced hyperglycemia

Type-I DM

735
Q

What cells are responsible for producing myelin in the PNS v. CNS?

A

Peripheral nervous system: Schwann cells (implicated in acoustic neuromas)
Central nervous system: Oligodendrocytes

736
Q

What is a positive tourniquet test?

A

When a patient develops petechiae after BP cuff inflation on their arm for 5 min
Often seen in Dengue hemorrhagic fever

737
Q

When does surgery need to be done for ovarian masses in pregnant women?

A

If a mass is identified and is persistent, has complex features (septations), and/or is >10cm in diameter
Surgery should be done in the early second trimester to prevent complications.

738
Q

Who gets berry aneurysms?

A

EHLERS-DANLOS!!!!!!

Not Marfan, they get aortic dissection and lens dislocations and shit

739
Q

What has shown efficacy in targeting the negative sxs a/w schizophrenia?

A

Psychosocial intervention w/social skills training
Meds so far have not shown proven benefits in targeting negative sxs and mood stabilizers should not be added as negative sxs are not the same as depression.

740
Q

What are the absolute contraindications to combined hormonal contraceptives (12)?

A
Migraine w/aura
15+ cigs/d AND age 35+
HTN >160/100
Heart disease
DM w/end-organ damage
Hx of thromboembolic disease
Antiphospholipid-Ab syndrome
Hx of Stroke
Breast ca
Cirrhosis and liver ca
Major surgery w/prolonged immobilization
Use <3wks postpartum
741
Q

How does ventilator-associated pneumonia commonly present?

A

New onset fever, increased secretions, new/worsening pulmonary infiltrates and increased requirement for ventilatory support in a patient ventilated for 48+ hrs
Commonly occurs as a complication of ARDS

Other signs: leukocytosis, tachypnea, and decreased oxygenation

respiratory sampling (tracheobronchial aspirate/BAL) is necessary for culture and microscopy to tailor abx

742
Q

What are common organisms implicated in VAP and how are they treated?

A

Often caused by: E. coli, Strep spp., MRSA, Pseudomonas (microaspiration of virulent oropharyngeal organisms)
Tx: Imipenem or meropenem, pip-tazo or cefepime, gentamicin AND vancomycin or linezolid
- Tracheobronchial aspiration or BAL must be done for culture/microscopy to tailor abx regimen d/t increased resistance of VAP-associated organisms

743
Q

What drugs can increase the risk of hospital-acquired pneumonia?

A

PPIs

744
Q

What should be suspected in an elderly patient with non-exertional syncope w/o an autonomic prodrome of sxs and no neurological sxs?

A

Cariogenic syncope – can happen in any age, but commonly in elderly w/structural heart disease. Often have no signs/sxs by time of presentation to ED or office
Can be exertional (d/t AS or HCM), have preceding sxs like fatigue/dizziness (sick sinus syndrome), or nonexertional w/no preceding sxs (Vtach, TdP)
These patients need inpatient monitoring w/tele to detect the arrhythmia + echo to look for structural heart disease

745
Q

What are risk factors for neural tube defects?

A
Folate deficiency – #1
Pregestational DM
Maternal fever in 1st trimester
Maternal obesity
Genetic factors
746
Q

What is a common complication of Spina Bifida/NTD repair?

A

NTDs require urgent neonatal surgical repair, and over half of infants who undergo repair of an NTD get hydrocephalus requiring a VP shunt

747
Q

When is daily abx suppression warranted during pregnancy?

A

If the pregnant mother had an episode of acute pyelonephritis – they need immediate IV abx during the episode and then once it has resolved require daily abx suppression until after delivery to prevent pyelo-associated cxs (preterm labor, sepsis, ARDS)

748
Q

What are the side effects and contraindications to progestin-subdermal implant?

A

Side Effects: unscheduled bleeding (most common), weight gain, HA
Contraindication: progesterone receptor+ breast cancer
This is the most effective form of contraception (even higher than sterilization and IUDs)

749
Q

What should be done to test for pernicious anemia?

A

Initial test should be for detection of Anti-IF Abs (anti-parietal Abs are not commonly tested for as they’re much less specific than anti-IF in diagnosing pernicious anemia)
Schilling can be done as a 2nd-line if anti-IF is negative

750
Q

What are the likely findings seen on gastric endoscopy in pernicious anemia?

A

Pernicious anemia is a/w autoimmune metaplastic atrophic gastritis (AMAG) – immune response mainly directed against oxyntic cells and IF.
There are 3 main components of AMAG:
1. Absent rugae in the fundus and sometimes body/glandular atrophy
2. Intestinal metaplasia
3. Inflammation
The gastric body and fundus are the main areas affected; typically see little/no changes in the antrum

751
Q

How to differentiate n-REM from REM sleep disorders:

A
n-REM disorders (sleep walking, sleep terrors), occur during the first 1/3 of sleep/slow wave sleep, the patients have amnesia of the event
REM disorders (nightmares), occur during second ½ of sleep, the patients have detailed dream recall or act out their dreams during the event
Don’t need tx unless episodes are frequent, persistent &amp; distressing – give low-dose benzo
752
Q

What are the common features and risk factors of candida endophthalmitis?

A

Often in neutropenic patients, those w/CVCs used for TPN, and in severely ill pts in the ICU
Sxs: fever, decreased visual acuity, and eye pain
Fundoscopy: focal, glistening white, mound-like lesions on the retina that may extend into the vitreous w/resultant vitreous haze

753
Q

What is the tx of candida endophthalmitis?

A

Vitrectomy + intravitreal antifungal injection + systemic antifungal (amphotericin B; can consider using fluconazole or voriconazole instead, but not ketoconazole)

754
Q

How do tuberculous effusions often present?

A

With fever, cough, pleurisy and weight loss
Thoracentesis often shows lymphocyte-predominate, exudative effusion w/elevated ADA
Often require pleural biopsy to diagnose as pleural fluid smear is usually aseptic

755
Q

How are HIV+ patients likely to present w/TB?

A

HIV patients w/high or normal CD4 counts typically present as expected w/apical cavitary lesions
Patients w/low CD4 counts cannot mount a sufficient cell-mediated defense to create cavitations and often present w/lobar, pleural, or disseminated infections.

756
Q

What is the typical course of lower extremity alignment in children?

A

Physiologic genu varum from 6mos up to 3yrs (after 3 yrs need investigation)
Straight legs are typical around age 2
Physiologic genu valgum from 4yrs on
Straight legs by >7yrs, if not need imaging and investigation

757
Q

What vessel is likely to cause CN-III palsy?

A

Aneurysms of the posterior communicating a. or rarely cavernous-carotid aneurysms
SAH d/t rupture of these aneurysms is typically what causes the palsy, but can get prodromal sxs (diplopia) from their mass effects prior to rupture

758
Q

What is primary v. secondary mitral regurgitation?

A

Primary is caused by an intrinsic defect of the MV apparatus – leaflets, chordae tendineae (MVP is one of the most common causes)
Secondary/Functional occurs d/t a disease process involving the LV (MI, DCMP, etc.)

759
Q

What is considered impaired LV systolic function?

A

Most healthy patients LVEF 50% or less is considered impaired systolic function
In patients w/severe, chronic MR, LVEF 60% or less is considered impaired function

760
Q

When is chronic MR considered severe?

A

In the presence of associated sxs – dyspnea on exertion, HF
Or specific echo findings – LA and LV enlargement, regurgitant jet prominence
LVEF <60% is considered systolic dysfunction in these patients bc a large portion of the LVEF flows back into the LA and underestimates the EF.

761
Q

What thyroid disorders will show decreased radioiodine uptake on thyroid scintigraphy?

A
Subacute (de Quervain, subacute granulomatous) thyroiditis
Silent (painless) thyroiditis
Postpartum thyroiditis
Surreptitious thyroid hormone abuse
Iodine-induced thyroiditis
762
Q

What is the treatment of Subacte thyroiditis?

A

Typically NSAIDs are enough, and relieve the associated pain; may give glucocorticoids for severe or refractory cases
BBs can also be added to minimize the sxs (sweating, palpitations)
Anti-thyroid meds (PTU, MTZ) have no role

763
Q

What conditions can be treated with radioiodine thyroid ablation?

A

Graves and nodular thyroid disease

764
Q

What anti-DM med is most helpful in obese patients and those w/NASH?

A

Metformin

In contrast, sulfonylureas will worsen obesity and do not improve lipid profiles

765
Q

What are the Rabies prophylaxis guidelines?

A

Pre-exposure pphx: Rabies vaccine on days 0, 7 & 21 or 28
Post-exposure pphx; unvaccinated: Rabies vax on days 0, 3, 7 & 14 + Rabies Ig on day 0
Post-exposure pphx; previously vaccinated: Rabies vax on days 0 & 3

766
Q

What are the common manifestations of early neurosyphilis?

A

Can have any or all of the following:
Meningitis – HA, confusion, N/V, stiff neck, photophobia (more subacute presentation than bacterial meningitis)
Ocular – posterior uveitis, decreased visual acuity, photophobia
Meningovascular – infectious CNS arteritis causing ischemia and/or infarction
Otosyphilis – tinnitus, sensorineural hearing loss (often unilateral)
Cranial neuropathies – most commonly of the optic, facial or auditory nerves

These most commonly occur during the secondary stage of syphilis and will also see signs of this – generalized maculopapular rash involving palms/soles, LAD

767
Q

What laxatives are safe for long-term use in pediatric patients?

A

Osmotic laxatives
Stimulant laxatives can be used for acute disimpaction as well as enemas but these should not be used everyday as part of a long-term therapy

768
Q

What does recall bias cause?

biostats

A

Often leads to misclassification of exposure

769
Q

What are the components to diagnosing brain death?

A

First: clinical criteria – imaging evidence, absence of confounding factors, etc.
Second: neuro exam showing coma w/absent cerebral and brainstem reflexes
Third: apnea test to confirm brainstem failure
If all of these are positive then brain death can be diagnosed; if any are inconclusive then ancillary testing should be performed (EEG, CTA, transcranial Doppler, etc.)

770
Q

1st line tx in PCP intoxication?

A
Benzos
Antipsychotics (haloperidol) can be used if benzos fail but should not be first line
771
Q

What are the causes, features and treatments of Acute hemolytic transfusion reactions?

A

Cause: ABO incompatibility (more common in those requiring multiple transfusions – can develop Abs to common Rh, Kell, or other blood group Ags)
Timing: within 1hr of transfusion start
Features: fever, flank pain, hemoglobinuria, + Coombs test
Cxs: DIC, renal failure (d/t immune complex deposition)
Tx: stop transfusion and aggressively hydrate w/NS (not ringers or dextrose) – treats HoTN and prevents renal failure

772
Q

What is the logic behind plasma exchange tx in a patient w/TTP?

A

To increase the amount and activity of ADAMTS13, a plasma metalloprotease

773
Q

How to distinguish TTP from ITP:

A

Both will cause thrombocytopenia, bruising and petechiae, but only TTP will cause MAHA leading to schistocytes on PBS, elevated direct BR, LDH and aminotransferases

774
Q

Causes of TTP v. ITP:

A

TTP – auto antibodies against ADAMTS13, a metalloprotease, that cleaves vWF
ITP – auto antibodies against platelet antigens

775
Q

What are the disadvantages to using Metoclopramide as an anti-emetic?

A

In high doses often needed in chemo patients it can cause EPS and drug induced parkinsonism

776
Q

What are some disorders that increase the risk of pediatric thromboembolic events?

A

Homocystinuria – presents w/Marfan habitus, fair complexion, developmental delay, lens dislocation, and hypercoagulability. Cystathionine synthase def.

Fabry disease – presents w/angiokeratomas, peripheral neuropathy, asx corneal dystrophy, increased risk for renal and heart failure as well as thromboembolic events. a-Galactosidase def.

777
Q

What are the common manifestations of scabies and how is it treated?

A

Itchy rash, worse at night, involvement of the webbed-spaces on the hand
May also be seen on the forearms, elbows, axilla, waist, genitalia, knees, thighs and feet
Tx: topical permethrin (1 application) or 1-2 doses oral ivermectin

778
Q

What are the common features of an amebic liver abscess?

A

Often d/t protozoal infection w/Entamoeba histolytica
Manifestations begin 8-20wks after inoculation and include: fever, RUQ pain, nonspecific systemic sxs (malaise, nausea); May or may not have recent hx of dysentery
US will show round, well-defined hypoechoic mass in the R hepatic lobe.
Dx w/blood serology and antigen detection; aspiration not required to diagnose but often resembles “anchovy paste” (thick, dark brown fluid) and is aseptic w/neg gram stain

779
Q

How to differentiate pyogenic v. amebic liver abscesses:

A

Both typically present w/the same sxs and appear similar on imaging
Differentiation must be done w/E histolytica serologic or antigen testing
If testing is negative aspiration can be done – pyogenic abscesses will typically have positive cultures and gram stains, whereas amebic abscesses will likely be negative and aseptic

780
Q

Mgmt of esophageal coin ingestion:

A

Ingestion time <24hrs AND asymptomatic – observation + repeat XR in 12-24hrs
Ingestion time 24+hrs, or unknown OR symptomatic – endoscopic coin removal

781
Q

Most common causes of small bowel obstruction:

A

Post-op adhesions, hernias (incarcerated), and tumors

782
Q

What is the non-surgical mgmt. of primary hyperparathyroidism?

A

For those who do not have indications for surgery, the mgmt. should be close monitoring of the serum Ca2+, creatinine and DEXA testing

783
Q

What are the high-intensity statins?

A

Atorvastatin and Rosuvastatin

784
Q

What are the common features and causes of Erythema multiforme?

A

Erythematous plaques w/central clearing; Usually begins on the extremities
Most occur d/t underlying infections (>90%), common causes: HSV (#1 cause), M. pneumoniae
Other causes: drugs (sulfas, B-lactams, phenytoin), cancers and AI diseases

785
Q

What cells does HCC arise from in the liver?

A

HCC arises from hepatocytes/liver parenchyma

Liver interstitial cells play no role in the development of HCC

786
Q

What will the lab findings show in pertussis?

A

Lymphocyte-dominant leukocytosis – aka will look like virus but needs abx (macrolide)

787
Q

Mgmt of pediatric inguinal hernias:

A

Asymptomatic – elective surgery in 1-2wks (regardless of age)
Immediate surgical repair for incarceration

788
Q

When should HZV vax be given?

A

Age 50 or greater to all immunocompetent individuals

789
Q

What is likely the cause in a patient with a new-onset bleeding disorder?

A

Presence of coagulation factor inhibitor – antibodies against coagulation factors
Common Abs: antiphospholipid Abs, inhibitors of factors VIII, IX, and XI
VIII inhibitors cause “acquired hemophilia” and lab results will mimic inherited hemophilia. Just as dangerous
These can occur independently or be a/w malignancy, pregnancy, lymphoproliferative disorders or rheumatic disease

790
Q

What should be ruled out in patients who present w/appendicitis-like sxs on warfarin tx?

A

Retroperitoneal bleed – can have acute, severe RLQ pain and +psoas sign
Hemorrhage can occur even if the INR is w/in the therapeutic range
Need a CT abdomen STAT

791
Q

What reverses heparin?

A

Protamine sulfate

792
Q

Effect of calcium on the QT interval:

A

Hypercalcemia – shortened interval

Hypocalcemia – prolonged interval

793
Q

Findings of choanal atresia:

A

Unilateral (most common) – chronic nasal discharge and sxs begin in childhood
Bilateral – cyanosis that worsens w/feeding, improves w/crying, noisy breathing (stertor), sxs present shortly after birth
Both may be a/w CHARGE syndrome
Dx by inability to pass catheter past nasopharynx; confirm w/CT or nasal endoscopy

794
Q

How should patients w/a malignant pleural or pericardial effusion be managed?

A

Malignant effusions automatically makes the cancer stage IV/incurable and therefore care should be palliative – recurrent thoracocenteses for slow accumulating effusions, chemical pleurodesis for more aggressive/rapidly accumulating effusions. Pleural catheter is another option but has risk of infection.

795
Q

What can long QT lead to?

A

Ventricular arrhythmias

796
Q

What will AV conduction delay cause on EKG?

A

Prolonged PR interval

797
Q

Single greatest risk factor for developing pancreatic cancer:

A

Cigarette smoking

798
Q

What are the indications for implantable cardioverter-defibrillator placement?

A

Primary prevention:
Prior MI w/LVEF 30% or less
NYHA class II or III sxs w/LVEF 35% or less
Secondary prevention:
Prior VF or unstable VT w/o reversible cause
Prior sustained VT w/underlying cardiomyopathy

799
Q

What patient would benefit from cardiac resynchronization therapy w/biventricular pacemaker?

A

Those with moderate-severe HF, an LVEF 35% or less, and a widened QRS (>120msec)

800
Q

Most common inherited thrombophilia:

A

Activated protein C resistance caused by Factor V Leiden

Account for about 50% of all inherited thrombophilias

801
Q

What drugs should be used and avoided in TCA toxicity?

A

Sodium Bicarb is the #1 choice to stabilize the cardiac membrane and decrease QRS, but Lidocaine may also be used is Sodium bicarb is ineffective
Mag Sulfate is often used to decrease QRS prolongation but is not first line, can be added later if there is persistent arrhythmia

Physostigmine is used in isolated anticholinergic toxicity, but TCAs have mixed MoAs and therefore it is contraindicated as it can cause cardiac arrest in TCA toxicity
Flecainide is contraindicated and will worsen QRS prolongation

802
Q

What are the different MoAs or TCAs:

A

NE and Serotonin reuptake inhibitors (antidepressant effects)
Antihistamines (results in sedation)
A1-antagonists (results in HoTN, worsens BPH/BOO)
Cardiac Na+ channel blockers (results in conduction delay/QRS prolongation)
Anticholinergics (dry mucous membranes, pupillary dilation)

803
Q

What should be used to treat Torsades de Pointes?

A

Mag Sulfate – will decrease QRS prolongation

804
Q

What should be included in the initial assessment of obesity?

A

Hx and sxs of obesity and obesity related cxs: Back pain, OA, atherosclerotic CD, sleep apnea
Biometric measurements: BP and pulse, Weight, BMI, Waist circumference
Lab studies: Glucose (or HbA1c), TSH, lipids, hepatic enzymes

must assess for complications and reversible causes when overweight/obesity is diagnosed

805
Q

How should obese patients be managed?

A

Step 1: lifestyle modifications – exercise 20-30min/d, 5-7d/wk, diet low in calories and fat or Mediterranean diet, decrease portion sizes
*If fail to lose wt + have BMI 30+ or 27-29 and have comorbidity move to step 2

Step 2: Drug therapy options – orlistat (often 1st line), phentermine/topiramate, buprorion/naltrexone, liraglutide
**If fail to lose wt and have BMI 40+ or 35+ and comorbidity proceed to step 3

Step 3: Bariatric surgery

806
Q

When can bariatric surgery be considered?

A

If a patient is obese (BMI 40+ or 35+ and has a comorbidity) and has already failed lifestyle modifications and drug therapy

comorbidities/obesity-related cxs include: HTN, impaired glucose tolerance, DM, dyslipidemia, sleep apnea

807
Q

How to differentiate EHEC v. Shigella sonnei infection:

A

Both will present w/dysentery and abdominal cramps
EHEC is often afebrile and is a/w animal exposure (farms, petting zoos), or ingestion of undercooked beef
Shigella is commonly febrile and is not a/w animal exposure, but is contracted through contaminated food or water

both will have shiga toxin present

808
Q

What are the common causes of diarrhea a/w pets and animals?

A

Salmonella – a/w pets, poultry and turtles; often does not produce dysentery and is seen as non-bloody diarrhea, but can be bloody
EHEC – a/w farms, petting zoos, etc.; almost always bloody and afebrile

809
Q

How to distinguish EHEC from other strains of E. coli:

A

EHEC does NOT ferment sorbitol which is evident by growing it on sorbitol-MacConey agar

810
Q

When should abx be avoided in patients w/dysentery?

A

If they have proven infection with EHEC – increased chance of developing HUS

811
Q

Normal values for serum transferrin saturation:

A

Aka TIBC
20%-50%
In Fe-deficient anemia levels typically drop below 10%

812
Q

What are the common features of anemia of chronic disease?

A

Increased Hepcidin in setting of inflammation leads to decreased release of Fe from macrophages and decreased Fe absorption from the gut.
Most often it is normocytic but can become microcytic
Always nonhemolytic so will have normal BR levels
Labs: decreased Fe, decreased TIBC (opposite of Fe-def), and increased ferritin (acute phase reactant)

Only time it should be treated is in setting of CKD – give EPO, otherwise just correct underlying disease; Fe plays no role in tx as they have normal iron stores they just can’t mobilize them properly

813
Q

Causes of aplastic anemia:

A

Radiation and Drugs – benzene, chloramphenicol, alkylating agents, antimetabolites, phenytoin
Viruses – parvoB19, EBV, HIV, hepatitis viruses
Faconi anemia – DNA repair defect leading to bone marrow failure
Idiopathic

All cell lines will be deficient, but will have normal cell morphology on PBS

814
Q

Causes of dry bone marrow tap:

A

Hairy Cell leukemia – fibrosis of bone marrow
Aplastic anemia – fatty infiltration of bone marrow
Both will cause pancytopenia and have all cell lines down

815
Q

What are the polyomaviruses?

A

circular, naked, dsDNA viruses
JC virus – causes PML in HIV pts
BK virus – common in transplant patients, attacks kidneys and causes nephritis
Has basophilic intranuclear inclusions like CMV and HSV

816
Q

Proportion of Medicaid enrollees to expenditures:

A

Children comprise about 50% of enrollees but only about 15% of the expenditures
Elderly and disabled comprise much smaller percentages but consume a disproportionately larger portion of expenditures.

Medicare is only for 65+ and disabled, low-income adults and children are not covered

817
Q

When should diabetic patients get C-sections?

A

If they have an estimated fetal weight >9.9lb by US – do C-section at 39 weeks to avoid risks of shoulder dystocia

818
Q

Preventative meds for migraines:

A

BBs (Metoprolol), TCAs (amitriptyline), and anticonvulsants (valproate)

819
Q

Abortive/acute meds for migraines:

A

Dopamine antagonsits (metoclopramide, chlorpromazine) – help w/N, V and pain
Ergotamines +/- caffeine or analgesics
Selective serotonin agonists – Triptans (sumatriptan)

820
Q

What should the ventilator settings be in patients w/ARDS?

A

Goal is to sustain PaO2 at 55-80, and O2 saturation 88-95%

Low tidal volume is most important – prevents alveolar overdistention and barotrauma
FiO2 should be lowered <60% as quickly as possible to prevent O2 toxicity
High PEEP (up to 15-20) – prevents alveolar collapse and improves oxygenation when FiO2 is <60%
Higher respiratory rates (35 or less) to maintain adequate minute ventilation
Plateau pressure 30 or less

821
Q

What are the endocrine manifestations of hereditary hemochromatosis?

A

DM
Secondary hypogonadism – see low/normal testosterone and decreased sex drive
Hypothyroidism

822
Q

Tx of vulvovaginal candidiasis in pregnancy:

A

Vaginal clotrimazole, miconazole and nystatin – all are safe in all trimesters

823
Q

What can help distinguish b/w the major causes of metabolic alkalosis w/hypokalemia?

A

Urine chloride level
Appropriately low urine Cl levels (<20): External loss of gastric acid – vomiting, NG suctioning
Inappropriately elevated levels: Diuretic therapy, Inherited sodium wasting disorders – Gitelman and Bartter syndromes

824
Q

Tx of furuncle and carbuncle:

A

Furuncle is infection of one single hair follicle, carbuncle involves multiple and often has systemic sxs as well.
Most common cause is S. aureus and often MRSA
Abx w/MRSA coverage are required: Clindamycin, TMP-SMX, or doxycycline
I&D is also warranted a well

825
Q

What imaging is warranted in patients w/S. aureus bacteremia?

A

TTE or TEE to assess for IE
Even if the patients have clear evidence of osteomyelitis, biopsy of bone for culture is not warranted, but echo is always needed

826
Q

How to confirm diagnosis of Primary sclerosing cholangitis:

A

Endoscopic cholangiogram or MRCP
Often though lab abnormalities are enough – show cholestatic pattern w v. high ALP and BR
90% of pts. w/PSC have UC

827
Q

What are the ductal-dependent congenital heart defects?

A

Hypoplastic left heart syndrome
Severe coarctation of the aorta

Differentiate by cyanosis and HoTN in all extremities in HLHS v. only lower extremities in coarctation
ToF and Truncus arteriosus are also cyanotic defects but are not ductal dependent and will not worsen w/its closure around day1 of life

828
Q

What is one of the most dangerous pulmonary cxs of TNF-a inhibitor therapy?

A

Severe necrotizing pneumonia caused by S. aureus
Often presents w/acute pulmonary sxs, rapid decompensation and a lower lobe infiltrate + cavitation

Common TNF inhibitors: etanercept, adalimumab, certolizumab, infliximab, golimumab

829
Q

How should pregnant mothers who have undergone alloimmunization be treated?

A

If a pregnant woman has any type of positive anti-Rh(D) Ab titer (even as low as 1:1, 1:2) then alloimmunization has already occurred and therefore they should not receive anti-D Ig as it will not be effective at preventing alloimmunization

830
Q

What causes Gaucher Disease?

A

It is an AR inherited lysosomal storage disorder d/t glucocerebrosidase deficiency
Glycolipids (glucocerebrosides) accumulate w/in the lysosomes of macrophages, which infiltrate and disrupt various organs
Type I GD is most common and has varying severities which can present at any time from early childhood to late adulthood.

831
Q

What are the common amino acid disorders?

A

Maple syrup urine disease and phenylketonuria
Can present in infancy w/acute decompensation after protein feeding or later in childhood w/developmental delay or regression

832
Q

What are common nucleotide metabolism disorders?

A

Lesch-Nyhan
Gout
ADA deficiency

833
Q

What is the primary goal of drug therapy in shingles?

A

To prevent postherpetic neuralgia

834
Q

What are unique features of atheroemboli-induced injury to the kidneys?

A

Eosinophilia and eosinophiluria – help differentiate it from contrast-induced nephropathy
Will not see the cholesterol crystals a/w atheroemboli as they remain in the blood vessels and don’t enter the urine

835
Q

What is a common cause of abdominal mass that moves w/respiration?

A

RCCa – often palpable in the flank region or abdomen, nontender and moves w/respiration

In contrast, colon and ovarian masses may be palpable in similar areas, but typically do not move w/respiration.

836
Q

Chronic mgmt. of gout:

A

Need a urate-lowering drug – allopurinol is DoC
While initiating therapy patients should also be placed on a prophylactic drug to prevent flares during this period – low dose colchicine is 1st line, but NSAIDs can also be used

837
Q

What are the common presenting features of Gaucher disease?

A

Onset may be delayed and present in mid-late adolescents
Bone marrow infiltration – anemia and thrombocytopenia
Splenomegaly – typically severe and more prominent than hepatomegaly
Bony pains d/t skeletal involvement – often mistaken for “growing pains”
May have osteopenia and pathologic fractures following minimal trauma
Failure to thrive – height and weight <5th percentile
Delayed puberty (tanner stage I in a 16yo)

838
Q

Rxs that cause pill-esophagitis:

A

Abx – tetracyclines
Anti-inflammatory agents – aspirin and many NSAIDs
Bisphosphonates – alendronate, risedronate
Others – potassium chloride, iron

839
Q

Endoscopic appearance of pill-esophagitis:

A

Circumferential deep ulceration w/relatively normal surrounding mucosa. Normally in mid-esophagus.

840
Q

What screening tests can be done to asses for aneuploidy in the 1st trimester?

A

Cell-free fetal DNA – has high sensitivity and specificity.
If the results of this are abnormal then the more invasive chorionic villus sampling can be taken and confirm the diagnosis w/fetal karyotyping.

841
Q

When can amniocentesis be performed?

A

Second trimester (15-20 weeks)

842
Q

When can chorionic villus sampling be performed?

A

First trimester (10-13 weeks)

843
Q

When can cell-free fetal DNA be performed?

A

First trimester (10+ weeks) in patients at risk for aneuploidies (>35)

844
Q

What pattern on quadruple screen will suggest Trisomy 21?

A

Decreased AFP
Increased hCG
Decreased estriol
Increased inhibin A

845
Q

What pattern on quadruple screen will suggest Trisomy 18?

A

Decreased AFP
Decreased BhCG
Decreased estriol
Normal or low inhibin A

846
Q

When should NSAIDs not be used in an acute gout attack?

A

Contraindicated in pts w/PUD and should be avoided in renal failure

847
Q

Features of Central precocious puberty v. peripheral:

A

CPP: early maturation of HPG axis; see typical pubertal sequence w/breast or testicular development first, followed by pubic and axillary hair development

PPP: d/t excess sex hormone; see pubic and axillary hair development first, and often no development of breast or testes. Often have other features of adrenarche such as acne or hirsutism and oligomenorrhea in girls.

Both present w/advanced bone age

848
Q

Common causes of peripheral precocious puberty:

A
Nonclassic CAH
Estrogen-secreting ovarian cysts
Exogenous estrogen exposure
DHEAS producing adrenal tms.
Aromatase excess
McCune-Albright syndrome
Leydig-cell testicular tms. (produce androgens or estrogen)
849
Q

Common causes of Central Precocious Puberty:

A

Hypothalamic or pituitary tms.
Idiopathic precocious puberty
Primary Hypothyroidism (TSH activates FSH)
Tuberous sclerosis (d/t brain hamartomas)
NF1 (rare, but optic gliomas can effect the hypothalamus)

850
Q

What are the typical basal-insulin options for Type I diabetics?

A

2x/d NPH insulin or 1x/d insulin glargine at bedtime.

If a patient is experiencing hypoglycemic episodes it is likely these that will need to be adjusted

851
Q

Do RBCs express HLA antigens?

A

NO! Only organs, bone marrow, and platelets

852
Q

What is contamination bias?

biostats

A

When the control group in a controlled trial unintentionally receives the tx or intervention, thereby reducing the difference in outcomes b/w the control and treatment groups.
Not a bias seen in observational studies

853
Q

What are the physical exam findings a/w Mitral Stenosis?

A

Mitral facies – pink/purple patches on cheeks
Loud S1, loud P2 if pHTN is present
Opening snap (high-freq early diastolic sound)
Mid-diastolic rumble (low-pitched, best heard at apex)

Sxs reported: dyspnea, orthopnea, PND, hemoptysis, aFib, thromboembolisms, hoarseness from RLN compression d/t LA enlargement

854
Q

What investigations do all patients w/Medullary thyroid cancer require?

A

Serum calcitonin and CEA measurements
Neck US
Genetic testing for RET mutations: if positive need metanephrine measurements before thyroidectomy to rule out pheo and cxs it can cause during surgery

855
Q

In what toxicity syndrome is mechanical ventilation avoided?

A

Salicylate toxicity – the sedation and paralysis in prep for intubation can acutely worsen acidosis and exacerbate the toxicity. In addition normal ventilation strategies often cannot mimic the high RR providing beneficial alkalosis in these patients.
Intubation should be reserved for those w/significant hypoventilation and respiratory failure

856
Q

What kind of medication is Cilostazol?

A

A PDE-3 inhibitor – aka antiplatelet

Can be used in PVD and intermittent claudication when lifestyle and exercise interventions fail

857
Q

How does thyroid hormone effect serum calcium levels?

A

Hyperthyroidism may cause mild hypercalcemia as a result of the increased bone turnover a/w hyperthyroidism

858
Q

What is the most common cause of culture negative endocarditis?

A

Q fever – caused by coxiella burnetii; spores inhaled as aerosols and a/w cattle or sheep amniotic fluid
May also present as pneumonia

859
Q

What are common lab values seen in small intestinal bacterial overgrowth syndrome?

A

Macrocytic anemia and B12 deficiency

Will also have +Lactulose breath test

860
Q

Tx of Dermatitis Herpetiformis:

A

Dapsone + Gluten-free diet

861
Q

When should IV glucocorticoids be used in spinal cord compression/cauda equina syndrome?

A

In the setting of malingnancy or trauma

They are NOT recommended in the setting of suspected infection/epidural abscess

862
Q

How is incidence rate calculated?

biostats

A

It is the number of new cases of disease occurring in a specified population in a given period
IR = (# of new cases of disease during a period) / (Total person times contributed by the at-risk population)

863
Q

What is the difference in SCD between structural heart diseases and those w/conduction abnormalities?

A

Most commonly seen in young patients
Those w/conduction abnormalities (Brugada, Congenital long QT) are more typically to suffer from non-exertional SCD
Those w/structural abnormalities (HOCM, AAOCA) often experience exertional SCD

864
Q

What is Lofgren syndrome?

A

Associated w/Sarcoidosis – get erythema nodosum, hilar adenopathy, migratory polyarthralgia and fever

865
Q

What are the CNS/endocrine manifestations seen in Sarcoidosis?

A

Facial n. palsy
Central DI
Hypercalcemia
Can also cause adrenal insufficiency

866
Q

What is the gold-standard confirmatory test for Heparin-induced thrombocytopenia?

A

Serotonin release assay

867
Q

What is the most common cause of non-gonococcal urethritis not eradicated by azithromycin?

A

Mycoplasma genitalium – tx w/moxifloxacin

868
Q

How to dx Microscopic colitis and differentiate the 2 types:

A

Dx w/colonoscopic bx – lymphocytic infiltration of lamina propria
Collagenous type – thickened subepithelial collagen band
Lymphocytic type – high levels of intraepithelial lymphocytes (>20 for every 100 epithelial cells)

869
Q

What are the features and triggers of Microscopic colitis?

A

MC is a chronic, immune-mediated colitis.
Features: watery, non-bloody diarrhea (secretory), fecal urgency & incontinence, nocturnal diarrhea (classic sign)
Less common sxs: abdP (50%), fatigue and wt. loss.
Triggers: smoking, Rxs – NSAIDs, PPIs, SSRIs, Ranitidine

870
Q

How will CNS tms manifest based on their location?

A

Supratentorial: Increased ICP, weakness, sensory changes, and seizures
- Astrocytoma, Glioblastoma, Craniopharyngioma

Posterior fossa (infratentorial): Increased ICP, cerebellar dysfxn – dysmetria, ataxia, clumsiness
     - Astrocytoma, Ependymoma, Medulloblastoma

Brainstem: ataxia, clumsiness, CN palsies

Spinal cord: back pain, weakness, abnormal gait
- Ependymoma (much less common than post. fossa)

871
Q

What Rx is used to diagnose and manage narrow-QRS-complex tachycardia?

A

Adenosine.

It slows the sinus rate, increases AVN conduction delay or can cause transient AVN block.

872
Q

How should developmental dysplasia of the hip be managed?

A

Needs referral to ortho for tx – most need hip in brace that flexes and abducts it for 3+mos, but needs close monitoring by ortho for cxs of this harness position
Most infants who are tx’d early have no long term sequelae but need monitoring until skeletal maturity to monitor for recurrent dysplasia

873
Q

Labyrinthitis v. vestibular neuritis:

A

Labyrinthitis is vestibular neuritis + hearing loss

Often post-viral

874
Q

What is the most effective single treatment for allergic rhinitis and its cxs?

A

Intranasal glucocorticoids – often cause epistaxis, can be prevented by adding nasal saline rinses

875
Q

How to differentiate croup v. pertussis:

A

Croup has short prodrome of rhinorrhea and fever followed by abrupt onset of stridor, hoarseness and harsh, barking cough
Pertussis has longer prodrome (10-14d) of rhinorrhea, cough +/- fever followed by weeks of increasingly severe cough. Not likely to have stridor or abrupt onset of cough.

876
Q

When should abx be considered in acute rhino-sinusitis?

A

If ARS does not improve w/in 7-10d of symptomatic tx or if it worsens acutely after initial improvement

877
Q

How is ADHF d/t peripartum cardiomyopathy managed?

A

Basically the same as any other cause of ADHF
First initiate loop diuretic to get prompt symptom relief
Then need to decreased both preload and afterload
Direct arterial dilator (Hydralazine) decreases afterload
Long acting nitrate (isosorbide mononitrate) decreases preload
These will lessen contractile demands of left ventricle

Once the acute decompensation is adequately treated a BB should be added, and digoxin can be used for conduction abnormalities or persistent sxs despite adequate diuresis and vasodilator tx

878
Q

What should be considered in an acutely delirious and lethargic patient with known psychiatric history?

A

Psychogenic polydipsia – check serum Na+ levels for possible hyponatremia causing the delirium, may also lead to seizures although this is uncommon

879
Q

Which SLE medication is safe during pregnancy?

A

Hydroxychloroquine

MTX, leflunomide, cyclophosphamide and mycophenolate are all contraindicated

880
Q

What antibodies increase the risk of developing neonatal lupus?

A

Anti-SSA (Ro) and anti-SSB (La) – these also increase risk of congenital heart block

881
Q

What is the treatment of spontaneous pneumomediastinum?

A

Analgesics + supplemental oxygen

Common in young males w/hx of lung disease, respiratory infection or hx of inhalational drug use

882
Q

What is the major risk factor for more rapid CKD progression?

A

Proteinuria – higher urine protein concentrations are a/w more rapid decline in renal function
HTN, hyperglycemia and African American and Asian decent are also risk factors

883
Q

What are common features of distal (Type I) renal tubular acidosis?

A

Impaired H+ excretion causes hyperchloremic, hypokalemic non-anion gap metabolic acidosis.
Hypercalciuria from chronic acidosis and a urine pH >5.5 predispose to recurrent stones

884
Q

What are the causes of painful genital ulcers?

A

HSV and H. ducreyi

lymphogranuloma venereum and syphilis are PAINLESS

885
Q

What is the management of breast pain?

A

If it is cyclic, bilateral and diffuse, patients can be observed unless a mass is palpated, then get imaging

If it is noncyclic, unilateral and focal w/o a mass – need imaging; if mass is present then biopsy and refer to breast surgeon

886
Q

Mgmt of hypercalcemia of malignancy:

A

IVF to increase renal excretion + calcitonin for short-term reductions
Long-term need to be treated w/bisphosphonates (zolendronic acid)

887
Q

When does further workup need to be done for a patient w/hypospadias?

A

If the hypospadias is accompanied by cryptorchidism – do pelvic US to look for uterus and karyotype to identify sex chromosomes

If accompanied by other organ system abnormalities (CHD, cleft lip) then need upper tract imaging w/renal US

888
Q

What should be considered in an HIV+ pt. w/TB sxs but labs and imaging that do not support classic TB?

A

Miliary TB
Will see multiple organs effected – pulmonary (cough, night sweats), liver (RUQ pain, vomiting, increased transaminases), CNS and adrenal glands can also be involved

More common in recently incarcerated individuals

889
Q

What preventive imaging should be done in patients w/Sickle Cell disease?

A

Trancranial Doppler US – assess risk of stroke
Done from age 2-16
Those w/high TCD velocity need chronic transfusion therapy to prevent stroke

890
Q

CVS complications independently a/w OSA:

A

Resistant HTN
Coronary artery disease
Cardiac arrhythmias (aFib, bradycardia, ventricular ectopy)
HF

891
Q

What do each of the ventilator settings achieve and what are cxs a/w them?

A

Tidal volumes and respiratory rate affect ventilation – will optimize the pH and PaCO2
FiO2 and PEEP affect oxygenation – will change the PaO2 and O2 sat

FiO2 >60% can cause oxygen toxicity, tidal volumes >8mL/kg predicted weight can cause alveolar overdistention and barotrauma

892
Q

When should an ARDS patient be given a spontaneous breathing trial in prep for extubation?

A

If they are able to maintain adequate ventilation (pH >7.25) and oxygenation (PaO2 55-80) w/minimal ventilator support (FiO2 40% or less, and PEEP 8 or less)

893
Q

Long-term consequences of exercise-induced hypothalamic amenorrhea:

A

Decreased bone mineral density

Increased total cholesterol and TGs

894
Q

Mgmt of Splenic sequestration in SCD patients:

A

First step is aggressive IVF resuscitation (NS or Ringers)
After resuscitation can give pRBCs to return Hct to normal but should not be first step as RBCs will release back into circulation w/IVF and over-transfusing can cause HF
Splenectomy can be done electively after recovery from the initial event

895
Q

What is the tx of acute angle-closure glaucoma?

A

Lower intraocular P w/topical BBs (timolol), miotic agents (pilocarpine), and a2-agonsits (apraclonidine) + oral or IV acetazolamide and IV mannitol

Pts may present w/o increased intraocular P, but still need tx

896
Q

What is the preferred tx of Lyme carditis?

A

IV ceftriaxone is DoC (cefotaxime and Pen G are alternatives) until AV block resolves, then tx w/3-4 wk course of Doxy or amoxicillin

897
Q

What should be used to control dyspnea experienced at the end of life?

A

Opiates – particularly morphine; this is part of comfort care when patients are DNR/DNI

898
Q

What are the manifestations and tx of Acalculous cholecystitis?

A

Primarily occurs in critically ill patients
Signs/Sxs: unexplained fever, jaundice, leukocytosis, RUQ pain, increased ALP, BR and transaminases
See GB wall thickening w/o stones on CT or US
Tx: percutaneous cholecystostomy (aka GB drainage) + abx; cholecystectomy if perforation or necrosis occurs

899
Q

Meds used to prevent opioid induced constipation:

A

Senna + Docusate or Lactulose alone

Methylnaltrexone can be used to tx refractory OIC but is not a preventative

900
Q

What lab values need to be monitored in polycythemia of the newborn?

A

Glucose and BR – can develop hypoglycemia and hyperbilirubinemia d/t increased RBC volume. May require tx w/IVF, glucose and partial exchange transfusion in symptomatic newborns, but most are asx and do not require tx

901
Q

Cxs of sickle cell trait:

A
Hematuria/papillary necrosis
Hyposthenuria
Splenic infarction (esp. at higher altitudes)
Venous TE
Priapism
Exertional rhabdomyolysis
902
Q

Manifestations of Hypophosphatemia:

A

Typically occur once phosphate drops below 1
Generalized weakness, diminished reflexes, paresthesias, ileus, and/or metabolic encephalopathy
IV Phosphate for symptomatic pts, oral for asx

903
Q

What cxs can occur after intrauterine fetal demise?

A

Coagulopathy (DIC) after several weeks of fetal retention

904
Q

What lobe is Wernicke’s area in?

A

Dominant temporal

905
Q

When should phototherapy be initiated in neonatal jaundice?

A

If BR climbs >12; >25 needs exchange transfusion and intensive phototherapy
BR <12 needs q8h serum total and indirect BR checks and can be monitored

906
Q

What is the mgmt. of Irritable bowel syndrome?

A
Lactose free diet
High fibre diet
Loperamide
Biofeedback
Reassurance
Relaxation exercise
907
Q

2 main types of dysphagia, their features and initial mgmt.:

A
  1. Oropharyngeal dysphagia – difficulty initiating a swallow, often a/w coughing, drooling or aspiration. May also have referred ear pain. Need Nasopharyngeal laryngoscopy assessment or barium esophagram
  2. Esophageal dysphagia – delayed sensations of food sticking in the upper or lower chest. Need EGD assessment.
908
Q

Most likely carcinoma based on location in esophagus:

A

Adeno – more likely in mid to distal, caused by Barrett’s

Squamous – more likely in upper esophagus, caused by tobacco and alcohol

909
Q

What is the order of therapy in managing HF?

A

1: add ACEI or ARB if ACEIs are not tolerated
2: Diuretic therapy (furosemide)
BB (once euvolemic, if EF is 40% or less)
Spironolactone (if EF is 35% or less), plus continue above
Defibrillators (for EF <30%), plus continue above
3: Isosorbide dinitrate + Hydralazine (if AfAm)
Digoxin (if sxs w/spironolactone)
Cardiac resynch is QRS >150
4: Transplant/VAD evaluation

910
Q

When do you give Vanc in pediatric sepsis?

A

ONLY if the patient is >28d old and there is suspicion of meningeal involvement
Ceftriaxone should also not be given before 28d, can cause kernicterus

911
Q

Characteristics of Acute Interstitial Nephritis:

A

Maculopapular rash, fever, new Rx exposure, +/- arthralgias.
Mostly caused by Rxs – Pens (Naficilin common), TMP-SMX, cephalosporins, NSAIDs, omeprazole
Labs: AKI, pyuria, hematuria, WBC casts, +/- eosinophilia
Renal bx: inflammatory infiltrates and edema

912
Q

Infectious causes of Acute Interstitial Nephritis:

A

Legionella, TB, Streptococcus

These are uncommon causes. Rxs are most common cause of AIN.

913
Q

What is the timeline of different monozygotic twins?

A

0-4 days: dichorionic, diamniotic (25%)
4-8 days: monochorionic, diamniotic (most common – 75%)
8-12 days: monochorionic, monoamniotic (rare)
>13 days: conjoined monochorionic, monoamniotic (rare)
All types will have 2 cords