IM Essentials Flashcards

1
Q

Listeria monocytogenes: gram stain

A

gram + rods

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2
Q

L. monocytogenes meningitis tx

A

ampicillin

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3
Q

Common groups infected w/L. monocytogenes meningitis

A

-elderly-neonates-immunocompromised

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4
Q

Most sensitive/specific test for HSV encephalitis

A

Cerebrospinal fluid polymerase chain reaction assay is the most sensitive and specific test for the diagnosis of herpes simplex encephalitis.

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5
Q

S. pneumo: gram stain

A

gram + diplococci

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6
Q

S. pneumo meningitis empiric therapy

A

-vanc + 3rd gen. ceph (e.g. ceftriaxone)

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7
Q

Imaging in suspicion of stroke

A
  1. Non-contrast CT Head ==> r/o hemorrhagic stroke2. MRI if CT negative
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8
Q

Important medication in resolving acute ischemic stroke

A

-aspirin vs. clopidogrel

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9
Q

Dx testing suspected subarachnoid hemorrhage

A
  1. CT w/out contrast2. if neg. ==> lumbar puncture-RBCs or xanthochromia indicate signs of SAH
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10
Q

Method of estimating GFR

A

-equation-based calculation of GFR-CKD-EPI (CKD epidemiology collaboration)-Cr clearance overestimates GFR (because some is excreted), but approximates true GFR in patients w/out kidney disease

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11
Q

Histology in rapidly-progressing glomerulonephritis

A

-most commonly crescentic glomerulonephritis

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12
Q

glomerulonephritis characteristics

A

-nephritic syndrome- ==> hematuria, oliguria, HTN, acute kidney failure- ==> pyuria, hematuria, cellular/granular casts+/- proteinuria

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13
Q

Examples of nephrotic syndromes

A

-MCD-FSGS-membranous glomerulonephropathy==> edema, hypoalbuminemia, proteinuria, bland sediement (no casts, RBCs, leuks)

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14
Q

MCD disease type

A

nephrotic syndrome

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15
Q

FSGS disease type

A

nephrotic syndrome

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16
Q

Membranous disease type

A

nephrotic syndrome

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17
Q

Dysmorphic erythrocytes or acanthocytes on urine micro ==>

A

-glomerular hematuria-indication of glomerulonephritis

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18
Q

Evaluation/work-up with glomerular hematuria

A
  1. urine protein-cr ratio/serum cr measurement2. serum complement3. hepatitis panel4. blood cx5. ANA, ANCA, anti-GBM, antistreptolysin
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19
Q

Evaluations of hematuria

A

repeat UA>40yo ==> lower/upper urinary tract workup

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20
Q

Evaluation of sustained, isolated proteinuria

A
  1. split urine collection ==> r/o orthostatic proteinuria2. imaging vs. kidney biopsy
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21
Q

Tx of rhabdomyolysis

A

rapid NS

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22
Q

Lab findings in rhabdo

A

-serum CK > 5000-blood on urine dip w/out sig. hematuria (myoglobin from m. breakdown)- ==> hypocalcemia, hyperphosphatemia, hyperkalemia, hyperuricemia, metablic acidosis-AK

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23
Q

Serum osmolality concentration

A

serum osm = 2[Na] + [BUN]/2.8 + [glucose]/18

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24
Q

Types/categories of hypo-osmolol hyponatremia

A

-hypovolemic-euvolemic-hypervolemic

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25
Q

Causes of hyperosmolal hyponatremia

A

-extreme hyperglycemia-exogenously administered solutes: mannitol or sucrose

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26
Q

Cuases of isosmotic hyponatremia

A

-glycine-sorbitol-pseudohyponatremia (lab artifact w/hyperglobulinemia or severe hyperlipidemia)

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27
Q

Tx of symptomatic hyponatremia 2/2 SIADH

A

-3% (hypertonic) saline-NS ==> excretion of most of infused sodium and retention of water ==> positive water balance

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28
Q

Causes of SIADH

A

-antidepressants-xx

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29
Q

Tx of significant hypernatremia

A

correct water deficit w/5% dextrose

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30
Q

Potential causes of nephrogenic diabetes insipidus

A

-medications (for example, lithium)-hypokalemia-hypercalcemia-sickle cell disease and trait-amyloidosis

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31
Q

Tx of nephrogenic DI

A

-adequate water intake-salt restriction-thiazide diuretic

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32
Q

Sodium polystyrene use/characteristics

A

-cation exchange resin-removes K from body ==> use in long-term control of hyperkalemia-slow onset; not useful in acute setting-contraindicated in pt.s w/recent bowel surgery

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33
Q

Characteristics of refeeding sydnrome

A

-occurs during reintro of nutrition after period of (relative) starvation==> hypophosphatemia, hypokalemia, and hypomagnesemia

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34
Q

Tx of hypoparathyroidism

A

calcium

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35
Q

Tx of acute hypercalcemia

A

normalization of intravascular volume with saline will improve delivery of calcium to the renal tubule and aid in excretion of calcium.

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36
Q

Urine anion gap (UAG)

A

Urine anion gap (UAG) = ([urine sodium] + [urine potassium]) – [urine chloride]Normal = 30-50

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37
Q

Type 2 RTA characteristics

A

-Type 2 (proximal) RTA = defect in regenerating bicarbonate in the proximal tubule-normal anion gap metabolic acidosis-hypokalemiaglycosuria (w/normal plasma glucose)-low-molecular-weight proteinuria-kidney phosphate wasting-urine pH is less than 5.5 -no nephrocalcinosis/nephroliths

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38
Q

Type 1 RTA characteristics

A

-Hypokalemic distal (type 1) renal tubular acidosis-normal anion gap metabolic acidosis-hypokalemia-urine pH > 6.0-nephrocalcinosis**no ability to excrete H+ ions

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39
Q

Possible causes of type 1 RTA

A

-autoimmune: Sjögren syndrome, systemic lupus erythematosus, or rheumatoid arthritis-drugs: lithium or amphotericin B-hypercalciuria-hyperglobulinemia

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40
Q

Expected compensation in respiratory alkalosis

A

PCO2 decrease by 10 ==> HCO3 decrease by 2

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41
Q

Expected compensation in respiratory acidosis

A

**predicted increase in the serum bicarbonate level is calculated as 1 mEq/L (1 mmol/L) for each 10 mm Hg (1.3 kPa) increase in Pco2 (acute) **4 mEq/L (4 mmol/L) for each 10 mm Hg (1.3 kPa) increase in Pco2 (chronic).

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42
Q

Evaluation of metabolic alkalosis

A
  1. clinical assessment of volume status and blood pressure; hypovolemic = “saline-responsive”2. measurement of urine sodium and chloride levels can help distinguish the various causes.
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43
Q

Urine chloride use in evaluation of metabolic alkalosis

A

-low urine chloride levels ( vomiting vs. decreased effective arterial blood (diuretics or low cardiac output)-high urine chloride levels (>15 mEq/L [15 mmol/L]) ==> diuretics vs. (rare) genetic tubular disorder (Bartter syndrome or Gitelman syndrome)

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44
Q

Compensation in metabolic acidosis

A

Winter’s formula:Expected Pco2 = (1.5 × [HCO3] + 8) ± 2 = 26 ± 2

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45
Q

Calculation of corrected bicarbonate in AG metabolic acidosis

A

-Corrected [HCO3] = measured [HCO3] + (measured anion gap – 12)-if corrected serum bircarb deviates from expected then there is another metabolic process in play

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46
Q

Correction in metabolic alkalosis

A

Pco2 would be expected to increase by 0.7 mm Hg (0.09 kPa) for each 1 mEq/L (1 mmol/L) increase in the serum bicarbonate level

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47
Q

FENa use

A

-distinguish source of AKI-prerenal vs. infrarenal vs. postrenal-xx

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48
Q

Evaluation of AKI

A

-Kidney imaging, typically US, considered in all patients w/ AKI esp. w/ risk factors for obstruction are present-FENa can be useful, but is variable in obstruction

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49
Q

Tx for acute pericarditis

A
  1. NSAIDs/antiinflamatory meds + observation/supportive ==> most cases resolve w/in 24 hours2. steroids only if other anti-inflam contraindicated or refractory cases (==> increase risk recurrence)
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50
Q

Tx of pituitary apoplexy

A
  1. glucocorticoids2. neurosurgery/tumor removal
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51
Q

Thyroid d/o w/low RAIU

A

-subacute/lymphocytic thyroiditis ==>1. hyperthyroid x weeks2. hypothyroid x weeks3. euthyroid

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52
Q

TSH goal in hypothyroidism

A

0.1 - 2.5

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53
Q

Hypothyroid in preg.

A

-levothyroxine dose need increases by 30-50%-test/increase dose in first semester followed by repeat testing in 2-4 weeks

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54
Q

Testing in incidental adenoma

A

Nearly 10% of adrenal incidentalomas are functional, and testing is usually necessary to identify functional tumors secreting catecholamines, cortisol, or aldosterone.

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55
Q

Screening in T1DM

A
  1. lipid panel @ puberty2. urine albumin-creatinine ratio @ 10yo+ AND dx of DM1 for 5 or more years3. dilated funduscopic examination @ 10 years of age or older AND dx with type 1 diabetes for 3 to 5 years.
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56
Q

Dx of DM

A

-A1c > 6.5-Fasting Gluc > 120If results of two different diagnostic tests for diabetes mellitus are discordant, the test that is diagnostic of diabetes should be repeated.

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57
Q

Modifiable risk factors for osteoporosis

A

-adequate amounts of both calcium and vitamin D-regular exercise-cessation of cigarette smoking-avoidance of alcohol abuse

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58
Q

Contraindication to oral bisphosphonates and alternative therapies

A

-GERD==> IV bisphosphonates (zoledronic acid)

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59
Q

Who should receive osteoporosis therapy?

A
  1. dx of osteo via DEXA/fragility fx OR2. (FRAX) risk of major osteoporotic fracture over the next 10 years is 20% OR3. risk of hip fracture over the next 10 years is 3% or greater
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60
Q

Outpatient vs. Inpatient management of diverticulitis

A

-most ==> outpatient + oral abx (metro + cipro-hospitalization/IV abx are generally reserved for patients with evidence of peritonitis, those with significant comorbidities, or those who cannot tolerate oral intake.

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61
Q

Indications of upper endoscopy in dyspepsia

A

-symptom onset after age 50 years-anemia-dysphagia-odynophagia-vomiting-weight loss-fhx of upper gastrointestinal malignancypersonal history of peptic ulcer disease, gastric surgery, or gastrointestinal malignancy-abdominal mass or lymphadenopathy on exam

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62
Q

Characteristics of gilbert syndrome

A

Gilbert syndrome is a common and frequently incidentally discovered cause of indirect (unconjugated) hyperbilirubinemia that usually does not require evaluation or treatment.

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63
Q

Acute viral hepatitis presentation

A

-elevations of liver aminotransferase levels-increased direct hyperbilirubinemia

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64
Q

Elevated alk phos ==>

A

cholestatic pattern of liver injury

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65
Q

Primary biliary cirrhosis presentation

A

-PBC = immune-mediated cause of chronic liver inflammation-elevated serum alkaline phosphatase and bilirubin levels disproportionately higher than the aminotransferase elevation

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66
Q

Hep C therapy

A

-peginterferon + ribavirin-addition of an NS3/4A protease inhibitor for patients with genotype 1 hepatitis C virus.

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67
Q

Management of chronic hep B

A

-as long as no elevation in LFTs ==> monitor-serial LFTs q3-6mo.

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68
Q

Immune-tolerant hep B

A

-immune-tolerant, identified by the presence of a circulating viral level in the absence of markers of liver inflammation-typically occurs in patients born in hepatitis B–endemic areas such as Southeast Asia or Africa in whom HBV was likely acquired perinatally

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69
Q

Dx of SBP

A

In patients with cirrhosis and ascites, an ascitic fluid neutrophil count of ≥250/µL (250 × 106/L) is diagnostic for spontaneous bacterial peritonitis.

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70
Q

Anemia of inflammation lab values

A

-Inflammatory cytokines ==> decrease transferrin saturation and calculated serum total iron-binding capacity (TIBC) levels-ferritin = acute phase reactant ==> serum ferritin levels tend to increase-Serum ferritin levels less than 100 to120 ng/mL (100-120 µg/L) may reflect co-existing iron deficiency in patients with inflammatory states.

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71
Q

Iron deficiency anemia lab values

A

-decreased transferrin saturation-increased calculated serum TIBC levels-decreased serum ferritin levels

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72
Q

Most sensitive/specific test for dx of B12 deficiency

A

An elevated serum methylmalonic acid level is more sensitive and specific for diagnosing cobalamin (vitamin B12) deficiency than a low serum vitamin B12 level.

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73
Q

Indications of IV iron

A

Parenteral iron, either intramuscular iron dextran or intravenous iron sucrose, is reserved for patients receiving dialysis or for patients who cannot absorb or tolerate oral iron replacement.

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74
Q

Management of acute chest syndrome

A
  1. empiric broad-spectrum antibiotics2. supplemental oxygen3. pain medication4. avoidance of overhydration5. bronchodilators as needed5. **erythrocyte transfusion for persistent hypoxia despite supplemental oxygen
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75
Q

Criteria for acute chest syndrome

A

-sickle cell disease-new infiltrate on a CXR that involves at least one lung segment AND 1+: -chest pain-temperature less than 38.3°C (100.9°F)-tachypnea-wheezing/cough/labored breathing-hypoxia relative to baseline

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76
Q

Presentation of thrombotic thrombocytopenic purpura

A

-(TTP) = abnormal activation of platelets and endothelial cells, deposition of fibrin in the microvasculature, and peripheral destruction of erythrocytes and platelets-microangiopathic hemolytic anemia-thrombocytopenia-peripheral smear = schistocytes.

77
Q

Dx of immune thrombocytopenic purpura

A

-isolated thrombocytopenia or thrombocytopenia and anemia from bleeding-otherwise normal peripheral blood smear-absence of additional organ dysfunction

78
Q

microangiopathic hemolytic anemia ==> elevated ___?

A

LDH

79
Q

Elevated LDH ==> ?

A

hemolysis

80
Q

Peripheral smear in warm autoimmune hemolytic anemia

A

spherocytes

81
Q

Coagulation lab values in TTP vs. DIC

A

-DIC ==> abnormal coagulation-TTP ==> normal coags

82
Q

Platelet clumping on peripheral smear ==> ?

A

-pseudothrombocytopenia = lab artifact- ==> repeat CBC

83
Q

Tx of ITP

A

-asx + platelets > 30-40,000 ==> repeat/f/u CBCs-sx OR platelets steriods

84
Q

Tx of PCV

A

Phlebotomy and aspirin are the initial treatments for patients with polycythemia vera.

85
Q

Indications of hydroxyurea in PCV

A

-increased risk for thrombosis: -age older than 60 years OR-history of a previous thrombotic event

86
Q

Dx of AML

A

peripheral blood smear showing myeloblasts that contain Auer rods

87
Q

MGUS presentation

A

-asx-serum monoclonal (M) protein level of less than 3 g/dL (30 g/L)-

88
Q

AL amyloidosis characteristics

A

-AL amyloid = deposition of monoclonal light chains1. nephrotic-range proteinuria w/worsening kidney fxn2. restrictive cardiomyopathy3. hepatomegaly4. neuro = symmetric distal sensorimotor neuropathy, carpal tunnel syndrome, and autonomic neuropathy with orthostatic hypotension5. Periorbital purpura and macroglossia

89
Q

Asymptomatic multiple myeloma

A

-Asymptomatic (smoldering) multiple myeloma = serum M protein level of 3 g/dL (30 g/L) or more OR-10% or more of clonal plasma cells on bone marrow examination-absence of myeloma-related end-organ damage

90
Q

Tests for determination of monoclonal protein production

A
  1. serum protein electrophoresis2. urine protein electrophoresis combined with immunofixation
91
Q

decreased anion gap + anemia + proteinuria, + hypercalcemia + kidney failure ==> dx?

A

multiple myeloma

92
Q

Milk-alkali syndrome labs

A

-hypercalcemia-metabolic alkalosis

93
Q

Timing of screening/testing for inherited thrombophilia

A

-factor V Leiden and the prothrombin gene mutation (PTG2021A) can be done at any time-antithrombin, protein C, protein S, and dysfibrinogenemia testing may be altered during acute thrombotic events and their treatment ==> wait until AFTER completion of tx

94
Q

Pes anserine bursitis presentation

A

-overuse/running-antero-medial pain-worse w/stair climbing & @ night

95
Q

IT band pain location

A

lateral knee

96
Q

PF pain syndrome presentation

A

-women

97
Q

Medical therapy for kidney stones

A

-stones

98
Q

Most common cause of obscure small intenstinal bleeding in older pt.s & dx

A

-angiectasia-dx w/tech-99 scan

99
Q

cough + SOB + glomerulonephritis ==> dx?

A

-Granulomatosis with polyangiitis (formerly known as Wegener granulomatosis) -systemic necrotizing vasculitis- ==> upper and lower respiratory tract sx and pauci-immune glomerulonephritis

100
Q

Tx of Bell’s Palsy

A

prednisone

101
Q

Typical joints of OA

A

DIPPIP1st MCP joint

102
Q

Presentation of pseudogout

A

-Ca-pyrophosphate dihydrate deposition disease-osteoarthritis-like arthritis in atypical joints (e.g. metacarpophalangeal joints)- AND chondrocalcinosis (calcification of cartilage)

103
Q

Solar lentigo vs. Lentigo meligna

A

-lentigo meligna = slow-growing melanoma-Solar lentigines = brown macules/patches in elderly fair-skinned persons in sun-damaged areas-SL = benign, usually more homogeneous pigmentation and lighter color-in equivocal cases, a biopsy is indicated.

104
Q

acute pancreatitis course/management

A
  1. bowel rest, opioids, iv fluids2. mild/mod ==> sx improvement @ 72-96H ==> resume PO3. severe = no improvement ==> CT scan + can consider NJ feedings
105
Q

Factors that affect BNP value

A

-increased by: kidney failure, older age, and female sex-decreased by: obesity

106
Q

Lambert-Eaton myasthenic syndrome (LEMS) characteristics

A

-autoimmune neuromuscular dz that is classically associated with small cell lung cancer-autoantibodies that target voltage-gated calcium channels @ NMJ- ==> proximal muscle weakness, autonomic symptoms, and loss of reflexes

107
Q

Normal response of HIV counts to HAART

A

-effective therapy x 24 wks ==> resistance/genotyping + consult ID specialist

108
Q

TMP-SMX prophylaxis in HIV

A

-@ CD4

109
Q

Hypersensitivty pneumonitis presentation

A

-inflammatory lung disease that is also called extrinsic allergic alveolitis-esults from exposure to airborne allergens that cause cell-mediated immunologic sensitization-Most patients who are exposed to an inhalational antigen have symptoms within 4 to 12 hours.

110
Q

Mitral stenosis murmur

A

opening snap followed by a diastolic murmur that is accentuated with atrial contraction. S1 is usually loud, and S2 may be variable in intensity.

111
Q

daily fever + salmon-colored rash + arthritis +multisystem involvement ==> dx?

A

adult-onset Still disease

112
Q

Labs in Still disease

A

-markedly elevated serum ferritin -leukocytosis-thrombocytosis-elevated erythrocyte sedimentation rate-anemia-abnormal liver chemistry tests

113
Q

Memantine: MOA, use

A

-N-methyl-D-aspartate receptor antagonist-first-line treatment of moderate to advanced Alzheimer disease

114
Q

Presentation/cause of delayed hemolytic transfusion rxn

A

-@ 5 to 10 days after transfusion ==> anemia, jaundice, and fever-cause = new alloantibody formation against non-abo antigen-tend to occur more frequently in sickle cell pt.s who receive multiple transfusion

115
Q

Risk factors for pseudomonal PNA

A

-smoking and chronic lung disease-broad-spectrum antibiotic use in the previous month-recent hospitalization-malnutrition-neutropenia-glucocorticoid use

116
Q

Tx/coverage for suspected pseudomonal PNA

A

-dual therapy: β-lactam and an aminoglycoside-e.g. pip-tazo + amikacin

117
Q

Blood products used with risk of anaphylaxis

A

“washed” erythrocytes/platelets

118
Q

γ-Irradiation of erythrocytes purpose

A

-minimize the incidence of graft-versus-host disease -eradicates any lymphocytes present in the transfusion when given to an immunocompromised recipien

119
Q

leukoreduction of erythrocytes purpose

A

decreases the incidence of febrile nonhemolytic transfusion reactions, CMV transmission, and alloimmunization

120
Q

Stage IA vs. IB NSCLC

A

1A 3cm tumor

121
Q

Tx of metastatic prostate cancer

A

-androgen deprivation-chemical (GnRH agonist) vs. surgical castration

122
Q

Tx of asx hyperuricemia

A

no tx needed

123
Q

Management of lesions suspicion for melanoma

A

excisional biopsy

124
Q

Indications for further workup of acute diarrhea

A

-bloody stools-diarrhea in pregnant, elderly, or immunocompromised patients-hospitalization-employment as a food handler-recent antibiotic use-volume depletion-significant abdominal pain

125
Q

Lung Cancer Screening

A

individuals age 55 to 79 years who have a 30-pack-year or greater smoking history either as current smokers or as former smokers who have quit within the past 15 years.

126
Q

Tx for resolving sx of ischemic stroke

A

aspirin

127
Q

Aortic regurgitation murmur

A

grade 2/6 high-pitched blowing diastolic decrescendo murmur is heard to the left of the sternum at the third intercostal space

128
Q

Features and tx of severe C. diff

A

-fever-leukocytosis-oral vancomyocin +/- IV metronidazole

129
Q

Indications for noninvasive positive pressure ventilation in COPD exacerbation

A

-moderate to severe dyspnea, -moderate to severe acidosis (pH 25/min

130
Q

Exclusion criteria for NNPV in COPD exacerbation

A

-respiratory arrest-cardiovascular instability (hypotension, arrhythmias, and myocardial infarction)-AMS -high aspiration risk/copious secretions-recent facial or gastroesophageal surgery-craniofacial trauma-fixed nasopharyngeal abnormalities-burns-extreme obesity

131
Q

Indication for intubation in COPD exacerbation

A

-Severe acidosis (pH 35/min

132
Q

Anticoagulants to avoid in advanced kidney disease

A

-LMWH

133
Q

Optimal medical therapy in severe systolic heart failure

A

-ACE-B-blocker-spiro

134
Q

Predictors of poor prognosis in acute pancreatitis

A

-APACHE II score-markers of hemoconcentration: elevated blood urea nitrogen, serum creatinine, or hematocrit levels-multiple medical comorbid, age > 70yrs, BMI > 30

135
Q

Polymyalgia rheumatica presentation

A

-hip and shoulder girdle stiffness and pain-elevated inflammatory markers-closely associated w/GCA ==> if any sx ==> temporal a. biopsy

136
Q

Prophylactic tx of tumor lysis syndrome

A

-aggressive hydration + diuresis -allopurinol and rasburicase- if necessary, hemodialysis before initiation of antineoplastic therapy.

137
Q

CURB-65 criteria

A

ConfusionUrea > 20RR > 30BP ward3 criteria ==> consider ICU

138
Q

Indications for endocarditis prophylaxis

A

-prosthetic cardiac valve-history of infective endocarditis-unrepaired cyanotic congenital heart disease-congenital heart disease repair with prosthetic material or device within the last 6 months-palliative shunts and conduits-cardiac valvulopathy in cardiac transplant recipients

139
Q

Tx of Raynauds

A

dihydropyridine ca-channel blocker (amlodipine)q

140
Q

Characteristic findings in hodgkin lymphoma

A

-B sx: fever, weight loss, night sweats-lymphadenopathy-Reed sternberg cell: abundant pale cytoplasm and two or more oval lobulated nuclei containing large nucleoli

141
Q

Tx of fibromuscular dysplasia

A

revascularization with kidney angioplasty

142
Q

Tx of early-stage large B-cell lymphoma

A
  1. abbreviated course of chemotherapy2. immunotherapy: rituximab2. involved-field radiation therapy
143
Q

Lymphangioleiomyomatosis classic presentation

A

young woman w/emphysema or chylothorax or tuberous sclerosis

144
Q

Respiratory bronchiolitis-associated interstitial lung disease characteristics

A

micronodular disease that causes mild symptoms and typically presents in active smokers with subacute progressive cough and dyspnea.

145
Q

Churg-Strauss syndrome presentation

A

-vasculitis that typically occurs in patients with a history of asthma-peripheral eosinophilia-perinuclear antineutrophil cytoplasmic antibody (pANCA).

146
Q

Microscopic polyangiitis presentation

A

-involves small arterioles and may be associated with glomerulonephritis and purpuric skin lesions-no immune deposits in the skin -positive p-ANCA titer.

147
Q

Polyarteritis nodosa

A

-small- to medium-vessel vasculitis -may be associated with renal artery involvement and hypertension-Purpura with skin biopsy findings of immune deposits is not a characteristic cutaneous feature.

148
Q

Goal of pressors

A

-maintain MAP > 65-MAP = [(2xdbp) + sbp]/3

149
Q

Tx in high grade carotid stenosis

A

carotid endarterectomy

150
Q

de Quervain tenosynovitis presentation

A

-inflammation of the abductor pollicis longus and extensor pollicis brevis tendons-associated with repetitive use of the thumb -also assoc. w/ pregnancy, RA, and calcium deposition disease. -pain on the radial aspect of the wrist that occurs when the thumb is used to pinch or grasp. -Examination: localized tenderness @ distal radial styloid process + pain with resisted thumb abduction and extension.

151
Q

Prevention of migraines

A

-b-blcokers-TCAs-anticonvulsants

152
Q

SVC syndrome initial w/u

A

biopsy to guide tx

153
Q

Ventricular interdependence/”to-and-fro diastolic motion of the ventricular septum” ==> dx?

A

constrictive pericarditis

154
Q

Constrictive pericarditis presentation

A

Dyspnea, pedal edema, clear lung fields, and jugular vein engorgement with inspiration

155
Q

initial tx in uncomplicated cystitis

A

-TMP-SMX-nitrofurantoin

156
Q

abx to avoid in kidney disease

A

aminoglycoside

157
Q

burning distal extremity pain + sensory loss ==> dx?

A

-small-fiber peripheral neuropathy==> glucose tolerance testing

158
Q

Tx of severe sx of PVCs

A

b-blockers

159
Q

Stage III colon cancer tx

A
  1. surgery/resection2. adjuvant chemo: 5-fluorouracil and leucovorin x 6 mo.
160
Q

Tx of recurrent gout w/hyperuricemia

A

allopurinol + colchicine

161
Q

Indication for PPX tx in migraine

A

sx > 10 days/month (limit of use of triptan)

162
Q

Threshold for thoracentesis for pleural effusion

A

-unexplained- > 1cm - ? loculated

163
Q

Late complication of gastric bypass

A

-Small intestinal bacterial overgrowth - ==> diarrhea, bloating, and features of malabsorption

164
Q

Characteristics of Acral lentiginous melanoma

A

unevenly darkly pigmented patch that most often arises on the palmar, plantar, or subungual surfaces

165
Q

Ca-channel blocker to add for HTN in heart failure

A

amlodipine

166
Q

Criteria for exudative pleural effusion

A
  1. pleural fluid total protein–serum total protein ratio greater than 0.52. pleural fluid lactate dehydrogenase level greater than two thirds of the upper limit of normal (or a pleural fluid–serum lactate dehydrogenase ratio >0.6)
167
Q

Workup in suspected CLL?

A

flow cytometry

168
Q

PFTs in respiratory m. weakness

A

-reduced total lung capacity-increased residual volume

169
Q

Cholangitis presentation

A

-fever, jaundice, and altered mental status-abdominal pain is usually present

170
Q

Management of cholangitis

A
  1. broad-spectrum antibiotics directed against gram-negative bacteria, enterococci, and gut anaerobes2. ductal decompression = urgent endoscopic retrograde cholangiopancreatography
171
Q

Synovial fluid in inflammatory arthritis

A

synovial fluid leukocyte count greater than 5000/µL (5 × 109/L)

172
Q

Churg-Strauss sx/presentation

A

-antecedent asthma, allergic rhinitis, or sinusitis-eosinophilia, migratory pulmonary infiltrates-purpuric skin rash-mononeuritis multiplex-fever, arthralgia, and myalgia-kidney disease- (+) pANCA

173
Q

Tx of essential tremor

A
  1. Lifestyle changes: getting enough sleep and reduction of caffeine2. Meds: β-blockers (such as propranolol) or anticonvulsants (such as primidone)
174
Q

Prostate cancer monitoring s/p remission

A

serial DRE + PSA q6-12 mo.

175
Q

Tactile fremitus

A

increased ==> consolidationdecreased ==> pleural effusion

176
Q

Indications for surgical intervention for spinal osteo

A
  1. abscess drainage2. removal of an orthopedic implant3. stabilization of the spine.
177
Q

Signs/sx of CAP that persist after a course of abx ==> dx?

A

cryptogenic organizing pneumonia

178
Q

Indications for valve replacement in endocarditis

A

endocarditis complicated by heart failure, abscess, severe regurgitation, or hemodynamic derangements ==> urgent surgery w/out waiting for response to abx

179
Q

LeMierre syndrome presentation

A

-fever, leukocytosis, sore throat-unilateral neck tenderness-multiple densities on CXR (septic emboli)

180
Q

Treatment of Lemierre syndrome

A

-abx that cover streptococci, anaerobes, and β-lactamase-producing organisms. -Penicillin with a β-lactamase inhibitor (eg, ampicillin-sulbactam, piperacillin-tazobactam, ticarcillin-clavulanate) OR-carbapenem

181
Q

Positive skin TB test

A

-5mm @ HIV+, recent contacts, CXR w/evidence of past TB, immunosuppresed-10mm @ recent from high-risk country, IVDUs, high-risk settings-15mm @ everyone else

182
Q

Management of calcium oxalate stones

A

increased dietary calcium intake and avoidance of oxalate-rich foods such as rhubarb, peanuts, spinach, beets, and chocolate

183
Q

Contraindication to B-blockers in management of MI

A

heart failure, systolic blood pressure of less than 90 mm Hg, bradycardia (

184
Q

Mitral valve prolapse murmur

A

The auscultatory feature of mitral valve prolapse is a midsystolic click followed by a late systolic murmur. Performing the Valsalva maneuver and standing from a squatting position move the click-murmur complex closer to S1.

185
Q

Management of acute afib

A

The acute management of atrial fibrillation in symptomatic but hemodynamically stable patients includes rate control with a β-blocking agent, such as metoprolol, or a calcium channel blocker, such as diltiazem.

186
Q

Adenosine: MOA, use

A

-Adenosine = IV agent that transiently blocks atrioventricular nodal conduction-tx of supraventricular tachycardia (whne dependent on the av node) -may be used to break the reentrant rhythm in atrioventricular nodal reentrant tachycardia, or orthodromic atrioventricular reciprocating tachycardia.

187
Q

first-line treatment for a hemodynamically stable ventricular tachycardia

A
  1. intravenous antiarrhythmic agent such as amiodarone, procainamide or sotalol2. lidocaine can be used as a second-line agent.
188
Q

Multifocal atrial tachycardia characteristics

A

Multifocal atrial tachycardia is characterized on electrocardiograms by three or more P wave morphologic patterns and variable P-R intervals.

189
Q

Characteristics of Lyme carditis

A

Lyme carditis is manifested by acute-onset, high-grade atrioventricular conduction defects that occasionally may be associated with myocarditis.