2025 Daily read Step2 CK Flashcards

1
Q

SvO2 is ↓ in all types of shock, except which?

A

distributive (septic [anphylax] + neurogenic)

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2
Q

Can give HPV vaccine to patients as young as which age?

A

age 9

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3
Q

Cervical cancer screening with pap test begins at which age?

A

age 21

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4
Q

What is the ML diagnosis in a patient post-gastrectomy with symptoms sounding like c.diff but also with symptoms like palpitations, sweating, or tachy?

A

Dumping syndrome has vasomotor sx (eg, palpitations, tachy), diarrhea. Seen post-gastrectomy, prolonged abx. Can seem like c.diff. Tx: Dietary mods.

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5
Q

What is the treatment for dumping syndrome?

A

Dietary mods

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6
Q

What is the treatment for specific phobia?

A

Exposure therapy

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7
Q

Which drugs improve mortality in heart failure with reduced ejection fraction?

A
  1. ACEi’s or ARBs
  2. B-blockers
  3. mineralocorticoid-R antagonists (*eplerenone, spironolactone)
  4. SGLUT-2 inhibitors
  5. Sacubitril- valsartan
  6. Hydralazine w isosorbide dinitrate in black patients
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8
Q

What intervention is most likely to improve cardiovascular and overall long-term mortality in patients with acute STEMI?

A

Prompt restoration of coronary blood flow (e.g., PCI, fibrinolysis)

  • Percutaneous coronary intervention (PCI) = angioplasty + stent
  • Early reperfusion also reduces likelihood of complications such as peri-infarction pericarditis
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9
Q

What is the recommended pharmacological therapy to reduce overall cardiovascular mortality in patients with peripheral arterial disease?

A

Anti-platelet agent (e.g., aspirin) and statin

  • Recommended to prevent stroke and heart attack due to strong association between PAD and atherosclerosis
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10
Q

What are the skin findings in someone with PAD

A

Pale (no blood)
Hairless
Scaly, dry
Thin skin (no blood = no nutrients)

Ulcers = round and ‘punched-out’

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11
Q

In septic shock, all paramers are ↓ except for ___

A

CO

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12
Q

↓ breath sounds + dullness to percussion

A

Can be either pleural effusion, or hemothorax

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13
Q

Describe how late decelerations look in relation to a contraction

A

Late decelerations begin at the peak of a contraction.

The peak of the decel is at end of contraction.

(Note: late decels are d/t uteroplacental insuff and subseq fetal hypoxemia)

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14
Q

This is a fetal heart tracing showing what?

A

Late decelerations

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15
Q

Which type(s) of deceleration(s) may indicate fetal hypoxia and/or acidosis?

A

Late and recurrent variable decelerations

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16
Q

Which type of study is useful for calculating relative risk (RR)?

A
  • CohoRt = Relative Risk
  • Case contrOl = Odds ratio
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17
Q

What statistical test is used to compare 2 categorical values?

A

Chi-squared

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18
Q

What statistical test is used to compare 3 or more means (numerical) values?

A

ANOVA

Compared to:
- Checking differences between the means of 2 more groups = t-test
- Checking differences between two categorical groups = Chi-square (χ2 ) test

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19
Q

Hypercalcemia + ↓ PTH =

A

Malignancy - paraneoplastic syndrome PTHrP in SCC of the lung

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20
Q

Hypercalcemia + ↑ PTH =

A

Primary hyperparathyroidism

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21
Q

What is the FeNa+ in pre-renal azotemia?

A

FeNa+ < 1%

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22
Q

What is the FeNa+ in intra-renal azotemia?

A

FeNa+ >2%

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23
Q

What is a normal FEV1/FVC ratio?

A

FEV1/FVC > 70%

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24
Q

What is FEV1/FVC ratio in obstructive disease?

A

FEV1/FVC = ↓↓ / ↓ ➞ ratio ↓

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25
Q

If a patient is pulseless but we are getting a rhythm, what are the 3 potential diagnoses?

A
  1. PEA (has a nl rhythm!)
  2. Asystole (flatline)
  3. V-tach (can be pulseless or have pulse)
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26
Q

What is the treatment for:

VT + pulse + HDUS

A

Synchronized cardioversion

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27
Q

What is the treatment for:

VT + no pulse

A

UNsynchronized cardioversion (defibrillator)

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28
Q

What is the treatment for:

VT + pulse + HDS

A

Amiodarone (or sotolol or lodocaine or procainamide)

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29
Q

What is the treatment for:

SVT + HDS

A

Adenosine (or B-block or CCB)

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30
Q

AVNRT is a type of ___

A

SVT

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31
Q

What is a normal glucose level in CSF?

A

40-70

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32
Q

Low glucose level in CSF means ______

A

it could either be bacterial or TB meningitis

(viral has normal glucose level)

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33
Q

What is the CD4+ count in an HIV patient that would put them at risk for toxoplasmosis

A

CD4+ <100

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34
Q

What is the treatment for toxoplasmosis

A

Sulfadiazine + pyrimethamine

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35
Q

What do you give for prophylaxis against toxoplasmosis?
When do you give it?

A

TMP-SMX

Give if CD4+ count < 100

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36
Q

Tender erythematous streaks extending from wound + regional LAD =

A

Lymphangiitis

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37
Q

What is the treatment for HSV?

A

Acyclovir or valacyclovir

(not ganicyclovir - that’s CMV)

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38
Q

What are clinical features of genital herpes?

A

Group of painful ulcers/vesicles
Systemic sx (fever, malaise)
*Regional LAD
+/- Dysuria + sterile pyuria (can seem like UTI)

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39
Q

What is the treatment for CMV?

A

Ganicyclovir

(NOT acyclovir - that’s HSV)

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40
Q

Which pulmonary condition do you confuse with cardiac tamponade?

A

Exacerbation of COPD (can have JVD, muffled breath sounds, but non hypotension)

Tamponade has triad JVD + muffled heart sounds + hypotensionn

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41
Q

In which pediatric syndrome is subependymal nodules a characteristic feature?

A

Tuberous sclerosis

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42
Q

In which pediatric syndrome do you see hypopigmented macules?

A

Tuberous sclerosis
(ash-leaf spots)

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43
Q

In which pediatric syndrome do you see big red blotch on the face?

A

Sturge-Weber syndrome
(port wine stain)

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44
Q

Cardiac rhabdomyoma is a cardiac tumor associate with which pediatric condition?

A

Tuberous Sclerosis

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45
Q

In which pediatric syndrome do you see inguinal and axillary freckling?

A

Neurofibromatosis type 1

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46
Q

In which pediatric syndrome do you see Cafe-au-lait macules?

A

Neurofibromatosis type 1

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47
Q

In which pediatric syndrome do you see optic gliomas?

A

Neurofibromatosis type 1

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48
Q

What annual screenings do NF-1 patients need?

A

Annual ophthalmological screening exam + MRI brain / orbits for any new onset vision changes

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49
Q

In which pediatric syndrome do you see schwannomas

A

Neurofibromatosis type 2

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50
Q

↑ tactile fremitus + dullness to percussion =

A

Consilodation

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51
Q

How long does a patient need to have symptoms to be diagnosed with acute stress disorder?

If symptoms last longer than this, what is the diagnosis?

A

Symptoms for < 1 month after traumatic event

(If sx ≥1 mo it’s PTSD)

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52
Q

What is the treatment for transient synovitis?

A

Supportive, NSAIDs

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53
Q

How long does a patient need to have symptoms to be diagnosed with panic disorder?

A

Symptoms for ≥1 momnth

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54
Q

Kids aged 3-8 after viral illness. Poss fever (but low-grade, can be 100.1). Typ hip/thigh pain + limp +/- hip eff.

Diagnosis?

A

Transient synovitis

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55
Q

What is the likely diagnosis in a child that presents with hip pain and limp several days after a viral URI with normal physical exam, labs, and X-ray?

A

Transient synovitis (AKA toxic synovitis)

  • Ultrasound reveals small unilateral or bilateral effusions (even when symptoms are confined to one hip)
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56
Q

What is the next best step in management of a patient with overlapping clinical features between transient synovitis and septic arthritis?

A

Bilateral ultrasound ± arthrocentesis

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57
Q

Most lung conditions have ↓/absent breath sounds, except which one?

A

Consolidation (has ↑ breath sounds)

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58
Q

Something is hypotonic is if _____ mOsm ; hypertonic is ______

A

< 275 mOsm. ; >295 mOsm

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59
Q

What is the treatment for empyema?

A

Chest tube (or video assist) AND abx

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60
Q

What is the pleural fluid like in a patient with empyema?

A

Thick, purulent, foul-smelling

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61
Q

What is lights criteria for exudative pleural effusions?

A

pl protein : ser protein > 0.5
pl LDH: ser LDH > 0.6
pl LDH > 133 (2/3 ULN)

Only has to meet 1 of the above criterias

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62
Q

What comes first in the ratio we calculate in lights criteria for pleural effusionn

A

always pleural fluid / serum

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63
Q

What is the ULN that LDH must be greater than in exudative pleural effusion

A

> 133

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64
Q

Which type of parapneumonic effusion is characterized by the following values:

pH < 7.2
Glucose < 60 mg/dl
WBC > 50,000/mm3
Gram stain/culture: negative

A

Complicated parapneumonic

  • Bacteria eat the sugar (low glucose) and generate lactate (low pH)
  • Ddx. with empyema which has a (+) pleural gram stain / culture
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65
Q

Which type of parapneumonic effusion is characterized by the following values:

pH < 7.2
Glucose < 60 mg/dl
WBC > 50,000/mm3
Gram stain/culture: positive

A

Empyema

  • Ddx. with complicated parapneumonic effusion which has a (-) pleural gram stain / culture
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66
Q

Which type of parapneumonic effusion is characterized by the following values:

pH ≥ 7.2
Glucose ≥ 60 mg/dl
WBC ≤ 50,000/mm3
Gram stain/culture: negative

A

Uncomplicated parapneumonic

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67
Q

Which type of parapneumonic effusion, uncomplicated or complicated, is characterized by pH < 7.2?

A

Complicated

(bacterial generate lactate)

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68
Q

Complicated or uncomplicated parapneumonic pleural effusion has the following:

  • Leukocyte counts > 50,000
  • pH < 7.2
  • Glucose < 60
A

Complicated

  • Glucose is lower since the bacteria are eating the sugar
  • Empyema = if (+) gram stain showing bacteria / pus
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69
Q

What are the potential paraneoplastic syndromes in lung squamous cell carcinoma?

A

Hypercalcemia (↑ PTHrP, stones bones groans)
Hypertroph pulmonary osteoarthropathy (diffuse jt pains)

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70
Q

What are the potential paraneoplastic syndromes in small cell lung cancer?

A

SIADH (hyponatremia)
Cushings (↑ ACTH)
LEMS

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71
Q

SIADH is a paraneoplastic syndrome in which type of lung cancer?

A

Small cell lung cancer

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72
Q

Hypercalcemia is a paraneoplastic syndrome in which type of lung cancer?

A

Squamous cell carcinoma of the lung

Hypercalcemia (↑ PTHrP, stones bones groans),

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73
Q

What is the treatment for exacerbation of COPD?

A

IV abx + steroids (systemmic, not ICS) + inhaled bronchodilators

74
Q

What statistical test is used to check differences between the means (numerical) of TWO groups ?

(e.g., comparing the mean blood pressure between men and women)

A

t-test

Compared to:
- Checking differences between the means of ≥3 groups = ANOVA
- Checking differences between two categorical groups = Chi-square (χ2 ) test

75
Q

What is ambulation?

A

the act/action of moving about or walking

76
Q

Where is a, b, c, d in the biostats table

77
Q

How do you distinguish between syringomyelia and anterior cord syndrome

A

Syringomyelina = Cape-like distrib (upper extremities, neck), loss of pain/temp, preserved DCML. Poss weakness.

Ant cord syndrome = also preserved DCML. Also urinary incont. Here it’s everything below lesion affected, wouldn’t just be arms.

78
Q

What happens to acetylcholine with a drug that inhibits acetylcholinesterase

A

↑ acetylcholine

(***OPPOSITE of anti-cholinergic toxicity symptoms!!)

79
Q

↑ Preload = ↑ or ↓ intensity of HOCM murmur?

A

Decreased intensity

(Increased preload [blood return] means less obstruction = softer HOCM murmur)

80
Q

What are the parameters in septic shock?

A

everything ↓, except CO and svO2(↑)

81
Q

What is the treatment for shingles?

A

Antiviral agents (eg, acyclovir, famciclovir, valacyclovir)

-Not steroids

82
Q

Hypotonic hyponatremia + low urine osm (<100 mOsm/kg) is diagnostic for _____ ?

A

Primary polydipsiaa

83
Q

What value is considered low for urine osm?

84
Q

Describe the HOCM murmur.

How is this differentiated from the AS murmur?

A

HOCM murmur = SEM, crescendo-decrescendo @ LSB. No carotid radiation

(AS radiates carotids, heard in R-2nd ICS, also cresc-decresc)

85
Q

When calcium level is >14
What is the most like etio of the hypercalcemia?

A

Malignancy

86
Q

Is the SN hearing loss in congenital infections B/L or U/L or either?

A

Can be either

87
Q

Girl with yellow-green cervical discharge, friable cervix. She was treated for UTI but is having refractory symptoms.

Dx?

A

Chlamydia/ gonorrhea

(acute cervicitis +/- urethritis [dysuria, sterile pyuria])

Note: If cervical motion tenderness present - means PID

88
Q

Microcytic anemia ↓Hb + ↓ ferritin = ACD or iron deficiency anemia?

A

Iron deficiency anemia

(ACD has ↑ ferritin)

89
Q

Which blistering skin disorder presents as groups of itchy rash with vesicles (or papules) & some crusted over on extensor surfaces (forearms, elbows, knees)

A

Dermatitis herpetiformis (Celiac’s)

90
Q

Is hypersensitivity pneumonitis an obstructive or restrictive lung disease?

A

Restrictive

91
Q

What are the 3 potential causes of hyponatremia in a euvolemic patient?

A
  1. SIADH
  2. Primary polydipsia
  3. Beer potomania (malnutrition)
92
Q

What is the triad seen in congential rubella?

A
  1. Cataracts
  2. PDA
  3. SN hearing loss
93
Q

↓ breath sounds L-lung base with dullness to percussion =

A
  1. Pleural eff
  2. Atelectasis (eg, mucus plugging)
  3. Hemothorax
94
Q

What is a common complication of mature cystic teratoma (dermoid cyst)

A

Ovarian torsion

95
Q

Ultrasound findings that can include: heterogeneous, solid components, thin echogenic bands/hyperechogenic nodules, partial calcifications

Describe which pathology?

A

Mature cystic teratoma (dermoid cyst)

(Thin echogenic bands [hair] /hyper-echogenic nodules, partial calcifications [teeth])

96
Q

Treatment for acute (<48h sx) symptomatic hyponatremia.

What does the Na+ level need to be to receive treatment?

A

hypertonic 3% saline if Na <130 ?or is it <120?

97
Q

Treatment for chronic (≥48h) symptomatic hyponatremia

What does the Na+ level need to be to receive treatment?

A

Hypertonic 3% saline is reserved for those with severe hyponatremia (Na <120) with severe sx (seizures)

because chronic has lower risk brain issues.

98
Q

How do you manage a newborn to hepB(+) mom?

A

Give HepB immune globulin + hepB vaccine (within 12h of birth) to the neonate

99
Q

If you suspect septic arthritis in a kid or overlapping symptoms with transient synovitis, what is the NBS?

A

B/L hip ultrasound

100
Q

Hypopigmented elliptical macule on chest =

A

Ash-leaf spot in tuberous sclerosis

101
Q

What are charcot bouchard aneurysms?

A

Tiny aneurysm bubbles on lenticulostriate A.s ➞ affect deep brain structure

102
Q

What virus do a lot of transplant patients get?

103
Q

Treatment for botulism?

A

Equine anti-toxin (even before diagnostic confirmation testing)

104
Q

What are some causes of conductive hearing loss?

A

Otosclerosis, Cholesteatoma
Chronic otitis media Foreign body

105
Q

Which drug should be given to all SAH patients in order to prevent the complication of cerebral vasospasm ?

A

CCB

(Cerebral vasospasm = delayed cerebral ischemia/stroke - FNDs)

106
Q

Management for peritonsillar abscess?

A

needle aspiration

107
Q

Trismus, muffled voice, deviated uvula, unilateral swelling =

A

Peritonsillar abscess

(Treatment is needle aspiration)

108
Q

Presence of WBC casts on urinalysis means it’s always either one of two things =

A

AIN or pyelonephritis!

109
Q

ADHD/autism symptoms, long face w large ears =

A

Fragile X

(Also macroorchidism if >8yo)

110
Q

Adolescent initially presenting with a single salmon-colored plaque that develops into a generalized rash with multiple, oval, scaly papules and plaques in a characteristic “christmas-tree” pattern on the trunk

A

Pityriasis rosacea

single salmon-colored plaque = herald patch

____
- Adolescent/young adult
- Self-limited
- Image on the right is a herald patch

111
Q

With derm condition has the dandruff association?

A

Seborrheic dermatitis

112
Q

CHF symptoms + holosytolic murmur @ LSB =

A

Tricuspid regurg

113
Q

Normal PT

A

11-15 seconds

114
Q

Normal PTT

A

25 - 40 seconds

115
Q

Polyarteritis nodosa

A

Renal insuff/↑Cr (100%)
GI - abdo pain
Mononeuritis multiplex (70%)
Spares the lungs
(-)ANCA

116
Q

Transient synovitis treatment

A

Supportive, NSAIDs

117
Q

When testing hearing loss, the tuning fork lateralizes to the left ear. Then AC > BC in both ears.

=

A

Right SN hearing loss

(Weber test localizes to the unaffected hear)

118
Q

Toxoplasomsis treatment

A

sulfadiazine + pyrimethamine

(note: CD4+ < 100)

119
Q

Toxoplasmosis prophylaxis

A

TMP-SMX when CD4<100

120
Q

Tender erythem streaks extending from wound + regional LAD =

A

Lymphangitis

121
Q

Hyperaldosteronism presents with the following findings:

(write hyper- or hypo-
______tension
______natremia
______kalemia

______ (metab/resp) ______ (acidosis/alkalosis)

A

Hypertension
Hypernatremia
Hypokalemia
Metabolic alkalosis

122
Q

Resistant hypertension, hypokalemia and abdominal bruit is suggestive of

A

Renal artery stenosis

(Due to hyperaldosteronism: low renal perfusion → activation of the RAAS → induces aldosterone secretion → augments potassium excretion → hypokalemia)

123
Q

Treatment of primary hyperaldosteronism (conn’s)

A

Aldosterone antagonists such as spironolactone or eplerenone

124
Q

Urinary chloride in metabolic alkalosis:

Vomiting + nasogastric aspiration causes metabolic alkalosis with ↑ or ↓ urinary Cl?

A

Decreased urinary Cl- (<10)
(volume loss, saline responsive)

(vs Mineralocorticoid excess state will result in a high urine chloride [>20] and hypervolemia that thus will not be saline responsive)

125
Q

The next step in the workup of metabolic alkalosis is

A

Check urine Cl-

_______________
-Saline responsive (urine chloride low [<10] because low vol): think about volume loss, activation of RAAS, causing Na+ in and H+/K+ out; Cl- is lost through gastric secretions

  • Saline resistant: think about other random causes (urine chloride high [>20] because hypervolemia) (e.g., hyperaldosteronism, Cushing’s, genetic stuff)
126
Q

What acid-base disorder may be caused by thiazide diuretics?

A

Metabolic alkalosis

(same with loops)

127
Q

What acid-base disorder may be caused by loop diuretics?

A

Metabolic alkalosis

(same with thiazides)

128
Q

What acid-base disturbance is classically found in patients with laxative abuse?

A

Metabolic alkalosis

In laxative abuse, osmotic losses of potassium → hypokalemia → cellular buffering → H+ moves into cell → alkalosis

(vs. the metabolic acidosis typically found with diarrhea)

129
Q

What is the likely diagnosis in a patient taking HCTZ, levothyroxine, and OTC mineral supplements (for osteoporosis) that develops symptomatic hypercalcemia, metabolic alkalosis, and AKI?

A

Milk-alkali syndrome

(Hypercalcemia causes renal vasoconstriction with ↓ GFR and also causes diuresis due to impaired ADH activity, with hypovolemia and contraction alkalosis)

130
Q

What is the likely diagnosis in a young female with hypokalemia, metabolic alkalosis, normotension, and low urine Cl-?

A

Surreptitious vomiting

  • Lose HCl and KCl via stomach

(Low urine Cl- helps distinguish vomiting from other causes of hypokalemia, alkalosis, and normotension (e.g., diuretic abuse, Bartter syndrome, and Gitelman syndrome which all have high urinary chloride)

131
Q

What is the likely diagnosis in a young patient with hypertension that develops severe hypokalemia after beginning a low-dose thiazide diuretic (eg, muscle weakness, leg cramps)?

A

PRIMARY hyperaldosteronism

(Volume depletion → ↑ aldosterone → more Na+ in, H+/K+ out)

132
Q

_______ is the probability that when the test is negative, the disease is absent

A

NPV

(vs - Specificity is the probability that when the disease is absent, the test is negative)

133
Q

______ is the probability that when the disease is absent, the test is negative

A

Specificity

(vs- NPV is the probability that when the test is negative, the disease is absent)

134
Q

What is the recommended primary prophylaxis against MAC for HIV patients with CD4 count < 50 for:

  1. Patient on or starting cART?
  2. Patient NOT on cART?
A

Patient on or starting cART = None

Patient NOT on cART = Macrolide (azithromycin or clarithromycin)

135
Q

HIV with CD4 < 50, high fever, and watery diarrhea is suggestive of

136
Q

Is primary prophylaxis against CMV recommended for patients with HIV?

A

No

(it’s coccidiomycosis not cryptococcus)

137
Q

Pneumocystis jirovecii prophylaxis in HIV patients should be started at CD4 counts < ______ with TMP-SMX.

138
Q

What is the likely diagnosis in an HIV patient with a CD4+ count of 25 that presents with 3 weeks of fever, night sweats, abdominal pain, diarrhea, and weight loss? CXR, CMV serology, and PPD are all negative

A

Disseminated MAC

(TB and CMV are less likely given the normal CXR, induration, and negative CMV IgG)

139
Q

Normal ABG ranges for:
1. pH
2. pCO2
3. pO2

A
  1. pH = 7.35 - 7.45
  2. pCO2 = 33 - 45
  3. pO2 = 75 - 105
140
Q

Normal serum calcium range

A

8.4 - 10.2

141
Q

How do the following labvalues change in primary hyperparathyroidism?

PTH:
Ca2+:
Phosphorus:

A

PTH: ↑ or inappropriately normal
Ca2+: ↑
Phosphorus: ↓

142
Q

Normal serum phosphorus range

143
Q

How do the following labvalues change in secondary hyperparathyroidism due to chronic kidney disease ?

PTH:
Ca2+:
Phosphorus:

A

PTH: ↑
Ca2+: ↓
Phosphorus: ↑

144
Q

Hypercalcemia + elevated PTH + high urine Ca2+ =

A

Primary hyperparathyroidism

  • High urine Ca2+ helps distinguish from familial hypocalciuric hypercalcemia
145
Q

In primary hyperparathyroidism, is serum phosphate ↑ or ↓ ?

A

Decreased (hypophosphatemia)

  • Due to ↑ PTH secretion (the primary defect)
  • Can be normal in mild disease (↓ in moderate to severe)
146
Q

What is the likely diagnosis in a patient presenting asymptomatically with mild hypercalcemia, hypocalciuria and normal / increased PTH levels?

A

Familial hypocalciuric hypercalcemia (FHH)

  • Due to defective Ca2+-sensing receptor (CaSR)
  • Higher than normal Ca2+ needed to suppress PTH
  • Hypocalciuria = want to reabsorb more Ca2+ to suppress the PTH
  • Low urine Ca2+ helps distinguish from primary hyperparathyroidism
147
Q

↑ HbA2 and ↑ HbF = alpha or beta thalassemia?

A

Beta

(↑ HbA2 and ↑ HbF is result of having little/no HbA)

-HbH and Hb Barts = alpha thalassemia

148
Q

Ventilator settings:
If ↓ PaCO2 and ↑ pH → should _____(↑/↓) the RR or TV?

A

decrease RR or TV

149
Q

How do SVR and afterload change during cardiogenic and obstructive shock?

150
Q

How do the following pressures change with pulmonary embolism?

RA pressure:
Pulmonary A. pressure:
LAP:

A

RA pressure: increased
Pulmonary A. pressure: increased
LAP: decreased or normal

151
Q

How does cardiac index change in septic shock?

A

Increased

-Important distinguishing feature from cardiogenic and hypovolemic shock;

152
Q

How does cardiac output change during cardiogenic and obstructive shock?

A

severely ↓

153
Q

How does cardiogenic shock affect the following?

CVP:
PCWP:
Cardiac index:
SVR:
SvO2:

A

CVP: increased
PCWP: increased
Cardiac index: decreased
SVR: increased
SvO2: decreased

154
Q

In cardiac tamponade, cardiac output decreases due to ________ (↓ / ↑ ) left ventricular _________

A

↓ CO due to: ↓ LV preload

155
Q

What is the likely diagnosis in a patient on post-MI day 5 that presents with sudden-onset cardiogenic shock and a harsh holosystolic murmur at the left sternal border with a palpable thrill?

A

Interventricular septal rupture

  • Compare with papillary muscle rupture, leading to MR (no thrill, soft murmur)
  • Left-to-right shunt may manifest as an ↑ in O2sat from the right atrium to the right ventricle; signs of left and right heart failure are present (e.g., pulmonary edema, JVD)
156
Q

What is the likely diagnosis in a patient s/p lung biopsy who presents with severe SOB and chest pain with a ↓ cardiac output and ↑ PCWP?

A

Cardiogenic shock (2/2 MI)

  • ↑ PCWP is indicative of cardiac etiology (helps rule out pulmonary etiologies, such as pneumothorax and PE since less blood is flowing to the LA)
  • Backup of blood into the lungs causes pulmonary edema
  • Peri-operative MI is common in patients undergoing noncardiac surgery; intra-operative hemorrhage requiring blood transfusion ↑ the risk
157
Q
A

Electrical alternans
is specific but poorly sensitive finding for pericardial effusion w cardiac tamponade; it results from heart changing position within the fluid-filled pericardial sac w each heartbeat.

  • Tx: emerg pericardiocentesis(to relieve pericardial pressure).
158
Q

Young boy presents with advanced bone age, coarse pubic hair, and severe cystic acne with low basal LH levels and normal testicular exam.

Diagnosis?

A

Late-onset (nonclassic) congenital adrenal hyperplasia

-Due to 21-hydroxylase deficiency → shunting to adrenal androgen production → peripheral precocious puberty

159
Q
A

Late decelerations

160
Q
A

Early decelerations

161
Q

_______ measures ability of a test to correctly identify those with the disease

A

Sensitivity

  • answers how often a test misses a dz
  • It measures ability of a test to correctly identify those w the dz. A test w high sensitivity has low likelihood of missing dz.
  • NBME Q: Pt concerned about the accuracy of a test and if could have missed the ca. Basically questioning the failure rate in detecting her breast ca.

disting from:
PPV: measures the probability that a person with positive test actually has the disease. Doesn’t tell you how often thw disease is missed.

162
Q

Treatment?

A

Amiodarone

163
Q
A
  • MC benign bone tumor
164
Q

Mgmt for stone retained in CBD (ie, choledocholithiasis)

A

ERCP immediately

165
Q

If signs of cholecystitis + pericholecystic fluid (edema in gallbladder wall) or wall thicken.

Next best step?

A

Antibiotics first
Then cholecystectomy within 72h (gives time for abx to kick in)

166
Q

Ascending cholangitis management

A

Antibiotics first
Then ERCP (within 24-48h)

167
Q

Why do you see no/minimal breast development in Turner’s?

A

Ovarian dysgenesis causes EST deficiency → no breast development

(girl will be like 15yo w tanner 1 breasts).

-gpt: no breast devel means the ovaries are not functioning

168
Q

What are the only times we do ERCP?

A
  1. Choledocholithiasis (stone in CBD)
  2. Ascending cholangitis: After antibiotics
169
Q

Give magnesium sulfate for preterm labor if < _____ weeks gestation

A

<32 weeks gestation

170
Q

Distinguish between:

  1. Chronic hypertension
  2. Gestational hypertension
  3. Preeclampsia
A

≥20 weeks = gestational HTN or preeclampsia. (preeclampsia if proteinuria or end-organ signs

<20 weeks = chronic HTN

171
Q

Management for preterm labor if <32 weeks gestation?

A
  • Tocolytics (nifedipine, terbutaline) ➞ delay delivery
    • Corticosteroids (betamethasone) ➞ fetal lung maturity
    • Magnesium sulfate ➞ neuroprotection, ↓ risk cerebral palsy
    • If unknown GBS status/ no prenatal care ➞ GBS prophylaxis
172
Q

What is the recommended management for
pregnant patient 35 weeks gestation presenting with preterm labor + fetus in vertex presentation on ultrasound?

A

Expectant management

  • Betamethasone ± penicillin may be administered
173
Q

Low serum osm
+ low urine osm(<300 mOsm)
+ hyponatremia

Diagnosis =

A

Primary polydipsia (ie, psychogenic)

174
Q

Low ser osm
+ ↓ urine osm(<300 mOsm)
+ nl or ↑ Na+

Diagnosis =

A

DI (ADH deficient/resistant)

175
Q

What level is considered low urine osmolarity?

176
Q

What level is considered high urine osmolarity?

What does that indicate?

A

> 600 mOsm

Indicates solute diuresis/ concentrated urine (if also ↑ glu, it’s d/t hyperglycemia)
- don’t confuse this w SIADH, both can be w head injury, and have ↓ Na+

177
Q

↑ HbA2 and ↑ HbF =

A

B-thalassemia

  • Will have little/no HbA
178
Q

Post-MI complication that looks like another MI several months later

A

LV aneurysm

179
Q

How do the following laboratory values change in a patient with hypovolemia?

ADH:
Renin:
Aldosterone:

A

ADH: ↑
Renin: ↑
Aldosterone: ↑

  • ↑ ADH due to angiotensin II, hypovolemia and hypotension. [goal is to replete volume]
  • ↑ Renin/aldosterone due to decreased renal perfusion → RAAS
180
Q

Hyponatremia, low plasma osmolality (< 280) and low urine osmolality (< 250) is suggestive of which diagnosis?

A

Primary polydipsia

  • Hypo-osmolarity (< 280 mM) → ↓↓ ADH → pee out H2O → dilute urine - everything is diluted
181
Q

NNT formula

A

NNT = 1/ARR

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