Nephrology 3 Flashcards

1
Q

Presentation of PD-associated peritonitis

A

abdominal pain + nausea

*often don’t have a fever or white count

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2
Q

PD-associated peritonitis diagnosis

A

Peritoneal fluid with over 100 WBCs or 50% PMNs

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3
Q

Treatment of PD-associated peritonitis

A
  • Intraperitoneal vancomycin and cefepime

treat empirically for both gram-positive and gram-negative organisms

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4
Q

Why recurrent urolithiasis occurs in gastric bypass patients

A
  • hyperoxaluria and hypocitraturia (malabsorption causes more intenstinal fatty acid binding to calcium, which increases colonic oxalate absorption and renal oxalate excretion)
  • applies to all malabsorption
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5
Q

Management of recurrent calcium oxalate stones in patients with malabsorption (Crohn’s)

A
  • low oxalate diet + exogenous citrate supplementation
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6
Q

significance of blood clots with hematuria

A
  • non-glomerular source of urinary tract bleeding (glomerular bleeding presents with dysmorphic RBCs-casts)
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7
Q

Significance of hematuria in a patient with previous cyclophosphamide exposure

A
  • high risk for bladder cancer, patient needs cyclophosphamide
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8
Q

Key feature of rhabdo

A

blood on dipstick (3-4+) but no RBCs on microscopic urinalysis

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9
Q

cystinuria clinical features

A
  • hexagonal (benzene ring) crystals in a *young patient with multiple stones
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10
Q

Treatment of nephrogenic DI

A
  • stop lithium
    IF patient can’t stop lithium – salt restriction + trial of diuretics (amiloride blocks sodium channels in collecting ducts to prevent lithiums entry, thiazides promote hypovolemia which increases proximal sodium and water reabsorption)
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11
Q

What is amiloride?

A

a diuretic

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12
Q

Management of Simple renal cyst

A

observation, no need for imaging unless symptomatic

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13
Q

Lab features of surreptitious diuretic use

A
  • intermittent hypokalemia
  • metabolic alkalosis
  • variable urinary chloride (diuretics cause a high urine chloride but urine chloride returns to low levels once effect wears office, thus level is variable)
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14
Q

Lab features of surreptitious vomiting

A
  • metabolic alkalosis + low urinary chloride
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15
Q

Management of hypercalcemic patient with nephrolithiasis

A

Repeat BMP + obtain PTH (rule out primary hyperparathyroidism)

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16
Q

Clinical features of anti phospholipid antibody syndrome

A
  • CVA or VTE in a young patient

- recurrent miscarriage and or fetal loss

17
Q

lab features of anti phospholipid antibody syndrome

A
  • thrombocytopenia (more than 25% of patients)
  • prolonged PTT
  • lupus anticoagulant
  • anticardiolipin antibody
  • anti-beta-2 glycoprotein antibody
18
Q

First step before anticoagulation patient with anti phospholipid antibody syndrome

A
  • MRI brain (risk stratification)
19
Q

other presentation of TTP

A

Fever

20
Q

Major side effect of hydroxychloroquine

A

retinopathy

21
Q

pathogen that is the cause of anal pruritus

A
  • enterobius vermicularis (pinworm)
22
Q

First line treatment of listeriosis

A

ampicillin

23
Q

Presentation of listeriosis in immunocompromised or elderly patient

A
  • invasive disease (bacteremia, sepsis, meningitis)
24
Q

diabetic nephropathy features vs. GN

A

DN = albuminuria + bland UA (but can occasionally see RBC casts and hematuria) +
*slowly progressive (takes years to develop)
GN = active sediment (hematuria, RBC casts) + HTN + *rapidly progressive

25
Q

management of patient with features of diabetic nephropathy but also GN features

A

biopsy

26
Q

When to call urology for nephrolithiasis

A
  • stone greater than 10 mm
  • no passage within 4-6 weeks
  • complicated nephrolithiasis (AKI, sepsis, complete obstruction, uncontrolled pain)
27
Q

initial workup of suspected nephrolithiasis

A
  • noncon CT scan
28
Q

Management of fulminant cdiff

A

add IV flagyl

29
Q

treatment of first recurrence of cdiff

A
  • prolonged course of oral vanc pulse dosed (QID for 10-14 days) and then slowly tapered over 2-8 weeks
  • can also use fidaxomicin
30
Q

Management of cholecystitis in patient with high surgical risk (elderly with multiple comorbidities)

A
  • percutaneous cholecytostomy
31
Q

Dietary modifications for reducing calcium-containing kidney stone formation in patients with hypercalciuria

A
  • low sodium (increased proximal tubule calcium and sodium reabsorption and reduced calcium excretion)
  • low animal protein diet (decreases acid load and urinary calcium excretion)
  • increase calcium intake
  • increase citrate intake
  • increase fluids, fruits, and vegetables
32
Q

Management of bilateral urinary obstruction complicated by post-obstructive diuresis

A
  • Volume repletion at significantly *lower rate than urine volume loss (matching volume repletion with UOP can worsen diuresis)
33
Q

bilateral urinary obstruction with post-obstructive diuresis physiology

A
  • patient has underlying bilateral obstruction (typically due to intrabdominal disease, mets), which when relieved leads to post obstructive diuresis (kidneys attempt to excrete retained fluid)
34
Q

Initial steps in suspected hepatorenal syndrome

A
  • albumin + *48 hour trial of diuretic cessation
35
Q

hepatorenal syndrome management

A
  • midodrine, octreotide, albumin
  • levophed in ICU
  • transplant (best definitive treatment)
36
Q

Renovascular HTN due to renal artery stenosis clinical features

A
  • recurrent flash pulmonary edema + severe HTN + AKI + underlying atherosclerosis