Nephrology Flashcards

1
Q

Contrast-associated nephropathy prophylaxis for patients who have an estimated GFR < 30 or AKI

A

IV NS pre- and post-procedure

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2
Q

Initial step in the management of newly diagnosed membranous nephropathy

A

Evaluation for secondary forms of the disease, including cancer screening in patient’s > 65 years of age

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3
Q

Most appropriate treatment for myeloma cast nephropathy aimed at reducing the concentration of free light chains

A

Chemotherapy

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4
Q

Indications for kidney biopsy

A

1) glomerular hematuria
2) severely increase albuminuria
3) acute or chronic kidney disease
4) Kidney transplant dysfunction or monitoring

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5
Q

Initial therapy for severe preeclampsia

A

Magnesium, antihypertensive medication, immediate delivery of the fetus

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6
Q

Management for kidney stone > 10 mm

A

Removal, ie via lithotripsy

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7
Q

Indication for management of chronic hypertension in pregnant women

A

Persistent systolic > 160 mmHg or diastolic > 110 mmHg blood pressure in the absence of end-organ damage to avoid over treatment of hypertension and associated fetal risk

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8
Q

Management for symptomatic hypermagnesemia

A

Immediate treatment with IV calcium gluconate while awaiting HD

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9
Q

NAGMA + negative urine anion gap

A

GI loss (diarrhea)

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10
Q

Primary therapeutic intervention in most patients with renal artery stenosis

A

Medical management, including correction of modifiable cardiovascular risk factors

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11
Q

Initial management of hyperphosphatemia in CKD

A

Low phosphate diet

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12
Q

NAGMA, hypokalemia, glycosuria (without hyperglycemia), low-molecular-weight proteinuria, and renal phosphate wasting.

A

Type 2 (proximal) RTA

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13
Q

Most common form of nephrotic syndrome in black patients

A

Focal segmental glomerulosclerosis

likely mediated in large part by variants in the APOL1 gene

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14
Q

Bacteria associated with struvite crystals (coffin-lid appearance)

A

Urea-splitting organisms (Proteus, Klebsiella, Pseudomonas

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15
Q

Most appropriate management for lithium -induced nephrogenic DI

A

Amiloride

Blocks the epithelial sodium channel in the collecting tubule and prevents the uptake of lithium by these cells

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16
Q

Appropriate management for recurrent gross hematuria and URI in younger patients with IgA nephropathy in the absence of proteinuria

A

Clinical observation

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17
Q

Appropriate management for salicylate toxicity in an otherwise well-appearing patient

A

IV sodium bicarbonate

18
Q

Definitive diagnostic test for lupus nephritis

A

Kidney biopsy

19
Q

Calcifications in the dermal arterioles resulting in painful ischemic skin lesions and has an increasingly recognized complication of ESRD. Many patients have severe secondary hyperparathyroidism and elevated calcium-phosphorus product

A

Calciphylaxis (calcific uremic arteriolopathy)

20
Q

Preferred initial agent for hypertension in black patients

A

Calcium channel blocker or thiazide diuretic

21
Q

Appropriate management for adults with stage 1 hypertension (SBP 130-139 or DBP 80-89) who have an estimated 10-year ASCVD event risk of < 10%

A

Non-pharmacological therapy

22
Q

Appropriate management for adults with stage 1 hypertension (SBP 130-139 or DBP 80-89) who have an estimated 10-year ASCVD event risk of > 10%

A

Nonpharmacological and antihypertensive drug therapy

23
Q

Most effective treatment to facilitate the passage of uric acid stones

A

Urinary alkalinization with potassium citrate

24
Q

Necrotizing and crescenteric glomerular nephritis with linear staining for IgG on immunoflorescence

A

Anti-glomerular basement membrane antibody disease

25
Q

Chronic interstitial nephritis with fibrosis and dense lymphoplasmacytic infiltrates

A

IgG4-related kidney disease

26
Q

Most appropriate management for acute tumor lysis syndrome

A

Isotonic fluids and rasburicase

27
Q

Gold standard for diagnosis of kidney stones

A

Noncontrast helical CT of the abdomen and pelvis

28
Q

Serum bicarbonate level in which metabolic acidosis should be treated with alkaline therapy in patients with CKD

A

< 22 mEq/L

29
Q

Autosomal dominant type IV collagen abnormality that causes thinning of the GBM, resulting IN hematuria but usually without proteinuria or abnormal kidney function. Diagnosis can be made by kidney biopsy, although this is not usually required and the setting of a good clinical in family history

A

Thin glomerular basement membrane disease, a.k.a. benign familial hematuria

30
Q

Serological testing which diagnosis primary membranous nephropathy

A

Anti-phospholipase A2 receptor (Anti-PLA2R)

31
Q

Leading cause of death among patients with CKD

A

Cardiovascular disease

32
Q

Electrolyte abnormality associated with ferric carboxymaltose, IV iron preparation

A

Hypophosphatemia caused by renal phosphate wasting

33
Q

Appropriate management for primary hyperaldosteronism

A

Aldosterone receptor antagonist, such as eplerenone

34
Q

Hepatitis virus associated with cryoglobulinemic glomerulonephritis

A

Hepatitis C virus

35
Q

hypokalemic metabolic alkalosis and frequently hypomagnesemia and high-normal serum calcium levels

A

Gitelman syndrome

36
Q

Most common etiology of immune complex MPGN

A

Hepatitis C virus infection

37
Q

Management for infection-related glomerulonephritis

A

Supportive and aimed at the infectious etiology

38
Q

Gold standard for pathologic diagnosis of amyloidosis

A

apple-green birefringence with congo red stain

39
Q

Pharmaceutical management that can slow kidney function decline in adults at risk for progressive autosomal dominant polycystic kidney disease

A

Tolvaptan, blockade of the renin-aldosterone system

40
Q

Resistant hypertension, metabolic alkalosis, hypokalemia

A

Primary hyperaldosteronism

41
Q

Etiology of hypokalemia with PPI use

A

Hypomagnesemia