Renal Flashcards

1
Q

Why are patients with chronic pancreatitis at increased risk of calcium oxalate stones?

A

Diarrhea –> volume depletion which increased quantity of calcium and oxalate in urine. Often have a metabolic acidosis which decreases urinary citrate. In fat malabsorption, calcium binds fat instead of oxalate leaving oxalate to precipitate in the urine.

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2
Q

Secondary causes membranous glomerulopathy

A

Hep B, Hep C, lupus, syphilis, about 25% of patients older than 65 will have a malignancy diagnosed within 1 year of diagnosis of membranous glomerulopathy. So all should undergo age appropriate screening at diagnosis.

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3
Q

When to immunosuppress in membranous glomerulopathy?

A

Need to rule out secondary causes. Then should wait at least 3-6months post initial diagnosis as up to 1/3 of patients have spontaneous remission

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4
Q

Heparin and hyperkalemia?

A

Heparin use is associated with decreased aldosterone synthesis. This then leads to hyperkalemia. IT is more likely in patients iwth CKD, on diabetes, on ACEi or ARBs

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5
Q

Pyroglutamic acidosis

A

presents with mental status changes and an increased anion gap in patients on chronic acetaminophen. Susceptible with critical illness, poor nutrition, CKD or liver disease

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6
Q

Conditions with reset osmostat mild hyponatremia

A

pregnancy, quadriplegia, chronic malnutrition, advanced age, tuberculosis, and psychiatric disorders

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7
Q

Lab test for primary membranous glomerulopathy

A

anti-phospholipase A2 Receptor (PLA2R) approaches 100% specificity for primary form

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8
Q

Treatment for atherosclerotic renovascular disease

A

ARB/ACEi - studies have not shown benefit to angioplasty/stenting in patients with stable kidney function on optimized medication regimen. There is some benefit in patients who cannot tolerate ACEi/ARBs, patients with flash pulmonary edema and resistant HTN despite maximal HTN therapies

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9
Q

Type 1 RTA

A

distal acidification defect. low bicarb, compensatory elevated chloride (leading to normal AG). Unable to acidify urine (so pH >6) and an elevated urine AG. Also hypokalemic

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10
Q

Most common disease associated with type 1 RTA

A

Sjogren Syndrome

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11
Q

Type 2 RTA

A

proximal defect in reclaiming bicarb. Normal AG metabolic acidosis, hypokalemia, glycosuria (Without hyperglycemia), low molecular weight proteinuria and phosphate wasting. DISTAL acidification is intact, so pH <5.5

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12
Q

Type 4 RTA

A

Associated with aldosterone deficiency or resistance. Hyperkalemic and urine pH <5.5

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13
Q

Subnephrotic proteinuria with no clinical symptoms

A

Likely FSGS

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14
Q

Nephrotic syndrome with greatest risk for VTE

A

Membranous glomerulopathy

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15
Q

Main causes of distal RTA’s in adults

A

autoimmune diseases (Sjogren’s RA), drugs (amphotericin) or toxin ingestion (toluene)

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16
Q

Factors that increase the Cr without decreasing the GFR

A

Trimethoprim, cimetidine, ketone bodies, cefoxitin and flucytosine. Cr increase usuall 0.1-0.2mg/dL, but can be up to 0.5mg/dL

17
Q

Treatment of salicylate poisoning

A

Supportive care, often intubation as salicylates act in medulla and cause marked increase in minute ventilation. Alkalinzation of the urine with IV bicarb which traps the ionic form of salicylic acid in tubular fluid and enhances renal elimiation. OK even though alkalemic from respiratory status. HD for AMS, pulmonary/cerebral edema, renal failure and salicylate level >100

18
Q

Recommended IVFs in post-obstructive diureses

A

Aim for replacing about 50% of the urine output volume with 0.45 or 0.9% NS

19
Q

Simple renal cysts features on US and management

A

Round, thin, smooth, regular border. No septa, calcifications or solid components. Posterior enhancement on US. no Contrast enhancement or CT/MRI. Reassurance is all that’s needed <1% malignancy risk

20
Q

Complex renal cysts features on US and management

A

Few septa, calcifications. No contrast enhancement on CT/MRI. If less than 3 CM Category II and reassurance is all that’s needed. If >3 cm, repeat imaging in 6-12 months (5-10% malignancy risk)

21
Q

Cystic Mass features on US and management

A

Thick, irregular wall. Mulitple thick septa, often with calcifications. Enhancement on CT/MRI. Surgical excision of mass or nephrectomy. 90% malignant risk

22
Q

When do you refer to urology for evaluation of abnormal prostate testing?

A

Men with PSA >7 or abnormal DRE should be referred to urology for possible biopsy. If PSA 3-7, it should be repeated in a few weeks and referred to urology if remains >3

23
Q

Treatemtn for scleroderma renal crisis

A

ACEi regardless of current Cr at time of diagnosis

24
Q

Treatment to reduce recurrence of calcium oxalate stones

A

Increase free water fluid intake, decrease sodium and animal protein intake, increase dietary calcium intake (binds GI oxalate),

25
Q

Empiric antibiotics for prostatitis

A

TMP-SMX or fluoroquinolones

26
Q

Isolated proteinuria (up to 3g/day) without hematuria or elevated Cr or other symptoms in a young health individual

A

Orthostatic proteinuria. Check a spot urine Pro/Cr ration first hting in AM and in PM

27
Q

Post renal transplant presenting with rising Cr and tubulointerstitial nephritis typically 10-15 months post transplant. Often with intranuclear inclusions on urine cytology

A

BK polyoma virus. Need biopsy + positive immunohistochemical testing using Ab directed against BK virus for diagonsis

28
Q

Envelope shaped crystals in urine

A

Calcium oxalate stones

29
Q

Rhomboid crystals, radiolucent stones

A

Uric acid stones

30
Q

Staghorn calculi. Coffin lid crystals

A

Struvite stones

31
Q

Hexagonal green/yellow crystals. Large branched calculi

A

Cystine stones

32
Q

Next steps with K >8, but no EKG changes

A

Consider pseudohyperkalemia and recheck value with free flowing arterial draw

33
Q

Initial management of bilateral renal artery stenosis

A

Medical management with a diuretic and an ACEi or ARB. If fail this - or recurrent flash pulmonary edema then should undergo angioplasty with stenting