Awesome Review Flashcards

(50 cards)

1
Q

Which type of AGMA causes nephrolithiasis?

A

Ethylene Gycol making glycolic acid; calcium phosphate kidney stones
Tx- Fomepizole

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2
Q

Which type of AGMA can cause blindness and papilledema?

A

Methanol from too much formic acid

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3
Q

If osmolol gap is greater than 20?

What if osmolol gap is greater than 50?

A

Give Fomepizole

Hemodialysis

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4
Q

Tx Type 2 RTA

A

Thiazides and alkali depletion
Problem with proximal CT, can’t reabsorb bicarbonate or NaCl

Looks like Fanconi Syndrome

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5
Q

Tx Type 1 RTA

A

Give potassium citrate

Distal CT can’t acidfy urine, urine pH > 6 and hypocitaturia

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6
Q

Features of type 4 RTA

A

Aldosterone deficiency or resistance causing hyperkalemia

Tx- try fludrocortisone

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7
Q

Features of Barter’s syndrome

A

Like loop diuretic
Hypokalemia, low BP, urine Cl > 15

Tx- inhibit prostaglandin production with indomethacin and ibuprofen

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8
Q

Features of Gitelman syndrome

A

Like thiazides
Problem with DCT sodium receptor
Hypokalemia, low BP, urine Cl > 15
Uric acid

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9
Q

Salicylate overdose causes…?

A

Respiratory alkalosis followed by metabolic acidosis

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10
Q

Features of Liddles Syndrome

A

Increased transport defect in distal tubule causing hyperaldosteronism
High BP

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11
Q

If you see hyponatremia and urine sodium

A

Hepatorenal syndrome

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12
Q

Lab findings in SIADH

A

Low serum sodium
High urine sodium
High urine osmolarity

Tx: demeclocycline or tolvaptan
(Demeclocycline in CI in liver cirrhosis)

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13
Q

How to fix it when you overcorrect hyponatremia?

A

Desmopressin with Dextrose 5%

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14
Q

When to give calcium gluconate in hyperkalemia?

A

Flattened P waves or wide QRS

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15
Q

Best test to measure microalbuminuria

A

spot urine protein/urine creatinine ratio, if >0.3

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16
Q

List 5 causes of papillary necrosis

A
Analgesics
Sickle cell trait 
Sickle cell disease
DM
Pyelonephritis 
Obstruction
TB
Chronic EtOH
RV thrombosis
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17
Q

Treat ADPKD-

Autosomal Dominant Polycystic Kidney Disease

A

Tolvaptan (also used to treat SIADH)

Associated with Hepatic Cysts and Berry Aneurysms and mitral Valve Prolapse and elevated hematocrit

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18
Q

Fatty Oval Bodies associated with

A

Nephrotic Syndrome

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19
Q

Light Microscopy Finding of

Focal Segmental

A

Sclerosis in some parts of some glomeruli

Focal/segmental

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20
Q

Etiology of

Focal Segmental

A

Obese Black patient with HIV and Sickle Disease using Heroin

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21
Q

Electron Microscopy Finding of

Membranous

A

Subepithelial deposits

LM- thickened capillary loops

22
Q

Etiology of Membranous

A

Hep B, Hep C, Syphillis, Solid Tumor, Lymphoma, malaria, NSAIDs, SLE, ACE-I, Gold, Pencillamine

23
Q

Etiology of Minimal Change Disease

A

Hodgkin’s lymphoma, thymoma, leukemia, NSAIDs, Lithium

24
Q

Electron Microscopy of Minimal Change

A

Effacement of Epithelial Foot Processes

25
Etiology of MembranoProliferative
Hep B, Hep C, SLE, Cryoglubinemia, SBE, monoclonal gammopathy
26
Which nephrotic syndrome has low Complement levels?
MembranoProliferative
27
Treatment for Nephrotic Syndrome
Steroids | Then consider cyclophosphamide, calcineurin inhibitors, mycophenolate,rituximab
28
IM finding of Rapidly Progressive Glomerulonephritis
Linear IgG deposition along glomerular basement membrane
29
Treatment of Rapidly Progressive Glomerulonephritis | Hint- Goodpastures
Plasmapheresis to remove the antibody | Cyclophosamide and steroids
30
Biopsy finding of IgA nephropathy
Mesangial Proliferation
31
Treatment of IgA Nephropathy
Fish Oil with omega 3 Fatty Acid
32
Lab findings with Infection Related GN (Hint- complement)
Low C3 Low CH50 Normal C4
33
Lab Findings in pre-renal Azotemia
BUN:Cr >20:1 Urine Osm >500 Urine Na
34
Anemia goal in CKD | Hgb, ferritin, transferrin sat
Hgb -10 Transferrin sat >30% Ferritin >500
35
Compensation for Metabolic Acidosis
1.5 (HCO3) + 8
36
Compensation for Metabolic Alkalosis
40 + 0.7(change in HCO3)
37
Compensation for Respiratory Acidosis
Acute- increase by 1 for 10 mmHg in PCO2 | Chronic- increase by 3.5 for 10 mmHg in PCO2
38
Compensation for Respiratory Alkalosis
Acute: decrease in 2 for 10 mmHg decrease in PCO2 Chronic: decrease in 5 for 10 mmHg decrease in PCO2
39
Serum Complement levels decreased in which nephritic syndrome?
Post Streptococcal GN MembranoProliferative (SLE, SBE, Cryoglobulinemia) Atheroembolism (livedo reticularis/blue toe syndrome, eosinophilia, eosinophiluria)
40
Name 5 causes of Acute Tubular Necrosis
``` Aminoglycosides Amphotericin B Cyclosporine Tumor Lysis Rhabdo Atheroembolism Ethylene glycol Calcium oxalate crystals Contrast ```
41
5 cause (Meds) of Acute Tubulointersitial Nephritis
``` Beta Lactam PCN Sulfa Phenytoin Quinolone Mesalamine NSAIDs PPI ```
42
Which macrolide causes AKI?
Clarithomycin
43
Difference btwn Rhabdo and Tumor Lysis Syndrome
Heme dipstick is positive in Rhabdo ``` Both have increased CPK Increased Uric acid Increased Potassium Low calcium Increased phosphate ```
44
Treatment of Uric Acid Stones
Adequate urine output of 2 liters in 24 hours Alkalinize urine (potassium citrate or potassium bicarbonate) Allopurinol only if hyperuricososuria
45
Acquired Cystic Kidney Disease have high risk of ... What?
Renal Cell Carcinoma
46
Which VEGF causes Thrombotic Microangiography?
Bevacizumab and Sunitinib
47
Orliastat causes which type of nephrolithiasis?
Calcium Oxalate due to hyperoxaluria | Bonds intestinal calcium so more oxalate is absorbed intestinally and more peed out (enteric hyperoxaluria)
48
Post transplant kidney patients have higher risk of which cancer?
Squamous cell cancer (skin)
49
Pneumococcal vaccine administration in CKD
``` 23 valent 1 year 13 valent 5 years 23 valent ```
50
Treatment for calcium Oxalate stones
Avoid oral oxalate Calcium carbonate/calcium citrate to bind intestinal oxalate Cholestyramine to bind oxalate as bile salts (Pyridoxine only for rare primary hyperoxaluria)