PA urinalysis Flashcards

1
Q

What electrolyte disorder to ARBs and ACEi’s cause?

A

Hyperkalemia

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2
Q

What electrolyte disorder to most diuretics cause?

A

Hypokalemia

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3
Q

Red/brown urine with NO blood/RBCs suggests:

A

Rhabdomyalysis

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4
Q

What electrolyte disturbance often accompanies Rhabdomyalysis?

A

Hyperkalemia (due to muscle cell lysis)

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5
Q

Muddy brown granular casts are pathognomonic for:

A

Acute tubular necrosis

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6
Q

WBC casts are suggestive of:

A

Pylonephritis OR Allergic Interstitial Nephritis

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7
Q

Fatty casts and oval fat bodies are pathognomonic for:

A

Nephrotic syndrome

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8
Q

Calculate FENa:

A

PcrUna/PnaUcr

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9
Q

What does a FENa<1% suggest in AKI?

A

PreRenal origin.

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10
Q

What can diphenhydramine do to the kidneys?

A

Damage them via post-renal obstruction. Prevents passage of urine. Tx with Foley.

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11
Q

What can you always expect Furosemide (Lasix) to do to BMP?

A

Increase serum Cr (dilutional)

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12
Q

RBC casts are pathognomonic for:

A

Glomerulonephritis (nephritic syndrome)

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13
Q

Kid comes in with nephritic syndrome after having a sore throat…what is it?

A

Post-streptococcal glomerulonephritis.

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14
Q

Kid comes in with swollen feet (no blood in urine). What is it?

A

Minimal change disease (until proven otherwise)

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15
Q

What causes AKI and elevated serum Ca?

A

Multiple myeloma

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16
Q

How do you treat someone with HTN and elevated sCR (or albuminuria)?

A

Ace inhibitor! Will lower BP AND decrease albumin in urine. (Check K at 2 weeks though).

17
Q

What will ACE inhibitors and ARBs due to SCr?

A

Increase up to 20-30%

18
Q

What must you always do to a serum Na in diabetic patients with high glucose?

A

Correct it for blood glucose. they are competitive.

19
Q

A young (20-40 yo), healthy patient with blood in urine but no casts, WBCs, or protein probably has:

A

IgA nephropathy. Don’t be fooled by lack of protein in urine. Sometimes it’s just blood. It’s a nephritic syndrome.

20
Q

How does increased distal Na delivery cause K+ wasting?

A

Increased distal Na will increase activity of Aldosterone and ENaC channels which will make the endothelial cells less polarized and encourage K+ secretion.

21
Q

Liddle’s syndrome

A

Hypokalemia, metabolic alkalosis and HTN. Due to overactive Na channel in CD (and compensatory K+ excretion)

22
Q

Bartter’s syndrome

A

Hypokalemia, NO HTN. Also associated with hypercalciuria. mutation in transporter in thick ascending loop causes decreased Na absorption. (like a loop diuretic)

23
Q

Gitelman’s syndrome

A

Mutation in thiazide-sensitive Na-Cl transporter in DCL causes decreased Na reabsorption, increased K secretion, DECREASED calcium secretion.
Pt. has hypokalemia but is normotensive with HYPOcalciuria.

24
Q

Licorice toxicity presents like which other disease?

A

Liddle’s

25
Q

How is serum K affected by acidosis?

A

Cells act as buffer. So H+ is taken in, K+, na+ are excreted into ECF.

26
Q

How is serum K affected by alkalosis?

A

Cells act as buffer. H+ leaves cells, K+ and Na+ are absorbed to compensate for electronegativity change.

27
Q

Steps for workup of suspected metabolic acidosis:

A
  1. Is there a normal or high anion gap (>11)?
  2. Is it compensated?
  3. Is there a high anion gap and a normal anion gap process occurring (delta gap)? Should be 1. If >2 a metabolic alkalosis coexists. If <1, a non-anion gap metabolic acidosis coexists.
  4. Is it adequately compensated? If not, mixed!
28
Q

What are some causes of high anion gap metabolic acidosis?

A

Uremia, Ketoacidosis, Lactic Acidosis, Salicylate poisoning. ethylene glycol

29
Q

What are some normal anion gap causes of metabolic acidosis?

A

Renal tubular acidosis

30
Q

What are type I, II, III, and IV RTAs?

A

I- HCO3 wasting in proximal tubule
II- impaired H+ excretion at Distal tubule
III-mixed
IV- due to aldosterone deficiency or aldosterone resistance (less H+ secretion in DT and CD).

31
Q

List some causes of metabolic alkalosis:

A
  1. Volume depletion (high bicarb)
  2. Hypokalemia (K+ moves into cells, H+ out to compensate)
  3. Hypercalcemia (increases H+ secretion)
  4. GI/Renal H+ losses (diuretics, vomiting)
  5. Refeeding syndrome (Insulin spike causes intracellular movement of H+)
  6. Hyperaldosteronism (increases H+ ATPase activity and enhances Na+ reabsorption