renal acid/base Flashcards

1
Q

how do you calculate the predicted respiratory compensation for a simple metabolic acidosis?

A

PCO2 should = 1.5[HCO3-] + 8 (plus or minus 2).

if the PCO2 is significantly different from that, then a mixed acid-base disorder is likely present.

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2
Q

acidemia vs. acidosis

A

acidema: the pH of the blood is low
acidosis: the process that could lead to a low pH

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3
Q

causes of metabolic acidosis

A

if you detect a metabolic acidosis, check the ANION GAP.
Anion Gap = [Na+] - ([HCO3-] + [Cl-]). normal is 8-12
Positive anion gap: something is there that shouldn’t be. MUDPILES: methanol, uremia, diabetic ketoacidosis, propylene glycol, iron tablets or isoniazid, lactic acidosis, ethylene glycol, salicylates (late).
Normal anion gap:
HARD-ASS:
hyperalimentation, addison disease, renal tubular acidosis, diarrhea, acetazolamide, spironolactone, saline infusion

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4
Q

causes of metabolic alkalosis

A

loop diuretics, vomiting, antacid use, hyperaldosteronism

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5
Q

causes of respiratory acidosis

A

hypoventilation: airway obstruction, acute or chronic lung disease, opioids, weakened resp. muscles.

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6
Q

causes of respiratory alkalosis

A

hypoxemia (ie high altitude), early salicylates, tumor, pulmonary emobolism

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7
Q

renal tubular acidosis

A

a defect in the renal tubules that leads to a non-anion gap hyperchloremic metabolic acidosis.

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8
Q

type I renal tubular acidosis

A

distal problem; pH > 5.5. I assume this is urine pH?
there is a defect in alpha intercalated cells to secrete H+. new HCO3- is not generated. associated with HYPOKALEMIA. incr. risk of calcium phosphate kidney stones due to incr. urine pH and incr. bone turnover.
causes: amphotericin B toxicity, analgesic nephropathy, multiple myeloma (light chains), congenital obstuctions of the urinary tract

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9
Q

type II renal tubular acidosis

A

urine pH < 5.5.
defect in proximal tubule HCO3- resorption causes an increase in excretion of HCO3- in the urine –> metabolic acidosis. urine is acidified by alpha intercalated cells in collecting tubule. associated with hypokalemia. incr. risk for hypophosphatemic rickets.
causes: Fanconi syndrome (eg. Wilson’s disease), chemicals toxic to the proximal tubule (lead, aminoglycosides), and carbonic anhydrase inhibitors

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10
Q

type IV renal tubular acidosis

A

hypoaldosteronism or aldosterone resistance or K sparing diuretics. resulting hyperkalemia impairs ammoniagenesis in the proximal tubule. decr. buffering capacity and decr. H+ excretion into urine.

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11
Q

RBC casts, RBCs in urine

A

RBCs in urine have many causes, including bladder cancer or kidney stones. however, casts indicates that the hematuria is of renal (vs. bladder) origin. RBC casts are seen in glomerulonephritis, ischemia, or malignant HTN.

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12
Q

WBC casts ddx

A

tubulointerstitial inflammation, acute pyelonephritis, transplant rejection

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13
Q

fatty cast ddx

A

aka oval fat bodies. seen in nephrotic syndrome

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14
Q

waxy casts ddx

A

advanced renal disease/chronic renal failure

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15
Q

granular casts

A

aka muddy brown casts. indicate acute tubular necrosis.

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