Renal Tubular Acidosis Flashcards

1
Q

What acid/base disorder is associated with all forms of renal tubular acidoses?

A

normal anion gap metabolic acidosis w/ hyperchloremia

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2
Q

What is the defect in Type 1?

A

alpha intercalated cells of the collecting duct cannot secrete H+. –> metabolic acidosis.

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3
Q

Is K+ high or low in Type 1?

A

hypokalemia.

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4
Q

What kind of kidney stones may form with RTA type one?

A

Calcium phosphate (increased urine pH), increased bone turnover.

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5
Q

What are the causes of RTA 1?

A

amphotericin B, analgesics, congenital obstruction of urinary tract

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6
Q

urine pH in RTA 1?

A

ph > 5.5

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7
Q

What is the defect in RTA type 2?

A

Defect in PCT bicarb reabsorption. Increased bicarb excretion in urine and subsequent metabolic acidosis.

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8
Q

Is K+ high or low in Type 2?

A

hypokalemia.

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9
Q

What disease is there an increased for with type 2?

A

hypophosphatemic rickets.

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10
Q

what is the urine pH in RTA 2?

A
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11
Q

What are causes of RTA 2?

A

Fanconi syndrome and carbonic anhydrase inhibitors.

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12
Q

What is the defect in RTA type 4?

A

Hypoaldosteronism.

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13
Q

Why does decreased aldosterone create acidosis?

A

Aldo normally upregs Enac channels and brings in more Na+, leading to greater excretion of potassium…without it, there is hyperkalemia–> potassium inhibits NH3 synth in the PCT, so hyperkalemia causes decreased NH3 synthesis in PCT –> decreased NH4 excretion. W/ decreased NH4 secretion, more H+ is reabsorbed.

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14
Q

What are some causes of decreased aldosterone production?

A

diabetic hyporeninism, ACEis/ARBs, NSAIDs, heparin, cyclosporine, adrenal insufficiency

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15
Q

What are some causes aldosterone resistance?

A

K+ sparing diuretics (spironolactone etc), nephropathy due to obstruction, TMP-SMX

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