Diuretics Flashcards

1
Q

Carbonic anhydrase inhibitor:

A

Acetazolamide

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2
Q

Carbonic anhydrase inhibitor effects (4):

A
  • Weak diuretic
  • Na+ excretion (5% filtered load Na+, H2O)
  • HCO3- excretion –> metabolic acidosis
  • K+ excretion
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3
Q

Carbonic anhydrase inhibitor therapeutic uses (3):

A
  • Decrease intraocular pressure (OA glaucoma)
  • Urinary alkalization
  • Mountain sickness prophylaxis
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4
Q

Carbonic anhydrase inhibitor adverse effects (4):

A
  • Metabolic acidosis
  • Hypokalemia
  • Drowsiness
  • Hypersensitivity (sulfonamides)
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5
Q

Thiazide MOA:

A

Inhibition of luminal Na+, Cl- cotransport

- Binds to Cl- binding site

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6
Q

Thiazide site of action:

A

Distal tubule

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7
Q

Thiazide effects on urine composition (4):

A
  • Na+ and H2O excretion (10% filtered load - modest)
  • K+, Cl-, HCO3- excretion
  • Decreased Ca2+ excretion
  • Decreased uric acid excretion
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8
Q

Thiazide therapeutic uses (5):

A
  • HTN (main use)
  • CHF, other edema states
  • Hypercalciuric renal stones
  • Nephrogenic DI
  • Nephrotic syndrome (with spironolactone)
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9
Q

Only thiazide-related drugs effect at lower GFR rates (2):

A
  • Metolazone

- Inadapamide

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10
Q

Thiazide ADRs (7):

A
  • Hypokalemia (digitalis interaction)
  • Hypovolemia (rare)
  • Hyperglycemia (diabetics)
  • Hyperuricemia (gout pts)
  • Hypercalcemia
  • Hypersensitivity (sulfonamide)
  • Hyperlipidemia
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11
Q

Loop diuretic that is NOT a sulfonamide:

A

Ethacrynic acid

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12
Q

Loop diuretics MOA:

A

Inhibit Na+, K+, 2Cl- cotransport (at Cl- binding site)

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13
Q

Loop diuretics site of action:

A

Ascending limb of loop of Henle

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14
Q

Loop diuretic effects (4):

A
  • Na+ and H20 excretion (25%)
  • K+, Cl- excretion
  • Ca2+ excretion
  • +/- HCO3- excretion (higher doses)
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15
Q

Loop diuretic therapeutic uses (4):

A
  • Acute pulmonary edema (IV use)
  • Edema (CHF, renal, hepatic)
  • HTN (low GFR)
  • Hypercalcemia
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16
Q

Loop diuretic ADRs (7):

A
  • Hypovolemia
  • Hypokalemia
  • Ototoxicity (hearing loss, additive)
  • Hyperuricemia
  • Hyperglycemia
  • Hypersensitivity (Sulfa - not EA)
  • Hyperlipidemia
17
Q

Potassium-sparing diuretics (4):

A
  • Triamterene
  • Amiloride
  • Spionolactone
  • Eplerenone
18
Q

Aldosterone receptor antagonists (2):

A
  • Spironolactone

- Eplerenone

19
Q

Aldosterone receptor antagonist MOA:

A

Competitive antagonist at renal aldosterone receptors

- Decreased Na+/K+ exchange in distal tubule and collecting duct

20
Q

Aldosterone receptor antagonist effect on urine composition (2):

A
  • Increased Na+, Cl-, H2O excretion (2-3%)

- Decreased K+, H+

21
Q

Spironolactone therapeutic uses (4):

A
  • Primary hyperaldosteronism
  • Prevent hypokalemia with K+ depleting diuretics
  • Edema from hepatic cirrhosis and nephrotic syndrome (DoC)
  • CHF
22
Q

Eplerenone therapeutic uses (2):

A
  • HTN

- CHF post-MI

23
Q

Aldosterone receptor antagonist ADRs (2):

A
  • Hyperkalemia

- Altered hormonal activity

24
Q

Sodium channel blockers (2):

A
  • Triamterene

- Amiloride

25
Q

Sodium channel blockers MOA:

A

Decrease Na+/K+ exchange in distal tubule and collecting duct

26
Q

Sodium channel blocker effects (2):

A
  • Decreased K+, H+ secretion

- Increased Na+, Cl-, H2O excretion (2-3%)

27
Q

Sodium channel blocker therapeutic uses (2):

A
  • Secondary hyperaldosteronism

- Prevent hyokalemia of K+ depleting diuretics

28
Q

Osmotic diuretic effects (3):

A
  • Increased urinary flow
  • Slight Na+ excretion
  • Decreased urine osmolarity
29
Q

Osmotic diuretic therapeutic uses (4):

A
  • Maintain urine flow
  • Acute renal failure
  • Reduce intracranial pressure
  • Glaucoma (decreases intraocular pressure)