Diuretics Flashcards

1
Q

formulas for free H2O clearance,osmolar clearance and FE of X and filtered load of X

A
  • CH2O= V - Cosm
  • where Cosm = (Uosm x V)/Posm
  • FEx = Cx/GFR (where GFR = Cin)
  • Filtered load of X = GFR x plasma concentration of X
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2
Q

potassium sparing diuretics

A
  • spironolactone (aldo-dependent)
  • **spironolactone is the only one that does not depend on GFR and tubular fluid concentration
  • amiloride and triamterene (aldo-independent) –> block Na channels in luminal membrane –> lowers intracell Na –> slows down Na/K ATPase on BL membrane –> less K secretion
  • act in late DT and CD
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3
Q

SE of thiazides

A
  • induce ECF volume contraction –> hyponatremia (higher risk), alkalosis, hyperuricemia, hypomagnesemia, azotemia
  • increased lipids
  • hypokalemia –> caution in PTs taking digitalis and quinidine (increased risk of arryhthmia)
  • hypokalemia further increased when taking corticosteroids or amphotericin B
  • diminshed activity with NSAIDs
  • reduce absorption from gut with resins
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3
Q

transcellular proximal tubule organic anion and cation secretion

A
  • loops and thiazides = weak acids (anions)
  • triamterence and amiloride= weak bases (cations)
  • anions: active transport across BL and passive across luminal membrane
  • cations: passive transport across BL membrane and active across lumenal
  • with kidney disease, GFR decreases and the clearance of anionic metabolites decreases–> higher concentrations of anionic metabolites compete with anionic diuretics so you need to give a higher dose of diuretic
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4
Q

loops

A
  • furosemide, bumetanide, torsemide, ethacrynic acid
  • acts in tALH (Na-2Cl-K transporter)
  • also inhibits reabsorption of Mg and Ca indirectly by decreasing the (+) lumen potential
  • when volume expanded, CH2O is decreased (blocks kidney’s ability to dilute the urine)
  • when PT is volume contracted loops also prevent H20 from leaving CD (osmotic gradient isnt as steep) –> block kidney’s abilit to concentrate the urine
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4
Q

uses and contraindications of K+ sparing diuretics

A
  • in combo with loops or thiazides to prevent hypokalemia
  • amiloride can tx Li-induced polyuria without increasing Li reabsorption
  • can’t use in renal failure or with ACEI/ARBs
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7
Q

aminophylline (theophylline)

A
  • acts in proximal tubule
  • PDE inhibitor –> increases levels of cAMP –> decreased Na reabsorption
  • not really used as a diuretic but is used in PTs with asthma
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7
Q

other uses of thiazides

A
  • treat idiopathic hypercalciuria (increase the reabsorption of Ca – opp of loops!)
  • nephrogenic diabetes insipidus(inability to respond to ADH) –> contract ECF volume –> decrease volume of tubular fluid and volume of urine
  • tx Li-induced nephrogenic diabetes insipidus by same mechanism as above (but be careful of compensatory increase in solute and water reabsorption –> increased Li absorption and toxicity!)
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9
Q

uses of loops

A
  • edema
  • hypercalcemia
  • drug toxcities
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10
Q

SE of loops

A
  • hyponatremia
  • hyperuricemia
  • contraction alkalosis (further increases K+ secretion)
  • azotemia
  • hypokalemia
  • possible onset of diabetes mellitus
  • hypomagnesemia (lost in urine)
  • ototoxicity
  • NSAIDS decrease their effectiveness
  • increased concentration of clotting factors
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11
Q

osmotic diuretics

A
  • mannitol, glucose, urea, isorbide
  • greatest effect is on proximal tubule
  • freely filtered, non-reabsorbeable solutes in tubular fluid increases osmotic pressure to oppose isotonic reabsorption of Na and H20
  • administered IV (mannitol does not cross cell membrane so its volume of distribution is limited to ECF) –> increased ECF osmolarity –> increases renal medullary blood flow
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12
Q

Thiazides

A
  • chlorothiazide, hydrochlorothiazide, chlorthalidone, metolazone, indapamide
  • act on early distal tubule (inhibit Na-Cl cotransporter)
  • limit kidney’s ability to dilute the urine but not concentrate it –> greater risk of hyponatremia
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13
Q

carbonic anhydrase inhibitors

A
  • acetazolamide, methazolamide, dichlorphenamide (“-amide”)
  • act in proximal tubule
  • less CO2 diffusion ino the cell –> less bicarb available to couple with H+ –> slows H+/Na+ exchanger down –> less Na+ reabsorption
  • SE: hypokalemia and metabolic acidosis (via increases loss of bicarb in urine)
  • however, body compensates by becoming refractory to CAI and prevents greater loss of bicarb in urine when metabolic acidosis ensues decreases elimination of ammonia –> ammonia builds up in blood –> hepatic encephalopathy
  • tx glaucoma and acute mtn sickness
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14
Q

uses of osmotics and cautions

A
  • induce diuresis for drug OD, shock (prevent renal failure), diff dx of oliguria
  • reduce intraocular and intracranial pressure (induces absorption of water from intraocular and intracranial space into ECF)
  • may induce pulmonary edema (IV infusion increases ECF volume –> transient increase in hydrostatic P)
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15
Q

body fluid compartments

A
  • TBW = 60% of person’s weight
  • TBW = 1/3 ECF and 2/3 ICF
  • ECF = 1/4 intravascular and 3/4 interstitial
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