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
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
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
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
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
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
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
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!)
9
Q
uses of loops
A
- edema
- hypercalcemia
- drug toxcities
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
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
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
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
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)
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