HEART
FAILURE
Clinical Overview
Pharmacotherapy
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Heart failure patients with signs and symptoms of significant
volume overload should be immediately started on a diuretic.1
Diuretics are very effective in relieving the signs and symptoms of
volume overload in heart failure, but their effects on survival and
disease progression are not known. Diuretic therapy can be started
before, with, or after ACE inhibitors.
Loop diuretics => more severe symptoms
Intravenous therapy => marked volume overload
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Monitoring electrolyte disturbances
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Agent |
Initial Maximum dose (mg) |
Major Adverse Reactions |
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Thiazide |
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Hydrochlorothiazide |
12.5 - 50 QD |
Postural hyotension; increased glucose; uric acid; decreased K+ |
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Chlorthalidone |
12.5 - 25 QD |
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Loop |
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Furosemide |
10 - 40 QD to 240 BID |
Same |
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Bumetanide |
0.5 - 1 to 10 QD |
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Torsemide |
5 - 10 QD - 100 QD |
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Thiazide-related |
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Metolazone |
2.5 - 10 QD |
Same |
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Indapamide |
1.25 - 5 QD |
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Potassium Sparing |
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Spironolactone |
25 QD - 100 BID |
Increased K+ (especially w/ ACE inhibitor), rash, gynecomastia (spironolactone only) |
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Triamterene |
50 QD - 100 QD |
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Amiloride |
5 QD or QOD - 20 QD |
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Proper dosing depends on patient size, age, renal function,
dietary sodium intake, and severity of edema.1
Most common adverse effects are postural hypotension, hypokalemia,
hyperglycemia, hyperuricemia, and rash. Hyperkalemia can occur with
K+ sparing diuretics.
Clinical Trials
The RALES study (Randomized Aldactone Evaluation Study)5 was designed to examine the effect of adding spironolactone to an established drug therapy regimen for heart failure. Since even high doses of ACE inhibitors may not be able to completely suppress the renin-angiotensin-aldosterone system, the addition of the spironolactone further suppressed the system by blocking aldosterone, The study was concluded 18 months early, in June 1998, because the results were so clinically significant that it was considered unethical to continue. The trial included 1663 patients with NYHA Class III or IV heart failure, who were followed for a mean of 24 months. The patients that were randomized to receive the spironolactone therapy showed a 27% decrease in mortality as compared to those patients receiving placebo.
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