Congestive heart failure drug interactions: Difference between revisions
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==Overview== | ==Overview== | ||
Polypharmacy is common in the management of the patient with congestive heart failure. Efforts should be made to assure that there are few if any adverse drug interactions. It should be noted that the volume of drug distribution and the clearance of drugs in heart failure is often altered due to impaired renal function, poor drug absorption due to gut edema, and impaired drug metabolism due to hepatic insufficiency. | Polypharmacy is common in the management of the patient with congestive heart failure. Efforts should be made to assure that there are few if any adverse drug interactions. It should be noted that the volume of drug distribution and the clearance of drugs in heart failure is often altered due to impaired renal function, poor drug absorption due to gut edema, and impaired drug metabolism due to hepatic insufficiency. |
Revision as of 00:29, 24 April 2013
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Polypharmacy is common in the management of the patient with congestive heart failure. Efforts should be made to assure that there are few if any adverse drug interactions. It should be noted that the volume of drug distribution and the clearance of drugs in heart failure is often altered due to impaired renal function, poor drug absorption due to gut edema, and impaired drug metabolism due to hepatic insufficiency.
Digoxin
Verapamil and amiodarone can increase serum digoxin levels. Hypokalemia can exacerbate digitalis toxicity.
Triple therapy with in Angiotensin-converting enzyme inhibitor, an Angiotensin Receptor Blocker, and Spironolactone
The combination of these three agents can lead to severe hyperkalemia and the use of all three agents together is not recommended.