Key result
A review of optimal drug treatment in chronic heart failure proposes a hierarchy of drugs and individualized therapy based on clinical and genetic factors to manage polypharmacy.
Why the study?
How can drug therapy be optimized and individualized in patients with chronic heart failure to manage polypharmacy?
How can drug therapy be optimized and individualized in patients with chronic heart failure to manage polypharmacy?
This review highlights the challenges of polypharmacy in chronic heart failure and proposes individualized treatment strategies based on clinical and genetic factors.
May support tailored drug hierarchies to ease polypharmacy in chronic HF; leaves open prospective validation of clinical-genetic algorithms.
Angiotensin-converting enzyme (ACE) inhibitors and beta-blockers are the cornerstone for treatment of patients with chronic heart failure (CHF), and are usually combined with diuretics, with or without digoxin. With the development of new, additional treatments, the problem of polypharmacy becomes relevant, and strategies to individualize treatment are warranted. This review considers optimal drug treatment in patients with CHF, focusing on the possible problems that can occur when combining drugs. A hierarchy of drugs is suggested, starting from the assumption of a central role for early and widespread use of ACE inhibitors and beta-blockers. A model of drug therapy is proposed that is based on each patient's individual clinical and genetic considerations, which might serve to further optimize treatment.
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Boer et al. (2002) conducted a review in chronic heart failure. Angiotensin-converting enzyme (ACE) inhibitors, beta-blockers, and other drugs was evaluated. A review of optimal drug treatment in chronic heart failure proposes a hierarchy of drugs and individualized therapy based on clinical and genetic factors to manage polypharmacy.
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