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What is the optimal angiotensin-converting enzyme inhibitor dose in heart failure?
1Division of Cardiology, Barnes-Jewish Hospital and Washington University School of Medicine, St. Louis, MO 63110, USA.
Insights
Doses of angiotensin-converting enzyme (ACE) inhibitors for heart failure survival benefit are often not achieved in practice. Higher doses improve outcomes, but optimal dosing remains uncertain, necessitating efforts to reach target levels.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Landmark trials show survival benefits with angiotensin-converting enzyme (ACE) inhibitors in heart failure.
- Current clinical practice rarely achieves the high doses used in these pivotal trials.
Purpose of the Study:
- To review literature on optimal ACE inhibitor dosing in heart failure.
- Focus on neurohormonal, functional capacity, and clinical outcomes.
Main Methods:
- Literature review of studies on ACE inhibitor dosing in heart failure.
- Analysis of neurohormonal, functional, and clinical endpoints.
Main Results:
- Lower ACE inhibitor doses may inadequately suppress the renin-angiotensin-aldosterone system.
- Higher doses correlate with improved exercise capacity and functional status.
- High-dose ACE inhibitors significantly reduce mortality and hospitalizations, including heart failure-specific events.
Conclusions:
- Optimal ACE inhibitor dosing in heart failure remains debated due to conflicting evidence.
- Insufficient evidence supports lower doses; limited data exist for doses exceeding landmark trial levels.
- Clinicians should strive to administer target ACE inhibitor doses in heart failure patients when feasible.
Abstract:
Doses of angiotensin-converting enzyme (ACE) inhibitors used in the landmark heart failure trials that demonstrated survival benefit are rarely reached in routine practice. The authors review the current literature regarding optimal dosing of ACE inhibitors in heart failure with specific focus on neurohormonal, functional capacity, and clinical outcomes. Neurohormonal studies have shown that lower ACE inhibitor dosing may provide inadequate suppression of the renin-angiotensin-aldosterone system. Higher doses of ACE inhibitors have resulted in greater increments in exercise and functional capacity. Clinically, patients on high-dose ACE inhibitor therapy had significant reductions in all-cause mortality or hospitalization, cardiovascular hospitalizations, and heart failure-specific hospitalizations. There is, however, conflicting evidence, and so continued uncertainty exists regarding optimal dosing. Despite underutilization of ACE inhibitors, there is insufficient evidence to support lower doses. Likewise, limited data exist for doses higher than those used in the landmark trials. Clinicians should therefore attempt to reach target doses in heart failure whenever possible.
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