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Angiotensin converting enzyme (ACE) inhibitors and heart failure. The consequences of underprescribing

F Andersson1, C Cline, T Rydén-Bergsten

  • 1Department of Health Economics & QoL, Astra Draco AB, Lund, Sweden. fredrik.andersson@draco.se.astra.com

Pharmacoeconomics
|October 28, 1999
PubMed

Insights

Underprescribing Angiotensin Converting Enzyme (ACE) inhibitors for heart failure (HF) leads to preventable deaths and hospitalizations. Optimizing ACE inhibitor use in HF patients, particularly those with chronic HF and post-myocardial infarction (MI) LVSD, is highly cost-effective.

Area of Science:

  • Cardiology
  • Health Economics

Background:

  • Heart failure (HF) is a significant cardiovascular burden, associated with high mortality and healthcare costs.
  • Angiotensin Converting Enzyme (ACE) inhibitors demonstrably reduce mortality and hospitalizations in HF patients.
  • Current prescription rates and dosages of ACE inhibitors for HF fall below optimal evidence-based guidelines.

Purpose of the Study:

  • To estimate the economic and human consequences of underprescribing ACE inhibitors in patients with heart failure.
  • To analyze the cost-effectiveness of ACE inhibitor therapy across different HF patient subgroups.
  • To evaluate the impact of increasing ACE inhibitor dosages to trial-recommended levels.

Main Methods:

  • Analysis of data stratified by patient groups: asymptomatic left ventricular systolic dysfunction (LVSD), chronic HF, and post-myocardial infarction (MI) LVSD (both asymptomatic and chronic HF).
  • Estimation of cost-effectiveness for adding ACE inhibitors to current treatment regimens.
  • Inclusion of patient populations where large trials demonstrated significant mortality benefits from ACE inhibition.

Main Results:

  • Increasing ACE inhibitor use in eligible Swedish HF patients could save over 3700 lives and prevent 8400 hospitalizations annually, at an additional cost of 101.5 million SEK.
  • Chronic HF patients represent the most cost-effective group for ACE inhibitor treatment, potentially yielding cost savings.
  • Extending ACE inhibitor use to asymptomatic LVSD patients could avert an additional 6700 hospitalizations.

Conclusions:

  • ACE inhibitor therapy in HF and LVSD is proven to be highly cost-effective, comparable to treatments for hypertension and hypercholesterolemia.
  • Suboptimal utilization of ACE inhibitors in HF persists despite clear evidence of benefit and cost-effectiveness.
  • Maximizing the use of cost-effective treatments like ACE inhibitors in HF and post-MI LVSD is crucial, especially within constrained healthcare resources.

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