Effect of Angiotensin Receptor Blocker Dose in Myocardial Infarction With Preserved Left Ventricular Systolic

Hee-Yeol Kim1, Jisu Mok1,2, Jae-Young Kim3

  • 1Department of Cardiology, College of Medicine, Bucheon St. Mary's Hospital, The Catholic University of Korea, Bucheon, Republic of Korea.

Insights

Higher doses of angiotensin receptor blockers (ARBs) did not improve outcomes for myocardial infarction (MI) patients with preserved left ventricular function. Dosing strategies did not significantly impact cardiac death or recurrent MI risk.

Area of Science:

  • Cardiology
  • Pharmacology
  • Clinical Research

Background:

  • Myocardial infarction (MI) with preserved left ventricular (LV) systolic function is common.
  • Optimal dosing of angiotensin receptor blockers (ARBs) in this patient population remains understudied.
  • Previous research has not clearly defined the benefits of varying ARB doses post-MI with preserved LV function.

Purpose of the Study:

  • To investigate the association between different doses of ARBs and clinical outcomes in patients following MI with preserved LV systolic function.
  • To determine if higher ARB doses are associated with improved outcomes compared to lower doses or no ARB therapy.
  • To evaluate the impact of ARB dosing on the composite endpoint of cardiac death or recurrent MI.

Main Methods:

  • A multicenter registry of MI patients with preserved LV systolic function was utilized.
  • Patients were grouped based on ARB dose indexed to target doses used in clinical trials: >0%-25%, >25%, and no ARB.
  • Primary outcome was the composite of cardiac death or MI, analyzed using multivariable adjustment and propensity score analysis.

Main Results:

  • Univariate analysis indicated lower mortality with any ARB use compared to no ARB.
  • Multivariable and propensity score analyses showed no significant difference in cardiac death or MI risk between patients receiving >25% of target ARB dose versus those receiving ≤25% or no ARB.
  • Hazard ratios for >25% target dose vs. ≤25% or no ARB were consistently around 1.0, indicating similar risk.

Conclusions:

  • Treatment with >25% of target ARB dose does not confer better clinical outcomes than lower doses (≤25%) or no ARB in MI patients with preserved LV systolic function.
  • Current ARB dosing strategies may not need adjustment for this specific patient group based on these findings.
  • Further research may explore other therapeutic targets or individualized treatment approaches for MI patients with preserved LV function.

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