Angiotensin II receptor blockers for the treatment of heart failure: a class effect?

Marie Hudson1, Karin Humphries, Jack V Tu

  • 1Division of Clinical Epidemiology, Research Institute of the McGill University Health Centre, Montreal, Quebec. marie.hudson@mcgill.ca

Pharmacotherapy
|March 27, 2007
PubMed

Insights

Elderly heart failure patients prescribed losartan had worse survival rates than those on other angiotensin II receptor blockers (ARBs). This suggests ARBs do not have a universal class effect due to distinct drug properties.

Area of Science:

  • Cardiology
  • Pharmacology
  • Geriatrics

Background:

  • Heart failure (HF) affects millions of elderly individuals globally.
  • Angiotensin II receptor blockers (ARBs) are commonly prescribed for HF management.
  • Understanding the class effect of ARBs on mortality in older adults is crucial for clinical practice.

Purpose of the Study:

  • To investigate the class effect of angiotensin II receptor blockers (ARBs) on all-cause mortality.
  • To compare the survival rates of elderly patients (≥65 years) with heart failure (HF) based on the specific ARB prescribed.

Main Methods:

  • A retrospective, population-based study utilizing administrative healthcare data from Canadian provinces.
  • Included 6876 elderly patients (mean age 78 years) discharged with heart failure and prescribed an ARB within 90 days.
  • Compared mortality rates between patients receiving different ARBs, adjusting for various demographic, clinical, and treatment factors.

Main Results:

  • Losartan was the most frequently prescribed ARB (61%).
  • Irbesartan, valsartan, and candesartan were associated with significantly better survival rates compared to losartan (HRs 0.65-0.71).
  • Telmisartan showed no significant difference in mortality compared to losartan (HR 0.92).

Conclusions:

  • Elderly heart failure patients prescribed losartan experienced worse survival outcomes than those on other ARBs.
  • The findings indicate a lack of a class effect for ARBs in this population.
  • Pharmacologic variations among ARBs likely contribute to the observed differences in survival.
Abstract

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