The CHARM program: study design leads to findings of clinical and public health importance

J Cardiovasc Pharmacol Ther. 2007 Jun;12(2):124-6. doi: 10.1177/1074248407301131.

Abstract

In large-scale randomized trials and their meta-analyses, beta-adrenergic blockers and angiotensin-converting enzyme inhibitors provide statistically significant and clinically important additive mortality and morbidity benefits in the treatment of heart failure. The CHARM trials were designed to test whether the angiotensin-receptor blocker candesartan would provide statistically significant and clinically important additive mortality and morbidity benefits to patients with heart failure as an alternative or in addition to angiotensin-converting enzyme inhibitors. CHARM demonstrated that an angiotensin-receptor blocker at a proven dose is an effective and safe therapy as an alternative or in addition to angiotensin-converting enzyme inhibitors in patients with heart failure, 55% of whom were receiving beta-adrenergic blockers. These benefits include reductions in cardiovascular mortality rate as well as in hospitalization for heart failure. Such patients have a 50% mortality rate at 5 years, and heart failure is the leading cause of hospitalization for patients 65 years of age and older.

MeSH terms

  • Adrenergic beta-Antagonists
  • Aged
  • Angiotensin II Type 1 Receptor Blockers / therapeutic use*
  • Angiotensin-Converting Enzyme Inhibitors / therapeutic use
  • Benzimidazoles / therapeutic use*
  • Biphenyl Compounds
  • Cardiac Output, Low / drug therapy*
  • Cardiac Output, Low / mortality
  • Drug Therapy, Combination
  • Hospitalization
  • Humans
  • Meta-Analysis as Topic
  • Randomized Controlled Trials as Topic
  • Tetrazoles / therapeutic use*

Substances

  • Adrenergic beta-Antagonists
  • Angiotensin II Type 1 Receptor Blockers
  • Angiotensin-Converting Enzyme Inhibitors
  • Benzimidazoles
  • Biphenyl Compounds
  • Tetrazoles
  • candesartan