Long-acting calcium antagonists in patients with coronary artery disease: a meta-analysis

Sripal Bangalore1, Sanobar Parkar, Franz H Messerli

  • 1Department of Medicine, Division of Cardiology, St. Luke's Roosevelt Hospital and Columbia University College of Physicians and Surgeons, New York, NY 10019, USA.

Insights

Long-acting calcium channel blockers (CCBs) do not increase mortality in coronary artery disease patients. These CCBs reduce the risk of stroke, angina, and heart failure.

Area of Science:

  • Cardiology
  • Pharmacology
  • Clinical Trials

Background:

  • Coronary artery disease (CAD) treatment with calcium channel blockers (CCBs) is controversial due to potential risks.
  • Short-acting CCBs have adverse hemodynamic effects, but the role of long-acting CCBs in CAD is unclear.

Purpose of the Study:

  • To evaluate the efficacy and safety of long-acting CCBs in patients with coronary artery disease.
  • To assess the impact of long-acting CCBs on mortality and major cardiovascular events.

Main Methods:

  • Systematic review and meta-analysis of randomized controlled trials (RCTs) from 1966 to August 2008.
  • Included studies involved long-acting CCBs in CAD patients with at least 1-year follow-up.
  • Extracted data on all-cause mortality, cardiovascular mortality, nonfatal myocardial infarction, stroke, angina, and heart failure.

Main Results:

  • 15 RCTs with 47,694 patients met the inclusion criteria.
  • Long-acting CCBs showed no increased risk for all-cause mortality, cardiovascular mortality, nonfatal myocardial infarction, or heart failure compared to control groups.
  • Significant reductions were observed in stroke (21%) and angina pectoris (18%), and heart failure (28%) compared to placebo.

Conclusions:

  • Long-acting CCBs, including dihydropyridines and nondihydropyridines, are safe for patients with coronary artery disease.
  • These agents are associated with reduced risks of stroke, angina pectoris, and heart failure.
  • Outcomes for other cardiovascular events were comparable to control groups.
Abstract

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