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Published on: June 2, 2022
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.
Background:
The use of calcium channel blockers (CCBs) in patients with coronary artery disease remains controversial, with reports of increased risk of myocardial infarction and all-cause mortality. Short-acting CCBs have an unfavorable hemodynamic profile. The role of long-acting CCBs in patients with coronary artery disease is unknown.
Methods:
MEDLINE/CENTRAL/EMBASE database were searched from 1966 to August 2008 for randomized controlled trials of long-acting CCBs in patients with coronary artery disease with follow-up for at least 1 year. We extracted from the studies the baseline characteristics and 6 outcomes: all-cause mortality, cardiovascular mortality, nonfatal myocardial infarction, stroke, angina pectoris, and heart failure.
Results:
Of the 100 randomized controlled trials of CCBs in patients with coronary artery disease, 15 studies evaluating 47,694 patients fulfilled our inclusion criteria. When compared with the comparison group (including placebo), CCBs were not associated with an increased risk of all-cause mortality (relative risk [RR] 0.99; 95% confidence interval [CI], 0.94-1.05), cardiovascular mortality (RR 1.03; 95% CI, 0.95-1.11), nonfatal myocardial infarction (RR 0.96; 95% CI, 0.87-1.06), or heart failure (RR 0.86; 95% CI, 0.71-1.05), and with a 21% reduction in the risk of stroke (95% CI, 0.70-0.89) and 18% reduction in the risk of angina pectoris (95% CI, 0.72-0.94). When compared with placebo, CCBs resulted in a 28% reduction in the risk of heart failure (95% CI, 0.73-0.92). The results were similar for both dihydropyridines and nondihydropyridine CCBs.
Conclusions:
In patients with coronary artery disease, long-acting CCBs (either dihydropyridines or nondihydropyridines), were associated with a reduction in the risk of stroke, angina pectoris, and heart failure, with similar outcomes for other cardiovascular events as the comparison group.
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