Key result
Aspirin chemoprevention in patients without known cardiovascular disease reduces the risk of nonfatal myocardial infarction and fatal coronary heart disease (OR 0.72; 95% CI 0.60-0.87).
Why the study?
Does aspirin chemoprevention reduce the combined end point of nonfatal myocardial infarction and fatal coronary heart disease in patients without previously known cardiovascular disease?
Population
Patients without previously known cardiovascular disease (5 trials)
Design
Meta-analysis
Follow-up
at least 1 year
Authors
Loading...
Supports targeted aspirin use in higher-risk primary prevention; confirms MI/CHD benefit while underscoring individualized bleeding risk assessment.
Meta-Analysis
Does aspirin chemoprevention reduce the combined end point of nonfatal myocardial infarction and fatal coronary heart disease in patients without previously known cardiovascular disease?
Effect estimate: OR 0.72 (95% CI 0.60-0.87)
Aspirin for primary prevention reduces nonfatal MI and fatal CHD but increases hemorrhagic stroke and major GI bleeding, meaning net benefit depends on baseline cardiovascular risk.
Hayden et al. (2002) conducted a meta-analysis in Primary prevention of cardiovascular events. Aspirin was evaluated on combined end point of nonfatal myocardial infarction and fatal coronary heart disease (OR 0.72, 95% CI 0.60-0.87). Aspirin chemoprevention in patients without known cardiovascular disease reduces the risk of nonfatal myocardial infarction and fatal coronary heart disease (OR 0.72; 95% CI 0.60-0.87).
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: