Aspirin for the Primary Prevention of Cardiovascular Events: A Summary of the Evidence for the U.S. Preventive Services Task Force
Top Cited Papers
Open Access
- 15 January 2002
- journal article
- research article
- Published by American College of Physicians in Annals of Internal Medicine
- Vol. 136 (2), 161-172
- https://doi.org/10.7326/0003-4819-136-2-200201150-00016
Abstract
The use of aspirin to prevent cardiovascular disease events in patients without a history of cardiovascular disease is controversial. To examine the benefits and harms of aspirin chemoprevention. MEDLINE (1966 to May 2001). 1] Randomized trials at least 1 year in duration that examined aspirin chemoprevention in patients without previously known cardiovascular disease and 2) systematic reviews, recent trials, and observational studies that examined rates of hemorrhagic strokes and gastrointestinal bleeding secondary to aspirin use. One reviewer read and extracted data from each included article and constructed evidence tables. A second reviewer checked the accuracy of the data extraction. Discrepancies were resolved by consensus. Meta-analysis was performed, and the quantitative results of the review were then used to model the consequences of treating patients with different levels of baseline risk for coronary heart disease. Five trials examined the effect of aspirin on cardiovascular events in patients with no previous cardiovascular disease. For patients similar to those enrolled in the trials, aspirin reduces the risk for the combined end point of nonfatal myocardial infarction and fatal coronary heart disease (summary odds ratio, 0.72 [95% CI, 0.60 to 0.87]). Aspirin increased the risk for hemorrhagic strokes (summary odds ratio, 1.4 [CI, 0.9 to 2.0]) and major gastrointestinal bleeding (summary odds ratio, 1.7 [CI, 1.4 to 2.1]). All-cause mortality (summary odds ratio, 0.93 [CI, 0.84 to 1.02]) was not significantly affected. For 1000 patients with a 5% risk for coronary heart disease events over 5 years, aspirin would prevent 6 to 20 myocardial infarctions but would cause 0 to 2 hemorrhagic strokes and 2 to 4 major gastrointestinal bleeding events. For patients with a risk of 1% over 5 years, aspirin would prevent 1 to 4 myocardial infarctions but would cause 0 to 2 hemorrhagic strokes and 2 to 4 major gastrointestinal bleeding events. The net benefit of aspirin increases with increasing cardiovascular risk. In the decision to use aspirin chemoprevention, the patient's cardiovascular risk and relative utility for the different clinical outcomes prevented or caused by aspirin use must be considered.Keywords
This publication has 10 references indexed in Scilit:
- Aspirin for primary prevention of coronary heart disease: safety and absolute benefit related to coronary risk derived from meta-analysis of randomised trialsHeart, 2001
- An overview of the 4 randomized trials of aspirin therapy in the primary prevention of vascular disease.Archives of Internal Medicine, 2000
- Risk of gastrointestinal haemorrhage with long term use of aspirin: meta-analysisBMJ, 2000
- Determination of who may derive most benefit from aspirin in primary prevention: subgroup results from a randomised controlled trialBMJ, 2000
- Risk of primary intracerebral haemorrhage associated with aspirin and non-steroidal anti-inflammatory drugs: case-control studyBMJ, 1999
- Aspirin: benefit and risk in thromboprophylaxisQJM: An International Journal of Medicine, 1998
- Prediction of Coronary Heart Disease Using Risk Factor CategoriesCirculation, 1998
- Risk of aspirin-associated major upper-gastrointestinal bleeding with enteric-coated or buffered productThe Lancet, 1996
- Prophylactic aspirin and risk of peptic ulcer bleedingBMJ, 1995
- The gastrointestinal toxicity of aspirin: an overview of randomised controlled trials.British Journal of Clinical Pharmacology, 1993