Randomised trial of prophylactic daily aspirin in British male doctors

Randomised trial of prophylactic daily aspirin in British male doctors

30 JANUARY 1988 | R PETO, R GRAY, R COLLINS, K WHEATLEY, C HENNEKENS, K JAMROZIK, C WARLOW, B HAFNER, E THOMPSON, S NORTON, J GILLILAND, R DOLL
A six-year randomized trial involving 5139 healthy male British doctors was conducted to assess whether daily aspirin (500 mg) would reduce the incidence and mortality from stroke, myocardial infarction, or other vascular conditions. The study found that total mortality was 10% lower in the aspirin group, but this difference was not statistically significant. There was no significant difference in the incidence of non-fatal myocardial infarction or stroke, though disabling strokes were somewhat more common in the aspirin group. However, the lower confidence limit for the effect of aspirin on non-fatal stroke or myocardial infarction was a substantial 25% reduction. Migraine and certain musculoskeletal pains were reported less frequently in the aspirin group, but the lack of a placebo control made these findings difficult to assess. There was no apparent reduction in cataract incidence. The study found no significant reduction in disabling stroke or vascular death, contrasting with the known benefits of antiplatelet treatment after vascular disease. The study aimed to determine if daily aspirin could prevent thrombotic events in apparently healthy individuals. Due to the low incidence of vascular events in healthy people, large trials were needed to detect even a small reduction. Two large trials were conducted, one among British doctors and another among Americans. The British trial found that aspirin did not significantly reduce the risk of stroke or vascular death, though there was a potential 25% reduction in non-fatal stroke or myocardial infarction. The study also found that aspirin was associated with a lower incidence of migraines and musculoskeletal pain, but these findings were not conclusively supported due to the lack of a placebo control. The study concluded that the benefits of aspirin in preventing vascular events in healthy individuals were not definitively proven, and further research was needed. The results were compared with those from a similar trial in the United States, which suggested that aspirin might prevent about one-third of non-fatal myocardial infarctions. However, the results from the United Kingdom trial did not show a significant benefit. The study also noted that aspirin may have side effects, such as gastrointestinal issues, which could be mitigated by using enteric-coated aspirin. The study highlighted the need for further research to determine the true benefits and risks of aspirin in preventing vascular events in healthy individuals.A six-year randomized trial involving 5139 healthy male British doctors was conducted to assess whether daily aspirin (500 mg) would reduce the incidence and mortality from stroke, myocardial infarction, or other vascular conditions. The study found that total mortality was 10% lower in the aspirin group, but this difference was not statistically significant. There was no significant difference in the incidence of non-fatal myocardial infarction or stroke, though disabling strokes were somewhat more common in the aspirin group. However, the lower confidence limit for the effect of aspirin on non-fatal stroke or myocardial infarction was a substantial 25% reduction. Migraine and certain musculoskeletal pains were reported less frequently in the aspirin group, but the lack of a placebo control made these findings difficult to assess. There was no apparent reduction in cataract incidence. The study found no significant reduction in disabling stroke or vascular death, contrasting with the known benefits of antiplatelet treatment after vascular disease. The study aimed to determine if daily aspirin could prevent thrombotic events in apparently healthy individuals. Due to the low incidence of vascular events in healthy people, large trials were needed to detect even a small reduction. Two large trials were conducted, one among British doctors and another among Americans. The British trial found that aspirin did not significantly reduce the risk of stroke or vascular death, though there was a potential 25% reduction in non-fatal stroke or myocardial infarction. The study also found that aspirin was associated with a lower incidence of migraines and musculoskeletal pain, but these findings were not conclusively supported due to the lack of a placebo control. The study concluded that the benefits of aspirin in preventing vascular events in healthy individuals were not definitively proven, and further research was needed. The results were compared with those from a similar trial in the United States, which suggested that aspirin might prevent about one-third of non-fatal myocardial infarctions. However, the results from the United Kingdom trial did not show a significant benefit. The study also noted that aspirin may have side effects, such as gastrointestinal issues, which could be mitigated by using enteric-coated aspirin. The study highlighted the need for further research to determine the true benefits and risks of aspirin in preventing vascular events in healthy individuals.
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