Aspirin, cardiovascular events, and major bleeding in older adults: extended follow-up of the ASPREE trial
Primary result · MACE, entire in-trial and post-trial periodResult — go to the resultHazard ratio 1.04 95% CI .94, 1.15Authors' conclusion
The present study provides novel evidence concerning long-term MACE and haemorrhage following aspirin use in initially healthy older adults.
Study context
- Population
- Adults aged ≥70 years (≥65 years for US minorities) without prior CV events, dementia or independence-limiting physical disability15,668 in post-trial follow-up
- Participants
- 19,114 adults
- Comparison
- Low-dose aspirin vs placebo
- Aspirinn = 9,525
- Placebon = 9,589reference
- Primary endpoint
- Major adverse cardiovascular events (MACE) and major haemorrhage (long-term and post-trial effects)
- Follow-up
- Entire in-trial (2010-17) and post-trial (2017-22) period
Methodological detailsplacebo-controlled, in-trial and post-trial follow-up
- Placebo-controlled
- In-trial and post-trial follow-up
Primary result
MACE, entire in-trial and post-trial period
Hazard ratio
1.04
95% CI .94, 1.15
Aspirinvs Placebo
HR 1.04 (95% CI .94, 1.15)
As reported in the abstract
Further findings
| Outcome | HR (95% CI) | |
|---|---|---|
| MACE, post-trial period · median 4.3 yearsHigher rate with aspirin | 1.17 (1.01–1.36) | |
| 0.512Hazard ratio (log scale) |
Safety
| Outcome | HR (95% CI) | |
|---|---|---|
| Major haemorrhage, entire periodHigher rate with aspirin | 1.24 (1.10–1.39) | |
| 0.512Hazard ratio (log scale) |
Original publication
Aspirin, cardiovascular events, and major bleeding in older adults: extended follow-up of the ASPREE trial. Eur Heart J. Published 12 August 2025. doi:10. 1093/ eurheartj/ ehaf514
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