Prevention & lipids

Aspirin, cardiovascular events, and major bleeding in older adults: extended follow-up of the ASPREE trial

Eur Heart JPublished Extended follow-up of the ASPREE randomised trial

Primary result · MACE, entire in-trial and post-trial periodResult — go to the resultHazard ratio 1.04 95% CI .94, 1.15

Authors' 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

OutcomeHR (95% CI)
MACE, post-trial period · median 4.3 yearsHigher rate with aspirin1.17 (1.01–1.36)

Safety

OutcomeHR (95% CI)
Major haemorrhage, entire periodHigher rate with aspirin1.24 (1.10–1.39)

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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