2018
DOI: 10.1016/s0140-6736(18)31924-x
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Use of aspirin to reduce risk of initial vascular events in patients at moderate risk of cardiovascular disease (ARRIVE): a randomised, double-blind, placebo-controlled trial

Abstract: Bayer.

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Cited by 698 publications
(677 citation statements)
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“…However, controversies have been existed about whether, and if so in whom, aspirin is appropriate for the primary prevention of CVD till the recent three trials of low‐dose aspirin versus placebo in populations at increased risk but without established CVD were reported. In the ARRIVE trial for people at low risk of CVD, aspirin had no effect on major CV events but increased gastrointestinal bleeding . In the ASCEND trial for patients with diabetes mellitus and no evidence of vascular disease, the benefits of aspirin on serious vascular events reduction were totally offset by the increased risk of major bleeding .…”
Section: Management Of Associated Cvd Risk Factorsmentioning
confidence: 99%
“…However, controversies have been existed about whether, and if so in whom, aspirin is appropriate for the primary prevention of CVD till the recent three trials of low‐dose aspirin versus placebo in populations at increased risk but without established CVD were reported. In the ARRIVE trial for people at low risk of CVD, aspirin had no effect on major CV events but increased gastrointestinal bleeding . In the ASCEND trial for patients with diabetes mellitus and no evidence of vascular disease, the benefits of aspirin on serious vascular events reduction were totally offset by the increased risk of major bleeding .…”
Section: Management Of Associated Cvd Risk Factorsmentioning
confidence: 99%
“…Since the submission of this letter for publication three modern trials of primary preventative aspirin have been published. Aspirin was associated with no cardiovascular benefit in the elderly, but low‐risk (3.45–3.88% 5‐year event‐rate) ASPirin in Reducing Events in the Elderly (ASPREE) population (hazard ratio (HR) 0.95, 95% CI 0.83–1.08, P > 0.05) or the low‐to‐moderate‐risk (4.29–4.48% 5‐year event‐rate) Aspirin to Reduce Risk of Initial Vascular Events (ARRIVE) trial (HR 0.96, 95% CI 0.81–1.13, P = 0.604) . The high‐risk (8.5–9.6% 7.4‐year event‐rate) A Study of Cardiovascular Events iN Diabetes (ASCEND) trial did show a benefit (RR 0.88, 95% CI 0.79–0.97, P = 0.01), but at the cost of increased major bleeding (RR 1.29, 95% CI 1.09–1.52, P = 0.003) .…”
mentioning
confidence: 99%
“…The ASPREE trial was in healthy elderly subjects, and the ARRIVE trial was in subjects at moderate risk of cardiovascular disease. The results of the three studies were broadly similar …”
mentioning
confidence: 52%