Aspirin for Primary Prevention of Cardiovascular Events

Hesham K Abdelaziz1, Marwan Saad2, Naga Venkata K Pothineni3

  • 1Lancashire Cardiac Center, Blackpool Victoria Hospital, Blackpool, United Kingdom; Department of Cardiovascular Medicine, Ain Shams University, Cairo, Egypt.

Insights

Aspirin use for primary prevention of cardiovascular disease (CVD) reduces nonfatal myocardial infarctions and strokes but increases major bleeding events. The overall benefit-risk profile remains under investigation for widespread recommendation.

Area of Science:

  • Cardiology
  • Preventive Medicine
  • Clinical Trials

Background:

  • The use of aspirin for primary prevention of cardiovascular disease (CVD) is a topic of ongoing debate.
  • Recent large-scale trials have added significant data, necessitating an updated analysis of aspirin's efficacy and safety.

Purpose of the Study:

  • To evaluate the clinical outcomes associated with aspirin for primary CVD prevention.
  • To incorporate data from over 45,000 new participants from recent large trials.

Main Methods:

  • A systematic review and meta-analysis of randomized controlled trials (RCTs) with a follow-up of at least one year.
  • Included efficacy outcomes (all-cause death, CV death, MI, stroke, TIA, MACE) and safety outcomes (major bleeding, intracranial bleeding, fatal bleeding, GI bleeding).
  • Calculated risk ratios (RRs) using random-effects DerSimonian-Laird models.

Main Results:

  • Analysis of 15 RCTs with 165,502 participants revealed aspirin was associated with a reduced risk of nonfatal myocardial infarction (MI), transient ischemic attack (TIA), and ischemic stroke.
  • However, aspirin significantly increased the risk of major bleeding, intracranial bleeding, and major gastrointestinal (GI) bleeding.
  • No significant differences were observed in all-cause death, cardiovascular death, or fatal bleeding between aspirin and control groups.

Conclusions:

  • Aspirin for primary prevention demonstrates a dual effect: reducing nonfatal ischemic events while increasing nonfatal bleeding events.
  • The findings highlight a trade-off between ischemic benefits and bleeding risks, impacting the decision for primary CVD prevention.
Abstract

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