1. Aspirin in Patients With Previous Percutaneous Coronary Intervention Undergoing Noncardiac Surgery.
- Author
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Graham MM, Sessler DI, Parlow JL, Biccard BM, Guyatt G, Leslie K, Chan MTV, Meyhoff CS, Xavier D, Sigamani A, Kumar PA, Mrkobrada M, Cook DJ, Tandon V, Alvarez-Garcia J, Villar JC, Painter TW, Landoni G, Fleischmann E, Lamy A, Whitlock R, Le Manach Y, Aphang-Lam M, Cata JP, Gao P, Terblanche NCS, Ramana PV, Jamieson KA, Bessissow A, Mendoza GR, Ramirez S, Diemunsch PA, Yusuf S, and Devereaux PJ
- Subjects
- Aged, Antihypertensive Agents therapeutic use, Aspirin adverse effects, Biomarkers blood, Clonidine therapeutic use, Drug Administration Schedule, Drug Therapy, Combination, Female, Hemorrhage chemically induced, Humans, Male, Middle Aged, Myocardial Infarction prevention & control, Platelet Aggregation Inhibitors adverse effects, Postoperative Complications chemically induced, Postoperative Complications prevention & control, Treatment Outcome, Aspirin therapeutic use, Percutaneous Coronary Intervention, Platelet Aggregation Inhibitors therapeutic use, Surgical Procedures, Operative
- Abstract
Background: Uncertainty remains about the effects of aspirin in patients with prior percutaneous coronary intervention (PCI) having noncardiac surgery., Objective: To evaluate benefits and harms of perioperative aspirin in patients with prior PCI., Design: Nonprespecified subgroup analysis of a multicenter factorial trial. Computerized Internet randomization was done between 2010 and 2013. Patients, clinicians, data collectors, and outcome adjudicators were blinded to treatment assignment. (ClinicalTrials.gov: NCT01082874)., Setting: 135 centers in 23 countries., Patients: Adults aged 45 years or older who had or were at risk for atherosclerotic disease and were having noncardiac surgery. Exclusions were placement of a bare-metal stent within 6 weeks, placement of a drug-eluting stent within 1 year, or receipt of nonstudy aspirin within 72 hours before surgery., Intervention: Aspirin therapy (overall trial, n = 4998; subgroup, n = 234) or placebo (overall trial, n = 5012; subgroup, n = 236) initiated within 4 hours before surgery and continued throughout the perioperative period. Of the 470 subgroup patients, 99.9% completed follow-up., Measurements: The 30-day primary outcome was death or nonfatal myocardial infarction; bleeding was a secondary outcome., Results: In patients with prior PCI, aspirin reduced the risk for the primary outcome (absolute risk reduction, 5.5% [95% CI, 0.4% to 10.5%]; hazard ratio [HR], 0.50 [CI, 0.26 to 0.95]; P for interaction = 0.036) and for myocardial infarction (absolute risk reduction, 5.9% [CI, 1.0% to 10.8%]; HR, 0.44 [CI, 0.22 to 0.87]; P for interaction = 0.021). The effect on the composite of major and life-threatening bleeding in patients with prior PCI was uncertain (absolute risk increase, 1.3% [CI, -2.6% to 5.2%]). In the overall population, aspirin increased the risk for major bleeding (absolute risk increase, 0.8% [CI, 0.1% to 1.6%]; HR, 1.22 [CI, 1.01 to 1.48]; P for interaction = 0.50)., Limitation: Nonprespecified subgroup analysis with small sample., Conclusion: Perioperative aspirin may be more likely to benefit rather than harm patients with prior PCI., Primary Funding Source: Canadian Institutes of Health Research.
- Published
- 2018
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