TY - JOUR
T1 - Aspirin in patients with previous percutaneous coronary intervention undergoing noncardiac surgery
AU - Graham, Michelle M.
AU - Sessler, Daniel I.
AU - Parlow, Joel L.
AU - Biccard, Bruce M.
AU - Guyatt, Gordon
AU - Leslie, Kate
AU - Chan, Matthew T.V.
AU - Meyhoff, Christian S.
AU - Xavier, Denis
AU - Sigamani, Alben
AU - Kumar, Priya A.
AU - Mrkobrada, Marko
AU - Cook, Deborah J.
AU - Tandon, Vikas
AU - Alvarez-Garcia, Jesus
AU - Villar, Juan Carlos
AU - Painter, Thomas W.
AU - Landoni, Giovanni
AU - Fleischmann, Edith
AU - Lamy, Andre
AU - Whitlock, Richard
AU - Le Manach, Yannick
AU - Aphang-Lam, Meylin
AU - Cata, Juan P.
AU - Gao, Peggy
AU - Terblanche, Nicolaas C.S.
AU - Ramana, Pamidimukkala V.
AU - Jamieson, Kim A.
AU - Bessissow, Amal
AU - Mendoza, Gabriela R.
AU - Ramirez, Silvia
AU - Diemunsch, Pierre A.
AU - Yusuf, Salim
AU - Devereaux, P. J.
N1 - Publisher Copyright:
© 2018 American College of Physicians.
PY - 2018/2/20
Y1 - 2018/2/20
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85042326412&partnerID=8YFLogxK
U2 - 10.7326/M17-2341
DO - 10.7326/M17-2341
M3 - Artículo Científico
C2 - 29132159
AN - SCOPUS:85042326412
SN - 0003-4819
VL - 168
SP - 237
EP - 244
JO - Annals of Internal Medicine
JF - Annals of Internal Medicine
IS - 4
ER -