Background Atherosclerotic peripheral arterial disease is associatedwith an increased risk of myocardial infarction, stroke, anddeath from cardiovascular causes. Antiplatelet drugs reducethis risk, but the role of oral anticoagulant agents in theprevention of cardiovascular complications in patients withperipheral arterial disease is unclear.
Methods We assigned patients with peripheral arterial diseaseto combination therapy with an antiplatelet agent and an oralanticoagulant agent (target international normalized ratio [INR],2.0 to 3.0) or to antiplatelet therapy alone. The first coprimaryoutcome was myocardial infarction, stroke, or death from cardiovascularcauses; the second coprimary outcome was myocardial infarction,stroke, severe ischemia of the peripheral or coronary arteriesleading to urgent intervention, or death from cardiovascularcauses.
Results A total of 2161 patients were randomly assigned to therapy.The mean follow-up time was 35 months. Myocardial infarction,stroke, or death from cardiovascular causes occurred in 132of 1080 patients receiving combination therapy (12.2%) and in144 of 1081 patients receiving antiplatelet therapy alone (13.3%)(relative risk, 0.92; 95% confidence interval [CI], 0.73 to1.16; P=0.48). Myocardial infarction, stroke, severe ischemia,or death from cardiovascular causes occurred in 172 patientsreceiving combination therapy (15.9%) as compared with 188 patientsreceiving antiplatelet therapy alone (17.4%) (relative risk,0.91; 95% CI, 0.74 to 1.12; P=0.37). Life-threatening bleedingoccurred in 43 patients receiving combination therapy (4.0%)as compared with 13 patients receiving antiplatelet therapyalone (1.2%) (relative risk, 3.41; 95% CI, 1.84 to 6.35; P<0.001).
Conclusions In patients with peripheral arterial disease, thecombination of an oral anticoagulant and antiplatelet therapywas not more effective than antiplatelet therapy alone in preventingmajor cardiovascular complications and was associated with anincrease in life-threatening bleeding. (ClinicalTrials.gov number,NCT00125671
[ClinicalTrials.gov]
.)
Source Information
The members of the writing group (Sonia Anand, M.D., Ph.D., F.R.C.P., Salim Yusuf, D.Phil., Changchun Xie, Ph.D., Janice Pogue, M.Sc., and John Eikelboom, M.B., B.S., McMaster University, Hamilton, ON, Canada; Andrzej Budaj, M.D., Ph.D., Grochowski Hospital, Warsaw, Poland; Bruce Sussex, M.D., M.B., B.S., Memorial University of Newfoundland, St. John's, Canada; Lisheng Liu, M.D., National Center of Cardiovascular Disease, Beijing; Randy Guzman, M.D., F.R.C.S., University of Manitoba, Winnipeg, Canada; Claudio Cina, M.D., Sp.Chir.It., F.R.C.S., Hamilton Health Sciences and St. Joseph's Hospital, Hamilton, ON, Canada; Richard Crowell, M.D., F.R.C.P., Queen Elizabeth II Health Sciences Centre, Halifax, NS, Canada; Matyas Keltai, M.D., Ph.D., Hungarian Institute of Cardiology, Semmelweis University, Budapest, Hungary; and Gilbert Gosselin, M.D., Montreal Heart Institute, Montreal) assume responsibility for the overall content and integrity of the article.
Address reprint requests to Dr. Anand at Hamilton General Hospital, Hamilton Health Sciences, 237 Barton St. East, Hamilton, ON L8L 2X2, Canada, or at anands{at}mcmaster.ca.
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