Inhibition of complement activation by pexelizumab reduces death in patients undergoing combined aortic valve replacement and coronary artery bypass surgery

被引:32
|
作者
Carrier, M
Ménasché, P
Levy, JH
Newman, MF
Taylor, KM
Haverich, A
Chen, JC
Shernan, SK
Van de Werf, F
van der Laan, M
Todaro, TG
Adams, PX
Verrier, ED
机构
[1] Montreal Heart Inst, Res Ctr, Montreal, PQ H1T 1C8, Canada
[2] Hammersmith Hosp, NHLI Imperial Coll Sch Med, London, England
[3] Hannover Med Sch, D-3000 Hannover, Germany
[4] Univ Hawaii, Kaiser Permanente Med Ctr, Honolulu, HI 96822 USA
[5] Harvard Univ, Brigham & Womens Hosp, Sch Med, Boston, MA 02115 USA
[6] Duke Univ, Duke Clin ResIinst, Durham, NC USA
[7] Emory Univ, Emory Univ Hosp, Atlanta, GA 30322 USA
[8] Univ Hosp Gasthuisberg, B-3000 Louvain, Belgium
[9] Procter & Gamble Co, Pharmaceut, Egham, Surrey, England
[10] Procter & Gamble Co, Mason, OH USA
[11] Alexion Pharmaceut Inc, Cheshire, CT USA
[12] Univ Washington, Sch Med, Seattle, WA USA
[13] Hop Georges Pompidou, Dept Cardiovasc Surg, Paris, France
来源
关键词
D O I
10.1016/j.jtcvs.2005.10.011
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: We sought to evaluate the effects of pexelizumab, a C5 complement inhibitor, on death and myocardial infarction in patients undergoing combined aortic valve replacement and coronary artery bypass grafting surgery. Methods: The Pexelizumab for Reduction in Myocardial Infarction and Mortality in Coronary Artery Bypass Graft surgery trial, a phase III prospective, randomized, double-blind, placebo-controlled study, enrolled 3099 patients at 205 centers. The primary end point was the composite of death, myocardial infarction, or both at postoperative day 30 in patients undergoing coronary artery bypass grafting without valve surgery. Postoperative myocardial infarction was defined as a creatine kinase MB fraction value of 100 ng/mL or greater, Q-wave myocardial infarction with a creatine kinase MB fraction value of 70 ng/mL or greater, or new Q-wave evidence of myocardial infarction by postoperative day 30. Because patients undergoing coronary artery bypass grafting with a valve procedure were not included in the primary population, separate analysis of death and myocardial infarction was conducted in 218 patients undergoing combined aortic valve replacement and coronary artery bypass grafting surgery. Results: Of the 353 patients randomized to any valve procedure, 106 (61%) underwent combined aortic valve replacement and coronary artery bypass grafting in the pexelizumab treatment group compared with 112 (63%) patients in the placebo group. Coronary artery bypass grafting was performed with 1 or more internal thoracic artery grafts in 139 (64%) patients and with 1 or more saphenous vein grafts in 179 (82%) patients. There were 4 (3.8%) deaths in the pexelizumab group versus 11 (9.9%) in the placebo group by postoperative day 30 and 6 (5.7%) deaths in the active group versus 16 (14.4%) in the placebo group by postoperative day 180 (P =.107 and P =.043, respectively, Fisher exact test). The incidence of myocardial infarction 30 days after surgical intervention was identical in the 2 groups, but the study was not designed to detect differences in this cohort of patients. Conclusions: Inhibition of complement activation by pexelizumab resulted in a decreased mortality at 180 days among 218 patients who underwent combined aortic valve replacement and coronary artery bypass grafting surgery. Additional studies are warranted to confirm this decrease in mortality with pexelizumab in combined aortic valve replacement and coronary artery bypass grafting procedures.
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页码:352 / 356
页数:5
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