A subgroup analysis of the impact of prerandomization antithrombin therapy on outcomes in the SYNERGY trial: Enoxaparin versus unfractionated heparin in non-ST-segment elevation acute coronary syndromes

被引:69
作者
Cohen, Marc
Mahaffey, Kenneth W.
Pieper, Karen
Pollack, Charles V.
Antman, Elliott M.
Hoekstra, James
Goodman, Shaun G.
Langer, Anatoly
Col, Jacques J.
White, Harvey D.
Califf, Robert M.
Ferguson, James J.
机构
[1] Duke Clin Res Inst, Durham, NC USA
[2] Newark Beth Israel Med Ctr, HEART Hosp New Jersey, Newark, NJ USA
[3] Wake Forest Univ, Winston Salem, NC 27109 USA
[4] Univ Penn, Sch Med, Penn Hosp, Philadelphia, PA 19104 USA
[5] Brigham & Womens Hosp, Boston, MA 02115 USA
[6] Univ Toronto, Canadian Heart Res Ctr, Toronto, ON, Canada
[7] Univ Toronto, Terrence Donnelly Heart Ctr, St Michaels Hosp, Toronto, ON, Canada
[8] Clin Univ St Luc, B-1200 Brussels, Belgium
[9] Green Lane Hosp, Auckland 3, New Zealand
[10] St Lukes Episcopal Hosp, Texas Heart Inst, Houston, TX 77030 USA
关键词
D O I
10.1016/j.jacc.2006.05.058
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVES The purpose of this study was to compare the effect of receiving pretreatment with antithrombin before randomization as well as overall efficacy and safety of enoxaparin versus unfractionated heparin (UFH) in the SYNERGY (Superior Yield of the New Strategy of Enoxaparin, Revascularization, and Glycoprotein IIb/IIIa Inhibitors) trial. BACKGROUND The SYNERGY trial results demonstrated noninferiority in outcomes with enoxaparin compared with UFH. Randomized treatment was independent of prerandornization treatment. METHODS Analyses were first performed on the 4 prerandomization subgroups: patients who received no antithrombin therapy and those who were treated with enoxaparin or UFH or both. Then, we focused on the subgroup of patients who received no pretreatment or were pretreated with and randomized to the same drug. Of the 9,978 patients, 2,440 did not receive prerandomization therapy and 6,138 received consistent therapy through randomization. The primary end point was the composite of death and nonfatal myocardial infarction (MI) at 30 days. RESULTS After adjustment for differences among the subgroups, no significant difference in the association between the 4 pretreatment groups and death or MI remained (p = 0.171). The randomized treatment effect on 30-day death or MI tended to vary with pretreatment (p = 0.055 for interaction test after adjustment). Patients who received consistent therapy with enoxaparin had significantly less death or MI than patients randomized to UFH (adjusted p = 0.041) with a trend toward increased bleeding. CONCLUSIONS Treatment with antithrombin therapy before randomization had potential impact on comparison of study drug effects. After adjustment for differences in baseline characteristics between subgroups, consistent therapy with enoxaparin might be superior to UFH in reducing death or nonfatal MI, with a modest excess in bleeding.
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收藏
页码:1346 / 1354
页数:9
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