Effects of angiotensin-converting enzyme inhibition in low-risk patients early after coronary artery bypass surgery

被引:127
作者
Rouleau, Jean L. [1 ,2 ]
Warnica, Wayne J. [3 ]
Baillot, Richard [4 ]
Block, Pierre J. [5 ]
Chocron, Sidney [6 ]
Johnstone, David [7 ]
Myers, Martin G. [8 ]
Calciu, Cristina-Dana [9 ]
Dalle-Ave, Sonia [10 ]
Martineau, Pierre [9 ]
Mormont, Christine [9 ]
van Gilst, Wiek H. [11 ]
机构
[1] Montreal Heart Inst, Res Ctr, Montreal, PQ H1T 1C8, Canada
[2] Univ Montreal, Montreal, PQ, Canada
[3] Univ Calgary, Foothills Hosp, Dept Cardiol, Calgary, AB, Canada
[4] Univ Laval, Hop Laval, Dept Cardiol, Quebec City, PQ, Canada
[5] Vrije Univ Brussel, Acad Ziekenhuis, Dept Cardiol, Brussels, Belgium
[6] Univ Franche Comte, Dept Cardiol, F-25030 Besancon, France
[7] Dalhousie Univ, Queen Elizabeth Hosp 2, Walter C McKenzie Hlth Sci Ctr, Halifax, NS, Canada
[8] Univ Toronto, Sunnybrook & Womens Coll, Hlth Sci Ctr, Div Med, Toronto, ON, Canada
[9] Pfizer Canada, Div Med, Montreal, PQ, Canada
[10] Pfizer Canada, Div Med, Toronto, ON, Canada
[11] Univ Groningen, Univ Med Ctr, Med Ctr, Groningen, Netherlands
关键词
cardiopulmonary bypass; coronary disease; inhibitors; trials; vasodilation;
D O I
10.1161/CIRCULATIONAHA.106.685073
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background-Early after coronary artery bypass surgery (CABG), activation of numerous neurohumoral and endogenous vasodilator systems occurs that could be influenced favorably by angiotensin-converting enzyme inhibitors. Methods and Results-The Ischemia Management with Accupril post -bypass Graft via Inhibition of the coNverting Enzyme (IMAGINE) trial tested whether early initiation (<= 7 days) of an angiotensin-converting enzyme inhibitor after CABG reduced cardiovascular events in stable patients with left ventricular ejection fraction >= 40%. The trial was a double-blind, placebo-controlled study of 2553 patients randomly assigned to quinapril, target dose 40 mg/d, or placebo, who were followed up to a maximum of 43 months. The mean (SD) age was 61 (10) years. The incidence of the primary composite end point (cardiovascular death, resuscitated cardiac arrest, nonfatal myocardial infarction, coronary revascularization, unstable angina or heart failure requiring hospitalization, documented angina, and stroke) was 13.7% in the quinapril group and 12.2% in the placebo group (hazard ratio 1.15, 95% confidence interval 0.92 to 1.42, P = 0.212) over a median follow-up of 2.95 years. The incidence of the primary composite end point increased significantly in the first 3 months after CABG in the quinapril group (hazard ratio 1.52, 95% confidence interval 1.03 to 2.26, P = 0.0356). Adverse events also increased in the quinapril group, particularly during the first 3 months after CABG. Conclusions-In patients at low risk of cardiovascular events after CABG, routine early initiation of angiotensin-converting enzyme inhibitor therapy does not appear to improve clinical outcome up to 3 years after CABG; however, it increases the incidence of adverse events, particularly early after CABG. Thus, early after CABG, initiation of angiotensin-converting enzyme inhibitor therapy should be individualized and continually reassessed over time according to risk.
引用
收藏
页码:24 / 31
页数:8
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