This Article Free upon publication Full Text Full Text (PDF) Data Supplement All Versions of this Article: 117/1/24    most recent CIRCULATIONAHA.106.685073v1 Alert me when this article is cited Alert me if a correction is posted Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Request Permissions Citing Articles Citing Articles via HighWire Citing Articles via Google Scholar Google Scholar Articles by Rouleau, J. L. Search for Related Content PubMed PubMed Citation Articles by Rouleau, J. L. Related Collections Other Treatment CV surgery: coronary artery disease Related Article

(Circulation. 2008;117:24-31.)
© 2008 American Heart Association, Inc.

Cardiovascular Surgery

Effects of Angiotensin-Converting Enzyme Inhibition in Low-Risk Patients Early After Coronary Artery Bypass Surgery

Jean L. Rouleau, MD; Wayne J. Warnica, MD; Richard Baillot, MD; Pierre J. Block, MD; Sidney Chocron, MD, PhD; David Johnstone, MD; Martin G. Myers, MD; Cristina-Dana Calciu, MD; Sonia Dalle-Ave, MD; Pierre Martineau, PharmD; Christine Mormont, PhD; Wiek H. van Gilst, PhD, for the IMAGINE (Ischemia Management with Accupril post–bypass Graft via Inhibition of the coNverting Enzyme) Investigators

From the Research Center, Montreal Heart Institute and University of Montreal (J.L.R.), Montreal, Quebec, Canada; Department of Cardiology, Foothills Hospital, University of Calgary (W.J.W.), Calgary, Alberta, Canada; Department of Cardiology, Hôpital Laval, Laval University (R.B.), Quebec City, Quebec, Canada; Department of Cardiology, Academisch Ziekenhuis Vrije Universiteit (P.J.B.), Brussels, Belgium; Department of Cardiology, Université of Franche-Comté (S.C.), Besançon, France; Walter C. McKenzie Health Sciences Center, Queen Elizabeth II Hospital, Dalhousie University (D.J.), Halifax, Nova Scotia, Canada; Medical Division, Sunnybrook and Women’s College Health Science Centre, University of Toronto (M.G.M.), Toronto, Ontario, Canada; Medical Division, Pfizer Canada (C.D.C., P.M., C.M.), Montreal, Quebec, Canada; Medical Division, Pfizer Canada (S.D.A.), Toronto, Ontario, Canada; and Medical Center, University Medical Center, University of Groningen (W.H.v.G.), Groningen, the Netherlands.

Correspondence to Jean-Lucien Rouleau, MD, Research Center, Montreal Heart Institute, 5000 Belanger St East, Montreal, Quebec, H1T 1C8, Canada. E-mail jean.rouleau{at}umontreal.ca

Received December 18, 2006; accepted October 15, 2007.

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.

---

 

CLINICAL PERSPECTIVE

Related Article:

Clinical Summaries
Circulation 2008 117: 1-3. [Extract] [Full Text]

This article has been cited by other articles:

				A. Miceli, R. Capoun, C. Fino, P. Narayan, A. J. Bryan, G. D. Angelini, and M. Caputo Effects of Angiotensin-Converting Enzyme Inhibitor Therapy on Clinical Outcome in Patients Undergoing Coronary Artery Bypass Grafting J. Am. Coll. Cardiol., November 3, 2009; 54(19): 1778 - 1784. [Abstract] [Full Text] [PDF]

				S. Chocron, R. Baillot, J. L. Rouleau, W. J. Warnica, P. Block, D. Johnstone, M. G. Myers, C. D. Calciu, A. Nozza, P. Martineau, et al. Impact of previous percutaneous transluminal coronary angioplasty and/or stenting revascularization on outcomes after surgical revascularization: insights from the imagine study Eur. Heart J., March 1, 2008; 29(5): 673 - 679. [Abstract] [Full Text] [PDF]

				H. L. Lazar All Coronary Artery Bypass Graft Surgery Patients Will Benefit From Angiotensin-Converting Enzyme Inhibitors Circulation, January 1, 2008; 117(1): 6 - 8. [Full Text] [PDF]