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Vivek Rao
George T. Christakis
Richard D. Weisel
Michael A. Borger
Gideon Cohen
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J Thorac Cardiovasc Surg 2002;123:928-935
© 2002 The American Association for Thoracic Surgery


Cardiopulmonary Support and Physiology (CSP)

The Insulin Cardioplegia Trial: Myocardial protection for urgent coronary artery bypass grafting

Vivek Rao, MD, PhD, George T. Christakis, MD, Richard D. Weisel, MD, Joan Ivanov, PhD, Michael A. Borger, MD, PhD, Gideon Cohen, MD, PhD For the ICT Investigators

From the Division of Cardiovascular Surgery, Toronto General Hospital and Sunnybrook and Women's College Health Centre, University of Toronto, Toronto, Ontario, Canada.

Supported by the Medical Research Council of Canada (grant MT13513) and the Heart and Stroke Foundation of Ontario (grants NA3767 and NA4189).

Received for publication May 29, 2001. Revisions requested July 11, 2001; revisions received Nov 2, 2001. Accepted for publication Nov 12, 2001. Address for reprints: Vivek Rao, MD, PhD, Division of Cardiovascular Surgery, EN 14-222, Toronto General Hospital, 200 Elizabeth St, Toronto, Ontario, Canada M5G 2C4 (E-mail: Vivek.Rao{at}uhn.on.ca).

Background: Small, nonrandomized clinical trials have demonstrated a beneficial effect of solutions containing insulin and glucose on the recovery of myocardial metabolism and ventricular function after cardioplegic arrest and reperfusion. However, no large, blinded, randomized study has yet determined the effects of insulin-enhanced cardioplegia on clinical outcomes after coronary artery bypass grafting.
Methods: The Insulin Cardioplegia Trial was designed to evaluate the clinical impact of insulin-enhanced cardioplegia on patients at high risk undergoing isolated coronary artery bypass grafting for unstable angina. A total of 1127 patients were randomly assigned at operation to receive cardioplegic solution supplemented with 10 IU/L insulin (n = 557) or placebo (n = 570). All personnel with direct patient contact were blinded to randomization group.
Results: Overall operative mortality was 2.2%, with no significant differences between groups. The prevalences of postoperative low output syndrome (insulin 10.4%, placebo 9.7%, P = .7) and enzymatic myocardial infarction (insulin 21.0%, placebo 18.8%, P = .3) were not different between groups. The primary composite outcome of low output syndrome and/or enzymatic myocardial infarction revealed no difference between groups (insulin 30.0%, placebo 26.3%, P = .2).
Conclusions: Despite encouraging results from smaller, nonrandomized studies, the Insulin Cardioplegia Trial failed to demonstrate a clinical benefit of insulin-enhanced cardioplegic solution for patients undergoing high-risk isolated coronary artery bypass grafting.


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