American Journal of Cardiology
Volume 102, Issue 5 , Pages 546-551, 1 September 2008

Impact of Perioperative Myocardial Infarction on Angiographic and Clinical Outcomes Following Coronary Artery Bypass Grafting (from PRoject of Ex-vivo Vein graft ENgineering via Transfection [PREVENT] IV)

  • James M. Yau, MD

      Affiliations

    • Duke University Medical Center, Durham, North Carolina
  • ,
  • John H. Alexander, MD, MHS

      Affiliations

    • Duke University Medical Center, Durham, North Carolina
    • Duke Clinical Research Institute, Durham, North Carolina
    • Corresponding Author InformationCorresponding author: Tel: 919-668-8955; Fax: 919-668-7085
  • ,
  • Gail Hafley, MS

      Affiliations

    • Duke Clinical Research Institute, Durham, North Carolina
  • ,
  • Kenneth W. Mahaffey, MD

      Affiliations

    • Duke University Medical Center, Durham, North Carolina
    • Duke Clinical Research Institute, Durham, North Carolina
  • ,
  • Michael J. Mack, MD

      Affiliations

    • Cardiopulmonary Research Science & Technology Institute, Dallas, Texas
  • ,
  • Nicholas Kouchoukos, MD

      Affiliations

    • Missouri Baptist Medical Center, St. Louis, Missouri
  • ,
  • Abhinav Goyal, MD, MHS

      Affiliations

    • Duke University Medical Center, Durham, North Carolina
    • Duke Clinical Research Institute, Durham, North Carolina
  • ,
  • Eric D. Peterson, MD, MPH

      Affiliations

    • Duke University Medical Center, Durham, North Carolina
    • Duke Clinical Research Institute, Durham, North Carolina
  • ,
  • C. Michael Gibson, MD

      Affiliations

    • PERFUSE Angiographic Laboratory, Boston, Massachusetts
  • ,
  • Robert M. Califf, MD

      Affiliations

    • Duke University Medical Center, Durham, North Carolina
    • Duke Clinical Research Institute, Durham, North Carolina
  • ,
  • Robert A. Harrington, MD

      Affiliations

    • Duke University Medical Center, Durham, North Carolina
    • Duke Clinical Research Institute, Durham, North Carolina
  • ,
  • T. Bruce Ferguson, MD

      Affiliations

    • East Carolina State University, Greenville, North Carolina
  • ,
  • PREVENT IV Investigators

Received 11 February 2008; received in revised form 17 April 2008; accepted 17 April 2008. published online 07 July 2008.

Myocardial infarction (MI) after coronary artery bypass grafting (CABG) is associated with significant morbidity and mortality. Frequency, management, mechanisms, and angiographic and clinical outcomes associated with perioperative MI remain poorly understood. PREVENT IV was a multicenter, randomized, placebo-controlled trial of edifoligide in 3,014 patients undergoing CABG. Angiographic and 2-year clinical follow-up were complete for 1,920 and 2,956 patients, respectively. Perioperative MI was defined as creatinine kinase-MB increase ≥10 times the upper limit of normal or ≥5 times the upper limit of normal with new 30-ms Q waves within 24 hours of surgery. Baseline characteristics, in-hospital management, and angiographic and clinical outcomes of patients with and without perioperative MI were compared. Perioperative MI occurred in 294 patients (9.8%). Patients with perioperative MI had longer surgery (250 vs 230 minutes; p <0.001), more on-pump surgery (83% vs 78%; p = 0.048), and worse target-artery quality (p <0.001). Patients with perioperative MI more frequently underwent angiography within 30 days of enrollment (1.7% vs 0.6%; p = 0.021). One-year angiographic vein graft failure occurred in 62.4% of patients with and 43.8% of patients without perioperative MI (p <0.001). Two-year composite clinical outcome (death, MI, or revascularization) was worse in patients with perioperative MI before (19.4% vs 15.2%; p = 0.039) and after (hazard ratio 1.33, 95% confidence interval 1.00 to 1.76, p = 0.046) adjusting for differences in significant predictors. In conclusion, perioperative MI was relatively common, was associated with worse outcomes, and mechanisms other than vein graft failure accounted for a substantial proportion of these MIs. Further research is needed into the prevention and treatment of perioperative MI in patients undergoing CABG.

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 This work was supported by the Duke Clinical Research Institute, Durham, North Carolina. The PREVENT-IV Trial was supported by Corgentech Inc., South San Francisco, California. Dr. Alexander, G. Hafley, Dr. Mahaffey, Dr. Mack, Dr. Kouchoukos, Dr. Goyal, Dr. Peterson, Dr. Gibson, Dr. Califf, Dr. Harrington, and Dr. Ferguson received research funding from Corgentech Inc. for their participation in PREVENT IV.

PII: S0002-9149(08)00748-0

doi:10.1016/j.amjcard.2008.04.069

American Journal of Cardiology
Volume 102, Issue 5 , Pages 546-551, 1 September 2008