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Publication Detail
Cold blood cardioplegia or intermittent cross-clamping in coronary artery bypass grafting?
  • Publication Type:
    Journal article
  • Publication Sub Type:
    Clinical Trial
  • Authors:
    Liu Z, Valencia O, Treasure T, Murday AJ
  • Publication date:
    08/1998
  • Pagination:
    462, 465
  • Journal:
    Ann Thorac Surg
  • Volume:
    66
  • Issue:
    2
  • Status:
    Published
  • Country:
    Netherlands
  • Print ISSN:
    0003-4975
  • PII:
    S0003-4975(98)00446-9
  • Language:
    eng
  • Keywords:
    Aorta, Cold Temperature, Coronary Artery Bypass, Elective Surgical Procedures, Emergencies, Female, Heart Arrest, Induced, Humans, Intra-Aortic Balloon Pumping, Male, Middle Aged, Prospective Studies, Random Allocation, Ventricular Function
Abstract
BACKGROUND: We determined that cold blood cardioplegia and intermittent ventricular fibrillation with ischemia were associated with similar enzyme and myocardial protein leakage in a randomized, prospective study of 40 patients. We have continued to use both methods in our unit, according to surgeons' preference. METHODS: In our database we have reviewed 1,923 patients who have undergone first-time elective or urgent coronary artery bypass grafting from January 1992 to May 1997. RESULTS: Five hundred seventy-eight patients underwent coronary artery bypass grafting with cold blood cardioplegia and 1,345 had ventricular fibrillation and aortic cross-clamping. The preoperative factors were virtually identical. Intraoperative differences were only those inherent to the two techniques: temperature and cross-clamp time. Mortality was 2.5% for ventricular fibrillation and aortic cross-clamping arrest and 2.1% for cardioplegia (p=0.55 by chi2 test). There was a higher use of the intraaortic balloon pump in the ventricular fibrillation and aortic cross-clamping group (2.4% versus 1.0%; p=0.04), but no other differences in outcome were detected. CONCLUSIONS: A truly randomized trial to demonstrate which technique is superior is impractical at this level of difference because it would require 37,000 patients to avoid a beta error. We have to base our practice on the retrospective data available. Each technique has its merits in practice, which are discussed.
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