Hancock, and Carpentier-Edwards heart valve prostheses

From 1975 to 1979, 540 patients undergoing valve replacement were entered into a randomized trial and received either a Bjdrk-Shiley (273 patients) or a porcine heterograft prosthesis (initially a Hancock valve [107 patients] and later a Carpentier-Edwards prosthesis [ 160 patients]). Two hundred and sixty-two patients required mitral valve replacement, 210 required aortic valve replacement, 60 required mitral and aortic valve replacement, and eight also required associated tricuspid valve replacement (six mitral valve replacement; two mitral plus aortic valve replacement). Analysis of 34 preoperative and operative variables showed the treatment groups to be well randomized. In-hospital mortality was not significantly different among patients receiving the three prostheses for aortic valve replacement (7.6% overall) and mitral plus aortic valve replacement (10% overall), but there was a higher in-hospital mortality for patients undergoing mitral valve replacement with the CarpentierEdwards prosthesis (15.5% compared with 8.8% overall; p = .03). This difference could not be explained on the basis of any preoperative or operative variable. Median follow-up was 5.6 (range 2.8 to 8.3) years. Actuarial survival after mitral valve replacement was 56.7 + 7.0% at 7 years, that after aortic valve replacement was 69.6 ± 9.6% at 7 years, and that after mitral plus aortic valve replacement was 62.5 ± 20.0% at 7 years. There was no significant difference in actuarial survival of patients receiving the three prostheses within the mitral, aortic, and mitral plus aortic valve replacement groups, nor was there a difference when these groups were amalgamated. Thirty-seven patients required reoperation for valve failure (15 with Bjbrk-Shiley, 12 with Hancock, and 10 with Carpentier-Edwards valves; p = NS) and 11 died at reoperation (four with Bjdrk-Shiley, four with Hancock, and three with Carpentier-Edwards valves; overall operative mortality 29.7%). Up to 7 years after surgery, there was no significant difference in the incidence of thromboembolism in patients with the different prostheses undergoing mitral or aortic valve replacement. There were too few patients undergoing mitral plus aortic valve replacement for meaningful comparison. There was no significant beneficial effect of anticoagulants in patients undergoing mitral or aortic valve replacement with porcine prostheses, but patients were not randomly allocated to anticoagulant treatment. All patients with Bjdrk-Shiley prostheses received anticoagulants. Multivariate analysis of factors associated with embolism identified atrial fibrillation with mitral valve replacement (p < .001) and age less than 65 years (p < .01) and a rheumatic cause of valvular disease (p < .01) with aortic valve replacement. The risks of anticoagulation were low, with an overall incidence of complications of approximately one per 100 years treatment. To date no significant advantage of any of the three prostheses has been observed, but further follow-up is necessary because important differences may yet emerge. Circulation 73, No. 6, 1213-1222, 1986. From the Departments of Cardiology and Cardiac Surgery, Royal IN THE EARLY 1970s glutaraldehyde-treated porcine Infirmary, the Department of Cardiology, Western General Hospital, valves mounted on a wire stent were introduced for and the Medical Computing and Statistics Unit, University of Edincardiac valve replacement and appeared in initial burgh, Edinburgh, Scotland. Supported by a grant from the Scottish Home and Health Department. short-term studies to be durable and to carry a reduced Address for correspondence: Dr. Hugh C. Miller, Department of risk of thromboembolism compared with mechanical Cardiology, Royal Infirmary, Edinburgh, Scotland. ls e Received Oct. 17, 1985; revision accepted Jan. 23, 1986. prostheses. Presented in part at the 58th Scientific Sessions of the American Heart However, in 1975 the long-term results with porcine Association, Washington, D.C., November 1985. heterograft prostheses had not been evaluated in a pro*Current address: Department of Cardiac Surgery, Glasgow Royal Infirmary, Glasgow, Scotland. spective trial, so we commenced a prospective ran1213 Vol. 73, No. 6, June 1986 by gest on N ovem er 2, 2017 http://ciajournals.org/ D ow nladed from