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Comparison of the Carpentier-Edwards Perimount™ and St. Jude Medical Epic™ Bioprostheses for Aortic Valve Replacement—A Retrospective Echocardiographic Short-Term Study
Authors:Andreas Goetzenich,M.D.,&dagger  ,Georg Langebartels,M.D.,&Dagger  ,Stefan Christiansen,M.D.,Ph.D.,§  ,Nima Hatam,M.D.,Rü  diger Autschbach,M.D.,Ph.D., Guido Dohmen,M.D.
Affiliation:Department of Cardiothoracic Surgery, University of Aachen, Aachen, Germany;;Department of Anaesthesiology, University of Aachen, Aachen, Germany;;Department of Cardiothoracic Surgery, University of Cologne, Cologne, Germany;;and Department of Cardiac Surgery, University of Lübeck, Lübeck, Germany
Abstract:Abstract   Objective: Stented biological prostheses show different performance related to their design and ultrastructure. Therefore, we compared the Carpentier-Edwards Perimount™ (Edwards Lifesciences, Irvine, CA, USA) and the St. Jude Medical Epic™ (SJM Epic™; St. Jude Medical Inc., St. Paul, MN, USA) prostheses with respect to their hemodynamic features. Methods: Eighty-six patients underwent aortic valve replacement for severe aortic stenosis (50 patients), aortic regurgitation (seven patients), or mixed lesion (29 patients) with these randomly assigned bioprostheses (Perimount™: 39 patients; SJM Epic™: 47 patients). Following informed consent, patients were examined postoperatively (mean 9.7 ± 4 months after surgery) with a detailed echocardiographic study, quality of life was determined by a standardized questionnaire. Results: Comparing the indexed effective orifice area (0.77 cm2/m2 vs. 0.64 cm2/m2; p = 0.019), the mean pressure gradient (11.15 mmHg vs. 14.80 mmHg; p = 0.004) and the stroke-work loss (6.95% vs. 8.49%; p = 0.025), the Carpentier-Edwards Perimount™ demonstrated significantly better hemodynamic features than the SJM Epic™ prosthesis. These effects were more pronounced in the smaller prosthetic sizes. Conclusion: The Carpentier-Edwards Perimount™ prosthesis was less obstructive than the SJM Epic™ in echocardiographic controls. Patient-prosthesis mismatch as determined by indexed effective orifice area showed no impact on functional recovery.
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