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  • Oral presentation
  • Open Access

Patient-prosthesis mismatch did not impact postoperative course and hemodynamics after biosthetic mitral valve replacement

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Journal of Cardiothoracic Surgery20138 (Suppl 1) :O277

  • Published:


  • Public Health
  • Hospital Stay
  • Mitral Valve
  • Valve Replacement
  • Hospital Mortality


The clinical risk of patient-prosthesis mismatch (PPM) after mitral valve replacement (MVR) is still a matter of controversy. We investigated whether PPM in mitral bioprothesis affects the operative results or hemodynamic parameters.


From 2004 to 2012, 34 patients underwent MVR with bioprosthesis in our institution. Patient’s age was 74±4 years old and male/female ratio was 23/11.

We implanted three valves; Epic Supra® (SJM, Minnesota) in 8 (25mm;5, 27mm;3), Mosaic® (Medtronic, Minneapolis) in 15 (25mm;5, 27mm;8, 29mm;2), Carpentier Edwards Perimount® (Edwards, Los Angeles) in 11 patients (25mm;1, 27mm;8, 29mm;2). Sixteen patients (group P) had small indexed effective orifice area (EOAI ≤1.2 cm2/m2), and the remaining 18 patients (group N) had acceptable EOAI. We compared operative results and hemodynamic parameters recorded by echocardiography between both groups. We also evaluated correlation between predicted EOAI and hemodynamic parameters after MVR.


Hospital mortality was 0% in both groups. Hospital stay was 26.5±15.6 days in group P and 34.2±20.7 in group N (p:NS). There was no difference between both groups in postoperative EF (p=0.92), max PG (p=0.38), mean PG (p=0.59), and measured EOAI from pressure half time (p=0.18). No correlation was found between predicted EOAI and measured EOAI (R2=0.0011), mean PG (R2=0.0000) and max PG (R2=0.0004).


PPM did not affect operative results and postoperative hemodynamics in biopsoethetic MVR. Smaller valve might be alternative when large bioprosthesis is difficult to implant.

Authors’ Affiliations

Cardiovascular Surgery, Shinshu University, Matsumoto, Nagano, Japan


© Ichimura et al; licensee BioMed Central Ltd. 2013

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.