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Eur J Cardiothorac Surg 2006;30:1
© 2006 Elsevier Science NL
Editorial |
a University of Southern California, 2025 Zonal Avenue, Los Angeles, CA 90033, USA
b Griffith Center, Division of Cardiovascular Medicine, Department of Medicine, LAC+USC Medical Center, Keck School of Medicine at USC, Los Angeles, CA, USA
* Corresponding author. Tel.: +1 323 226 7264; fax: +1 323 221 4428. (Email: rahimtoo{at}usc.edu).
Two papers in the current issue of the journal questioned whether valve prosthesis-patient mismatch (VP-PM) [1] is associated with an increased mortality and have come to different conclusions.
Howell et al. [2] have classified severe VP-PM as prosthetic aortic valve area (PHVA) <0.6 cm2/m2, which was determined at the time of valve implantation from the manufacturer's in vitro data. The survival (all-cause mortality) was not significantly different at 3 and 5 years from the reference group (PHVA
0.6 cm2/m2).
Walther et al. [3] have also classified PHVA from the manufacturer's effective office area. They have classified severe VP-PM as PHVA < 0.65 cm2/m2and moderate VP-PM as PHVA 0.650.85 cm2/m2. In their study, moderate VP-PM was independently predictive for short-term and long-term mortality.
Three recent studies have documented an increased mortality with VP-PM:
0.60 cm2/m2) was associated with lower survival (from all-cause mortality) than those with moderate or mild VP-PM. VP-PM was calculated from prosthesis internal orifice diameter, as provided by the manufacturer. The problem with these studies as with other similar studies is the use of the manufacturer stated orifice size, using different criteria for grading severity of VP-PM and not determining the causes of death. To be able to address correctly the issue of mortality in patients with VP-PM the following data should be obtained:
0.6 cm2/m2 (it is not possible to measure PHVA with any degree of precision to a hundredth of a centimeter) [7]; and References
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