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The Annals of Thoracic Surgery, Vol 51, 683-684, Copyright © 1991 by The Society of Thoracic Surgeons
LH Cohn
The Hancock porcine xenograft valve was the first commercially prepared,
quality-controlled tissue valve. The National Institutes of Health group
began implantation of this valve in 1970 and reported on the first 5 years
of their results, which was one of the longest follow- ups of that valve at
that particular time. Since then there have been a number of centers that
have had long-term experience with thousands of these valves. In
retrospect, it is now clear that some of the conclusions made by the
National Institutes of Health group have not come to pass, such as this
valve being the "valve of choice" for all patients. "Valve of choice" is a
relative term and may be one valve for one patient and another valve for
another patient. This report was important in bringing together some of the
first medium-term data and pointing out that, even in this valve, there was
some small degree of thromboembolism. The paper also provided a historical
look at the methods of data analysis that were in use in the early 1970s
compared with those now used in 1991. Actuarial curves were not yet
commonly used, nor were percent/patient-year linearized results. Valve
types were mixed as well. Hemodynamic data, always a strong point of
National Institutes of Health data analysis, were excellent. The use of
this valve became a fairly standard device and has been retrospectively
analyzed by a number of centers, suggesting that now it is better used in
the older patient or in patients who cannot take warfarin sodium.(ABSTRACT
TRUNCATED AT 250 WORDS)
ARTICLES
Atrioventricular valve replacement with a Hancock porcine xenograft
Department of Surgery, Harvard Medical School, Boston, Massachusetts.
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