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The Annals of Thoracic Surgery, Vol 48, 280-283, Copyright © 1989 by The Society of Thoracic Surgeons
VJ DiSesa, JJ Collins Jr and LH Cohn
We examined hematological complications in 415 patients having valve
replacement with the St. Jude mechanical prosthesis (212, aortic valve
replacement [AVR]; 159, mitral valve replacement [MVR]; and 44, AVR + MVR).
There were 164 men and 251 women with a mean age of 59 years (range, 20 to
88 years). Preoperatively 386 patients were in New York Heart Association
functional classes III and IV. There were 154 associated procedures (37%),
the most common being myocardial revascularization. Overall hospital
mortality was 7.5% (31/415), 7% after AVR, 8% after MVR, and 7% after AVR +
MVR. All operative survivors were anticoagulated with Coumadin (crystalline
warfarin sodium) to maintain the prothrombin time at 1.5 times control.
During a mean follow-up of 21 months (range, 6 to 60 months), there were 29
late deaths (7.6%) and 5 patients (1.3%) lost to follow-up. No patient
experienced structural valve degeneration. At 48 months, actuarial freedom
from thromboembolism was 87% +/- 3% after AVR and 91% +/- 9% after MVR;
from anticoagulation-related hemorrhage, 97% +/- 3% after AVR and 91% +/-
3% after MVR; and from hemolysis, 100% after AVR and 98% +/- 2% after MVR.
Freedom from all valve-related morbidity at 4 years was 82% +/- 5% after
AVR and 75% +/- 10% after MVR. Actuarial survival at 48 months was 80% +/-
4% after AVR and 65% +/- 7% after MVR.
ARTICLES
Hematological complications with the St. Jude valve and reduced-dose Coumadin
Division of Cardiac Surgery, Brigham and Women's Hospital, Boston, Massachusetts 02115.
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