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Hematological complications with the St. Jude valve and reduced-dose Coumadin
Journal article   Open access   Peer reviewed

Hematological complications with the St. Jude valve and reduced-dose Coumadin

Verdi J. DiSesa, John J. Collins and Lawrence H. Cohn
The Annals of thoracic surgery, v 48(2), 280
01 Aug 1989
PMID: 2764619
url
https://europepmc.org/articles/pmc4698073View
Accepted (AM)Open Access (License Unspecified) Open

Abstract

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% alter 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; front 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.

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Web of Science research areas
Cardiac & Cardiovascular Systems
Respiratory System
Surgery
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