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European Journal of Cardio-Thoracic Surgery, Vol 5, 592-597, Copyright © 1991 by European Association for Cardio-thoracic Surgery
JB Garcia-Bengoechea, JR Gonzalez-Juanatey, J Rubio, D Duran and J Sierra
Between January 1977 and January 1989, 465 pericardial bioprostheses were
implanted in 424 patients. The mean age of patients was 59.1 years (range
16-81 y.) At the time of surgery, 68% of the patients suffered from chronic
atrial fibrillation. Mitral valve replacement was performed in 167
patients, aortic valve replacement in 216, multiple replacement in 40 (36
mitral and aortic, 3 mitral and tricuspid, and 1 mitral, aortic and
tricuspid), and 1 pulmonary valve replacement. The different types of
pericardial valve used were: Ionescu-Shiley 408, Mitral Medical 23, Bioflo
30, and Hancock 4. Hospital mortality was 10.1% with an attrition rate of
1.8 episodes per 100 patients/year. The 12-year actuarial survival rate was
65.1%. No patient underwent long- term anticoagulant treatment. The first
144 patients undergoing mitral and multiple valve replacements received
temporary anticoagulation for the first 8 weeks after surgery. There was no
valve thrombosis observed. Altogether 19 thromboembolic events (6 early and
13 late) were clinically documented. One patient died after an embolic
event. The linearized rates of thromboembolism were 1.64 episodes per 100
patients/year for mitral and multiple valve replacements and 0.33 episodes
per 100 patients/year for aortic valve replacement, with an overall rate of
1.0 episodes per 100 patients/year. Excluding early thromboembolism, the
linearized rate was 1.02 episodes per 100 patients/year overall. The
actuarial freedom from embolism was 92.4% overall, 88.2% for the mitral and
multiple valve replacement group, and 97.6% for the aortic valve
replacement group at a maximum follow-up of 12 years.(ABSTRACT TRUNCATED AT
250 WORDS)
ARTICLES
Thromboembolism in patients with pericardial valves in the absence of chronic anticoagulation: 12 years' experience
Department of Cardiac Surgery, Hospital Xeral de Galicia, University of Santiago, School of Medicine, Spain.
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