Abstract |
In 434 operations for valvular heart disease, patients were randomised to receive Björk-Shiley, Edwards-Duromedics, or Medtronic-Hall mechanical prostheses. At a median follow-up time of 37.5 months there were no differences in hazard of death or non-embolic events. In the first six postoperative months the incidence of thromboembolism was about the same for the three valves. Subsequently, however, the incidence of thromboembolism for the Edwards-Duromedics valve was 3.9 times higher than for the Björk-Shiley valve, and for the Medtronic-Hall valve 2.6 times higher than for the Björk-Shiley valve.
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Authors | C E Kuntze, T Ebels, A Eijgelaar, J N Homan van der Heide |
Journal | Lancet (London, England)
(Lancet)
Vol. 1
Issue 8637
Pg. 514-7
(Mar 11 1989)
ISSN: 0140-6736 [Print] England |
PMID | 2564058
(Publication Type: Clinical Trial, Comparative Study, Journal Article, Randomized Controlled Trial)
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Topics |
- Adult
- Aged
- Aortic Valve
- Evaluation Studies as Topic
- Female
- Follow-Up Studies
- Heart Valve Prosthesis
(adverse effects, classification, mortality)
- Humans
- Male
- Middle Aged
- Mitral Valve
- Prospective Studies
- Random Allocation
- Thromboembolism
(etiology, mortality)
- Time Factors
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