Abstract
The incidence of thrombotic and thromboembolic (TE) complications after Hancock valve replacement was reviewed in 140 patients with mitral valve prostheses and 150 patients with aortic valve prostheses. In patients with aortic valves, 1 embolus occurred and another patient was found at autopsy to have thrombi on a degenerated valve. Both patients had been on aspirin treatment. There was no TE event in patients receiving no anticoagulant therapy.
In patients with mitral valves, 16 showed pre- and/or postoperative low output syndrome (Group A); 8 of these patients died and 6 had autopsies that showed major thrombi in the heterograft. In 126 long-term survivors, 9 thromboembolic events occurred (TE incidence 5.4% per patient year). All patients with emboli had atrial fibrillation. The majority (7/9) of emboli occurred during the first 3 postoperative months. Five occurred in patients who were not on anticoagulation (Group B), and 2 occurred in patients receiving warfarin therapy (Group C). There was no thromboembolic event in patients receiving aspirin treatment (Group D).
It is concluded that patients with Hancock aortic valves have a very small risk of TE, and do not need anticoagulation. Patients with Hancock mitral valves with stable hemodynamics have a decreased risk of TE and do not require anticoagulation. Patients with atrial fibrillation have an increased risk of TE and should be on warfarin for 3 months after surgery and then on aspirin therapy.
Résumé
Nous avons revu la fréquence des thromboses et des thrombo-embolies (TE) après remplacement valvulaire par valve de Hancock, chez 140 patients porteurs d'une prothèse mitrale et 150 avec prothèse aortique. Chez les malades avec valve aortique, nous avons observé un embol et, à l'autopsie d'un autre cas, une thrombose sur une valve dégénérée. Les 2 malades avaient reçu de l'aspirine. Il n'y a pas eu de TE chez les patients ne recevant pas d'anticoagulants. Parmi les patients avec valve mitrale, 16 avaient, avant et/ou après l'opération, un syndrome de débit bas (groupe A): 8 sont décédés, dont 6 avaient, à l'autopsie, des thrombi importants sur l'hétérogreffe. Parmi 126 survivants à long terme, 9 accidents thrombo-emboliques ont été observés (fréquence: 5.4% par patient/année). Tous les malades qui ont fait une embolie avaient une fibrillation auriculaire. La majorité des embolies (7/9) sont survenues dans les 3 mois post-opératoires, dont 5 chez les malades ne recevant pas d'anticoagulants (groupe B) et 2 chez les patients sous warfarine (groupe C). Il n'y a pas eu d'accident thrombo-embolique chez les malades recevant de l'aspirine (groupe D).
On peut donc conclure que les malades porteurs d'une valve aortique de Hancock ont un risque de TE très faible; ils n'ont pas besoin d'anticoagulation. Chez las malades porteurs d'une valve mitrale de Hancock, stables au point de vue hémodynamique, le risque de TE est réduit; l'anticoagulation n'est pas nécessaire. Chez les malades avec fibrillation auriculaire, le risque de TE est accru: ces patients doivent être mis sous warfarine pendant les 3 premiers mois post-opératoires, puis sous aspirine.
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Hetzer, R., Gerbode, F., Kerth, W.J. et al. Thrombotic complications after valve replacement with porcine heterografts. World J. Surg. 3, 505–510 (1979). https://doi.org/10.1007/BF01556120
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DOI: https://doi.org/10.1007/BF01556120