Literature DB >> 308120

Aortic valve replacement in von Willebrand's disease.

P H Young, J D Bouhasin, H B Barner.   

Abstract

A patient with von Willebrand's disease having aortic valve replacement was managed with cryoprecipitate infusions and monitoring of factor VIII levels. This disorder is associated with low factor VIII levels and abnormal platelet function. There may be no history of bleeding, as the severity of the bleeding tendency varies greatly and fluctuates temporally. The partial thromboplastin time is frequently prolonged, but more detailed studies are necessary to establish a diagnosis (bleeding time, platelet adhesiveness to glass beads and ristocetin, von Willebrand's antigen, ristocetin-von Willebrand's factor, and factor VIII clotting activity). Elevation of factor VIII levels to 50 to 100% of normal allows adequate clotting and is best accomplished with cryoprecipitate or fresh frozen plasma rather than commercial concentrates of factor VIII, whose activity is unpredictable.

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Year:  1978        PMID: 308120

Source DB:  PubMed          Journal:  J Thorac Cardiovasc Surg        ISSN: 0022-5223            Impact factor:   5.209


  2 in total

1.  Atherosclerosis and a coronary artery bypass operation in a woman with von Willebrand disease.

Authors:  R A Moss; R R Mena; R J Morin
Journal:  West J Med       Date:  1980-12

2.  Surgical correction of coarctation of the aorta and ventricular septal defect in an infant with inherited factor V deficiency.

Authors:  J Losay; J P Binet; Y Bogaty; M Samama
Journal:  Pediatr Cardiol       Date:  1983 Apr-Jun       Impact factor: 1.655

  2 in total

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