Literature DB >> 316311

Surgery in von Willebrand's disease.

I M Nilsson, S E Bergentz, S A Larsson.   

Abstract

Fifty-eight major surgical procedures were performed in 38 patients with von Willebrand's disease (VWD), one of the most common of the inheritable hemorrhagic disorders. Specific treatment with fraction I-0, (AHF-Kabi) in addition to a fibrinolytic inhibitor, was given to all patients. The effect of the treatment was checked by measuring the Duke bleeding time and factor VIII:C level. A marked difference between hemophilia and VWD from a surgical point of view is demonstrated. While most of the surgery in hemophiliacs is performed for severe joint deformities, contractures and blood cysts, surgery in VWD is mostly general surgery, often necessitated by massive hemorrhages from mucous membranes.

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Year:  1979        PMID: 316311      PMCID: PMC1345635          DOI: 10.1097/00000658-197912000-00014

Source DB:  PubMed          Journal:  Ann Surg        ISSN: 0003-4932            Impact factor:   12.969


  26 in total

1.  THE DUKE AND IVY METHODS FOR DETERMINATION OF THE BLEEDING TIME.

Authors:  I M NILSSON; S MAGNUSSON; C BORCHGREVINK
Journal:  Thromb Diath Haemorrh       Date:  1963-11-01

2.  Transfusion studies in von Willebrand's disease: effect on bleeding time and factor VIII.

Authors:  P CORNU; M J LARRIEU; J CAEN; J BERNARD
Journal:  Br J Haematol       Date:  1963-04       Impact factor: 6.998

3.  v. Willebrand's disease in Sweden; its pathogenesis and treatment.

Authors:  I M NILSSON; M BLOMBACK; B BLOMBACK
Journal:  Acta Med Scand       Date:  1959-06-30

4.  Von Willebrand's disease and its correction with human plasma fraction 1-0.

Authors:  I M NILSSON; M BLOMBACK; E JORPES; B BLOMBACK; S A JOHANSSON
Journal:  Acta Med Scand       Date:  1957-11-29

5.  von Willebrand's Disease : A Cause for Massive Postoperative Bleeding-Report of a Case.

Authors:  J E Arrants; P H Jordan; T F Newcomb
Journal:  Ann Surg       Date:  1962-11       Impact factor: 12.969

6.  Surgery of hemophiliacs--20 years' experience.

Authors:  I M Nilsson; U Hedner; A Ahlberg; S A Larsson; S E Bergentz
Journal:  World J Surg       Date:  1977-01       Impact factor: 3.352

7.  Characteristics of various factor VIII concentrates used in treatment of haemophilia A.

Authors:  I M Nilsson; U Hedner
Journal:  Br J Haematol       Date:  1977-12       Impact factor: 6.998

8.  A method for measuring plasma ristocetin cofactor activity. Normal distribution and stability during storage.

Authors:  M Zuzel; I M Nilsson; M Aberg
Journal:  Thromb Res       Date:  1978-05       Impact factor: 3.944

9.  The secondary bleeding time; a new method for the differentiation of hemorrhagic diseases.

Authors:  C F BORCHGREVINK; B A WAALER
Journal:  Acta Med Scand       Date:  1958-11-27

10.  On an inherited autosomal hemorrhagic diathesis with antihemophilic globulin (AHG) deficiency and prolonged bleeding time.

Authors:  I M NILSSON; M BLOMBACK; I VON FRANCKEN
Journal:  Acta Med Scand       Date:  1957-10-30
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  4 in total

1.  Management of intraventricular haemorrhage secondary to ruptured arteriovenous malformation in a child with von Willebrand's disease.

Authors:  R K Osenbach; C M Loftus; A H Menezes; J Biller; R Tannous; W T Yuh
Journal:  J Neurol Neurosurg Psychiatry       Date:  1989-12       Impact factor: 10.154

2.  The use of blood components in the treatment of congenital coagulation disorders.

Authors:  I M Nilsson; S A Larsson; S E Bergentz
Journal:  World J Surg       Date:  1987-02       Impact factor: 3.352

3.  Medical evaluation before operation.

Authors:  D L Elliot; D H Linz; J A Kane
Journal:  West J Med       Date:  1982-10

Review 4.  Disorders of platelet function: mechanisms, diagnosis and management.

Authors:  L B Huebsch; L A Harker
Journal:  West J Med       Date:  1981-02
  4 in total

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