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Publication year
2002Source
Nederlands Tijdschrift voor Geneeskunde, 146, 12, (2002), pp. 545-548ISSN
Publication type
Article / Letter to editor

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Organization
Gynaecology
Journal title
Nederlands Tijdschrift voor Geneeskunde
Volume
vol. 146
Issue
iss. 12
Page start
p. 545
Page end
p. 548
Subject
Alle HP's en lijnenAbstract
Two women aged 39 and 30 years were investigated for possible coagulation disorders because of menorrhagia, anaemia and postoperative haemorrhages. These investigations revealed that they had type 1 Von Willebrand's disease. During the treatment with desmopressin, factor VIII and Von Willebrand factor (VWF) activity normalised. About one third of the patients referred to a gynaecologist for menorrhagia have an inherited bleeding disorder, of which type 1 Von Willebrand's disease is the most prevalent. Once a gynaecological cause of the menorrhagia has been excluded, or in the case of an increased risk on the basis of the medical history, a limited haemostatic investigation can establish or exclude an inherited coagulation disorder. For women with a coagulation disorder the menorrhagia can be treated. Surgical interventions can be carried out safely following treatment with desmopressin or factor VIII/VWF concentrates.
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