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Differentiation of patients with subtype IIb‐like von Willebrand's disease by means of perfusion experiments with reconstituted blood
Author(s) -
Sakariassen Kjell S.,
Nieuwenhuis H. Karel,
Sixma Jan J.
Publication year - 1985
Publication title -
british journal of haematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.907
H-Index - 186
eISSN - 1365-2141
pISSN - 0007-1048
DOI - 10.1111/j.1365-2141.1985.tb07333.x
Subject(s) - platelet , ristocetin , von willebrand factor , von willebrand disease , bleeding diathesis , medicine , perfusion , bleeding time , cryoprecipitate , coagulopathy , endocrinology , immunology , gastroenterology , chemistry , platelet aggregation
S ummary Four unrelated patients with a bleeding diathesis (bleeding time longer than 30 min), some spontaneous platelet aggregation, thrombocytopenia and large platelets, had decreased levels of factor VIII‐von Willebrand factor (FVIII‐VWF) related properties and impaired platelet adherence to human artery subendothelium. The largest multimers of plasma FVIII‐VWF were absent and enhanced ristocetin induced platelet aggregation in platelet‐rich plasma was observed. ‘Pseudo‐von Willebrand's disease’ was excluded, because FVIII‐VWF from normal subjects did not initiate platelet aggregation. Perfusion studies with reconstituted blood, consisting of respectively patient platelets in normal plasma or normal platelets in patient plasma, yielded evidence for an intrinsic platelet abnormality in two out of the four patients and a plasma defect in the other two patients. Similar experiments with platelets and plasma from four patients with von Willebrand's disease (VWD) subtype I and four patients with VWD subtype IIa showed that the impaired platelet adherence in blood from these patients was caused by a plasma defect. These experiments indicate that patients with laboratory findings in many respects similar to those originally reported for patients with VWD subtype IIb may represent a heterogeneous group of individuals. The data derived from our study imply that perfusion experiments with reconstituted blood offer a new approach in characterization of these patients, which may be more relevant for the treatment of the patients than characterization by ristocetin induced adsorption of FVIII‐VWF to platelets.