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Human von Willebrand factor/factor VIII concentrates in the management of pediatric patients with von Willebrand disease/hemophilia A

Authors :
Castaman G
Linari S
Source :
Therapeutics and Clinical Risk Management, Vol 2016, Iss Issue 1, Pp 1029-1037 (2016)
Publication Year :
2016
Publisher :
Dove Medical Press, 2016.

Abstract

Giancarlo Castaman, Silvia Linari Department of Oncology, Center for Bleeding Disorders, Careggi University Hospital, Florence, ItalyAbstract: Several plasma-derived intermediate and high-purity concentrates containing von Willebrand factor (VWF) and factor VIII (FVIII) are currently available. The main role of these products in the management of pediatric the population is represented by the replacement therapy in patients with severe or intermediate forms of von Willebrand disease, in whom other treatments are ineffective or contraindicated. Another important role of VWF/FVIII concentrates in children may be their use in immune tolerance induction (ITI) protocols. ITI is particularly recommended for hemophilia A children who have developed an inhibitor against FVIII, currently the most serious complication of substitutive treatment in hemophilia. Although recombinant concentrates may represent the preferred option in children with hemophilia A, VWF/FVIII concentrates may offer an advantage in rescuing patients who failed previous ITI.Keywords: von Willebrand factor, factor VIII, plasma-derived concentrates, children, von Willebrand disease, hemophilia A

Details

Language :
English
ISSN :
1178203X
Volume :
2016
Issue :
Issue 1
Database :
Directory of Open Access Journals
Journal :
Therapeutics and Clinical Risk Management
Publication Type :
Academic Journal
Accession number :
edsdoj.57aca2fd779b4b4eabd54cb7234f269d
Document Type :
article