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Title: [Inhibitor development after changing FVIII/IX products in patients with haemophilia]. Author: Kocher S, Asmelash G, Makki V, Müller S, Krekeler S, Alesci S, Miesbach W. Journal: Hamostaseologie; 2012; 32 Suppl 1():S39-42. PubMed ID: 22961330. Abstract: UNLABELLED: The retrospective observational study surveys the relationship between development of inhibitors in the treatment of haemophilia patients and risk factors such as changing FVIII products. A total of 119 patients were included in this study, 198 changes of FVIII products were evaluated. RESULTS: During the observation period of 12 months none of the patients developed an inhibitor, which was temporally associated with a change of FVIII products. A frequent change of FVIII products didn't lead to an increase in inhibitor risk. The change between plasmatic and recombinant preparations could not be confirmed as a risk factor. Furthermore, no correlation between treatment regimens, severity, patient age and comorbidities of the patients could be found.[Abstract] [Full Text] [Related] [New Search]