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pubmed-article:9873861pubmed:abstractTextThirty-six haemophilia A, HIV-negative, previously treated patients were changed therapy to a highpurity and double-inactivated (solvent/detergent and dry-heating) previously unused factor VIII concentrate. The mean age of these patients was 27 years at the time of the change. Twenty-three patients were severe haemophiliacs (FVIII:C < 0.02 IU mL-1), seven moderate (FVIII:C between 0.02 and 0.05 IU mL-1) and six mild (FVIII:C > 0.05 IU mL-1). The mean follow-up with this single product was 16 months, with 82 accumulated exposure days and the mean consumption was 117,300 IU of FVIII corresponding to a mean of six batches per patient. No patient developed FVIII inhibitors (upper limit of the CI95: 7.98%), resulting in an incidence rate of 0/48 patient-years (upper limit of the CI95: 77/1000 patient-years). The change in therapy to this new factor VIII concentrate was not associated with the appearance of inhibitors.lld:pubmed
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pubmed-article:9873861pubmed:pagination21-4lld:pubmed
pubmed-article:9873861pubmed:dateRevised2009-10-21lld:pubmed
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pubmed-article:9873861pubmed:articleTitleZero incidence of inhibitor development in previously treated haemophilia A, HIV-negative patients upon exposure to a plasma-derived high-purity and double viral inactivated factor VIII concentrate.lld:pubmed
pubmed-article:9873861pubmed:affiliationUnidad de Coagulopatías Congénitas, Hospital La Fe, Valencia, Spain.lld:pubmed
pubmed-article:9873861pubmed:publicationTypeJournal Articlelld:pubmed