| Literature DB >> 16411390 |
Sam Schulman1, Geir E Tjønnfjord, Richard Wallensten, Uri Martinowitz, Gill Kenet.
Abstract
The administration of recombinant activated factor VII (rFVIIa) by continuous infusion has provided a safe and convenient alternative to bolus injections in haemophiliacs with inhibitors, but it has only been reported in a single case with congenital factor VII (FVII) deficiency. The results of 12 consecutive surgical procedures in 7 patients with congenital FVII deficiency are reported here. rFVIIa was always given in continuous infusion,aiming at plasma FVII activity of 0.5 IU/mL. Treatment was given for 2 to 7 days with a mean total dose of 7.8 mg rFVIIa. Blood loss was as expected from the different types of procedures and the only thromboembolic complication was a superficial thrombophlebitis at the infusion site. This mode of substitution was therefore safe, effective and well tolerated.Entities:
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Year: 2005 PMID: 16411390 DOI: 10.1160/TH05-05-0342
Source DB: PubMed Journal: Thromb Haemost ISSN: 0340-6245 Impact factor: 5.249