Continuous infusion of recombinant activated factor VII during caesarean section delivery in a patient with congenital factor VII deficiency
- 1 September 2000
- journal article
- case report
- Published by Wiley in Haemophilia
- Vol. 6 (5), 588-590
- https://doi.org/10.1046/j.1365-2516.2000.00424.x
Abstract
Recombinant activated factor VII (rFVIIa) can be used as an alternative therapy in patients with FVII deficiency. However, as the drug has a very short half-life, continuous infusion could be a meaningful administration modality. We report the case of a 30-year-old woman with moderate FVII deficiency and human immunodeficiency virus infection who underwent a caesarean section delivery. She was treated with a continuous infusion of rFVIIa and did not suffer any bleeding complication. The continuous infusion of rFVIIa was a safe and effective therapeutic approach for our patient, maintaining her levels of FVII:C and avoiding bleeding during caesarean section and afterwards.Keywords
This publication has 10 references indexed in Scilit:
- Treatment with recombinant activated factor VII in a patient with hemophilia A and an inhibitorBlood Coagulation & Fibrinolysis, 1999
- Clinical picture and treatment strategies in factor VII deficiencyHaemophilia, 1998
- Safety, efficacy and lessons from continuous infusion with rFVIIaHaemophilia, 1998
- A Longitudinal Study of the Factor VII Rise during PregnancyThrombosis and Haemostasis, 1998
- Clinical manifestations in 28 Italian and Iranian patients with severe factor VII deficiencyHaemophilia, 1997
- Use of recombinant factor VIIa in surgery in factor‐VII‐deficient patientsHaemophilia, 1997
- PKRD: a pharmacokinetic program for least-squares and bayesian analysis of repeated-dose pharmacokinetic curvesComputer Methods and Programs in Biomedicine, 1992
- Hereditary factor VII deficiency in pregnancy: Peripartum treatment with factor VII concentrateAmerican Journal of Hematology, 1992
- The Design and Analysis of Half-Life and Recovery Studies for Factor VIII and Factor IXThrombosis and Haemostasis, 1991
- Hereditary factor VII deficiency: heterogeneity defined by combined functional and immunochemical analysisBlood, 1985