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Berntorp, ErikLund University,Lunds universitet,Klinisk koagulationsmedicin, Malmö,Forskargrupper vid Lunds universitet,Clinical Coagulation, Malmö,Lund University Research Groups
(author)
New Approaches to Using FEIBA in the Treatment of Inhibitor Patients.
- Article/chapterEnglish2006
Publisher, publication year, extent ...
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Georg Thieme Verlag KG,2006
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LIBRIS-ID:oai:lup.lub.lu.se:bb529c58-0e2a-4890-94b8-aa8558de7b5c
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https://lup.lub.lu.se/record/158071URI
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https://doi.org/10.1055/s-2006-946911DOI
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Language:English
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Summary in:English
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Subject category:art swepub-publicationtype
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Subject category:ref swepub-contenttype
Notes
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Managing hemophilia becomes particularly difficult in patients with inhibitory antibodies, especially in those requiring surgery or with refractory bleeding events. Equally challenging are those patients who develop autoantibodies against factor VIII (FVIII) in the absence of a prior history of FVIII deficiency (acquired hemophilia). Physicians seeking both short- and long-term treatment strategies for bleeding events must often rely on FVIII-bypassing agents such as activated prothrombin complex concentrate (e.g., factor eight bypassing activity [FEIBA VH, Baxter BioScience, Westlake Village, CA]) or recombinant factor VIIa (rFVIIa [NovoSeven, NovoNordisk, Bagsvaerd, Denmark]). Surgical procedures in patients with inhibitors present a considerable challenge, from both a risk-benefit and a cost-benefit aspect. Hemostasis is difficult to achieve in these patients and new treatment options are being explored. Similarly challenging are refractory bleeds, the management of which is likely to benefit from a systematic treatment approach.
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Gringeri, Alessandro
(author)
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Leissinger, Cindy
(author)
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Négrier, Claude
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Key, Nigel
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Klinisk koagulationsmedicin, MalmöForskargrupper vid Lunds universitet
(creator_code:org_t)
Related titles
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In:Seminars in Thrombosis and Hemostasis: Georg Thieme Verlag KG32:Suppl 2, s. 22-271098-90640094-6176
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