| Literature DB >> 26674816 |
Silva Zupančić Šalek1, Günter Auerswald2, Gary Benson3, Gerry Dolan4, Anne Duffy5, Cedric Hermans6, Victor Jiménez-Yuste7, Rolf Ljung8, Massimo Morfini9, Elena Santagostino10, Thierry Lambert11.
Abstract
Preventing haemarthroses and arthropathy is a major challenge in patients with haemophilia and inhibitors, as treatment options are limited. One potential strategy is short-term episodic prophylaxis, which extends bypassing agent therapy beyond the resolution of bleeding to include the post-bleed inflammatory phase. At the 13th Zürich Haemophilia Forum, an expert panel reviewed the rationale behind this strategy, explored its current use with recombinant activated factor VII (rFVIIa) and considered treatment monitoring and optimisation. Two protocols are currently used for short-term episodic prophylaxis, both of which stipulate on-demand rFVIIa until resolution of bleeding, followed by daily dosing for ≥3 days to prevent re-bleeds. Short-term episodic prophylaxis should be individualised to optimise outcomes, perhaps through early treatment initiation or by combining rFVIIa with other treatments (e.g. factor VIII, tranexamic acid). Encouraging treatment compliance can also improve outcomes. Additionally, there is a need to develop objective clinical outcome measures, biomarkers and imaging protocols that can monitor treatment outcomes and joint disease in patients with inhibitors. A proactive approach incorporating a systematic package of care is needed. Currently, short-term episodic prophylaxis with rFVIIa may be an alternative treatment option to on-demand treatment for patients with inhibitors.Entities:
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Year: 2015 PMID: 26674816 PMCID: PMC5269432 DOI: 10.2450/2015.0127-15
Source DB: PubMed Journal: Blood Transfus ISSN: 1723-2007 Impact factor: 3.443