| Literature DB >> 25899749 |
Shin-Young Na1, Eva Mracsko1, Joanne van Ryn2, Roland Veltkamp1,3.
Abstract
Lack of specific antidotes is a major concern in intracerebral hemorrhage (ICH) related to direct anticoagulants including dabigatran (OAC-ICH). We examined the efficacy of idarucizumab, an antibody fragment binding to dabigatran, in a mouse model of OAC-ICH. Dabigatran etexilate (DE) dose-dependently prolonged diluted thrombin time and tail-vein bleeding time, which were reversed by idarucizumab. Pretreatment with DE increased intracerebral hematoma volume and cerebral hemoglobin content. Idarucizumab in equimolar dose prevented excess hematoma expansion for both DE doses. In more extensive ICH, idarucizumab significantly reduced mortality. Thus, idarucizumab prevents excess intracerebral hematoma formation in mice anticoagulated with dabigatran and reduces mortality.Entities:
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Year: 2015 PMID: 25899749 DOI: 10.1002/ana.24421
Source DB: PubMed Journal: Ann Neurol ISSN: 0364-5134 Impact factor: 10.422