Recombinant activated factor VII in clinical practice: a 2014 update
Recombinant activated factor VII (rFVIIa) was initially developed to treat bleeding episodes in patients with congenital hemophilia and inhibitors. Due to the initial success in this clinical setting, its use has been extended to other coagulopathies characterized by impaired thrombin generation, i....
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| Veröffentlicht in: | Journal of thrombosis and thrombolysis Jg. 39; H. 2; S. 235 - 240 |
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| Hauptverfasser: | , , , , |
| Format: | Journal Article |
| Sprache: | Englisch |
| Veröffentlicht: |
Boston
Springer US
01.02.2015
Springer Nature B.V |
| Schlagworte: | |
| ISSN: | 0929-5305, 1573-742X, 1573-742X |
| Online-Zugang: | Volltext |
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| Zusammenfassung: | Recombinant activated factor VII (rFVIIa) was initially developed to treat bleeding episodes in patients with congenital hemophilia and inhibitors. Due to the initial success in this clinical setting, its use has been extended to other coagulopathies characterized by impaired thrombin generation, i.e. acquired hemophilia, inherited factor VII deficiency and Glanzmann’s thrombasthenia, for which it is currently licensed. Extensive research in the last decade has increased our knowledge of the mechanisms utilized by rFVIIa to restore normal hemostasis. This paper reviews current understanding of the mechanisms of action of rFVIIa before summarizing the clinical experience, in terms of safety and efficacy, to date in its licensed indications. |
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| Bibliographie: | SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 14 ObjectType-Article-1 ObjectType-Feature-2 ObjectType-Review-3 content type line 23 |
| ISSN: | 0929-5305 1573-742X 1573-742X |
| DOI: | 10.1007/s11239-014-1114-1 |