Brown Racquel
University of Kentucky, Lexington, Kentucky, USA.
Blood Coagul Fibrinolysis. 2017 Oct;28(7):570-575. doi: 10.1097/MBC.0000000000000632.
: A recombinant von Willebrand factor (rVWF) was recently approved in the United States for on-demand treatment and control of bleeding episodes in adults with von Willebrand disease (VWD). In contrast to plasma-derived VWF products available in the United States, rVWF does not contain factor VIII (FVIII). To date, there is no published experience of rVWF in clinical practice. We report the acute and prophylactic use of rVWF in a patient with VWD type 2A and severe gastrointestinal bleeding. Dosing with plasma-derived VWF/FVIII concentrates was constrained by FVIII accumulation; the bleeding was unresponsive, and multiple red blood cell transfusions were required. After initiation of rVWF (4200 IU every other day), bleeding symptoms subsided, and no red blood cell transfusions were required during more than 3 months of prophylactic therapy (most recent dosage: 2800 IU every other day). rVWF may be effective in the prevention, as well as treatment, of severe bleeding symptoms in VWD.
一种重组血管性血友病因子(rVWF)最近在美国被批准用于按需治疗和控制血管性血友病(VWD)成人患者的出血发作。与美国现有的血浆源性VWF产品不同,rVWF不含有因子VIII(FVIII)。迄今为止,尚无rVWF在临床实践中的公开经验。我们报告了rVWF在一名2A型VWD和严重胃肠道出血患者中的急性和预防性应用。使用血浆源性VWF/FVIII浓缩物进行给药受到FVIII蓄积的限制;出血未得到缓解,需要多次输注红细胞。开始使用rVWF(每隔一天4200 IU)后,出血症状消退,在超过3个月的预防性治疗期间无需输注红细胞(最新剂量:每隔一天2800 IU)。rVWF在预防和治疗VWD的严重出血症状方面可能有效。