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The international prospective Glanzmann Thrombasthenia Registry: treatment modalities and outcomes of non-surgical bleeding episodes in patients with Glanzmann thrombasthenia

机译:国际前瞻性Glanzmann血小板减少症注册中心:Glanzmann血虚症患者的治疗方式和非手术性出血发作的结局

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摘要

Standard treatment for Glanzmann thrombasthenia is platelet transfusion. Recombinant activated factor VII has been shown to be successful in patients with Glanzmann thrombasthenia with platelet antibodies or who are refractory to platelet transfusions. The Glanzmann Thrombasthenia Registry prospectively collected worldwide information on the effectiveness and safety of platelet transfusion, recombinant activated factor VII and/or antifibrinolytics for the treatment of bleeds in patients with Glanzmann thrombasthenia. Data relating to 829 non-surgical bleeding episodes were entered into the Glanzmann Thrombasthenia Registry (severe/moderate: 216/613; spontaneous/post-traumatic: 630/199). Recombinant activated factor VII alone was used in 124/829 bleeds, recombinant activated factor VII+antifibrinolytics in 107/829, platelets±antifibrinolytics in 312/829, antifibrinolytics alone in 219/829, and recombinant activated factor VII+platelets±antifibrinolytics in 67/829. The proportion of successful treatments to stop bleeding was 91.0% in cases treated with recombinant activated factor VII only, 82.7% for recombinant activated factor VII+antifibrinolytics, 72.7% for treatment with recombinant activated factor VII+platelets±antifibrinolytics, 78.8% for platelets±antifibrinolytics and 84.7% for antifibrinolytics alone. Treatment failure was documented in 18 bleeding events (2% of the total treatments), the majority of which were in patients receiving treatment with antifibrinolytics; bleeding re-started in 6% of bleeds after initial effective treatment. Thirty-five adverse events were reported, none of which was a thromboembolic event. Among treatments that included recombinant activated factor VII, only one patient reported three possibly drug-related non-serious adverse events (nausea, dyspnea and headache). To conclude, non-surgical bleeds were common and often severe in Glanzmann thrombasthenia; both platelets and recombinant activated factor VII appeared to be effective, and with good safety profiles, for the treatment of non-surgical bleeds. This trial was registered at identifier: .
机译:格兰茨曼性血小板减少症的标准治疗方法是血小板输注。重组活化因子VII已被证明在患有血小板抗体的格兰茨曼血虚症患者或血小板输注困难的患者中是成功的。 Glanzmann血小板减少症注册中心前瞻性地收集了有关血小板输注,重组活化的VII因子和/或抗纤溶蛋白治疗血小板减少性血小板减少症患者出血的有效性和安全性的全球信息。将与829次非手术性出血发作相关的数据输入Glanzmann血小板减少症登记册(严重/中度:216/613;自发性/创伤后:630/199)。仅在124/829出血中使用重组活化因子VII,在107/829中使用重组活化因子VII +抗纤溶蛋白,在312/829中使用血小板±抗纤溶蛋白,在219/829中仅使用抗纤溶蛋白,在67/67中使用重组活化因子VII +血小板±抗纤溶蛋白/ 829。仅用重组活化因子VII治疗的成功止血疗法的比例为91.0%,重组活化因子VII +抗纤溶药物的治疗率为82.7%,重组活化因子VII +血小板治疗的为72.7%±纤溶酶,血小板为78.8%抗纤维蛋白溶解药,单独使用抗纤维蛋白溶解药占84.7%。在18个出血事件(占总治疗的2%)中记录了治疗失败的情况,其中大多数是接受抗纤溶剂治疗的患者。最初的有效治疗后,有6%的出血重新开始出血。报告了35例不良事件,其中没有一个是血栓栓塞事件。在包括重组激活因子VII的治疗中,只有一名患者报告了三种可能与药物相关的非严重不良事件(恶心,呼吸困难和头痛)。总而言之,非手术性出血在Glanzmann血虚症中很常见,而且常常很严重。血小板和重组活化因子VII均可有效治疗非手术性出血,并具有良好的安全性。该试验已在标识符处注册。

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