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

被引:52
|
作者
Di Minno, Giovanni [1 ]
Zotz, Rainer B. [2 ]
d'Oiron, Roseline [3 ]
Bindslev, Niels [4 ]
Di Minno, Matteo Nicola Dario [1 ,5 ]
Poon, Man-Chiu [6 ,7 ,8 ]
机构
[1] Univ Naples Federico II, Reg Reference Ctr Coagulat Disorders, Dept Clin Med & Surg, Naples, Italy
[2] Ctr Blood Coagulat & Transfus Med CBT, Dusseldorf, Germany
[3] Univ Paris 11, Hop Bicetre, AP HP, Reg Reference Ctr Hemophilia & Constitut Bleeding, Le Kremlin Bicetre, France
[4] Novo Nordisk AS, Biostat, DK-2860 Soborg, Denmark
[5] IRCCS, Ctr Cardiol Monzino, Unit Cell & Mol Biol Cardiovasc Dis, Milan, Italy
[6] Univ Calgary, Dept Med, Foothills Hosp, Southern Alberta Rare Blood & Bleeding Disorders, Calgary, AB, Canada
[7] Univ Calgary, Dept Pediat, Foothills Hosp, Southern Alberta Rare Blood & Bleeding Disorders, Calgary, AB T2N 1N4, Canada
[8] Univ Calgary, Dept Oncol, Foothills Hosp, Southern Alberta Rare Blood & Bleeding Disorders, Calgary, AB, Canada
关键词
RECOMBINANT FACTOR VIIA; DEFECTS; ITGA2B;
D O I
10.3324/haematol.2014.121475
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
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 clinicaltrials.gov identifier: NCT01476423.
引用
收藏
页码:1031 / 1037
页数:7
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