Patch: platelet transfusion in cerebral haemorrhage: study protocol for a multicentre, randomised, controlled trial

被引:52
作者
de Gans, Koen [1 ]
de Haan, Rob J. [2 ]
Majoie, Charles B. [3 ]
Koopman, Maria M. [4 ]
Brand, Anneke [5 ,6 ]
Dijkgraaf, Marcel G. [7 ]
Vermeulen, Marinus [1 ]
Roos, Yvo B. [1 ,2 ]
机构
[1] Acad Med Ctr, Dept Neurol, NL-1100 DD Amsterdam, Netherlands
[2] Acad Med Ctr, Clin Res Unit, NL-1100 DD Amsterdam, Netherlands
[3] Acad Med Ctr, Dept Radiol, NL-1100 DD Amsterdam, Netherlands
[4] Sanquin Blood Bank, NL-1006 AC Amsterdam, Netherlands
[5] Sanquin Blood Bank, Dept Res & Dev, Leiden, Netherlands
[6] Leiden Univ, Dept Immune Haematol & Transfus Med, Med Ctr, Leiden, Netherlands
[7] Acad Med Ctr, Dept Clin Epidemiol & Biostat, NL-1100 DD Amsterdam, Netherlands
来源
BMC NEUROLOGY | 2010年 / 10卷
关键词
ACUTE INTRACEREBRAL HEMORRHAGE; ACTIVATED FACTOR-VII; INDEPENDENT PREDICTOR; ANTIPLATELET THERAPY; HEMOSTATIC THERAPY; 30-DAY MORTALITY; HEMATOMA; GROWTH; SAFETY; ONSET;
D O I
10.1186/1471-2377-10-19
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Patients suffering from intracerebral haemorrhage have a poor prognosis, especially if they are using antiplatelet therapy. Currently, no effective acute treatment option for intracerebral haemorrhage exists. Limiting the early growth of intracerebral haemorrhage volume which continues the first hours after admission seems a promising strategy. Because intracerebral haemorrhage patients who are on antiplatelet therapy have been shown to be particularly at risk of early haematoma growth, platelet transfusion may have a beneficial effect. Methods/Design: The primary objective is to investigate whether platelet transfusion improves outcome in intracerebral haemorrhage patients who are on antiplatelet treatment. The PATCH study is a prospective, randomised, multi-centre study with open treatment and blind endpoint evaluation. Patients will be randomised to receive platelet transfusion within six hours or standard care. The primary endpoint is functional health after three months. The main secondary endpoints are safety of platelet transfusion and the occurrence of haematoma growth. To detect an absolute poor outcome reduction of 20%, a total of 190 patients will be included. Discussion: To our knowledge this is the first randomised controlled trial of platelet transfusion for an acute haemorrhagic disease.
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页数:6
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