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[欧洲急性输血性肝炎干扰素研究(EATHIS)]

[European Acute Transfusion Hepatitis Interferon Study (EATHIS)].

作者信息

Jullien A M, Dejean A M, Janot C, Trepo C

机构信息

Centre National de Transfusion Sanguine, Hôpital Saint-Antoine, Paris.

出版信息

Rev Fr Transfus Hemobiol. 1992 Jul;35(3):199-204. doi: 10.1016/s1140-4639(05)80123-6.

Abstract

Since 1989, a prospective, multicentric and collaborative study, named European Acute Transfusion Hepatitis Interferon Study (EATHIS), involving 16 blood centres in France is coordinated by a task force in collaboration with the Viral Hepatitis and Recipients working groups of the French National Society of Blood Transfusion. A phase of recipient screening may be completed by a therapeutic interferon protocol. Among 1,476 transfused recipients receiving an average of 4.4 blood components, 1,011 were followed up at least four months. The incidence of non-A, non-B post-transfusion hepatitis (PTH) was varying from 0.1 to 6% at the different locations. Out of 15 hepatitis cases, 10 were diagnosed as post-transfusional. These preliminary data indicate a reduced incidence of PTH, with a mean of 1% for the period 1989-1991. It emphasises the importance of a transfusion vigilance program including follow up and testing for transaminases and specific viral markers.

摘要

自1989年以来,一项名为欧洲急性输血性肝炎干扰素研究(EATHIS)的前瞻性、多中心合作研究在法国的16个血液中心开展,该研究由一个特别工作组与法国国家输血协会的病毒性肝炎及受血者工作组合作进行协调。受血者筛查阶段可通过治疗性干扰素方案完成。在1476名平均接受4.4个血液成分的输血受血者中,1011人接受了至少四个月的随访。不同地点的非甲非乙型输血后肝炎(PTH)发病率在0.1%至6%之间。在15例肝炎病例中,10例被诊断为输血后肝炎。这些初步数据表明PTH发病率有所降低,1989 - 1991年期间的平均发病率为1%。这强调了输血监测计划的重要性,该计划包括随访以及检测转氨酶和特定病毒标志物。

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