Suppr超能文献

急性缺血性卒中血液稀释的随机临床试验。

Randomized clinical trials of hemodilution in acute ischemic stroke.

作者信息

Asplund K

机构信息

Department of Medicine, University Hospital, Umeå, Sweden.

出版信息

Acta Neurol Scand Suppl. 1989;127:22-30. doi: 10.1111/j.1600-0404.1989.tb01807.x.

Abstract

The effects of hemodilution in acute ischemic stroke have been investigated, first in a single-center, then in a multicenter trial. Patients with hematocrit levels of 38-50% were randomized, within 48 h of onset of symptoms, to treatment with repeated venesections (total 250-1000 ml) and concomitant dextran 40 administration, or to a control group. The single-center study, performed in a research-oriented stroke unit, involved 102 patients. Case fatality rate was not grossly affected by hemodilution. In survivors, hemodilution improved neurological outcome. More hemodiluted patients were independent in walking and more were at home 3 months after the stroke. The ensuing multicenter trial involved 383 patients in 15 Scandinavian centers. Three-month case fatality rate was 16% in hemodiluted and 12% in control patients. Neurological scoring and ADL performance at 3 months was not improved by hemodilution. No subgroup with beneficial effects was discerned. It is concluded that the present standardized hemodilution regime cannot be recommended for general use in patients with ischemic stroke.

摘要

急性缺血性卒中血液稀释的效果已得到研究,先是在单中心研究,然后是多中心试验。血细胞比容水平在38%-50%的患者在症状发作48小时内被随机分组,一组接受重复放血治疗(总量250-1000毫升)并同时给予右旋糖酐40,另一组为对照组。在一个以研究为导向的卒中单元进行的单中心研究纳入了102例患者。血液稀释对病死率没有明显影响。在幸存者中,血液稀释改善了神经功能结局。血液稀释程度更高的患者在卒中后3个月时能独立行走,且更多患者在家中生活。随后的多中心试验在15个斯堪的纳维亚中心纳入了383例患者。血液稀释组3个月病死率为16%,对照组为12%。血液稀释并未改善3个月时的神经功能评分和日常生活活动能力表现。未发现有获益的亚组。结论是,目前标准化的血液稀释方案不推荐普遍用于缺血性卒中患者。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验