Asplund K, Israelsson K, Schampi I
Department of Medicine, University Hospital, S-901 85 Umea, Sweden.
Cochrane Database Syst Rev. 2000(2):CD000103. doi: 10.1002/14651858.CD000103.
Ischaemic stroke interrupts the flow of blood to part of the brain. Haemodilution is thought to improve the flow of blood to the affected areas of the brain.
The objective of this review was to assess the effects of haemodilution in acute ischaemic stroke.
We searched the Cochrane Stroke Group trials register, Medline and conference abstracts. We contacted manufactures and investigators in the field.
Randomised trials of haemodilution treatment in people with acute ischaemic stroke. Only trials where treatment was started within 72 hours of stroke onset were included.
Two reviewers assessed trial quality and independently extracted the data.
Sixteen trials were included. A combination of venesection and plasma volume expander was used in eight trials. Eight trials used plasma volume expander alone. The plasma volume expander was dextran 40 in 11 trials, hydroxyethyl starch in four trials and albumin in one trial. Two trials tested haemodilution in combination with another therapy. Evaluation was blinded in 11 trials. Five trials probably included some patients with intracerebral haemorrhage. Haemodilution did not significantly reduce deaths within seven to 28 days (odds ratio 1.12, 95% confidence interval 0.88 to 1.43). Similarly, haemodilution did not influence deaths within three to six months (odds ratio 1.02, 95% confidence interval 0.85 to 1.23), or death and dependency or institutionalisation (odds ratio 1.01, 95% confidence interval 0.86 to 1.19). The results were similar in confounded and unconfounded trials, in trials of isovolaemic and hypervolaemic haemodilution, and in trials using different types of hemodiluting agents. Six trials reported venous thromboembolic events. There was a tendency towards reduction in deep venous thrombosis and/or pulmonary embolism at three to six months follow-up (odds ratio 0.59, 95% confidence interval 0.33 to 1.06).
REVIEWER'S CONCLUSIONS: The overall results of this review are compatible both with a modest benefit and a moderate harm of haemodilution therapy for acute ischaemic stroke. As used in the randomised trials, this therapy has not been proven to improve survival or functional outcome.
缺血性中风会中断流向大脑部分区域的血液。血液稀释被认为可改善流向大脑受影响区域的血流。
本综述的目的是评估血液稀释对急性缺血性中风的影响。
我们检索了Cochrane中风组试验注册库、Medline和会议摘要。我们联系了该领域的制造商和研究人员。
急性缺血性中风患者血液稀释治疗的随机试验。仅纳入在中风发作72小时内开始治疗的试验。
两名评价员评估试验质量并独立提取数据。
纳入了16项试验。8项试验使用了放血术和血浆容量扩充剂的联合治疗。8项试验仅使用了血浆容量扩充剂。11项试验中的血浆容量扩充剂为右旋糖酐40,4项试验为羟乙基淀粉,1项试验为白蛋白。2项试验测试了血液稀释与另一种疗法的联合应用。11项试验的评价采用了盲法。5项试验可能纳入了一些脑出血患者。血液稀释在7至28天内未显著降低死亡率(比值比1.12,95%置信区间0.88至1.43)。同样,血液稀释在3至6个月内未影响死亡率(比值比1.02,95%置信区间0.85至1.23),也未影响死亡、依赖或入住机构的情况(比值比1.01,95%置信区间0.86至1.19)。在有混杂因素和无混杂因素的试验中、在等容性和高容性血液稀释试验中以及在使用不同类型血液稀释剂的试验中,结果相似。6项试验报告了静脉血栓栓塞事件。在3至6个月的随访中,有降低深静脉血栓形成和/或肺栓塞的趋势(比值比0.59,95%置信区间0.33至1.06)。
本综述的总体结果表明,血液稀释疗法对急性缺血性中风可能既有适度益处,也有中度危害。在随机试验中使用的这种疗法尚未被证明能改善生存率或功能结局。