Ricci S, Celani M G, Cantisani A T, Righetti E
Stroke Service, USL 2, Via Guerra 17, 06127 Perugia, Italy.
Cochrane Database Syst Rev. 2000(2):CD000419. doi: 10.1002/14651858.CD000419.
Piracetam has neuroprotective and antithrombotic effects which may help to reduce death and disability in people with acute stroke.
The objective of this review was to assess the effects of piracetam in acute presumed ischaemic stroke.
We searched the Cochrane Stroke Review Group trials register, Medline (from 1965), Embase (from 1980), BIDIS ISI (from 1981). We also contacted manufacturers and handsearched 15 journals.
Randomised trials comparing piracetam with control, with at least mortality reported and entry to the trial within approximately 48 hours of stroke onset.
Two reviewers extracted data and assessed trial quality and this was checked by the other two reviewers. Study authors were contacted for missing information.
Three trials involving 1002 people were included, with one trial contributing 97% of the data. Participants' ages ranged from 40 to 85, and both sexes were equally represented. Piracetam was associated with a statistically non significant increase in death (31% increase, 95% confidence interval 81% increase to 5% reduction). This trend was no longer apparent in the large trial after correction for imbalance in stroke severity. Limited data showed no difference between the treatment and control groups for functional outcome, dependency or proportion of patients dead or dependent. Adverse effects were not reported.
REVIEWER'S CONCLUSIONS: There is some suggestion of an unfavourable effect of piracetam on early death, but this may have been caused by baseline differences in stroke severity in the trials. Piracetam does not appear to reduce dependency for stroke patients.
吡拉西坦具有神经保护和抗血栓形成作用,可能有助于降低急性中风患者的死亡率和残疾率。
本综述旨在评估吡拉西坦对急性疑似缺血性中风的疗效。
我们检索了Cochrane中风综述组试验注册库、Medline(始于1965年)、Embase(始于1980年)、BIDIS ISI(始于1981年)。我们还联系了制造商并手工检索了15种期刊。
将吡拉西坦与对照组进行比较的随机试验,至少报告了死亡率,且在中风发作后约48小时内进入试验。
两名综述员提取数据并评估试验质量,另外两名综述员进行核对。联系研究作者获取缺失信息。
纳入了三项涉及1002人的试验,其中一项试验贡献了97%的数据。参与者年龄在40至85岁之间,男女比例均等。吡拉西坦与死亡人数的统计学非显著增加相关(增加31%,95%置信区间为增加81%至减少5%)。在校正中风严重程度的不平衡后,这一趋势在大型试验中不再明显。有限的数据显示,治疗组和对照组在功能结局、依赖程度或死亡或依赖患者比例方面没有差异。未报告不良反应。
有迹象表明吡拉西坦对早期死亡有不利影响,但这可能是由试验中中风严重程度的基线差异导致的。吡拉西坦似乎并未降低中风患者的依赖程度。