Sandercock P, Counsell C, Stobbs S L
Department of Clinical Neurosciences, Neurosciences Trials Unit, Bramwell Dott Building, Western General Hospital, Crewe Road, Edinburgh, UK, EH4 2XU.
Cochrane Database Syst Rev. 2005 Apr 18(2):CD000119. doi: 10.1002/14651858.CD000119.pub2.
Low-molecular-weight heparins and heparinoids are anticoagulants that may be associated with lower risks of haemorrhage and more powerful antithrombotic (anti-clotting) effects than standard unfractionated heparin.
The objective of this review was to compare the effects of low-molecular-weight heparins or heparinoids with those of unfractionated heparin in people with acute, confirmed or presumed, ischaemic stroke (sudden blockage of an artery carrying blood to the brain).
We searched the Cochrane Stroke Group trials register (last searched November 2003). In addition we searched the Cochrane Central Register of Controlled Trials (The Cochrane Library Issue 4, 2003), MEDLINE (1966 to October 2003) and EMBASE (1980 to October 2003). For previous versions of this review we searched MedStrategy (1995) and also contacted pharmaceutical companies.
Randomised trials comparing heparinoids or low-molecular-weight heparins with standard unfractionated heparin in people with acute ischaemic stroke. Only trials where treatment was started within 14 days of stroke onset were included.
Two reviewers independently selected studies for inclusion, assessed trial quality and extracted the data.
Six trials involving 740 people were included. Four trials compared a heparinoid (danaparoid), one trial compared a low-molecular-weight heparin (enoxaparin), and one trial compared an unspecified low-molecular-weight heparin with standard unfractionated heparin. Allocation a to low-molecular-weight heparin or heparinoid was associated with a significant reduction in the odds of deep vein thrombosis (Peto odds ratio 0.52, 95% confidence interval 0.56 to 0.79). However, the number of more major events (pulmonary embolism, death, intra-cranial or extra-cranial haemorrhage) was too small to provide a reliable estimate of more important benefits and risks. No information was reported for recurrent stroke or functional outcome.
AUTHORS' CONCLUSIONS: Treatment with a low-molecular-weight heparin or heparinoid after acute ischaemic stroke appears to decrease the occurrence of deep vein thrombosis compared to standard unfractionated heparin, but there are too few data to provide reliable information on their effects on other important outcomes, including death and intracranial haemorrhage.
低分子量肝素和类肝素是抗凝剂,与标准普通肝素相比,它们可能具有更低的出血风险和更强的抗血栓形成(抗凝血)作用。
本综述的目的是比较低分子量肝素或类肝素与普通肝素对急性、确诊或疑似缺血性卒中(向大脑供血的动脉突然阻塞)患者的影响。
我们检索了Cochrane卒中小组试验注册库(最后检索时间为2003年11月)。此外,我们还检索了Cochrane对照试验中央注册库(《Cochrane图书馆》2003年第4期)、MEDLINE(1966年至2003年10月)和EMBASE(1980年至2003年10月)。对于本综述的以往版本,我们检索了MedStrategy(1995年)并联系了制药公司。
比较类肝素或低分子量肝素与标准普通肝素对急性缺血性卒中患者影响的随机试验。仅纳入在卒中发作14天内开始治疗的试验。
两名综述作者独立选择纳入研究、评估试验质量并提取数据。
纳入了6项涉及740人的试验。4项试验比较了一种类肝素(达那肝素),1项试验比较了一种低分子量肝素(依诺肝素),1项试验比较了一种未指明的低分子量肝素与标准普通肝素。使用低分子量肝素或类肝素与深静脉血栓形成几率的显著降低相关(Peto比值比0.52,95%置信区间0.56至0.79)。然而,更严重事件(肺栓塞、死亡、颅内或颅外出血)的数量过少,无法对更重要的益处和风险提供可靠估计。未报告复发性卒中或功能结局的信息。
与标准普通肝素相比,急性缺血性卒中后使用低分子量肝素或类肝素治疗似乎可降低深静脉血栓形成的发生率,但数据过少,无法提供关于其对包括死亡和颅内出血在内的其他重要结局影响的可靠信息。