De Schryver E L L M, Algra A, van Gijn J
Cochrane Database Syst Rev. 2006 Apr 19(2):CD001820. doi: 10.1002/14651858.CD001820.pub2.
Patients with limited cerebral ischaemia of arterial origin are at risk of serious vascular events (4% to 11% annually). Aspirin reduces that risk by 13%. In one trial, adding dipyridamole to aspirin was associated with a 22% risk-reduction compared with aspirin alone. However, a systematic review of all trials of antiplatelet agents by the Antithrombotic Trialists' Collaboration showed that, in high-risk patients, there was virtually no difference between the aspirin-dipyridamole combination and aspirin alone.
To assess the efficacy and safety of dipyridamole versus control in the secondary prevention of vascular events in patients with vascular disease.
We searched the Cochrane Stroke Group trials register (searched November 2005), the Cochrane Central Register of Controlled Trials (CENTRAL) (The Cochrane Library Issue 3, 2005), MEDLINE (1966 to November 2005) and EMBASE (1980 to November 2005).
Randomised long-term secondary prevention trials with concealed treatment allocation, treatment for more than one month, starting within six months after presentation of an arterial vascular disease were selected. Treatment consisted of dipyridamole with or without other antiplatelet drugs compared with no drug or an antiplatelet drug other than dipyridamole.
Two authors independently selected trials for inclusion, assessed trial quality and extracted data. Data were analysed according to the intention-to-treat principle.
Twenty-seven trials were included, with 20242 patients, among whom 1399 vascular deaths and 3090 fatal and non-fatal vascular events occurred during follow up. Compared with control, dipyridamole had no clear effect on vascular death (relative risk (RR) 1.02, 95% confidence internal (CI) 0.90 to 1.17). This result was not influenced by the dose of dipyridamole or type of presenting vascular disease. In the presence of aspirin, dipyridamole appeared to reduce the risk of vascular events compared with control (RR 0.90, 95% CI 0.82 to 0.97), due to a single large trial in patients presenting with cerebral ischaemia.
AUTHORS' CONCLUSIONS: For patients who presented with arterial vascular disease, there was no evidence that dipyridamole, in the presence or absence of another antiplatelet drug reduced the risk of vascular death, though it may reduce the risk of further vascular events. However, this benefit was found in only one single large trial and only in patients presenting after cerebral ischaemia. There was no evidence that dipyridamole alone was more efficacious than aspirin. Further trials comparing the effects of the combination of dipyridamole with aspirin versus aspirin alone are justified.
动脉源性局限性脑缺血患者有发生严重血管事件的风险(每年4%至11%)。阿司匹林可将该风险降低13%。在一项试验中,与单用阿司匹林相比,阿司匹林联用双嘧达莫可使风险降低22%。然而,抗栓治疗协作组对所有抗血小板药物试验进行的系统评价表明,在高危患者中,阿司匹林 - 双嘧达莫联合用药与单用阿司匹林之间几乎没有差异。
评估双嘧达莫与对照相比在血管疾病患者二级预防血管事件中的疗效和安全性。
我们检索了Cochrane卒中组试验注册库(2005年11月检索)、Cochrane对照试验中央注册库(CENTRAL)(《Cochrane图书馆》2005年第3期)、MEDLINE(1966年至2005年11月)和EMBASE(1980年至2005年11月)。
入选采用隐匿治疗分配的随机长期二级预防试验,治疗时间超过1个月,在出现动脉血管疾病后6个月内开始。治疗包括双嘧达莫加或不加其他抗血小板药物,与无药物或双嘧达莫以外的抗血小板药物进行比较。
两位作者独立选择纳入试验、评估试验质量并提取数据。数据根据意向性分析原则进行分析。
纳入27项试验,共20242例患者,随访期间发生1399例血管性死亡和3090例致命及非致命血管事件。与对照相比,双嘧达莫对血管性死亡无明显影响(相对危险度(RR)1.02,95%可信区间(CI)0.90至1.17)。该结果不受双嘧达莫剂量或所患血管疾病类型的影响。在使用阿司匹林的情况下,与对照相比,双嘧达莫似乎可降低血管事件风险(RR 0.90,95%CI 0.82至0.97),这是由于一项针对脑缺血患者的大型试验得出的结果。
对于患有动脉血管疾病的患者,没有证据表明双嘧达莫无论是否联用另一种抗血小板药物都能降低血管性死亡风险,不过它可能降低进一步发生血管事件的风险。然而,这种益处仅在一项大型试验中发现,且仅在脑缺血后就诊的患者中存在。没有证据表明单用双嘧达莫比阿司匹林更有效。进一步比较双嘧达莫与阿司匹林联用和单用阿司匹林效果的试验是合理的。