Duley L, Henderson-Smart D J, Knight M, King J F
Resource Centre for Randomised Trials, Institute of Health Sciences, Old Road, Headington, Oxford, UK, OX3 7LF.
Cochrane Database Syst Rev. 2004(1):CD004659. doi: 10.1002/14651858.CD004659.
Pre-eclampsia is associated with deficient intravascular production of prostacyclin, a vasodilator, and excessive production of thromboxane, a platelet-derived vasoconstrictor and stimulant of platelet aggregation. These observations led to the hypotheses that antiplatelet agents, low-dose aspirin in particular, might prevent or delay the development of pre-eclampsia.
To assess the effectiveness and safety of antiplatelet agents when given to women at risk of developing pre-eclampsia.
We searched the Cochrane Pregnancy and Childbirth Group trials register (September 2003), the Cochrane Central Register of Controlled Trials (The Cochrane Library, Issue 2, 2003), EMBASE (1994 to 2003) and we handsearched the congress proceedings of the International and European Societies for the Study of Hypertension in Pregnancy.
All randomised trials comparing antiplatelet agents with either placebo or no antiplatelet agent during pregnancy. Quasi-random study designs were excluded. Participants were pregnant women considered to be at risk of developing pre-eclampsia. Interventions were any comparisons of an antiplatelet agent (such as low-dose aspirin or dipyridamole) with either placebo or no antiplatelet agent.
Two reviewers assessed trials for inclusion in the review and extracted data. We entered data into the Review Manager software and double checked.
Fifty-one trials involving 36,500 women are included in this review. There is a 19% reduction in the risk of pre-eclampsia associated with the use of antiplatelet agents ((43 trials, 33,439 women; relative risk (RR) 0.81, 95% confidence interval (CI) 0.75 to 0.88); number needed to treat (NNT) 69 (51, 109)).Twenty-eight trials (31,845 women) reported preterm birth. There is a small (7%) reduction in the risk of delivery before 37 completed weeks ((RR 0.93, 95% CI 0.89 to 0.98); NNT 83 (50, 238)). Fetal or neonatal deaths were reported in 38 trials (34,010 women). Overall there is a 16% reduction in baby deaths in the antiplatelet group (RR 0.84, 95% CI 0.74 to 0.96); NNT 227 (128, 909)). Small-for-gestational age babies were reported in 32 trials (24,310 women), with an 8% reduction in risk (RR 0.92, 95% CI 0.85 to 1.00). There were no significant differences between treatment and control groups in any other measures of outcome.
REVIEWER'S CONCLUSIONS: Antiplatelet agents, in this review largely low-dose aspirin, have small-moderate benefits when used for prevention of pre-eclampsia. Further information is required to assess which women are most likely to benefit, when treatment is best started, and at what dose.
子痫前期与血管内扩血管物质前列环素生成不足以及血小板源性血管收缩剂和血小板聚集刺激剂血栓素生成过多有关。这些观察结果引发了如下假说:抗血小板药物,尤其是小剂量阿司匹林,可能预防或延缓子痫前期的发生。
评估给予有子痫前期发病风险的女性抗血小板药物的有效性和安全性。
我们检索了Cochrane妊娠与分娩组试验注册库(2003年9月)、Cochrane对照试验中心注册库(《Cochrane图书馆》,2003年第2期)、EMBASE(1994年至2003年),并手工检索了国际和欧洲妊娠期高血压研究学会的会议论文集。
所有在孕期比较抗血小板药物与安慰剂或不使用抗血小板药物的随机试验。排除半随机研究设计。参与者为被认为有子痫前期发病风险的孕妇。干预措施为抗血小板药物(如小剂量阿司匹林或双嘧达莫)与安慰剂或不使用抗血小板药物的任何比较。
两名综述作者评估试验是否纳入本综述并提取数据。我们将数据录入Review Manager软件并进行了双重核对。
本综述纳入了51项涉及36,500名女性的试验。使用抗血小板药物可使子痫前期风险降低19%(43项试验,33,439名女性;相对危险度(RR)0.81,95%置信区间(CI)0.75至0.88);需治疗人数(NNT)为69(51,109)。28项试验(31,845名女性)报告了早产情况。在妊娠满37周前分娩的风险有小幅(7%)降低(RR 0.93,95% CI 0.89至0.98);NNT为83(50,238)。38项试验(34,010名女性)报告了胎儿或新生儿死亡情况。总体而言,抗血小板药物组婴儿死亡风险降低了16%(RR 0.84,95% CI 0.74至0.96);NNT为227(128,909)。32项试验(24,310名女性)报告了小于胎龄儿情况,风险降低了8%(RR 0.92,95% CI 0.85至1.00)。在任何其他结局指标方面,治疗组与对照组之间均无显著差异。
在本综述中,抗血小板药物主要是小剂量阿司匹林,用于预防子痫前期时有中度益处。需要进一步的信息来评估哪些女性最可能受益、何时开始治疗最佳以及使用何种剂量。