Duley L, Henderson-Smart D J, Meher S, King J F
University of Leeds, Centre for Epidemiology and Biostatistics, Academic Unit, Fieldhouse, Bradford Teaching Hospitals Foundation Trust, Bradford Royal Infirmary, Duckworth Lane, Bradford, West Yorkshire, UK BD9 6RJ.
Cochrane Database Syst Rev. 2007 Apr 18(2):CD004659. doi: 10.1002/14651858.CD004659.pub2.
Pre-eclampsia is associated with deficient intravascular production of prostacyclin, a vasodilator, and excessive production of thromboxane, a vasoconstrictor and stimulant of platelet aggregation. These observations led to the hypotheses that antiplatelet agents, low-dose aspirin in particular, might prevent or delay development of pre-eclampsia.
To assess the effectiveness and safety of antiplatelet agents for women at risk of developing pre-eclampsia.
We searched the Cochrane Pregnancy and Childbirth Group's Trials Register (July 2006), the Cochrane Central Register of Controlled Trials (The Cochrane Library 2005, Issue 1), EMBASE (1994 to November 2005) and handsearched 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 were included. Quasi-random studies were excluded. Participants were pregnant women 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.
Two authors assessed trials for inclusion and extracted data independently.
Fifty-nine trials (37,560 women) are included. There is a 17% reduction in the risk of pre-eclampsia associated with the use of antiplatelet agents ((46 trials, 32,891 women, relative risk (RR) 0.83, 95% confidence interval (CI) 0.77 to 0.89), number needed to treat (NNT) 72 (52, 119)). Although there is no statistical difference in RR based on maternal risk, there is a significant increase in the absolute risk reduction of pre-eclampsia for high risk (risk difference (RD) -5.2% (-7.5, -2.9), NNT 19 (13, 34)) compared with moderate risk women (RD -0.84 (-1.37, -0.3), NNT 119 (73, 333)). Antiplatelets were associated with an 8% reduction in the relative risk of preterm birth (29 trials, 31,151 women, RR 0.92, 95% CI 0.88 to 0.97); NNT 72 (52, 119)), a 14% reduction in fetal or neonatal deaths (40 trials, 33,098 women, RR 0.86, 95% CI 0.76 to 0.98); NNT 243 (131, 1,666) and a 10% reduction in small-for-gestational age babies (36 trials, 23,638 women, RR 0.90, 95% CI0.83 to 0.98). There were no statistically significant differences between treatment and control groups for any other outcomes.
AUTHORS' CONCLUSIONS: Antiplatelet agents, largely low-dose aspirin, have moderate benefits when used for prevention of pre-eclampsia and its consequences. Further information is required to assess which women are most likely to benefit, when treatment is best started, and at what dose.
子痫前期与血管舒张剂前列环素的血管内生成不足以及血管收缩剂和血小板聚集刺激剂血栓素的过度生成有关。这些观察结果引发了如下假设:抗血小板药物,尤其是低剂量阿司匹林,可能预防或延缓子痫前期的发展。
评估抗血小板药物对有子痫前期发病风险女性的有效性和安全性。
我们检索了Cochrane妊娠与分娩组试验注册库(2006年7月)、Cochrane对照试验中央注册库(Cochrane图书馆2005年第1期)、EMBASE(1994年至2005年11月),并手工检索了国际和欧洲妊娠高血压研究学会的会议论文集。
纳入所有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。参与者为有子痫前期发病风险的孕妇。干预措施为抗血小板药物(如低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之间的任何比较。
两位作者独立评估试验是否纳入并提取数据。
纳入59项试验(37560名女性)。使用抗血小板药物使子痫前期风险降低17%(46项试验,32891名女性,相对危险度(RR)0.83,95%置信区间(CI)0.77至0.89),需治疗人数(NNT)为72(52,119)。尽管基于母亲风险的RR无统计学差异,但与中度风险女性相比,高风险女性子痫前期的绝对风险降低显著增加(风险差(RD)-5.2%(-7.5,-2.9),NNT 19(13,34))(中度风险女性RD -0.84(-1.37,-0.3),NNT 11