Duley Lelia, Gülmezoglu A Metin, Henderson-Smart David J, Chou Doris
Centre for Epidemiology and Biostatistics, University of Leeds, Bradford Institute for Health Research, Bradford Royal Infirmary, Duckworth Lane, Bradford, West Yorkshire, UK, BD9 6RJ.
Cochrane Database Syst Rev. 2010 Nov 10;2010(11):CD000025. doi: 10.1002/14651858.CD000025.pub2.
Eclampsia, the occurrence of a seizure (fit) in association with pre-eclampsia, is rare but potentially life-threatening. Magnesium sulphate is the drug of choice for treating eclampsia. This review assesses its use for preventing eclampsia.
To assess the effects of magnesium sulphate, and other anticonvulsants, for prevention of eclampsia.
We searched the Cochrane Pregnancy and Childbirth Group's Trials Register (4 June 2010), and the Cochrane Central Register of Controlled Trials Register (The Cochrane Library 2010, Issue 3).
Randomised trials comparing anticonvulsants with placebo or no anticonvulsant, or comparisons of different drugs, for pre-eclampsia.
Two authors assessed trial quality and extracted data independently.
We included 15 trials. Six (11,444 women) compared magnesium sulphate with placebo or no anticonvulsant: magnesium sulphate more than a halved the risk of eclampsia (risk ratio (RR) 0.41, 95% confidence interval (CI) 0.29 to 0.58; number needed to treat for an additional beneficial outcome (NNTB) 100, 95% CI 50 to 100), with a non-significant reduction in maternal death (RR 0.54, 95% CI 0.26 to 1.10) but no clear difference in serious maternal morbidity (RR 1.08, 95% CI 0.89 to 1.32). It reduced the risk of placental abruption (RR 0.64, 95% CI 0.50 to 0.83; NNTB 100, 95% CI 50 to 1000), and increased caesarean section (RR 1.05, 95% CI 1.01 to 1.10). There was no clear difference in stillbirth or neonatal death (RR 1.04, 95% CI 0.93 to 1.15). Side effects, primarily flushing, were more common with magnesium sulphate (24% versus 5%; RR 5.26, 95% CI 4.59 to 6.03; number need to treat for an additional harmful outcome (NNTH) 6, 95% CI 5 to 6).Follow-up was reported by one trial comparing magnesium sulphate with placebo: for 3375 women there was no clear difference in death (RR 1.79, 95% CI 0.71 to 4.53) or morbidity potentially related to pre-eclampsia (RR 0.84, 95% CI 0.55 to 1.26) (median follow-up 26 months); for 3283 children exposed in utero there was no clear difference in death (RR 1.02, 95% CI 0.57 to 1.84) or neurosensory disability (RR 0.77, 95% CI 0.38 to 1.58) at age 18 months.Magnesium sulphate reduced eclampsia compared to phenytoin (three trials, 2291 women; RR 0.08, 95% CI 0.01 to 0.60) and nimodipine (one trial, 1650 women; RR 0.33, 95% CI 0.14 to 0.77).
AUTHORS' CONCLUSIONS: Magnesium sulphate more than halves the risk of eclampsia, and probably reduces maternal death. There is no clear effect on outcome after discharge from hospital. A quarter of women report side effects with magnesium sulphate.
子痫是指与子痫前期相关的惊厥(抽搐)发作,虽罕见但有潜在生命危险。硫酸镁是治疗子痫的首选药物。本综述评估其预防子痫的用途。
评估硫酸镁及其他抗惊厥药物预防子痫的效果。
我们检索了Cochrane妊娠与分娩组试验注册库(2010年6月4日)以及Cochrane对照试验中心注册库(《Cochrane图书馆》2010年第3期)。
比较抗惊厥药物与安慰剂或不使用抗惊厥药物,或不同药物用于子痫前期的随机试验。
两位作者独立评估试验质量并提取数据。
我们纳入了15项试验。6项试验(11444名女性)比较了硫酸镁与安慰剂或不使用抗惊厥药物:硫酸镁使子痫风险降低超过一半(风险比(RR)0.41,95%置信区间(CI)0.29至0.58;获得额外有益结果所需治疗人数(NNTB)100,95%CI 50至100),孕产妇死亡有非显著性降低(RR 0.54,95%CI 0.26至1.10),但严重孕产妇发病率无明显差异(RR 1.08,95%CI 0.89至1.32)。它降低了胎盘早剥风险(RR 0.64,95%CI 0.50至0.83;NNTB 100,95%CI 50至1000),并增加了剖宫产率(RR(1.05),95%CI 1.01至1.10)。死产或新生儿死亡无明显差异(RR 1.04,95%CI 0.93至1.15)。副作用主要为潮红,硫酸镁组更常见(24%对5%;RR 5.26,95%CI 4.59至6.03;获得额外有害结果所需治疗人数(NNTH)6,95%CI 5至6)。一项比较硫酸镁与安慰剂的试验报告了随访情况:3375名女性在死亡(RR 1.79,95%CI 0.71至4.53)或可能与子痫前期相关的发病率(RR 0.84,95%CI 0.55至1.26)方面无明显差异(中位随访26个月);3283名宫内暴露儿童在18个月时死亡(RR 1.02,95%CI 0.57至1.84)或神经感觉残疾(RR 0.77,95%CI 0.38至1.58)方面无明显差异。与苯妥英钠相比(3项试验,2291名女性;RR 0.08,95%CI 0.01至0.60)以及与尼莫地平相比(1项试验,1650名女性;RR 0.33,95%CI 0.14至0.77),硫酸镁降低了子痫风险。
硫酸镁使子痫风险降低超过一半,且可能降低孕产妇死亡风险。对出院后的结局无明显影响。四分之一的女性报告有硫酸镁相关的副作用。