Churchill D, Beevers G D G, Meher S, Rhodes C
Royal Wolverhampton Hospitals NHS Trust, Department of Obstetrics and Gynaecology, New Cross Hospital, Wednesfield, Wolverhampton, West Midlands, UK, WV10 0QP.
Cochrane Database Syst Rev. 2007 Jan 24;2007(1):CD004451. doi: 10.1002/14651858.CD004451.pub2.
Diuretics are used to reduce blood pressure and oedema in non-pregnant individuals. Formerly, they were used in pregnancy with the aim of preventing or delaying the development of pre-eclampsia. This practice became controversial when concerns were raised that diuretics may further reduce plasma volume in women with pre-eclampsia, thereby increasing the risk of adverse effects on the mother and baby, particularly fetal growth.
To assess the effects of diuretics on prevention of pre-eclampsia and its complications.
We searched the Cochrane Pregnancy and Childbirth Group's Trials Register (April 2005), the Cochrane Central Register of Controlled Trials (The Cochrane Library 2005, Issue 2) and EMBASE (2002 to April 2005).
Randomised trials evaluating the effects of diuretics for preventing pre-eclampsia and its complications.
Three review authors independently selected trials for inclusion and extracted data. We analysed and double checked data for accuracy.
Five studies (1836 women) were included. All were of uncertain quality. The studies compared thiazide diuretics with either placebo or no intervention. There were no clear differences between the diuretic and control groups for any reported pregnancy outcomes including pre-eclampsia (four trials, 1391 women; relative risk (RR) 0.68, 95% confidence interval (CI) 0.45 to 1.03), perinatal death (five trials,1836 women; RR 0.72, 95% CI 0.40 to 1.27), and preterm birth (two trials, 465 women; RR 0.67, 95% CI 0.32 to 1.41). There were no small-for-gestational age babies in the one trial that reported this outcome, and there was insufficient evidence to demonstrate any clear differences between the two groups for birthweight (one trial, 20 women; weighted mean difference 139 grams, 95% CI -484.40 to 762.40). Thiazide diuretics were associated with an increased risk of nausea and vomiting (two trials, 1217 women; RR 5.81, 95% CI 1.04 to 32.46), and women allocated diuretics were more likely to stop treatment due to side-effects compared to those allocated placebo (two trials, 1217 women; RR 1.85, 95% CI 0.81 to 4.22).
AUTHORS' CONCLUSIONS: There is insufficient evidence to draw reliable conclusions about the effects of diuretics on prevention of pre-eclampsia and its complications. However, from this review, no clear benefits have been found from the use of diuretics to prevent pre-eclampsia. Taken together with the level of adverse effects found, the use of diuretics for the prevention of pre-eclampsia and its complications cannot be recommended.
利尿剂用于降低非妊娠个体的血压和水肿。以前,利尿剂曾用于妊娠,目的是预防或延缓子痫前期的发展。当有人担心利尿剂可能会进一步降低子痫前期女性的血容量,从而增加对母婴尤其是胎儿生长产生不良影响的风险时,这种做法就变得有争议了。
评估利尿剂对预防子痫前期及其并发症的效果。
我们检索了Cochrane妊娠与分娩组试验注册库(2005年4月)、Cochrane对照试验中心注册库(《Cochrane图书馆》2005年第2期)和EMBASE(2002年至2005年4月)。
评估利尿剂预防子痫前期及其并发症效果的随机试验。
三位综述作者独立选择纳入试验并提取数据。我们对数据进行了分析并进行了双重核对以确保准确性。
纳入了五项研究(1836名女性)。所有研究质量均不确定。这些研究将噻嗪类利尿剂与安慰剂或不干预进行了比较。在任何报告的妊娠结局方面,利尿剂组和对照组之间均无明显差异,包括子痫前期(四项试验,1391名女性;相对危险度(RR)0.68,95%置信区间(CI)0.45至1.03)、围产期死亡(五项试验,1836名女性;RR 0.72,95%CI 0.40至1.27)和早产(两项试验,465名女性;RR 0.67,95%CI 0.32至1.41)。在报告了该结局的一项试验中,没有小于胎龄儿,并且没有足够的证据表明两组在出生体重方面有任何明显差异(一项试验,20名女性;加权平均差139克,95%CI -484.40至762.40)。噻嗪类利尿剂与恶心和呕吐风险增加相关(两项试验,1217名女性;RR 5.81,95%CI 1.04至32.46),与分配到安慰剂组的女性相比,分配到利尿剂组的女性因副作用而更有可能停止治疗(两项试验,1217名女性;RR 1.85,95%CI 0.81至4.22)。
没有足够的证据就利尿剂对预防子痫前期及其并发症的效果得出可靠结论。然而,从本综述来看,未发现使用利尿剂预防子痫前期有明显益处。综合所发现的不良反应程度,不建议使用利尿剂预防子痫前期及其并发症。