Van Teeffelen Stijn, Pajkrt Eva, Willekes Christine, Van Kuijk Sander M J, Mol Ben Willem J
Department of Obstetrics and Gynaecology, Maastricht University Medical Centre, P. Debyelaan 25, Maastricht, Netherlands, 6229 HX.
Cochrane Database Syst Rev. 2013 Aug 3;2013(8):CD009952. doi: 10.1002/14651858.CD009952.pub2.
Preterm prelabour rupture of membranes (PPROM) before 26 weeks can delay lung development and can cause pulmonary hypoplasia, as a result of oligohydramnios. Restoring the amniotic fluid volume by transabdominal amnioinfusion might prevent abnormal lung development and might have a protective effect for neurological complications, fetal deformities and neonatal sepsis.
To assess the effectiveness of transabdominal amnioinfusion in improving perinatal outcome in women with oligohydramnios secondary to rupture of fetal membranes before 26 weeks.
We searched the Cochrane Pregnancy and Childbirth Group's Trials Register (30 April 2013).
All randomised controlled trials comparing transabdominal amnioinfusion with no transabdominal amnioinfusion. Cluster- or quasi-randomised trials were not eligible for inclusion. In cases where only an abstract was available, we attempted to find the full articles.
Two review authors assessed trials for inclusion. No eligible trials were identified.
There are no included studies.
AUTHORS' CONCLUSIONS: There is currently no evidence to evaluate the use of transabdominal amnioinfusion in women with oligohydramnios secondary to rupture of fetal membranes before 26 weeks for improving perinatal outcome. Further research examining the effects of this intervention is needed. Two randomised controlled trials are ongoing but final data have not yet been published.
孕26周前胎膜早破(PPROM)可因羊水过少而延迟肺发育并导致肺发育不全。经腹羊膜腔灌注恢复羊水量可能预防肺发育异常,并可能对神经并发症、胎儿畸形及新生儿败血症具有保护作用。
评估经腹羊膜腔灌注对改善孕26周前胎膜破裂继发羊水过少孕妇围产期结局的有效性。
我们检索了Cochrane妊娠和分娩组试验注册库(2013年4月30日)。
所有比较经腹羊膜腔灌注与未进行经腹羊膜腔灌注的随机对照试验。整群随机或半随机试验不符合纳入标准。若仅有摘要可用,我们会尝试查找全文。
两名综述作者评估纳入试验。未识别出符合条件的试验。
无纳入研究。
目前尚无证据评估经腹羊膜腔灌注用于改善孕26周前胎膜破裂继发羊水过少孕妇围产期结局的效果。需要进一步研究该干预措施的效果。两项随机对照试验正在进行,但最终数据尚未发表。