Hofmeyr G Justus
Department of Obstetrics and Gynaecology, East London Hospital Complex, University of the Witwatersrand, University of FortHare, Eastern Cape Department of Health, East London, South Africa.
Cochrane Database Syst Rev. 2012 Jun 13;2012(6):CD000004. doi: 10.1002/14651858.CD000004.pub2.
Abdominal decompression was developed as a means of pain relief during labour. It has also been used for complications of pregnancy, and in healthy pregnant women in an attempt to improve fetal wellbeing and intellectual development.
The objective of this review was to assess the effects of antenatal abdominal decompression for maternal hypertension or impaired fetal growth, on perinatal outcome.
The Cochrane Pregnancy and Childbirth Group's Trials Register (2 February 2012).
Randomised or quasi-randomised trials comparing abdominal decompression with no decompression in women with pre-eclampsia and/or fetuses thought to be compromised.
Eligibility and trial quality were assessed by one review author.
Three studies were included, all with the possibility of containing serious bias. Therapeutic abdominal decompression was associated with the following reductions: persistent pre-eclampsia (relative risk 0.36, 95% confidence interval 0.18 to 0.72); fetal distress in labour (relative risk 0.37, 95% confidence interval 0.19 to 0.71); low birthweight (relative risk 0.50, 95% confidence interval 0.40 to 0.63); Apgar scores less than six at one minute (relative risk 0.26, 95% confidence interval 0.12 to 0.56); and perinatal mortality (relative risk 0.39, 95% confidence interval 0.22 to 0.71).
AUTHORS' CONCLUSIONS: Due to the methodological limitations of the studies, the effects of therapeutic abdominal decompression are not clear. The apparent improvements in birthweight and perinatal mortality warrant further evaluation of abdominal decompression where there is impaired fetal growth and possibly for women with pre-eclampsia.
腹部减压作为分娩时缓解疼痛的一种方法而被采用。它也被用于治疗妊娠并发症,以及用于健康孕妇以试图改善胎儿健康状况和智力发育。
本综述的目的是评估产前腹部减压对患有妊娠高血压或胎儿生长受限的孕妇围产期结局的影响。
Cochrane妊娠与分娩组试验注册库(2012年2月2日)。
比较子痫前期和/或被认为有问题的胎儿的孕妇进行腹部减压与不进行减压的随机或半随机试验。
由一位综述作者评估纳入标准和试验质量。
纳入了三项研究,所有研究都有可能存在严重偏倚。治疗性腹部减压与以下情况的减少相关:持续性子痫前期(相对危险度0.36,95%置信区间0.18至0.72);分娩时胎儿窘迫(相对危险度0.37,95%置信区间0.19至0.71);低出生体重(相对危险度0.50,95%置信区间0.40至0.63);1分钟时阿氏评分低于6分(相对危险度0.26,95%置信区间0.12至0.56);以及围产期死亡率(相对危险度0.39,95%置信区间0.22至0.71)。
由于研究的方法学局限性,治疗性腹部减压的效果尚不清楚。出生体重和围产期死亡率的明显改善值得在胎儿生长受限的情况下以及可能在子痫前期妇女中对腹部减压进行进一步评估。