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首页> 外文期刊>Acta Obstetricia et Gynecologica Scandinavica: Official Publication of the Nordisk Forening for Obstetrik och Gynekologi >Induction of labor at full‐term in pregnant women with uncomplicated singleton pregnancy: A systematic review and meta‐analysis of randomized trials
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Induction of labor at full‐term in pregnant women with uncomplicated singleton pregnancy: A systematic review and meta‐analysis of randomized trials

机译:在孕妇的孕妇诱导患有简单的单身妊娠的劳动:系统评价和随机试验的荟萃分析

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摘要

Abstract Introduction The lowest incidence of perinatal morbidity and mortality occurs around 39‐40?weeks. Therefore, some have advocated induction of uncomplicated singleton gestations once they reach full‐term. The aim of the study was to evaluate the risk of cesarean delivery, and any maternal and perinatal effects of a policy of induction of labor in women with full‐term uncomplicated singleton gestations. Material and methods We performed an electronic search from inception of each database to August 2018. All results were then limited to randomized trial. No restrictions for language or geographic location were applied. Inclusion criteria were randomized clinical trials of asymptomatic women with uncomplicated, singleton gestations at full‐term (ie, between 39 +0 and 40 +6 ?weeks) who were randomized to either planned induction of labor or control (ie, expectant management). Only trials on asymptomatic singleton gestations without premature rupture of membranes or any other indications for induction evaluating the effectiveness of planned induction of labor in full‐term singleton gestations were included. The primary outcome was the incidence of cesarean delivery. Results Seven randomized clinical trials, including 7598 participants were analyzed. Three studies enrolled only women with favorable cervix, defined as a Bishop score of ≥5 in nulliparous women or ≥4 in multiparous women. One trial included only women aged 35?years or older. Women randomized to the planned induction of labor, received scheduled induction usually at 39 +0 to 39 +6 ?weeks of gestation, whereas women in the control group received expectant management usually until 41‐42?weeks of gestation, or earlier if medically indicated. Methods of induction usually included cervical ripening, with either misoprostol or Foley catheter, in conjunction with or followed by oxytocin for women with unfavorable cervix, and oxytocin and artificial rupture of membranes for those with favorable cervix. Five trials also used artificial rupture of membranes as a method for induction. Uncomplicated full‐term singleton gestations that were randomized to receive induction of labor had similar incidence of cesarean delivery compared with controls (18.6% vs 21.4%; relative risk 0.96, 95% CI 0.78‐1.19). Regarding neonatal outcomes, induction of labor at full‐term was associated with a significantly lower rate of meconium‐stained amniotic fluid (4.0% vs 13.5%; relative risk 0.32, 95% CI 0.18‐0.57), and lower mean birthweight (mean difference ?98.96?g, 95% CI ?126.29 to ?71.63) compared with the control group. There were no between‐group differences in other adverse neonatal outcomes. Conclusions Induction of labor at about 39?weeks is not associated with increased risk of cesarean delivery.
机译:摘要引言围产期发病率最低和死亡率发生在39-40左右约为39-40周。因此,一旦达到全术,他们就有一些倡导的诱导简单的单身孕产。该研究的目的是评估剖腹产的风险,以及具有全学期简单的单例妊娠的妇女委托劳动政策的任何孕产妇和围产期影响。材料和方法我们从每个数据库开始到2018年8月的电子搜索。然后所有结果都限于随机试验。没有应用语言或地理位置的限制。纳入标准是随机的,无症状妇女随机临床试验,具有简单的单例妊娠(即39 + 0和40 + 6?周),其被随机分为计划诱导劳动或控制(即预期管理)。只有在没有过早破裂的无症状单身妊娠的试验,或对诱导血液诱导劳动中劳动造成的有效性的任何其他适应性的妊娠期妊娠。主要结果是剖宫产的发病率。结果分析了七项随机临床试验,包括7598名参与者。三项研究只注册了子宫颈的女性,被定义为无数妇女的无流动女性≥5的主教得分或≥4。一项审判仅包括35岁的女性年龄或以上。妇女随机向计划诱导劳动,通常在妊娠的39 + 0到39 + 6?周周内接受预定诱导,而对照组的妇女通常在41-42?妊娠周期之前接受预期管理,如果医学表明,或更早的妊娠。诱导方法通常包括颈椎熟化,用缺氧或粪便导管,与具有不利子宫颈的妇女的催产素,以及催产素和人工破裂的膜,用于患有贫困的子宫颈。五项试验还使用人造破裂的膜作为诱导方法。随机以接受劳动诱导的未复杂的全术术语妊娠与对照组相比具有类似的剖宫产的发病率(18.6%vs 21.4%;相对风险0.96,95%CI 0.78-1.19)。关于新生儿结果,全术语促进劳动率与膀胱染色液体的显着较低(4.0%Vs 13.5%;相对风险为0.32,95%CI 0.18-0.57),较低的平均分批(平均差异与对照组相比,98.96?G,95%CI?126.29至10.63)。其他不良新生儿结果没有组差异。结论植入诱导约39〜周与剖宫产递送的风险增加无关。

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