Romero R, Conde-Agudelo A, El-Refaie W, Rode L, Brizot M L, Cetingoz E, Serra V, Da Fonseca E, Abdelhafez M S, Tabor A, Perales A, Hassan S S, Nicolaides K H
Perinatology Research Branch, Program for Perinatal Research and Obstetrics, Division of Intramural Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Department of Health and Human Services, Bethesda, MD and Detroit, MI, USA.
Department of Obstetrics and Gynecology, University of Michigan, Ann Arbor, MI, USA.
Ultrasound Obstet Gynecol. 2017 Mar;49(3):303-314. doi: 10.1002/uog.17397.
To assess the efficacy of vaginal progesterone for the prevention of preterm birth and neonatal morbidity and mortality in asymptomatic women with a twin gestation and a sonographic short cervix (cervical length ≤ 25 mm) in the mid-trimester.
This was an updated systematic review and meta-analysis of individual patient data (IPD) from randomized controlled trials comparing vaginal progesterone with placebo/no treatment in women with a twin gestation and a mid-trimester sonographic cervical length ≤ 25 mm. MEDLINE, EMBASE, POPLINE, CINAHL and LILACS (all from inception to 31 December 2016), the Cochrane Central Register of Controlled Trials, Research Registers of ongoing trials, Google Scholar, conference proceedings and reference lists of identified studies were searched. The primary outcome measure was preterm birth < 33 weeks' gestation. Two reviewers independently selected studies, assessed the risk of bias and extracted the data. Pooled relative risks (RRs) with 95% confidence intervals (CI) were calculated.
IPD were available for 303 women (159 assigned to vaginal progesterone and 144 assigned to placebo/no treatment) and their 606 fetuses/infants from six randomized controlled trials. One study, which included women with a cervical length between 20 and 25 mm, provided 74% of the total sample size of the IPD meta-analysis. Vaginal progesterone, compared with placebo/no treatment, was associated with a statistically significant reduction in the risk of preterm birth < 33 weeks' gestation (31.4% vs 43.1%; RR, 0.69 (95% CI, 0.51-0.93); moderate-quality evidence). Moreover, vaginal progesterone administration was associated with a significant decrease in the risk of preterm birth < 35, < 34, < 32 and < 30 weeks' gestation (RRs ranging from 0.47 to 0.83), neonatal death (RR, 0.53 (95% CI, 0.35-0.81)), respiratory distress syndrome (RR, 0.70 (95% CI, 0.56-0.89)), composite neonatal morbidity and mortality (RR, 0.61 (95% CI, 0.34-0.98)), use of mechanical ventilation (RR, 0.54 (95% CI, 0.36-0.81)) and birth weight < 1500 g (RR, 0.53 (95% CI, 0.35-0.80)) (all moderate-quality evidence). There were no significant differences in neurodevelopmental outcomes at 4-5 years of age between the vaginal progesterone and placebo groups.
Administration of vaginal progesterone to asymptomatic women with a twin gestation and a sonographic short cervix in the mid-trimester reduces the risk of preterm birth occurring at < 30 to < 35 gestational weeks, neonatal mortality and some measures of neonatal morbidity, without any demonstrable deleterious effects on childhood neurodevelopment. Published 2017. This article is a U.S. Government work and is in the public domain in the USA.
评估阴道用黄体酮对孕中期双胎妊娠且超声检查宫颈短(宫颈长度≤25mm)的无症状女性预防早产及新生儿发病率和死亡率的疗效。
这是一项对个体患者数据(IPD)进行的系统评价和荟萃分析,这些数据来自随机对照试验,比较了阴道用黄体酮与安慰剂/不治疗在双胎妊娠且孕中期超声检查宫颈长度≤25mm的女性中的效果。检索了MEDLINE、EMBASE、POPLINE、CINAHL和LILACS(均从创刊至2016年12月31日)、Cochrane对照试验中央注册库、正在进行试验的研究注册库、谷歌学术、会议论文集以及已识别研究的参考文献列表。主要结局指标是妊娠<33周的早产。两名研究者独立选择研究、评估偏倚风险并提取数据。计算了合并相对风险(RR)及95%置信区间(CI)。
来自6项随机对照试验的303名女性(159名被分配至阴道用黄体酮组,144名被分配至安慰剂/不治疗组)及其606名胎儿/婴儿的IPD数据可用。一项纳入宫颈长度在20至25mm之间女性的研究,提供了IPD荟萃分析总样本量的74%。与安慰剂/不治疗相比,阴道用黄体酮与妊娠<33周早产风险的统计学显著降低相关(31.4%对43.1%;RR,0.69(95%CI,0.51 - 0.93);中等质量证据)。此外,阴道用黄体酮给药与妊娠<35、<34、<32和<30周早产风险的显著降低相关(RR范围为0.47至0.83)、新生儿死亡(RR,0.53(95%CI,0.35 - 0.81))、呼吸窘迫综合征(RR,0.70(95%CI,0.56 - 0.89))、新生儿复合发病率和死亡率(RR,0.61(95%CI,0.34 - 0.98))、机械通气的使用(RR,0.54(9%CI,0.36 - 0.81))以及出生体重<1500g(RR,0.53(95%CI,0.35 - )(均为中等质量证据)。阴道用黄体酮组和安慰剂组在4至5岁时的神经发育结局无显著差异。
对孕中期双胎妊娠且超声检查宫颈短的无症状女性给予阴道用黄体酮可降低妊娠<30至<35周早产、新生儿死亡及一些新生儿发病率指标的风险,且对儿童神经发育无任何明显有害影响。2017年发表。本文为美国政府作品,在美国属于公共领域。