Impact of early versus late artificial rupture of membranes during oxytocin induction of labour on the incidence of chorioamnionitis: a randomised controlled trial (ARM trial).

IF 2 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Trials Pub Date : 2025-01-22 DOI:10.1186/s13063-025-08722-z
Meghan G Hill, Michelle R Wise, Emmanuelle Pauleau, Beatrice Treadwell, Lynn Sadler
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Abstract

Background: The approach to induction of labour differs internationally, with timing of amniotomy being controversial. Some institutions favour performing artificial rupture of membranes prior to commencement of oxytocin infusion, with the belief that the labour will progress more efficiently. In other institutions, the approach recommended is for oxytocin infusion with intact amniotic membranes until the person has reached the active phase of labour, citing risk of infection with early amniotomy. Current evidence is inconclusive. We are performing a randomised controlled trial assessing whether delaying amniotomy until the active phase of labour can decrease the rate of chorioamnionitis.

Methods: This is a randomised controlled trial at a single centre in New Zealand. Pregnant people undergoing induction of labour at ≥ 37 weeks gestational age with intact membranes and a singleton gestation are eligible for the trial. Participants are randomised to 'Early' amniotomy, at the commencement of oxytocin infusion, or to 'Late' amniotomy, when they have reached a cervical dilation of 6 or more centimetres or when they have been receiving oxytocin infusion for 12 h. The primary outcome of the trial is chorioamnionitis. To detect a decrease in chorioamnionitis from 9 to 3% with a power of 80% and a 95% CI, we will require 488 participants in total, randomised in a 1:1 ratio.

Discussion: If delaying amniotomy reduces the rate of chorioamnionitis, this is important to inform future practice. Chorioamnionitis entails risk to both the pregnant person and the fetus and is an important contributor to neonatal sepsis, neonatal intensive care unit admission, maternal sepsis, caesarean, wound infection and postoperative infective complications. Conversely, if the rate of chorioamnionitis is not affected by timing of amniotomy, this will allow for safe individualization of care.

Trial registration: The trial is registered on the Australian and New Zealand Clinical Trials Registry, anzctr.org.au. Full registry title is 'Impact of early versus late artificial rupture of membranes during oxytocin induction of labour on the incidence of chorioamnionitis: A randomised controlled trial'.

Trial id: ACTRN12621000405819. Date registered 14 April 2021.

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催产素引产过程中早期和晚期人工破膜对羊膜炎发生率的影响:一项随机对照试验(ARM试验)。
背景:引产的方法在国际上是不同的,羊膜切开的时机是有争议的。一些机构倾向于在开始注射催产素之前进行人工破膜术,相信分娩过程会更有效。在其他机构中,推荐的方法是用完整的羊膜输注催产素,直到人达到产程活动性阶段,引用早期羊膜切开感染的风险。目前的证据尚无定论。我们正在进行一项随机对照试验,评估将羊膜切开推迟到产程活动性阶段是否可以降低羊膜炎的发生率。方法:这是一项新西兰单中心随机对照试验。孕龄≥37周引产且胎膜完整且单胎妊娠的孕妇符合试验条件。参与者被随机分配到“早期”羊膜切开术,在催产素输注开始时,或“晚期”羊膜切开术,当他们已经达到6厘米或更多的宫颈扩张或当他们已经接受催产素输注12小时。试验的主要结果是绒毛膜羊膜炎。为了检测绒毛膜羊膜炎的发生率从9%下降到3%,幂次为80%,95%可信区间为95%,我们总共需要488名参与者,按1:1的比例随机分组。讨论:如果延迟羊膜切开术可以降低羊膜炎的发生率,这对未来的实践是很重要的。绒毛膜羊膜炎对孕妇和胎儿都有风险,是新生儿败血症、新生儿重症监护病房住院、产妇败血症、剖腹产、伤口感染和术后感染并发症的重要因素。相反,如果绒毛膜羊膜炎的发生率不受羊膜切开时间的影响,这将允许安全的个体化护理。试验注册:该试验在澳大利亚和新西兰临床试验注册中心anzctr.org.au注册。完整的注册标题是“催产素引产过程中早期和晚期人工破膜对绒毛膜羊膜炎发生率的影响:一项随机对照试验”。试用号:ACTRN12621000405819。注册日期2021年4月14日。
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来源期刊
Trials
Trials 医学-医学:研究与实验
CiteScore
3.80
自引率
4.00%
发文量
966
审稿时长
6 months
期刊介绍: Trials is an open access, peer-reviewed, online journal that will encompass all aspects of the performance and findings of randomized controlled trials. Trials will experiment with, and then refine, innovative approaches to improving communication about trials. We are keen to move beyond publishing traditional trial results articles (although these will be included). We believe this represents an exciting opportunity to advance the science and reporting of trials. Prior to 2006, Trials was published as Current Controlled Trials in Cardiovascular Medicine (CCTCVM). All published CCTCVM articles are available via the Trials website and citations to CCTCVM article URLs will continue to be supported.
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