OASI2:英国产科单位可持续实施产科肛门括约肌损伤护理包策略的聚类随机混合评估。

Magdalena Jurczuk, Posy Bidwell, Dorian Martinez, Louise Silverton, Jan Van der Meulen, Daniel Wolstenholme, Ranee Thakar, Ipek Gurol-Urganci, Nick Sevdalis
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引用次数: 5

摘要

背景:产科肛门括约肌损伤(OASI)护理包包括四个一级和二级预防措施,针对分娩期间严重会阴撕裂率上升,这可能对妇女造成严重的衰弱后果。在英国的OASI1项目(2017-2018年)中,OASI护理包在16个产科单位实施,证明了护理包在降低OASI比率方面的有效性。在OASI2中,在一项效果与实施的混合研究中,护理包将扩大到20个国家卫生服务(NHS)产科单位,该研究将审查用于引入、实施和维持护理包的战略的有效性。方法:OASI2是一项在英格兰、苏格兰和威尔士的产科病房进行的双组随机对照试验(C-RCT),另外还有一个非随机研究组。C-RCT第1组(同伴支持,n = 10个单位)将由“伙伴”单位提供支持,以实施OASI护理包。C-RCT组2(精益实施,n = 10个单位)将在没有外部支持的情况下实施。额外的研究组(可持续性,n = 10个单位)将包括一些原始的OASI1单位,以评估从OASI1之前到OASI2结束期间护理包的可持续性和OASI率。所有三个研究组的单位都将获得一个包含培训资源和实施支持的实施工具包。C-RCT组将在OASI率降低(主要效果结果)和临床医生对护理包的采用(主要实施结果)方面进行比较。将从产妇信息系统中整理临床数据;实施数据将通过对妇女和临床医生的有效调查收集,并辅以定性方法。描述性统计和回归模型将用于分析。从定性数据的紧急主题将使用框架分析进行评估。讨论:OASI2将研究用于引入和维持OASI护理包的各种实施策略的影响,以及这些策略如何影响护理包的临床效果。这项研究将有助于了解如何有效地扩大和维持产科单位对类似干预措施的吸收和覆盖。将制定一份适合当地情况的“实施蓝图”,为未来预防会阴创伤指南的制定提供信息。试验注册:ISRCTN26523605。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

OASI2: a cluster randomised hybrid evaluation of strategies for sustainable implementation of the Obstetric Anal Sphincter Injury Care Bundle in maternity units in Great Britain.

OASI2: a cluster randomised hybrid evaluation of strategies for sustainable implementation of the Obstetric Anal Sphincter Injury Care Bundle in maternity units in Great Britain.

OASI2: a cluster randomised hybrid evaluation of strategies for sustainable implementation of the Obstetric Anal Sphincter Injury Care Bundle in maternity units in Great Britain.

OASI2: a cluster randomised hybrid evaluation of strategies for sustainable implementation of the Obstetric Anal Sphincter Injury Care Bundle in maternity units in Great Britain.

Background: The Obstetric Anal Sphincter Injury (OASI) Care Bundle comprises four primary and secondary prevention practices that target the rising rates of severe perineal tearing during childbirth, which can have severe debilitating consequences for women. The OASI Care Bundle was implemented in 16 maternity units in Britain in the OASI1 project (2017-2018), which demonstrated the care bundle's effectiveness in reducing OASI rates. In OASI2, the care bundle will be scaled up to 20 additional National Health Service (NHS) maternity units in a hybrid effectiveness-implementation study that will examine the effectiveness of strategies used to introduce, implement and sustain the care bundle.

Methods: OASI2 is a two-arm cluster-randomised control trial (C-RCT) of maternity units in England, Scotland and Wales, with an additional non-randomised study arm. C-RCT arm 1 (peer support, n = 10 units) will be supported by 'buddy' units to implement the OASI Care Bundle. C-RCT arm 2 (lean implementation, n = 10 units) will implement without external support. The additional study arm (sustainability, n = 10 units) will include some original OASI1 units to evaluate the care bundle's sustainability and OASI rates over time, from before OASI1 and through the end of OASI2. Units in all three study arms will receive an Implementation Toolkit with training resources and implementation support. The C-RCT arms will be compared in terms of OASI rate reduction (primary effectiveness outcome) and clinicians' adoption of the care bundle (primary implementation outcome). Clinical data will be collated from maternity information systems; implementation data will be collected through validated surveys with women and clinicians, supplemented by qualitative methods. Descriptive statistics and regression modelling will be used for analysis. Emergent themes from the qualitative data will be assessed using framework analysis.

Discussion: OASI2 will study the impact of various implementation strategies used to introduce and sustain the OASI Care Bundle, and how these strategies affect the bundle's clinical effectiveness. The study will generate insights into how to effectively scale-up and sustain uptake and coverage of similar interventions in maternity units. A locally adaptable 'implementation blueprint' will be produced to inform development of future guidelines to prevent perineal trauma.

Trial registration: ISRCTN26523605.

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