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经阴道分娩并发伤口裂开后会阴缝合与期待治疗(PREVIEW):一项先导性和可行性随机对照试验

Perineal resuturing versus expectant management following vaginal delivery complicated by a dehisced wound (PREVIEW): a pilot and feasibility randomised controlled trial.

作者信息

Dudley L, Kettle C, Thomas P W, Ismail K M K

机构信息

The Maternity Centre, Royal Stoke, University Hospitals of North Midlands, Staffordshire, UK.

Faculty of Health, Staffordshire University, Stafford, UK.

出版信息

BMJ Open. 2017 Feb 10;7(2):e012766. doi: 10.1136/bmjopen-2016-012766.

Abstract

OBJECTIVE

To establish the feasibility of conducting a definitive randomised controlled trial (RCT) comparing the effectiveness of resuturing versus expectant management for dehisced perineal wounds.

DESIGN

A multicentre pilot and feasibility RCT.

SETTING

Ten UK maternity units from July 2011 to July 2013.

POPULATION

Eligible women with a dehisced perineal wound within 2 weeks of childbirth.

METHODS

The interventions were resuturing or expectancy. Randomisation was via web or telephone, stratified by participating centre. Blinding was not possible due to the nature of the interventions. Analysis was by intention-to-treat.

OUTCOME

The primary outcome measure was wound healing at 6-8 weeks.

RESULTS

The study revealed a number of feasibility issues, particularly strong patient and clinician preference for treatment options at recruiting centres and the timing of the primary outcome measure. Thirty-four women were randomised (17 in each arm). Data from 33 women were analysed on an intention-to-treat analysis to obtain preliminary estimates of effect size. There was a difference in wound healing at 2 weeks favouring resuturing (OR 20.00, 95% CI 2.04 to 196.37, p=0.004). However, by 6-8 weeks all but one wound in both groups had healed.

CONCLUSIONS

PREVIEW revealed a number of feasibility issues, which impacted on recruitment rate. These will have to be taken into account in the design of any future definitive study. In this feasibility study, resuturing was associated with quicker wound healing and women reported higher satisfaction rates with the outcome at 3 months.

TRIAL REGISTRATION NUMBER

ISRCTN05754020.

摘要

目的

确定开展一项确定性随机对照试验(RCT)的可行性,该试验旨在比较会阴伤口裂开后缝合与期待疗法的效果。

设计

多中心预试验及可行性RCT。

地点

2011年7月至2013年7月期间英国的10个产科单位。

研究对象

分娩后2周内会阴伤口裂开的符合条件的女性。

方法

干预措施为缝合或期待疗法。通过网络或电话进行随机分组,按参与中心分层。由于干预措施的性质,无法实施盲法。采用意向性分析。

结局

主要结局指标为6 - 8周时伤口愈合情况。

结果

该研究揭示了一些可行性问题,特别是在招募中心患者和临床医生对治疗方案有强烈偏好,以及主要结局指标的时间安排。34名女性被随机分组(每组17名)。对33名女性的数据进行意向性分析,以获得效应大小的初步估计值。2周时伤口愈合情况存在差异,缝合组更具优势(比值比20.00,95%可信区间2.04至196.37,p = 0.004)。然而,到6 - 8周时,两组除1例伤口外均已愈合。

结论

PREVIEW研究揭示了一些可行性问题,这些问题影响了招募率。在未来任何确定性研究的设计中都必须考虑这些问题。在这项可行性研究中,缝合与伤口愈合更快相关,且女性在3个月时对结局的满意度更高。

试验注册号

ISRCTN05754020。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e7d/5306527/9409998f4020/bmjopen2016012766f01.jpg

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