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环形聚乙二醇手术巾预防手术部位感染(COVER 试验):一项随机对照试验的研究方案。

Circular pOlyethylene drape in preVEntion of suRgical site infection (COVER trial): study protocol for a randomised controlled trial.

机构信息

Surgery, St. Vincent's Hospital, The Catholic University of Korea, Suwon, The Republic of Korea.

Surgery, Uijeongbu St. Mary's Hospital. The Catholic University of Korea, Uijeongbu, The Republic of Korea.

出版信息

BMJ Open. 2020 Jan 22;10(1):e034687. doi: 10.1136/bmjopen-2019-034687.

Abstract

INTRODUCTION

Surgical site infection (SSI) after abdominal surgery remains a significant cause of morbidity and is associated with an increased socioeconomic burden and a reduced quality of life. Circular wound protectors have been expected to reduce the risk of SSI, but previous studies reported conflicting results on their protective effects. The purpose of this study was to evaluate the efficacy of circular wound protectors in reducing SSI in open abdominal surgery.

METHODS AND ANALYSIS

The circular pOlyethylen drape in preVEntion of suRgical site infection (COVER) trial investigates whether the application of a dual-ring circular plastic wound protector reduces the rate of SSI in patients undergoing elective or emergent open abdominal surgery related to the gastrointestinal tract, regardless of the type of wound classified by the Centers for Disease Control. The COVER trial is a multicentre, randomised controlled clinical trial with two parallel arms-one using a dual-ring wound protector with circular polyethylene drape and the other using conventional surgical dressing gauze. The primary outcome will measure the rate of SSI within 30 days after surgery in two groups. Statistical analysis of the primary end point will be based on the intention-to-treat population. The sample size was determined to achieve a study power of 80% with 95% two-sided confidence limits. Considering a dropout rate of up to 5%, a total of 458 patients, 229 patients in each group, will be enrolled in this study.

ETHICS AND DISSEMINATION

The trial protocol and informed consent document have been reviewed and approved by the institutional review board at each participating centre. Written informed consent will be obtained from each study participant. The clinical outcomes of this trial will be submitted to an international peer-reviewed journal and presented at international conferences.

TRIAL REGISTRATION NUMBER

NCT03170843.

摘要

简介

腹部手术后的手术部位感染(SSI)仍然是发病率的一个重要原因,并且与增加的社会经济负担和降低的生活质量有关。环形伤口保护器有望降低 SSI 的风险,但以前的研究报告对其保护作用的结果存在矛盾。本研究旨在评估环形伤口保护器在减少开放性腹部手术中 SSI 的效果。

方法与分析

环形聚乙烯罩在预防手术部位感染(COVER)试验中调查了在接受择期或紧急开放性腹部手术的患者中,应用双环环形塑料伤口保护器是否能降低与胃肠道相关的 SSI 发生率,而不论由疾病控制中心分类的伤口类型如何。COVER 试验是一项多中心、随机对照临床试验,有两个平行组-一个使用带环形聚乙烯罩的双环伤口保护器,另一个使用常规手术敷料纱布。主要结局将在两组中测量手术后 30 天内的 SSI 发生率。主要终点的统计分析将基于意向治疗人群。根据 80%的研究效能和 95%的双侧置信区间确定了样本量。考虑到高达 5%的脱落率,总共将招募 458 名患者,每组 229 名患者参加这项研究。

伦理和传播

该试验方案和知情同意书已经在每个参与中心的机构审查委员会进行了审查和批准。将从每个研究参与者那里获得书面知情同意书。本试验的临床结果将提交给国际同行评议期刊,并在国际会议上进行报告。

试验注册号

NCT03170843。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3894/7044988/b3571aedb52e/bmjopen-2019-034687f01.jpg

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