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肠道清洁剂的比较安全性:系统评价与网状Meta分析方案

Comparative safety of bowel cleansers: protocol for a systematic review and network meta-analysis.

作者信息

Barbeau Pauline, Wolfe Dianna, Yazdi Fatemeh, Rice Danielle B, Dube Catherine, Kanji Salmaan, Rostom Alaa, Skidmore Becky, Moher David, Hutton Brian

机构信息

Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.

Department of Clinical Psychology, McGill University, Montreal, Quebec, Canada.

出版信息

BMJ Open. 2018 Jun 27;8(6):e021892. doi: 10.1136/bmjopen-2018-021892.

Abstract

INTRODUCTION

The US Food and Drug Administration has withdrawn the bowel cleansing kit HalfLytely (PEG 3500) with 10 mg bisacodyl tablets due to an increased risk of ischaemic colitis compared with the same kit with only 5 mg bisacodyl. This is of interest in Canada given that the bowel cleansing kit Bi-Peglyte (PEG 3500) with 15 mg bisacodyl is currently approved for use. The objective is to assess the comparative safety of various bowel cleansers with or without bisacodyl, with a primary interest inpolyethylene glycol (PEG)-based and sodium-picosulfate-based products.

METHODS AND ANALYSIS

Given the existing volume of the literature, the review will be conducted in two stages. Stage 1 will consist of a scoping exercise by searching MEDLINE, Embase and the Cochrane Library (up to 21 November 2017) to identify randomised controlled trials, quasirandomised studies and non-randomised studies in which any bowel cleanser regimens were compared among persons undergoing colonoscopy. The outcomes will be mapped to establish a listing of the studies and their comparisons and outcomes currently available in the literature. From this, a data synthesis plan will be determined. In stage 2, a systematic review with meta-analyses will be pursued, focused on the bowel cleanser comparisons and outcomes of interest identified in stage 1. Two reviewers will screen, extract and quality assess the articles. Outcomes of interest include ischaemic colitis, electrolyte imbalances and their consequences, seizures, bowel perforation and patient tolerability. If sufficient data exist and studies are of sufficient homogeneity, network meta-analyses (NMAs) will be performed.

ETHICS AND DISSEMINATION

Ethics approval was not necessary due to study design. Updating the safety profile of bowel cleansers among the generally healthy population undergoing colonoscopy is pertinent given recent approval changes. This will be the first NMA within this population. Policy considerations may be reconsidered to minimise risk during bowel cleanser use.

PROSPERO REGISTRATION NUMBER

CRD42018084720.

摘要

引言

美国食品药品监督管理局已撤回含10毫克比沙可啶片的肠道清洗套装HalfLytely(聚乙二醇3500),因为与仅含5毫克比沙可啶的同一套装相比,其缺血性结肠炎风险增加。鉴于含15毫克比沙可啶的肠道清洗套装Bi - Peglyte(聚乙二醇3500)目前在加拿大已获批准使用,这一点在加拿大受到关注。目的是评估含或不含比沙可啶的各种肠道清洗剂的相对安全性,主要关注基于聚乙二醇(PEG)和基于匹可硫酸钠的产品。

方法与分析

鉴于现有文献量,本综述将分两个阶段进行。第一阶段将通过检索MEDLINE、Embase和Cochrane图书馆(截至2017年11月21日)进行范围界定,以识别在接受结肠镜检查的人群中比较任何肠道清洗剂方案的随机对照试验、半随机研究和非随机研究。将对结果进行梳理,以建立文献中现有研究及其比较和结果的清单。据此确定数据综合计划。在第二阶段,将进行系统综述和荟萃分析,重点关注第一阶段确定的肠道清洗剂比较和感兴趣的结果。两名评审员将筛选、提取并对文章进行质量评估。感兴趣的结果包括缺血性结肠炎、电解质失衡及其后果、癫痫发作、肠穿孔和患者耐受性。如果有足够的数据且研究具有足够的同质性,将进行网状荟萃分析(NMA)。

伦理与传播

由于研究设计,无需伦理批准。鉴于最近的批准变化,更新接受结肠镜检查的一般健康人群中肠道清洗剂的安全性概况具有相关性。这将是该人群中的首个NMA。可能会重新考虑政策因素,以尽量减少使用肠道清洗剂期间的风险。

PROSPERO注册号:CRD42018084720。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e59b/6020982/683a0f8e4b93/bmjopen-2018-021892f01.jpg

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