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利那洛肽联合聚乙二醇用于中国行结肠镜息肉切除术患者肠道准备的疗效:一项随机对照试验方案。

Efficacy of linaclotide in combination with polyethylene glycol for bowel preparation in Chinese patients undergoing colonoscopy polypectomy: protocol for a randomised controlled trial.

机构信息

Department of Nursing, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.

Department of Colorectal Surgery, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.

出版信息

BMJ Open. 2024 Jul 23;14(7):e080723. doi: 10.1136/bmjopen-2023-080723.

Abstract

BACKGROUND

Adequate bowel preparation is essential for successful colonoscopy and polypectomy procedures. However, a significant proportion of patients still exhibit suboptimal bowel preparation, ranging from 18% to 35%. The effectiveness of bowel preparation agents can be hampered by volume and taste, adversely affecting patient compliance and tolerance. Therefore, exploring strategies to minimise laxative volume and improve patient tolerance and adherence is imperative to ensure optimal bowel preparation quality.

METHODS AND ANALYSIS

This study is a two-arm, single-blinded, parallel-group randomised controlled trial designed to compare the efficacy of 2 L polyethylene glycol (PEG) combined with linaclotide with 4 L PEG in bowel cleansing. A total of 422 participants will be randomly assigned in a 1:1 ratio to either the intervention group (2 L PEG combined with 580 µg linaclotide) or the control group (4 L PEG). The primary outcome measure is bowel cleansing efficacy, which is assessed using the Boston Bowel Preparation Scale. Secondary outcomes include evaluating the tolerability and safety of the bowel preparation regimens, bowel diary assessments, postpolypectomy complications (such as bleeding and perforation) and the size and number of removed polyps.

ETHICS AND DISSEMINATION

The study has received approval from the Clinical Research Ethics Committee of The First Affiliated Hospital, Zhejiang University School of Medicine. The findings of this trial will serve as a valuable resource for clinicians and patients undergoing colonoscopy polypectomy by guiding the selection of appropriate bowel preparation regimens. Study findings will be disseminated to participants, presented at professional society meetings, and published in peer-reviewed journals. This trial was registered on the Chinese Clinical Trial Registry with registration number ChiCTR2300075410.

摘要

背景

充分的肠道准备对于成功进行结肠镜检查和息肉切除术至关重要。然而,仍有相当一部分患者的肠道准备不理想,比例在 18%至 35%之间。肠道准备剂的效果可能会受到容量和口感的影响,从而对患者的依从性和耐受性产生不利影响。因此,探索减少泻药用量、提高患者耐受性和依从性的策略对于确保最佳肠道准备质量至关重要。

方法和分析

这是一项双臂、单盲、平行组随机对照试验,旨在比较 2L 聚乙二醇(PEG)联合利那洛肽与 4L PEG 在肠道清洁中的疗效。总共将有 422 名参与者以 1:1 的比例随机分配到干预组(2L PEG 联合 580µg 利那洛肽)或对照组(4L PEG)。主要结局测量指标是肠道清洁效果,使用波士顿肠道准备量表进行评估。次要结局包括评估肠道准备方案的耐受性和安全性、肠道日记评估、息肉切除术后并发症(如出血和穿孔)以及切除的息肉大小和数量。

伦理和传播

该研究已获得浙江大学医学院第一附属医院临床研究伦理委员会的批准。本试验的结果将为接受结肠镜息肉切除术的临床医生和患者提供有价值的资源,指导选择合适的肠道准备方案。研究结果将分发给参与者,在专业学会会议上展示,并在同行评议的期刊上发表。该试验在中国临床试验注册中心注册,注册号为 ChiCTR2300075410。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58d9/11733793/9546e3487a2d/bmjopen-14-7-g001.jpg

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