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B-腺瘤研究:使用内套优化黏膜异常的肠道镜检查检测准确性:随机对照试验研究方案

The B-ADENOMA Study: Bowelscope - Accuracy of Detection using Endocuff Optimisation of Mucosal Abnormalities: Study Protocol for randomised controlled trial.

作者信息

Ngu Wee Sing, Walls Martin, Bhandari Pradeep, Stokes Clive, Totton Nikki, Hoare Zoe, Bastable Lexi, Rees Colin

机构信息

South Tyneside NHS Foundation Trust - Gastroenterology, South Shields, Tyne and Wear, United Kingdom of Great Britain and Northern Ireland.

Queen Alexandra Hospital - Gastroenterology, Portsmouth, Portsmouth, United Kingdom of Great Britain and Northern Ireland.

出版信息

Endosc Int Open. 2018 Jul;6(7):E872-E877. doi: 10.1055/a-0591-9308. Epub 2018 Jul 4.

Abstract

BACKGROUND AND STUDY AIMS

UK Bowel Cancer Screening flexible sigmoidoscopy (BowelScope) currently offers patients aged 55 a one-off flexible sigmoidoscopy for adenoma clearance to decrease colorectal cancer incidence by interrupting the adenoma-carcinoma sequence. Recent evidence has shown maximum benefit in increasing adenoma detection rate (ADR) using the Endocuff Vision device in the left side of the colon and in screening patients. Currently, ADR is low and shows unacceptable variation in BowelScope. ADR is a quality indicator in screening sigmoidoscopy and higher rates have been shown to reduce colorectal cancer incidence.

PATIENTS AND METHODS

This will be a prospective, multicenter, UK-based randomized controlled trial (RCT) comparing ADR in Endocuff-assisted versus standard bowel cancer screening flexible sigmoidoscopy (BowelScope). All patients aged 55 to 61 years invited to BowelScope screening and able to give informed consent will be eligible for recruitment. Exclusion criteria include absolute contraindications to flexible sigmoidoscopy, known or suspected large bowel obstruction or pseudo-obstruction, colonic strictures or polyposis syndromes, known severe diverticular segment, active colitis, inability to give informed consent, anticoagulation precluding polypectomy and pregnancy. Patients will be randomized on the day of procedure to Endocuff-assisted flexible sigmoidoscopy or standard flexible sigmoidoscopy, stratified by age group and sex. Baseline, endoscopy and polyp data were collected as well as nurse and patient assessment of comfort. Polyp histology was collected when available. Patients will be asked to return a comfort questionnaire the following day and were followed up for 14 days for complications.

RESULTS

The ADENOMA trial will be designed to demonstrate a significant improvement in ADR with maximal effect in the left colon and in fecal occult blood test-positive screening patients. This trial will be the first RCT to look at Endocuff Vision in bowel cancer screening flexible sigmoidoscopy. We will aim to establish whether Endocuff vision improves ADR in this population.

摘要

背景与研究目的

英国肠癌筛查柔性乙状结肠镜检查(肠道镜检查)目前为55岁的患者提供一次性柔性乙状结肠镜检查以清除腺瘤,通过中断腺瘤 - 癌序列来降低结直肠癌发病率。最近的证据表明,使用Endocuff Vision设备在结肠左侧及筛查患者中提高腺瘤检出率(ADR)的获益最大。目前,肠道镜检查中的ADR较低且存在不可接受的差异。ADR是筛查乙状结肠镜检查的质量指标,较高的ADR已被证明可降低结直肠癌发病率。

患者与方法

这将是一项基于英国的前瞻性、多中心随机对照试验(RCT),比较Endocuff辅助与标准肠癌筛查柔性乙状结肠镜检查(肠道镜检查)中的ADR。所有受邀参加肠道镜检查且能够给予知情同意的55至61岁患者均有资格入选。排除标准包括柔性乙状结肠镜检查的绝对禁忌症、已知或疑似大肠梗阻或假性梗阻、结肠狭窄或息肉病综合征、已知严重憩室段、活动性结肠炎、无法给予知情同意、抗凝治疗妨碍息肉切除术以及妊娠。患者将在手术当天随机分为Endocuff辅助柔性乙状结肠镜检查组或标准柔性乙状结肠镜检查组,按年龄组和性别分层。收集基线、内镜检查和息肉数据以及护士和患者对舒适度的评估。如有可用,收集息肉组织学检查结果。患者将被要求在第二天返回一份舒适度问卷,并随访14天以观察并发症。

结果

腺瘤试验旨在证明ADR有显著改善,在左结肠及粪便潜血试验阳性的筛查患者中效果最大。该试验将是首个在肠癌筛查柔性乙状结肠镜检查中研究Endocuff Vision的RCT。我们旨在确定Endocuff Vision是否能改善该人群的ADR。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adfc/6032634/ec1cec296350/10-1055-a-0591-9308-i1086ei1.jpg

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