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全谱内镜在结直肠癌筛查中的作用:随机试验。

Role of Full-spectrum Endoscopy in Colorectal Cancer Screening: Randomized Trial.

机构信息

Gastroenterology Department.

Investigation Department, Rio Hortega Hospital.

出版信息

J Clin Gastroenterol. 2019 Mar;53(3):191-196. doi: 10.1097/MCG.0000000000000975.

DOI:10.1097/MCG.0000000000000975
PMID:29283904
Abstract

GOALS

The aim of this study was to compare a new, full-spectrum endoscope (Fuse; EndoChoice, Alpharetta, GA) to standard forward-viewing colonoscopy in the detection of colorectal neoplasms.

BACKGROUND

Colonoscopy, the gold standard for the detection of colorectal cancer, fails to detect 22% to 28% of polyps, increasing the risk of interval cancer. Endoscopic improvement of the adenoma detection rate decrease interval carcinomas. Full-spectrum endoscopy (FUSE) (330-degree field of view), in a tandem study, has been shown to reduce the adenoma miss rate.

STUDY

Prospective, randomized study of 249 patients in patients referred from the colorectal screening program with a positive fecal occult blood test (FOBT). Patients were randomized to standard forward-viewing colonoscopy (170 degrees) or to full-spectrum colonoscopy with the Fuse system (330 degrees). Study variables were the adenoma detection rate, the polyp detection rate, the mean number of adenomas per procedure, the lesions detected according to the location, morphology and size, cecal intubation rate, total procedure time, insertion time to the cecum, therapeutic success, and adverse events.

RESULTS

The Fuse system did not produce a significantly higher adenoma detection rate than standard forward-viewing colonoscopy (FUSE 73.1% vs. standard colonoscopy 68.1%; P=0.47) but did have a significantly longer insertion time (FUSE 6.2 min vs. standard colonoscopy 4.2 min; P< 0.001). Further analysis failed to reveal any significant difference in polyp/adenoma detection rates by lesion size or colonic section.

CONCLUSIONS

FUSE did not detect significantly more colorectal neoplasia than forward viewing colonoscopy in a medium-risk CRC screening population with positive FOBT.

摘要

目的

本研究旨在比较新型全谱内镜(Fuse;EndoChoice,Alpharetta,GA)与标准前视结肠镜检查在结直肠肿瘤检测中的差异。

背景

作为结直肠癌检测的金标准,结肠镜检查未能检测到 22%至 28%的息肉,增加了间隔期癌症的风险。提高腺瘤检出率可降低间隔期癌的发生。全谱内镜(FUSE)(330 度视野)在前瞻性研究中已被证实可降低腺瘤漏诊率。

研究

对来自结直肠筛查计划的 249 例阳性粪便潜血试验(FOBT)患者进行前瞻性、随机研究。患者被随机分为标准前视结肠镜检查(170 度)或 FUSE 系统全谱结肠镜检查(330 度)。研究变量包括腺瘤检出率、息肉检出率、每个手术的平均腺瘤数、根据位置、形态和大小检测到的病变、盲肠插管率、总手术时间、插入盲肠的时间、治疗成功率和不良事件。

结果

FUSE 系统并未显著提高腺瘤检出率(FUSE 73.1%比标准结肠镜检查 68.1%;P=0.47),但插入时间明显延长(FUSE 6.2 分钟比标准结肠镜检查 4.2 分钟;P<0.001)。进一步分析未能发现病变大小或结肠节段对息肉/腺瘤检出率的任何显著差异。

结论

在阳性 FOBT 的中危 CRC 筛查人群中,与标准前视结肠镜相比,FUSE 并未显著检测到更多的结直肠肿瘤。

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