Impact of withdrawal time on adenoma detection rate: results from a prospective multicenter trial

医学 四分位间距 置信区间 优势比 退出时间 腺瘤 随机对照试验 多中心试验 前瞻性队列研究 多中心研究 内科学 癌症 结肠镜检查 结直肠癌
作者
Madhav Desai,Douglas K. Rex,Matthew Bohm,Perica Davitkov,John M. DeWitt,Monika Fischer,Gregory Faulx,Ryan D. Heath,Timothy D. Imler,Toyia N. James-Stevenson,Charles J. Kahi,William R. Kessler,Divyanshoo R. Kohli,Lee McHenry,Tarun Rai,Nicholas Rogers,Sashidhar Sagi,Anjana Sathyamurthy,Prashanth Vennalaganti,Suneha Sundaram,Harsh K. Patel,April D. Higbee,Kevin F. Kennedy,Rachel E. Lahr,Gjorgie Stojadinovikj,Carlissa Campbell,Chandra S. Dasari,Sravanthi Parasa,Ashley L. Faulx,Prateek Sharma
出处
期刊:Gastrointestinal Endoscopy [Elsevier]
卷期号:97 (3): 537-543.e2 被引量:10
标识
DOI:10.1016/j.gie.2022.09.031
摘要

Performing a high-quality colonoscopy is critical for optimizing the adenoma detection rate (ADR). Colonoscopy withdrawal time (a surrogate measure) of ≥6 minutes is recommended; however, a threshold of a high-quality withdrawal and its impact on ADR are not known.We examined withdrawal time (excluding polyp resection and bowel cleaning time) of subjects undergoing screening and/or surveillance colonoscopy in a prospective, multicenter, randomized controlled trial. We examined the relationship of withdrawal time in 1-minute increments on ADR and reported odds ratio (OR) with 95% confidence intervals. Linear regression analysis was performed to assess the maximal inspection time threshold that impacts the ADR.A total of 1142 subjects (age, 62.3 ± 8.9 years; 80.5% men) underwent screening (45.9%) or surveillance (53.6%) colonoscopy. The screening group had a median withdrawal time of 9.0 minutes (interquartile range [IQR], 3.3) with an ADR of 49.6%, whereas the surveillance group had a median withdrawal time of 9.3 minutes (IQR, 4.3) with an ADR of 63.9%. ADR correspondingly increased for a withdrawal time of 6 minutes to 13 minutes, beyond which ADR did not increase (50.4% vs 76.6%, P < .01). For every 1-minute increase in withdrawal time, there was 6% higher odds of detecting an additional subject with an adenoma (OR, 1.06; 95% confidence interval, 1.02-1.10; P = .004).Results from this multicenter, randomized controlled trial underscore the importance of a high-quality examination and efforts required to achieve this with an incremental yield in ADR based on withdrawal time. (Clinical trial registration number: NCT03952611.).
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