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Prolonged cecal insertion time is associated with decreased adenoma detection

医学 退出时间 结肠镜检查 四分位间距 腺瘤 四分位数 插入时间 结直肠癌 内科学 胃肠病学 外科 泌尿科 癌症 置信区间 气道
作者
Daniel von Renteln,Douglas J. Robertson,Steve Bensen,Heiko Pohl
出处
期刊:Gastrointestinal Endoscopy [Elsevier BV]
卷期号:85 (3): 574-580 被引量:51
标识
DOI:10.1016/j.gie.2016.08.021
摘要

The adenoma detection rate (ADR) is an important colonoscopy quality parameter. A longer withdrawal time is associated with increased adenoma detection; however, the effect of cecal insertion time on adenoma detection is unclear. The aim of this study was to evaluate if cecal insertion time is associated with adenoma detection.The study included 50- to 89-year-old subjects undergoing an elective outpatient colonoscopy as part of a randomized trial on cap-assisted colonoscopy. The primary outcome was the adjusted mean number of adenomas per patient across quartiles of lengthening patient insertion times. Secondary outcomes included the mean number of advanced adenomas, ADR, and advanced ADR. Adjusted regression analysis was applied to assess for a possible trend.Among 1043 included study subjects, the median cecal insertion time was 5.3 minutes (interquartile range [IQR], 3.5-8.1) and the median withdrawal time was 8.6 minutes (IQR, 7.1-10.7). Cecal insertion time was not associated with withdrawal time (P = .950). The mean number of adenomas per patient decreased across increasing insertion time quartiles from 1.1 to .7, corresponding to a 11% decline per quartile (P = .031). Similarly, the number of advanced adenomas decreased from .15 to .06, corresponding to a 7% decline per quartile (P = .013). The observed decrease in adenoma detection was similar for proximal and distal adenomas. Endoscopists' individual insertion times were not associated with adenoma detection.A longer cecal insertion time was associated with a decreased detection of adenomas and advanced adenomas. A long insertion time may be a marker for a more difficult examination that requires a longer withdrawal time to assure adequate examination and adenoma detection. (Clinical trial registration number: NCT01935180.).

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