Retrograde-viewing device improves adenoma detection rate in colonoscopies for surveillance and diagnostic workup

被引:32
作者
Siersema, Peter D. [1 ]
Rastogi, Amit [2 ]
Leufkens, Anke M. [1 ]
Akerman, Paul A. [3 ]
Azzouzi, Kassem [4 ]
Rothstein, Richard I. [5 ]
Vleggaar, Frank P. [1 ]
Repici, Alessandro [6 ]
Rando, Giacomo [6 ]
Okolo, Patrick I. [7 ]
Dewit, Olivier [4 ]
Ignjatovic, Ana [8 ]
Odstrcil, Elizabeth [9 ]
East, James [8 ]
Deprez, Pierre H. [4 ]
Saunders, Brian P. [8 ]
Kalloo, Anthony N. [7 ]
Creel, Bradley [9 ]
Singh, Vikas [2 ]
Lennon, Anne Marie [7 ]
DeMarco, Daniel C. [9 ]
机构
[1] Univ Med Ctr Utrecht, Dept Gastroenterol & Hepatol, NL-3508 GA Utrecht, Netherlands
[2] Kansas City Vet Adm Med Ctr, Div Gastroenterol & Hepatol, Kansas City, MO 64128 USA
[3] Bayside Endoscopy Ctr, Dept Gastroenterol, Providence, RI 02905 USA
[4] Catholic Univ Louvain, Clin Univ St Luc, Dept Gastroenterol, B-1200 Brussels, Belgium
[5] Dartmouth Hitchcock Med Ctr, Dept Gastroenterol & Hepatol, Lebanon, NH 03756 USA
[6] Ist Clin Humanitas, Dept Gastroenterol, I-20089 Rozzano, Italy
[7] Johns Hopkins Univ Hosp, Dept Internal Med, Div Gastroenterol & Hepatol, Baltimore, MD 21205 USA
[8] St Marks Hosp, Wolfson Unit Endoscopy, Harrow HA1 3UJ, Middx, England
[9] Baylor Univ, Med Ctr, Dept Internal Med, Div Gastroenterol, Dallas, TX 75246 USA
关键词
Colonoscopy; Colorectal cancer; Adenomas; Miss rates; Retrograde-viewing; RANDOMIZED CONTROLLED-TRIAL; CAP-ASSISTED COLONOSCOPY; SOCIETY TASK-FORCE; COLORECTAL-CANCER; MISS RATES; SCREENING COLONOSCOPY; STANDARD COLONOSCOPY; WITHDRAWAL TECHNIQUE; VIRTUAL COLONOSCOPY; PREPARATION QUALITY;
D O I
10.3748/wjg.v18.i26.3400
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AIM: To determine which patients might benefit most from retrograde viewing during colonoscopy through subset analysis of randomized, controlled trial data. METHODS: The Third Eye (R) Retroscope (R) Randomized Clinical Evaluation (TERRACE) was a randomized, controlled, multicenter trial designed to evaluate the efficacy of a retrograde-viewing auxiliary imaging device that is used during colonoscopy to provide a second video image which allows viewing of areas on the proximal aspect of haustral folds and flexures that are difficult to see with the colonoscope's forward view. We performed a post-hoc analysis of the TERRACE data to determine whether certain subsets of the patient population would gain more benefit than others from use of the device. Subjects were patients scheduled for colonoscopy for screening, surveillance or diagnostic workup, and each underwent same-day tandem examinations with standard colonoscopy (SC) and Third Eye colonoscopy (TEC), randomized to SC followed by TEC or vice versa. RESULTS: Indication for colonoscopy was screening in 176/345 subjects (51.0%), surveillance after previous polypectomy in 87 (25.2%) and diagnostic workup in 82 (23.8%). In 4 subjects no indication was specified. Previously reported overall results had shown a net additional adenoma detection rate (ADR) with TEC of 23.2% compared to SC. Relative risk (RR) of missing adenomas with SC vs TEC as the initial procedure was 1.92 (P = 0.029). Post-hoc subset analysis shows additional ADRs for TEC compared to SC were 4.4% for screening, 35.7% for surveillance, 55.4% for diagnostic and 40.7% for surveillance and diagnostic combined. The RR of missing adenomas with SC vs TEC was 1.11 (P = 0.815) for screening, 3.15 (P = 0.014) for surveillance, 8.64 (P = 0.039) for diagnostic and 3.34 (P = 0.003) for surveillance and diagnostic combined. Although a multivariate Poisson regression suggested gender as a possibly significant factor, subset analysis showed that the difference between genders was not statistically significant. Age, bowel prep quality and withdrawal time did not significantly affect the RR of missing adenomas with SC vs TEC. Mean sizes of adenomas detected with TEC and SC were similar at 0.59 cm and 0.56 cm, respectively (P = NS). CONCLUSION: TEC allows detection of significantly more adenomas compared to SC in patients undergoing surveillance or diagnostic workup, but not in screening patients (ClinicalTrials.gov Identifier: NCT01044732). (C) 2012 Baishideng. All rights reserved.
引用
收藏
页码:3400 / 3408
页数:9
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