Linked color imaging versus white light imaging colonoscopy for colorectal adenoma detection: A randomized controlled trial.


Journal

Journal of gastroenterology and hepatology
ISSN: 1440-1746
Titre abrégé: J Gastroenterol Hepatol
Pays: Australia
ID NLM: 8607909

Informations de publication

Date de publication:
Oct 2021
Historique:
revised: 27 04 2021
received: 19 08 2020
accepted: 07 05 2021
pubmed: 12 5 2021
medline: 11 2 2022
entrez: 11 5 2021
Statut: ppublish

Résumé

The adenoma detection rate is an important indicator of colonoscopy quality and colorectal cancer incidence. We compared the adenoma detection rates between white light imaging (WLI) and linked color imaging (LCI) colonoscopy. Patients undergoing colonoscopy for positive fecal immunochemical tests, follow-up of colon polyps, and abdominal symptoms at three institutions were randomly assigned to the LCI or WLI groups. Mean adenoma number per patient (including based on endoscopists' experience), adenoma detection rate, cecal intubation time, withdrawal time, mean adenoma number per location, and adenoma size were compared. The LCI and WLI groups comprised 494 and 501 patients, respectively. No significant differences in the cecal intubation rate (LCI vs WLI: 99.5% vs 99.4%), cecal intubation time, and withdrawal time were noted between groups. The mean adenoma number per patient was significantly higher in the LCI group than in the WLI group (1.07 vs 0.88, P = 0.04), particularly in the descending [0.12 (58/494) vs 0.07 (35/501), P = 0.01] and sigmoid colon [0.41 (201/494) vs 0.30 (149/501), P ≤ 0.001]. However, the adenoma detection rate was 47.1% in the LCI group and 46.9% in the WLI group, with no significant difference (P = 0.93). The total number of sessile-type adenomas was significantly higher in the LCI group than in the WLI group (346/494 vs 278/501, P = 0.04). As for polyp size, small polyps (≤ 5 mm) were detected at a significantly higher rate in the LCI group (271/494 vs 336/501, P = 0.04). Linked color imaging is significantly superior to WLI in terms of mean adenoma number per patient.

Sections du résumé

BACKGROUND AND AIM OBJECTIVE
The adenoma detection rate is an important indicator of colonoscopy quality and colorectal cancer incidence. We compared the adenoma detection rates between white light imaging (WLI) and linked color imaging (LCI) colonoscopy.
METHODS METHODS
Patients undergoing colonoscopy for positive fecal immunochemical tests, follow-up of colon polyps, and abdominal symptoms at three institutions were randomly assigned to the LCI or WLI groups. Mean adenoma number per patient (including based on endoscopists' experience), adenoma detection rate, cecal intubation time, withdrawal time, mean adenoma number per location, and adenoma size were compared.
RESULTS RESULTS
The LCI and WLI groups comprised 494 and 501 patients, respectively. No significant differences in the cecal intubation rate (LCI vs WLI: 99.5% vs 99.4%), cecal intubation time, and withdrawal time were noted between groups. The mean adenoma number per patient was significantly higher in the LCI group than in the WLI group (1.07 vs 0.88, P = 0.04), particularly in the descending [0.12 (58/494) vs 0.07 (35/501), P = 0.01] and sigmoid colon [0.41 (201/494) vs 0.30 (149/501), P ≤ 0.001]. However, the adenoma detection rate was 47.1% in the LCI group and 46.9% in the WLI group, with no significant difference (P = 0.93). The total number of sessile-type adenomas was significantly higher in the LCI group than in the WLI group (346/494 vs 278/501, P = 0.04). As for polyp size, small polyps (≤ 5 mm) were detected at a significantly higher rate in the LCI group (271/494 vs 336/501, P = 0.04).
CONCLUSION CONCLUSIONS
Linked color imaging is significantly superior to WLI in terms of mean adenoma number per patient.

Identifiants

pubmed: 33973300
doi: 10.1111/jgh.15539
doi:

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

2778-2784

Informations de copyright

© 2021 Journal of Gastroenterology and Hepatology Foundation and John Wiley & Sons Australia, Ltd.

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Auteurs

Kazuya Miyaguchi (K)

Department of General Internal Medicine, Saitama Medical University, Saitama, Japan.

Kaoru Takabayashi (K)

Center for Diagnostic and Therapeutic Endoscopy, School of Medicine, Keio University, Tokyo, Japan.

Daisuke Saito (D)

Department of Gastroenterology, Kyorin University Hospital, Tokyo, Japan.

Yoshikazu Tsuzuki (Y)

Department of Gastroenterology, Saitama Medical University, Saitama, Japan.

Nobutaka Hirooka (N)

Department of General Internal Medicine, Saitama Medical University, Saitama, Japan.

Naoki Hosoe (N)

Center for Diagnostic and Therapeutic Endoscopy, School of Medicine, Keio University, Tokyo, Japan.

Hideki Ohgo (H)

Department of Gastroenterology, Saitama Medical University, Saitama, Japan.

Keigo Ashitani (K)

Department of General Internal Medicine, Saitama Medical University, Saitama, Japan.

Hiromitsu Soma (H)

Department of General Internal Medicine, Saitama Medical University, Saitama, Japan.

Ryoichi Miyanaga (R)

Division of Gastroenterology and Hepatology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan.

Kayoko Kimura (K)

Center for Diagnostic and Therapeutic Endoscopy, School of Medicine, Keio University, Tokyo, Japan.

Sotaro Tokunaga (S)

Department of Gastroenterology, Kyorin University Hospital, Tokyo, Japan.

Tatsuya Mitsui (T)

Department of Gastroenterology, Kyorin University Hospital, Tokyo, Japan.

Miki Miura (M)

Department of Gastroenterology, Kyorin University Hospital, Tokyo, Japan.

Ryo Ozaki (R)

Department of Gastroenterology, Kyorin University Hospital, Tokyo, Japan.

Hidetomo Nakamoto (H)

Department of General Internal Medicine, Saitama Medical University, Saitama, Japan.

Takanori Kanai (T)

Division of Gastroenterology and Hepatology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan.

Tadakazu Hisamatsu (T)

Department of Gastroenterology, Kyorin University Hospital, Tokyo, Japan.

Haruhiko Ogata (H)

Center for Diagnostic and Therapeutic Endoscopy, School of Medicine, Keio University, Tokyo, Japan.

Hiroyuki Imaeda (H)

Department of Gastroenterology, Saitama Medical University, Saitama, Japan.

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