Digital Cholangioscopic Interpretation: When North Meets the South.

Cholangioscopy Indeterminate biliary stricture Monaco criteria Single-operator digital cholangioscopy Video cholangioscopy

Journal

Digestive diseases and sciences
ISSN: 1573-2568
Titre abrégé: Dig Dis Sci
Pays: United States
ID NLM: 7902782

Informations de publication

Date de publication:
04 2022
Historique:
received: 03 11 2020
accepted: 15 03 2021
pubmed: 31 3 2021
medline: 6 4 2022
entrez: 30 3 2021
Statut: ppublish

Résumé

Digital single-operator cholangioscopy (DSOC) (SpyGlass DS™, Boston Scientific, MA, USA) allows for high-definition imaging of the biliary tree. The superior visualization has led to the development of two different sets of criteria to evaluate and classify indeterminate biliary strictures: the Monaco criteria and the criteria in Carlos Robles-Medranda's publication (CRM). Our objective was to assess the interrater agreement (IA) of DSOC interpretation for indeterminate biliary strictures using the two newly published criteria. Forty de-identified DSOC video recordings were sent to 15 interventional endoscopists with experience in cholangioscopy. They were asked to score the videos based on the presence of Monaco Classification criteria: stricture, lesion, mucosal changes, papillary projections, ulceration, white linear bands or rings, and vessels. Next, they scored the videos using CRM criteria: villous pattern, polypoid pattern, inflammatory pattern, flat pattern, ulcerate pattern and honeycomb pattern. The endoscopists then diagnosed the recordings as neoplastic or non-neoplastic based on the criteria. Intraclass correlation (ICC) analysis was done to evaluate interrater agreement for both criteria set and final diagnosis. Recordings of 26 malignant lesions and 14 benign lesions were scored. The IA using both the Monaco criteria and CRM criteria ranged from poor to excellent (range 0.1-0.76) and (range 0.1-0.62), respectively. Within the Monaco criteria, IA was excellent for lesion (0.75) and fingerlike papillary projections (0.74); good for tortuous vessels (0.7), mucosal features (0.62), uniform papillary projections (0.53), and ulceration (0.58); and fair for white linear bands (0.4). Within the CRM criteria, the IA was good for villous pattern (0.62), flat pattern (0.62), and honeycomb pattern; fair for ulcerated pattern (0.56), polypoid pattern (0.52) and inflammatory pattern (0.54). The diagnostic IA using Monaco criteria was good (0.65), while the diagnostic IA using CRM was fair (0.58). The overall diagnostic accuracy using the Monaco classification was 61% and CRM criteria were 57%. The IOA and accuracy rate of DSOC using visual criteria from both Monaco Criteria and CRM are similar. However, some criteria from both sets suffer from poor IA, thus affecting the overall diagnostic accuracy. More formal training and refinements in visual criteria with additional validation are needed to improve diagnostic accuracy. ClinicalTrials.gov Identifier: NCT02166099.

Sections du résumé

BACKGROUND
Digital single-operator cholangioscopy (DSOC) (SpyGlass DS™, Boston Scientific, MA, USA) allows for high-definition imaging of the biliary tree. The superior visualization has led to the development of two different sets of criteria to evaluate and classify indeterminate biliary strictures: the Monaco criteria and the criteria in Carlos Robles-Medranda's publication (CRM). Our objective was to assess the interrater agreement (IA) of DSOC interpretation for indeterminate biliary strictures using the two newly published criteria.
METHODS
Forty de-identified DSOC video recordings were sent to 15 interventional endoscopists with experience in cholangioscopy. They were asked to score the videos based on the presence of Monaco Classification criteria: stricture, lesion, mucosal changes, papillary projections, ulceration, white linear bands or rings, and vessels. Next, they scored the videos using CRM criteria: villous pattern, polypoid pattern, inflammatory pattern, flat pattern, ulcerate pattern and honeycomb pattern. The endoscopists then diagnosed the recordings as neoplastic or non-neoplastic based on the criteria. Intraclass correlation (ICC) analysis was done to evaluate interrater agreement for both criteria set and final diagnosis.
RESULTS
Recordings of 26 malignant lesions and 14 benign lesions were scored. The IA using both the Monaco criteria and CRM criteria ranged from poor to excellent (range 0.1-0.76) and (range 0.1-0.62), respectively. Within the Monaco criteria, IA was excellent for lesion (0.75) and fingerlike papillary projections (0.74); good for tortuous vessels (0.7), mucosal features (0.62), uniform papillary projections (0.53), and ulceration (0.58); and fair for white linear bands (0.4). Within the CRM criteria, the IA was good for villous pattern (0.62), flat pattern (0.62), and honeycomb pattern; fair for ulcerated pattern (0.56), polypoid pattern (0.52) and inflammatory pattern (0.54). The diagnostic IA using Monaco criteria was good (0.65), while the diagnostic IA using CRM was fair (0.58). The overall diagnostic accuracy using the Monaco classification was 61% and CRM criteria were 57%.
CONCLUSION
The IOA and accuracy rate of DSOC using visual criteria from both Monaco Criteria and CRM are similar. However, some criteria from both sets suffer from poor IA, thus affecting the overall diagnostic accuracy. More formal training and refinements in visual criteria with additional validation are needed to improve diagnostic accuracy.
TRIAL REGISTRATION
ClinicalTrials.gov Identifier: NCT02166099.

Identifiants

pubmed: 33783691
doi: 10.1007/s10620-021-06961-z
pii: 10.1007/s10620-021-06961-z
doi:

Banques de données

ClinicalTrials.gov
['NCT02166099']

Types de publication

Clinical Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1345-1351

Informations de copyright

© 2021. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

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Auteurs

Michel Kahaleh (M)

Department of Medicine, Rutgers Robert Wood Johnson Medical School, Robert Wood Johnson University Hospital, Rutgers University, 1 RWJ Place, MEB 464, New Brunswick, NJ, 08901, USA. mkahaleh@gmail.com.

Isaac Raijman (I)

Gastroenterology, Greater Houston Gastroenterology, Houston, USA.

Monica Gaidhane (M)

Department of Medicine, Rutgers Robert Wood Johnson Medical School, Robert Wood Johnson University Hospital, Rutgers University, 1 RWJ Place, MEB 464, New Brunswick, NJ, 08901, USA.

Amy Tyberg (A)

Department of Medicine, Rutgers Robert Wood Johnson Medical School, Robert Wood Johnson University Hospital, Rutgers University, 1 RWJ Place, MEB 464, New Brunswick, NJ, 08901, USA.

Amrita Sethi (A)

Columbia University Medical Center, New York, USA.

Adam Slivka (A)

Gastroenterology, University of Pittsburgh Medical Center, Pittsburgh, USA.

Douglas G Adler (DG)

Gastroenterology, University of Utah Health, Salt Lake City, USA.

Divyesh Sejpal (D)

Baylor College of Medicine Houston, Long Island, USA.

Haroon Shahid (H)

Department of Medicine, Rutgers Robert Wood Johnson Medical School, Robert Wood Johnson University Hospital, Rutgers University, 1 RWJ Place, MEB 464, New Brunswick, NJ, 08901, USA.

Avik Sarkar (A)

Department of Medicine, Rutgers Robert Wood Johnson Medical School, Robert Wood Johnson University Hospital, Rutgers University, 1 RWJ Place, MEB 464, New Brunswick, NJ, 08901, USA.

Fernanda Martins (F)

Hospital Israelita Albert Einstein, São Paulo, Brazil.

Christine Boumitri (C)

Saint Louis University School of Medicine, St. Louis, MO, USA.

Samuel Burton (S)

Saint Louis University School of Medicine, St. Louis, MO, USA.

Helga Bertani (H)

NuovoOspedale Civile S. Agostino Endoscopy Unit, Dr., Baggiovara, Italy.

Paul Tarnasky (P)

Digestive Health Associates of Texas, Dallas, USA.

Frank Gress (F)

Division of Digestive and Liver Diseases, Columbia University, New York, USA.

Ian Gan (I)

Vancouver General Hospital, GI, Vancouver, Canada.

Jose C Ardengh (JC)

HCFMRP-USP Department of Surgery and Anatomy, Surgery and Anatomy of HCFMRP-USP, São Paulo, Brazil.

Prashant Kedia (P)

Digestive Health Associates of Texas, Dallas, USA.

Urban Arnelo (U)

Department of Upper Gastrointestinal Diseases, Division of Surgery, CLINTEC, Karolinska Institutet, Stockholm, Sweden.

Priya Jamidar (P)

Gastroenterology/Medicine, Yale University, Guilford, USA.

Raj J Shah (RJ)

Gastroenterology, University of Colorado, Aurora, USA.

Carlos Robles-Medranda (C)

Instituto Ecuatoriano De Enfermedades Digestivas (IECED)-University Hospital Omni, Espiritu Santo University, Guayaquil, Ecuador.

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