TY - JOUR
T1 - Digital Cholangioscopic Interpretation
T2 - When North Meets the South
AU - Kahaleh, Michel
AU - Raijman, Isaac
AU - Gaidhane, Monica
AU - Tyberg, Amy
AU - Sethi, Amrita
AU - Slivka, Adam
AU - Adler, Douglas G.
AU - Sejpal, Divyesh
AU - Shahid, Haroon
AU - Sarkar, Avik
AU - Martins, Fernanda
AU - Boumitri, Christine
AU - Burton, Samuel
AU - Bertani, Helga
AU - Tarnasky, Paul
AU - Gress, Frank
AU - Gan, Ian
AU - Ardengh, Jose C.
AU - Kedia, Prashant
AU - Arnelo, Urban
AU - Jamidar, Priya
AU - Shah, Raj J.
AU - Robles-Medranda, Carlos
N1 - Publisher Copyright:
© 2021, The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.
PY - 2022/4
Y1 - 2022/4
N2 - 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.
AB - 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.
KW - Cholangioscopy
KW - Indeterminate biliary stricture
KW - Monaco criteria
KW - Single-operator digital cholangioscopy
KW - Video cholangioscopy
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U2 - 10.1007/s10620-021-06961-z
DO - 10.1007/s10620-021-06961-z
M3 - Article
C2 - 33783691
AN - SCOPUS:85103371775
SN - 0163-2116
VL - 67
SP - 1345
EP - 1351
JO - Digestive diseases and sciences
JF - Digestive diseases and sciences
IS - 4
ER -