Validation of choledocholithiasis predictors from the "2019 ASGE Guideline for the role of endoscopy in the evaluation and management of choledocholithiasis."


Journal

Surgical endoscopy
ISSN: 1432-2218
Titre abrégé: Surg Endosc
Pays: Germany
ID NLM: 8806653

Informations de publication

Date de publication:
06 2022
Historique:
received: 23 02 2021
accepted: 27 09 2021
pubmed: 17 10 2021
medline: 14 5 2022
entrez: 16 10 2021
Statut: ppublish

Résumé

Identifying patients likely to have CDL is an important clinical dilemma because endoscopic retrograde cholangiopancreatography (ERCP), carries a 5-7% risk of adverse events. The purpose of this study was to compare the diagnostic test performance of the 2010 and 2019 ASGE criteria used to help risk stratify patients with suspected CDL. Consecutive patients evaluated for possible CDL from 2013 to 2019 were identified from surgical, endoscopic, and radiologic databases at a single academic center. Inclusion criteria included all patients who underwent ERCP and/or cholecystectomy with intraoperative cholangiogram (IOC) for suspected CDL. We calculated the diagnostic test performance of criteria from both guidelines and compared their discrimination using the receiver operator curve. Univariate and multivariate analysis was used to identify the strongest component predictors. 1098 patients [age 57.9 ± 19.0 years, 62.8% (690) F] were included. 66.3% (728) were found to have CDL on ERCP and/or IOC. When using the 2019 guidelines, the sensitivity, specificity, PPV, NPV, and accuracy are 65.8, 78.9, 86.3, 54.1, and 70.4%, respectively. Using the 2010 guidelines, the sensitivity, specificity, PPV, NPV, and accuracy are 50.5, 78.9, 82.5, 44.8, and 60.1%, respectively. The AUC for high-risk criteria using the 2019 guidelines [0.726 (0.695, 0.758)] was greater than for the 2010 guidelines [0.647 (0.614, 0.681)]. The key difference providing the increased discrimination was the inclusion of stones on any imaging modality, which increased the sensitivity to 55.0% from 29.1%. Not including CDL on imaging or cholangitis, a dilated CBD was the strongest individual predictor of CDL on multivariate analysis (OR 3.70, CI 2.80, 4.89). Compared to 2010, the 2019 high-risk criterion improves diagnostic test performance, but still performs suboptimally. Less invasive tests, such as EUS or MRCP, should be considered in patients with suspected CDL prior to ERCP.

Sections du résumé

BACKGROUND AND AIMS
Identifying patients likely to have CDL is an important clinical dilemma because endoscopic retrograde cholangiopancreatography (ERCP), carries a 5-7% risk of adverse events. The purpose of this study was to compare the diagnostic test performance of the 2010 and 2019 ASGE criteria used to help risk stratify patients with suspected CDL.
METHODS
Consecutive patients evaluated for possible CDL from 2013 to 2019 were identified from surgical, endoscopic, and radiologic databases at a single academic center. Inclusion criteria included all patients who underwent ERCP and/or cholecystectomy with intraoperative cholangiogram (IOC) for suspected CDL. We calculated the diagnostic test performance of criteria from both guidelines and compared their discrimination using the receiver operator curve. Univariate and multivariate analysis was used to identify the strongest component predictors.
RESULTS
1098 patients [age 57.9 ± 19.0 years, 62.8% (690) F] were included. 66.3% (728) were found to have CDL on ERCP and/or IOC. When using the 2019 guidelines, the sensitivity, specificity, PPV, NPV, and accuracy are 65.8, 78.9, 86.3, 54.1, and 70.4%, respectively. Using the 2010 guidelines, the sensitivity, specificity, PPV, NPV, and accuracy are 50.5, 78.9, 82.5, 44.8, and 60.1%, respectively. The AUC for high-risk criteria using the 2019 guidelines [0.726 (0.695, 0.758)] was greater than for the 2010 guidelines [0.647 (0.614, 0.681)]. The key difference providing the increased discrimination was the inclusion of stones on any imaging modality, which increased the sensitivity to 55.0% from 29.1%. Not including CDL on imaging or cholangitis, a dilated CBD was the strongest individual predictor of CDL on multivariate analysis (OR 3.70, CI 2.80, 4.89).
CONCLUSION
Compared to 2010, the 2019 high-risk criterion improves diagnostic test performance, but still performs suboptimally. Less invasive tests, such as EUS or MRCP, should be considered in patients with suspected CDL prior to ERCP.

Identifiants

pubmed: 34654972
doi: 10.1007/s00464-021-08752-z
pii: 10.1007/s00464-021-08752-z
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

4199-4206

Subventions

Organisme : NCATS NIH HHS
ID : UL1 TR000448
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA091842
Pays : United States

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

Stephen Hasak (S)

Division of Gastroenterology, Washington University School of Medicine, 660 South Euclid Ave., Campus, Box 8124, Saint Louis, MO, 63110, USA.

Scott McHenry (S)

Division of Gastroenterology, Washington University School of Medicine, 660 South Euclid Ave., Campus, Box 8124, Saint Louis, MO, 63110, USA.

Bradley Busebee (B)

Division of Gastroenterology, Washington University School of Medicine, 660 South Euclid Ave., Campus, Box 8124, Saint Louis, MO, 63110, USA.

Shahroz Fatima (S)

Division of Gastroenterology, Washington University School of Medicine, 660 South Euclid Ave., Campus, Box 8124, Saint Louis, MO, 63110, USA.

Ian Sloan (I)

Division of Gastroenterology, Washington University School of Medicine, 660 South Euclid Ave., Campus, Box 8124, Saint Louis, MO, 63110, USA.

Michael Weaver (M)

Division of Gastroenterology, Washington University School of Medicine, 660 South Euclid Ave., Campus, Box 8124, Saint Louis, MO, 63110, USA.

Vivek Hansalia (V)

Division of Gastroenterology, Washington University School of Medicine, 660 South Euclid Ave., Campus, Box 8124, Saint Louis, MO, 63110, USA.

Arvind Rengarajan (A)

Division of Gastroenterology, Washington University School of Medicine, 660 South Euclid Ave., Campus, Box 8124, Saint Louis, MO, 63110, USA.

Aymen Almuhaidb (A)

Division of Gastroenterology, Washington University School of Medicine, 660 South Euclid Ave., Campus, Box 8124, Saint Louis, MO, 63110, USA.

Abdullah Al-Shahrani (A)

Division of Gastroenterology, Washington University School of Medicine, 660 South Euclid Ave., Campus, Box 8124, Saint Louis, MO, 63110, USA.

Thomas Hollander (T)

Division of Gastroenterology, Washington University School of Medicine, 660 South Euclid Ave., Campus, Box 8124, Saint Louis, MO, 63110, USA.

Dayna Early (D)

Division of Gastroenterology, Washington University School of Medicine, 660 South Euclid Ave., Campus, Box 8124, Saint Louis, MO, 63110, USA.

Gabriel Lang (G)

Division of Gastroenterology, Washington University School of Medicine, 660 South Euclid Ave., Campus, Box 8124, Saint Louis, MO, 63110, USA.

Koushik Das (K)

Division of Gastroenterology, Washington University School of Medicine, 660 South Euclid Ave., Campus, Box 8124, Saint Louis, MO, 63110, USA.

Natalie Cosgrove (N)

Division of Gastroenterology, Washington University School of Medicine, 660 South Euclid Ave., Campus, Box 8124, Saint Louis, MO, 63110, USA.

Daniel Mullady (D)

Division of Gastroenterology, Washington University School of Medicine, 660 South Euclid Ave., Campus, Box 8124, Saint Louis, MO, 63110, USA.

Daniel R Ludwig (DR)

Mallinckrodt Institute of Radiology, Washington University School of Medicine, Saint Louis, MO, USA.

Chet Hammill (C)

Hepatobiliary-Pancreatic and Gastrointestinal Surgery Section, Department of Surgery, Washington University School of Medicine, Saint Louis, MO, USA.

Vladimir Kushnir (V)

Division of Gastroenterology, Washington University School of Medicine, 660 South Euclid Ave., Campus, Box 8124, Saint Louis, MO, 63110, USA. vkushnir@wustl.edu.

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