Development and validation of a practical clinical risk prediction model for post‐endoscopic retrograde cholangiopancreatography pancreatitis

Author:

Meng Zhao Wu12,Ruan Yibing34,Fisher Stacey5,Bishay Kirles12,Chau Millie2,Howarth Megan2,Cartwright Shane2,Chen Yen‐I6ORCID,Dixon Elijah17,Heitman Steven J.12,Brenner Darren R.13,Forbes Nauzer12ORCID

Affiliation:

1. Department of Community Health Sciences University of Calgary Calgary Canada

2. Department of Medicine Division of Gastroenterology and Hepatology University of Calgary Calgary Canada

3. Department of Oncology Cumming School of Medicine University of Calgary Calgary Canada

4. Department of Cancer Epidemiology and Prevention Research Cancer Care Alberta, Alberta Health Services Calgary Canada

5. Ottawa Hospital Research Institute Ottawa Canada

6. Department of Medicine, Division of Gastroenterology and Hepatology McGill University Health Centre Montreal Canada

7. Department of Surgery University of Calgary Calgary Canada

Abstract

AbstractBackgroundPancreatitis following endoscopic retrograde cholangiopancreatography (ERCP) can lead to significant morbidity and mortality. We aimed to develop an accurate post‐ERCP pancreatitis risk prediction model using easily obtainable variables.MethodsUsing prospective multi‐center ERCP data, we performed logistic regression using stepwise selection on several patient‐, procedure‐, and endoscopist‐related factors that were determined a priori. The final model was based on a combination of the Bayesian information criterion and Akaike's information criterion performance, balancing the inclusion of clinically relevant variables and model parsimony. All available data were used for model development, with subsequent internal validation performed on bootstrapped data using 10‐fold cross‐validation.ResultsData from 3021 ERCPs were used to inform models. There were 151 cases of post‐ERCP pancreatitis (5.0% incidence). Variables included in the final model included female sex, pancreatic duct cannulation, native papilla status, pre‐cut sphincterotomy, increasing cannulation time, presence of biliary stricture, patient age, and placement of a pancreatic duct stent. The final model was discriminating, with a receiver operating characteristic curve statistic of 0.79, and well‐calibrated, with a predicted risk‐to‐observed risk ratio of 1.003.ConclusionsWe successfully developed and internally validated a promising post‐ERCP pancreatitis clinical prediction model using easily obtainable variables that are known at baseline or observed during the ERCP procedure. The model achieved an area under the curve of 0.79. External validation is planned as additional data becomes available.

Publisher

Wiley

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