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Updated: Jan 12, 2026

Endoscopic Ultrasound-Guided Biliary Drainage: Endoscopic Ultrasound-Guided Hepaticogastrostomy in Malignant Biliary Obstruction
Published on: March 25, 2022
The role of ROSE-enhanced ERCP-guided biopsy in diagnosing biliary stricture
Chengyu Lv1, Yinchao Zhang2, Tong Bai1
1Department of ERCP Diagnosis and Treatment Center of Hepatobiliary Surgery, The Third Central Hospital of Tianjin, Tianjin, 300170, China.
Abstract:
To evaluate the diagnostic efficacy of rapid on-site evaluation (ROSE)-enhanced endoscopic retrograde cholangiopancreatography (ERCP)-guided biopsy for biliary strictures, and develop a predictive model for diagnostic accuracy. This retrospective study included 200 patients undergoing ERCP-guided biopsy (ROSE cohort, n = 100; NON-ROSE cohort, n = 100). Diagnostic performance metrics (accuracy, sensitivity, specificity, positive predictive value [PPV], negative predictive value [NPV]), specimen adequacy, biopsy attempts, procedure duration, and complications were compared between groups. Logistic regression identified independent predictors of diagnostic accuracy. A prediction model was developed and internally validated through receiver operating characteristic (ROC) curve analysis, calibration curves, decision curve analysis (DCA), and constructed as a nomogram. The ROSE cohort demonstrated significantly higher accuracy (92.0% vs. 78.0%), sensitivity (97.2% vs. 74.7%), and NPV (91.6% vs. 48.7%) (all P < 0.05). ROSE required fewer biopsy passes (2.43 vs. 3.61; P < 0.001), shorter sampling time (2.71 vs. 4.33 min; P < 0.001), without increased complications (P > 0.05). Multivariate analysis confirmed ROSE as an independent predictor (OR≈4.0, P = 0.032). The validated predictive model showed good discrimination (AUC≈0.80) and clinical utility. ROSE significantly enhances diagnostic yield and procedural efficiency in ERCP-guided biopsy for biliary strictures. The developed nomogram provides an evidence-based tool for individualized prediction, supporting clinical decision-making.
