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Published on: September 1, 2023
Validation of models using basic parameters to differentiate intestinal tuberculosis from Crohn's disease: A
Julajak Limsrivilai1,2, Choon Kin Lee3, Piyapan Prueksapanich4
1Division of Gastroenterology, Department of Medicine, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
External validation of models for distinguishing Crohn's disease (CD) from intestinal tuberculosis (ITB) is limited. The Limsrivilai clinical-endoscopy-pathology (CEP) model showed superior performance in differentiating CD from ITB, reducing misdiagnosis rates.
Area of Science:
- Gastroenterology
- Internal Medicine
- Diagnostic Accuracy
Background:
- Limited external validation data exists for models differentiating Crohn's disease (CD) from intestinal tuberculosis (ITB).
- Accurate differentiation between CD and ITB is crucial for appropriate patient management.
Purpose of the Study:
- To externally validate and compare existing models for distinguishing CD from ITB.
- To assess the diagnostic performance of models utilizing clinical, endoscopic, and pathology data.
Main Methods:
- Retrospective collection of data from newly diagnosed ITB and CD patients across 5 centers in Thailand and Hong Kong.
- Application of data to established models: Lee et al., Makharia et al., Jung et al., and Limsrivilai et al.
- Comparison of model performance using Area Under the Receiver Operating Characteristic Curve (AUROC) and misdiagnosis rates.
Main Results:
- Limsrivilai's clinical-endoscopy-pathology (CEP) model achieved an AUROC of 0.887, outperforming other models.
- The CEP model demonstrated significantly better performance than the clinical-endoscopy (CE) model (AUROC: 0.824) and Jung's model (AUROC: 0.798).
- Misdiagnosis of ITB as CD was lowest with Limsrivilai's CEP model (9.6%) compared to Jung's (15.7%) and Makharia's (66.3%) models.
Conclusions:
- Models incorporating more diagnostic modalities and parameters exhibit superior performance.
- Despite improved accuracy, clinical application remains challenging due to persistent misdiagnosis rates, particularly of ITB as CD.
- Future models should integrate additional modalities like imaging and serological tests for enhanced diagnostic accuracy.
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