AI Article Synopsis

  • This study aimed to validate various models that differentiate Crohn's disease (CD) from intestinal tuberculosis (ITB) using clinical, endoscopic, and pathology data from patients in Thailand and Hong Kong.
  • The Limsrivilai clinical-endoscopy (CE) model and Jung's model showed similar performance in differentiating CD from ITB, while both outperformed Lee's endoscopy-only approach, highlighting the value of incorporating multiple data types.
  • Despite improvements in diagnostic accuracy with combined models, misdiagnosis rates remain a concern; further development of models that include additional diagnostic methods like imaging and serological tests is necessary for better clinical application.

Article Abstract

Background: Data on external validation of models developed to distinguish Crohn's disease (CD) from intestinal tuberculosis (ITB) are limited. This study aimed to validate and compare models using clinical, endoscopic, and/or pathology findings to differentiate CD from ITB.

Methods: Data from newly diagnosed ITB and CD patients were retrospectively collected from 5 centers located in Thailand or Hong Kong. The data was applied to Lee, et al., Makharia, et al., Jung, et al., and Limsrivilai, et al. model.

Results: Five hundred and thirty patients (383 CD, 147 ITB) with clinical and endoscopic data were included. The area under the receiver operating characteristic curve (AUROC) of Limsrivilai's clinical-endoscopy (CE) model was 0.853, which was comparable to the value of 0.862 in Jung's model (p = 0.52). Both models performed significantly better than Lee's endoscopy model (AUROC: 0.713, p<0.01). Pathology was available for review in 199 patients (116 CD, 83 ITB). When 3 modalities were combined, Limsrivilai's clinical-endoscopy-pathology (CEP) model performed significantly better (AUROC: 0.887) than Limsrivilai's CE model (AUROC: 0.824, p = 0.01), Jung's model (AUROC: 0.798, p = 0.005) and Makharia's model (AUROC: 0.637, p<0.01). In 83 ITB patients, the rate of misdiagnosis with CD when used the proposed cutoff values in each original study was 9.6% for Limsrivilai's CEP, 15.7% for Jung's, and 66.3% for Makharia's model.

Conclusions: Scoring systems with more parameters and diagnostic modalities performed better; however, application to clinical practice is still limited owing to high rate of misdiagnosis of ITB as CD. Models integrating more modalities such as imaging and serological tests are needed.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7703980PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0242879PLOS

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