Division of Gastroenterology, Department of Medicine, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Division of Gastroenterology, Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, United States of America.
PLoS One. 2020 Nov 30;15(11):e0242879. doi: 10.1371/journal.pone.0242879. eCollection 2020.
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.
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.
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.
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.
用于区分克罗恩病(CD)和肠结核(ITB)的模型的外部验证数据有限。本研究旨在验证和比较使用临床、内镜和/或病理发现来区分 CD 和 ITB 的模型。
从位于泰国或香港的 5 个中心回顾性收集新诊断的 ITB 和 CD 患者的数据。将这些数据应用于 Lee 等人、Makharia 等人、Jung 等人和 Limsrivilai 等人的模型。
共纳入 530 例(383 例 CD,147 例 ITB)具有临床和内镜数据的患者。Limsrivilai 的临床-内镜(CE)模型的受试者工作特征曲线下面积(AUROC)为 0.853,与 Jung 模型的 0.862 值相当(p = 0.52)。这两个模型的表现均明显优于 Lee 的内镜模型(AUROC:0.713,p<0.01)。199 例患者(116 例 CD,83 例 ITB)可进行病理复查。当 3 种方式结合时,Limsrivilai 的临床-内镜-病理(CEP)模型的表现明显优于 Limsrivilai 的 CE 模型(AUROC:0.887,p = 0.01)、Jung 模型(AUROC:0.798,p = 0.005)和 Makharia 模型(AUROC:0.637,p<0.01)。在 83 例 ITB 患者中,当使用每个原始研究中提出的截断值时,将 CD 误诊为 ITB 的比率分别为 Limsrivilai 的 CEP 模型为 9.6%、Jung 模型为 15.7%和 Makharia 模型为 66.3%。
具有更多参数和诊断方式的评分系统表现更好;然而,由于 ITB 误诊为 CD 的比率较高,因此其在临床实践中的应用仍然有限。需要整合更多的方式,如影像学和血清学检查的模型。