区分儿童多系统炎症综合征的诊断预测模型。

ACR Open Rheumatology Pub Date : 2022-12-01 Epub Date: 2022-11-01 DOI:10.1002/acr2.11509
Matthew T Clark, Danielle A Rankin, Lauren S Peetluk, Alisa Gotte, Alison Herndon, William McEachern, Andrew Smith, Daniel E Clark, Edward Hardison, Adam J Esbenshade, Anna Patrick, Natasha B Halasa, James A Connelly, Sophie E Katz
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摘要

目的:儿童多系统炎症综合征(MIS-C儿童多系统炎症综合征(MIS-C)的特征与其他综合征重叠,给临床医生的诊断带来困难。我们旨在比较临床诊断为 MIS-C 和未诊断为 MIS-C 的患者之间的临床差异,并建立一个诊断预测模型,以帮助临床医生在患者入院后 24 小时内识别 MIS-C 患者:方法:对127名患者进行队列分析(结果:127名患儿中,有1名被确诊为MIS-C:结果:在本院收治的127名疑似MIS-C患儿中,45人被临床诊断为MIS-C,82人被诊断为其他疾病。我们发现,一个包含四个变量(出现低血压和/或液体复苏、腹痛、新皮疹和血清钠值)的模型在识别 MIS-C 患者方面显示出极佳的辨别力(一致性指数 0.91;95% 置信区间:0.85-0.96)和良好的校准性:结论:具有早期临床和实验室特征的诊断预测模型显示出卓越的辨别能力,可帮助临床医生区分 MIS-C 患者。该模型在广泛使用前需要进行外部和前瞻性验证。
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A Diagnostic Prediction Model to Distinguish Multisystem Inflammatory Syndrome in Children.

Objective: Features of multisystem inflammatory syndrome in children (MIS-C) overlap with other syndromes, making the diagnosis difficult for clinicians. We aimed to compare clinical differences between patients with and without clinical MIS-C diagnosis and develop a diagnostic prediction model to assist clinicians in identification of patients with MIS-C within the first 24 hours of hospital presentation.

Methods: A cohort of 127 patients (<21 years) were admitted to an academic children's hospital and evaluated for MIS-C. The primary outcome measure was MIS-C diagnosis at Vanderbilt University Medical Center. Clinical, laboratory, and cardiac features were extracted from the medical record, compared among groups, and selected a priori to identify candidate predictors. Final predictors were identified through a logistic regression model with bootstrapped backward selection in which only variables selected in more than 80% of 500 bootstraps were included in the final model.

Results: Of 127 children admitted to our hospital with concern for MIS-C, 45 were clinically diagnosed with MIS-C and 82 were diagnosed with alternative diagnoses. We found a model with four variables-the presence of hypotension and/or fluid resuscitation, abdominal pain, new rash, and the value of serum sodium-showed excellent discrimination (concordance index 0.91; 95% confidence interval: 0.85-0.96) and good calibration in identifying patients with MIS-C.

Conclusion: A diagnostic prediction model with early clinical and laboratory features shows excellent discrimination and may assist clinicians in distinguishing patients with MIS-C. This model will require external and prospective validation prior to widespread use.

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