A Diagnostic Prediction Model to Distinguish Multisystem Inflammatory Syndrome in Children

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Abstract

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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APA

Clark, M. T., Rankin, D. A., Peetluk, L. S., Gotte, A., Herndon, A., McEachern, W., … Katz, S. E. (2022). A Diagnostic Prediction Model to Distinguish Multisystem Inflammatory Syndrome in Children. ACR Open Rheumatology, 4(12), 1050–1059. https://doi.org/10.1002/acr2.11509

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