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A Diagnostic Prediction Model to Distinguish Multisystem Inflammatory Syndrome in Children.
Clark, Matthew T; Rankin, Danielle A; Peetluk, Lauren S; Gotte, Alisa; Herndon, Alison; McEachern, William; Smith, Andrew; Clark, Daniel E; Hardison, Edward; Esbenshade, Adam J; Patrick, Anna; Halasa, Natasha B; Connelly, James A; Katz, Sophie E.
Afiliación
  • Clark MT; Vanderbilt University Medical Center, Tennessee, Nashville.
  • Rankin DA; Vanderbilt University Medical Center and Vanderbilt University School of Medicine, Tennessee, Nashville.
  • Peetluk LS; Vanderbilt University Medical Center, Tennessee, Nashville.
  • Gotte A; Vanderbilt University Medical Center, Tennessee, Nashville.
  • Herndon A; Vanderbilt University Medical Center, Tennessee, Nashville.
  • McEachern W; Vanderbilt University Medical Center, Tennessee, Nashville.
  • Smith A; Johns Hopkins All Children's Hospital, Florida, St. Petersburg.
  • Clark DE; Vanderbilt University Medical Center, Tennessee, Nashville.
  • Hardison E; Vanderbilt University Medical Center, Tennessee, Nashville.
  • Esbenshade AJ; Vanderbilt University Medical Center, Tennessee, Nashville.
  • Patrick A; Vanderbilt University Medical Center, Tennessee, Nashville.
  • Halasa NB; Vanderbilt University Medical Center, Tennessee, Nashville.
  • Connelly JA; Vanderbilt University Medical Center, Tennessee, Nashville.
  • Katz SE; Vanderbilt University Medical Center, Tennessee, Nashville.
ACR Open Rheumatol ; 4(12): 1050-1059, 2022 Dec.
Article en En | MEDLINE | ID: mdl-36319189
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.

Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: ACR Open Rheumatol Año: 2022 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: ACR Open Rheumatol Año: 2022 Tipo del documento: Article