Revista Paulista de Pediatria (Nov 2022)

Multisystem Inflammatory Syndrome in Children (MIS-C) temporally related to COVID-19: the experience at a pediatric reference hospital in Colombia

  • Diego Alejandro Lozano-Espinosa,
  • Germán Camacho-Moreno,
  • Juan Francisco López-Cubillos,
  • Adriana Soraya Díaz-Maldonado,
  • Oscar Javier León-Guerra,
  • Diego Mauricio Galvis-Trujillo,
  • Roy Sanguino-Lobo,
  • Oscar Guillermo Arévalo-Leal,
  • Ana María Eraso-Díaz del Castillo,
  • María Fernanda Reina-Ávila,
  • Vicky Carolina Cárdenas-Hernández,
  • Gabriela Ivankovich-Escoto,
  • Adriana H Tremoulet,
  • Rolando Ulloa-Gutiérrez

DOI
https://doi.org/10.1590/1984-0462/2023/41/2021267
Journal volume & issue
Vol. 41

Abstract

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Abstract Objective: This study aimed to describe the clinical characteristics and the different phenotypes of children with multisystem inflammatory syndrome in children (MIS-C) temporally related to COVID-19 and to evaluate the risk conditions that favored a greater severity of the disease during a 12-month period at a pediatric reference hospital in Colombia. Methods: A 12-month retrospective observational study of children under the age of 18 years who met criteria for MIS-C. Results: A total of 28 children presented MIS-C criteria. The median age was 7 years. Other than fever (100%) (onset 4 days prior to admission), the most frequent clinical features were gastrointestinal (86%) and mucocutaneous (61%). Notably, 14 (50%) children had Kawasaki-like symptoms. The most frequent echocardiographic abnormalities were pericardial effusion (64%), valvular involvement (68%), ventricular dysfunction (39%), and coronary artery abnormalities (29%). In addition, 75% had lymphopenia. All had at least one abnormal coagulation test. Most received intravenous immunoglobulin (89%), glucocorticoids (82%), vasopressors (54%), and antibiotics (64%). Notably, 61% had a more severe form of the disease and were admitted to an intensive care unit (median 4 days, mean 6 days); the severity predictors were patients with the inflammatory/MIS-C phenotype (OR 26.5; 95%CI 1.40–503.7; p=0.029) and rash (OR 14.7; 95%CI 1.2–178.7; p=0.034). Two patients had macrophage activation syndrome. Conclusions: Coronary artery abnormalities, ventricular dysfunction, and intensive care unit admission were frequent, which needs to highlight the importance of early clinical suspicion.

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