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Chest radiograph features of multisystem inflammatory syndrome in children (MIS-C) compared to pediatric COVID-19

BACKGROUND: Although the radiographic features of coronavirus disease 2019 (COVID-19) in children have been described, the distinguishing features of multisystem inflammatory syndrome in children (MIS-C) associated with COVID-19 are not well characterized. OBJECTIVE: We compared the chest radiograph...

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Autores principales: Rostad, Bradley S., Shah, Jay H., Rostad, Christina A., Jaggi, Preeti, Richer, Edward J., Linam, Leann E., Alazraki, Adina L., Riedesel, Erica L., Milla, Sarah S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7785920/
https://www.ncbi.nlm.nih.gov/pubmed/33404786
http://dx.doi.org/10.1007/s00247-020-04921-9
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author Rostad, Bradley S.
Shah, Jay H.
Rostad, Christina A.
Jaggi, Preeti
Richer, Edward J.
Linam, Leann E.
Alazraki, Adina L.
Riedesel, Erica L.
Milla, Sarah S.
author_facet Rostad, Bradley S.
Shah, Jay H.
Rostad, Christina A.
Jaggi, Preeti
Richer, Edward J.
Linam, Leann E.
Alazraki, Adina L.
Riedesel, Erica L.
Milla, Sarah S.
author_sort Rostad, Bradley S.
collection PubMed
description BACKGROUND: Although the radiographic features of coronavirus disease 2019 (COVID-19) in children have been described, the distinguishing features of multisystem inflammatory syndrome in children (MIS-C) associated with COVID-19 are not well characterized. OBJECTIVE: We compared the chest radiographic findings of MIS-C with those of COVID-19 and described other distinguishing imaging features of MIS-C. MATERIALS AND METHODS: We performed a retrospective case series review of children ages 0 to 18 years who were hospitalized at Children’s Healthcare of Atlanta from March to May 2020 and who either met the Centers for Disease Control and Prevention (CDC) case definition for MIS-C (n=11) or who had symptomatic, laboratory-confirmed COVID-19 (n=16). Two radiologists reviewed the most severe chest radiographs for each patient. The type and distribution of pulmonary opacities and presence or absence of pleural effusions were recorded. The chest radiographs were categorized based on potential COVID-19 imaging findings as typical, indeterminate, atypical or negative. An imaging severity score was also assigned using a simplified version of the Radiographic Assessment of Lung Edema Score. Findings were statistically compared between patients with MIS-C and those with COVID-19. Additional imaging findings of MIS-C were also described. RESULTS: Radiographic features of MIS-C included pleural effusions (82% [9/11]), pulmonary consolidations (73% [8/11]) and ground glass opacities (91% [10/11]). All of the lung opacities (100% [10/10]) were bilateral, and the majority of the pleural effusions (67% [6/9]) were bilateral. Compared to children with COVID-19, children with MIS-C were significantly more likely to develop pleural effusions on chest radiograph (82% [9/11] vs. 0% [0/0], P-value <0.01) and a lower zone predominance of pulmonary opacifications (100% [10/10] vs. 38% [5/13], P-value <0.01). Children with MIS-C who also had abdominal imaging had intra-abdominal inflammatory changes. CONCLUSION: Key chest radiographic features of MIS-C versus those of COVID-19 were pleural effusions and lower zone pulmonary opacifications as well as intra-abdominal inflammation. Elucidating the distinguishing radiographic features of MIS-C may help refine the case definition and expedite diagnosis and treatment. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00247-020-04921-9.
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spelling pubmed-77859202021-01-06 Chest radiograph features of multisystem inflammatory syndrome in children (MIS-C) compared to pediatric COVID-19 Rostad, Bradley S. Shah, Jay H. Rostad, Christina A. Jaggi, Preeti Richer, Edward J. Linam, Leann E. Alazraki, Adina L. Riedesel, Erica L. Milla, Sarah S. Pediatr Radiol Original Article BACKGROUND: Although the radiographic features of coronavirus disease 2019 (COVID-19) in children have been described, the distinguishing features of multisystem inflammatory syndrome in children (MIS-C) associated with COVID-19 are not well characterized. OBJECTIVE: We compared the chest radiographic findings of MIS-C with those of COVID-19 and described other distinguishing imaging features of MIS-C. MATERIALS AND METHODS: We performed a retrospective case series review of children ages 0 to 18 years who were hospitalized at Children’s Healthcare of Atlanta from March to May 2020 and who either met the Centers for Disease Control and Prevention (CDC) case definition for MIS-C (n=11) or who had symptomatic, laboratory-confirmed COVID-19 (n=16). Two radiologists reviewed the most severe chest radiographs for each patient. The type and distribution of pulmonary opacities and presence or absence of pleural effusions were recorded. The chest radiographs were categorized based on potential COVID-19 imaging findings as typical, indeterminate, atypical or negative. An imaging severity score was also assigned using a simplified version of the Radiographic Assessment of Lung Edema Score. Findings were statistically compared between patients with MIS-C and those with COVID-19. Additional imaging findings of MIS-C were also described. RESULTS: Radiographic features of MIS-C included pleural effusions (82% [9/11]), pulmonary consolidations (73% [8/11]) and ground glass opacities (91% [10/11]). All of the lung opacities (100% [10/10]) were bilateral, and the majority of the pleural effusions (67% [6/9]) were bilateral. Compared to children with COVID-19, children with MIS-C were significantly more likely to develop pleural effusions on chest radiograph (82% [9/11] vs. 0% [0/0], P-value <0.01) and a lower zone predominance of pulmonary opacifications (100% [10/10] vs. 38% [5/13], P-value <0.01). Children with MIS-C who also had abdominal imaging had intra-abdominal inflammatory changes. CONCLUSION: Key chest radiographic features of MIS-C versus those of COVID-19 were pleural effusions and lower zone pulmonary opacifications as well as intra-abdominal inflammation. Elucidating the distinguishing radiographic features of MIS-C may help refine the case definition and expedite diagnosis and treatment. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00247-020-04921-9. Springer Berlin Heidelberg 2021-01-06 2021 /pmc/articles/PMC7785920/ /pubmed/33404786 http://dx.doi.org/10.1007/s00247-020-04921-9 Text en © Springer-Verlag GmbH Germany, part of Springer Nature 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Original Article
Rostad, Bradley S.
Shah, Jay H.
Rostad, Christina A.
Jaggi, Preeti
Richer, Edward J.
Linam, Leann E.
Alazraki, Adina L.
Riedesel, Erica L.
Milla, Sarah S.
Chest radiograph features of multisystem inflammatory syndrome in children (MIS-C) compared to pediatric COVID-19
title Chest radiograph features of multisystem inflammatory syndrome in children (MIS-C) compared to pediatric COVID-19
title_full Chest radiograph features of multisystem inflammatory syndrome in children (MIS-C) compared to pediatric COVID-19
title_fullStr Chest radiograph features of multisystem inflammatory syndrome in children (MIS-C) compared to pediatric COVID-19
title_full_unstemmed Chest radiograph features of multisystem inflammatory syndrome in children (MIS-C) compared to pediatric COVID-19
title_short Chest radiograph features of multisystem inflammatory syndrome in children (MIS-C) compared to pediatric COVID-19
title_sort chest radiograph features of multisystem inflammatory syndrome in children (mis-c) compared to pediatric covid-19
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7785920/
https://www.ncbi.nlm.nih.gov/pubmed/33404786
http://dx.doi.org/10.1007/s00247-020-04921-9
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