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Clinical features and outcome of MIS-C patients: an experience from Central Anatolia

BACKGROUND: Multisystem inflammatory syndrome in children (MIS-C) is a new clinical condition characterized by signs of inflammation and multiorgan dysfunction due to cytokine storm associated with SARS-CoV-2. The clinical spectrum of MIS-C ranges from mild to severe, and even to mortal multisystem...

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Autores principales: Alkan, Gulsum, Sert, Ahmet, Oz, Sadiye Kubra Tuter, Emiroglu, Melike, Yılmaz, Resul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8100744/
https://www.ncbi.nlm.nih.gov/pubmed/33956250
http://dx.doi.org/10.1007/s10067-021-05754-z
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author Alkan, Gulsum
Sert, Ahmet
Oz, Sadiye Kubra Tuter
Emiroglu, Melike
Yılmaz, Resul
author_facet Alkan, Gulsum
Sert, Ahmet
Oz, Sadiye Kubra Tuter
Emiroglu, Melike
Yılmaz, Resul
author_sort Alkan, Gulsum
collection PubMed
description BACKGROUND: Multisystem inflammatory syndrome in children (MIS-C) is a new clinical condition characterized by signs of inflammation and multiorgan dysfunction due to cytokine storm associated with SARS-CoV-2. The clinical spectrum of MIS-C ranges from mild to severe, and even to mortal multisystem involvement. To guide clinicians, we evaluated detailed demographic characteristics, clinical features, laboratory findings, and outcomes of MIS-C cases. METHODS: We performed a retrospective study of patients with MIS-C who were managed in the Department of Pediatric Infectious Disease in the Selcuk University Faculty of Medicine, Konya, Turkey. MIS-C patients were divided into three clinical severity groups (mild, moderate, and severe) and separated into three age groups (< 5 years, 5–10 years, > 10 years). We compared the characteristics of MIS-C cases according to the severity of the disease and by age groups. RESULT: Thirty-six children with MIS-C were evaluated (52.8% male, median age of 7.8 years). A clinical spectrum overlapping with Kawasaki disease (KD) was the most common presentation (69.4%) in all age groups. The most common clinical symptoms were fever (100%), mucocutaneous rash (69.4%), and gastrointestinal symptoms (66.6%). There was no statistically significant difference in echocardiographic abnormality between KD-like and the other clinical spectra (p > 0.05). All life-threatening rhythm disturbances were observed in severe cases. No patients died. CONCLUSION: It is important to increase the awareness of physicians about the MIS-C disease, which can present with different combinations of different systemic findings, so that patients can be diagnosed and treated in a timely manner.
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spelling pubmed-81007442021-05-06 Clinical features and outcome of MIS-C patients: an experience from Central Anatolia Alkan, Gulsum Sert, Ahmet Oz, Sadiye Kubra Tuter Emiroglu, Melike Yılmaz, Resul Clin Rheumatol Original Article BACKGROUND: Multisystem inflammatory syndrome in children (MIS-C) is a new clinical condition characterized by signs of inflammation and multiorgan dysfunction due to cytokine storm associated with SARS-CoV-2. The clinical spectrum of MIS-C ranges from mild to severe, and even to mortal multisystem involvement. To guide clinicians, we evaluated detailed demographic characteristics, clinical features, laboratory findings, and outcomes of MIS-C cases. METHODS: We performed a retrospective study of patients with MIS-C who were managed in the Department of Pediatric Infectious Disease in the Selcuk University Faculty of Medicine, Konya, Turkey. MIS-C patients were divided into three clinical severity groups (mild, moderate, and severe) and separated into three age groups (< 5 years, 5–10 years, > 10 years). We compared the characteristics of MIS-C cases according to the severity of the disease and by age groups. RESULT: Thirty-six children with MIS-C were evaluated (52.8% male, median age of 7.8 years). A clinical spectrum overlapping with Kawasaki disease (KD) was the most common presentation (69.4%) in all age groups. The most common clinical symptoms were fever (100%), mucocutaneous rash (69.4%), and gastrointestinal symptoms (66.6%). There was no statistically significant difference in echocardiographic abnormality between KD-like and the other clinical spectra (p > 0.05). All life-threatening rhythm disturbances were observed in severe cases. No patients died. CONCLUSION: It is important to increase the awareness of physicians about the MIS-C disease, which can present with different combinations of different systemic findings, so that patients can be diagnosed and treated in a timely manner. Springer International Publishing 2021-05-06 2021 /pmc/articles/PMC8100744/ /pubmed/33956250 http://dx.doi.org/10.1007/s10067-021-05754-z Text en © International League of Associations for Rheumatology (ILAR) 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
Alkan, Gulsum
Sert, Ahmet
Oz, Sadiye Kubra Tuter
Emiroglu, Melike
Yılmaz, Resul
Clinical features and outcome of MIS-C patients: an experience from Central Anatolia
title Clinical features and outcome of MIS-C patients: an experience from Central Anatolia
title_full Clinical features and outcome of MIS-C patients: an experience from Central Anatolia
title_fullStr Clinical features and outcome of MIS-C patients: an experience from Central Anatolia
title_full_unstemmed Clinical features and outcome of MIS-C patients: an experience from Central Anatolia
title_short Clinical features and outcome of MIS-C patients: an experience from Central Anatolia
title_sort clinical features and outcome of mis-c patients: an experience from central anatolia
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8100744/
https://www.ncbi.nlm.nih.gov/pubmed/33956250
http://dx.doi.org/10.1007/s10067-021-05754-z
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