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542. SARS CoV-2-Associated Multisystem Inflammatory Syndrome of Children (MIS-C) in the Washington DC Metropolitan Region

BACKGROUND: Background: Multi-system Inflammatory Syndrome of Children (MIS-C) has recently emerged internationally as a serious inflammatory complication of SARS-CoV-2 infection with significant morbidity for the pediatric population. METHODS: This observational retrospective cohort study includes...

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Autores principales: DeBiasi, Roberta L, Smith, Karen L, Bell, Michael, Berul, Charles, Ansusinha, Emily, Bundy, Vanessa, Delaney, Meghan, Diab, Yaser, Hahn, Andrea, Hamdy, Rana F, Hanisch, Benjamin, Harik, Nada, Harahsheh, Ashraf S, Herstek, Jessica, Kline, Jaclyn, Koay, Wei Li A, Krishnan, Anita, Jantausch, Barbara, Majumdar, Suvankar, Parikh, Kavita, Pershad, Jay, Ronis, Tova, Sadler, Eleanor D, Sharma, Hemant, Sharron, Matthew P, Srinivasalu, Hemalatha, Sule, Sangeeta, Wells, Elizabeth, Wessel, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7776150/
http://dx.doi.org/10.1093/ofid/ofaa439.736
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author DeBiasi, Roberta L
Smith, Karen L
Bell, Michael
Berul, Charles
Ansusinha, Emily
Bundy, Vanessa
Delaney, Meghan
Diab, Yaser
Hahn, Andrea
Hamdy, Rana F
Hanisch, Benjamin
Harik, Nada
Harahsheh, Ashraf S
Herstek, Jessica
Kline, Jaclyn
Koay, Wei Li A
Krishnan, Anita
Jantausch, Barbara
Majumdar, Suvankar
Parikh, Kavita
Pershad, Jay
Ronis, Tova
Sadler, Eleanor D
Sharma, Hemant
Sharron, Matthew P
Srinivasalu, Hemalatha
Sule, Sangeeta
Wells, Elizabeth
Wessel, David
author_facet DeBiasi, Roberta L
Smith, Karen L
Bell, Michael
Berul, Charles
Ansusinha, Emily
Bundy, Vanessa
Delaney, Meghan
Diab, Yaser
Hahn, Andrea
Hamdy, Rana F
Hanisch, Benjamin
Harik, Nada
Harahsheh, Ashraf S
Herstek, Jessica
Kline, Jaclyn
Koay, Wei Li A
Krishnan, Anita
Jantausch, Barbara
Majumdar, Suvankar
Parikh, Kavita
Pershad, Jay
Ronis, Tova
Sadler, Eleanor D
Sharma, Hemant
Sharron, Matthew P
Srinivasalu, Hemalatha
Sule, Sangeeta
Wells, Elizabeth
Wessel, David
author_sort DeBiasi, Roberta L
collection PubMed
description BACKGROUND: Background: Multi-system Inflammatory Syndrome of Children (MIS-C) has recently emerged internationally as a serious inflammatory complication of SARS-CoV-2 infection with significant morbidity for the pediatric population. METHODS: This observational retrospective cohort study includes 33 children meeting CDC criteria for MIS-C treated between March 15 and June 17, 2020 at Children’s National Hospital in Washington DC. Clinical and demographic data were extracted from medical records and are summarized. RESULTS: Of 33 hospitalized MIS-C patients, 42% were critically ill, and 58% were non-critically ill. The median age was 8.9 years (0.7–18.7 years). More males (58 %) than females (43 %) were represented in the MIS-C cohort. The majority (75%) of children had no underlying medical condition. Criteria for incomplete or complete Kawasaki Disease (KD) were present in 39% of patients, while an additional 9% had some features of KD. However the remaining 52% of MIS-C patients presented with other sub-phenotypes including prominent severe abdominal pain and/or nonspecific multiorgan dysfunction. 30% presented with shock requiring volume and/or inotropic support. SARS-CoV-2 antibodies were present in 61% of patients. Virus was detectable by PCR in 36% of patients. At the time of initial evaluation, 39% (13/33) of children had identified cardiac abnormalities including myocardial dysfunction (5/33; 15%), coronary ectasia (4/33; 12%), coronary aneurysm (3/33; 9%), or pericardial effusion 5/33; 15%) either alone or in combination. Cytokine profiling identified elevation of several cytokines in this cohort, including IL-6. Treatment has included intravenous immunoglobulin, aspirin, anakinra and other immunomodulatory therapies, with overall rapid response to therapy. No deaths have occurred. CONCLUSION: The emergence of MIS-C late in the surge of SARS-CoV-2 circulation in the Washington DC metropolitan region has added to the already significant burden of hospitalized and critically ill children in our region. A significant percentage of these children present with cardiac dysfunction and abnormalities, whether or not with KD features at presentation. Detailed characterization of immune responses and long term outcome of these patients is a priority. DISCLOSURES: Andrea Hahn, MD, MS, Johnson and Johnson (Consultant)
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spelling pubmed-77761502021-01-07 542. SARS CoV-2-Associated Multisystem Inflammatory Syndrome of Children (MIS-C) in the Washington DC Metropolitan Region DeBiasi, Roberta L Smith, Karen L Bell, Michael Berul, Charles Ansusinha, Emily Bundy, Vanessa Delaney, Meghan Diab, Yaser Hahn, Andrea Hamdy, Rana F Hanisch, Benjamin Harik, Nada Harahsheh, Ashraf S Herstek, Jessica Kline, Jaclyn Koay, Wei Li A Krishnan, Anita Jantausch, Barbara Majumdar, Suvankar Parikh, Kavita Pershad, Jay Ronis, Tova Sadler, Eleanor D Sharma, Hemant Sharron, Matthew P Srinivasalu, Hemalatha Sule, Sangeeta Wells, Elizabeth Wessel, David Open Forum Infect Dis Poster Abstracts BACKGROUND: Background: Multi-system Inflammatory Syndrome of Children (MIS-C) has recently emerged internationally as a serious inflammatory complication of SARS-CoV-2 infection with significant morbidity for the pediatric population. METHODS: This observational retrospective cohort study includes 33 children meeting CDC criteria for MIS-C treated between March 15 and June 17, 2020 at Children’s National Hospital in Washington DC. Clinical and demographic data were extracted from medical records and are summarized. RESULTS: Of 33 hospitalized MIS-C patients, 42% were critically ill, and 58% were non-critically ill. The median age was 8.9 years (0.7–18.7 years). More males (58 %) than females (43 %) were represented in the MIS-C cohort. The majority (75%) of children had no underlying medical condition. Criteria for incomplete or complete Kawasaki Disease (KD) were present in 39% of patients, while an additional 9% had some features of KD. However the remaining 52% of MIS-C patients presented with other sub-phenotypes including prominent severe abdominal pain and/or nonspecific multiorgan dysfunction. 30% presented with shock requiring volume and/or inotropic support. SARS-CoV-2 antibodies were present in 61% of patients. Virus was detectable by PCR in 36% of patients. At the time of initial evaluation, 39% (13/33) of children had identified cardiac abnormalities including myocardial dysfunction (5/33; 15%), coronary ectasia (4/33; 12%), coronary aneurysm (3/33; 9%), or pericardial effusion 5/33; 15%) either alone or in combination. Cytokine profiling identified elevation of several cytokines in this cohort, including IL-6. Treatment has included intravenous immunoglobulin, aspirin, anakinra and other immunomodulatory therapies, with overall rapid response to therapy. No deaths have occurred. CONCLUSION: The emergence of MIS-C late in the surge of SARS-CoV-2 circulation in the Washington DC metropolitan region has added to the already significant burden of hospitalized and critically ill children in our region. A significant percentage of these children present with cardiac dysfunction and abnormalities, whether or not with KD features at presentation. Detailed characterization of immune responses and long term outcome of these patients is a priority. DISCLOSURES: Andrea Hahn, MD, MS, Johnson and Johnson (Consultant) Oxford University Press 2020-12-31 /pmc/articles/PMC7776150/ http://dx.doi.org/10.1093/ofid/ofaa439.736 Text en © The Author 2020. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Poster Abstracts
DeBiasi, Roberta L
Smith, Karen L
Bell, Michael
Berul, Charles
Ansusinha, Emily
Bundy, Vanessa
Delaney, Meghan
Diab, Yaser
Hahn, Andrea
Hamdy, Rana F
Hanisch, Benjamin
Harik, Nada
Harahsheh, Ashraf S
Herstek, Jessica
Kline, Jaclyn
Koay, Wei Li A
Krishnan, Anita
Jantausch, Barbara
Majumdar, Suvankar
Parikh, Kavita
Pershad, Jay
Ronis, Tova
Sadler, Eleanor D
Sharma, Hemant
Sharron, Matthew P
Srinivasalu, Hemalatha
Sule, Sangeeta
Wells, Elizabeth
Wessel, David
542. SARS CoV-2-Associated Multisystem Inflammatory Syndrome of Children (MIS-C) in the Washington DC Metropolitan Region
title 542. SARS CoV-2-Associated Multisystem Inflammatory Syndrome of Children (MIS-C) in the Washington DC Metropolitan Region
title_full 542. SARS CoV-2-Associated Multisystem Inflammatory Syndrome of Children (MIS-C) in the Washington DC Metropolitan Region
title_fullStr 542. SARS CoV-2-Associated Multisystem Inflammatory Syndrome of Children (MIS-C) in the Washington DC Metropolitan Region
title_full_unstemmed 542. SARS CoV-2-Associated Multisystem Inflammatory Syndrome of Children (MIS-C) in the Washington DC Metropolitan Region
title_short 542. SARS CoV-2-Associated Multisystem Inflammatory Syndrome of Children (MIS-C) in the Washington DC Metropolitan Region
title_sort 542. sars cov-2-associated multisystem inflammatory syndrome of children (mis-c) in the washington dc metropolitan region
topic Poster Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7776150/
http://dx.doi.org/10.1093/ofid/ofaa439.736
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