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  1. Article ; Online: American College of Rheumatology Clinical Guidance for Multisystem Inflammatory Syndrome in Children Associated With SARS-CoV-2 and Hyperinflammation in Pediatric COVID-19: Version 1.

    Henderson, Lauren A / Canna, Scott W / Friedman, Kevin G / Gorelik, Mark / Lapidus, Sivia K / Bassiri, Hamid / Behrens, Edward M / Ferris, Anne / Kernan, Kate F / Schulert, Grant S / Seo, Philip / F Son, Mary Beth / Tremoulet, Adriana H / Yeung, Rae S M / Mudano, Amy S / Turner, Amy S / Karp, David R / Mehta, Jay J

    Arthritis & rheumatology (Hoboken, N.J.)

    2020  Volume 72, Issue 11, Page(s) 1791–1805

    Abstract: ... associated with SARS-CoV-2 and hyperinflammation in COVID-19. The task force was composed of 9 pediatric ... Objective: To provide guidance on the management of multisystem inflammatory syndrome in children ... of SARS-CoV-2-related syndromes in the pediatric population continues to evolve. The guidance provided ...

    Abstract Objective: To provide guidance on the management of multisystem inflammatory syndrome in children (MIS-C), a condition characterized by fever, inflammation, and multiorgan dysfunction that manifests late in the course of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, and to provide recommendations for children with hyperinflammation during coronavirus disease 2019 (COVID-19), the acute, infectious phase of SARS-CoV-2 infection.
    Methods: A multidisciplinary task force was convened by the American College of Rheumatology (ACR) to provide guidance on the management of MIS-C associated with SARS-CoV-2 and hyperinflammation in COVID-19. The task force was composed of 9 pediatric rheumatologists, 2 adult rheumatologists, 2 pediatric cardiologists, 2 pediatric infectious disease specialists, and 1 pediatric critical care physician. Preliminary statements addressing clinical questions related to MIS-C and hyperinflammation in COVID-19 were developed based on evidence reports. Consensus was built through a modified Delphi process that involved 2 rounds of anonymous voting and 2 webinars. A 9-point scale was used to determine the appropriateness of each statement (median scores of 1-3 for inappropriate, 4-6 for uncertain, and 7-9 for appropriate), and consensus was rated as low, moderate, or high based on dispersion of the votes along the numeric scale. Approved guidance statements were those that were classified as appropriate with moderate or high levels of consensus, as prespecified prior to voting.
    Results: The ACR task force approved a total of 128 guidance statements addressing the management of MIS-C and hyperinflammation in pediatric COVID-19. These statements were refined into 40 final clinical guidance statements, accompanied by a flow diagram depicting the diagnostic pathway for MIS-C.
    Conclusion: Our understanding of SARS-CoV-2-related syndromes in the pediatric population continues to evolve. The guidance provided in this "living document" reflects currently available evidence, coupled with expert opinion, and will be revised as further evidence becomes available.
    MeSH term(s) COVID-19/complications ; COVID-19/etiology ; COVID-19/therapy ; Consensus ; Humans ; Systemic Inflammatory Response Syndrome/etiology ; Systemic Inflammatory Response Syndrome/therapy
    Keywords covid19
    Language English
    Publishing date 2020-10-03
    Publishing country United States
    Document type Journal Article ; Practice Guideline
    ZDB-ID 2756371-6
    ISSN 2326-5205 ; 2326-5191
    ISSN (online) 2326-5205
    ISSN 2326-5191
    DOI 10.1002/art.41454
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: American College of Rheumatology Clinical Guidance for Multisystem Inflammatory Syndrome in Children Associated With SARS-CoV-2 and Hyperinflammation in Pediatric COVID-19: Version 1

    Henderson, Lauren A / Canna, Scott W / Friedman, Kevin G / Gorelik, Mark / Lapidus, Sivia K / Bassiri, Hamid / Behrens, Edward M / Ferris, Anne / Kernan, Kate F / Schulert, Grant S / Seo, Philip / F Son, Mary Beth / Tremoulet, Adriana H / Yeung, Rae S M / Mudano, Amy S / Turner, Amy S / Karp, David R / Mehta, Jay J

    Arthritis rheumatol. (Malden. Online)

    Abstract: ... by the American College of Rheumatology (ACR) to provide guidance on the management of MIS-C associated with SARS ... CoV-2 and hyperinflammation in COVID-19. The task force was composed of 9 pediatric rheumatologists, 2 ... OBJECTIVE: To provide guidance on the management of multisystem inflammatory syndrome in children ...

    Abstract OBJECTIVE: To provide guidance on the management of multisystem inflammatory syndrome in children (MIS-C), a condition characterized by fever, inflammation, and multiorgan dysfunction that manifests late in the course of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, and to provide recommendations for children with hyperinflammation during coronavirus disease 2019 (COVID-19), the acute, infectious phase of SARS-CoV-2 infection. METHODS: A multidisciplinary task force was convened by the American College of Rheumatology (ACR) to provide guidance on the management of MIS-C associated with SARS-CoV-2 and hyperinflammation in COVID-19. The task force was composed of 9 pediatric rheumatologists, 2 adult rheumatologists, 2 pediatric cardiologists, 2 pediatric infectious disease specialists, and 1 pediatric critical care physician. Preliminary statements addressing clinical questions related to MIS-C and hyperinflammation in COVID-19 were developed based on evidence reports. Consensus was built through a modified Delphi process that involved 2 rounds of anonymous voting and 2 webinars. A 9-point scale was used to determine the appropriateness of each statement (median scores of 1-3 for inappropriate, 4-6 for uncertain, and 7-9 for appropriate), and consensus was rated as low, moderate, or high based on dispersion of the votes along the numeric scale. Approved guidance statements were those that were classified as appropriate with moderate or high levels of consensus, as prespecified prior to voting. RESULTS: The ACR task force approved a total of 128 guidance statements addressing the management of MIS-C and hyperinflammation in pediatric COVID-19. These statements were refined into 40 final clinical guidance statements, accompanied by a flow diagram depicting the diagnostic pathway for MIS-C. CONCLUSION: Our understanding of SARS-CoV-2-related syndromes in the pediatric population continues to evolve. The guidance provided in this "living document" reflects currently available evidence, coupled with expert opinion, and will be revised as further evidence becomes available.
    Keywords covid19
    Publisher WHO
    Document type Article
    Note WHO #Covidence: #670553
    Database COVID19

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  3. Article ; Online: American College of Rheumatology Clinical Guidance for Pediatric Patients with Multisystem Inflammatory Syndrome in Children (MIS‐C) Associated with SARSCoV2 and Hyperinflammation in COVID19. Version 1

    Henderson, Lauren A. / Canna, Scott W. / Friedman, Kevin G. / Gorelik, Mark / Lapidus, Sivia K. / Bassiri, Hamid / Behrens, Edward M. / Ferris, Anne / Kernan, Kate F. / Schulert, Grant S. / Seo, Philip / F. Son, Mary Beth / Tremoulet, Adriana H. / Yeung, Rae S.M. / Mudano, Amy S. / Turner, Amy S. / Karp, David R. / Mehta, Jay J.

    Arthritis & Rheumatology ; ISSN 2326-5191 2326-5205

    2020  

    Keywords covid19
    Language English
    Publisher Wiley
    Publishing country us
    Document type Article ; Online
    DOI 10.1002/art.41454
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  4. Article ; Online: American College of Rheumatology Clinical Guidance for Multisystem Inflammatory Syndrome in Children Associated With SARS-CoV-2 and Hyperinflammation in Pediatric COVID-19: Version 3.

    Henderson, Lauren A / Canna, Scott W / Friedman, Kevin G / Gorelik, Mark / Lapidus, Sivia K / Bassiri, Hamid / Behrens, Edward M / Kernan, Kate F / Schulert, Grant S / Seo, Philip / Son, Mary Beth F / Tremoulet, Adriana H / VanderPluym, Christina / Yeung, Rae S M / Mudano, Amy S / Turner, Amy S / Karp, David R / Mehta, Jay J

    Arthritis & rheumatology (Hoboken, N.J.)

    2022  Volume 74, Issue 4, Page(s) e1–e20

    Abstract: Objective: To provide guidance on the management of Multisystem Inflammatory Syndrome in Children ... Our understanding of SARS-CoV-2-related syndromes in the pediatric population continues to evolve. This guidance ... with hyperinflammation during COVID-19, the acute, infectious phase of SARS-CoV-2 infection.: Methods: The Task Force ...

    Abstract Objective: To provide guidance on the management of Multisystem Inflammatory Syndrome in Children (MIS-C), a condition characterized by fever, inflammation, and multiorgan dysfunction that manifests late in the course of SARS-CoV-2 infection. Recommendations are also provided for children with hyperinflammation during COVID-19, the acute, infectious phase of SARS-CoV-2 infection.
    Methods: The Task Force is composed of 9 pediatric rheumatologists and 2 adult rheumatologists, 2 pediatric cardiologists, 2 pediatric infectious disease specialists, and 1 pediatric critical care physician. Preliminary statements addressing clinical questions related to MIS-C and hyperinflammation in COVID-19 were developed based on evidence reports. Consensus was built through a modified Delphi process that involved anonymous voting and webinar discussion. A 9-point scale was used to determine the appropriateness of each statement (median scores of 1-3 for inappropriate, 4-6 for uncertain, and 7-9 for appropriate). Consensus was rated as low, moderate, or high based on dispersion of the votes. Approved guidance statements were those that were classified as appropriate with moderate or high levels of consensus, which were prespecified before voting.
    Results: The guidance was approved in June 2020 and updated in November 2020 and October 2021, and consists of 41 final guidance statements accompanied by flow diagrams depicting the diagnostic pathway for MIS-C and recommendations for initial immunomodulatory treatment of MIS-C.
    Conclusion: Our understanding of SARS-CoV-2-related syndromes in the pediatric population continues to evolve. This guidance document reflects currently available evidence coupled with expert opinion, and will be revised as further evidence becomes available.
    MeSH term(s) Adult ; COVID-19/complications ; Child ; Humans ; Rheumatology ; SARS-CoV-2 ; Systemic Inflammatory Response Syndrome/therapy ; United States
    Language English
    Publishing date 2022-02-03
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2756371-6
    ISSN 2326-5205 ; 2326-5191
    ISSN (online) 2326-5205
    ISSN 2326-5191
    DOI 10.1002/art.42062
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: American College of Rheumatology Clinical Guidance for Multisystem Inflammatory Syndrome in Children Associated With SARS-CoV-2 and Hyperinflammation in Pediatric COVID-19: Version 2.

    Henderson, Lauren A / Canna, Scott W / Friedman, Kevin G / Gorelik, Mark / Lapidus, Sivia K / Bassiri, Hamid / Behrens, Edward M / Ferris, Anne / Kernan, Kate F / Schulert, Grant S / Seo, Philip / Son, Mary Beth F / Tremoulet, Adriana H / Yeung, Rae S M / Mudano, Amy S / Turner, Amy S / Karp, David R / Mehta, Jay J

    Arthritis & rheumatology (Hoboken, N.J.)

    2021  Volume 73, Issue 4, Page(s) e13–e29

    Abstract: Objective: To provide guidance on the management of Multisystem Inflammatory Syndrome in Children ... Conclusion: Our understanding of SARS-CoV-2-related syndromes in the pediatric population continues ... Recommendations are also provided for children with hyperinflammation during coronavirus disease 2019 (COVID-19 ...

    Abstract Objective: To provide guidance on the management of Multisystem Inflammatory Syndrome in Children (MIS-C), a condition characterized by fever, inflammation, and multiorgan dysfunction that manifests late in the course of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. Recommendations are also provided for children with hyperinflammation during coronavirus disease 2019 (COVID-19), the acute, infectious phase of SARS-CoV-2 infection.
    Methods: The Task Force was composed of 9 pediatric rheumatologists and 2 adult rheumatologists, 2 pediatric cardiologists, 2 pediatric infectious disease specialists, and 1 pediatric critical care physician. Preliminary statements addressing clinical questions related to MIS-C and hyperinflammation in COVID-19 were developed based on evidence reports. Consensus was built through a modified Delphi process that involved anonymous voting and webinar discussion. A 9-point scale was used to determine the appropriateness of each statement (median scores of 1-3 for inappropriate, 4-6 for uncertain, and 7-9 for appropriate). Consensus was rated as low, moderate, or high based on dispersion of the votes. Approved guidance statements were those that were classified as appropriate with moderate or high levels of consensus, which were prespecified before voting.
    Results: The first version of the guidance was approved in June 2020, and consisted of 40 final guidance statements accompanied by a flow diagram depicting the diagnostic pathway for MIS-C. The document was revised in November 2020, and a new flow diagram with recommendations for initial immunomodulatory treatment of MIS-C was added.
    Conclusion: Our understanding of SARS-CoV-2-related syndromes in the pediatric population continues to evolve. This guidance document reflects currently available evidence coupled with expert opinion, and will be revised as further evidence becomes available.
    MeSH term(s) Adolescent ; Advisory Committees ; Anticoagulants/therapeutic use ; Antirheumatic Agents/therapeutic use ; COVID-19/diagnosis ; COVID-19/therapy ; Child ; Child, Preschool ; Delphi Technique ; Diagnosis, Differential ; Glucocorticoids/therapeutic use ; Humans ; Immunoglobulins, Intravenous/therapeutic use ; Immunologic Factors/therapeutic use ; Infant ; Infant, Newborn ; Inflammation ; Interleukin 1 Receptor Antagonist Protein/therapeutic use ; Mucocutaneous Lymph Node Syndrome/diagnosis ; Platelet Aggregation Inhibitors/therapeutic use ; Rheumatology ; SARS-CoV-2 ; Systemic Inflammatory Response Syndrome/diagnosis ; Systemic Inflammatory Response Syndrome/therapy ; Young Adult
    Chemical Substances Anticoagulants ; Antirheumatic Agents ; Glucocorticoids ; Immunoglobulins, Intravenous ; Immunologic Factors ; Interleukin 1 Receptor Antagonist Protein ; Platelet Aggregation Inhibitors
    Language English
    Publishing date 2021-02-15
    Publishing country United States
    Document type Consensus Development Conference ; Journal Article ; Practice Guideline
    ZDB-ID 2756371-6
    ISSN 2326-5205 ; 2326-5191
    ISSN (online) 2326-5205
    ISSN 2326-5191
    DOI 10.1002/art.41616
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: American College of Rheumatology Clinical Guidance for Multisystem Inflammatory Syndrome in Children Associated With SARS-CoV-2 and Hyperinflammation in Pediatric COVID-19

    Henderson, Lauren A / Canna, Scott W / Friedman, Kevin G / Gorelik, Mark / Lapidus, Sivia K / Bassiri, Hamid / Behrens, Edward M / Ferris, Anne / Kernan, Kate F / Schulert, Grant S / Seo, Philip / F Son, Mary Beth / Tremoulet, Adriana H / Yeung, Rae SM / Mudano, Amy S / Turner, Amy S / Karp, David R / Mehta, Jay J

    Version 1.

    2020  

    Abstract: ... by the American College of Rheumatology (ACR) to provide guidance on the management of MIS-C associated with SARS ... CoV-2 and hyperinflammation in COVID-19. The task force was composed of 9 pediatric rheumatologists, 2 ... OBJECTIVE:To provide guidance on the management of multisystem inflammatory syndrome in children ...

    Abstract OBJECTIVE:To provide guidance on the management of multisystem inflammatory syndrome in children (MIS-C), a condition characterized by fever, inflammation, and multiorgan dysfunction that manifests late in the course of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, and to provide recommendations for children with hyperinflammation during coronavirus disease 2019 (COVID-19), the acute, infectious phase of SARS-CoV-2 infection. METHODS:A multidisciplinary task force was convened by the American College of Rheumatology (ACR) to provide guidance on the management of MIS-C associated with SARS-CoV-2 and hyperinflammation in COVID-19. The task force was composed of 9 pediatric rheumatologists, 2 adult rheumatologists, 2 pediatric cardiologists, 2 pediatric infectious disease specialists, and 1 pediatric critical care physician. Preliminary statements addressing clinical questions related to MIS-C and hyperinflammation in COVID-19 were developed based on evidence reports. Consensus was built through a modified Delphi process that involved 2 rounds of anonymous voting and 2 webinars. A 9-point scale was used to determine the appropriateness of each statement (median scores of 1-3 for inappropriate, 4-6 for uncertain, and 7-9 for appropriate), and consensus was rated as low, moderate, or high based on dispersion of the votes along the numeric scale. Approved guidance statements were those that were classified as appropriate with moderate or high levels of consensus, as prespecified prior to voting. RESULTS:The ACR task force approved a total of 128 guidance statements addressing the management of MIS-C and hyperinflammation in pediatric COVID-19. These statements were refined into 40 final clinical guidance statements, accompanied by a flow diagram depicting the diagnostic pathway for MIS-C. CONCLUSION:Our understanding of SARS-CoV-2-related syndromes in the pediatric population continues to evolve. The guidance provided in this "living document" reflects currently available evidence, coupled with expert opinion, and will be revised as further evidence becomes available.
    Keywords COVID-19 ; MIS-C ; SARS-CoV-2 ; pediatrics ; covid19
    Subject code 610
    Publishing date 2020-07-23
    Publisher eScholarship, University of California
    Publishing country us
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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