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Intravenous administration of anakinra in children with macrophage activation syndrome
BACKGROUND: Subcutaneous anakinra is an interleukin-1 inhibitor used to treat juvenile idiopathic arthritis. Recent reports suggest anakinra can be a valuable addition to the treatment of COVID-19 associated cytokine storm syndrome and the related multisystem inflammatory syndrome (MIS-C) in childre...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8240425/ https://www.ncbi.nlm.nih.gov/pubmed/34187503 http://dx.doi.org/10.1186/s12969-021-00585-3 |
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author | Phadke, Omkar Rouster-Stevens, Kelly Giannopoulos, Helen Chandrakasan, Shanmuganathan Prahalad, Sampath |
author_facet | Phadke, Omkar Rouster-Stevens, Kelly Giannopoulos, Helen Chandrakasan, Shanmuganathan Prahalad, Sampath |
author_sort | Phadke, Omkar |
collection | PubMed |
description | BACKGROUND: Subcutaneous anakinra is an interleukin-1 inhibitor used to treat juvenile idiopathic arthritis. Recent reports suggest anakinra can be a valuable addition to the treatment of COVID-19 associated cytokine storm syndrome and the related multisystem inflammatory syndrome (MIS-C) in children. Herein, we describe our experience with intravenously administered anakinra. FINDINGS: 19 Patients (9 male) received intravenous (IV) anakinra for treatment of macrophage activation syndrome (MAS) secondary to systemic lupus erythematosus (SLE), systemic JIA (SJIA) or secondary hemophagocytic lymphohistiocytosis (sHLH). In most cases the general trend of the fibrinogen, ferritin, AST, and platelet count (Ravelli criteria) improved after initiation of IV anakinra. There were no reports of anaphylaxis or reactions associated with administration of IV anakinra. CONCLUSION: Intravenous administration of anakinra is an important therapeutic option for critically ill patients with MAS/HLH. It is also beneficial for those with thrombocytopenia, subcutaneous edema, neurological dysfunction, or very young, hospitalized patients who need multiple painful subcutaneous injections. |
format | Online Article Text |
id | pubmed-8240425 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-82404252021-06-29 Intravenous administration of anakinra in children with macrophage activation syndrome Phadke, Omkar Rouster-Stevens, Kelly Giannopoulos, Helen Chandrakasan, Shanmuganathan Prahalad, Sampath Pediatr Rheumatol Online J Short Report BACKGROUND: Subcutaneous anakinra is an interleukin-1 inhibitor used to treat juvenile idiopathic arthritis. Recent reports suggest anakinra can be a valuable addition to the treatment of COVID-19 associated cytokine storm syndrome and the related multisystem inflammatory syndrome (MIS-C) in children. Herein, we describe our experience with intravenously administered anakinra. FINDINGS: 19 Patients (9 male) received intravenous (IV) anakinra for treatment of macrophage activation syndrome (MAS) secondary to systemic lupus erythematosus (SLE), systemic JIA (SJIA) or secondary hemophagocytic lymphohistiocytosis (sHLH). In most cases the general trend of the fibrinogen, ferritin, AST, and platelet count (Ravelli criteria) improved after initiation of IV anakinra. There were no reports of anaphylaxis or reactions associated with administration of IV anakinra. CONCLUSION: Intravenous administration of anakinra is an important therapeutic option for critically ill patients with MAS/HLH. It is also beneficial for those with thrombocytopenia, subcutaneous edema, neurological dysfunction, or very young, hospitalized patients who need multiple painful subcutaneous injections. BioMed Central 2021-06-29 /pmc/articles/PMC8240425/ /pubmed/34187503 http://dx.doi.org/10.1186/s12969-021-00585-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Short Report Phadke, Omkar Rouster-Stevens, Kelly Giannopoulos, Helen Chandrakasan, Shanmuganathan Prahalad, Sampath Intravenous administration of anakinra in children with macrophage activation syndrome |
title | Intravenous administration of anakinra in children with macrophage activation syndrome |
title_full | Intravenous administration of anakinra in children with macrophage activation syndrome |
title_fullStr | Intravenous administration of anakinra in children with macrophage activation syndrome |
title_full_unstemmed | Intravenous administration of anakinra in children with macrophage activation syndrome |
title_short | Intravenous administration of anakinra in children with macrophage activation syndrome |
title_sort | intravenous administration of anakinra in children with macrophage activation syndrome |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8240425/ https://www.ncbi.nlm.nih.gov/pubmed/34187503 http://dx.doi.org/10.1186/s12969-021-00585-3 |
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