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Systemic Inflammation Is Associated With Neurologic Involvement in Pediatric Inflammatory Multisystem Syndrome Associated With SARS-CoV-2
OBJECTIVE: Pediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2 (PIMS-TS) is a severe immune-mediated disorder. We aim to report the neurologic features of children with PIMS-TS. METHODS: We identified children presenting to a large children's hospital with PIMS-TS...
Autores principales: | , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8054962/ https://www.ncbi.nlm.nih.gov/pubmed/33850037 http://dx.doi.org/10.1212/NXI.0000000000000999 |
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author | Sa, Mario Mirza, Luwaiza Carter, Michael Carlton Jones, Lalani Gowda, Vasantha Handforth, Jennifer Hedderly, Tammy Kenny, Julia Lascelles, Karine Lin, Jean-Pierre Lumsden, Daniel McDougall, Marilyn Miller, Owen Rossor, Thomas Shivamurthy, Vinay Siddiqui, Ata Singh, Rahul Tang, Shan White, Marie Byrne, Susan Lim, Ming |
author_facet | Sa, Mario Mirza, Luwaiza Carter, Michael Carlton Jones, Lalani Gowda, Vasantha Handforth, Jennifer Hedderly, Tammy Kenny, Julia Lascelles, Karine Lin, Jean-Pierre Lumsden, Daniel McDougall, Marilyn Miller, Owen Rossor, Thomas Shivamurthy, Vinay Siddiqui, Ata Singh, Rahul Tang, Shan White, Marie Byrne, Susan Lim, Ming |
author_sort | Sa, Mario |
collection | PubMed |
description | OBJECTIVE: Pediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2 (PIMS-TS) is a severe immune-mediated disorder. We aim to report the neurologic features of children with PIMS-TS. METHODS: We identified children presenting to a large children's hospital with PIMS-TS from March to June 2020 and performed a retrospective medical note review, identifying clinical and investigative features alongside short-term outcome of children presenting with neurologic symptoms. RESULTS: Seventy-five patients with PIMS-TS were identified, 9 (12%) had neurologic involvement: altered conciseness (3), behavioral changes (3), focal neurology deficits (2), persistent headaches (2), hallucinations (2), excessive sleepiness (1), and new-onset focal seizures (1). Four patients had cranial images abnormalities. At 3-month follow-up, 1 child had died, 1 had hemiparesis, 3 had behavioral changes, and 4 completely recovered. Systemic inflammatory and prothrombotic markers were higher in patients with neurologic involvement (mean highest CRP 267 vs 202 mg/L, p = 0.05; procalcitonin 30.65 vs 13.11 μg/L, p = 0.04; fibrinogen 7.04 vs 6.17 g/L, p = 0.07; d-dimers 19.68 vs 7.35 mg/L, p = 0.005). Among patients with neurologic involvement, these markers were higher in those without full recovery at 3 months (ferritin 2284 vs 283 μg/L, p = 0.05; d-dimers 30.34 vs 6.37 mg/L, p = 0.04). Patients with and without neurologic involvement shared similar risk factors for PIMS-TS (Black, Asian and Minority Ethnic ethnicity 78% vs 70%, obese/overweight 56% vs 42%). CONCLUSIONS: Broad neurologic features were found in 12% patients with PIMS-TS. By 3-month follow-up, half of these surviving children had recovered fully without neurologic impairment. Significantly higher systemic inflammatory markers were identified in children with neurologic involvement and in those who had not recovered fully. |
format | Online Article Text |
id | pubmed-8054962 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-80549622021-04-20 Systemic Inflammation Is Associated With Neurologic Involvement in Pediatric Inflammatory Multisystem Syndrome Associated With SARS-CoV-2 Sa, Mario Mirza, Luwaiza Carter, Michael Carlton Jones, Lalani Gowda, Vasantha Handforth, Jennifer Hedderly, Tammy Kenny, Julia Lascelles, Karine Lin, Jean-Pierre Lumsden, Daniel McDougall, Marilyn Miller, Owen Rossor, Thomas Shivamurthy, Vinay Siddiqui, Ata Singh, Rahul Tang, Shan White, Marie Byrne, Susan Lim, Ming Neurol Neuroimmunol Neuroinflamm Article OBJECTIVE: Pediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2 (PIMS-TS) is a severe immune-mediated disorder. We aim to report the neurologic features of children with PIMS-TS. METHODS: We identified children presenting to a large children's hospital with PIMS-TS from March to June 2020 and performed a retrospective medical note review, identifying clinical and investigative features alongside short-term outcome of children presenting with neurologic symptoms. RESULTS: Seventy-five patients with PIMS-TS were identified, 9 (12%) had neurologic involvement: altered conciseness (3), behavioral changes (3), focal neurology deficits (2), persistent headaches (2), hallucinations (2), excessive sleepiness (1), and new-onset focal seizures (1). Four patients had cranial images abnormalities. At 3-month follow-up, 1 child had died, 1 had hemiparesis, 3 had behavioral changes, and 4 completely recovered. Systemic inflammatory and prothrombotic markers were higher in patients with neurologic involvement (mean highest CRP 267 vs 202 mg/L, p = 0.05; procalcitonin 30.65 vs 13.11 μg/L, p = 0.04; fibrinogen 7.04 vs 6.17 g/L, p = 0.07; d-dimers 19.68 vs 7.35 mg/L, p = 0.005). Among patients with neurologic involvement, these markers were higher in those without full recovery at 3 months (ferritin 2284 vs 283 μg/L, p = 0.05; d-dimers 30.34 vs 6.37 mg/L, p = 0.04). Patients with and without neurologic involvement shared similar risk factors for PIMS-TS (Black, Asian and Minority Ethnic ethnicity 78% vs 70%, obese/overweight 56% vs 42%). CONCLUSIONS: Broad neurologic features were found in 12% patients with PIMS-TS. By 3-month follow-up, half of these surviving children had recovered fully without neurologic impairment. Significantly higher systemic inflammatory markers were identified in children with neurologic involvement and in those who had not recovered fully. Lippincott Williams & Wilkins 2021-04-12 /pmc/articles/PMC8054962/ /pubmed/33850037 http://dx.doi.org/10.1212/NXI.0000000000000999 Text en Copyright © 2021 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Article Sa, Mario Mirza, Luwaiza Carter, Michael Carlton Jones, Lalani Gowda, Vasantha Handforth, Jennifer Hedderly, Tammy Kenny, Julia Lascelles, Karine Lin, Jean-Pierre Lumsden, Daniel McDougall, Marilyn Miller, Owen Rossor, Thomas Shivamurthy, Vinay Siddiqui, Ata Singh, Rahul Tang, Shan White, Marie Byrne, Susan Lim, Ming Systemic Inflammation Is Associated With Neurologic Involvement in Pediatric Inflammatory Multisystem Syndrome Associated With SARS-CoV-2 |
title | Systemic Inflammation Is Associated With Neurologic Involvement in Pediatric Inflammatory Multisystem Syndrome Associated With SARS-CoV-2 |
title_full | Systemic Inflammation Is Associated With Neurologic Involvement in Pediatric Inflammatory Multisystem Syndrome Associated With SARS-CoV-2 |
title_fullStr | Systemic Inflammation Is Associated With Neurologic Involvement in Pediatric Inflammatory Multisystem Syndrome Associated With SARS-CoV-2 |
title_full_unstemmed | Systemic Inflammation Is Associated With Neurologic Involvement in Pediatric Inflammatory Multisystem Syndrome Associated With SARS-CoV-2 |
title_short | Systemic Inflammation Is Associated With Neurologic Involvement in Pediatric Inflammatory Multisystem Syndrome Associated With SARS-CoV-2 |
title_sort | systemic inflammation is associated with neurologic involvement in pediatric inflammatory multisystem syndrome associated with sars-cov-2 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8054962/ https://www.ncbi.nlm.nih.gov/pubmed/33850037 http://dx.doi.org/10.1212/NXI.0000000000000999 |
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