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1325. Neurodevelopmental outcomes in preschoolers following viral meningitis is Canterbury, New Zealand

BACKGROUND: Most childhood meningitis nowadays is caused by viruses in countries with widespread use of conjugate vaccines. There is limited knowledge about outcomes following childhood viral meningitis, necessary to inform clinical guidelines. METHODS: Children aged 19-42 months in Canterbury New Z...

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Autores principales: Martin, Natalie G, Williman, Jonathan, Walls, Tony, Sadarangani, Manish, Grant, Cameron
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10676827/
http://dx.doi.org/10.1093/ofid/ofad500.1163
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author Martin, Natalie G
Williman, Jonathan
Walls, Tony
Sadarangani, Manish
Grant, Cameron
author_facet Martin, Natalie G
Williman, Jonathan
Walls, Tony
Sadarangani, Manish
Grant, Cameron
author_sort Martin, Natalie G
collection PubMed
description BACKGROUND: Most childhood meningitis nowadays is caused by viruses in countries with widespread use of conjugate vaccines. There is limited knowledge about outcomes following childhood viral meningitis, necessary to inform clinical guidelines. METHODS: Children aged 19-42 months in Canterbury New Zealand, who had enterovirus (EV) or human parechovirus (HPEV) meningitis as infants were included. Clinical data was collected. Comprehensive neurodevelopmental assessments were completed using the Bayley Scale for Infant Development (BSID) Third Edition. Mean composite and scaled scores, and proportion below cutoff were assessed in each domain. Normative mean composite scores for any domain is 100. Expected scaled score range is 8-12. Mean scores between EV and HPEV meningitis were compared by t-tests, with P< 0.05 considered significant. RESULTS: BSID assessments were completed for 33 children (55% male) of mean age 31 months, from 2019-22, including 23 with EV and 10 with HPEV meningitis. There were 24 children of NZ European, 4 Māori, 4 Asian, and 1 Middle Eastern ethnicity. Mean age at diagnosis was 43 days, and mean length of admission was 2.79 days (CI 1.74-3.15). Of 33 children, 32 (97%) received intravenous or intramuscular antibiotics, 6 (18%) received a fluid bolus on arrival at hospital, and 9 (27%) required high dependency or intensive care. Following viral meningitis, parents reported developmental speech concerns in 6 children, and delayed motor milestones in 1 child. There was no reported sensorineural hearing loss. BSID mean composite scores were in expected range for cognition 102 (CI 98-106), language 96 (93-100) and motor 102 (98-106) domains. Mean scaled scores were in expected range for receptive language 9 (9-10), expressive language 9 (9-10), fine motor 11 (11-12) and gross motor 9 (9-10) domains. Overall, 12/33 (36%) children had below expected scores in one area of development including cognition (2/33; 6%), receptive language (6/33; 18%), expressive language (5/33; 15%), and gross motor (6/33; 18%). There were no significant differences between BSID scores in EV and HPEV meningitis. CONCLUSION: Following viral meningitis, 36% percent of preschool children had findings below expected in at least one developmental domain, suggesting targeted follow-up should be considered. DISCLOSURES: Manish Sadarangani, BM BCh, FRCPC, DPhil, GlaxoSmithKline: Grant/Research Support|Merck: Grant/Research Support|Moderna: Grant/Research Support|Pfizer: Grant/Research Support|Sanofi Pasteur: Grant/Research Support|Seqirus: Grant/Research Support|Symvivo: Grant/Research Support|VBI Vaccines: Grant/Research Support
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spelling pubmed-106768272023-11-27 1325. Neurodevelopmental outcomes in preschoolers following viral meningitis is Canterbury, New Zealand Martin, Natalie G Williman, Jonathan Walls, Tony Sadarangani, Manish Grant, Cameron Open Forum Infect Dis Abstract BACKGROUND: Most childhood meningitis nowadays is caused by viruses in countries with widespread use of conjugate vaccines. There is limited knowledge about outcomes following childhood viral meningitis, necessary to inform clinical guidelines. METHODS: Children aged 19-42 months in Canterbury New Zealand, who had enterovirus (EV) or human parechovirus (HPEV) meningitis as infants were included. Clinical data was collected. Comprehensive neurodevelopmental assessments were completed using the Bayley Scale for Infant Development (BSID) Third Edition. Mean composite and scaled scores, and proportion below cutoff were assessed in each domain. Normative mean composite scores for any domain is 100. Expected scaled score range is 8-12. Mean scores between EV and HPEV meningitis were compared by t-tests, with P< 0.05 considered significant. RESULTS: BSID assessments were completed for 33 children (55% male) of mean age 31 months, from 2019-22, including 23 with EV and 10 with HPEV meningitis. There were 24 children of NZ European, 4 Māori, 4 Asian, and 1 Middle Eastern ethnicity. Mean age at diagnosis was 43 days, and mean length of admission was 2.79 days (CI 1.74-3.15). Of 33 children, 32 (97%) received intravenous or intramuscular antibiotics, 6 (18%) received a fluid bolus on arrival at hospital, and 9 (27%) required high dependency or intensive care. Following viral meningitis, parents reported developmental speech concerns in 6 children, and delayed motor milestones in 1 child. There was no reported sensorineural hearing loss. BSID mean composite scores were in expected range for cognition 102 (CI 98-106), language 96 (93-100) and motor 102 (98-106) domains. Mean scaled scores were in expected range for receptive language 9 (9-10), expressive language 9 (9-10), fine motor 11 (11-12) and gross motor 9 (9-10) domains. Overall, 12/33 (36%) children had below expected scores in one area of development including cognition (2/33; 6%), receptive language (6/33; 18%), expressive language (5/33; 15%), and gross motor (6/33; 18%). There were no significant differences between BSID scores in EV and HPEV meningitis. CONCLUSION: Following viral meningitis, 36% percent of preschool children had findings below expected in at least one developmental domain, suggesting targeted follow-up should be considered. DISCLOSURES: Manish Sadarangani, BM BCh, FRCPC, DPhil, GlaxoSmithKline: Grant/Research Support|Merck: Grant/Research Support|Moderna: Grant/Research Support|Pfizer: Grant/Research Support|Sanofi Pasteur: Grant/Research Support|Seqirus: Grant/Research Support|Symvivo: Grant/Research Support|VBI Vaccines: Grant/Research Support Oxford University Press 2023-11-27 /pmc/articles/PMC10676827/ http://dx.doi.org/10.1093/ofid/ofad500.1163 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Abstract
Martin, Natalie G
Williman, Jonathan
Walls, Tony
Sadarangani, Manish
Grant, Cameron
1325. Neurodevelopmental outcomes in preschoolers following viral meningitis is Canterbury, New Zealand
title 1325. Neurodevelopmental outcomes in preschoolers following viral meningitis is Canterbury, New Zealand
title_full 1325. Neurodevelopmental outcomes in preschoolers following viral meningitis is Canterbury, New Zealand
title_fullStr 1325. Neurodevelopmental outcomes in preschoolers following viral meningitis is Canterbury, New Zealand
title_full_unstemmed 1325. Neurodevelopmental outcomes in preschoolers following viral meningitis is Canterbury, New Zealand
title_short 1325. Neurodevelopmental outcomes in preschoolers following viral meningitis is Canterbury, New Zealand
title_sort 1325. neurodevelopmental outcomes in preschoolers following viral meningitis is canterbury, new zealand
topic Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10676827/
http://dx.doi.org/10.1093/ofid/ofad500.1163
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