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Clinical features and prognostic factors in adults with viral meningitis

Clinical features applicable to the entire spectrum of viral meningitis are limited, and prognostic factors for adverse outcomes are undetermined. This nationwide population-based prospective cohort study included all adults with presumed and microbiologically confirmed viral meningitis in Denmark f...

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Autores principales: Petersen, Pelle Trier, Bodilsen, Jacob, Jepsen, Micha Phill Grønholm, Larsen, Lykke, Storgaard, Merete, Hansen, Birgitte Rønde, Helweg-Larsen, Jannik, Wiese, Lothar, Lüttichau, Hans Rudolf, Andersen, Christian Østergaard, Nielsen, Henrik, Brandt, Christian Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10473559/
https://www.ncbi.nlm.nih.gov/pubmed/36929167
http://dx.doi.org/10.1093/brain/awad089
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author Petersen, Pelle Trier
Bodilsen, Jacob
Jepsen, Micha Phill Grønholm
Larsen, Lykke
Storgaard, Merete
Hansen, Birgitte Rønde
Helweg-Larsen, Jannik
Wiese, Lothar
Lüttichau, Hans Rudolf
Andersen, Christian Østergaard
Nielsen, Henrik
Brandt, Christian Thomas
author_facet Petersen, Pelle Trier
Bodilsen, Jacob
Jepsen, Micha Phill Grønholm
Larsen, Lykke
Storgaard, Merete
Hansen, Birgitte Rønde
Helweg-Larsen, Jannik
Wiese, Lothar
Lüttichau, Hans Rudolf
Andersen, Christian Østergaard
Nielsen, Henrik
Brandt, Christian Thomas
author_sort Petersen, Pelle Trier
collection PubMed
description Clinical features applicable to the entire spectrum of viral meningitis are limited, and prognostic factors for adverse outcomes are undetermined. This nationwide population-based prospective cohort study included all adults with presumed and microbiologically confirmed viral meningitis in Denmark from 2015 until 2020. Prognostic factors for an unfavourable outcome (Glasgow Outcome Scale score of 1–4) 30 days after discharge were examined by modified Poisson regression. In total, 1066 episodes of viral meningitis were included, yielding a mean annual incidence of 4.7 episodes per 100 000 persons. Pathogens were enteroviruses in 419/1066 (39%), herpes simplex virus type 2 in 171/1066 (16%), varicella-zoster virus in 162/1066 (15%), miscellaneous viruses in 31/1066 (3%) and remained unidentified in 283/1066 (27%). The median age was 33 years (IQR 27–44), and 576/1066 (54%) were females. In herpes simplex virus type 2 meningitis, 131/171 (77%) were females. Immunosuppression [32/162 (20%)] and shingles [90/149 (60%)] were frequent in varicella-zoster virus meningitis. The triad of headache, neck stiffness and hyperacusis or photophobia was present in 264/960 (28%). The median time until lumbar puncture was 3.0 h (IQR 1.3–7.1), and the median CSF leucocyte count was 160 cells/µl (IQR 60–358). The outcome was unfavourable in 216/1055 (20%) 30 days after discharge. Using unidentified pathogen as the reference, the adjusted relative risk of an unfavourable outcome was 1.34 (95% CI 0.95–1.88) for enteroviruses, 1.55 (95% CI 1.00–2.41) for herpes simplex virus type 2, 1.51 (95% CI 0.98–2.33) for varicella-zoster virus and 1.37 (95% CI 0.61–3.05) for miscellaneous viruses. The adjusted relative risk of an unfavourable outcome was 1.34 (95% CI 1.03–1.75) for females. Timing of acyclovir or valacyclovir was not associated with the outcome in meningitis caused by herpes simplex virus type 2 or varicella-zoster virus. In summary, the outcome of viral meningitis was similar among patients with different aetiologies, including those with presumed viral meningitis but without an identified pathogen. Females had an increased risk of an unfavourable outcome. Early antiviral treatment was not associated with an improved outcome in meningitis caused by herpes simplex virus type 2 or varicella-zoster virus.
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spelling pubmed-104735592023-09-02 Clinical features and prognostic factors in adults with viral meningitis Petersen, Pelle Trier Bodilsen, Jacob Jepsen, Micha Phill Grønholm Larsen, Lykke Storgaard, Merete Hansen, Birgitte Rønde Helweg-Larsen, Jannik Wiese, Lothar Lüttichau, Hans Rudolf Andersen, Christian Østergaard Nielsen, Henrik Brandt, Christian Thomas Brain Original Article Clinical features applicable to the entire spectrum of viral meningitis are limited, and prognostic factors for adverse outcomes are undetermined. This nationwide population-based prospective cohort study included all adults with presumed and microbiologically confirmed viral meningitis in Denmark from 2015 until 2020. Prognostic factors for an unfavourable outcome (Glasgow Outcome Scale score of 1–4) 30 days after discharge were examined by modified Poisson regression. In total, 1066 episodes of viral meningitis were included, yielding a mean annual incidence of 4.7 episodes per 100 000 persons. Pathogens were enteroviruses in 419/1066 (39%), herpes simplex virus type 2 in 171/1066 (16%), varicella-zoster virus in 162/1066 (15%), miscellaneous viruses in 31/1066 (3%) and remained unidentified in 283/1066 (27%). The median age was 33 years (IQR 27–44), and 576/1066 (54%) were females. In herpes simplex virus type 2 meningitis, 131/171 (77%) were females. Immunosuppression [32/162 (20%)] and shingles [90/149 (60%)] were frequent in varicella-zoster virus meningitis. The triad of headache, neck stiffness and hyperacusis or photophobia was present in 264/960 (28%). The median time until lumbar puncture was 3.0 h (IQR 1.3–7.1), and the median CSF leucocyte count was 160 cells/µl (IQR 60–358). The outcome was unfavourable in 216/1055 (20%) 30 days after discharge. Using unidentified pathogen as the reference, the adjusted relative risk of an unfavourable outcome was 1.34 (95% CI 0.95–1.88) for enteroviruses, 1.55 (95% CI 1.00–2.41) for herpes simplex virus type 2, 1.51 (95% CI 0.98–2.33) for varicella-zoster virus and 1.37 (95% CI 0.61–3.05) for miscellaneous viruses. The adjusted relative risk of an unfavourable outcome was 1.34 (95% CI 1.03–1.75) for females. Timing of acyclovir or valacyclovir was not associated with the outcome in meningitis caused by herpes simplex virus type 2 or varicella-zoster virus. In summary, the outcome of viral meningitis was similar among patients with different aetiologies, including those with presumed viral meningitis but without an identified pathogen. Females had an increased risk of an unfavourable outcome. Early antiviral treatment was not associated with an improved outcome in meningitis caused by herpes simplex virus type 2 or varicella-zoster virus. Oxford University Press 2023-03-16 /pmc/articles/PMC10473559/ /pubmed/36929167 http://dx.doi.org/10.1093/brain/awad089 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the Guarantors of Brain. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Article
Petersen, Pelle Trier
Bodilsen, Jacob
Jepsen, Micha Phill Grønholm
Larsen, Lykke
Storgaard, Merete
Hansen, Birgitte Rønde
Helweg-Larsen, Jannik
Wiese, Lothar
Lüttichau, Hans Rudolf
Andersen, Christian Østergaard
Nielsen, Henrik
Brandt, Christian Thomas
Clinical features and prognostic factors in adults with viral meningitis
title Clinical features and prognostic factors in adults with viral meningitis
title_full Clinical features and prognostic factors in adults with viral meningitis
title_fullStr Clinical features and prognostic factors in adults with viral meningitis
title_full_unstemmed Clinical features and prognostic factors in adults with viral meningitis
title_short Clinical features and prognostic factors in adults with viral meningitis
title_sort clinical features and prognostic factors in adults with viral meningitis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10473559/
https://www.ncbi.nlm.nih.gov/pubmed/36929167
http://dx.doi.org/10.1093/brain/awad089
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