Herpes Simplex Virus 2 Meningitis in Adults: A Prospective, Nationwide, Population-Based Cohort Study.

HSV-2 Herpes simplex virus 2 acyclovir adults cohort incidence meningitis nationwide population-based prognosis prognostic factors risk factors virus

Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
14 09 2022
Historique:
received: 28 10 2021
pubmed: 4 1 2022
medline: 20 9 2022
entrez: 3 1 2022
Statut: ppublish

Résumé

Data on the clinical presentation are scarce and prognostic factors of herpes simplex virus type 2 (HSV-2) meningitis remain unknown. Prospective, nationwide, population-based database identifying all adults treated for HSV-2 meningitis at departments of infectious diseases in Denmark from 2015 to 2020. Unfavorable outcome was defined as Glasgow Outcome Scale (GOS) scores of 1-4 and Extended GOS scores of 1-6. Modified Poisson regression was used to compute relative risks with 95% confidence intervals for unfavorable outcome. HSV-2 meningitis was diagnosed in 205 patients (76% female; median age [interquartile range (IQR)], 35 [27-49] years) yielding an incidence of 0.7/100 000 population/y. Common symptoms were headache (195 of 204 patients [95%]), photophobia or phonophobia (143 of 188 [76%]), and neck stiffness (106 of 196 [54%]). The median (IQR) time to lumbar puncture was 2.0 (1-4.8) hours, and the median cerebrospinal fluid (CSF) leukocyte count was 360 (166-670) × 10 × 6/L, with a mononuclear predominance of 97% (91%-99%). Lumbar puncture was preceded by brain imaging in 61 of 205 patients (30%). Acyclovir or valacyclovir was administered in 197 of 205 patients (96%) for a median (IQR) of 10 (7-14) days. Unfavorable outcome was observed in 64 of 205 patients (31%) at discharge and 19 of 181 (11%) after 6 months and was not associated with female sex (relative risk [95% confidence interval], 1.08 [.65-1.79]), age ≥35 years (1.28 [.83-1.97]), immunocompromise (1.07 [.57-2.03]), or CSF leukocyte count >1000 × 10 × 6/L (0.78 [.33-1.84]). HSV-2 meningitis often presented as meningeal symptoms in younger women. Unfavorable outcome at discharge was common and was not associated with sex, age, immunocompromise, or CSF leukocyte count. Sequelae persisted beyond 6 months in one-tenth of patients.

Sections du résumé

BACKGROUND
Data on the clinical presentation are scarce and prognostic factors of herpes simplex virus type 2 (HSV-2) meningitis remain unknown.
METHODS
Prospective, nationwide, population-based database identifying all adults treated for HSV-2 meningitis at departments of infectious diseases in Denmark from 2015 to 2020. Unfavorable outcome was defined as Glasgow Outcome Scale (GOS) scores of 1-4 and Extended GOS scores of 1-6. Modified Poisson regression was used to compute relative risks with 95% confidence intervals for unfavorable outcome.
RESULTS
HSV-2 meningitis was diagnosed in 205 patients (76% female; median age [interquartile range (IQR)], 35 [27-49] years) yielding an incidence of 0.7/100 000 population/y. Common symptoms were headache (195 of 204 patients [95%]), photophobia or phonophobia (143 of 188 [76%]), and neck stiffness (106 of 196 [54%]). The median (IQR) time to lumbar puncture was 2.0 (1-4.8) hours, and the median cerebrospinal fluid (CSF) leukocyte count was 360 (166-670) × 10 × 6/L, with a mononuclear predominance of 97% (91%-99%). Lumbar puncture was preceded by brain imaging in 61 of 205 patients (30%). Acyclovir or valacyclovir was administered in 197 of 205 patients (96%) for a median (IQR) of 10 (7-14) days. Unfavorable outcome was observed in 64 of 205 patients (31%) at discharge and 19 of 181 (11%) after 6 months and was not associated with female sex (relative risk [95% confidence interval], 1.08 [.65-1.79]), age ≥35 years (1.28 [.83-1.97]), immunocompromise (1.07 [.57-2.03]), or CSF leukocyte count >1000 × 10 × 6/L (0.78 [.33-1.84]).
CONCLUSIONS
HSV-2 meningitis often presented as meningeal symptoms in younger women. Unfavorable outcome at discharge was common and was not associated with sex, age, immunocompromise, or CSF leukocyte count. Sequelae persisted beyond 6 months in one-tenth of patients.

Identifiants

pubmed: 34979025
pii: 6494530
doi: 10.1093/cid/ciab1071
doi:

Substances chimiques

Valacyclovir MZ1IW7Q79D
Acyclovir X4HES1O11F

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

753-760

Commentaires et corrections

Type : ErratumIn

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.

Déclaration de conflit d'intérêts

Potential conflicts of interests. M. M. T. reports grants or contracts from Independent Research Fund Denmark for a PhD scholarship (12 months) and was an invited speaker for Nordic Society of Clinical Microbiology and Infectious Diseases 2021 (paid flight and hotel). H. N. reports receiving grants or contracts from NovoNordiskFoundation for a randomized controlled trial for brain abscess in adults and receiving personal fees for serving on Advisory Board Denmark for MSD and GlaxoSmithKline, on the subject of coronavirus 2019 therapeutics. All other authors report no potential conflicts. All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Conflicts that the editors consider relevant to the content of the manuscript have been disclosed.

Auteurs

Anna Jakobsen (A)

Department of Infectious Diseases, Aalborg University Hospital, Aalborg, Denmark.

Marie Thaarup Skov (MT)

Department of Infectious Diseases, Aalborg University Hospital, Aalborg, Denmark.

Lykke Larsen (L)

Research Unit for Infectious Diseases, Odense University Hospital, Odense, Denmark.
University of Southern Denmark, Odense, Denmark.

Pelle Trier Petersen (P)

Department of Pulmonary and Infectious Diseases, Nordsjællands Hospital, Hillerød, Denmark.

Christian Brandt (C)

Department of Pulmonary and Infectious Diseases, Nordsjællands Hospital, Hillerød, Denmark.
Department of Infectious Diseases, Sjælland University Hospital, Roskilde, Denmark.

Lothar Wiese (L)

Department of Infectious Diseases, Sjælland University Hospital, Roskilde, Denmark.

Birgitte Rønde Hansen (BR)

Department of Infectious Diseases, Hvidovre University Hospital, Hvidovre, Denmark.

Hans Rudolf Lüttichau (HR)

Department of Medicine and Infectious Diseases, Herlev Gentofte Hospital, Copenhagen, Denmark.

Malte Mose Tetens (MM)

Department of Infectious Diseases, Rigshospitalet, Copenhagen, Denmark.

Jannik Helweg-Larsen (J)

Department of Infectious Diseases, Rigshospitalet, Copenhagen, Denmark.

Merete Storgaard (M)

Department of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmarkand.

Henrik Nielsen (H)

Department of Infectious Diseases, Aalborg University Hospital, Aalborg, Denmark.
Department of Clinical Medicine, Aalborg University, Aalborg, Denmark.

Jacob Bodilsen (J)

Department of Infectious Diseases, Aalborg University Hospital, Aalborg, Denmark.

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