Clinical features and prognostic factors in adults with viral meningitis

Author:

Petersen Pelle Trier12ORCID,Bodilsen Jacob34ORCID,Jepsen Micha Phill Grønholm1,Larsen Lykke5,Storgaard Merete6,Hansen Birgitte Rønde7,Helweg-Larsen Jannik8,Wiese Lothar9ORCID,Lüttichau Hans Rudolf10,Andersen Christian Østergaard11,Nielsen Henrik34ORCID,Brandt Christian Thomas9,

Affiliation:

1. Department of Pulmonary and Infectious Diseases, Nordsjællands Hospital , 3400 Hillerød , Denmark

2. Faculty of Health and Medical Sciences, University of Copenhagen , 2200 Copenhagen , Denmark

3. Department of Infectious Diseases, Aalborg University Hospital , 9000 Aalborg , Denmark

4. Department of Clinical Medicine, Aalborg University , 9000 Aalborg , Denmark

5. Department of Infectious Diseases, Odense University Hospital , 5000 Odense , Denmark

6. Department of Infectious Diseases, Aarhus University Hospital , 8200 Aarhus , Denmark

7. Department of Infectious Diseases, Hvidovre Hospital , 2650 Hvidovre , Denmark

8. Department of Infectious Diseases, Rigshospitalet , 2100 Copenhagen , Denmark

9. Department of Medicine, Sjællands University Hospital , 4000 Roskilde , Denmark

10. Department of Infectious Diseases, Herlev Hospital , 2730 Herlev , Denmark

11. Department of Clinical Microbiology, Hvidovre Hospital , 2650 Hvidovre , Denmark

Abstract

Abstract 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.

Funder

Helsefonden

Helen Rudes Fond

A & J C Tvergaards Fond

Minister Erna Hamiltons Legat for Videnskab og Kunst

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

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