Evidence map›Paper›PMID 37611003›Full record

Observational studyPloS one2023

Clinical predictors of encephalitis in UK adults-A multi-centre prospective observational cohort study.

Sylviane Defres, Kukatharmini Tharmaratnam, Benedict D Michael, Mark Ellul, Nicholas W S Davies, Ava Easton, Michael J Griffiths, Maneesh Bhojak, Kumar Das, Hayley Hardwick and 10 more

Open access · goldAbstract readObservational StudyMulticenter Study
In one paragraph

Observational study in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.7field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Herpes Simplex Virus Type 1 Encephalitis: A Prospective Population-Based Cohort Study.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors at 5 institutions in 1 country.

Sylviane DefresDepartment of Clinical Infection Microbiology and Immunology, Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, United Kingdom.ORCID 0000-0002-4729-7505
Kukatharmini TharmaratnamDepartment of Biostatistics, Institute of Translational Medicine, University of Liverpool, Liverpool, United Kingdom.
Benedict D MichaelDepartment of Clinical Infection Microbiology and Immunology, Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, United Kingdom.ORCID 0000-0002-8693-8926
Mark EllulDepartment of Clinical Infection Microbiology and Immunology, Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, United Kingdom.
Nicholas W S DaviesDepartment of Neurology, Chelsea and Westminster NHS Trust, London, United Kingdom.
Ava EastonDepartment of Clinical Infection Microbiology and Immunology, Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, United Kingdom.
Michael J GriffithsDepartment of Clinical Infection Microbiology and Immunology, Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, United Kingdom.
Maneesh BhojakDepartment of Neurology, The Walton Centre NHS Foundation Trust, Liverpool, United Kingdom.
Kumar DasDepartment of Neurology, The Walton Centre NHS Foundation Trust, Liverpool, United Kingdom.
Hayley HardwickDepartment of Clinical Infection Microbiology and Immunology, Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, United Kingdom.
Chris CheyneDepartment of Biostatistics, Institute of Translational Medicine, University of Liverpool, Liverpool, United Kingdom.
Rachel KneenDepartment of Clinical Infection Microbiology and Immunology, Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, United Kingdom.
Antonieta Medina-LaraHealth Economics Group, University of Exeter Medical School, Exeter, United Kingdom.
Anne Christine SalterPatient Representative, Encephalitis Society, Malton, United Kingdom.
Nicholas J BeechingTropical and Infectious Disease Unit, Liverpool University Hospitals NHS Foundation Trust, Liverpool, United Kingdom.
Enitan CarrolDepartment of Clinical Infection Microbiology and Immunology, Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, United Kingdom.
Angela VincentNuffield Department of Clinical Neurosciences, University of Oxford, Oxford, United Kingdom.
ENCEPH UK study group
Marta Garcia-FinanaDepartment of Biostatistics, Institute of Translational Medicine, University of Liverpool, Liverpool, United Kingdom.
Tom SolomonDepartment of Clinical Infection Microbiology and Immunology, Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, United Kingdom.
University of Liverpool · GBChelsea and Westminster Hospital NHS Foundation Trust · GBEncephalitis Society · GBUniversity of Exeter · GBUniversity of Oxford · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesEncephalitis, brain inflammation and swelling, most often caused by an infection or the body's immune defences, can have devastating consequences, especially if diagnosed late. We looked for clinical predictors of different types of encephalitis to help clinicians consider earlier treatment.

methodsWe conducted a multicentre prospective observational cohort study (ENCEPH-UK) of adults (> 16 years) with suspected encephalitis at 31 UK hospitals. We evaluated clinical features and investigated for infectious and autoimmune causes.

results341 patients were enrolled between December 2012 and December 2015 and followed up for 12 months. 233 had encephalitis, of whom 65 (28%) had HSV, 38 (16%) had confirmed or probable autoimmune encephalitis, and 87 (37%) had no cause found. The median time from admission to 1st dose of aciclovir for those with HSV was 14 hours (IQR 5-50); time to 1st dose of immunosuppressant for the autoimmune group was 125 hours (IQR 45-250). Compared to non-HSV encephalitis, patients with HSV more often had fever, lower serum sodium and lacked a rash. Those with probable or confirmed autoimmune encephalitis were more likely to be female, have abnormal movements, normal serum sodium levels and a cerebrospinal fluid white cell count < 20 cells x106/L, but they were less likely to have a febrile illness.

conclusionsInitiation of treatment for autoimmune encephalitis is delayed considerably compared with HSV encephalitis. Clinical features can help identify patients with autoimmune disease and could be used to initiate earlier presumptive therapy.

Indexed as

Autoimmune Diseases of the Nervous SystemEncephalitisAdultFemaleHashimoto DiseaseHumansMaleProspective StudiesSodiumUnited KingdomSodium

Identifiers

PMID37611003
PMCPMC10446234
OpenAlexW4386086160

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.