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

Kumar Das, Tom Solomon, Marta Garcia-Finana, Enitan Carrol, Nicholas J Beeching, Anne Christine Salter, Antonieta Medina-Lara, Rachel Kneen, Chris Cheyne, Hayley Hardwick, Angela Vincent, Maneesh Bhojak, Michael J Griffiths, Ava Easton, Nicholas W S Davies, Mark Ellul, Benedict D Michael, Kukatharmini Tharmaratnam, Sylviane Defres

Journal: PloS one 2023;18(8):e0282645

PMID: 37611003

Abstract

OBJECTIVES

Encephalitis, 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.

METHODS

We 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.

RESULTS

341 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.

CONCLUSIONS

Initiation 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.

Copyright: © 2023 Defres et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Address: Department of Clinical Infection Microbiology and Immunology, Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, United Kingdom.; Tropical and Infectious Disease Unit, Liverpool University Hospitals NHS Foundation Trust, Liverpool, United Kingdom.; National Institute for Health Research (NIHR) Health Protection Research Unit (HPRU) in Emerging and Zoonotic Infections, Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, United Kingdom.; Department of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.; Department of Biostatistics, Institute of Translational Medicine, University of Liverpool, Liverpool, United Kingdom.; Department of Neurology, The Walton Centre NHS Foundation Trust, Liverpool, United Kingdom.; Department of Neurology, Chelsea and Westminster NHS Trust, London, United Kingdom.; Encephalitis Society, Malton, United Kingdom.; Department of Paediatric Neurology, Alder Hey Hospital Children's NHS Foundation Trust, Liverpool, United Kingdom.; Health Economics Group, University of Exeter Medical School, Exeter, United Kingdom.; Patient Representative, Encephalitis Society, Malton, United Kingdom.; Department of Paediatric Infectious Diseases, Alder Hey Hospital Children's NHS Foundation Trust, Liverpool, United Kingdom.; Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, United Kingdom.
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