Evidence map›Paper›PMID 39870668›Full record

ArticleScientific reports2025

Patients with neurological or psychiatric complications of COVID-19 have worse long-term functional outcomes: COVID-CNS-A multicentre case-control study.

Rajish S K Shil, Adam Seed, Nkongho Egbe Franklyn, Brendan F Sargent, Greta K Wood, Yun Huang, Katherine C Dodd, James B Lilleker, Thomas A Pollak, Sylviane Defres and 19 more

Abstract readMulticenter Study
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
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

29 authors.

Rajish S K ShilClinical Infection, Microbiology & Immunology, Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, UK. rajishsk@liverpool.ac.uk.ORCID http://orcid.org/0000-0001-9100-6114
Adam SeedLiverpool University Hospitals NHS Foundation Trust, Liverpool, UK.ORCID http://orcid.org/0009-0008-3314-471X
Nkongho Egbe FranklynClinical Infection, Microbiology & Immunology, Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, UK.ORCID http://orcid.org/0000-0002-9547-4609
Brendan F SargentClinical Infection, Microbiology & Immunology, Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, UK.ORCID http://orcid.org/0000-0003-2262-7755
Greta K WoodClinical Infection, Microbiology & Immunology, Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, UK.ORCID http://orcid.org/0000-0001-6098-2331
Yun HuangClinical Infection, Microbiology & Immunology, Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, UK.ORCID http://orcid.org/0000-0001-7843-9126
Katherine C DoddManchester Centre for Clinical Neurosciences, Northern Care Alliance NHS Foundation Trust, Manchester Academic Health Science Centre, Salford, M6 8HD, UK.ORCID http://orcid.org/0000-0002-0491-7030
James B LillekerManchester Centre for Clinical Neurosciences, Northern Care Alliance NHS Foundation Trust, Manchester Academic Health Science Centre, Salford, M6 8HD, UK.ORCID http://orcid.org/0000-0002-9230-4137
Thomas A PollakDepartment of Psychosis Studies, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, SE5 4AF, UK.ORCID http://orcid.org/0000-0002-6171-0810
Sylviane DefresClinical Infection, Microbiology & Immunology, Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, UK.ORCID http://orcid.org/0000-0002-4729-7505
Thomas M JenkinsCurtin University, Kent Street, Bentley, Perth, WA, 6102, Australia.ORCID http://orcid.org/0000-0003-0342-7184
Nicholas W S DaviesDepartment of Neurology, Charing Cross Hospital, London, UK.ORCID http://orcid.org/0000-0003-4095-4549
David A CousinsTranslational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Campus for Ageing and Vitality, Newcastle Upon Tyne, NE4 5PL, UK.ORCID http://orcid.org/0000-0001-5682-7507
Michael S ZandiUCL Queen Square Institute of Neurology, University College London, London, WC1N 3BG, UK.ORCID http://orcid.org/0000-0002-9612-9401
Thomas A JacksonMRC-Versus Arthritis Centre for Musculoskeletal Ageing Research, Institute of Inflammation and Ageing, University of Birmingham, Birmingham, UK.ORCID http://orcid.org/0000-0001-6320-9600
Laura A BenjaminInstitute of Infection, Veterinary and Ecological Sciences, National Institute for Health and Care Research Health Protection Research Unit in Emerging and Zoonotic Infections, University of Liverpool, Liverpool, UK.ORCID http://orcid.org/0000-0002-9685-1664
Ava EastonClinical Infection, Microbiology & Immunology, Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, UK.ORCID http://orcid.org/0000-0002-1739-2915
Tom SolomonClinical Infection, Microbiology & Immunology, Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, UK.ORCID http://orcid.org/0000-0001-7266-6547
John R BradleyNIHR BioResource, Cambridge University Hospitals NHS Foundation, Cambridge Biomedical Campus, Cambridge, UK.ORCID http://orcid.org/0000-0002-7774-8805
Patrick F ChinneryDepartment of Clinical Neurosciences, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0002-7065-6617
Craig J SmithManchester Centre for Clinical Neurosciences, Northern Care Alliance NHS Foundation Trust, Manchester Academic Health Science Centre, Salford, M6 8HD, UK.ORCID http://orcid.org/0000-0002-4828-2700
Timothy R NicholsonDepartment of Psychosis Studies, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, SE5 4AF, UK.ORCID http://orcid.org/0000-0002-4367-3956
Alan CarsonCentre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, EH16 4SB, UK.ORCID http://orcid.org/0000-0002-7425-0964
Rhys H ThomasTranslational and Clinical Research, Newcastle University, Newcastle, NE1 7RU, UK.ORCID http://orcid.org/0000-0003-2062-8623
Mark Alexander EllulClinical Infection, Microbiology & Immunology, Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, UK.ORCID http://orcid.org/0000-0002-6115-8245
Nicholas W WoodDepartment of Molecular Neuroscience, UCL Institute of Neurology, London, UK.ORCID http://orcid.org/0000-0002-9500-3348
Gerome BreenClinical Infection, Microbiology & Immunology, Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, UK.ORCID http://orcid.org/0000-0003-2053-1792
Benedict Daniel MichaelClinical Infection, Microbiology & Immunology, Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, UK. benmic@liverpool.ac.uk.ORCID http://orcid.org/0000-0002-8693-8926
COVID-CNS Study Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is established that patients hospitalised with COVID-19 often have ongoing morbidity affecting activity of daily living (ADL), employment, and mental health. However, little is known about the relative outcomes in patients with COVID-19 neurological or psychiatric complications. We conducted a UK multicentre case-control study of patients hospitalised with COVID-19 (controls) and those who developed COVID-19 associated acute neurological or psychiatric complications (cases). Among the 651 patients, [362 (55%) cases and 289 (45%) controls], a higher proportion of cases had impairment in ADLs (199 [68.9%] vs 101 [51.8%], OR 2.06, p < 0.0002) and reported symptoms impacting employment (159 [58.2%] vs 69 [35.6%] OR 2.53, p < 0.0001). There was no significant difference in the proportion with depression or anxiety between case and control groups overall. For cases, impairment of ADLs was associated with increased risk in female sex, age > 50 years and hypertension (OR 5.43, p < 0.003, 3.11, p = 0.02, 3.66, p = 0.04). Those receiving either statins or angiotensin converting enzyme (ACE) inhibitors had a lower risk of impairment in ADLs (OR 0.09, p = 0.0006, 0.17, p = 0.03). Patients with neurological or psychiatric complications of COVID-19 had worse functional outcomes than those with respiratory COVID-19 alone in terms of ADLs and employment. Female sex, age > 50 years, and hypertension were associated with worse outcomes, and statins or ACE inhibitors with better outcomes.

Indexed as

COVID-19Mental DisordersNervous System DiseasesActivities of Daily LivingAdultAgedCase-Control StudiesEmploymentFemaleHospitalizationHumansMaleMiddle AgedSARS-CoV-2United Kingdom

Identifiers

PMID39870668
PMCPMC11772688

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