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dc.contributor.authorSorrell, Lexy
dc.contributor.authorLeta, V
dc.contributor.authorBarnett, Anton
dc.contributor.authorStevens, K
dc.contributor.authorKing, A
dc.contributor.authorInches, J
dc.contributor.authorKobylecki, C
dc.contributor.authorWalker, R
dc.contributor.authorChaudhuri, KR
dc.contributor.authorMartin, H
dc.contributor.authorRideout, J
dc.contributor.authorSneyd, John
dc.contributor.authorCampbell, S
dc.contributor.authorCarroll, Camille
dc.date.accessioned2023-08-04T10:22:02Z
dc.date.available2023-08-04T10:22:02Z
dc.date.issued2023-07-31
dc.identifier.issn1932-6203
dc.identifier.issn1932-6203
dc.identifier.othere0285349
dc.identifier.urihttps://pearl.plymouth.ac.uk/handle/10026.1/21157
dc.description.abstract

Background Parkinson’s disease has been identified as a risk factor for severe Coronavirus disease 2019 (COVID-19) outcomes. However, whether the significant high risk of death from COVID-19 in people with Parkinson’s disease is specific to the disease itself or driven by other concomitant and known risk factors such as comorbidities, age, and frailty remains unclear. Objective To investigate clinical profiles and outcomes of people with Parkinson’s disease and atypical parkinsonian syndromes who tested positive for COVID-19 in the hospital setting in a multicentre UK-based study. Methods A retrospective cohort study of Parkinson’s disease patients with a positive SARS-CoV-2 test admitted to hospital between February 2020 and July 2021. An online survey was used to collect data from clinical care records, recording patient, Parkinson’s disease and COVID-19 characteristics. Associations with time-to-mortality and severe outcomes were analysed using either the Cox proportional hazards model or logistic regression models, as appropriate. Results Data from 552 admissions were collected: 365 (66%) male; median (inter-quartile range) age 80 (74–85) years. The 34-day all-cause mortality rate was 38.4%; male sex, increased age and frailty, Parkinson’s dementia syndrome, requirement for respiratory support and no vaccination were associated with increased mortality risk. Community-acquired COVID-19 and co-morbid chronic neurological disorder were associated with increased odds of requiring respiratory support. Hospital-acquired COVID-19 and delirium were associated with requiring an increase in care level post-discharge. Conclusions This first, multicentre, UK-based study on people with Parkinson’s disease or atypical parkinsonian syndromes, hospitalised with COVID-19, adds and expands previous findings on clinical profiles and outcomes in this population.

dc.format.extente0285349-e0285349
dc.format.mediumElectronic-eCollection
dc.languageen
dc.publisherPublic Library of Science (PLoS)
dc.subjectHumans
dc.subjectMale
dc.subjectAged, 80 and over
dc.subjectFemale
dc.subjectCOVID-19
dc.subjectSARS-CoV-2
dc.subjectParkinson Disease
dc.subjectRetrospective Studies
dc.subjectFrailty
dc.subjectAftercare
dc.subjectPatient Discharge
dc.subjectParkinsonian Disorders
dc.subjectUnited Kingdom
dc.titleClinical features and outcomes of hospitalised patients with COVID-19 and Parkinsonian disorders: A multicentre UK-based study
dc.typejournal-article
dc.typeMulticenter Study
dc.typeJournal Article
dc.typeResearch Support, Non-U.S. Gov't
plymouth.author-urlhttps://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:001041473900021&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=11bb513d99f797142bcfeffcc58ea008
plymouth.issue7
plymouth.volume18
plymouth.publication-statusPublished online
plymouth.journalPLOS ONE
dc.identifier.doi10.1371/journal.pone.0285349
plymouth.organisational-group|Plymouth
plymouth.organisational-group|Plymouth|Faculty of Health
plymouth.organisational-group|Plymouth|Users by role
plymouth.organisational-group|Plymouth|Users by role|Academics
plymouth.organisational-group|Plymouth|Faculty of Health|Peninsula Medical School
dc.publisher.placeUnited States
dcterms.dateAccepted2023-07-18
dc.date.updated2023-08-04T10:21:50Z
dc.rights.embargodate2023-8-5
dc.identifier.eissn1932-6203
dc.rights.embargoperiodforever
rioxxterms.versionofrecord10.1371/journal.pone.0285349


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