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Clinical features and outcomes of hospitalised patients with COVID-19 and Parkinsonian disorders: A multicentre UK-based study
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...
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Published in: | PloS one 2023-07, Vol.18 (7), p.e0285349-e0285349 |
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creator | Sorrell, Lexy Leta, Valentina Barnett, Anton Stevens, Kara King, Angela Inches, Jemma Kobylecki, Christopher Walker, Richard Chaudhuri, K Ray Martin, Hannah Rideout, Jane Sneyd, J Robert Campbell, Sarah Carroll, Camille |
description | 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.
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.
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.
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.
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. |
doi_str_mv | 10.1371/journal.pone.0285349 |
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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.
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.
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.
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.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0285349</identifier><identifier>PMID: 37523365</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Aftercare ; Age ; Aged, 80 and over ; Basal ganglia ; Biology and Life Sciences ; Cardiovascular disease ; Central nervous system diseases ; Comorbidity ; Complications and side effects ; Coronaviruses ; COVID-19 ; COVID-19 - epidemiology ; COVID-19 vaccines ; Data collection ; Dementia ; Dementia disorders ; Diabetes ; Diagnosis ; Disorders ; Drug dosages ; Ethnicity ; Female ; Frailty ; Health risks ; Hospitals ; Humans ; Hypertension ; Immunization ; Infections ; Male ; Males ; Medical records ; Medical research ; Medicine and Health Sciences ; Medicine, Experimental ; Mental disorders ; Missing data ; Mortality ; Movement disorders ; Nervous system diseases ; Neurodegenerative diseases ; Neurological diseases ; Pandemics ; Parkinson Disease - complications ; Parkinson Disease - epidemiology ; Parkinson's disease ; Parkinsonian Disorders - complications ; Parkinsonian Disorders - epidemiology ; Patient Discharge ; Patient outcomes ; Patients ; Regression analysis ; Regression models ; Retrospective Studies ; Risk factors ; SARS-CoV-2 ; Severe acute respiratory syndrome coronavirus 2 ; Statistical models ; Statistical significance ; United Kingdom ; United Kingdom - epidemiology ; Vaccination ; Viral diseases</subject><ispartof>PloS one, 2023-07, Vol.18 (7), p.e0285349-e0285349</ispartof><rights>Copyright: © 2023 Sorrell 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.</rights><rights>COPYRIGHT 2023 Public Library of Science</rights><rights>2023 Sorrell et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2023 Sorrell et al 2023 Sorrell et al</rights><rights>2023 Sorrell et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c627t-99a7965e2555755b5c791f968c3762f735e2342eef7b6e077784bf37d23086a13</citedby><cites>FETCH-LOGICAL-c627t-99a7965e2555755b5c791f968c3762f735e2342eef7b6e077784bf37d23086a13</cites><orcidid>0000-0001-8044-3706 ; 0000-0003-3546-9856 ; 0000-0001-7867-8469 ; 0000-0002-7797-0756</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2844073333/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2844073333?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,38516,43895,44590,53791,53793,74412,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37523365$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Kenmoe, Sebastien</contributor><creatorcontrib>Sorrell, Lexy</creatorcontrib><creatorcontrib>Leta, Valentina</creatorcontrib><creatorcontrib>Barnett, Anton</creatorcontrib><creatorcontrib>Stevens, Kara</creatorcontrib><creatorcontrib>King, Angela</creatorcontrib><creatorcontrib>Inches, Jemma</creatorcontrib><creatorcontrib>Kobylecki, Christopher</creatorcontrib><creatorcontrib>Walker, Richard</creatorcontrib><creatorcontrib>Chaudhuri, K Ray</creatorcontrib><creatorcontrib>Martin, Hannah</creatorcontrib><creatorcontrib>Rideout, Jane</creatorcontrib><creatorcontrib>Sneyd, J Robert</creatorcontrib><creatorcontrib>Campbell, Sarah</creatorcontrib><creatorcontrib>Carroll, Camille</creatorcontrib><creatorcontrib>COVID-19 PD UK study team</creatorcontrib><creatorcontrib>on behalf of the COVID-19 PD UK study team</creatorcontrib><title>Clinical features and outcomes of hospitalised patients with COVID-19 and Parkinsonian disorders: A multicentre UK-based study</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>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.
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.
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.
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.
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.</description><subject>Aftercare</subject><subject>Age</subject><subject>Aged, 80 and over</subject><subject>Basal ganglia</subject><subject>Biology and Life Sciences</subject><subject>Cardiovascular disease</subject><subject>Central nervous system diseases</subject><subject>Comorbidity</subject><subject>Complications and side effects</subject><subject>Coronaviruses</subject><subject>COVID-19</subject><subject>COVID-19 - epidemiology</subject><subject>COVID-19 vaccines</subject><subject>Data collection</subject><subject>Dementia</subject><subject>Dementia disorders</subject><subject>Diabetes</subject><subject>Diagnosis</subject><subject>Disorders</subject><subject>Drug dosages</subject><subject>Ethnicity</subject><subject>Female</subject><subject>Frailty</subject><subject>Health risks</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Hypertension</subject><subject>Immunization</subject><subject>Infections</subject><subject>Male</subject><subject>Males</subject><subject>Medical records</subject><subject>Medical research</subject><subject>Medicine and Health Sciences</subject><subject>Medicine, Experimental</subject><subject>Mental disorders</subject><subject>Missing data</subject><subject>Mortality</subject><subject>Movement disorders</subject><subject>Nervous system diseases</subject><subject>Neurodegenerative diseases</subject><subject>Neurological diseases</subject><subject>Pandemics</subject><subject>Parkinson Disease - complications</subject><subject>Parkinson Disease - epidemiology</subject><subject>Parkinson's disease</subject><subject>Parkinsonian Disorders - complications</subject><subject>Parkinsonian Disorders - epidemiology</subject><subject>Patient Discharge</subject><subject>Patient outcomes</subject><subject>Patients</subject><subject>Regression analysis</subject><subject>Regression models</subject><subject>Retrospective Studies</subject><subject>Risk factors</subject><subject>SARS-CoV-2</subject><subject>Severe acute respiratory syndrome coronavirus 2</subject><subject>Statistical models</subject><subject>Statistical significance</subject><subject>United Kingdom</subject><subject>United Kingdom - epidemiology</subject><subject>Vaccination</subject><subject>Viral 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Collection</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sorrell, Lexy</au><au>Leta, Valentina</au><au>Barnett, Anton</au><au>Stevens, Kara</au><au>King, Angela</au><au>Inches, Jemma</au><au>Kobylecki, Christopher</au><au>Walker, Richard</au><au>Chaudhuri, K Ray</au><au>Martin, Hannah</au><au>Rideout, Jane</au><au>Sneyd, J Robert</au><au>Campbell, Sarah</au><au>Carroll, Camille</au><au>Kenmoe, Sebastien</au><aucorp>COVID-19 PD UK study team</aucorp><aucorp>on behalf of the COVID-19 PD UK study team</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinical features and outcomes of hospitalised patients with COVID-19 and Parkinsonian disorders: A multicentre UK-based study</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2023-07-31</date><risdate>2023</risdate><volume>18</volume><issue>7</issue><spage>e0285349</spage><epage>e0285349</epage><pages>e0285349-e0285349</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>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.
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.
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.
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.
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.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>37523365</pmid><doi>10.1371/journal.pone.0285349</doi><tpages>e0285349</tpages><orcidid>https://orcid.org/0000-0001-8044-3706</orcidid><orcidid>https://orcid.org/0000-0003-3546-9856</orcidid><orcidid>https://orcid.org/0000-0001-7867-8469</orcidid><orcidid>https://orcid.org/0000-0002-7797-0756</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2023-07, Vol.18 (7), p.e0285349-e0285349 |
issn | 1932-6203 1932-6203 |
language | eng |
recordid | cdi_plos_journals_2844073333 |
source | Publicly Available Content Database; PubMed Central; Coronavirus Research Database |
subjects | Aftercare Age Aged, 80 and over Basal ganglia Biology and Life Sciences Cardiovascular disease Central nervous system diseases Comorbidity Complications and side effects Coronaviruses COVID-19 COVID-19 - epidemiology COVID-19 vaccines Data collection Dementia Dementia disorders Diabetes Diagnosis Disorders Drug dosages Ethnicity Female Frailty Health risks Hospitals Humans Hypertension Immunization Infections Male Males Medical records Medical research Medicine and Health Sciences Medicine, Experimental Mental disorders Missing data Mortality Movement disorders Nervous system diseases Neurodegenerative diseases Neurological diseases Pandemics Parkinson Disease - complications Parkinson Disease - epidemiology Parkinson's disease Parkinsonian Disorders - complications Parkinsonian Disorders - epidemiology Patient Discharge Patient outcomes Patients Regression analysis Regression models Retrospective Studies Risk factors SARS-CoV-2 Severe acute respiratory syndrome coronavirus 2 Statistical models Statistical significance United Kingdom United Kingdom - epidemiology Vaccination Viral diseases |
title | Clinical features and outcomes of hospitalised patients with COVID-19 and Parkinsonian disorders: A multicentre UK-based study |
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