Long-term functioning status of COVID-19 survivors: a prospective observational evaluation of a cohort of patients surviving hospitalisation.


Journal

BMJ open
ISSN: 2044-6055
Titre abrégé: BMJ Open
Pays: England
ID NLM: 101552874

Informations de publication

Date de publication:
27 07 2022
Historique:
entrez: 27 7 2022
pubmed: 28 7 2022
medline: 30 7 2022
Statut: epublish

Résumé

The study investigated the long-term functional status of hospitalised COVID-19 survivors to explore and document their functional situation. This prospective observational study assessed 801 COVID-19 survivors at 3-11 months after hospital discharge. It analyses participants' sociodemographic background, COVID-19 clinical manifestations, and clinical and functional evaluations. Tertiary-level university hospital in São Paulo, Brazil. Study participants are COVID-19 survivors admitted to hospital care for at least 24 hours to treat acute SARS-CoV-2 infection. Epworth Sleepiness Scale, EuroQoL-5 Dimensions-5 Levels, Functional Assessment of Chronic Illness Therapy-Fatigue, Functional Independence Measure, Functional Oral Intake Scale, Handgrip Strength, Insomnia Severity Index, Medical Research Council (MRC) Dyspnea Scale, MRC sum score, Modified Borg Dyspnea Scale, pain Visual Analogue Scale, Post-COVID-19 Functional Status, Timed Up and Go, WHO Disability Assessment Schedule 2.0, 1-Minute Sit to Stand Test. Many participants required invasive mechanical ventilation (41.57%, 333 of 801). Mean age was 55.35±14.58 years. With a mean of 6.56 (SD: 1.58; 95% CI: 6.45 to 6.67) months after hospital discharge, 70.86% (567 of 800) reported limited daily activities, which were severe in 5.62% (45 of 800). They also reported pain and discomfort (64.50%, 516 of 800), breathlessness (64.66%, 514 of 795), and anxiety and depression (57.27%, 457 of 798). Daytime sleepiness and insomnia evaluations showed subthreshold results. Most (92.85%, 727 of 783) participants reported unrestricted oral intake. Data indicated no generalised fatigue (mean score: 39.18, SD: 9.77; 95% CI: 38.50 to 39.86). Assessments showed poor handgrip strength (52.20%, 379 of 726) and abnormal Timed Up and Go results (mean 13.07 s, SD: 6.49). The invasive mechanical ventilation group seemed to have a better handgrip strength however. We found no clear trends of change in their functional status during months passed since hospital discharge. Muscle weakness, pain, anxiety, depression, breathlessness, reduced mobility, insomnia and daytime sleepiness were the most prevalent long-term conditions identified among previously hospitalised COVID-19 survivors.

Identifiants

pubmed: 35896292
pii: bmjopen-2021-057246
doi: 10.1136/bmjopen-2021-057246
pmc: PMC9334693
doi:

Types de publication

Journal Article Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e057246

Informations de copyright

© Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

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Auteurs

Linamara Rizzo Battistella (LR)

Faculdade de Medicina FMUSP, Universidade de Sao Paulo, São Paulo, SP, Brazil.
Instituto de Medicina Física e Reabilitação, Hospital das Clinicas HCFMUSP, São Paulo, SP, Brazil.

Marta Imamura (M)

Faculdade de Medicina FMUSP, Universidade de Sao Paulo, São Paulo, SP, Brazil marta.imamura@fm.usp.br.
Instituto de Medicina Física e Reabilitação, Hospital das Clinicas HCFMUSP, São Paulo, SP, Brazil.

Lucas Ramos De Pretto (LR)

Center for Lasers and Applications, Energy and Nuclear Research Institute, São Paulo, SP, Brazil.

Simon K H A A Van Cauwenbergh (SKHAA)

Faculdade de Medicina FMUSP, Universidade de Sao Paulo, São Paulo, SP, Brazil.

Vinicius Delgado Ramos (V)

Instituto de Medicina Física e Reabilitação, Hospital das Clinicas HCFMUSP, São Paulo, SP, Brazil.

Sabrina Saemy Tome Uchiyama (S)

Instituto de Medicina Física e Reabilitação, Hospital das Clinicas HCFMUSP, São Paulo, SP, Brazil.

Denise Matheus (D)

Instituto de Medicina Física e Reabilitação, Hospital das Clinicas HCFMUSP, São Paulo, SP, Brazil.

Flavia Kuhn (F)

Instituto de Medicina Física e Reabilitação, Hospital das Clinicas HCFMUSP, São Paulo, SP, Brazil.

Ana Alice Amaral de Oliveira (AA)

Instituto de Medicina Física e Reabilitação, Hospital das Clinicas HCFMUSP, São Paulo, SP, Brazil.

Gabriella Souza Naves (G)

Instituto de Medicina Física e Reabilitação, Hospital das Clinicas HCFMUSP, São Paulo, SP, Brazil.

Aline Rossetti Mirisola (A)

Instituto de Medicina Física e Reabilitação, Hospital das Clinicas HCFMUSP, São Paulo, SP, Brazil.

Fernando de Quadros Ribeiro (F)

Instituto de Medicina Física e Reabilitação, Hospital das Clinicas HCFMUSP, São Paulo, SP, Brazil.

Andre Tadeu Sugawara (A)

Instituto de Medicina Física e Reabilitação, Hospital das Clinicas HCFMUSP, São Paulo, SP, Brazil.

Mauricio Cantarino (M)

Instituto de Medicina Física e Reabilitação, Hospital das Clinicas HCFMUSP, São Paulo, SP, Brazil.

Rafael Andrade Santos Antunes Cavalca (R)

Instituto de Medicina Física e Reabilitação, Hospital das Clinicas HCFMUSP, São Paulo, SP, Brazil.

Vanessa Pagano (V)

Instituto de Medicina Física e Reabilitação, Hospital das Clinicas HCFMUSP, São Paulo, SP, Brazil.

Melina Valentim Marques (M)

Instituto de Medicina Física e Reabilitação, Hospital das Clinicas HCFMUSP, São Paulo, SP, Brazil.

Elizabeth Mendes da Silva (E)

Instituto de Medicina Física e Reabilitação, Hospital das Clinicas HCFMUSP, São Paulo, SP, Brazil.

Alessandra Pereira Gomes (A)

Instituto de Medicina Física e Reabilitação, Hospital das Clinicas HCFMUSP, São Paulo, SP, Brazil.

Felipe Fregni (F)

Department of Physical Medicine and Rehabilitation, Massachusetts General Hospital, Boston, Massachusetts, USA.
Harvard Medical School, Boston, Massachusetts, USA.
Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA.

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