What items should be included in an early warning score for remote assessment of suspected COVID-19? qualitative and Delphi study.


Journal

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

Informations de publication

Date de publication:
12 11 2020
Historique:
entrez: 13 11 2020
pubmed: 14 11 2020
medline: 20 11 2020
Statut: epublish

Résumé

To develop items for an early warning score (RECAP: REmote COVID-19 Assessment in Primary Care) for patients with suspected COVID-19 who need escalation to next level of care. The study was based in UK primary healthcare. The mixed-methods design included rapid review, Delphi panel, interviews, focus groups and software development. Participants were 112 primary care clinicians and 50 patients recovered from COVID-19, recruited through social media, patient groups and snowballing. Using rapid literature review, we identified signs and symptoms which are commoner in severe COVID-19. Building a preliminary set of items from these, we ran four rounds of an online Delphi panel with 72 clinicians, the last incorporating fictional vignettes, collating data on R software. We refined the items iteratively in response to quantitative and qualitative feedback. Items in the penultimate round were checked against narrative interviews with 50 COVID-19 patients. We required, for each item, at least 80% clinician agreement on relevance, wording and cut-off values, and that the item addressed issues and concerns raised by patients. In focus groups, 40 clinicians suggested further refinements and discussed workability of the instrument in relation to local resources and care pathways. This informed design of an electronic template for primary care systems. The prevalidation RECAP-V0 comprises a red flag alert box and 10 assessment items: pulse, shortness of breath or respiratory rate, trajectory of breathlessness, pulse oximeter reading (with brief exercise test if appropriate) or symptoms suggestive of hypoxia, temperature or fever symptoms, duration of symptoms, muscle aches, new confusion, shielded list and known risk factors for poor outcome. It is not yet known how sensitive or specific it is. Items on RECAP-V0 align strongly with published evidence, clinical judgement and patient experience. The validation phase of this study is ongoing. NCT04435041.

Sections du résumé

BACKGROUND
To develop items for an early warning score (RECAP: REmote COVID-19 Assessment in Primary Care) for patients with suspected COVID-19 who need escalation to next level of care.
METHODS
The study was based in UK primary healthcare. The mixed-methods design included rapid review, Delphi panel, interviews, focus groups and software development. Participants were 112 primary care clinicians and 50 patients recovered from COVID-19, recruited through social media, patient groups and snowballing. Using rapid literature review, we identified signs and symptoms which are commoner in severe COVID-19. Building a preliminary set of items from these, we ran four rounds of an online Delphi panel with 72 clinicians, the last incorporating fictional vignettes, collating data on R software. We refined the items iteratively in response to quantitative and qualitative feedback. Items in the penultimate round were checked against narrative interviews with 50 COVID-19 patients. We required, for each item, at least 80% clinician agreement on relevance, wording and cut-off values, and that the item addressed issues and concerns raised by patients. In focus groups, 40 clinicians suggested further refinements and discussed workability of the instrument in relation to local resources and care pathways. This informed design of an electronic template for primary care systems.
RESULTS
The prevalidation RECAP-V0 comprises a red flag alert box and 10 assessment items: pulse, shortness of breath or respiratory rate, trajectory of breathlessness, pulse oximeter reading (with brief exercise test if appropriate) or symptoms suggestive of hypoxia, temperature or fever symptoms, duration of symptoms, muscle aches, new confusion, shielded list and known risk factors for poor outcome. It is not yet known how sensitive or specific it is.
CONCLUSIONS
Items on RECAP-V0 align strongly with published evidence, clinical judgement and patient experience. The validation phase of this study is ongoing.
TRIAL REGISTRATION NUMBER
NCT04435041.

Identifiants

pubmed: 33184088
pii: bmjopen-2020-042626
doi: 10.1136/bmjopen-2020-042626
pmc: PMC7662139
doi:

Banques de données

ClinicalTrials.gov
['NCT04435041']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e042626

Informations de copyright

© Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: MD’s company makes templates for general practice record systems. All other authors declare no competing interests.

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Auteurs

Trisha Greenhalgh (T)

Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK trish.greenhalgh@phc.ox.ac.uk.

Paul Thompson (P)

Department of Experimental Psychology, University of Oxford, Oxford, UK.

Sietse Weiringa (S)

Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK.

Ana Luisa Neves (AL)

Institute of Global Health Innovation, Imperial College London, London, UK.

Laiba Husain (L)

Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK.

Merlin Dunlop (M)

Ardens Ltd, Oxford, UK.

Alexander Rushforth (A)

Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK.

David Nunan (D)

Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK.

Simon de Lusignan (S)

Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK.

Brendan Delaney (B)

Institute of Global Health Innovation, Imperial College London, London, UK.

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