Protocol for the COG-UK hospital-onset COVID-19 infection (HOCI) multicentre interventional clinical study: evaluating the efficacy of rapid genome sequencing of SARS-CoV-2 in limiting the spread of COVID-19 in UK NHS hospitals.


Journal

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

Informations de publication

Date de publication:
19 04 2022
Historique:
entrez: 20 4 2022
pubmed: 21 4 2022
medline: 22 4 2022
Statut: epublish

Résumé

Nosocomial transmission of SARS-CoV-2 has been a significant cause of mortality in National Health Service (NHS) hospitals during the COVID-19 pandemic. The COG-UK Consortium Hospital-Onset COVID-19 Infections (COG-UK HOCI) study aims to evaluate whether the use of rapid whole-genome sequencing of SARS-CoV-2, supported by a novel probabilistic reporting methodology, can inform infection prevention and control (IPC) practice within NHS hospital settings. Multicentre, prospective, interventional, superiority study. 14 participating NHS hospitals over winter-spring 2020/2021 in the UK. Eligible patients must be admitted to hospital with first-confirmed SARS-CoV-2 PCR-positive test result >48 hour from time of admission, where COVID-19 diagnosis not suspected on admission. The projected sample size is 2380 patients. The intervention is the return of a sequence report, within 48 hours in one phase (rapid local lab processing) and within 5-10 days in a second phase (mimicking central lab), comparing the viral genome from an eligible study participant with others within and outside the hospital site. The primary outcomes are incidence of Public Health England (PHE)/IPC-defined SARS-CoV-2 hospital-acquired infection during the baseline and two interventional phases, and proportion of hospital-onset cases with genomic evidence of transmission linkage following implementation of the intervention where such linkage was not suspected by initial IPC investigation. Secondary outcomes include incidence of hospital outbreaks, with and without sequencing data; actual and desirable changes to IPC actions; periods of healthcare worker (HCW) absence. Health economic analysis will be conducted to determine cost benefit of the intervention. A process evaluation using qualitative interviews with HCWs will be conducted alongside the study. ISRCTN50212645. Pre-results stage. This manuscript is based on protocol V.6.0. 2 September 2021.

Identifiants

pubmed: 35440446
pii: bmjopen-2021-052514
doi: 10.1136/bmjopen-2021-052514
pmc: PMC9019828
doi:

Banques de données

ISRCTN
['ISRCTN50212645']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e052514

Subventions

Organisme : Medical Research Council
ID : MC_PC_19027
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/T005416/1
Pays : United Kingdom
Organisme : Department of Health
Pays : United Kingdom

Investigateurs

Joshua Singer (J)
Joseph Hughes (J)
Emma Thomson (E)
Matthew Parker (M)
Asif Tamuri (A)
Sunando Roy (S)
Stefan Piatek (S)

Informations de copyright

© Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

Références

Lancet Microbe. 2020 Jul;1(3):e99-e100
pubmed: 32835336
Antimicrob Resist Infect Control. 2021 Jan 6;10(1):7
pubmed: 33407833
Microb Genom. 2021 Jun;7(6):
pubmed: 34184982
J Hosp Infect. 2021 Feb;108:189-196
pubmed: 33259882
Clin Infect Dis. 2019 Jan 7;68(2):222-228
pubmed: 29800111
Elife. 2021 Jun 29;10:
pubmed: 34184637
Lancet Infect Dis. 2020 Nov;20(11):1263-1272
pubmed: 32679081
J Infect Dis. 2018 Sep 8;218(8):1261-1271
pubmed: 29917114
Clin Infect Dis. 2019 Oct 30;69(10):1649-1656
pubmed: 30993315

Auteurs

James Blackstone (J)

Comprehensive Clinical Trials Unit, University College London, London, UK.

Oliver Stirrup (O)

Institute for Global Health, University College London, London, UK.

Fiona Mapp (F)

Institute for Global Health, University College London, London, UK.

Monica Panca (M)

Comprehensive Clinical Trials Unit, University College London, London, UK.

Andrew Copas (A)

Institute for Global Health, University College London, London, UK.

Paul Flowers (P)

School of Psychology & Health, University of Strathclyde, Glasgow, UK.

Leanne Hockey (L)

Comprehensive Clinical Trials Unit, University College London, London, UK.

James Price (J)

Department of Infectious Disease, Imperial College London, London, UK.

David Partridge (D)

Department of Virology, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.

Christine Peters (C)

Queen Elizabeth University Hospital, NHS Greater Glasgow and Clyde, Glasgow, UK.

Thushan de Silva (T)

Department of Infection, Immunity and Cardiovascular Disease, The University of Sheffield, Sheffield, UK.

Gaia Nebbia (G)

Department of Infectious Diseases, Guy's and St Thomas' NHS Foundation Trust, London, UK.

Luke B Snell (LB)

Department of Infectious Diseases, Guy's and St Thomas' NHS Foundation Trust, London, UK.

Rachel McComish (R)

Comprehensive Clinical Trials Unit, University College London, London, UK.

Judith Breuer (J)

Institute of Child Health, University College London, London, UK j.breuer@ucl.ac.uk.

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Classifications MeSH