Evaluating the cost implications of integrating SARS-CoV-2 genome sequencing for infection prevention and control investigation of nosocomial transmission within hospitals.

COVID-19 Cost Healthcare-associated infection Infection prevention and control Micro-costing SARS-CoV-2

Journal

The Journal of hospital infection
ISSN: 1532-2939
Titre abrégé: J Hosp Infect
Pays: England
ID NLM: 8007166

Informations de publication

Date de publication:
Sep 2023
Historique:
received: 08 03 2023
revised: 30 05 2023
accepted: 01 06 2023
medline: 28 8 2023
pubmed: 13 6 2023
entrez: 12 6 2023
Statut: ppublish

Résumé

The COG-UK hospital-onset COVID-19 infection (HOCI) trial evaluated the impact of SARS-CoV-2 whole-genome sequencing (WGS) on acute infection, prevention, and control (IPC) investigation of nosocomial transmission within hospitals. To estimate the cost implications of using the information from the sequencing reporting tool (SRT), used to determine likelihood of nosocomial infection in IPC practice. A micro-costing approach for SARS-CoV-2 WGS was conducted. Data on IPC management resource use and costs were collected from interviews with IPC teams from 14 participating sites and used to assign cost estimates for IPC activities as collected in the trial. Activities included IPC-specific actions following a suspicion of healthcare-associated infection (HAI) or outbreak, as well as changes to practice following the return of data via SRT. The mean per-sample costs of SARS-CoV-2 sequencing were estimated at £77.10 for rapid and £66.94 for longer turnaround phases. Over the three-month interventional phases, the total management costs of IPC-defined HAIs and outbreak events across the sites were estimated at £225,070 and £416,447, respectively. The main cost drivers were bed-days lost due to ward closures because of outbreaks, followed by outbreak meetings and bed-days lost due to cohorting contacts. Actioning SRTs, the cost of HAIs increased by £5,178 due to unidentified cases and the cost of outbreaks decreased by £11,246 as SRTs excluded hospital outbreaks. Although SARS-CoV-2 WGS adds to the total IPC management cost, additional information provided could balance out the additional cost, depending on identified design improvements and effective deployment.

Sections du résumé

BACKGROUND BACKGROUND
The COG-UK hospital-onset COVID-19 infection (HOCI) trial evaluated the impact of SARS-CoV-2 whole-genome sequencing (WGS) on acute infection, prevention, and control (IPC) investigation of nosocomial transmission within hospitals.
AIM OBJECTIVE
To estimate the cost implications of using the information from the sequencing reporting tool (SRT), used to determine likelihood of nosocomial infection in IPC practice.
METHODS METHODS
A micro-costing approach for SARS-CoV-2 WGS was conducted. Data on IPC management resource use and costs were collected from interviews with IPC teams from 14 participating sites and used to assign cost estimates for IPC activities as collected in the trial. Activities included IPC-specific actions following a suspicion of healthcare-associated infection (HAI) or outbreak, as well as changes to practice following the return of data via SRT.
FINDINGS RESULTS
The mean per-sample costs of SARS-CoV-2 sequencing were estimated at £77.10 for rapid and £66.94 for longer turnaround phases. Over the three-month interventional phases, the total management costs of IPC-defined HAIs and outbreak events across the sites were estimated at £225,070 and £416,447, respectively. The main cost drivers were bed-days lost due to ward closures because of outbreaks, followed by outbreak meetings and bed-days lost due to cohorting contacts. Actioning SRTs, the cost of HAIs increased by £5,178 due to unidentified cases and the cost of outbreaks decreased by £11,246 as SRTs excluded hospital outbreaks.
CONCLUSION CONCLUSIONS
Although SARS-CoV-2 WGS adds to the total IPC management cost, additional information provided could balance out the additional cost, depending on identified design improvements and effective deployment.

Identifiants

pubmed: 37308063
pii: S0195-6701(23)00178-0
doi: 10.1016/j.jhin.2023.06.005
pmc: PMC10257337
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

23-32

Subventions

Organisme : Medical Research Council
ID : MC_UU_00034/6
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/W025140/1
Pays : United Kingdom

Informations de copyright

Copyright © 2023 The Authors. Published by Elsevier Ltd.. All rights reserved.

Auteurs

M Panca (M)

Comprehensive Clinical Trials Unit, Institute of Clinical Trials and Methodology, UCL, London, UK. Electronic address: m.panca@ucl.ac.uk.

J Blackstone (J)

Comprehensive Clinical Trials Unit, Institute of Clinical Trials and Methodology, UCL, London, UK.

O Stirrup (O)

Institute for Global Health, UCL, London, UK.

M-T Cutino-Moguel (MT)

Barts Health NHS Trust, London, UK.

E Thomson (E)

MRC-University of Glasgow Centre for Virus Research, Glasgow, UK.

C Peters (C)

NHS Greater Glasgow and Clyde, Glasgow, UK.

L B Snell (LB)

Guy's and St Thomas' Hospital NHS Foundation Trust, London, UK.

G Nebbia (G)

Guy's and St Thomas' Hospital NHS Foundation Trust, London, UK.

A Holmes (A)

Imperial College Healthcare NHS Trust, London, UK.

A Chawla (A)

Liverpool University Hospitals NHS Foundation Trust, Liverpool, UK.

N Machin (N)

Manchester University NHS Foundation Trust, Manchester, UK.

Y Taha (Y)

Departments of Virology and Infectious Diseases, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle, UK.

T Mahungu (T)

Royal Free NHS Foundation Trust, London, UK.

T Saluja (T)

Sandwell and West Birmingham NHS Trust, UK.

T I de Silva (TI)

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

K Saeed (K)

University Hospital Southampton NHS Foundation Trust, Southampton, UK.

C Pope (C)

St George's University Hospitals NHS Foundation Trust, London, UK; Institute for Infection and Immunity, St George's University of London, London, UK.

G Y Shin (GY)

University College London Hospitals NHS Foundation Trust, London, UK.

R Williams (R)

Department of Genetics & Genomic Medicine, UCL Great Ormond Street Institute of Child Health, UCL, London, UK.

A Darby (A)

Centre for Genomic Research, University of Liverpool, Liverpool, UK.

D L Smith (DL)

Department of Applied Sciences, Northumbria University, Newcastle, UK.

M Loose (M)

School of Life Sciences, University of Nottingham, Nottingham, UK.

S C Robson (SC)

Centre for Enzyme Innovation & School of Pharmacy and Biomedical Science, University of Portsmouth, Portsmouth, UK.

K Laing (K)

Institute for Infection and Immunity, St George's University of London, London, UK.

D G Partridge (DG)

Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.

J R Price (JR)

Imperial College Healthcare NHS Trust, London, UK.

J Breuer (J)

Department of Infection, Immunity and Inflammation, Great Ormond Street Institute of Child Health, UCL, London, UK.

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