Insights into the implementation of a whole genome sequencing report form (SRF) to reduce nosocomial SARS-CoV-2 within UK hospitals: a qualitative process evaluation using normalisation process theory

Author:

Leiser Ruth1,McLeod Julie1,Mapp Fiona2,Stirrup Oliver2,Blackstone James3,Illingwo Christopher JR4,Nebbia Gaia5,Price James R6,Snell Luke B5,Saluja Tranprit7,Breuer Judith8,Flowers Paul1

Affiliation:

1. University of Strathclyde

2. Institute for Global Health, UCL, London

3. Comprehensive Clinical Trials Unit, UCL

4. University of Glasgow Centre for Virus Research

5. Department of Infection, Guy’s and St Thomas’ Hospital NHS Trust

6. Department of Global Health and Infection

7. Sandwell & West Birmingham Hospitals NHS Trust

8. Department of Infection, Immunity and Inflammation, UCL

Abstract

Abstract Background Here we report on a process evaluation conducted as part of a large multisite non-randomised trial of the effectiveness of a whole genome sequence report form (SRF) to reduce nosocomial SARS-CoV-2 through changing infection prevention and control (IPC) behaviours during the COVID − 19 pandemic. We detail how the SRF was implemented across a heterogeneous purposive sub-sample of hospital trial sites (n = 5/14). Methods We conducted in-depth interviews from diverse professional staff (N = 39). Inductive thematic analysis initially explored participants’ accounts of implementing the SRF. The resulting data driven themes, concerning the way the SRF was used within sites, were then coded in relation to the key tenets of normalisation process theory (NPT). Results Factors that enabled the implementation of the SRF included: elements of the context such as health care professional passion; the existence of whole genome sequencing (WGS) infrastructure; effective communication channels, the creation of new connections across professionals and teams; the integration of SRF-led discussions within pre-existing meetings and the ability of a site to achieve a rapid turnaround time. In contrast, we found factors that constrained the use of the SRF included elements of the context such as the impact of the Alpha-variant overwhelming hospitals. In turn, dealing with COVID-19 breached the limited capacity of infection prevention and control (IPC) to respond to the SRF and ensure its routinisation. Conclusion We show preliminary support for the SRF being an acceptable, useable and potentially scalable way of enhancing existing IPC activities. However, the context of both the trial and the alpha wave of COVID-19 limit these insights. Clinical trial number https://www.isrctn.com/ISRCTN50212645, Registration date 20/05/2020

Publisher

Research Square Platform LLC

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