4.5 Article

Factors affecting turnaround time of SARS-CoV-2 sequencing for inpatient infection prevention and control decision making: analysis of data from the COG-UK HOCI study

Journal

JOURNAL OF HOSPITAL INFECTION
Volume 131, Issue -, Pages 34-42

Publisher

W B SAUNDERS CO LTD
DOI: 10.1016/j.jhin.2022.09.022

Keywords

Infection control; Sequencing; SARS-CoV-2 Turnaround time

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This study identifies challenges in achieving a rapid turnaround time (TAT) in COVID-19 sequencing. The main delay comes from the time between COVID-19 PCR results and sample arrival at the sequencing laboratory. Integrating pathogen sequencing into diagnostic laboratories can improve sequencing TAT and make sequence data valuable for infection control practice.
Background: Barriers to rapid return of sequencing results can affect the utility of sequence data for infection prevention and control decisions.Aim: To undertake a mixed-methods analysis to identify challenges that sites faced in achieving a rapid turnaround time (TAT) in the COVID-19 Genomics UK Hospital-Onset COVID-19 Infection (COG-UK HOCI) study.Methods: For the quantitative analysis, timepoints relating to different stages of the sequencing process were extracted from both the COG-UK HOCI study dataset and surveys of study sites. Qualitative data relating to the barriers and facilitators to achieving rapid TATs were included from thematic analysis.Findings: The overall TAT, from sample collection to receipt of sequence report by infection control teams, varied between sites (median 5.1 days, range 3.0-29.0 days). Most variation was seen between reporting of a positive COVID-19 polymerase chain reaction (PCR) result to sequence report generation (median 4.0 days, range 2.3-27.0 days). On deeper analysis, most of this variability was accounted for by differences in the delay between the COVID-19 PCR result and arrival of the sample at the sequencing lab-oratory (median 20.8 h, range 16.0-88.7 h). Qualitative analyses suggest that closer proximity of sequencing laboratories to diagnostic laboratories, increased staff flexibility and regular transport times facilitated a shorter TAT.Conclusion: Integration of pathogen sequencing into diagnostic laboratories may help to improve sequencing TAT to allow sequence data to be of tangible value to infection control practice. Adding a quality control step upstream to increase capacity further down the workflow may also optimize TAT if lower quality samples are removed at an earlier stage. 2022 The Author(s). Published by Elsevier Ltd on behalf of The Healthcare Infection Society. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

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