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Routine molecular point-of-care testing for SARS-CoV-2 reduces hospital-acquired COVID-19

OBJECTIVES: Risk of hospital-acquired COVID-19 (HA-COVID-19) infection is increased by cohorting infected and non-infected patients together in assessment areas, whist awaiting laboratory PCR results. Molecular point-of-care tests (mPOCT) reduce time to results and improve patient flow but the impac...

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Autores principales: Livingstone, Robert, Lin, Hlaing, Brendish, Nathan J., Poole, Stephen, Tanner, Alex R., Borca, Florina, Smith, Trevor, Stammers, Matthew, Clark, Tristan W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The British Infection Association. Published by Elsevier Ltd. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8802147/
https://www.ncbi.nlm.nih.gov/pubmed/35108599
http://dx.doi.org/10.1016/j.jinf.2022.01.034
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author Livingstone, Robert
Lin, Hlaing
Brendish, Nathan J.
Poole, Stephen
Tanner, Alex R.
Borca, Florina
Smith, Trevor
Stammers, Matthew
Clark, Tristan W.
author_facet Livingstone, Robert
Lin, Hlaing
Brendish, Nathan J.
Poole, Stephen
Tanner, Alex R.
Borca, Florina
Smith, Trevor
Stammers, Matthew
Clark, Tristan W.
author_sort Livingstone, Robert
collection PubMed
description OBJECTIVES: Risk of hospital-acquired COVID-19 (HA-COVID-19) infection is increased by cohorting infected and non-infected patients together in assessment areas, whist awaiting laboratory PCR results. Molecular point-of-care tests (mPOCT) reduce time to results and improve patient flow but the impact on HA-COVID-19 is unknown. METHODS: In this pre and post implementation study patients were evaluated across two time periods: March 1st to August 13th 2020, prior to the introduction of mPOCT in medical admissions areas, and 14th August 2020 to 1st April 2021, after mPOCT introduction. The primary outcome was proportion of HA-COVID-19 infection among all COVID-19 positive patients. Secondary outcome measures included time to SARS-CoV-2 results, length of time spent in the medical assessment area and comparison of local, regional and national proportions of HA-COVID-19. RESULTS: 1988 patients were admitted through the acute medicine admission cohorting area and tested for SARS-CoV-2 prior to introducing mPOCT and 4640 afterwards. Median (IQR) time to SARS-CoV-2 result was 6.5 (2.1–17.9) hours prior to introducing mPOCT and 1.0 (0.8–1.3) hours afterwards (p < 0.0001). Median (IQR) duration in the assessment cohort area was 12.0 (4.8–20.6) hours prior to introduction of POCT and 3.2 (2.0–5.6) hours afterwards (p < 0.0001). The proportion of hospital-acquired COVID-19 cases was 108 (16.5%) of 654 prior to introducing mPOCT compared with 168 (9.4%) of 1782 afterwards, (HR 0.55, 95%CI 0.43–0.70; p < 0.0001). In the period following the introduction of mPOCT up to 1st April 2021 the median proportion of HA-COVID-19 was 13.6% (95%CI 8.2–18.9%) locally, compared with 43.8% (95%CI 37.8–49.9%) for all acute NHS trusts regionally and 30.9% (95%CI 28.4–33.5%) for all NHS trusts nationally. CONCLUSIONS: Routine mPOCT for SARS-CoV-2 was associated with reduced time to results, time spent in admission cohort areas, and hospital-acquired COVID-19, compared to laboratory PCR.
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spelling pubmed-88021472022-01-31 Routine molecular point-of-care testing for SARS-CoV-2 reduces hospital-acquired COVID-19 Livingstone, Robert Lin, Hlaing Brendish, Nathan J. Poole, Stephen Tanner, Alex R. Borca, Florina Smith, Trevor Stammers, Matthew Clark, Tristan W. J Infect Article OBJECTIVES: Risk of hospital-acquired COVID-19 (HA-COVID-19) infection is increased by cohorting infected and non-infected patients together in assessment areas, whist awaiting laboratory PCR results. Molecular point-of-care tests (mPOCT) reduce time to results and improve patient flow but the impact on HA-COVID-19 is unknown. METHODS: In this pre and post implementation study patients were evaluated across two time periods: March 1st to August 13th 2020, prior to the introduction of mPOCT in medical admissions areas, and 14th August 2020 to 1st April 2021, after mPOCT introduction. The primary outcome was proportion of HA-COVID-19 infection among all COVID-19 positive patients. Secondary outcome measures included time to SARS-CoV-2 results, length of time spent in the medical assessment area and comparison of local, regional and national proportions of HA-COVID-19. RESULTS: 1988 patients were admitted through the acute medicine admission cohorting area and tested for SARS-CoV-2 prior to introducing mPOCT and 4640 afterwards. Median (IQR) time to SARS-CoV-2 result was 6.5 (2.1–17.9) hours prior to introducing mPOCT and 1.0 (0.8–1.3) hours afterwards (p < 0.0001). Median (IQR) duration in the assessment cohort area was 12.0 (4.8–20.6) hours prior to introduction of POCT and 3.2 (2.0–5.6) hours afterwards (p < 0.0001). The proportion of hospital-acquired COVID-19 cases was 108 (16.5%) of 654 prior to introducing mPOCT compared with 168 (9.4%) of 1782 afterwards, (HR 0.55, 95%CI 0.43–0.70; p < 0.0001). In the period following the introduction of mPOCT up to 1st April 2021 the median proportion of HA-COVID-19 was 13.6% (95%CI 8.2–18.9%) locally, compared with 43.8% (95%CI 37.8–49.9%) for all acute NHS trusts regionally and 30.9% (95%CI 28.4–33.5%) for all NHS trusts nationally. CONCLUSIONS: Routine mPOCT for SARS-CoV-2 was associated with reduced time to results, time spent in admission cohort areas, and hospital-acquired COVID-19, compared to laboratory PCR. The British Infection Association. Published by Elsevier Ltd. 2022-04 2022-01-31 /pmc/articles/PMC8802147/ /pubmed/35108599 http://dx.doi.org/10.1016/j.jinf.2022.01.034 Text en © 2022 The British Infection Association. Published by Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Livingstone, Robert
Lin, Hlaing
Brendish, Nathan J.
Poole, Stephen
Tanner, Alex R.
Borca, Florina
Smith, Trevor
Stammers, Matthew
Clark, Tristan W.
Routine molecular point-of-care testing for SARS-CoV-2 reduces hospital-acquired COVID-19
title Routine molecular point-of-care testing for SARS-CoV-2 reduces hospital-acquired COVID-19
title_full Routine molecular point-of-care testing for SARS-CoV-2 reduces hospital-acquired COVID-19
title_fullStr Routine molecular point-of-care testing for SARS-CoV-2 reduces hospital-acquired COVID-19
title_full_unstemmed Routine molecular point-of-care testing for SARS-CoV-2 reduces hospital-acquired COVID-19
title_short Routine molecular point-of-care testing for SARS-CoV-2 reduces hospital-acquired COVID-19
title_sort routine molecular point-of-care testing for sars-cov-2 reduces hospital-acquired covid-19
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8802147/
https://www.ncbi.nlm.nih.gov/pubmed/35108599
http://dx.doi.org/10.1016/j.jinf.2022.01.034
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