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  1. Article ; Online: Rapid feedback on hospital onset SARS-CoV-2 infections combining epidemiological and sequencing data.

    Stirrup, Oliver / Hughes, Joseph / Parker, Matthew / Partridge, David G / Shepherd, James G / Blackstone, James / Coll, Francesc / Keeley, Alexander / Lindsey, Benjamin B / Marek, Aleksandra / Peters, Christine / Singer, Joshua B / Tamuri, Asif / de Silva, Thushan I / Thomson, Emma C / Breuer, Judith

    eLife

    2021  Volume 10

    Abstract: ... important for suppression of SARS-CoV-2, but the infection source for hospital onset COVID-19 infections ... evaluation. The integration of epidemiological and sequence data is important given the low mutation rate ... of SARS-CoV-2 and its variable incubation period.: Funding: COG-UK HOCI funded by COG-UK consortium ...

    Abstract Background: Rapid identification and investigation of healthcare-associated infections (HCAIs) is important for suppression of SARS-CoV-2, but the infection source for hospital onset COVID-19 infections (HOCIs) cannot always be readily identified based only on epidemiological data. Viral sequencing data provides additional information regarding potential transmission clusters, but the low mutation rate of SARS-CoV-2 can make interpretation using standard phylogenetic methods difficult.
    Methods: We developed a novel statistical method and sequence reporting tool (SRT) that combines epidemiological and sequence data in order to provide a rapid assessment of the probability of HCAI among HOCI cases (defined as first positive test >48 hr following admission) and to identify infections that could plausibly constitute outbreak events. The method is designed for prospective use, but was validated using retrospective datasets from hospitals in Glasgow and Sheffield collected February-May 2020.
    Results: We analysed data from 326 HOCIs. Among HOCIs with time from admission ≥8 days, the SRT algorithm identified close sequence matches from the same ward for 160/244 (65.6%) and in the remainder 68/84 (81.0%) had at least one similar sequence elsewhere in the hospital, resulting in high estimated probabilities of within-ward and within-hospital transmission. For HOCIs with time from admission 3-7 days, the SRT probability of healthcare acquisition was >0.5 in 33/82 (40.2%).
    Conclusions: The methodology developed can provide rapid feedback on HOCIs that could be useful for infection prevention and control teams, and warrants further prospective evaluation. The integration of epidemiological and sequence data is important given the low mutation rate of SARS-CoV-2 and its variable incubation period.
    Funding: COG-UK HOCI funded by COG-UK consortium, supported by funding from UK Research and Innovation, National Institute of Health Research and Wellcome Sanger Institute.
    MeSH term(s) COVID-19/diagnosis ; COVID-19/epidemiology ; Cross Infection/diagnosis ; Cross Infection/epidemiology ; Disease Outbreaks/statistics & numerical data ; Genome, Viral ; Hospitals/statistics & numerical data ; Humans ; Population Surveillance/methods ; Probability ; Retrospective Studies ; SARS-CoV-2/genetics ; United Kingdom/epidemiology ; Whole Genome Sequencing
    Language English
    Publishing date 2021-06-29
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2687154-3
    ISSN 2050-084X ; 2050-084X
    ISSN (online) 2050-084X
    ISSN 2050-084X
    DOI 10.7554/eLife.65828
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Rapid feedback on hospital onset SARS-CoV-2 infections combining epidemiological and sequencing data

    Oliver Stirrup / Joseph Hughes / Matthew Parker / David G Partridge / James G Shepherd / James Blackstone / Francesc Coll / Alexander Keeley / Benjamin B Lindsey / Aleksandra Marek / Christine Peters / Joshua B Singer / The COVID-19 Genomics UK (COG-UK) consortium / Asif Tamuri / Thushan I de Silva / Emma C Thomson / Judith Breuer

    eLife, Vol

    2021  Volume 10

    Abstract: ... important for suppression of SARS-CoV-2, but the infection source for hospital onset COVID-19 infections ... evaluation. The integration of epidemiological and sequence data is important given the low mutation rate ... of SARS-CoV-2 and its variable incubation period. Funding: COG-UK HOCI funded by COG-UK consortium ...

    Abstract Background: Rapid identification and investigation of healthcare-associated infections (HCAIs) is important for suppression of SARS-CoV-2, but the infection source for hospital onset COVID-19 infections (HOCIs) cannot always be readily identified based only on epidemiological data. Viral sequencing data provides additional information regarding potential transmission clusters, but the low mutation rate of SARS-CoV-2 can make interpretation using standard phylogenetic methods difficult. Methods: We developed a novel statistical method and sequence reporting tool (SRT) that combines epidemiological and sequence data in order to provide a rapid assessment of the probability of HCAI among HOCI cases (defined as first positive test >48 hr following admission) and to identify infections that could plausibly constitute outbreak events. The method is designed for prospective use, but was validated using retrospective datasets from hospitals in Glasgow and Sheffield collected February–May 2020. Results: We analysed data from 326 HOCIs. Among HOCIs with time from admission ≥8 days, the SRT algorithm identified close sequence matches from the same ward for 160/244 (65.6%) and in the remainder 68/84 (81.0%) had at least one similar sequence elsewhere in the hospital, resulting in high estimated probabilities of within-ward and within-hospital transmission. For HOCIs with time from admission 3–7 days, the SRT probability of healthcare acquisition was >0.5 in 33/82 (40.2%). Conclusions: The methodology developed can provide rapid feedback on HOCIs that could be useful for infection prevention and control teams, and warrants further prospective evaluation. The integration of epidemiological and sequence data is important given the low mutation rate of SARS-CoV-2 and its variable incubation period. Funding: COG-UK HOCI funded by COG-UK consortium, supported by funding from UK Research and Innovation, National Institute of Health Research and Wellcome Sanger Institute.
    Keywords COVID-19 ; healthcare associated ; nosocomial ; SARS-CoV-2 ; whole genome sequencing ; outbreak ; Medicine ; R ; Science ; Q ; Biology (General) ; QH301-705.5
    Subject code 360
    Language English
    Publishing date 2021-06-01T00:00:00Z
    Publisher eLife Sciences Publications Ltd
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  3. Article ; Online: Rapid feedback on hospital onset SARS-CoV-2 infections combining epidemiological and sequencing data

    Stirrup, O. T. / Hughes, J. / Parker, M. / Partridge, D. / Shepherd, J. G. / Blackstone, J. / Coll, F. / Keeley, A. J. / Lindsey, B. B. / Marek, A. / Peters, C. / Singer, J. B. / The COVID-19 Genomics UK consortium, / Tamuri, A. / de Silva, T. I. / Thomson, E. C. / Breuer, J. C.

    Abstract: ... important for suppression of SARS-CoV-2, but the infection source for hospital onset COVID-19 infections ... evaluation. The integration of epidemiological and sequence data is important given the low mutation rate ... of SARS-CoV-2 and its variable incubation period. ...

    Abstract Background: Rapid identification and investigation of healthcare-associated infections (HCAIs) is important for suppression of SARS-CoV-2, but the infection source for hospital onset COVID-19 infections (HOCIs) cannot always be readily identified based only on epidemiological data. Viral sequencing data provides additional information regarding potential transmission clusters, but the low mutation rate of SARS-CoV-2 can make interpretation using standard phylogenetic methods difficult. Methods: We developed a novel statistical method and sequence reporting tool (SRT) that combines epidemiological and sequence data in order to provide a rapid assessment of the probability of HCAI among HOCI cases (defined as first positive test >48 hours following admission) and to identify infections that could plausibly constitute outbreak events. The method is designed for prospective use, but was validated using retrospective datasets from hospitals in Glasgow and Sheffield collected February-May 2020. Results: We analysed data from 326 HOCIs. Among HOCIs with time-from-admission [≥]8 days the SRT algorithm identified close sequence matches from the same ward for 160/244 (65.6%) and in the remainder 68/84 (81.0%) had at least one similar sequence elsewhere in the hospital, resulting in high estimated probabilities of within-ward and within-hospital transmission. For HOCIs with time-from-admission 3-7 days, the SRT probability of healthcare acquisition was >0.5 in 33/82 (40.2%). Conclusions: The methodology developed can provide rapid feedback on HOCIs that could be useful for infection prevention and control teams, and warrants further prospective evaluation. The integration of epidemiological and sequence data is important given the low mutation rate of SARS-CoV-2 and its variable incubation period.
    Keywords covid19
    Publisher MedRxiv; WHO
    Document type Article ; Online
    DOI 10.1101/2020.11.12.20230326
    Database COVID19

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  4. Article ; Online: Rapid feedback on hospital onset SARS-CoV-2 infections combining epidemiological and sequencing data

    Stirrup, Oliver T / Hughes, Joseph / Parker, Matthew / Partridge, David / Shepherd, James G / Blackstone, James / Coll, Francesc / Keeley, Alexander James / Lindsey, Benjamin B / Marek, Aleksandra / Peters, Christine / Singer, Joshua B / The COVID-19 Genomics UK (COG-UK) consortium / Tamuri, Asif / de Silva, Thushan I / Thomson, Emma C / Breuer, Judith C

    medRxiv

    Abstract: ... important for suppression of SARS-CoV-2, but the infection source for hospital onset COVID-19 infections ... evaluation. The integration of epidemiological and sequence data is important given the low mutation rate ... of SARS-CoV-2 and its variable incubation period. ...

    Abstract Background: Rapid identification and investigation of healthcare-associated infections (HCAIs) is important for suppression of SARS-CoV-2, but the infection source for hospital onset COVID-19 infections (HOCIs) cannot always be readily identified based only on epidemiological data. Viral sequencing data provides additional information regarding potential transmission clusters, but the low mutation rate of SARS-CoV-2 can make interpretation using standard phylogenetic methods difficult. Methods: We developed a novel statistical method and sequence reporting tool (SRT) that combines epidemiological and sequence data in order to provide a rapid assessment of the probability of HCAI among HOCI cases (defined as first positive test >48 hours following admission) and to identify infections that could plausibly constitute outbreak events. The method is designed for prospective use, but was validated using retrospective datasets from hospitals in Glasgow and Sheffield collected February-May 2020. Results: We analysed data from 326 HOCIs. Among HOCIs with time-from-admission ≥8 days the SRT algorithm identified close sequence matches from the same ward for 160/244 (65.6%) and in the remainder 68/84 (81.0%) had at least one similar sequence elsewhere in the hospital, resulting in high estimated probabilities of within-ward and within-hospital transmission. For HOCIs with time-from-admission 3-7 days, the SRT probability of healthcare acquisition was >0.5 in 33/82 (40.2%). Conclusions: The methodology developed can provide rapid feedback on HOCIs that could be useful for infection prevention and control teams, and warrants further prospective evaluation. The integration of epidemiological and sequence data is important given the low mutation rate of SARS-CoV-2 and its variable incubation period.
    Keywords covid19
    Language English
    Publishing date 2020-11-15
    Publisher Cold Spring Harbor Laboratory Press
    Document type Article ; Online
    DOI 10.1101/2020.11.12.20230326
    Database COVID19

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