Home > Research > Publications & Outputs > The burden and dynamics of hospital-acquired SA...

Links

Text available via DOI:

View graph of relations

The burden and dynamics of hospital-acquired SARS-CoV-2 in England

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Published

Standard

The burden and dynamics of hospital-acquired SARS-CoV-2 in England. / Cooper, B.S.; Evans, S.; Jafari, Y. et al.
In: Nature, Vol. 623, No. 7985, 02.11.2023, p. 132-138.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Cooper, BS, Evans, S, Jafari, Y, Pham, TM, Mo, Y, Lim, C, Pritchard, MG, Pople, D, Hall, V, Stimson, J, Eyre, DW, Read, JM, Donnelly, CA, Horby, P, Watson, C, Funk, S, Robotham, JV & Knight, GM 2023, 'The burden and dynamics of hospital-acquired SARS-CoV-2 in England', Nature, vol. 623, no. 7985, pp. 132-138. https://doi.org/10.1038/s41586-023-06634-z

APA

Cooper, B. S., Evans, S., Jafari, Y., Pham, T. M., Mo, Y., Lim, C., Pritchard, M. G., Pople, D., Hall, V., Stimson, J., Eyre, D. W., Read, J. M., Donnelly, C. A., Horby, P., Watson, C., Funk, S., Robotham, J. V., & Knight, G. M. (2023). The burden and dynamics of hospital-acquired SARS-CoV-2 in England. Nature, 623(7985), 132-138. https://doi.org/10.1038/s41586-023-06634-z

Vancouver

Cooper BS, Evans S, Jafari Y, Pham TM, Mo Y, Lim C et al. The burden and dynamics of hospital-acquired SARS-CoV-2 in England. Nature. 2023 Nov 2;623(7985):132-138. Epub 2023 Oct 18. doi: 10.1038/s41586-023-06634-z

Author

Cooper, B.S. ; Evans, S. ; Jafari, Y. et al. / The burden and dynamics of hospital-acquired SARS-CoV-2 in England. In: Nature. 2023 ; Vol. 623, No. 7985. pp. 132-138.

Bibtex

@article{3e2834b1362243ffb7d606ca5dc2ab8b,
title = "The burden and dynamics of hospital-acquired SARS-CoV-2 in England",
abstract = "Hospital-based transmission had a dominant role in Middle East respiratory syndrome coronavirus (MERS-CoV) and severe acute respiratory syndrome coronavirus (SARS-CoV) epidemics1, 2, but large-scale studies of its role in the SARS-CoV-2 pandemic are lacking. Such transmission risks spreading the virus to the most vulnerable individuals and can have wider-scale impacts through hospital–community interactions. Using data from acute hospitals in England, we quantify within-hospital transmission, evaluate likely pathways of spread and factors associated with heightened transmission risk, and explore the wider dynamical consequences. We estimate that between June 2020 and March 2021 between 95,000 and 167,000 inpatients acquired SARS-CoV-2 in hospitals (1% to 2% of all hospital admissions in this period). Analysis of time series data provided evidence that patients who themselves acquired SARS-CoV-2 infection in hospital were the main sources of transmission to other patients. Increased transmission to inpatients was associated with hospitals having fewer single rooms and lower heated volume per bed. Moreover, we show that reducing hospital transmission could substantially enhance the efficiency of punctuated lockdown measures in suppressing community transmission. These findings reveal the previously unrecognized scale of hospital transmission, have direct implications for targeting of hospital control measures and highlight the need to design hospitals better equipped to limit the transmission of future high-consequence pathogens.",
keywords = "COVID-19/epidemiology, Communicable Disease Control, Cross Infection/epidemiology, Disease Transmission, Infectious/prevention & control, England/epidemiology, Hospitals, Humans, Inpatients, Pandemics/prevention & control, Quarantine/statistics & numerical data, SARS-CoV-2",
author = "B.S. Cooper and S. Evans and Y. Jafari and T.M. Pham and Y. Mo and C. Lim and M.G. Pritchard and D. Pople and V. Hall and J. Stimson and D.W. Eyre and J.M. Read and C.A. Donnelly and P. Horby and C. Watson and S. Funk and J.V. Robotham and G.M. Knight",
year = "2023",
month = nov,
day = "2",
doi = "10.1038/s41586-023-06634-z",
language = "English",
volume = "623",
pages = "132--138",
journal = "Nature",
issn = "0028-0836",
publisher = "Nature Publishing Group",
number = "7985",

}

RIS

TY - JOUR

T1 - The burden and dynamics of hospital-acquired SARS-CoV-2 in England

AU - Cooper, B.S.

AU - Evans, S.

AU - Jafari, Y.

AU - Pham, T.M.

AU - Mo, Y.

AU - Lim, C.

AU - Pritchard, M.G.

AU - Pople, D.

AU - Hall, V.

AU - Stimson, J.

AU - Eyre, D.W.

AU - Read, J.M.

AU - Donnelly, C.A.

AU - Horby, P.

AU - Watson, C.

AU - Funk, S.

AU - Robotham, J.V.

AU - Knight, G.M.

PY - 2023/11/2

Y1 - 2023/11/2

N2 - Hospital-based transmission had a dominant role in Middle East respiratory syndrome coronavirus (MERS-CoV) and severe acute respiratory syndrome coronavirus (SARS-CoV) epidemics1, 2, but large-scale studies of its role in the SARS-CoV-2 pandemic are lacking. Such transmission risks spreading the virus to the most vulnerable individuals and can have wider-scale impacts through hospital–community interactions. Using data from acute hospitals in England, we quantify within-hospital transmission, evaluate likely pathways of spread and factors associated with heightened transmission risk, and explore the wider dynamical consequences. We estimate that between June 2020 and March 2021 between 95,000 and 167,000 inpatients acquired SARS-CoV-2 in hospitals (1% to 2% of all hospital admissions in this period). Analysis of time series data provided evidence that patients who themselves acquired SARS-CoV-2 infection in hospital were the main sources of transmission to other patients. Increased transmission to inpatients was associated with hospitals having fewer single rooms and lower heated volume per bed. Moreover, we show that reducing hospital transmission could substantially enhance the efficiency of punctuated lockdown measures in suppressing community transmission. These findings reveal the previously unrecognized scale of hospital transmission, have direct implications for targeting of hospital control measures and highlight the need to design hospitals better equipped to limit the transmission of future high-consequence pathogens.

AB - Hospital-based transmission had a dominant role in Middle East respiratory syndrome coronavirus (MERS-CoV) and severe acute respiratory syndrome coronavirus (SARS-CoV) epidemics1, 2, but large-scale studies of its role in the SARS-CoV-2 pandemic are lacking. Such transmission risks spreading the virus to the most vulnerable individuals and can have wider-scale impacts through hospital–community interactions. Using data from acute hospitals in England, we quantify within-hospital transmission, evaluate likely pathways of spread and factors associated with heightened transmission risk, and explore the wider dynamical consequences. We estimate that between June 2020 and March 2021 between 95,000 and 167,000 inpatients acquired SARS-CoV-2 in hospitals (1% to 2% of all hospital admissions in this period). Analysis of time series data provided evidence that patients who themselves acquired SARS-CoV-2 infection in hospital were the main sources of transmission to other patients. Increased transmission to inpatients was associated with hospitals having fewer single rooms and lower heated volume per bed. Moreover, we show that reducing hospital transmission could substantially enhance the efficiency of punctuated lockdown measures in suppressing community transmission. These findings reveal the previously unrecognized scale of hospital transmission, have direct implications for targeting of hospital control measures and highlight the need to design hospitals better equipped to limit the transmission of future high-consequence pathogens.

KW - COVID-19/epidemiology

KW - Communicable Disease Control

KW - Cross Infection/epidemiology

KW - Disease Transmission, Infectious/prevention & control

KW - England/epidemiology

KW - Hospitals

KW - Humans

KW - Inpatients

KW - Pandemics/prevention & control

KW - Quarantine/statistics & numerical data

KW - SARS-CoV-2

U2 - 10.1038/s41586-023-06634-z

DO - 10.1038/s41586-023-06634-z

M3 - Journal article

C2 - 37853126

VL - 623

SP - 132

EP - 138

JO - Nature

JF - Nature

SN - 0028-0836

IS - 7985

ER -