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Impact of the Coronavirus Disease 2019 (COVID-19) Pandemic on Invasive Pneumococcal Disease and Risk of Pneumococcal Coinfection With Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2): Prospective National Cohort Study, England.

Amin-Chowdhury, Z; Aiano, F; Mensah, A; Sheppard, CL; Litt, D; Fry, NK; Andrews, N; Ramsay, ME; Ladhani, SN (2021) Impact of the Coronavirus Disease 2019 (COVID-19) Pandemic on Invasive Pneumococcal Disease and Risk of Pneumococcal Coinfection With Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2): Prospective National Cohort Study, England. Clin Infect Dis, 72 (5). e65-e75. ISSN 1537-6591 https://doi.org/10.1093/cid/ciaa1728
SGUL Authors: Ladhani, Shamez Nizarali

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Abstract

BACKGROUND: Streptococcus pneumoniae coinfection with influenza results in synergistic lethality, but there are limited data on pneumococcal coinfection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). METHODS: Public Health England conducts invasive pneumococcal disease (IPD) and SARS-CoV-2 surveillance in England. IPD trends during 2000/2001-2019/2020 epidemiological years were analyzed and cases during February-June 2020 linked with laboratory-confirmed SARS-CoV-2 infections. Multivariable logistic regression was used to assess risk factors for death. RESULTS: IPD incidence in 2019/2020 (7.6/100 000; n = 3964) was 30% (IRR, .70; 95% CI, .18-2.67) lower compared with 2018/2019 (10.9/100 000; n = 5666), with large reductions observed across all age groups during March-June 2020. There were 160 886 SARS-CoV-2 and 1137 IPD cases during February-June 2020, including 40 IPD/coronavirus disease 2019 (COVID-19) co-infections (.025% [95% CI, .018-.034] of SARS-CoV-2 infections; 3.5% [2.5-4.8] of IPD cases), 21 with COVID-19 diagnosed 3-27 days after IPD, and 27 who developed COVID-19 ≥28 days after IPD. Case-fatality rates (CFRs) were 62.5 (25/40), 47.6% (10/21), and 33.3% (9/27), respectively (P < .001). In addition to an independent association with increasing age and serotype group, CFR was 7.8-fold (95% CI, 3.8-15.8) higher in those with IPD/COVID-19 coinfection and 3.9-fold (95% CI, 1.4-10.7) higher in patients who developed COVID-19 3-27 days after IPD compared with patients with IPD only. CONCLUSIONS: Large declines in IPD were observed following COVID-19 lockdown. IPD/COVID-19 coinfections were rare but associated with high CFR, mainly in older adults. The rarity, age and serotype distribution of IPD/COVID-19 coinfections do not support wider extension of pneumococcal vaccination.

Item Type: Article
Additional Information: © Crown copyright 2020. This Open Access article contains public sector information licensed under the Open Government Licence v3.0 (http://www.nationalarchives.gov.uk/doc/open-government-licence/version/3/).
Keywords: bacterial coinfection, case fatality, nosocomial infection, pneumococcal disease, risk factor, Aged, COVID-19, Cohort Studies, Coinfection, Communicable Disease Control, England, Humans, Pandemics, Pneumococcal Infections, Prospective Studies, SARS-CoV-2, Streptococcus pneumoniae, Humans, Streptococcus pneumoniae, Pneumococcal Infections, Cohort Studies, Prospective Studies, Communicable Disease Control, Aged, England, Pandemics, Coinfection, COVID-19, SARS-CoV-2, pneumococcal disease, bacterial coinfection, nosocomial infection, case fatality, risk factor, bacterial coinfection, case fatality, nosocomial infection, pneumococcal disease, risk factor, Aged, COVID-19, Cohort Studies, Coinfection, Communicable Disease Control, England, Humans, Pandemics, Pneumococcal Infections, Prospective Studies, SARS-CoV-2, Streptococcus pneumoniae, 06 Biological Sciences, 11 Medical and Health Sciences, Microbiology
SGUL Research Institute / Research Centre: Academic Structure > Infection and Immunity Research Institute (INII)
Journal or Publication Title: Clin Infect Dis
ISSN: 1537-6591
Language: eng
Dates:
DateEvent
1 March 2021Published
16 November 2020Published Online
11 November 2020Accepted
PubMed ID: 33196783
Web of Science ID: WOS:000637029200001
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/113614
Publisher's version: https://doi.org/10.1093/cid/ciaa1728

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