Clinical Severity of SARS-CoV-2 Omicron Variant Compared with Delta among Hospitalized COVID-19 Patients in Belgium during Autumn and Winter Season 2021–2022
This retrospective multi-center matched cohort study assessed the risk for severe COVID-19 (combination of severity indicators), intensive care unit (ICU) admission, and in-hospital mortality in hospitalized patients when infected with the Omicron variant compared to when infected with the Delta var...
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MDPI AG
2022-06-01
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Online Access: | https://www.mdpi.com/1999-4915/14/6/1297 |
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author | Nina Van Goethem Pui Yan Jenny Chung Marjan Meurisse Mathil Vandromme Laurane De Mot Ruben Brondeel Veerle Stouten Sofieke Klamer Lize Cuypers Toon Braeye Lucy Catteau Louis Nevejan Joris A. F. van Loenhout Koen Blot |
author_facet | Nina Van Goethem Pui Yan Jenny Chung Marjan Meurisse Mathil Vandromme Laurane De Mot Ruben Brondeel Veerle Stouten Sofieke Klamer Lize Cuypers Toon Braeye Lucy Catteau Louis Nevejan Joris A. F. van Loenhout Koen Blot |
author_sort | Nina Van Goethem |
collection | DOAJ |
description | This retrospective multi-center matched cohort study assessed the risk for severe COVID-19 (combination of severity indicators), intensive care unit (ICU) admission, and in-hospital mortality in hospitalized patients when infected with the Omicron variant compared to when infected with the Delta variant. The study is based on a causal framework using individually-linked data from national COVID-19 registries. The study population consisted of 954 COVID-19 patients (of which, 445 were infected with Omicron) above 18 years old admitted to a Belgian hospital during the autumn and winter season 2021–2022, and with available viral genomic data. Patients were matched based on the hospital, whereas other possible confounders (demographics, comorbidities, vaccination status, socio-economic status, and ICU occupancy) were adjusted for by using a multivariable logistic regression analysis. The estimated standardized risk for severe COVID-19 and ICU admission in hospitalized patients was significantly lower (RR = 0.63; 95% CI (0.30; 0.97) and RR = 0.56; 95% CI (0.14; 0.99), respectively) when infected with the Omicron variant, whereas in-hospital mortality was not significantly different according to the SARS-CoV-2 variant (RR = 0.78, 95% CI (0.28–1.29)). This study demonstrates the added value of integrated genomic and clinical surveillance to recognize the multifactorial nature of COVID-19 pathogenesis. |
first_indexed | 2024-03-09T22:14:09Z |
format | Article |
id | doaj.art-4097a250a35248f9a50d4562588816be |
institution | Directory Open Access Journal |
issn | 1999-4915 |
language | English |
last_indexed | 2024-03-09T22:14:09Z |
publishDate | 2022-06-01 |
publisher | MDPI AG |
record_format | Article |
series | Viruses |
spelling | doaj.art-4097a250a35248f9a50d4562588816be2023-11-23T19:27:01ZengMDPI AGViruses1999-49152022-06-01146129710.3390/v14061297Clinical Severity of SARS-CoV-2 Omicron Variant Compared with Delta among Hospitalized COVID-19 Patients in Belgium during Autumn and Winter Season 2021–2022Nina Van Goethem0Pui Yan Jenny Chung1Marjan Meurisse2Mathil Vandromme3Laurane De Mot4Ruben Brondeel5Veerle Stouten6Sofieke Klamer7Lize Cuypers8Toon Braeye9Lucy Catteau10Louis Nevejan11Joris A. F. van Loenhout12Koen Blot13Scientific Directorate of Epidemiology and Public Health, Sciensano, J. Wytsmanstraat 14, 1050 Brussels, BelgiumScientific Directorate of Epidemiology and Public Health, Sciensano, J. Wytsmanstraat 14, 1050 Brussels, BelgiumScientific Directorate of Epidemiology and Public Health, Sciensano, J. Wytsmanstraat 14, 1050 Brussels, BelgiumScientific Directorate of Epidemiology and Public Health, Sciensano, J. Wytsmanstraat 14, 1050 Brussels, BelgiumScientific Directorate of Epidemiology and Public Health, Sciensano, J. Wytsmanstraat 14, 1050 Brussels, BelgiumScientific Directorate of Epidemiology and Public Health, Sciensano, J. Wytsmanstraat 14, 1050 Brussels, BelgiumScientific Directorate of Epidemiology and Public Health, Sciensano, J. Wytsmanstraat 14, 1050 Brussels, BelgiumScientific Directorate of Epidemiology and Public Health, Sciensano, J. Wytsmanstraat 14, 1050 Brussels, BelgiumClinical Department of Laboratory Medicine and National Reference Center for Respiratory Pathogens, University Hospitals Leuven, 3000 Leuven, BelgiumScientific Directorate of Epidemiology and Public Health, Sciensano, J. Wytsmanstraat 14, 1050 Brussels, BelgiumScientific Directorate of Epidemiology and Public Health, Sciensano, J. Wytsmanstraat 14, 1050 Brussels, BelgiumClinical Department of Laboratory Medicine and National Reference Center for Respiratory Pathogens, University Hospitals Leuven, 3000 Leuven, BelgiumScientific Directorate of Epidemiology and Public Health, Sciensano, J. Wytsmanstraat 14, 1050 Brussels, BelgiumScientific Directorate of Epidemiology and Public Health, Sciensano, J. Wytsmanstraat 14, 1050 Brussels, BelgiumThis retrospective multi-center matched cohort study assessed the risk for severe COVID-19 (combination of severity indicators), intensive care unit (ICU) admission, and in-hospital mortality in hospitalized patients when infected with the Omicron variant compared to when infected with the Delta variant. The study is based on a causal framework using individually-linked data from national COVID-19 registries. The study population consisted of 954 COVID-19 patients (of which, 445 were infected with Omicron) above 18 years old admitted to a Belgian hospital during the autumn and winter season 2021–2022, and with available viral genomic data. Patients were matched based on the hospital, whereas other possible confounders (demographics, comorbidities, vaccination status, socio-economic status, and ICU occupancy) were adjusted for by using a multivariable logistic regression analysis. The estimated standardized risk for severe COVID-19 and ICU admission in hospitalized patients was significantly lower (RR = 0.63; 95% CI (0.30; 0.97) and RR = 0.56; 95% CI (0.14; 0.99), respectively) when infected with the Omicron variant, whereas in-hospital mortality was not significantly different according to the SARS-CoV-2 variant (RR = 0.78, 95% CI (0.28–1.29)). This study demonstrates the added value of integrated genomic and clinical surveillance to recognize the multifactorial nature of COVID-19 pathogenesis.https://www.mdpi.com/1999-4915/14/6/1297SARS-CoV-2COVID-19OmicronDeltagenomic surveillance |
spellingShingle | Nina Van Goethem Pui Yan Jenny Chung Marjan Meurisse Mathil Vandromme Laurane De Mot Ruben Brondeel Veerle Stouten Sofieke Klamer Lize Cuypers Toon Braeye Lucy Catteau Louis Nevejan Joris A. F. van Loenhout Koen Blot Clinical Severity of SARS-CoV-2 Omicron Variant Compared with Delta among Hospitalized COVID-19 Patients in Belgium during Autumn and Winter Season 2021–2022 Viruses SARS-CoV-2 COVID-19 Omicron Delta genomic surveillance |
title | Clinical Severity of SARS-CoV-2 Omicron Variant Compared with Delta among Hospitalized COVID-19 Patients in Belgium during Autumn and Winter Season 2021–2022 |
title_full | Clinical Severity of SARS-CoV-2 Omicron Variant Compared with Delta among Hospitalized COVID-19 Patients in Belgium during Autumn and Winter Season 2021–2022 |
title_fullStr | Clinical Severity of SARS-CoV-2 Omicron Variant Compared with Delta among Hospitalized COVID-19 Patients in Belgium during Autumn and Winter Season 2021–2022 |
title_full_unstemmed | Clinical Severity of SARS-CoV-2 Omicron Variant Compared with Delta among Hospitalized COVID-19 Patients in Belgium during Autumn and Winter Season 2021–2022 |
title_short | Clinical Severity of SARS-CoV-2 Omicron Variant Compared with Delta among Hospitalized COVID-19 Patients in Belgium during Autumn and Winter Season 2021–2022 |
title_sort | clinical severity of sars cov 2 omicron variant compared with delta among hospitalized covid 19 patients in belgium during autumn and winter season 2021 2022 |
topic | SARS-CoV-2 COVID-19 Omicron Delta genomic surveillance |
url | https://www.mdpi.com/1999-4915/14/6/1297 |
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