TY - JOUR
T1 - Risk of intensive care unit admission and mortality in patients hospitalized due to influenza A or B and SARS‑CoV‑2 variants Omicron or Delta
AU - the COVID-19 Omicron Delta study group collaborators
AU - Rezahosseini, Omid
AU - Roed, Casper
AU - Sejdic, Adin
AU - Eiberg, Mads Frederik
AU - Nielsen, Lene
AU - Boel, Jonas
AU - Johannesen, Caroline Klint
AU - van Wijhe, Maarten
AU - Franck, Kristina Træholt
AU - Ostrowski, Sisse Rye
AU - Lindegaard, Birgitte
AU - Fischer, Thea K.
AU - Knudsen, Troels Bygum
AU - Holler, Jon Gitz
AU - Harboe, Zitta Barrella
AU - Lindgaard-Jensen, Betina
AU - Søborg, Christian
AU - Nielsen, Thyge Lynghøj
AU - Bernhard, Peter Haahr
AU - Pedersen, Emilie Marie Juelstorp
AU - Egelund, Gertrud Baunbæk
AU - Mathiesen, Inger Hee Mabuza
AU - Jespersen, Naja Zenius
AU - Petersen, Pelle Trier
AU - Seitz-Rasmussen, Hans Eric Sebastian
AU - Bertelsen, Barbara Bonnesen
AU - Bestle, Morten
AU - Andersen, Henrik
AU - Skram, Thomas Ulrik
AU - Altaraihi, Sarah
AU - Sivapalan, Pradeesh
AU - Jensen, Jens Ulrik Stæhr
AU - Bagge, Kristian
AU - Jørgensen, Kristina Melbardis
AU - Ahlström, Magnus Glindvad
AU - Rytter, Sofie
AU - le Dous, Nina
AU - Ravn, Pernille
AU - Reiter, Nanna
AU - Podlekareva, Daria
AU - Knudsen, Jesper Andreas
AU - Kristensen, Lars Erik
AU - Leding, Cæcilie
AU - Benfield, Thomas
AU - Kirk, Ole
AU - Sigurdsson, Sigurdur Thor
AU - Pedersen, Martin Schou
N1 - Funding Information:
The study was funded by Independent Research Fund (grant number 0134\u201000257B), the Lundbeck Foundation (grant number R349\u20102020\u2010835), the Helen Rudes Foundation, and the Danish Cancer Society (grant number KBVU\u2010MS R327\u2010A19137).
PY - 2024/7
Y1 - 2024/7
N2 - Background: Respiratory viral infections have significant global health impacts. We compared 30-day intensive care unit (ICU) admission and all-cause mortality risks in patients with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Delta and Omicron variants versus influenza A and B (A/B). Methods: Data from two retrospective inpatient cohorts in Copenhagen were analyzed. Cohorts included hospitalized influenza A/B patients (2017–2018) and SARS-CoV-2 Delta/Omicron patients (2021–2022), aged ≥18 years, admitted within 14 days of a positive real-time polymerase chain reaction test result. Cumulative ICU admission and mortality rates were estimated using the Aalen–Johansen estimator. Cox regression models calculated hazard ratios (HRs) for ICU admission and mortality. Results: The study encompassed 1459 inpatients (Delta: 49%; Omicron: 26%; influenza A: 6.4%; and influenza B: 18%). Cumulative incidence of ICU admission was 11%, 4.0%, 7.5%, and 4.1%, for Delta, Omicron, influenza A, and B, respectively. For ICU admission, adjusted HRs (aHRs) were 3.1 (p <.001) and 1.5 (p =.34) for Delta and Omicron versus influenza B, and 1.5 (p =.36) and 0.71 (p =.48) versus influenza A. For mortality, aHRs were 3.8 (p <.001) and 3.4 (p <.001) for Delta and Omicron versus influenza B, and 2.1 (p =.04) and 1.9 (p =.11) versus influenza A. Conclusion: Delta but not Omicron inpatients had an increased risk for ICU admission compared to influenza B; however, both variants were associated with higher risks of mortality than influenza B. Only Delta inpatients had a higher risk of mortality than influenza A inpatients.
AB - Background: Respiratory viral infections have significant global health impacts. We compared 30-day intensive care unit (ICU) admission and all-cause mortality risks in patients with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Delta and Omicron variants versus influenza A and B (A/B). Methods: Data from two retrospective inpatient cohorts in Copenhagen were analyzed. Cohorts included hospitalized influenza A/B patients (2017–2018) and SARS-CoV-2 Delta/Omicron patients (2021–2022), aged ≥18 years, admitted within 14 days of a positive real-time polymerase chain reaction test result. Cumulative ICU admission and mortality rates were estimated using the Aalen–Johansen estimator. Cox regression models calculated hazard ratios (HRs) for ICU admission and mortality. Results: The study encompassed 1459 inpatients (Delta: 49%; Omicron: 26%; influenza A: 6.4%; and influenza B: 18%). Cumulative incidence of ICU admission was 11%, 4.0%, 7.5%, and 4.1%, for Delta, Omicron, influenza A, and B, respectively. For ICU admission, adjusted HRs (aHRs) were 3.1 (p <.001) and 1.5 (p =.34) for Delta and Omicron versus influenza B, and 1.5 (p =.36) and 0.71 (p =.48) versus influenza A. For mortality, aHRs were 3.8 (p <.001) and 3.4 (p <.001) for Delta and Omicron versus influenza B, and 2.1 (p =.04) and 1.9 (p =.11) versus influenza A. Conclusion: Delta but not Omicron inpatients had an increased risk for ICU admission compared to influenza B; however, both variants were associated with higher risks of mortality than influenza B. Only Delta inpatients had a higher risk of mortality than influenza A inpatients.
KW - influenza A
KW - influenza B
KW - intensive care units
KW - Mortality
KW - SARS-CoV-2 Delta variants
KW - SARS-CoV-2 Omicron variant
KW - influenza A
KW - influenza B
KW - intensive care units
KW - Mortality
KW - SARS-CoV-2 Delta variants
KW - SARS-CoV-2 Omicron variant
U2 - 10.1002/iid3.1269
DO - 10.1002/iid3.1269
M3 - Journal article
AN - SCOPUS:85197802004
SN - 2050-4527
VL - 12
JO - Immunity, Inflammation and Disease
JF - Immunity, Inflammation and Disease
IS - 7
M1 - e1269
ER -