TY - JOUR
T1 - Assessment of mortality and hospital admissions associated with confirmed infection with SARS-CoV-2 Alpha variant
T2 - a matched cohort and time-to-event analysis, England, October to December 2020
AU - Dabrera, Gavin
AU - Allen, Hester
AU - Zaidi, Asad
AU - Flannagan, Joe
AU - Twohig, Katherine
AU - Thelwall, Simon
AU - Marchant, Elizabeth
AU - Aziz, Nurin Abdul
AU - Lamagni, Theresa
AU - Myers, Richard
AU - Charlett, André
AU - Capelastegui, Fernando
AU - Chudasama, Dimple
AU - Clare, Tom
AU - Coukan, Flavien
AU - Sinnathamby, Mary
AU - Ferguson, Neil
AU - Hopkins, Susan
AU - Chand, Meera
AU - Hope, Russell
AU - Kall, Meaghan
N1 - Publisher Copyright:
© 2022 European Centre for Disease Prevention and Control (ECDC). All rights reserved.
PY - 2022/5/19
Y1 - 2022/5/19
N2 - Background: The emergence of the SARS-CoV-2 Alpha variant in England coincided with a rapid increase in the number of PCR-confirmed COVID-19 cases in areas where the variant was concentrated. Aim: Our aim was to assess whether infection with Alpha was associated with more severe clinical outcomes than the wild type. Methods: Laboratory-confirmed infections with genomically sequenced SARS-CoV-2 Alpha and wild type between October and December 2020 were linked to routine healthcare and surveillance data-sets. We conducted two statistical analyses to compare the risk of hospital admission and death within 28 days of testing between Alpha and wild-type infections: a matched cohort study and an adjusted Cox proportional hazards model. We assessed differences in disease severity by comparing hospital admission and mortality, including length of hospitalisation and time to death. Results: Of 63,609 COVID-19 cases sequenced in England between October and December 2020, 6,038 had the Alpha variant. In the matched cohort analysis, we matched 2,821 cases with Alpha to 2,821 to cases with wild type. In the time-to-event analysis, we observed a 34% increased risk in hospitalisation associated with Alpha compared with wild type, but no significant difference in the risk of mortality. Conclusion: We found evidence of increased risk of hospitalisation after adjusting for key confounders, suggesting increased infection severity associated with the Alpha variant. Rapid assessments of the relative morbidity in terms of clinical outcomes and mortality associated with emerging SARS-CoV-2 variants compared with dominant variants are required to assess overall impact of SARS-CoV-2 mutations.
AB - Background: The emergence of the SARS-CoV-2 Alpha variant in England coincided with a rapid increase in the number of PCR-confirmed COVID-19 cases in areas where the variant was concentrated. Aim: Our aim was to assess whether infection with Alpha was associated with more severe clinical outcomes than the wild type. Methods: Laboratory-confirmed infections with genomically sequenced SARS-CoV-2 Alpha and wild type between October and December 2020 were linked to routine healthcare and surveillance data-sets. We conducted two statistical analyses to compare the risk of hospital admission and death within 28 days of testing between Alpha and wild-type infections: a matched cohort study and an adjusted Cox proportional hazards model. We assessed differences in disease severity by comparing hospital admission and mortality, including length of hospitalisation and time to death. Results: Of 63,609 COVID-19 cases sequenced in England between October and December 2020, 6,038 had the Alpha variant. In the matched cohort analysis, we matched 2,821 cases with Alpha to 2,821 to cases with wild type. In the time-to-event analysis, we observed a 34% increased risk in hospitalisation associated with Alpha compared with wild type, but no significant difference in the risk of mortality. Conclusion: We found evidence of increased risk of hospitalisation after adjusting for key confounders, suggesting increased infection severity associated with the Alpha variant. Rapid assessments of the relative morbidity in terms of clinical outcomes and mortality associated with emerging SARS-CoV-2 variants compared with dominant variants are required to assess overall impact of SARS-CoV-2 mutations.
UR - http://www.scopus.com/inward/record.url?scp=85130351468&partnerID=8YFLogxK
U2 - 10.2807/1560-7917.ES.2022.27.20.2100377
DO - 10.2807/1560-7917.ES.2022.27.20.2100377
M3 - Article
C2 - 35593163
AN - SCOPUS:85130351468
VL - 27
JO - Eurosurveillance
JF - Eurosurveillance
SN - 1025-496X
IS - 20
ER -