• FluTrackers.com Inc. does not provide medical advice. Information on this web site is collected from various internet resources, and the FluTrackers board of directors makes no warranty to the safety, efficacy, correctness or completeness of the information posted on this site by any author or poster. The information collated here is for instructional and/or discussion purposes only and is NOT intended to diagnose or treat any disease, illness, or other medical condition. Every individual reader or poster should seek advice from their personal physician/healthcare practitioner before considering or using any interventions that are discussed on this website. By continuing to access this website you agree to consult your personal physican before using any interventions posted on this website, and you agree to hold harmless FluTrackers.com Inc., the board of directors, the members, and all authors and posters for any effects from use of any medication, supplement, vitamin or other substance, device, intervention, etc. mentioned in posts on this website, or other internet venues referenced in posts on this website.
  • We are not asking for any donations. Do not donate to any entity who says they are raising funds for us.

J Infect Chemother . Clinical outcomes of COVID-19 caused by the Alpha variant compared with one by wild type in Kobe, Japan. A multi-center nested

tetano

Editor, Senior Moderator
J Infect Chemother


. 2022 Dec 6;S1341-321X(22)00321-X.
doi: 10.1016/j.jiac.2022.11.014. Online ahead of print.
Clinical outcomes of COVID-19 caused by the Alpha variant compared with one by wild type in Kobe, Japan. A multi-center nested case-control study


Asako Doi[SUP] 1 [/SUP], Kentaro Iwata[SUP] 2 [/SUP], Tadahiro Nakamura[SUP] 3 [/SUP], Koji Oh[SUP] 4 [/SUP], Kenichi Isome[SUP] 5 [/SUP], Kohei Hasegawa[SUP] 6 [/SUP], Hirokazu Kuroda[SUP] 6 [/SUP], Toshikazu Hasuike[SUP] 6 [/SUP], Ryutaro Seo[SUP] 7 [/SUP], Hisato Kohsai[SUP] 8 [/SUP], Noriko Nakanishi[SUP] 9 [/SUP], Ryohei Nomoto[SUP] 9 [/SUP], Riyo Fujiyama[SUP] 8 [/SUP], Nobuya Kusunoki[SUP] 8 [/SUP], Tomotada Iwamoto[SUP] 9 [/SUP], Hiroaki Nishioka[SUP] 6 [/SUP], Keisuke Tomii[SUP] 10 [/SUP], Yasuki Kihara[SUP] 11 [/SUP]



Affiliations

Abstract

Objectives: The emergence of the Alpha variant of novel coronavirus 2019 (SARS-CoV-2) is a concerning issue but their clinical implications have not been investigated fully.
Methods: We conducted a nested case-control study to compare severity and mortality caused by the Alpha variant (B.1.1.7) with the one caused by the wild type as a control from December 2020 to March 2021, using whole-genome sequencing. 28-day mortality and other clinically important outcomes were evaluated.
Results: Infections caused by the Alpha variant were associated with an increase in the use of oxygen (43.4% vs 26.3%. p = 0.017), high flow nasal cannula (21.2% vs 4.0%, p = 0.0007), mechanical ventilation (16.2% vs 6.1%, p = 0.049), ICU care (30.3% vs 14.1%, p = 0.01) and the length of hospital stay (17 vs 10 days, p = 0.031). More patients with the Alpha variant received medications such as dexamethasone. However, the duration of each modality did not differ between the 2 groups. Likewise, there was no difference in 28-day mortality between the 2 groups (12% vs 8%, p = 0.48), even after multiple sensitivity analyses, including propensity score analysis.
Conclusion: The Alpha variant was associated with a severe form of COVID-19, compared with the non-Alpha wild type, but might not be associated with higher mortality.

Keywords: Alpha variant; COVID-19; Clinical outcomes.
 
Back
Top Bottom