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Research Article

Association of coinfections with differences in outcomes across COVID-19 variants

, MDORCID Icon, , DO, , PhD, , MPH, , PhD, , MD, , MD & , MD show all
Received 02 May 2024, Accepted 02 Jul 2024, Published online: 31 Jul 2024
 

Abstract

Background

In previous studies, there was an increase in mortality with secondary coinfections in all COVID-19 variants. However, no prior study has explored the association of coinfection with outcomes of hospitalized patients among the COVID-19 variants (Alpha, Delta, and Omicron).

Methods

This observational cohort study involved 21,186 patients hospitalized with COVID-19 in 25 hospitals in Texas. Patients were divided into groups by surges of COVID-19: Alpha (November 1, 2020–February 10, 2021), Delta (July 10, 2021–October 14, 2021), and Omicron (December 21, 2021–March 3, 2022). Data were collected from electronic health records using methodology from the Viral Respiratory Illness Universal Study COVID-19 registry (NCT04323787) of COVID-19 hospitalizations. Multivariable Cox-proportional hazard regression model assessed the adjusted effect of different surge periods on mortality.

Results

Bacterial coinfections varied among hospitalization surges associated with Alpha (8.5%), Delta (11.7%), and Omicron (11.9%) variants. Adjusted analyses showed a higher 30-day and 90-day mortality in all variants when coinfections were present compared with isolated COVID-19 infection. In particular, 30-day and 90-day mortality were significantly worse with Delta compared to Alpha and Omicron.

Conclusions

All variants were associated with a higher mortality when bacterial coinfections were present. Delta was associated with a higher risk-adjusted mortality at 30 days and thereafter.

Disclosure statement/Funding

This work was partially funded by the Cardiovascular Research Review Committee of the Baylor Scott & White Health, Society of Critical Care Medicine, and the Gordon and Betty Moore Foundation. The authors report no conflicts of interest.

Additional information

Funding

This work was partially funded by the Cardiovascular Research Review Committee of the Baylor Scott & White Health, Society of Critical Care Medicine, and the Gordon and Betty Moore Foundation

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