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合并感染与不同新冠病毒变异株的预后差异之间的关联。

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

作者信息

Beltran Christian, Hood Jennifer, Danesh Valerie, Shrestha Anisha, Ogola Gerald, Boethel Carl, Arroliga Alejandro C, Ghamande Shekhar

机构信息

Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Baylor Scott & White Medical Center - Temple, Temple, Texas, USA.

Center for Applied Health Research, Baylor Scott & White Health, Dallas, Texas, USA.

出版信息

Proc (Bayl Univ Med Cent). 2024 Jul 31;37(5):750-754. doi: 10.1080/08998280.2024.2379723. eCollection 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.

摘要

背景

在先前的研究中,所有新冠病毒变异株的继发性合并感染都会导致死亡率上升。然而,此前尚无研究探讨新冠病毒变异株(阿尔法、德尔塔和奥密克戎)中合并感染与住院患者预后之间的关联。

方法

这项观察性队列研究纳入了德克萨斯州25家医院的21186例新冠病毒住院患者。患者按新冠病毒感染高峰分为几组:阿尔法组(2020年11月1日至2021年2月10日)、德尔塔组(2021年7月10日至2021年10月14日)和奥密克戎组(2021年12月21日至2022年3月3日)。使用新冠病毒住院患者的病毒呼吸道疾病通用研究新冠病毒注册库(NCT04323787)中的方法,从电子健康记录中收集数据。多变量Cox比例风险回归模型评估了不同感染高峰时期对死亡率的调整影响。

结果

与阿尔法变异株(8.5%)、德尔塔变异株(11.7%)和奥密克戎变异株(11.9%)相关的住院高峰期间,细菌合并感染情况有所不同。校正分析显示,与单纯新冠病毒感染相比,所有变异株出现合并感染时,30天和90天死亡率更高。特别是,与阿尔法和奥密克戎变异株相比,德尔塔变异株的30天和90天死亡率明显更高。

结论

出现细菌合并感染时,所有变异株都与较高的死亡率相关。德尔塔变异株在30天及之后与更高的风险调整死亡率相关。

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1
Association of coinfections with differences in outcomes across COVID-19 variants.合并感染与不同新冠病毒变异株的预后差异之间的关联。
Proc (Bayl Univ Med Cent). 2024 Jul 31;37(5):750-754. doi: 10.1080/08998280.2024.2379723. eCollection 2024.

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