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

Q3 Medicine Baylor University Medical Center Proceedings Pub Date : 2024-07-31 eCollection Date: 2024-01-01 DOI:10.1080/08998280.2024.2379723
Christian Beltran, Jennifer Hood, Valerie Danesh, Anisha Shrestha, Gerald Ogola, Carl Boethel, Alejandro C Arroliga, Shekhar Ghamande
{"title":"Association of coinfections with differences in outcomes across COVID-19 variants.","authors":"Christian Beltran, Jennifer Hood, Valerie Danesh, Anisha Shrestha, Gerald Ogola, Carl Boethel, Alejandro C Arroliga, Shekhar Ghamande","doi":"10.1080/08998280.2024.2379723","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>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).</p><p><strong>Methods: </strong>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.</p><p><strong>Results: </strong>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.</p><p><strong>Conclusions: </strong>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.</p>","PeriodicalId":8828,"journal":{"name":"Baylor University Medical Center Proceedings","volume":"37 5","pages":"750-754"},"PeriodicalIF":0.0000,"publicationDate":"2024-07-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11332641/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Baylor University Medical Center Proceedings","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/08998280.2024.2379723","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/1/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

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.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
合并感染与 COVID-19 变体的结果差异之间的关系。
背景:在以前的研究中,所有 COVID-19 变体的继发性合并感染都会增加死亡率。然而,此前没有研究探讨过 COVID-19 变体(Alpha、Delta 和 Omicron)中合并感染与住院患者预后的关系:这项观察性队列研究涉及德克萨斯州 25 家医院的 21,186 名 COVID-19 住院患者。根据 COVID-19 的突增情况将患者分为以下几组: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)和奥米克隆组(2021 年 12 月 21 日至 2022 年 3 月 3 日)。数据来自电子健康记录,采用的方法来自病毒性呼吸道疾病普遍研究 COVID-19 登记处(NCT04323787)的 COVID-19 住院病例。多变量 Cox 比例危险回归模型评估了不同激增期对死亡率的调整效应:与 Alpha(8.5%)、Delta(11.7%)和 Omicron(11.9%)变体相关的住院激增期的细菌合并感染率各不相同。调整后的分析表明,与孤立的 COVID-19 感染相比,所有变异株在合并感染时的 30 天和 90 天死亡率都较高。特别是,与阿尔法和奥米克隆相比,德尔塔变体的30天和90天死亡率明显更低:结论:当存在细菌合并感染时,所有变体都与较高的死亡率相关。结论:当存在细菌合并感染时,所有变异株都与较高的死亡率相关,Delta与30天及之后较高的风险调整死亡率相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
1.30
自引率
0.00%
发文量
245
期刊最新文献
The importance of screening and surveillance: Barrett's esophagus and esophageal cancer. A brief descriptive analysis of a pilot study of peer support training and supervision for Texas firefighters. Contrast-associated acute kidney injury: How can we do better? "In a word, partnership"-lessons from a student-led health fair. A review of professionalism in surgery.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1