• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

2019冠状病毒病患者中严重急性呼吸综合征冠状病毒2与甲型/乙型流感病毒的合并感染:一项系统评价和荟萃分析

Co-infection of SARS-CoV-2 and influenza A/B among patients with COVID-19: a systematic review and meta-analysis.

作者信息

Golpour Monireh, Jalali Hossein, Alizadeh-Navaei Reza, Talarposhti Masoumeh Rezaei, Mousavi Tahoora, Ghara Ali Asghar Nadi

机构信息

Cancer Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, Iran.

Thalassemia Research Center, Hemoglobinopathy Institute, Mazandaran University of Medical Sciences, Sari, Iran.

出版信息

BMC Infect Dis. 2025 Jan 31;25(1):145. doi: 10.1186/s12879-025-10521-5.

DOI:10.1186/s12879-025-10521-5
PMID:39891054
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11783914/
Abstract

BACKGROUND

The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) that causes coronavirus disease 2019 (COVID-19) is a public health problem and may result in co-infection with other pathogens such as influenza virus. This review investigates the co-infection of SARS-CoV-2 and influenza A/B among patients with COVID-19.

METHODS

This meta- analysis included 38 primary studies investigating co-infection of SARS-CoV-2 with influenza in confirmed cases of COVID-19. The global online databases were used to identify relevant studies published between December 2019 and July 2024. Data analysis was performed using STATA Ver. 17 software, and standard errors of prevalence were calculated using the binomial distribution formula. Heterogeneity of study results was evaluated using the I-square and Q index, and publication bias was examined using the Begg's and Egger's tests, as well as funnel plot. A random effects model was used to determine prevalence rates, and a forest plot diagram was used to present results with 95% confidence intervals. In addition, sensitivity analyses were performed to check the impact of each primary study on the overall estimate.

RESULT

The analysis found that the prevalence of influenza in co-infected patients at 95% confidence interval using a random effect model was 14% (95% CI: 8-20%). Significant heterogeneity was observed in the random-effects model for influenza A, 11% (95% CI: 5-18%) and B, 4% (95% CI: 2-7%) in co-infected patients. The highest prevalence of influenza A/B (21%), influenza A (17%) and influenza B (20%) was shown in Asia and Europe respectively. Subgroup analysis by study year showed that the co-prevalence of COVID-19 and influenza A/B was similar in the pre-2021 and post-2021 time periods, at 14% (95% CI: 5-23%) for pre-2021 and 6-22% for 2021 and post-2021. Also, the overall prevalence of influenza A and B in COVID-19 patients is 11% and 4%, and there was no significant difference between the time periods before and after 2021. Meta-regression with a random-effects model showed that the variables location, year group, and total patients showed only 2.71% of very high heterogeneity (I² = 99.92%), and none of these variables had a significant effect on the co-prevalence of COVID-19 and influenza A/B (p > 0.05). Also, meta-regression results showed that these variables had no significant effect on influenza A and B prevalence (p > 0.05) and showed only a small proportion of the very high heterogeneity (I² = 99.72%), (I² = 68.78%). In our study, Egger's test indicated that there was publication bias or small study effects in this meta-analysis (p = 0.0000).

CONCLUSION

The combination of SARS-CoV-2 with influenza and other respiratory viruses requires the best treatment protocols to reduce the severity of the disease. In this approach, high vaccination coverage against seasonal influenza and SARS-CoV-2 could reduce the risk of co-infection in the recent pandemic.

摘要

背景

导致2019冠状病毒病(COVID-19)的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)是一个公共卫生问题,可能导致与其他病原体如流感病毒的合并感染。本综述调查了COVID-19患者中SARS-CoV-2与甲型/乙型流感的合并感染情况。

方法

这项荟萃分析纳入了38项关于COVID-19确诊病例中SARS-CoV-2与流感合并感染情况的初步研究。使用全球在线数据库来识别2019年12月至2024年7月期间发表的相关研究。使用STATA 17软件进行数据分析,并使用二项分布公式计算患病率的标准误差。使用I²和Q指数评估研究结果的异质性,并使用Begg检验、Egger检验以及漏斗图来检查发表偏倚。采用随机效应模型确定患病率,并使用森林图展示结果及其95%置信区间。此外,进行敏感性分析以检查每项初步研究对总体估计值的影响。

结果

分析发现,采用随机效应模型,合并感染患者中流感的患病率在95%置信区间为14%(95%CI:8-20%)。在随机效应模型中,合并感染患者中甲型流感的患病率为11%(95%CI:5-18%),乙型流感的患病率为4%(95%CI:2-7%),观察到显著的异质性。甲型/乙型流感、甲型流感和乙型流感的患病率在亚洲和欧洲分别达到最高,分别为21%、17%和20%。按研究年份进行的亚组分析显示,2021年之前和2021年之后COVID-19与甲型/乙型流感的合并患病率相似,2021年之前为14%(95%CI:5-23%),2021年及之后为6-22%。此外,COVID-19患者中甲型和乙型流感的总体患病率分别为11%和4%,2021年前后各时间段之间无显著差异。随机效应模型的Meta回归显示,变量地点、年份组和患者总数仅显示出2.71%的极高异质性(I² = 99.92%),且这些变量均对COVID-19与甲型/乙型流感的合并患病率无显著影响(p>0.05)。此外,Meta回归结果显示,这些变量对甲型和乙型流感患病率无显著影响(p>0.05),仅显示出一小部分极高的异质性(I² = 99.72%),(I² = 68.78%)。在我们的研究中,Egger检验表明该荟萃分析存在发表偏倚或小型研究效应(p = 0.0000)。

结论

SARS-CoV-2与流感及其他呼吸道病毒的合并感染需要最佳治疗方案以降低疾病严重程度。通过这种方式,针对季节性流感和SARS-CoV-2的高疫苗接种覆盖率可降低近期大流行中合并感染的风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09f6/11783914/5c9b0afb6c27/12879_2025_10521_Fig14_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09f6/11783914/d4ea749e2acd/12879_2025_10521_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09f6/11783914/42a195ff22ec/12879_2025_10521_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09f6/11783914/6079c3b8928c/12879_2025_10521_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09f6/11783914/ef91da421d92/12879_2025_10521_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09f6/11783914/aaed3cf20317/12879_2025_10521_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09f6/11783914/fcbd1f9d495a/12879_2025_10521_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09f6/11783914/6ea988eefb8e/12879_2025_10521_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09f6/11783914/b3d777efa43c/12879_2025_10521_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09f6/11783914/22b5794c968b/12879_2025_10521_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09f6/11783914/04ffefbb0fc9/12879_2025_10521_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09f6/11783914/7f320cbcff25/12879_2025_10521_Fig11_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09f6/11783914/2567fd0396ab/12879_2025_10521_Fig12_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09f6/11783914/a6bdce4aa5f4/12879_2025_10521_Fig13_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09f6/11783914/5c9b0afb6c27/12879_2025_10521_Fig14_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09f6/11783914/d4ea749e2acd/12879_2025_10521_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09f6/11783914/42a195ff22ec/12879_2025_10521_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09f6/11783914/6079c3b8928c/12879_2025_10521_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09f6/11783914/ef91da421d92/12879_2025_10521_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09f6/11783914/aaed3cf20317/12879_2025_10521_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09f6/11783914/fcbd1f9d495a/12879_2025_10521_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09f6/11783914/6ea988eefb8e/12879_2025_10521_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09f6/11783914/b3d777efa43c/12879_2025_10521_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09f6/11783914/22b5794c968b/12879_2025_10521_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09f6/11783914/04ffefbb0fc9/12879_2025_10521_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09f6/11783914/7f320cbcff25/12879_2025_10521_Fig11_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09f6/11783914/2567fd0396ab/12879_2025_10521_Fig12_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09f6/11783914/a6bdce4aa5f4/12879_2025_10521_Fig13_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09f6/11783914/5c9b0afb6c27/12879_2025_10521_Fig14_HTML.jpg

相似文献

1
Co-infection of SARS-CoV-2 and influenza A/B among patients with COVID-19: a systematic review and meta-analysis.2019冠状病毒病患者中严重急性呼吸综合征冠状病毒2与甲型/乙型流感病毒的合并感染:一项系统评价和荟萃分析
BMC Infect Dis. 2025 Jan 31;25(1):145. doi: 10.1186/s12879-025-10521-5.
2
Folic acid supplementation and malaria susceptibility and severity among people taking antifolate antimalarial drugs in endemic areas.在流行地区,服用抗叶酸抗疟药物的人群中,叶酸补充剂与疟疾易感性和严重程度的关系。
Cochrane Database Syst Rev. 2022 Feb 1;2(2022):CD014217. doi: 10.1002/14651858.CD014217.
3
Antibody tests for identification of current and past infection with SARS-CoV-2.用于识别当前和既往感染新型冠状病毒2的抗体检测。
Cochrane Database Syst Rev. 2020 Jun 25;6(6):CD013652. doi: 10.1002/14651858.CD013652.
4
Physical interventions to interrupt or reduce the spread of respiratory viruses.中断或减少呼吸道病毒传播的物理干预措施。
Cochrane Database Syst Rev. 2020 Nov 20;11(11):CD006207. doi: 10.1002/14651858.CD006207.pub5.
5
The epidemiology and clinical characteristics of co-infection of SARS-CoV-2 and influenza viruses in patients during COVID-19 outbreak.新型冠状病毒肺炎大流行期间 SARS-CoV-2 和流感病毒合并感染患者的流行病学和临床特征。
J Med Virol. 2020 Nov;92(11):2870-2873. doi: 10.1002/jmv.26163. Epub 2020 Jul 6.
6
Immunopathological similarities between COVID-19 and influenza: Investigating the consequences of Co-infection.新型冠状病毒肺炎与流感的免疫病理学相似性:探讨合并感染的后果。
Microb Pathog. 2021 Mar;152:104554. doi: 10.1016/j.micpath.2020.104554. Epub 2020 Nov 3.
7
Antibody tests for identification of current and past infection with SARS-CoV-2.抗体检测用于鉴定 SARS-CoV-2 的现症感染和既往感染。
Cochrane Database Syst Rev. 2022 Nov 17;11(11):CD013652. doi: 10.1002/14651858.CD013652.pub2.
8
Physical interventions to interrupt or reduce the spread of respiratory viruses.物理干预措施以阻断或减少呼吸道病毒的传播。
Cochrane Database Syst Rev. 2023 Jan 30;1(1):CD006207. doi: 10.1002/14651858.CD006207.pub6.
9
Prevalence and associated outcomes of coinfection between SARS-CoV-2 and influenza: a systematic review and meta-analysis.SARS-CoV-2 与流感共感染的流行率及相关结局:系统评价和荟萃分析。
Int J Infect Dis. 2023 Nov;136:29-36. doi: 10.1016/j.ijid.2023.08.021. Epub 2023 Aug 28.
10
Prevalence of Co-Infections in Primary Care Patients with Medically Attended Acute Respiratory Infection in the 2022/2023 Season.2022/2023 年度初级保健中因急性呼吸道感染就诊患者的合并感染发生率。
Viruses. 2024 Aug 13;16(8):1289. doi: 10.3390/v16081289.

引用本文的文献

1
Prevalence of Viral and Bacterial Co-Infections in SARS-CoV-2-Positive Individuals in Cyprus 2020-2022.2020 - 2022年塞浦路斯新冠病毒检测呈阳性个体中病毒与细菌合并感染的患病率
Biomedicines. 2025 May 19;13(5):1236. doi: 10.3390/biomedicines13051236.
2
Fungal Pulmonary Coinfections in COVID-19: Microbiological Assessment, Inflammatory Profiles, and Clinical Outcomes.COVID-19患者的真菌肺部合并感染:微生物学评估、炎症特征及临床结局
Biomedicines. 2025 Apr 3;13(4):864. doi: 10.3390/biomedicines13040864.

本文引用的文献

1
Multiplex molecular assays for the laboratory-based and point-of-care diagnosis of infections caused by seasonal influenza, COVID-19, and RSV.基于实验室和即时检测的季节性流感、COVID-19 和 RSV 感染的多重分子检测。
Expert Rev Mol Diagn. 2024 Nov;24(11):997-1008. doi: 10.1080/14737159.2024.2408745. Epub 2024 Oct 4.
2
SARS-CoV-2, influenza A/B and respiratory syncytial virus positivity and association with influenza-like illness and self-reported symptoms, over the 2022/23 winter season in the UK: a longitudinal surveillance cohort.2022/23 年冬季英国纵向监测队列中 SARS-CoV-2、甲型/乙型流感病毒和呼吸道合胞病毒阳性率及其与流感样疾病和自我报告症状的关系。
BMC Med. 2024 Mar 26;22(1):143. doi: 10.1186/s12916-024-03351-w.
3
Nanostructures for prevention, diagnosis, and treatment of viral respiratory infections: from influenza virus to SARS-CoV-2 variants.用于预防、诊断和治疗病毒性呼吸道感染的纳米结构:从流感病毒到 SARS-CoV-2 变体。
J Nanobiotechnology. 2023 Jun 21;21(1):199. doi: 10.1186/s12951-023-01938-8.
4
Reciprocal enhancement of SARS-CoV-2 and influenza virus replication in human pluripotent stem cell-derived lung organoids.人多能干细胞衍生肺类器官中 SARS-CoV-2 和流感病毒复制的相互增强。
Emerg Microbes Infect. 2023 Dec;12(1):2211685. doi: 10.1080/22221751.2023.2211685.
5
Influenza and Respiratory Syncytial Virus Infections in Pediatric Patients during the COVID-19 Pandemic: A Single-Center Experience.新冠疫情期间儿科患者的流感和呼吸道合胞病毒感染:单中心经验
Children (Basel). 2023 Jan 7;10(1):126. doi: 10.3390/children10010126.
6
Coinfections with SARS-CoV-2 variants and influenza virus during the 2019 Coronavirus disease pandemic in Burkina Faso: A surveillance study.布基纳法索2019冠状病毒病大流行期间严重急性呼吸综合征冠状病毒2变种与流感病毒的合并感染:一项监测研究。
Health Sci Rep. 2023 Jan 4;6(1):e1041. doi: 10.1002/hsr2.1041. eCollection 2023 Jan.
7
Influenza viral infection is a risk factor for severe illness in COVID-19 patients: a nationwide population-based cohort study.流感病毒感染是 COVID-19 患者重症的危险因素:一项全国基于人群的队列研究。
Emerg Microbes Infect. 2023 Dec;12(1):2164215. doi: 10.1080/22221751.2022.2164215.
8
COVID-19 and Influenza Coinfection Outcomes among Hospitalized Patients in the United States: A Propensity Matched Analysis of National Inpatient Sample.美国住院患者中新冠病毒与流感病毒合并感染的结局:一项基于全国住院患者样本的倾向匹配分析
Vaccines (Basel). 2022 Dec 15;10(12):2159. doi: 10.3390/vaccines10122159.
9
SARS-CoV-2 and influenza co-infection: A cross-sectional study in central Missouri during the 2021-2022 influenza season.SARS-CoV-2 和流感合并感染:2021-2022 年流感季美国密苏里州中部的一项横断面研究。
Virology. 2022 Nov;576:105-110. doi: 10.1016/j.virol.2022.09.009. Epub 2022 Sep 30.
10
Human Respiratory Infections in Nigeria: Influenza and the Emergence of SARS-CoV-2 Pandemic.尼日利亚的人类呼吸道感染:流感与严重急性呼吸综合征冠状病毒2大流行的出现
Vaccines (Basel). 2022 Sep 17;10(9):1551. doi: 10.3390/vaccines10091551.