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ArticleEuropean journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology2025

Clinical characteristics and co-infection analysis of influenza a virus in pediatric respiratory infections: a study based on tNGS technology.

Chunyun Fu, Qiang Huang, Jiangyang Zhao, Lishai Mo, Wenting Tang, Junming Lu, Yili Zhang, Xiangjun Lu, Ya Huang, Yanhua Feng and 7 more

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Article in European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Chunyun Fu *Medical Science Laboratory, Children's Hospital, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, 530003, People's Republic of China.
Qiang Huang *Medical Science Laboratory, Children's Hospital, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, 530003, People's Republic of China.
Jiangyang Zhao *Medical Science Laboratory, Children's Hospital, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, 530003, People's Republic of China.
Lishai MoMedical Science Laboratory, Children's Hospital, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, 530003, People's Republic of China.
Wenting TangMedical Science Laboratory, Children's Hospital, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, 530003, People's Republic of China.
Junming LuMedical Science Laboratory, Children's Hospital, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, 530003, People's Republic of China.
Yili ZhangDepartment of Pediatric Respiratory Medicine, Children's Hospital, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, 530003, People's Republic of China.
Xiangjun LuMedical Science Laboratory, Children's Hospital, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, 530003, People's Republic of China.
Ya HuangDepartment of Pediatric Respiratory Medicine, Children's Hospital, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, 530003, People's Republic of China.
Yanhua FengDepartment of Pediatric Respiratory Medicine, Children's Hospital, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, 530003, People's Republic of China.
Xuehua HuMedical Science Laboratory, Children's Hospital, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, 530003, People's Republic of China.
Yanqing TangDepartment of Genetic Metabolism, Children's Hospital, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, 530003, People's Republic of China.
Shang YiDepartment of Genetic Metabolism, Children's Hospital, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, 530003, People's Republic of China.
Hao WeiDepartment of Genetic Metabolism, Children's Hospital, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, 530003, People's Republic of China.
Huiping HuangDepartment of Pediatric Respiratory Medicine, Children's Hospital, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, 530003, People's Republic of China. huiping.qz@foxmail.com.
Qifei LiDivision of Neonatology, Department of Pediatrics, University of Miami Miller School of Medicine and Holtz Children's Hospital, Jackson Health System, Miami, FL, 33136, USA. qxl368@med.miami.edu.
Jie TanDepartment of Pediatric Respiratory Medicine, Children's Hospital, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, 530003, People's Republic of China. tanjie273@163.com.

Funding

the Guangxi Medical and Health Appropriate Technology Development and Promotion Application Project S2024082
6 · The paper itself

Abstract

objectiveInfluenza A virus (IAV) represents a significant etiological agent of respiratory infections in pediatric populations. The primary objective of this research was to evaluate the infection status and clinical manifestations associated with IAV in these pediatric patients.

methodsFrom April 2021 to December 2024, 10,310 pediatric inpatients diagnosed with respiratory infections were enrolled at Guangxi Zhuang Autonomous Region Maternal and Child Health Hospital. Pathogen screening was systematically performed on biological specimens using targeted next-generation sequencing (tNGS) technologies.

resultsAmong 10,310 pediatric inpatients with respiratory infections screened by tNGS, 325 cases (3.2%) demonstrated IAV detection, predominantly distributed among preschool-aged children (3-5 years) and adolescents (5-11 years), with males predominating (male: female ratio 1.5:1). Monoinfection was observed in only 9 cases (2.8%), while 316 patients (97.2%) exhibited co-infections, primarily manifesting as IAV-bacterial-viral (97 cases, 29.8%) and IAV-bacterial (91 cases, 28.0%) co-infection patterns. Comprehensive pathogen profiling identified 41 distinct co-pathogens, with Haemophilus influenzae, Streptococcus pneumoniae, and Mycoplasma pneumoniae being the most common. Clinically, 33.2% developed respiratory complications (n = 108) and 41.2% extrapulmonary manifestations (n = 134), requiring median hospitalization of 6 days (IQR 5-8). Critical care needs included respiratory support in 20.6% (n = 67) and ICU admission in 4.6% (n = 15), underscoring the substantial disease burden associated with IAV co-infections in pediatric populations.

conclusionThis study delineates critical epidemiological and clinical patterns of pediatric IAV infections. A striking 97.2% of IAV-positive cases exhibited polymicrobial co-infections, necessitating implementation of comprehensive diagnostic panels. Clinically significant extrapulmonary complications developed in 41.2%, mandating vigilant multi-system monitoring beyond conventional respiratory surveillance. The 4.6% ICU admission rate, coupled with median hospitalization of 6 days (IQR 5-8), underscores the substantial healthcare burden imposed by IV-associated co-infections in pediatric populations.

Indexed as

CoinfectionInfluenza A virusInfluenza, HumanRespiratory Tract InfectionsAdolescentChildChild, PreschoolChinaFemaleHigh-Throughput Nucleotide SequencingHumansInfantMaleCo-infectionsInfluenza A virusPathogensPediatric patientstNGS

Identifiers

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.