Comprehensive insights into pathogen distribution, clinical features, and outcomes in pediatric severe pneumonia

Read full text
Authors: Chunyun Fu, Xiangjun Lu, Jiangyang Zhao, Ya Huang, Qiang Huang, Lishai Mo, Yanhua Feng, Wenting Tang, Cuihong Lu, Mengjun Li, Yubing Wei, Ruting Chen
+5 more Guangbing Liu, Jialing Ruan, Huiping Huang, Q. Li, Jie Tan
Cited by: 2
References: 30

Abstract

Objective Pediatric severe pneumonia is a life-threatening condition with high incidence and mortality rates. This study provides a comprehensive analysis of pathogen distribution, infection patterns, clinical manifestations, and prognosis associated with the disease. Methods This study involved 227 children with severe pneumonia and a control group of 227 with non-severe pneumonia. Targeted next-generation sequencing (tNGS) was applied to identify respiratory pathogens. Results The median age of children with severe pneumonia was 12 months, markedly younger than the median of 24 months in the non-severe group. The tNGS identified suspected pathogenic microorganisms in 99.12% of the severe pneumonia cases, with predominant pathogens including Human Respiratory Syncytial Virus (33.92%), Cytomegalovirus (33.04%), Mycoplasma pneumoniae (24.67%), and Rhinovirus (23.79%). Clinically, those with severe pneumonia exhibited markedly elevated procalcitonin levels and an increased prevalence of fever, wheezing, and dyspnea, alongside longer hospital stays, more protracted fever, and significantly higher hospitalization costs compared to their non-severe counterparts. Complications, including respiratory and other systemic issues, occurred in 96.04% and 59.47% of the severe pneumonia group, respectively, both significantly higher than in the non-severe pneumonia group; 99.12% required respiratory support and significantly more (56.83%) were admitted to the ICU, with a 9.69% incidence of poor outcomes. Conclusion Children with severe pneumonia tend to be younger than those with non-severe pneumonia. While significant differences are observed in the distribution of pathogens, complications, clinical manifestations, and prognosis between the two groups, no significant differences are noted in the number of infecting microorganisms or infection patterns.

Fields of Study & Subjects

Respiratory viral infections research Pneumonia and Respiratory Infections Immunodeficiency and Autoimmune Disorders

Publication details

Journal / source
Frontiers in Cellular and Infection Microbiology
Publisher
Frontiers Media SA
Volume
15
Pages
1681950–1681950
Publication date
7 January 2026
Language
EN