Clinical characteristics, co-detection patterns and prognostic risk factors of human metapneumovirus infection in
Wen Li1, Chi Zhu2, Mengfei Yu1
1Department of Pediatric Infectious Diseases, Hangzhou Children's Hospital, Hangzhou, China.
Insights
Human metapneumovirus (hMPV) infection in children is often co-detected with other viruses, particularly rhinovirus. Bacterial co-infections, especially Streptococcus pneumoniae, prolonged fever, and high procalcitonin levels increase severe pneumonia risk.
Area of Science:
- Pediatric infectious diseases
- Virology
- Respiratory infections
Background:
- Human metapneumovirus (hMPV) is a significant respiratory pathogen in children.
- Understanding co-detection patterns and risk factors is crucial for managing hMPV infections.
- Clinical characteristics and prognostic indicators for severe outcomes remain areas for investigation.
Purpose of the Study:
- To investigate the clinical features of hMPV infection in children.
- To analyze co-detection patterns, focusing on viral-viral and viral-bacterial co-infections.
- To identify independent risk factors for severe pneumonia in pediatric hMPV cases.
Main Methods:
- Retrospective analysis of 621 children with laboratory-confirmed hMPV infection.
- Evaluation of clinical data, laboratory results, and co-pathogen detection.
- Multivariate logistic regression to determine independent risk factors for severe pneumonia.
Main Results:
- hMPV infection predominantly affects preschool-aged children (median age 3.5 years).
- Viral-viral co-detection (68.9%) was more common than single detection (64.3%); rhinovirus was the most frequent co-pathogen (39.6%).
- Viral-bacterial co-detection correlated with longer hospital stays (6.5 days) and higher severe pneumonia rates (14.5%).
- Independent risk factors for severe pneumonia included *Streptococcus pneumoniae* co-detection (aOR=8.43), prolonged fever (aOR=1.19), and procalcitonin ≥0.5 ng/mL (aOR=4.27).
- Older age (>3 years) demonstrated a protective effect against severe pneumonia (aOR=0.20-0.03).
Conclusions:
- hMPV infection is common in preschool children, with frequent co-detections.
- Viral-bacterial co-infection, particularly with *S. pneumoniae*, significantly worsens clinical outcomes.
- Early identification of risk factors like prolonged fever and elevated procalcitonin aids in risk stratification for severe pneumonia.
- Older children exhibit reduced risk, suggesting age-specific disease severity patterns.
Objective:
To investigate clinical characteristics, co-detection patterns, and prognostic risk factors of human metapneumovirus (hMPV) infection in children.
Methods:
Retrospective study of 621 children with laboratory-detected hMPV infection. Clinical data, laboratory indicators, and co-detection status were analyzed. Multivariate logistic regression identified independent risk factors for severe pneumonia.
Results:
Median age was 3.50 years (IQR 1.75-4.75). Of 621 patients, 399 (64.3%) had Single-detection and 222 (35.7%) co-detection, with viral-viral co-detection dominant (68.9%) and rhinovirus the most common co-pathogen (39.6%). Only platelet count and aspartate aminotransferase differed significantly between groups (both P<0.01), with all inflammatory markers improving post-treatment (all P<0.001). Viral-bacterial co-detection was associated with longer hospitalization (median 6.5 days) and higher severe pneumonia rate (14.5%, both P<0.01). Multivariate analysis identified Streptococcus pneumoniae co-detection (aOR=8.43, 95%CI:1.50-47.32), prolonged fever duration (aOR=1.19, 95%CI:1.02-1.38), and procalcitonin ≥0.5 ng/mL (aOR=4.27, 95%CI:1.76-10.33) as independent risk factors for severe pneumonia. Older age (3-5 years: aOR=0.20; >5 years: aOR=0.03) showed significant protective effects.
Conclusion:
hMPV infection is most prevalent in preschool children. Viral-bacterial co-detection was associated with worse clinical outcomes. S. pneumoniae co-detection, prolonged fever, and elevated procalcitonin were independently associated with increased risk, while older age was associated with reduced risk. These findings support early risk stratification and targeted intervention.
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