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Published on: August 30, 2014
Influenza B associated paediatric acute respiratory infection hospitalization in central vietnam
Keisuke Yoshihara1, Minh Nhat Le1,2, Michiko Toizumi1
1Department of Paediatric Infectious Diseases, Institute of Tropical Medicine, Nagasaki University, Nagasaki, Japan.
Insights
Influenza B hospitalization incidence in Vietnamese children increased post-A/H1N1pdm09. Genetic variations in Influenza B Victoria lineage influenced clinical severity, highlighting the importance of viral evolution in pediatric acute respiratory infections.
Area of Science:
- Virology
- Pediatrics
- Epidemiology
Background:
- Influenza B is a significant cause of pediatric acute respiratory infections (ARIs) globally.
- Limited clinical-epidemiological data exists for influenza B-associated ARIs in children, particularly in central Vietnam.
Purpose of the Study:
- To investigate the hospitalization incidence of influenza B-associated ARIs in children in central Vietnam.
- To characterize the clinical-epidemiological features of these infections.
- To analyze the impact of influenza B lineages and WHO groups on disease presentation.
Main Methods:
- Collected clinical and epidemiological data from hospitalized children with ARIs.
- Utilized Multiplex-PCR to screen for 13 respiratory viruses.
- Genotyped influenza B cases using Haemagglutinin gene sequencing.
- Analyzed data based on pre- and post-A/H1N1pdm09 periods, and influenza B lineages (Victoria/Yamagata).
Main Results:
- Influenza B-associated ARI hospitalization incidence in children under five increased significantly after the A/H1N1pdm09 pandemic.
- The Victoria lineage became predominant (84%) between 2010-2013.
- Influenza B cases were slightly older with milder symptoms; however, Victoria lineage Group1 infections showed greater clinical severity than Group5.
Conclusions:
- The incidence of influenza B-related ARI hospitalizations has risen in Vietnamese children post-A/H1N1pdm09.
- Genetic variations within the influenza B Victoria lineage correlate with differences in clinical severity.
- These findings underscore the impact of influenza B genetic diversity on pediatric respiratory illness.
Background:
Influenza B is one of the major etiologies for acute respiratory infections (ARI) among children worldwide; however, its clinical-epidemiological information is limited. We aimed to investigate the hospitalization incidence and clinical-epidemiological characteristics of influenza B-associated paediatric ARIs in central Vietnam.
Methods:
We collected clinical-epidemiological information and nasopharyngeal swabs from ARI children hospitalized at Khanh Hoa General Hospital, Nha Trang, Vietnam from February 2007 through June 2013. Nasopharyngeal samples were screened for 13 respiratory viruses using Multiplex-PCRs. Influenza B-confirmed cases were genotyped by Haemagglutinin gene sequencing. We analyzed the clinical-epidemiological characteristics of influenza B Lineages (Victoria/Yamagata) and WHO Groups.
Results:
In the pre-A/H1N1pdm09 period, influenza B-associated ARI hospitalization incidence among children under five was low, ranging between 14.7 and 80.7 per 100 000 population. The incidence increased to between 51.4 and 330 in the post-A/H1N1pdm09. Influenza B ARI cases were slightly older with milder symptoms. Both Victoria and Yamagata lineages were detected before the A/H1N1pdm09 outbreak; however, Victoria lineage became predominant in 2010-2013 (84% Victoria vs 16% Yamagata). Victoria and Yamagata lineages did not differ in demographic and clinical characteristics. In Victoria lineage, Group1 ARI cases were clinically more severe compared to Group5, presenting a greater proportion of wheeze, tachypnea, and lower respiratory tract infection.
Conclusions:
The current results highlight the increased incidence of influenza B-related ARI hospitalization among children in central Vietnam in the post-A/H1N1pdm09 era. Furthermore, the difference in clinical severity between Victoria lineage Group1 and 5 implies the importance of influenza B genetic variation on clinical presentation.
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