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   Age-specificity of clinical dengue during primary and secondary infections  
   
نویسنده thai k.t.d. ,nishiura h. ,hoang p.l. ,tran n.t.t. ,phan g.t. ,le h.q. ,tran b.q. ,van nguyen n. ,de vries p.j.
منبع plos neglected tropical diseases - 2011 - دوره : 5 - شماره : 6
چکیده    Background: this study aims to estimate the age-specific risks of clinical dengue attack (i.e.,the risk of symptomatic dengue among the total number of dengue virus (denv) infections) during primary and secondary infections. methods: we analyzed two pieces of epidemiological information in binh thuan province,southern vietnam,i.e.,age-specific seroprevalence and a community-wide longitudinal study of clinical dengue attack. the latter data set stratified febrile patients with denv infection by age as well as infection parity. a simple modeling approach was employed to estimate the age-specific risks of clinical dengue attack during primary and secondary infections. results: using the seroprevalence data,the force of infection was estimated to be 11.7% (95% confidence intervals (ci): 10.8-12.7) per year. median age (and the 25-75 percentiles) of dengue fever patients during primary and secondary infections were 12 (9-20) and 20 (14-31) years,respectively. the estimated age-specific risk of clinical dengue increases as a function of age for both primary and secondary infections; the estimated proportion of symptomatic patients among the total number of infected individuals was estimated to be <7% for those aged <10 years for both primary and secondary infections,but increased as patients become older,reaching to 8-11% by the age of 20 years. conclusions/significance: for both primary and secondary infections,higher age at denv infection was shown to result in higher risk of clinical attack. age as an important modulator of clinical dengue explains recent increase in dengue notifications in ageing countries in southeast asia,and moreover,poses a paradoxical problem of an increase in adult patients resulting from a decline in the force of infection,which may be caused by various factors including time-dependent variations in epidemiological,ecological and demographic dynamics. © 2011 thai et al.
آدرس division of infectious diseases,tropical medicine and aids,academic medical center,amsterdam,netherlands,center for infection and inflammation research (cinima),academic medical center,university of amsterdam,amsterdam, Netherlands, theoretical epidemiology,university of utrecht,utrecht,netherlands,presto,japan science and technology agency,saitama, Japan, tropical diseases clinical research center,cho ray hospital,ho chi minh city, Viet Nam, department of virology,cho ray hospital,ho chi minh city, Viet Nam, tropical diseases clinical research center,cho ray hospital,ho chi minh city, Viet Nam, tropical diseases clinical research center,cho ray hospital,ho chi minh city, Viet Nam, tropical diseases clinical research center,cho ray hospital,ho chi minh city, Viet Nam, binh thuan medical college,phan thiet city, Viet Nam, division of infectious diseases,tropical medicine and aids,academic medical center,amsterdam,netherlands,center for infection and inflammation research (cinima),academic medical center,university of amsterdam,amsterdam, Netherlands
 
     
   
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