Dayan Gustavo, Arredondo Jose L, Carrasquilla Gabriel, Deseda Carmen C, Dietze Reynaldo, Luz Kleber, Costa Maria Selma N, Cunha Rivaldo V, Rey Luis C, Morales Javier, Reynales Humberto, Miranda Maria, Zambrano Betzana, Rivas Enrique, Garbes Pedro, Noriega Fernando
Am J Trop Med Hyg. 2015 Jul;93(1):18-23. doi: 10.4269/ajtmh.13-0663. Epub 2015 May 26.
To prepare for a Phase III dengue vaccine efficacy trial, 20 investigational sites were selected for this observational study to identify dengue infections in a closed cohort (N = 3,000 children 9-16 years of age). Of 255 acute febrile episodes experienced by 235 children, 50 (21.3%) were considered serologically probable dengue, and 18 (7.7%) were considered virologically confirmed (i.e., dengue NS1 antigen positive) dengue cases. Considering the disease-free and at-risk period from study start to onset of symptoms, the overall incidence density of acute febrile episodes was 17.7 per 100 person-years of follow-up, ranging from 15.3 in Colombia to 22.0 in Puerto Rico. This study showed that all sites were capable of capturing and following up acute febrile episodes within a specific timeframe among the established cohort and to detect dengue cases.
为筹备一项III期登革热疫苗效力试验,本观察性研究选取了20个研究地点,以确定一个封闭队列(3000名9至16岁儿童)中的登革热感染情况。在235名儿童经历的255次急性发热发作中,50次(21.3%)被认为血清学上可能为登革热,18次(7.7%)被认为是病毒学确诊(即登革热NS1抗原阳性)的登革热病例。考虑到从研究开始到症状出现的无病和危险期,急性发热发作的总体发病密度为每100人年随访17.7次,范围从哥伦比亚的15.3次到波多黎各的22.0次。这项研究表明,所有研究地点都有能力在既定队列中的特定时间范围内捕捉并随访急性发热发作情况,并检测登革热病例。