J. L. Arredondo-GarcíaS. R. HadinegoroH. ReynalesM. N. ChuaD. M. Rivera MedinaT. ChotpitayasunondhN. H. TranC. C. DesedaD. N. WirawanM. Cortés SupelanoC. FragoE. LangevinD. CoronelT. LaotA. P. PerroudL. SanchezM. BonaparteK. LimkittikulD. ChansinghakulS. GailhardouF. NoriegaT. A. WartelA. BouckenoogheB. ZambranoUniversitas UdayanaUniversity of Indonesia, RSUPN Dr. Cipto MangunkusumoSanofi Pasteur SAMahidol UniversityQueen Sirikit National Institute of Child HealthInstituto Nacional de PediatríaSanofi PasteurINVERIME SAInstitut Pasteur in Ho-Chi-Minh-CityCaribbean Travel Medicine ClinicCaimed SASSanofi PasteurSanofi PasteurSanofi PasteurSanofi PasteurSanofi PasteurSanofi PasteurChong Hua HospitalSanofi Pasteur2019-08-282019-08-282018-07-01Clinical Microbiology and Infection. Vol.24, No.7 (2018), 755-763146906911198743X2-s2.0-85042586862https://repository.li.mahidol.ac.th/handle/20.500.14594/46583© 2018 The Authors Objective: Our objective was to describe the risk of hospital admission for virologically confirmed dengue (VCD) and the risk of clinically severe hospitalized VCD occurring up to 4 years after the first dose (years 1 to 4) in three randomized clinical trials comparing tetravalent dengue vaccine with placebo. Methods: The relative risks (RR) for hospitalized VCD from first dose to year 4 were estimated by year and age-group in individual and combined studies. Results: Overall, from Year 1 to Year 4, 233 and 228 participants had at least one episode of hospitalized VCD in the vaccinated (n = 22 603) and placebo (n = 11 301) groups, respectively (RR = 0.511, 95% CI 0.42–0.62). Among these, 48 and 47 cases, respectively, were classified as clinically severe. In children aged ≥9 years, 88 and 136 participants had at least one episode of hospitalized VCD in the vaccinated (n = 17 629) and placebo (n = 8821) groups, respectively (RR = 0.324; 95% CI 0.24–0.43). In vaccinated participants aged <9 years, particularly in those aged 2–5 years, there were more hospitalized VCD cases compared with the control participants in Year 3 but not in Year 4. The overall RR in those aged <9 years for Year 1 to Year 4 was 0.786 (95% CI 0.60–1.03), with a higher protective effect in the 6–8 year olds than in the 2–5 year olds. Conclusions: The overall benefit-risk remained positive in those aged ≥9 years up to year 4, although the protective effect was lower in years 3 and 4 than in years 1 and 2.Mahidol UniversityMedicineArticleSCOPUS10.1016/j.cmi.2018.01.018