[HTML][HTML] Four-year safety follow-up of the tetravalent dengue vaccine efficacy randomized controlled trials in Asia and Latin America

JL Arredondo-García, SR Hadinegoro… - Clinical Microbiology …, 2018 - Elsevier
JL Arredondo-García, SR Hadinegoro, H Reynales, MN Chua, DMR Medina…
Clinical Microbiology and Infection, 2018Elsevier
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 …
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.
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