Publication: Four-year safety follow-up of the tetravalent dengue vaccine efficacy randomized controlled trials in Asia and Latin America
dc.contributor.author | J. L. Arredondo-García | en_US |
dc.contributor.author | S. R. Hadinegoro | en_US |
dc.contributor.author | H. Reynales | en_US |
dc.contributor.author | M. N. Chua | en_US |
dc.contributor.author | D. M. Rivera Medina | en_US |
dc.contributor.author | T. Chotpitayasunondh | en_US |
dc.contributor.author | N. H. Tran | en_US |
dc.contributor.author | C. C. Deseda | en_US |
dc.contributor.author | D. N. Wirawan | en_US |
dc.contributor.author | M. Cortés Supelano | en_US |
dc.contributor.author | C. Frago | en_US |
dc.contributor.author | E. Langevin | en_US |
dc.contributor.author | D. Coronel | en_US |
dc.contributor.author | T. Laot | en_US |
dc.contributor.author | A. P. Perroud | en_US |
dc.contributor.author | L. Sanchez | en_US |
dc.contributor.author | M. Bonaparte | en_US |
dc.contributor.author | K. Limkittikul | en_US |
dc.contributor.author | D. Chansinghakul | en_US |
dc.contributor.author | S. Gailhardou | en_US |
dc.contributor.author | F. Noriega | en_US |
dc.contributor.author | T. A. Wartel | en_US |
dc.contributor.author | A. Bouckenooghe | en_US |
dc.contributor.author | B. Zambrano | en_US |
dc.contributor.other | Universitas Udayana | en_US |
dc.contributor.other | University of Indonesia, RSUPN Dr. Cipto Mangunkusumo | en_US |
dc.contributor.other | Sanofi Pasteur SA | en_US |
dc.contributor.other | Mahidol University | en_US |
dc.contributor.other | Queen Sirikit National Institute of Child Health | en_US |
dc.contributor.other | Instituto Nacional de Pediatría | en_US |
dc.contributor.other | Sanofi Pasteur | en_US |
dc.contributor.other | INVERIME SA | en_US |
dc.contributor.other | Institut Pasteur in Ho-Chi-Minh-City | en_US |
dc.contributor.other | Caribbean Travel Medicine Clinic | en_US |
dc.contributor.other | Caimed SAS | en_US |
dc.contributor.other | Sanofi Pasteur | en_US |
dc.contributor.other | Sanofi Pasteur | en_US |
dc.contributor.other | Sanofi Pasteur | en_US |
dc.contributor.other | Sanofi Pasteur | en_US |
dc.contributor.other | Sanofi Pasteur | en_US |
dc.contributor.other | Sanofi Pasteur | en_US |
dc.contributor.other | Chong Hua Hospital | en_US |
dc.contributor.other | Sanofi Pasteur | en_US |
dc.date.accessioned | 2019-08-28T06:03:52Z | |
dc.date.available | 2019-08-28T06:03:52Z | |
dc.date.issued | 2018-07-01 | en_US |
dc.description.abstract | © 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. | en_US |
dc.identifier.citation | Clinical Microbiology and Infection. Vol.24, No.7 (2018), 755-763 | en_US |
dc.identifier.doi | 10.1016/j.cmi.2018.01.018 | en_US |
dc.identifier.issn | 14690691 | en_US |
dc.identifier.issn | 1198743X | en_US |
dc.identifier.other | 2-s2.0-85042586862 | en_US |
dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/46583 | |
dc.rights | Mahidol University | en_US |
dc.rights.holder | SCOPUS | en_US |
dc.source.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85042586862&origin=inward | en_US |
dc.subject | Medicine | en_US |
dc.title | Four-year safety follow-up of the tetravalent dengue vaccine efficacy randomized controlled trials in Asia and Latin America | en_US |
dc.type | Article | en_US |
dspace.entity.type | Publication | |
mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85042586862&origin=inward | en_US |