Four-year safety follow-up of the tetravalent dengue vaccine efficacy randomized controlled trials in Asia and Latin America.
Autor: | Arredondo-García JL; Instituto Nacional de Pediatria, México DF, Mexico., Hadinegoro SR; Department of Child Health, Cipto Mangunkusumo Hospital, Medical School, University of Indonesia, Jakarta, Indonesia., Reynales H; Centro de Atención e Investigación Médica-CAIMED, Bogotá, Colombia., Chua MN; Department of Paediatrics, Chong Hua Hospital, Cebu City, Philippines., Rivera Medina DM; Inversiones en Investigación Médica, INVERIME SA, Tegucigalpa, Honduras., Chotpitayasunondh T; Department of Paediatrics, Queen Sirikit National Institute of Child Health, Bangkok, Thailand., Tran NH; Infectious Diseases Department, Institut Pasteur in Ho-Chi-Minh-City, Ho-Chi-Minh-City, Viet Nam., Deseda CC; Caribbean Travel Medicine Clinic, San Juan, Puerto Rico., Wirawan DN; Department of Preventive Medicine, School of Medicine, Udayana University, Denpasar, Bali, Indonesia., Cortés Supelano M; Sanofi Pasteur, Bogota, Colombia., Frago C; Sanofi Pasteur, Singapore, Singapore., Langevin E; Sanofi Pasteur, Marcy-l'Étoile, France., Coronel D; Sanofi Pasteur, Mexico City, Mexico., Laot T; Sanofi Pasteur, Taguig, Philippines., Perroud AP; Sanofi Pasteur, São Paulo, Brazil., Sanchez L; Sanofi Pasteur, Taguig, Philippines., Bonaparte M; Sanofi Pasteur, Swiftwater, PA, USA., Limkittikul K; Faculty of Tropical Medicine, Mahidol University, Thailand., Chansinghakul D; Sanofi Pasteur, Bangkok, Thailand., Gailhardou S; Sanofi Pasteur, Lyon, France., Noriega F; Sanofi Pasteur, Swiftwater, PA, USA., Wartel TA; Sanofi Pasteur, Marcy-l'Étoile, France., Bouckenooghe A; Sanofi Pasteur, Singapore, Singapore., Zambrano B; Sanofi Pasteur, Montevideo, Uruguay. Electronic address: betzana.zambrano@sanofi.com. |
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Jazyk: | angličtina |
Zdroj: | Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases [Clin Microbiol Infect] 2018 Jul; Vol. 24 (7), pp. 755-763. Date of Electronic Publication: 2018 Feb 08. |
DOI: | 10.1016/j.cmi.2018.01.018 |
Abstrakt: | 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. (Copyright © 2018 The Authors. Published by Elsevier Ltd.. All rights reserved.) |
Databáze: | MEDLINE |
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