Cargando…
An integrated, multistudy analysis of the safety of Ann Arbor strain live attenuated influenza vaccine in children aged 2–17 years
Please cite this paper as: Ambrose et al. (2011) An integrated, multistudy analysis of the safety of Ann Arbor strain live attenuated influenza vaccine in children aged 2–17 years. Influenza and Other Respiratory Viruses 5(6), 389–397. Background Trivalent, Ann Arbor strain, live attenuated influen...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3256242/ https://www.ncbi.nlm.nih.gov/pubmed/21668683 http://dx.doi.org/10.1111/j.1750-2659.2011.00243.x |
_version_ | 1782221063345668096 |
---|---|
author | Ambrose, Christopher S. Yi, Tingting Falloon, Judith |
author_facet | Ambrose, Christopher S. Yi, Tingting Falloon, Judith |
author_sort | Ambrose, Christopher S. |
collection | PubMed |
description | Please cite this paper as: Ambrose et al. (2011) An integrated, multistudy analysis of the safety of Ann Arbor strain live attenuated influenza vaccine in children aged 2–17 years. Influenza and Other Respiratory Viruses 5(6), 389–397. Background Trivalent, Ann Arbor strain, live attenuated influenza vaccine (LAIV) is approved in several countries for use in eligible children aged ≥2 years. Objective To describe the safety of Ann Arbor strain LAIV in children aged 2–17 years. Methods An integrated analysis of randomized, controlled trials of LAIV. Results A total of 4245 and 10 693 children received ≥1 dose of LAIV in year 1 of 6 trivalent inactivated influenza vaccine (TIV)‐controlled and 14 placebo‐controlled studies, respectively; 3212 children were revaccinated in year 2 of 4 placebo‐controlled studies. Compared with placebo for days 0–10 post‐vaccination, LAIV recipients exhibited increased runny/stuffy nose (+7%), headache (+7%), and tiredness/decreased activity (+2%) after dose 1; and a higher rate of decreased appetite (+4%) after year 2 revaccination. Compared with TIV, only runny/stuffy nose was increased (dose 1, +12%; dose 2, +4%). Compared with initial vaccination, LAIV reactogenicity was lower after dose 2 in year 1 and revaccination in year 2. Unsolicited adverse events (AEs) increased with LAIV in some comparisons were headache, nasal congestion/rhinorrhea, rhinitis, and pyrexia; ear pain and lower respiratory illness were decreased. There was no evidence of an increase in any potential vaccine‐related serious AE in LAIV recipients. Among children aged 2–17 years and specifically aged 24–35 months, there was no evidence that lower respiratory illness or wheezing illness occurred at a higher rate in LAIV recipients. Conclusion This analysis supports the safety of Ann Arbor strain LAIV in children aged 2–17 years and provides a consensus assessment of events expected after vaccination. |
format | Online Article Text |
id | pubmed-3256242 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-32562422012-01-13 An integrated, multistudy analysis of the safety of Ann Arbor strain live attenuated influenza vaccine in children aged 2–17 years Ambrose, Christopher S. Yi, Tingting Falloon, Judith Influenza Other Respir Viruses Original Articles Please cite this paper as: Ambrose et al. (2011) An integrated, multistudy analysis of the safety of Ann Arbor strain live attenuated influenza vaccine in children aged 2–17 years. Influenza and Other Respiratory Viruses 5(6), 389–397. Background Trivalent, Ann Arbor strain, live attenuated influenza vaccine (LAIV) is approved in several countries for use in eligible children aged ≥2 years. Objective To describe the safety of Ann Arbor strain LAIV in children aged 2–17 years. Methods An integrated analysis of randomized, controlled trials of LAIV. Results A total of 4245 and 10 693 children received ≥1 dose of LAIV in year 1 of 6 trivalent inactivated influenza vaccine (TIV)‐controlled and 14 placebo‐controlled studies, respectively; 3212 children were revaccinated in year 2 of 4 placebo‐controlled studies. Compared with placebo for days 0–10 post‐vaccination, LAIV recipients exhibited increased runny/stuffy nose (+7%), headache (+7%), and tiredness/decreased activity (+2%) after dose 1; and a higher rate of decreased appetite (+4%) after year 2 revaccination. Compared with TIV, only runny/stuffy nose was increased (dose 1, +12%; dose 2, +4%). Compared with initial vaccination, LAIV reactogenicity was lower after dose 2 in year 1 and revaccination in year 2. Unsolicited adverse events (AEs) increased with LAIV in some comparisons were headache, nasal congestion/rhinorrhea, rhinitis, and pyrexia; ear pain and lower respiratory illness were decreased. There was no evidence of an increase in any potential vaccine‐related serious AE in LAIV recipients. Among children aged 2–17 years and specifically aged 24–35 months, there was no evidence that lower respiratory illness or wheezing illness occurred at a higher rate in LAIV recipients. Conclusion This analysis supports the safety of Ann Arbor strain LAIV in children aged 2–17 years and provides a consensus assessment of events expected after vaccination. Blackwell Publishing Ltd 2011-04-04 2011-11 /pmc/articles/PMC3256242/ /pubmed/21668683 http://dx.doi.org/10.1111/j.1750-2659.2011.00243.x Text en © 2011 Blackwell Publishing Ltd Open access. |
spellingShingle | Original Articles Ambrose, Christopher S. Yi, Tingting Falloon, Judith An integrated, multistudy analysis of the safety of Ann Arbor strain live attenuated influenza vaccine in children aged 2–17 years |
title | An integrated, multistudy analysis of the safety of Ann Arbor strain live attenuated influenza vaccine in children aged 2–17 years |
title_full | An integrated, multistudy analysis of the safety of Ann Arbor strain live attenuated influenza vaccine in children aged 2–17 years |
title_fullStr | An integrated, multistudy analysis of the safety of Ann Arbor strain live attenuated influenza vaccine in children aged 2–17 years |
title_full_unstemmed | An integrated, multistudy analysis of the safety of Ann Arbor strain live attenuated influenza vaccine in children aged 2–17 years |
title_short | An integrated, multistudy analysis of the safety of Ann Arbor strain live attenuated influenza vaccine in children aged 2–17 years |
title_sort | integrated, multistudy analysis of the safety of ann arbor strain live attenuated influenza vaccine in children aged 2–17 years |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3256242/ https://www.ncbi.nlm.nih.gov/pubmed/21668683 http://dx.doi.org/10.1111/j.1750-2659.2011.00243.x |
work_keys_str_mv | AT ambrosechristophers anintegratedmultistudyanalysisofthesafetyofannarborstrainliveattenuatedinfluenzavaccineinchildrenaged217years AT yitingting anintegratedmultistudyanalysisofthesafetyofannarborstrainliveattenuatedinfluenzavaccineinchildrenaged217years AT falloonjudith anintegratedmultistudyanalysisofthesafetyofannarborstrainliveattenuatedinfluenzavaccineinchildrenaged217years AT ambrosechristophers integratedmultistudyanalysisofthesafetyofannarborstrainliveattenuatedinfluenzavaccineinchildrenaged217years AT yitingting integratedmultistudyanalysisofthesafetyofannarborstrainliveattenuatedinfluenzavaccineinchildrenaged217years AT falloonjudith integratedmultistudyanalysisofthesafetyofannarborstrainliveattenuatedinfluenzavaccineinchildrenaged217years |