Vaccine effectiveness of live attenuated and trivalent inactivated influenza vaccination in 2010/11 to 2015/16: the SIVE II record linkage study

Background: There is good evidence of vaccine effectiveness in healthy individuals but less robust evidence for vaccine effectiveness in the populations targeted for influenza vaccination. The live attenuated influenza vaccine (LAIV) has recently been recommended for children in the UK. The trivalen...

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Main Authors: Colin R Simpson, Nazir I Lone, Kim Kavanagh, Tanya Englishby, Chris Robertson, Jim McMenamin, Beatrix von Wissman, Eleftheria Vasileiou, Christopher C Butler, Lewis D Ritchie, Rory Gunson, Jürgen Schwarze, Aziz Sheikh
Format: Article
Language:English
Published: NIHR Journals Library 2020-12-01
Series:Health Technology Assessment
Subjects:
Online Access:https://doi.org/10.3310/hta24670
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record_format Article
collection DOAJ
language English
format Article
sources DOAJ
author Colin R Simpson
Nazir I Lone
Kim Kavanagh
Tanya Englishby
Chris Robertson
Jim McMenamin
Beatrix von Wissman
Eleftheria Vasileiou
Christopher C Butler
Lewis D Ritchie
Rory Gunson
Jürgen Schwarze
Aziz Sheikh
spellingShingle Colin R Simpson
Nazir I Lone
Kim Kavanagh
Tanya Englishby
Chris Robertson
Jim McMenamin
Beatrix von Wissman
Eleftheria Vasileiou
Christopher C Butler
Lewis D Ritchie
Rory Gunson
Jürgen Schwarze
Aziz Sheikh
Vaccine effectiveness of live attenuated and trivalent inactivated influenza vaccination in 2010/11 to 2015/16: the SIVE II record linkage study
Health Technology Assessment
asthma
live attenuated influenza vaccine
trivalent influenza vaccine
hospitalisation
adverse effects
author_facet Colin R Simpson
Nazir I Lone
Kim Kavanagh
Tanya Englishby
Chris Robertson
Jim McMenamin
Beatrix von Wissman
Eleftheria Vasileiou
Christopher C Butler
Lewis D Ritchie
Rory Gunson
Jürgen Schwarze
Aziz Sheikh
author_sort Colin R Simpson
title Vaccine effectiveness of live attenuated and trivalent inactivated influenza vaccination in 2010/11 to 2015/16: the SIVE II record linkage study
title_short Vaccine effectiveness of live attenuated and trivalent inactivated influenza vaccination in 2010/11 to 2015/16: the SIVE II record linkage study
title_full Vaccine effectiveness of live attenuated and trivalent inactivated influenza vaccination in 2010/11 to 2015/16: the SIVE II record linkage study
title_fullStr Vaccine effectiveness of live attenuated and trivalent inactivated influenza vaccination in 2010/11 to 2015/16: the SIVE II record linkage study
title_full_unstemmed Vaccine effectiveness of live attenuated and trivalent inactivated influenza vaccination in 2010/11 to 2015/16: the SIVE II record linkage study
title_sort vaccine effectiveness of live attenuated and trivalent inactivated influenza vaccination in 2010/11 to 2015/16: the sive ii record linkage study
publisher NIHR Journals Library
series Health Technology Assessment
issn 1366-5278
2046-4924
publishDate 2020-12-01
description Background: There is good evidence of vaccine effectiveness in healthy individuals but less robust evidence for vaccine effectiveness in the populations targeted for influenza vaccination. The live attenuated influenza vaccine (LAIV) has recently been recommended for children in the UK. The trivalent influenza vaccine (TIV) is recommended for all people aged ≥ 65 years and for those aged < 65 years who are at an increased risk of complications from influenza infection (e.g. people with asthma). Objective: To examine the vaccine effectiveness of LAIV and TIV. Design: Cohort study and test-negative designs to estimate vaccine effectiveness. A self-case series study to ascertain adverse events associated with vaccination. Setting: A national linkage of patient-level general practice (GP) data from 230 Scottish GPs to the Scottish Immunisation & Recall Service, Health Protection Scotland virology database, admissions to Scottish hospitals and the Scottish death register. Participants: A total of 1,250,000 people. Interventions: LAIV for 2- to 11-year-olds and TIV for older people (aged ≥ 65 years) and those aged < 65 years who are at risk of diseases, from 2010/11 to 2015/16. Main outcome measures: The main outcome measures include vaccine effectiveness against laboratory-confirmed influenza using real-time reverse-transcription polymerase chain reaction (RT-PCR), influenza-related morbidity and mortality, and adverse events associated with vaccination. Results: Two-fifths (40%) of preschool-aged children and three-fifths (60%) of primary school-aged children registered in study practices were vaccinated. Uptake varied among groups [e.g. most affluent vs. most deprived in 2- to 4-year-olds, odds ratio 1.76, 95% confidence interval (CI) 1.70 to 1.82]. LAIV-adjusted vaccine effectiveness among children (aged 2–11 years) for preventing RT-PCR laboratory-confirmed influenza was 21% (95% CI –19% to 47%) in 2014/15 and 58% (95% CI 39% to 71%) in 2015/16. No significant adverse events were associated with LAIV. Among at-risk 18- to 64-year-olds, significant trivalent influenza vaccine effectiveness was found for four of the six seasons, with the highest vaccine effectiveness in 2010/11 (53%, 95% CI 21% to 72%). The seasons with non-significant vaccine effectiveness had low levels of circulating influenza virus (2011/12, 5%; 2013/14, 9%). Among those people aged ≥ 65 years, TIV effectiveness was positive in all six seasons, but in only one of the six seasons (2013/14) was significance achieved (57%, 95% CI 20% to 76%). Conclusions: The study found that LAIV was safe and effective in decreasing RT-PCR-confirmed influenza in children. TIV was safe and significantly effective in most seasons for 18- to 64-year-olds, with positive vaccine effectiveness in most seasons for those people aged ≥ 65 years (although this was significant in only one season). Future work: The UK Joint Committee on Vaccination and Immunisation has recommended the use of adjuvanted injectable vaccine for those people aged ≥ 65 years from season 2018/19 onwards. A future study will be required to evaluate this vaccine. Trial registration: Current Controlled Trials ISRCTN88072400. Funding: This project was funded by the National Institute for Health Research (NIHR) Health Technology Assessment programme and will be published in full in Health Technology Assessment; Vol. 24, No. 67. See the NIHR Journals Library website for further project information.
topic asthma
live attenuated influenza vaccine
trivalent influenza vaccine
hospitalisation
adverse effects
url https://doi.org/10.3310/hta24670
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spelling doaj-013fbaf4c5d444fc8263e1a0f751facb2020-12-01T09:41:38ZengNIHR Journals LibraryHealth Technology Assessment1366-52782046-49242020-12-01246710.3310/hta2467013/34/14Vaccine effectiveness of live attenuated and trivalent inactivated influenza vaccination in 2010/11 to 2015/16: the SIVE II record linkage studyColin R Simpson0Nazir I Lone1Kim Kavanagh2Tanya Englishby3Chris Robertson4Jim McMenamin5Beatrix von Wissman6Eleftheria Vasileiou7Christopher C Butler8Lewis D Ritchie9Rory Gunson10Jürgen Schwarze11Aziz Sheikh12School of Health, Faculty of Health, Victoria University of Wellington, Wellington, New ZealandAsthma UK Centre for Applied Research, Usher Institute of Population Health Sciences and Informatics, University of Edinburgh, Edinburgh, UKDepartment of Mathematics and Statistics, University of Strathclyde, Glasgow, UKDepartment of Mathematics and Statistics, University of Strathclyde, Glasgow, UKDepartment of Mathematics and Statistics, University of Strathclyde, Glasgow, UKHealth Protection Scotland, Glasgow, UKHealth Protection Scotland, Glasgow, UKAsthma UK Centre for Applied Research, Usher Institute of Population Health Sciences and Informatics, University of Edinburgh, Edinburgh, UKNuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UKCentre of Academic Primary Care, University of Aberdeen, Aberdeen, UKWest of Scotland Specialist Virology Centre, Glasgow Royal Infirmary, Glasgow, UKChild Life and Health, Medicine and Veterinary Medicine, University of Edinburgh, Edinburgh, UKAsthma UK Centre for Applied Research, Usher Institute of Population Health Sciences and Informatics, University of Edinburgh, Edinburgh, UKBackground: There is good evidence of vaccine effectiveness in healthy individuals but less robust evidence for vaccine effectiveness in the populations targeted for influenza vaccination. The live attenuated influenza vaccine (LAIV) has recently been recommended for children in the UK. The trivalent influenza vaccine (TIV) is recommended for all people aged ≥ 65 years and for those aged < 65 years who are at an increased risk of complications from influenza infection (e.g. people with asthma). Objective: To examine the vaccine effectiveness of LAIV and TIV. Design: Cohort study and test-negative designs to estimate vaccine effectiveness. A self-case series study to ascertain adverse events associated with vaccination. Setting: A national linkage of patient-level general practice (GP) data from 230 Scottish GPs to the Scottish Immunisation & Recall Service, Health Protection Scotland virology database, admissions to Scottish hospitals and the Scottish death register. Participants: A total of 1,250,000 people. Interventions: LAIV for 2- to 11-year-olds and TIV for older people (aged ≥ 65 years) and those aged < 65 years who are at risk of diseases, from 2010/11 to 2015/16. Main outcome measures: The main outcome measures include vaccine effectiveness against laboratory-confirmed influenza using real-time reverse-transcription polymerase chain reaction (RT-PCR), influenza-related morbidity and mortality, and adverse events associated with vaccination. Results: Two-fifths (40%) of preschool-aged children and three-fifths (60%) of primary school-aged children registered in study practices were vaccinated. Uptake varied among groups [e.g. most affluent vs. most deprived in 2- to 4-year-olds, odds ratio 1.76, 95% confidence interval (CI) 1.70 to 1.82]. LAIV-adjusted vaccine effectiveness among children (aged 2–11 years) for preventing RT-PCR laboratory-confirmed influenza was 21% (95% CI –19% to 47%) in 2014/15 and 58% (95% CI 39% to 71%) in 2015/16. No significant adverse events were associated with LAIV. Among at-risk 18- to 64-year-olds, significant trivalent influenza vaccine effectiveness was found for four of the six seasons, with the highest vaccine effectiveness in 2010/11 (53%, 95% CI 21% to 72%). The seasons with non-significant vaccine effectiveness had low levels of circulating influenza virus (2011/12, 5%; 2013/14, 9%). Among those people aged ≥ 65 years, TIV effectiveness was positive in all six seasons, but in only one of the six seasons (2013/14) was significance achieved (57%, 95% CI 20% to 76%). Conclusions: The study found that LAIV was safe and effective in decreasing RT-PCR-confirmed influenza in children. TIV was safe and significantly effective in most seasons for 18- to 64-year-olds, with positive vaccine effectiveness in most seasons for those people aged ≥ 65 years (although this was significant in only one season). Future work: The UK Joint Committee on Vaccination and Immunisation has recommended the use of adjuvanted injectable vaccine for those people aged ≥ 65 years from season 2018/19 onwards. A future study will be required to evaluate this vaccine. Trial registration: Current Controlled Trials ISRCTN88072400. Funding: This project was funded by the National Institute for Health Research (NIHR) Health Technology Assessment programme and will be published in full in Health Technology Assessment; Vol. 24, No. 67. See the NIHR Journals Library website for further project information.https://doi.org/10.3310/hta24670asthmalive attenuated influenza vaccinetrivalent influenza vaccinehospitalisationadverse effects