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Usability of daily SF36 questionnaires to capture the QALD variation experienced after vaccination with AS03A-adjuvanted monovalent influenza A (H5N1) vaccine in a safety and tolerability study.

Authors :
Standaert, B.
Dort, T.
Linden, J.
Madan, A.
Bart, S.
Chu, L.
Hayney, M. S.
Kosinski, M.
Kroll, R.
Malak, J.
Meier, G.
Segall, N.
Schuind, A.
Source :
Health & Quality of Life Outcomes. 5/6/2019, Vol. 17 Issue 1, pN.PAG-N.PAG. 1p.
Publication Year :
2019

Abstract

<bold>Background: </bold>This study aims to describe the short-term reactogenicity of the AS03-adjuvanted H5N1 vaccine expressed through adverse events (AEs) and quality-adjusted life-day (QALD) scores. The AEs are likely to be short-term and therefore the quality of life (QoL) questionnaire, SF-36v2, was administered daily to record changes over seven days. A more sensitive application of this instrument should allow for a better understanding of short-term tolerability of adjuvanted vaccines.<bold>Methods: </bold>Participants (N = 50) received a 2-dose vaccination schedule. Solicited (collected daily: days 0 to 7 [post dose 1] and 21 to 28 [post dose 2]) and unsolicited (collected weekly until day 21) AEs were collected via diary cards. The QoL questionnaires were completed daily (days 0-6) and weekly (days 0, 6, 21, 27) after dose one. Questionnaire data were transformed into SF-6D scores to report QALDs. It was hypothesized post-hoc that the QALD and daily AEs scores should correlate if discrete QoL-changes were captured.<bold>Results: </bold>Pain (92%) and muscle ache (66%) were the most commonly reported solicited local and general AEs respectively, neither increased in intensity nor in frequency after dose 2. No safety concerns were identified during the study. A correlation between the daily AEs and QALD scores existed (correlation coefficient, - 0.97 (p < 0.001)). The impact of the AEs scores on the QALD was marginal (- 0.02 max for one day).<bold>Conclusion: </bold>Similarly with other H5N1 studies, no safety concern was identified throughout the study. Some time-limited variations in QALD-scores were reported. Our results imply that daily administration of the SF-36v2 captures changes in QALD-scores.<bold>Trial Registration: </bold>ClinicalTrials.gov . NCT01788228. Registered 11 February 2013. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14777525
Volume :
17
Issue :
1
Database :
Academic Search Index
Journal :
Health & Quality of Life Outcomes
Publication Type :
Academic Journal
Accession number :
136255167
Full Text :
https://doi.org/10.1186/s12955-019-1147-4