Literature DB >> 22546331

Public perspectives on consent for the linkage of data to evaluate vaccine safety.

Jesia G Berry1, Michael S Gold, Philip Ryan, Katherine M Duszynski, Annette J Braunack-Mayer.   

Abstract

INTRODUCTION: We sought community opinion on consent alternatives when linking childhood immunisation and hospital attendance records for the purpose of vaccine safety surveillance.
METHODS: We conducted computer-assisted telephone interviewing (CATI) of a sample of rural and metropolitan residents of South Australia in 2011.
RESULTS: Of 2002 households interviewed (response rate 55.6%), 96.4% supported data linkage for postmarketing surveillance of vaccines; very few were completely opposed (1.5%) or undecided (2.2%). The majority (75.3%) trusted the privacy protections used in data linkage and most wished to have minimal or no direct involvement, preferring either opt-out consent (40.4%) or no consent (30.6%). A quarter of respondents (24.6%) favoured opt-in consent, but their preferences were divergent; half requested consent be sought prior to every use (11.4%) while the remainder preferred to give broad consent just once (3.4%) or renewed at periodic intervals (9.8%). Over half of the respondents gave higher priority to rapid vaccine safety surveillance (56.5%) rather than first seeking parental consent (26.6%) and one in seven was undecided (14.5%). Although 91.6% of respondents believed childhood vaccines are safe, over half (53.1%) were very or somewhat concerned that a vaccine could cause a serious reaction. Nevertheless, 92.4% of the parents in the sample (556/601) reported every child in their care as being fully immunised according to the National Immunisation Program schedule. Only 3.7% of parents (22/601) reported one or more children as under immunised, and 3.9% (23/601) reported that none of their children were immunised.
CONCLUSIONS: This survey demonstrates that data linkage for vaccine safety surveillance has substantial community support and that a system utilising opt-out consent or no consent was preferred to one using opt-in consent. These findings should inform public health policy and practice; data linkage should be established where feasible to address limitations in passive surveillance systems.
Copyright © 2012 Elsevier Ltd. All rights reserved.

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Year:  2012        PMID: 22546331     DOI: 10.1016/j.vaccine.2012.04.056

Source DB:  PubMed          Journal:  Vaccine        ISSN: 0264-410X            Impact factor:   3.641


  3 in total

1.  Consumer reporting of adverse events following immunization (AEFI): identifying predictors of reporting an AEFI.

Authors:  Adriana Parrella; Michael Gold; Annette Braunack-Mayer; Peter Baghurst; Helen Marshall
Journal:  Hum Vaccin Immunother       Date:  2014-01-09       Impact factor: 3.452

2.  Attitudes towards the collection and linkage of maltreatment data for research: A qualitative study.

Authors:  Gwenllian Moody; Rebecca Cannings-John; Kerenza Hood; Michael Robling
Journal:  Int J Popul Data Sci       Date:  2022-01-26

3.  Measuring trust in vaccination: A systematic review.

Authors:  Heidi J Larson; Richard M Clarke; Caitlin Jarrett; Elisabeth Eckersberger; Zachary Levine; Will S Schulz; Pauline Paterson
Journal:  Hum Vaccin Immunother       Date:  2018-05-10       Impact factor: 3.452

  3 in total

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