Postmarketing vaccine safety surveillance using data linkage: the issue of consent.

Background: Linked electronic administrative health care databases are a valuable resource that can be used for postmarketing safety surveillance of medicines and vaccines. Australian legislation mandates that individual consent is required for the collection, use and dissemination of health information. However, the requirement for consent is not absolute; a waiver of consent may be granted by an appropriately constituted human research ethics committee, provided certain qualifying criteria are met and the research (or other activity) is deemed to be substantially in the public interest. In Australia, data linkage research projects are recommended to abide by a best practice protocol, whereby individual privacy is preserved as researchers only receive files of pre-linked data with no personal identifiers. Ethical approval of a waiver of consent is required for the disclosure of identifiable demographic information to an authorised data linkage unit for the purpose of creating a master linkage key. However, some ethics committees and data custodians still require informed consent. Objective: The overall objective of this thesis was to examine the issue of consent in the context of postmarketing surveillance of vaccine safety using data linkage. A randomised controlled trial (RCT) was used for the primary aim of determining which method of obtaining parental consent (opt-in or opt-out) provided the highest participation rate. The secondary aims of the RCT were to examine reasons for participation and nonparticipation, socio-demographic factors, consent preferences and attitudes towards a data linkage study of vaccine safety. For this, a follow-up telephone interview of a parent from each family enrolled in the RCT was conducted. The generalisability of findings from the follow-up telephone interview was examined by repeating selected questions in a population-based survey sample of South Australians. Method: A total of 1129 families of children born at a South Australian hospital in 2009 were enrolled in a single-blind parallel group RCT of opt-in and opt-out consent at six weeks post-partum, with four weeks to respond by reply form, telephone or email. Interviews were conducted at 10 weeks post-partum (response rate 91%, n=1026). Computer-assisted telephone interviewing (CATI) of rural and metropolitan South Australian residents was conducted in 2010 (response rate 56%, n=2002). Results: The participation rate was 21% (n=120/564) in the opt-in arm and 96% (n=540/565) in the opt-out arm [χ² (1df) = 567.7, P<0.001]. Participants in the opt-in arm were more likely than non-participants to be older, married or in a de facto relationship, university educated and of higher socioeconomic status. Participants in the opt-out arm were similar to non-participants, except men were more likely to opt out. Substantial proportions did not receive, understand or properly consider study invitations, and opting in or opting out behaviour was often at odds with parents’ stated underlying intentions. Three-fifths of the parents in the opt-in and opt-out arms reported reading the information (63% vs 67%, P=0.11), but only two-fifths correctly identified the health records to be linked (43% vs 39%, P=0.21). Parents who actively consented (opted in) were more likely than those who passively consented (did not opt out) to correctly identify the data sources (60% vs 39%, P