Title

Consumer reporting of adverse events following immunization (AEFI): Identifying predictors of reporting an AEF

RIS ID

125760

Publication Details

Parella, A., MS Gold, M. S., Braunack-Mayer, A. J., Baghurst, P. & Marshall, H. S. (2014). Consumer reporting of adverse events following immunization (AEFI): Identifying predictors of reporting an AEF. Human Vaccines & Immunotherapeutics, 10 (3), 747-754.

Abstract

Surveillance of adverse events following immunisation (AEFI) is an essential component of vaccine safety monitoring. The most commonly utilized passive surveillance systems rely predominantly on reporting by health care providers (HCP). We reviewed adverse event reports received in Victoria, Australia since surveillance commencement in July 2007, to June 2013 (6 years) to ascertain the contribution of consumer (vaccinee or their parent/guardian) reporting to vaccine safety monitoring and to inform future surveillance system development directions. Categorical data included were: reporter type; serious and non-serious AEFI category; and, vaccinee age group. Chi-square test and 2-sample test of proportions were used to compare categories; trend changes were assessed using linear regression. Consumer reporting increased over the 6 years, reaching 21% of reports received in 2013 (P <0.001), most commonly for children aged less than 7 years. Consumer reports were 5% more likely to describe serious AEFI than HCP (P = 0.018) and 10% more likely to result in specialist clinic attendance (P <0.001). Although online reporting increased to 32% of all report since its introduction in 2010, 85% of consumers continued to report by phone. Consumer reporting of AEFI is a valuable component of vaccine safety surveillance in addition to HCP reporting. Changes are required to AEFI reporting systems to implement efficient consumer AEFI reporting, but may be justified for their potential impact on signal detection sensitivity.

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Link to publisher version (DOI)

http://dx.doi.org/10.4161/hv.27459