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https://hdl.handle.net/2440/131575
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Type: | Journal article |
Title: | Efficacy of m-Health for the detection of adverse events following immunization – the stimulated telephone assisted rapid safety surveillance (STARSS) randomised control trial |
Author: | Gold, M.S. Lincoln, G. Cashman, P. Braunack-Mayer, A. Stocks, N. |
Citation: | Vaccine, 2020; 39(2):332-342 |
Publisher: | Elsevier |
Issue Date: | 2020 |
ISSN: | 0264-410X 1873-2518 |
Statement of Responsibility: | lM.S. Golda, G. Lincolnb, P. Cashmanc, A. Braunack-Mayerd, N. Stocks |
Abstract: | Introduction: Passive surveillance is recommended globally for the detection of adverse events following immunisation (AEFI) but this has significant challenges. Use of Mobile health for vaccine safety surveillance enables a consumer-centred approach to reporting. The Stimulated Telephone Assisted Rapid Safety Surveillance (STARSS) a randomised control trial (RCT) sought to evaluate the efficacy and acceptability of SMS for AEFI surveillance. Methods: Multi-centre RCT, participants were adult vaccinees or parents of children receiving any vaccine at a trial site. At enrolment randomisation occurred to one of two SMS groups or a control group. Prompts on days 2, 7 and 14 post-immunisation, were sent to the SMS group, to ascertain if a medical event following immunisation (MEFI) had occurred. No SMS’s were sent to the control participants. Those in the SMS who notified an MEFI were pre-randomised to complete a computer assisted telephone interview or a web based report to determine if an AEFI had occurred whilst an AEFI in the controls was determined by a search for passive reports. The primary outcome was the AEFI detection rate in the SMS group compared to controls. Results: We enrolled 6,338 participants, who were equally distributed across groups and who received 11,675 vaccines. The SMS group (4,225) received 12,675 surveillance prompts with 9.8% being non-compliant and not responding. In those that responded 90% indicated that no MEFI had been experienced and 184 had a verified AEFI. 6 control subjects had a reported AEFI. The AEFI detection rate was 13 fold greater in the SMS group when compared with controls (4.3 vs 0.3%). Conclusion: We have demonstrated that the STARSS methodology improves AEFI detection. Our findings should inform the wider use of SMS-based surveillance which is particularly relevant since establishing robust and novel pharmacovigilance systems is critical to monitoring novel vaccines which includes potential COVID vaccines. |
Keywords: | Adverse events following immunisation; vaccine safety surveillance, pharmacovigilance; m-Health |
Rights: | © 2020 Published by Elsevier Ltd. All rights reserved. |
DOI: | 10.1016/j.vaccine.2020.11.056 |
Grant ID: | http://purl.org/au-research/grants/nhmrc/1067703 |
Appears in Collections: | Aurora harvest 4 Medicine publications |
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