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Published on: June 19, 2018
Adverse events following immunisation: Prospective cohort study evaluating Australian children presenting to
Hannah Stubbs1, Pamela Palasanthiran2, Archana Koirala3
1Faculty of Medicine, University of New South Wales, Sydney, Australia.
Insights
Revaccination is generally safe for children with a history of adverse events following immunisation. Most children with prior adverse events following immunisation did not experience recurrence, indicating safety for future vaccinations.
Area of Science:
- Pediatrics
- Immunology
- Public Health
Background:
- Adverse events following immunisation (AEFI) can deter vaccination.
- Limited Australian data exists on AEFI recurrence in children.
- Understanding recurrence risk is crucial for clinical decisions.
Purpose of the Study:
- To assess the recurrence rate of adverse events following immunisation in children with a history of AEFI.
- To evaluate if a family history of AEFI increases the risk of recurrence.
- To inform vaccination strategies for children with prior AEFI.
Main Methods:
- Prospective cohort study conducted between March and August 2023.
- Recruited children ≤16 years with prior AEFI (personal or family history).
- Collected AEFI outcomes via surveys at 3 and 8 days post-vaccination.
Main Results:
- 87.8% of enrolled children received further vaccines.
- 50.0% of those completing follow-up reported an AEFI.
- 23.3% experienced recurrence of prior AEFI; serious AEFI recurrence was 16.7% in those with prior serious AEFI.
- Neurological conditions were a risk factor for post-vaccination seizures.
- Family history did not correlate with post-vaccination AEFI.
Conclusions:
- Revaccination is safe for most children with a personal or family history of AEFI.
- The study provides valuable Australian data on AEFI recurrence.
- Findings support continued vaccination efforts in at-risk pediatric populations.
Objective:
Prior experience of an adverse event following immunisation is a known barrier to vaccination. Limited Australian data evaluating adverse event recurrence among children exists to inform clinical decisions. We aimed to assess adverse event following immunisation recurrence among children with prior adverse events and to evaluate if family history increased adverse event risk.
Methods:
A prospective cohort study was conducted from March 3rd until August 18th, 2023. Children ≤ 16 years with prior adverse events following immunisation in themselves or family were recruited from specialist immunisation clinics at two quaternary paediatric hospitals. Adverse event outcomes were collected via surveys administered at presentation, three, and eight days post vaccination, and analysed by key characteristics and potential risk factors.
Results:
Forty three of forty nine (43/49, 87.8 %) children enrolled received further vaccines. Of those who completed the follow up surveys, 50.0 % (16/32) reported an adverse event. Recurrence of prior adverse events occurred for 23.3 % (10/43, 95 % CI: 11.8 % - 38.6 %) of the cohort. Two of twelve (2/12, 16.7 %) participants with prior serious adverse events who received further vaccines reported a serious adverse event recurrence. No post review serious adverse events were observed in children with prior non serious adverse events. Neurological conditions were a risk factor for prior (neurological condition 3/3 versus no neurological condition 2/40, p < 0.001) and post review (neurological condition 2/3 versus no neurological condition 0/28, p = 0.006) post vaccination seizures. Family history had no relationship to post review adverse events (family history 5/8 versus no family history 11/23, p = 0.685).
Conclusion:
Revaccination is safe for the majority of children with a personal or family history of adverse event following immunisation.
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