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Revaccination outcomes of children with vaccine proximate seizures
Lucy Deng1, Margie Danchin2, Georgina Lewis3
1National Centre for Immunisation Research and Surveillance, Children's Hospital at Westmead, Westmead, Australia; The University of Sydney Children's Hospital Westmead Clinical School, Westmead, Australia.
Insights
Vaccine proximate seizures (VPSs) are uncommon in children with a history of a single VPS. However, children with multiple seizures after initial VPS are at higher risk for recurrence upon revaccination, especially if diagnosed with Dravet syndrome.
Area of Science:
- Pediatric Neurology
- Vaccinology
- Epilepsy Research
Background:
- Vaccine proximate seizures (VPSs) are defined as seizures occurring within 14 days of vaccination.
- While the risk of a first febrile VPS is known, the recurrence risk and outcomes of VPS are less understood.
Purpose of the Study:
- To investigate the recurrence of VPS and outcomes following revaccination in children.
- To compare outcomes between children with a single VPS and those with subsequent seizures.
Main Methods:
- Retrospective review of 119 children experiencing their first seizure as a VPS.
- Comparison of revaccination outcomes between children with a single VPS and those with multiple seizures (VPS+) prior to clinic review.
Main Results:
- 51% of children experienced further seizures (VPS+).
- Children with VPS+ were younger and more likely to have afebrile seizures.
- VPS recurrence on revaccination was uncommon but higher in VPS+ children (12.5% vs 2.4%).
- Dravet syndrome diagnosis was significantly associated with VPS recurrence (P < 0.001).
Conclusions:
- VPS recurrence is uncommon after a single VPS.
- Children with multiple seizures post-VPS, especially those under 12 months, are at higher risk for recurrence.
- Consider Dravet syndrome diagnosis and precautions for revaccination in high-risk children.
Background:
Seizures, whether febrile or afebrile, occurring within 14 days following vaccination can be considered as vaccine proximate seizures (VPSs). While the attributable risk and clinical severity of first febrile VPS is well known, the risk and clinical outcomes of VPS recurrence is less well defined.
Methods:
We conducted a retrospective review of revaccination management and outcomes in children who experienced a VPS as their first seizure seen in Australian Specialist Immunisation Clinics between 2013 and 2017. Vaccination outcomes were compared between children who had a VPS as their only seizure (VPS only) and children who had further non-vaccine proximate seizures following their initial VPS (VPS+) prior to review at the clinic.
Results:
We identified 119 children with a VPS as their first seizure, of which 61 (51%) went on to have other seizures (VPS+). Children with VPS+ were more likely to present at a younger age (6.2 vs 12.5 months, P = 0.03), with afebrile seizures (42.6% vs 15.5%, P = 0.002) compared to VPS only children. VPS recurrence on revaccination was uncommon in both groups, but more common in VPS+ children (12.5% vs 2.4%, P = 0.07). Having an epilepsy diagnosis, specifically Dravet syndrome, was associated with VPS recurrence (P < 0.001). Of the four children with Dravet syndrome who had VPS recurrence, all had status epilepticus following revaccination.
Conclusion:
In children who presented with a single VPS as their only seizure, VPS recurrence on revaccination was uncommon. Children who had multiple non-vaccine proximate seizures following their initial VPS (VPS+) were more likely to present with afebrile VPS, at a younger age and have a VPS recurrence with vaccination. In these children, particularly those aged < 12 months, assessment and investigation for diagnosis of Dravet syndrome should be considered and additional precautions for revaccination undertaken as they are at highest risk of VPS recurrence.
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