Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/29753
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dc.contributor.authorHood, Veronica-
dc.contributor.authorBerg, Anne T-
dc.contributor.authorKnupp, Kelly G-
dc.contributor.authorKoh, Sookyong-
dc.contributor.authorLaux, Linda-
dc.contributor.authorMeskis, Mary Anne-
dc.contributor.authorZulfiqar-Ali, Quratulain-
dc.contributor.authorPerry, M Scott-
dc.contributor.authorScheffer, Ingrid E-
dc.contributor.authorSullivan, Joseph-
dc.contributor.authorWirrell, Elaine-
dc.contributor.authorAndrade, Danielle M-
dc.date2022-
dc.date.accessioned2022-04-12T04:27:41Z-
dc.date.available2022-04-12T04:27:41Z-
dc.date.issued2022-
dc.identifier.citationEpilepsia 2022; 63(7): 1778-1786en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/29753-
dc.description.abstractVaccination against SARS-CoV-2 virus is a primary tool to combat the COVID-19 pandemic. However, vaccination is a common seizure trigger in individuals with Dravet syndrome (DS). Information surrounding COVID-19 vaccines side-effects in patients with DS would aid caregivers and providers in decisions for and management of COVID-19 vaccination. A survey was emailed to the Dravet Syndrome Foundation's (DSF) Family Network and posted to the Dravet Parent & Caregiver Support Group on Facebook between May and August 2021. Deidentified information obtained included demographics and vaccination status for individuals with DS. Vaccine type, side effects, preventative measures, and changes in seizure activity following COVID-19 vaccination were recorded. For unvaccinated individuals, caregivers were asked about intent to vaccinate and reasons for their decision. Of 278 survey responses, 120 represented vaccinated individuals with DS (median age 19.5 years) with 50% reporting no side effects from COVID-19 vaccination. Increased seizures following COVID-19 vaccination were reported in 16 individuals, but none had status epilepticus. Of the 158 individuals who had not received a COVID-19 vaccination, 37 were over the age of 12 (i.e., eligible at time of study) and only six of these caregivers indicated intent to seek vaccination. The remaining 121 responses were caregivers to children under the age of 12, 60 of whom indicated they would not seek COVID-19 vaccination when their child with DS is eligible. Reasons for vaccine-hesitancy were fear of increased seizure activity and concerns about vaccine safety. These results indicate COVID-19 vaccination is well-tolerated by individuals with DS. One main reason for vaccine hesitancy was fear of increased seizure activity, which only occurred in 13% of vaccinated individuals and none had status epilepticus. This study provides critical and reassuring insights for caregivers and healthcare providers making decisions about safety of COVID-19 vaccinations for individuals with DS.en
dc.language.isoeng-
dc.subject(max 6): Draveten
dc.subjectCOVID-19en
dc.subjectsurveyen
dc.subjectvaccineen
dc.titleCOVID-19 vaccine in patients with Dravet syndrome: Observations and real-world experiences.en
dc.typeJournal Articleen
dc.identifier.journaltitleEpilepsiaen
dc.identifier.affiliationDravet Syndrome Foundation, Cherry Hill, New Jersey, USA..en
dc.identifier.affiliationDepartment of Neurology, Northwestern Feinberg School of Medicine, Chicago, USA..en
dc.identifier.affiliationDepartment of Pediatrics and Neurology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA..en
dc.identifier.affiliationDepartment of Pediatric Neurology, University of Nebraska Medical Center, Omaha, Nebraska, USA..en
dc.identifier.affiliationEpilepsy Center, Department of Pediatrics, Ann & Robert H. Lurie Children's Hospital, Chicago, Illinois, USA..en
dc.identifier.affiliationAdult Genetic Epilepsy Program, University of Toronto, Toronto, Ontario, Canada..en
dc.identifier.affiliationAdult Epilepsy Genetics Program, Toronto Western Hospital, Krembil Brain Institute, Toronto, Canada..en
dc.identifier.affiliationJane and John Justin Neurosciences Center, Cook Children's Medical Center, Fort Worth, Texas, USA...en
dc.identifier.affiliationEpilepsy Research Centreen
dc.identifier.affiliationDepartment of Neurology & Pediatrics, University of California, San Francisco, California, USA..en
dc.identifier.affiliationChild and Adolescent Neurology, Mayo Clinic, Rochester, Minnesota, USA..en
dc.identifier.affiliationDivision of Neurology, Krembil Brain Institute, Toronto Western Hospital, University of Toronto, Toronto, Canada..en
dc.identifier.affiliationRoyal Children's Hospital, Florey Institute, Melbourne, Victoria, Australia..en
dc.identifier.affiliationMurdoch Children's Research Institute, Melbourne, Victoria, Australia..en
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/35383912/en
dc.identifier.doi10.1111/epi.17250en
dc.type.contentTexten
dc.identifier.orcidhttps://orcid.org/0000-0002-1988-4980en
dc.identifier.orcidhttps://orcid.org/0000-0002-0298-5523en
dc.identifier.orcidhttps://orcid.org/0000-0002-1967-0827en
dc.identifier.orcidhttps://orcid.org/0000-0002-1825-846Xen
dc.identifier.orcidhttps://orcid.org/0000-0002-2311-2174en
dc.identifier.orcidhttps://orcid.org/0000-0003-3015-8282en
dc.identifier.pubmedid35383912-
local.name.researcherScheffer, Ingrid E
item.grantfulltextnone-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.deptEpilepsy Research Centre-
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