Vaccination in Pediatric Movement Disorders, Immune-mediated/ Inflammatory Central Nervous System Disorders, and Developmental and Epileptic Encephalopathies: Current Evidence-Based Recommendations
DOI:
https://doi.org/10.31305/rrijm.2025.v10.n11.009Keywords:
Movement Disorders, Cerebral Palsy, progressive neurological disease, Anti-NMDA receptor encephalitis, Narcolepsy, Rasmussen encephalitis, Febrile Infection-Related Epilepsy Syndrome, Dravet Syndrome, Vaccine-Proximate Febrile Seizures, Children, Vaccination, RecommendationsAbstract
Certain vaccines themselves, or vaccine-proximate fevers have been reported to, or postulated to trigger or exacerbate Pediatric Movement Disorders (MDs) [including Acute Cerebellar Ataxia (ACA) and Opsoclonus-Myoclonus-Ataxia syndrome (OMA)]; Immune-mediated/inflammatory Central Nervous System (IICNS) disorders [including Narcolepsy, Anti-NMDA receptor encephalitis, Rasmussen encephalitis (RE) and Febrile Infection-Related Epilepsy Syndrome (FIRES)]; and Developmental and Epileptic Encephalopathies (DEE) including Dravet Syndrome (DS). The fear of triggering or exacerbating these conditions is an important reason for vaccine hesitancy, even with routine age-appropriate vaccines. This narrative review collates relevant level and grade evidence up to September 2025 pertaining to safety of various vaccines, and summarizes current recommendations for vaccination. Per current recommendations, in children with MDs, particularly in Cerebral Palsy, all vaccines are recommended, with no contraindication. Influenza and Pneumococcal vaccines are specifically recommended owing to vulnerability to respiratory infections; as also MMR, COVID-19 and Varicella vaccines. For ACA and OMS, epidemiologic evidence to establish a causal association with vaccination is lacking. For pertussis containing vaccines including acellular DTP, while the American CDC guidelines list progressive encephalopathy, infantile spasms and uncontrolled epilepsy as precautions and recommend deferment until neurologic status stabilization; the Australian guidelines recommend that these vaccines can be safely administered even to infants and children with active or progressive neurological diseases, since vaccination is the best prevention. The risk of narcolepsy has been definitely attributed to only one erstwhile Influenza vaccine brand (Pandemrix®). No convincing evidence implicates any vaccine in current use as directly causing any IICNS disorder. In the spectrum of DEEs, no consistent association with vaccination has been documented, other than in children with DS. Vaccine-Proximate Febrile Seizures (VP-FSs) could occur within 48 hours following inactivated (whole-cell DPT/influenza/Pneumococcal Conjugate) or 5–14 days following live-attenuated (MMR/varicella) vaccines, especially in DEE (DS); yet long-term neurodevelopmental outcomes are no different from unvaccinated. Overall, all scheduled vaccinations are recommended, but whole-cell DPT avoided and acellular DPT considered on case-to-case basis in progressive, unstable neurological disorders and VP-FSs/DS; and administered only under medical supervision. Vaccination during the phases of disease deterioration should be judiciously avoided.
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