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Published on: February 22, 2019
Pertussis vaccine and infantile spasms
Petros Lapatsanis1, Dimitris Lapatsanis
1University of Ioannina, Medical School, Department of Child Health, Ioannina 45110, Greece. plapatsanis@yahoo.com
Insights
This study investigated a potential link between childhood vaccines and epilepsy. The findings suggest that infantile spasms in one case were unlikely caused by the triple vaccine, despite family seizure history.
Area of Science:
- Neurology
- Pediatrics
- Immunology
Background:
- Epilepsy and infantile spasms are serious neurological conditions in children.
- The triple vaccine, including diphtheria, tetanus, and whole-cell pertussis, is a common childhood immunization.
- Family history of seizures can increase the risk of developing epilepsy.
Observation:
- Case 1: A 12-week-old boy developed spasms and hypsarrhythmia after the first triple vaccine dose, treated with ACTH and later sodium valproate for recurrent seizures at age 9.
- Case 2: A paternal cousin experienced blackouts at age 11 with EEG findings of idiopathic epilepsy, also treated with sodium valproate.
- Both cases belong to a family with a predisposition to seizures.
Findings:
- Electroencephalogram (EEG) in Case 1 confirmed hypsarrhythmia, a hallmark of infantile spasms.
- EEG in Case 2 indicated idiopathic epilepsy.
- The temporal association between vaccination and symptom onset in Case 1 does not confirm causation, especially given the family history.
Implications:
- The study questions the direct causal link between the triple vaccine and infantile spasms in the presented case.
- Highlights the importance of considering genetic predisposition and family history in diagnosing childhood epilepsy.
- Suggests further research into vaccine safety and potential triggers for neurological disorders in susceptible individuals.
Abstract:
The boy (case 1) at the age of 12 weeks started having attacks and jercked after the first injection of triple vaccine (diphtheria, retanus and whole cell pertussis) The electro-encephalogram (EEG) confirmed the typical features of hypsarrhythmia. Intramuscular ACTH was commenced for 2 weeks. No problem was reported until the age of 9 years when he started having attacks of jercking. He was treated with sodium valproate. The boy of the second case was a first cousin of case 1. At the age of 11 years the boy had momentary black outs. The EEG showed findings of idiopathic epilepsy. Treatment with sodium valproate was commenced. The children of both cases belong to a family in which there is a trendency to seizures. It seems unlikely the triple vaccine produced the infantile spasms in case 1.
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