Narrative
Research undertaken by Bromley and Clayton-Smith at The University of Manchester has been integral in reducing risks to fetal development from the treatment of epilepsy during pregnancy. We demonstrated that sodium valproate taken in pregnancy can lead to increased rates of physical birth defects and lifelong cognitive, behavioural and social difficulties in the offspring. Our research has contributed to regulatory interventions and policy changes which have seen the prescribing of valproate become severely restricted in women and girls, resulting in tens of thousands fewer children being affected worldwide. Diagnostic guidelines and both genetic and neuropsychological clinical pathways have been developed to improve management for those affected.Impact date | Aug 2013 → Dec 2020 |
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Category of impact | Health and wellbeing, Policy |
Impact level | Adoption |
Documents & Links
Related content
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Research output
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Fetal antiepileptic drug exposure and cognitive outcomes at age 6 years (NEAD study): A prospective observational study
Research output: Contribution to journal › Article › peer-review
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The prevalence of neurodevelopmental disorders in children prenatally exposed to antiepileptic drugs
Research output: Contribution to journal › Article › peer-review
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Cognitive function at 3 years of age after fetal exposure to antiepileptic drugs
Research output: Contribution to journal › Article › peer-review
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Treatment for epilepsy in pregnancy: neurodevelopmental outcomes in the child
Research output: Contribution to journal › Article › peer-review
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IQ at 6 years after in utero exposure to antiepileptic drugs: a controlled cohort study. A controlled cohort study
Research output: Contribution to journal › Article › peer-review
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Cognition in school-age children exposed to levetiracetam, topiramate, or sodium valproate
Research output: Contribution to journal › Article › peer-review