Diagnosis and management of individuals with Fetal Valproate Spectrum Disorder; a consensus statement from the

Jill Clayton-Smith1,2, Rebecca Bromley3,4, John Dean5

  • 1Division of Evolution and Genomic Sciences School of Biological Sciences, University of Manchester, Manchester, UK. Jill.Clayton-Smith@mft.nhs.uk.

Insights

Fetal Valproate Spectrum Disorder (FVSD) encompasses a range of effects from in utero sodium valproate (VPA) exposure, including congenital anomalies and neurodevelopmental issues. Expert consensus provides management guidance for this rare disorder.

Area of Science:

  • Teratology
  • Neurodevelopmental Disorders
  • Genetics and Rare Diseases

Background:

  • In utero exposure to sodium valproate (VPA) is associated with a spectrum of congenital anomalies and neurodevelopmental deficits.
  • Recognition of VPA's teratogenic risks, particularly neurodevelopmental effects, has evolved through prospective studies and registries.
  • Effects range from major malformations and intellectual disability to subtle facial dysmorphism and moderate neurodevelopmental impacts.

Purpose of the Study:

  • To establish clinical management recommendations for Fetal Valproate Spectrum Disorder (FVSD).
  • To address the lack of high-level evidence regarding optimal clinical management for FVSD.
  • To propose a standardized term, Fetal Valproate Spectrum Disorder (FVSD), to encompass the varied effects of in utero VPA exposure.

Main Methods:

  • Convening an expert group under ERN-ITHACA, including professionals and patient representatives.
  • Conducting a literature review of published and unpublished management data for FVSD, with evidence grading.
  • Utilizing an expert consensus meeting and iterative refinement for developing management recommendations.

Main Results:

  • Strong evidence exists for increased risks of major congenital malformations and neurodevelopmental difficulties.
  • A significant gap in high-level evidence was identified for other areas, especially optimal clinical management.
  • The expert consensus approach facilitated the formulation of management recommendations based on available evidence and best practices.

Conclusions:

  • Expert consensus is a viable method for developing clinical guidance for rare disorders like FVSD.
  • FVSD presents with medical, developmental, and neuropsychological impacts that can have lifelong consequences.
  • Multidisciplinary healthcare professional input is crucial for individuals diagnosed with FVSD.
Abstract

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