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Cognitive Outcome in Children with Myelomeningocele and Perinatal Hydrocephalus: A Longitudinal Perspective

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Abstract

Myelomeningocele, a form of spina bifida where the vertebrae fail to fuse during foetal development, is often associated with sensory deficits, reduced motor function and hydrocephalus. These complications may interfere with the development of the central nervous system affecting myelination of axons and formation of synaptic connections, and development of cognitive skills, particularly where complications occur within the first twelve months of life. This paper examines the long-term cognitive outcome in nineteen children with myelomeningocele, who were shunted for hydrocephalus within the first year of life. In comparison to a healthy control group matched for age and gender, the clinical sample were found to have globally compromised cognitive skills, including reduced intellectual and educational skills. Specific impairments were noted on measures of speed of processing, immediate registration of information, learning and memory, organisation and high level language, with greatest deficits on more complex, less structured tasks. Within the clinical group, there was a fall in IQ over time, suggesting a failure to acquire cognitive skills in the expected time frame. These results, reflecting a cumulative pattern of deficits over time, highlight the importance of long-term follow up in children with myelomeningocele and perinatal hydrocephalus.

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Authors and Affiliations

  1. Department of Psychology, Royal Children's Hospital, Melbourne, Australia

    Rani Jacobs, Elisabeth Northam & Vicki Anderson

  2. Murdoch Children's Research Institute, Melbourne, Australia

    Rani Jacobs

  3. University of Melbourne, Australia

    Vicki Anderson

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  2. Elisabeth Northam
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Jacobs, R., Northam, E. & Anderson, V. Cognitive Outcome in Children with Myelomeningocele and Perinatal Hydrocephalus: A Longitudinal Perspective. Journal of Developmental and Physical Disabilities 13, 389–405 (2001). https://doi.org/10.1023/A:1012289513829

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