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    Soft neurological signs and prenatal alcohol exposure: a population-based study in remote Australia

    Access Status
    Open access via publisher
    Authors
    Lucas, B.
    Latimer, J.
    Fitzpatrick, J.
    Doney, Robyn Michelle
    Watkins, R.
    Tsang, T.
    Jirikowic, T.
    Carmichael Olson, H.
    Oscar, J.
    Carter, M.
    Elliott, E.
    Date
    2016
    Type
    Journal Article
    
    Metadata
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    Citation
    Lucas, B. and Latimer, J. and Fitzpatrick, J. and Doney, R.M. and Watkins, R. and Tsang, T. and Jirikowic, T. et al. 2016. Soft neurological signs and prenatal alcohol exposure: a population-based study in remote Australia. Developmental Medicine and Child Neurology. 58 (8): pp. 861-867.
    Source Title
    Developmental Medicine and Child Neurology
    DOI
    10.1111/dmcn.13071
    ISSN
    0012-1622
    School
    School of Public Health
    URI
    http://hdl.handle.net/20.500.11937/36904
    Collection
    • Curtin Research Publications
    Abstract

    © 2016 Mac Keith PressAim: To identify soft neurological signs (SNS) in a population-based study of children living in remote Aboriginal communities in the Fitzroy Valley, Western Australia, born between 2002 and 2003 and explore the relationship between SNS, prenatal alcohol exposure (PAE), and fetal alcohol spectrum disorders (FASD). Method: The presence of SNS was assessed using the Quick Neurological Screening Test, 2nd edition (QNST-2), which has a total maximum score of 140. Higher scores indicated more SNS. ‘Severe discrepancy’ was defined as scores less than or equal to the fifth centile while ‘moderate discrepancy’ represented scores from the sixth to the 24th centile. Children were assigned FASD diagnoses using modified Canadian FASD diagnostic guidelines. Results: A total of 108 of 134 (80.6%) eligible children (mean age 8y 9mo, SD=6mo, 53% male) were assessed. The median QNST-2 Total Score for all participants was within the normal category (19.0, range 4–66). However, the median QNST-2 Total Score was higher in children with than without (1) PAE (r=0.2, p=0.045) and (2) FASD (r=0.3, p=0.004). Half (8/16) of children scoring ‘moderate discrepancy’ and all (2/2) children scoring ‘severe discrepancy’ had at least three domains of central nervous system impairment. Interpretation: SNS were more common in children with PAE or FASD, consistent with the known neurotoxic effect of PAE. The QNST-2 is a useful screen for subtle neurological dysfunction indicating the need for more comprehensive assessment in children with PAE or FASD.

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    • Gross motor performance in children prenatally exposed to alcohol and living in remote Australia
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