Use of the General Movements Assessment for the Early Detection of Cerebral Palsy in Infants with Congenital Anomalies Requiring Surgery
Autor: | Nadia Badawi, Cathryn Crowle, Iona Novak, Alison Loughran Fowlds |
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Jazyk: | angličtina |
Rok vydání: | 2019 |
Předmět: |
General movements assessment
medicine.medical_specialty Early detection lcsh:Medicine Article Cerebral palsy 03 medical and health sciences 0302 clinical medicine 030225 pediatrics medicine Prospective cohort study early detection general movements cerebral palsy business.industry congenital anomalies lcsh:R General Medicine medicine.disease Predictive value General movements Surgery Fidgety movements Gestation business 030217 neurology & neurosurgery |
Zdroj: | Journal of Clinical Medicine Volume 8 Issue 9 Journal of Clinical Medicine, Vol 8, Iss 9, p 1286 (2019) |
ISSN: | 2077-0383 |
DOI: | 10.3390/jcm8091286 |
Popis: | The general movements (GMs) assessment is recognised as one of the most important tools in the early detection of cerebral palsy (CP). However, there remains a paucity of data on its application to infants with congenital anomalies requiring surgery. This was a prospective study of 202 infants (mean gestation 38 weeks, SD 2.2) who had undergone major surgery for congenital anomalies in the neonatal period. Infants were assessed at three months of age (mean 12 weeks, SD 1.6) and GMs videos were independently rated by three clinicians, two blinded to clinical details. Developmental follow-up was at three years of age. Of the twenty-five infants (9%) rated as having an absence of fidgety movements, 22 were seen at 3 years, and 17 had an abnormal outcome: 11 with CP, and 6 with a developmental disability. Infants with absent fidgety movements were 21.5 (95% CI 7.3&ndash 63.8) times more likely to have an abnormal outcome including CP. None of the infants with normal fidgety movements had a diagnosis of CP and 86% were assessed to be developing normally. The GMs assessment has predictive value for cerebral palsy and neurodevelopment for infants with congenital anomalies, and should be incorporated into routine follow-up to facilitate early referral. |
Databáze: | OpenAIRE |
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