Please use this identifier to cite or link to this item: https://dora.health.qld.gov.au/qldresearchjspui/handle/1/5901
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dc.contributor.authorLuke, C.-
dc.contributor.authorMcNamara, L.-
dc.contributor.authorGordon, A.-
dc.contributor.authorFinn, C.-
dc.contributor.authorGibson, S.-
dc.contributor.authorMorris, K.-
dc.contributor.authorShannon, B.-
dc.contributor.authorCharlton, M.-
dc.contributor.authorOakes, E.-
dc.contributor.authorThomas, R.-
dc.contributor.authorGeorge, J.-
dc.contributor.authorKentish, M.-
dc.contributor.authorWare, R.-
dc.contributor.authorBoyd, R.-
dc.date.accessioned2024-06-20T00:28:37Z-
dc.date.available2024-06-20T00:28:37Z-
dc.date.issued2023-
dc.identifier.citationDevelopmental Medicine and Child Neurology, 2023 (65) p.65en
dc.identifier.urihttps://dora.health.qld.gov.au/qldresearchjspui/handle/1/5901-
dc.description.abstractIntroduction: The QEDIN-CP network supports implementation of the CP early detection guidelines; providing training, support for early screening, to fast-track infants to early intervention. This study evaluates the relationship between screening and outcomes in a prospective cohort of infants at risk of CP or adverse neurodevelopmental outcomes (NDO). Patients and methods: 574 clinicians, across 18 sites, were trained in (1) General Movements Assessment (GMA; n = 246) (2) Hammersmith Infant Neurological Examination (HINE; n = 328), over a 5-year period. Infants were screened at 0-12 months corrected age (CA) using GMA, Motor Optimality Score (MOS) and HINE with outcomes at 24 months CA on Ages and Stages Questionnaire (ASQ-3) and/or paediatrician diagnosis, classified as (a) typically developing, (b) CP or (c) adverse NDO (<2SD on ASQ-3). Results: 770 infants were referred with 637 (83%) consented, 439 (69%) were born preterm (mean GA = 33 wks) with 116 (18%) extreme preterm. Of these 46 3(73%) completed GMA, (n = 184, 40% writhing, n = 432, 93% fidgety), with 308 (71.3%) normal, 18 (4.2%) abnormal and 106 (24.5%) absent fidgety. At 3-12 months 290 (45%) infants completed HINE assessments (mean = 57.5, SD = 12.5). 95 (15%) infants received a diagnosis of CP at any age. Of 200 (87.7%) infants with completed outcomes, a further 37 (18%) were “high risk of CP” at 24 months. 118 (19%) infants were fast-tracked to early intervention studies. Conclusion: Large scale implementation of the CP early detection guidelines is feasible utilising a collaborative state-wide approach and clinical support network providing training, second opinions and calibration sessions. Early identification of high-risk infants promotes early access to CP specific supports and services..-
dc.language.isoEnglish-
dc.titleImplementation of the state-wide Queensland Early Detection Network (QEDIN-CP) -Prediction of outcomes for infants at risk of adverse neurodevelopmental outcomes-
dc.typeConference Abstract-
dc.identifier.doi10.1111/dmcn.15595-
dc.relation.urlhttps://www.embase.com/search/results?subaction=viewrecord&id=L641650070&from=export-
dc.relation.urlhttp://dx.doi.org/10.1111/dmcn.15595-
dc.identifier.journaltitleDevelopmental Medicine and Child Neurology-
dc.identifier.risid4608-
dc.description.pages65-
dc.description.volume65-
item.languageiso639-1English-
item.openairetypeConference Abstract-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
Appears in Sites:Children's Health Queensland Publications
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