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1.
Early Hum Dev ; 193: 106019, 2024 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-38718464

RESUMEN

BACKGROUND: Prechtl's General Movement Assessment (GMA) at fidgety age (3-5 months) is a widely used tool for early detection of cerebral palsy. Further to GMA classification, detailed assessment of movement patterns at fidgety age is conducted with the Motor Optimality Score-Revised (MOS-R). Inter-rater reliability and agreement are properties that inform test application and interpretation in clinical and research settings. This study aims to establish the inter-rater reliability and agreement of the GMA classification and MOS-R in a large population-based sample. METHODS: A cross-sectional study of 773 infants from birth-cohort in Perth, Western Australia. GMA was conducted on home-recorded videos collected between 12 + 0 and 16 + 6 weeks post term age. Videos were independently scored by two masked experienced assessors. Inter-rater reliability and agreement were assessed using intraclass correlation coefficient and limits of agreement respectively for continuous variables, and Cohen's Kappa and Gwet's Agreement Coefficient, and percentage agreement respectively for discrete variables. RESULTS: The classification of GMA showed almost perfect reliability (AC1 = 0.999) and agreement (99.9 %). Total MOS-R scores showed good-excellent reliability (ICC 0.857, 95 % CI 0.838-0.876) and clinically acceptable agreement (95 % limits of agreement of ±2.5 points). Substantial to almost perfect reliability and agreement were found for all MOS-R domain subscores. While MOS-R domains with higher redundancy in their categorisation have higher reliability and agreement, inter-rater reliability and agreement are substantial to almost perfect at the item level and are consistent across domains. CONCLUSION: GMA at fidgety age shows clinically acceptable inter-rater reliability and agreement for GMA classification and MOS-R for population-based cohorts assessed by experienced assessors.


Asunto(s)
Parálisis Cerebral , Variaciones Dependientes del Observador , Humanos , Femenino , Parálisis Cerebral/diagnóstico , Parálisis Cerebral/fisiopatología , Masculino , Lactante , Reproducibilidad de los Resultados , Movimiento/fisiología , Estudios Transversales , Australia Occidental , Destreza Motora/fisiología
2.
BMJ Open ; 11(4): e041695, 2021 04 09.
Artículo en Inglés | MEDLINE | ID: mdl-33837094

RESUMEN

INTRODUCTION: The current diagnostic pathways for cognitive impairment rarely identify babies at risk before 2 years of age. Very early detection and timely targeted intervention has potential to improve outcomes for these children and support them to reach their full life potential. Early Moves aims to identify early biomarkers, including general movements (GMs), for babies at risk of cognitive impairment, allowing early intervention within critical developmental windows to enable these children to have the best possible start to life. METHOD AND ANALYSIS: Early Moves is a double-masked prospective cohort study that will recruit 3000 term and preterm babies from a secondary care setting. Early Moves will determine the diagnostic value of abnormal GMs (at writhing and fidgety age) for mild, moderate and severe cognitive delay at 2 years measured by the Bayley-4. Parents will use the Baby Moves smartphone application to video their babies' GMs. Trained GMs assessors will be masked to any risk factors and assessors of the primary outcome will be masked to the GMs result. Automated scoring of GMs will be developed through applying machine-based learning to the data and the predictive value for an abnormal GM will be investigated. Screening algorithms for identification of children at risk of cognitive impairment, using the GM assessment (GMA), and routinely collected social and environmental profile data will be developed to allow more accurate prediction of cognitive outcome at 2 years. A cost evaluation for GMA implementation in preparation for national implementation will be undertaken including exploring the relationship between cognitive status and healthcare utilisation, medical costs, health-related quality of life and caregiver burden. ETHICS AND DISSEMINATION: Ethics approval has been granted by the Medical Research Ethics Committee of Joondalup Health Services and the Health Service Human Research Ethics Committee (1902) of Curtin University (HRE2019-0739). TRIAL REGISTRATION NUMBER: ACTRN12619001422112.


Asunto(s)
Disfunción Cognitiva , Calidad de Vida , Biomarcadores , Niño , Preescolar , Disfunción Cognitiva/diagnóstico , Estudios de Cohortes , Humanos , Lactante , Recién Nacido , Estudios Prospectivos
3.
BMJ Case Rep ; 12(6)2019 Jun 06.
Artículo en Inglés | MEDLINE | ID: mdl-31175114

RESUMEN

Tarsal-carpal coalition syndrome is a progressive condition involving synostosis of the wrist, ankle and digits. We describe a mother and her newborn that have this rare inherited condition where the diagnosis was made only after the baby's birth. The baby's condition was suspected on antenatal scanning, and he was born with reduced range of motion of his digits, elbows and ankles. The mother's condition has progressed to involve a fixed flexion deformity of her bilateral elbows, synostoses of her second to fifth digits and extensive coalition of her tarsal and carpal bones. She has required regular osteotomies to improve limb functioning and quality of life.


Asunto(s)
Huesos del Carpo/anomalías , Proteínas Portadoras/genética , Deformidades Congénitas del Pie/diagnóstico por imagen , Deformidades Congénitas del Pie/cirugía , Deformidades Congénitas de la Mano/diagnóstico por imagen , Deformidades Congénitas de la Mano/cirugía , Estribo/anomalías , Sinostosis/diagnóstico por imagen , Sinostosis/cirugía , Huesos Tarsianos/anomalías , Huesos del Carpo/diagnóstico por imagen , Huesos del Carpo/cirugía , Diagnóstico Precoz , Femenino , Deformidades Congénitas del Pie/genética , Deformidades Congénitas de la Mano/genética , Humanos , Recién Nacido , Masculino , Edad Materna , Osteotomía , Polimorfismo de Nucleótido Simple , Estribo/diagnóstico por imagen , Sinostosis/genética , Huesos Tarsianos/diagnóstico por imagen , Huesos Tarsianos/cirugía , Adulto Joven
4.
Early Hum Dev ; 124: 38-41, 2018 09.
Artículo en Inglés | MEDLINE | ID: mdl-30138737

RESUMEN

Studies on general movement assessments (GMs) have included small numbers of extremely preterm (EP) infants. We determined the GMs and motor optimality score (MOS) of 40 EP infants. Poor repertoire at writhing age normalising to fidgety movements was the most common finding. MOS was lower than for published term infants.


Asunto(s)
Recien Nacido Extremadamente Prematuro/fisiología , Actividad Motora/fisiología , Femenino , Humanos , Lactante , Masculino , Neonatología/métodos , Proyectos Piloto , Estudios Prospectivos , Reproducibilidad de los Resultados
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