Congenital anomalies and the severity of impairments for cerebral palsy
Autor: | Kristin Melheim Strand, Kari Klungsøyr, Solveig Bjellmo, Guro L. Andersen, Kjersti Postmyr Jystad, Jon Skranes, Stian Lydersen, Torstein Vik, Magne Stoknes |
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Jazyk: | angličtina |
Rok vydání: | 2017 |
Předmět: |
Male
Pediatrics medicine.medical_specialty Adolescent Cross-sectional study Gestational Age Nervous System Malformations Severity of Illness Index Community Health Planning Functional Laterality Cerebral palsy Cohort Studies 03 medical and health sciences Epilepsy 0302 clinical medicine Developmental Neuroscience Risk Factors Severity of illness Odds Ratio Spastic Humans Medicine 030212 general & internal medicine Child Norway business.industry Cerebral Palsy Gestational age medicine.disease Exact test Cross-Sectional Studies Pediatrics Perinatology and Child Health Female Neurology (clinical) business 030217 neurology & neurosurgery Cohort study |
Zdroj: | Developmental Medicine & Child Neurology |
Popis: | Aim: To study the prevalence of congenital anomalies among children with cerebral palsy (CP) born at term or late preterm, and if CP subtypes and clinical manifestations differ between children with and without congenital anomalies. Method: This was a cross-sectional study using data from the Cerebral Palsy Register of Norway and the Medical Birth Registry of Norway. All children with congenital CP born at and later than 34 weeks’ gestation in Norway from 1999 to 2009 were included. Anomalies were classified according to the European Surveillance of Congenital Anomalies classification guidelines. Groups were compared using Fisher's exact test, Kruskal–Wallis test, and the Mann–Whitney U test. Results: Among 685 children with CP, 169 (25%) had a congenital anomaly; 125 within the central nervous system. Spastic bilateral CP was more prevalent in children with anomalies (42%) than in children without (34%; p=0.011). Children with anomalies less frequently had low Apgar scores (p |
Databáze: | OpenAIRE |
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