IMDIndex and within the UK. [4][5][6][7][8][9][10][11][12] Applying and maintaining such standards, however, requires the collection and dissemination of high-quality data on existing best practice. The UK currently has no national data collection system to produce comprehensive population-based evidence of this kind. At present, such information can only be assembled by examining the provision and variation in care for disabled children with individual conditions where population-based data are already available.Cerebral palsies (CP) are the most common cause of physical disability in early childhood, affecting 2 to 3 per 1000 live births. 13 They are a group of permanent disorders of movement and posture resulting from non-progressive disturbances in the developing brain that cause activity limitation. These motor disorders are often accompanied by further disturbances of sensation, perception, cognition, communication, and behaviour, as well as by epilepsies, and by secondary musculoskeletal problems.14 The wideranging profile of disabilities arising from CP means they can serve as excellent exemplars of the range of disabling conditions that affect children and young people in general.The aim of this retrospective audit of medical records was to explore and describe the provision and variations in care over time, between districts and by socio-economic status (SES), for children and young people with CP in a defined geographical area of the UK.
METHOD PopulationThe North of England Collaborative Cerebral Palsy Survey (NECCPS), established in 1991, is a consented population-based register of children and young people with CP