UKCP: a collaborative network of cerebral palsy registers in the United Kingdom

Geraldine Surman, Sandra Bonellie, James Chalmers, Allan Colver, Helen Dolk, Karla Hemming, Andy King, Jennifer J Kurinczuk, Jackie Parkes, Mary Jane Platt

Research output: Contribution to journalArticlepeer-review

54 Citations (Scopus)

Abstract

Cerebral palsy (CP) is a relatively rare condition with enormous social and financial impact. Information about CP is not routinely collected in the United Kingdom. We have pooled non-identifiable data from the five currently active UK CP registers to form the UKCP database: birth years 1960-1997. This article describes the rationale behind this collaboration and the creation of the database. Data about 6910 children with CP are currently held. The mean annual prevalence rate was 2.1 [corrected] per 1000 live births for birth years 1986-1996. Where type is known, 91 per cent have spastic CP. Where data are available, nearly one-third of children have severely impaired lower limb function, and nearly a quarter have severely impaired upper limb function. As well as describing the range and complexity of motor and associated impairments, the pooled data from the UKCP database provide a platform for studies of aetiology, long-term outcomes, participation and service needs. The UKCP database is an important national resource for the surveillance of CP and the study of its epidemiology in the United Kingdom.
Original languageEnglish
Pages (from-to)148-56
Number of pages9
JournalJournal of Public Health
Volume28
Issue number2
DOIs
Publication statusPublished - Jun 2006

Keywords

  • Adolescent
  • Cerebral Palsy
  • Child
  • Child, Preschool
  • Cooperative Behavior
  • Great Britain
  • Health Services Needs and Demand
  • Humans
  • Infant
  • Registries

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