Epidemiology of cerebral palsy in England and Scotland, 1984-9
a FSID Unit of
Paediatric and Perinatal Epidemiology,
Department of Public Health,
University of Liverpool
Liverpool L69 3GB, b National Perinatal Epidemiology
Unit, Radcliffe Infirmary,
Oxford, c Public Health Research Unit,
University of Glasgow
Glasgow
Correspondence to: Professor Pharoah.
Accepted 31 December
1997
AIMS
To report
on the epidemiology of cerebral palsy in England and Scotland, to
provide information on the prevalence of cerebral palsy and the
severity of the disability or any co-morbidity.
METHODS
Cerebral
palsy registers were compiled from multiple sources of ascertainment
covering all of Scotland and the counties of Merseyside, Cheshire,
Berkshire, Buckinghamshire, Northamptonshire and Oxfordshire in
England. All cases of cerebral palsy born in 1984 to 1989, to mothers
resident in the area, were included. Denominator number of live births
and neonatal deaths for determining birthweight specific prevalence
were obtained from birth and death registrations. Learning, manual, and
ambulatory disabilities were graded for severity. Any co-existing
sensory (hearing or visual) morbidity was also graded for severity.
RESULTS
There
were 789 411 live births in 1984-9, with 3651 neonatal deaths
(neonatal mortality 4.6 per 1000 live births) and 1649 cases of
cerebral palsy
a cerebral palsy prevalence of 2.1 per 1000 neonatal
survivors. The birthweight specific cerebral palsy prevalence ranged
from 1.1 per 1000 neonatal survivors in infants weighing
2500 g to
78.1 in infants weighing <1000 g. There was no significant time trend
in prevalence of cerebral palsy in any of the birthweight groups, in
contrast to the fall in neonatal mortality observed in all birthweight
groups. Of the 1649 cases of cerebral palsy, 550 (33.4%) had severe
ambulatory disability (no independent walking), 390 (23.7%) had severe
manual disability (incapable of feeding or dressing unaided), 381 (23.1%) had severe learning disability (IQ <50), 146 (8.9%) had
severe visual disability (vision <6/60 in the better eye) and 12 had
severe hearing disability (>70 dB loss).
CONCLUSIONS
Registers
fill an important gap left by the lack of routine data on the
prevalence of disability in children. The ability to record trends in
the prevalence and the severity of the disability should inform those
who have responsibility for providing services for children with disabilities.
© 1998 by Archives of Disease in Childhood
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