AIM This study used data collected prospectively since 1986 from a population-based cerebral palsy registry to explore the rates, predictors, trends, and causes of mortality for individuals born in Victoria, Australia, between 1970 and 2004. METHOD Data were extracted for 3507 individuals (1972 males; 1535 females). The probability of survival before 31 May 2010 was determined using the Kaplan-Meier method; age-specific mortality rates were calculated per 1000 person-years and related to population rates. Using Cox proportional hazards regression, relative risks of mortality were estimated for different categories of chosen demographic and clinical variables. Causes were tabulated according to the direct cause of death.RESULTS There were 418 deaths. Crude mortality was 20% at the age of 40 years. Relative to the population, mortality was highest in children aged under 15 years and decreased to twice the population rate at the age of 35 years. The strongest independent predictor of mortality was no independent ambulation (adjusted hazard ratio 6.2 [95% confidence interval 3.3-11.8]); additional predictors were severe intellectual impairment Cerebral palsy (CP) is a diagnostic label that embraces a range of disorders of movement and posture. Substantial variation exists with regard to the type, topographical pattern, and severity of the movement disorder, the presence of associated conditions and impairments, and how these combine to impact on function, participation, and quality of life. Since the label 'CP' accommodates such a wide variety of possible clinical manifestations, information about survival with CP based on different combinations of clinical features is needed to counsel families about a child's prognosis, to plan for the provision of medical, educational, and social services, to inform public policy, and for medicolegal services relating to litigation. The aim of this study was to describe the rates, trends, predictors, and causes of mortality in individuals with nonpostneonatally acquired CP who were born in the Australian state of Victoria between 1970 and 2004. A number of groups have previously studied life expectancy in CP samples but many studies have had shortcomings. Recent studies of all CP cases from long-standing registers in Western Australia, 1 the UK, 2 and Denmark 3 have provided useful information on the long-term prognosis of all newly diagnosed children. The UK study noted regional differences in survival, but it was unclear whether these reflected regional variation in survival patterns, risk factor profiles, levels of care, or differences in definition, classification, or ascertainment.2 Severity of disability is the key factor influencing survival in CP. Immobility or severe motor impairment of all four limbs, 1-9 intellectual impairment, 1,2,4-7,10 epilepsy, 3,4,10 severe visual and hearing impairments, 2,7,11 hydrocephalus, 4 and an increasing number of impairments 1,2,5-7 have been associated with poorer survival. Although different severity profiles have been used by ea...