Health and social outcomes of children with cerebral palsy

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Health and social outcomes in children who have cerebral palsy (CP) depend on several factors, including the severity of the CP, medical interventions, and the child's environment. One of the hallmarks of cerebral palsy is its variability. Several formal methods of classifying persons with CP, such as the Gross Motor Function Classification System, have been developed to standardize that variability. Children and adults with CP must contend with increased mortality as well as many secondary conditions that can affect activities and participation in society. Predicting outcomes for children with CP, establishing realistic goals, and determining the best interventions to improve functioning are facilitated by applying research results to individual decisions. Many more such studies are needed—especially those performed with large representative samples. In addition, the childhood factors that affect outcomes in adults with CP still need to be elucidated.

Section snippets

Clinical factors and the classification of cerebral palsy

Lloyd and Gould4 noted that variability is the fundamental reality of nature. One of the striking characteristics of CP is its variability. CP can be classified according to the type of motor impairment, which includes spasticity, dyskinesia (dystonia and choreoathetosis), and ataxia. Sometimes hypotonia is included in this classification scheme. Many children have mixed CP that involves two or more of these elements. Another way to classify CP is by location—for instance, quadriplegia,

Secondary conditions

The International Classification of Functioning, Disability and Health10 provides a classification scheme for understanding outcomes that includes body function and structure (impairments), activities, and participation (Fig 2). Environmental and personal factors are postulated to affect outcomes in all categories. Children who have CP have outcomes in all three categories. They are likely to have comorbid conditions that accompany the primary diagnosis and affect outcome, as well as secondary

Mortality

Most children with CP survive to adulthood, although the death rate is higher than in children who do not have CP. Strauss et al20 found that children with severe impairment of mobility and feeding skills had the greatest risk of dying during childhood. Data from the Western Australian Cerebral Palsy Register of children with CP born between 1958 and 1994 showed a mortality rate greater than 1% per year in the first 5 years of life; it then declined to 0.35% over the period of the next 20 years.

Interventions to improve outcomes

Most children who have CP receive multimodal therapy—for example, physical, occupational, and speech therapies; orthopedic surgery; spasticity management; and special educational support services. These therapies tend to be complementary. For example, orthopedic interventions have no effect on spasticity but address secondary problems such as contractures and lever-arm dysfunction. On the other hand, reducing spasticity has no effect on existing bony problems. Neither can improve selective

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