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Cerebral Palsy

Cerebral palsy, also referred to as CP, is a term used to describe a group of chronic conditions affecting body movement and muscle coordination. It is caused by damage to one or more specific areas of the brain, usually occurring during fetal development; before, during or shortly after birth; or during infancy. “Cerebral” refers to the brain and “palsy” to muscle weakness/poor control. Cerebral palsy itself is not progressive (i.e., brain damage does not get worse); however, secondary conditions, such as muscle spasticity, can develop which may get better, get worse, or remain the same. Cerebral palsy is not communicable. It is not a disease and should not be referred to as such. Although cerebral palsy is not “curable” in the accepted sense, training and therapy can help improve function.

What are the effects?
Cerebral palsy is characterized by an inability to fully control motor function, particularly muscle control and coordination. Depending on which areas of the brain have been damaged, one or more of the following may occur: muscle tightness or spasticity; involuntary movement; disturbance in gait or mobility, difficulty in swallowing and problems with speech. In addition, the following may occur: abnormal sensation and perception; impairment of sight, hearing or speech; seizures; and/or mental retardation. Other problems that may arise are difficulties in feeding, bladder and bowel control, problems with breathing because of postural difficulties, skin disorders because of pressure sores, and learning disabilities.

What are the causes?
Cerebral palsy is not a disorder with a single cause, like chicken pox or measles. It is a group of disorders with similar problems in control of movement, but probably with a variety of causes.

Congenital cerebral palsy, results from brain injury during intra-uterine life. It is present at birth, although it may not be detected for months. It is responsible for about 70% of children who have cerebral palsy. An additional 20 % are diagnosed with congenital cerebral palsy due to a brain injury during the birthing process. In most cases, the cause of congenital cerebral palsy is unknown.

On the other hand, in the United States, about 10 percent of children who have cerebral palsy acquire the disorder after birth. (The figures are higher in underdeveloped countries.) Acquired cerebral palsy results from brain damage in the first few months or years of life and can follow brain infections, such as bacterial meningitis or viral encephalitis, or the results of head injury -- most often from a motor vehicle accident, a fall, or child abuse.

Risk factors for cerebral palsy include the following: premature birth; low birth weight; inability of the placenta to provide the developing fetus with oxygen and nutrients; lack of growth factors during intra-uterine life; RH or A-B-O blood type incompatibility between mother and infant; infection of the mother with German measles or other viral diseases in early pregnancy; bacterial infection of the mother, fetus or infant that directly or indirectly attack the infant's central nervous system; prolonged loss of oxygen during the birthing process and severe jaundice shortly after birth.

Are there different types of cerebral palsy?
There are three main types: spastic – characterized by stiff and difficult movement; athetoid – characterized by involuntary and uncontrolled movement; and ataxic – characterized by a disturbed sense of balance and depth perception. It is not unusual for patients to have symptoms of more than one of the previous three forms. The most common mixed form includes spasticity and athetoid movements, but other combinations are also possible.

How many people have cerebral palsy?
It is estimated that some 764,000 children and adults in the United States manifest one or more of the symptoms of cerebral palsy. Currently, about 8,000 babies and infants are diagnosed with the condition each year. In addition, some 1,200 - 1,500 preschool age children are recognized each year to have cerebral palsy.

Can it be prevented?
Yes. Measures of prevention are increasingly possible today. Pregnant women are tested routinely for the Rh factor and, if Rh negative, they can be immunized within 72 hours after the birth (or after the pregnancy terminates) and thereby prevent adverse consequences of blood incompatibility in a subsequent pregnancy. If the woman has not been immunized, the consequences of blood incompatibility in the newborn can be prevented by exchange transfusion in the baby. If a newborn baby has jaundice, this can be treated with phototherapy (light therapy) in the hospital nursery. Immunization against measles for all women who have not had measles and are susceptible to becoming pregnant is an essential preventive measure. Other preventive programs are directed towards the prevention of prematurity; reducing exposure of pregnant women to virus and other infections; recognition and treatment of bacterial infection of the maternal reproductive and urinary tracts; avoiding unnecessary exposure to X-rays, drugs and medications; and the control of diabetes, anemia and nutritional deficiencies. Of great importance are optimal well being prior to conception, adequate prenatal care, and protecting infants from accidents or injury.

Can cerebral palsy be treated?
"Management" is a better word than "treatment." Management consists of helping the child achieve maximum potential in growth and development. This should be started as early as possible with identification of the very young child who may have a developmental brain disorder. A management program can then be started promptly wherein programs, physicians, therapists, educators, nurses, social workers, and other professionals assist the family as well as the child. Certain medications, surgery, and braces may be used to improve nerve and muscle coordination and prevent or minimize dysfunction.

As individuals mature, they may require support services such as personal assistance services, continuing therapy, educational and vocational training, independent living services, counseling, transportation, recreation/leisure programs, and employment opportunities, all essential to the developing adult. People with cerebral palsy can go to school, have jobs, get married, raise families, and live in homes of their own. Most of all people with cerebral palsy need the opportunity for independence and full inclusion in our society.

Is research being done on cerebral palsy?
Yes. Active national programs of research are being vigorously pursued to prevent cerebral palsy and improve the quality of life for persons with cerebral palsy. The four organizations with major research programs are the United Cerebral Palsy Research and Educational Foundation in the private sector, and the National Institutes of Health, the Centers for Disease Control and Prevention and the National Institute of Disability and Rehabilitation Research in the government sector. The research questions being addressed include:

  • What are the factors that predispose the developing fetal brain to injury? Can these factors be eliminated or minimized?
     

  • What are the causes of injury to the developing fetal brain? Can the developing fetal and newborn brain be protected? What are the causes of developmental delays and failure to thrive?
     

  • Why are low birth weight in the full-term and the premature infant important risk factors for cerebral palsy?
     

  • Can cerebral palsy be diagnosed before birth and better diagnosed shortly after birth?
     

  • Which available treatments are most effective for specific disabilities of persons with cerebral palsy?
     

  • Based on new knowledge now available in the medical, surgical, behavioral and bioengineering sciences, what improvements can be made in the quality of life of people with cerebral palsy?
     

  • What are the effects of aging on a person with disabilities due to cerebral palsy?
     

  • Can the damaged brain be "repaired"?
     

What is UCP?
Founded in 1949, UCP is a nationwide network consisting of a central national organization, located in Washington, D.C. and over 100 independent, state and local non-profit affiliates. UCP is the leading source of information on cerebral palsy and is a pivotal advocate for the rights of all people with disabilities. In fact, 65% of the people UCP serves have a disability other than cerebral palsy. UCP is one of the nation’s most efficient charities, with a system wide average of 85% of all revenues going to programs.

UCP affiliates serve more than 170,000 children and adults with disabilities and their families every day. Together, with over 100,000 volunteers and an even larger number of professional staff, UCP serves people with disabilities and others, through the development of state-of-the-art programs, information and referral services, legislative advocacy, technology initiatives and research, and the delivery of a range of direct services tailored to local communities through programs such as assistive technology training, early intervention services, individual and family support services, and social and recreation programs. In addition, UCP provides supported living services, employment assistance and other supports as needed.


© October 2001 United Cerebral Palsy

 

 


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