Orthopedic surgery is often recommended when spasticity and stiffness are severe enough to make walking and moving about difficult or painful. For many people with cerebral palsy, improving the appearance of how they walk – their gait – is also important. A more upright gait with smoother transitions and foot placements is the primary goal for many children and young adults.
In the operating room, surgeons can lengthen muscles and tendons that are proportionately too short. But first, they have to determine the specific muscles responsible for the gait abnormalities. Finding these muscles can be difficult. It takes more than 30 major muscles working at the right time using the right amount of force to walk two strides with a normal gait. A problem with any of those muscles can cause an abnormal gait.
In addition, because the body makes natural adjustments to compensate for muscle imbalances, these adjustments could appear to be the problem, instead of a compensation. In the past, doctors relied on clinical examination, observation of the gait, and the measurement of motion and spasticity to determine the muscles involved. Now, doctors have a diagnostic technique known as gait analysis.
Gait analysis uses cameras that record how an individual walks, force plates that detect when and where feet touch the ground, a special recording technique that detects muscle activity (known as electromyography), and a computer program that gathers and analyzes the data to identify the problem muscles. Using gait analysis, doctors can precisely locate which muscles would benefit from surgery and how much improvement in gait can be expected.
The timing of orthopedic surgery has also changed in recent years. Previously, orthopedic surgeons preferred to perform all of the necessary surgeries a child needed at the same time, usually between the ages of 7 and 10. Because of the length of time spent in recovery, which was generally several months, doing them all at once shortened the amount of time a child spent in bed. Now most of the surgical procedures can be done on an outpatient basis or with a short inpatient stay. Children usually return to their normal lifestyle within a week.
Consequently, doctors think it is much better to stagger surgeries and perform them at times appropriate to a child's age and level of motor development. For example, spasticity in the upper leg muscles (the adductors), which causes a “scissor pattern” walk, is a major obstacle to normal gait. The optimal age to correct this spasticity with adduction release surgery is 2 to 4 years of age. On the other hand, the best time to perform surgery to lengthen the hamstrings or Achilles tendon is 7 to 8 years of age. If adduction release surgery is delayed so that it can be performed at the same time as hamstring lengthening, the child will have learned to compensate for spasticity in the adductors. By the time the hamstring surgery is performed, the child's abnormal gait pattern could be so ingrained that it might not be easily corrected.
With shorter recovery times and new, less invasive surgical techniques, doctors can schedule surgeries at times that take advantage of a child's age and developmental abilities for the best possible result.
Selective dorsal rhizotomy (SDR) is a surgical procedure recommended only for cases of severe spasticity when all of the more conservative treatments – physical therapy, oral medications, and intrathecal baclofen -- have failed to reduce spasticity or chronic pain. In the procedure, a surgeon locates and selectively severs overactivated nerves at the base of the spinal column.
Because it reduces the amount of stimulation that reaches muscles via the nerves, SDR is most commonly used to relax muscles and decrease chronic pain in one or both of the lower or upper limbs. It is also sometimes used to correct an overactive bladder. Potential side effects include sensory loss, numbness, or uncomfortable sensations in limb areas once supplied by the severed nerve.
Even though the use of microsurgery techniques has refined the practice of SDR surgery, there is still controversy about how selective SDR actually is. Some doctors have concerns since it is invasive and irreversible and may only achieve small improvements in function. Although recent research has shown that combining SDR with physical therapy reduces spasticity in some children, particularly those with spastic diplegia, whether or not it improves gait or function has still not been proven. Ongoing research continues to look at this surgery's effectiveness.
Spinal cord stimulation was developed in the 1980s to treat spinal cord injury and other neurological conditions involving motor neurons. An implanted electrode selectively stimulates nerves at the base of the spinal cord to inhibit and decrease nerve activity. The effectiveness of spinal cord stimulation for the treatment of cerebral palsy has yet to be proven in clinical studies. It is considered a treatment alternative only when other conservative or surgical treatments have been unsuccessful at relaxing muscles or relieving pain.
Articles On Cerebral Palsy
Even when the condition is present at birth, the signs of cerebral palsy (CP) may not be noticed until a child is between 1 and 3 years of age. This is due to the way children develop and mature. Health professionals and parents may not recognize that a baby's movements are irregular until they become more pronounced as a child grows. These babies and young children may retain newborn reflexes and fail to reach age-appropriate developmental milestones. Parents and caregivers usually are the first to notice that a baby has developmental delays that may be early signs of CP.
When CP is severe, signs are often noticed at birth or shortly thereafter. However, some early signs of severe CP vary according to the specific type present.
Common signs of severe CP that may be noticed shortly after birth include:
* Problems sucking and swallowing.
* A weak or shrill cry.
* Unusual positions. Often the body is either very relaxed and floppy or very stiff. When held, babies may arch their backs and extend their arms and legs. These postures are different from and more extreme than those that sometimes occur in babies with colic.
Some problems related to CP become more evident over time or develop as a child grows. These may include:
* Smaller muscles in affected arms or legs. Nervous system problems prevent movement in affected arms and legs. Inactivity affects muscle growth.
* Abnormal sensations and perceptions. Some people with CP feel pain when touched lightly. Even everyday activities, such as brushing teeth, may hurt. Abnormal sensations can also make it difficult to identify common objects by touch, such as feeling the difference between a soft foam ball and a hard baseball.
* Skin irritation. Drooling is common when facial and throat muscles are affected. Drooling irritates the skin, particularly around the mouth, chin, and chest.
* Dental problems. Children who have difficulty brushing their teeth have increased risk of developing cavities and gum disease (gingivitis). Seizure medications may also contribute toward developing gum disease.
* Accidents. Falls and other accidents are a risk, depending on muscle control, joint stiffness, and general physical strength. In addition, CP-related seizures can cause accidental injuries.
* Infections and long-term illnesses. Severe CP causes problems with eating. If food is inhaled into the lungs, a child's risk of developing pneumonia increases. Adults are at increased risk for heart and lung disease.
Some children with CP often also display a group of behavioral symptoms, such as excessive sleepiness, irritability, and little interest in their environment.
Expectations
All people with cerebral palsy (CP) have some problems with body movement and posture. However, many babies do not show signs of CP at birth. Parents and caregivers may notice the first signs of CP, such as the baby not rolling over, sitting, crawling, or walking at the expected ages.
Signs of CP may become more obvious as the child grows. Some developmental problems may not appear until after a baby's first year. The brain injury that causes CP does not get worse over time; however, its effects can appear, change, or become more severe as the child gets older.
The specific effects of CP depend on its type and severity, the level of mental impairment, and whether other complications develop or other medical conditions are present.
* The type of CP present and how much of the body that is affected will determine a child's mobility.
o Most people with CP have forms of spastic cerebral palsy, which affects only part of the body. For example, a child with spastic cerebral palsy may develop symptoms mostly in one leg or one side of the body. Most children usually learn ways to accommodate for their handicaps. Some people can live on their own; others live and work in situations that provide some level of assistance. When both legs are affected, children can move around with the help of a scooter board (a device used to self-propel while lying down), modified stroller, wheelchair, or other special equipment.
o Total body cerebral palsy causes the most severe problems. Severe spastic CP and athetoid (dyskinetic) CP are types of total body CP. Many of those affected are not able to take care of themselves, either because of severe physical disabilities or mental retardation. However, some people can live on their own with the help of family members and/or health care aides.
* Complications, such as seizures, and other long-term physical effects of CP can be difficult to predict until a child is between 1 and 3 years of age. Sometimes, however, such predictions are not possible until a child reaches school age when learning, communication skills, and other abilities can be measured. The amount of help and supervision needed depends on the number and severity of problems.
* The severity of mental impairment, if any, is a strong predictor of daily functioning. Approximately 75% of people with CP have some degree of cognitive impairment . 2 About 60% of these people are mentally retarded (ranging from mildly to severely); the remainder often function normally but have some type of learning disability. 2
* Other medical conditions, such as vision or hearing problems, are often associated with CP. Sometimes these conditions are known right away; in others they are not detected until a child gets older.
Also, just like people with normal physical development, people with CP have social and emotional concerns throughout their lives. Because their physical limitations may add to these concerns, people with CP need the awareness and consideration of others.
Of all children diagnosed with cerebral palsy, 90% live to adulthood (beyond 20 years old). 3 A more precise life expectancy can be estimated by evaluating the type of CP present, its severity, and the impact of any conditions that are often related to CP. Most adults with the mild or moderate form—and some with the severe form—live independently and have jobs. Opportunities for independent living and employment for adults with CP have improved. These opportunities are a result of better home support services and advances in technology, such as computers to assist with speech, powered wheelchairs, and other devices.
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