Hip Instability
Individuals with spina bifida commonly have hip instability or dislocation as
the muscles on one side of the joint may pull strongly while the other side
pulls weakly or not at all. This is due to the fact that hip flexors and
adductors are controlled primarily by L1 and L2 level nerves, whereas hip
extensors and abductors are controlled primarily by nerves at levels L5 to S1.
The main concern about the dislocated hip is not the effects on walking, but
rather the development of asymmetric (uneven) hips which causes the pelvis to
lie at an angle. The development of pelvic tilt can make seating difficult,
predispose an individual to pressure sores, and lead to
Scoliosis.
It is beneficial to intervene early with physical therapy in order to prevent
hip contractures. This occurs when the strong muscles cannot be stretched back
to their normal position, and the joint cannot be straightened. A Pavlik
harness, worn during sleep, may also be helpful for children up to 2 years of
age to encourage the joint to develop a normal shape.
Club Feet
Some children with spina bifida are born with clubbed feet, which cause the
child's feet to point down and inwards. It is important to make sure that the
feet are well aligned when a child is ready to stand and walk (with or without
braces). An orthopedic surgeon or physiotherapist may put casts on a baby's feet
to correct or partially correct their position. Sometimes surgery is required.
Scoliosis
Any muscle imbalance around the spine affects the position of the vertebrae
and can produce an abnormal spinal curve. Such a curve may make it difficult to
sit or stand comfortably. There are 3 types of abnormal spinal curves:
-
Lordosis - a hollow in the low back,
-
Kyphosis - excessive rounding of the upper back,
-
Scoliosis - a bend to the side.
Congenital scoliosis (present at birth) occurs in around 15-25 percent of
newborns with spina bifida, most commonly those with thoracic level lesions and
associated vertebral abnormalities. Paralytic scoliosis (that which develops
after birth) usually has a gradual onset between the ages of five and nine
years, although it may arise for the first time in the second decade of life.
The degree of scoliosis may be stable or progress slowly initially but has the
potential to increase rapidly, especially during puberty.
Although mild scoliosis can be quite insignificant to the overall function
and health of the child, more severe scoliosis can have dire consequences:
- increase in pressure on the ischium (the sit bone), can cause severe
pressure sores to develop
- interference with mobility by making walking more inefficient or even
impossible
- can cause back pain
- respiratory compromise - chest wall can become so misshapen that it
dangerously restricts the capacity of the lungs
The management of scoliosis aims to preserve symmetry and prevent
progression. For rapidly progressing scoliosis or curves in excess of 45
degrees, surgery may be considered. For slowly progressive curves under 45
degrees, it is generally possible to manage the problem with bracing. In many
cases, this will be sufficient to prevent progression or to allow the child to
reach the age of 9-12 years before surgery is necessary.
For more information, see our
Scoliosis links.
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