Spina Bifida Flashcards

1
Q

Spina bifida

A

spinal defect diagnosed by presence of an external sac on infant’s back

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2
Q

Most common location

A

lumbar region

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3
Q

Spina bifida occulta

A

involves nonfusion of the halves of the vertabral arches

without disturbance of underlying neural tissue

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4
Q

Myelocele

A

protruding sac containing meninges and cerebrospinal fluid
nerve roots and spinal cord remain intact and in normal positions
No motor deficits, associated hydrocephalus, or other CNS problems

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5
Q

Lipomeningocele

A

superficial fatty mass in low lumbar or sacral level of the spinal cord
significant neurologic deficits and hydrocephalus are not expected

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6
Q

Caudal end of neural tube closes on approximately day __ of gestation

A

26

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7
Q

Clinical signs

A

Absence of motor and sensory function below level of spinal defect
Higher motor or sensory level on one side than on the other
Functional deficits may be partial or complete

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8
Q

Hydrocephalus

A

Abnormal accumulation of CSF in cranial vault

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9
Q

Causes of hydrocephalus

A

Overproduction of CSF
Failure in absorption of CSF fluid
Obstruction in normal flow of CSF through the brain structures and spinal cord

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10
Q

Chiari Malformation

A

deformity of cerebellum, medulla, and cervical spinal cord

posterior cerebellum is herniated downward through foramen magnum, displacing brainstem in caudal direction

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11
Q

__% of infants develop hydrocephalus after back closure surgery

A

90%

Shunt will be placed withing first several days to 6 months

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12
Q

Ventriculoatrial (VA) shunt

A

mores excess CSF from one lateral ventricle to the right atrium of the heart

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13
Q

Ventriculoperitoneal (VP) shunt

A

preferred treatment for hydrocephalus, less severe complications

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14
Q

MMT should be performed…

A

preoperative, 10 days postop, 6 months post op, and yearly

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15
Q

Purpose of MMT

A

can provide level of function, motor level is defined as lowest level which has antigravity movement

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16
Q

Typical contractures in spina bifida

A

hip flexion due to unopposed hip flexors

ankle due to unopposed dorsiflexors

17
Q

Considerations for thoracic level paralysis

A

Flaccid LE
At risk for developing frog-legged deformity
Will have total contact body brace including lower leg section to hold ankle in neutral or plantigrade

18
Q

Considerations with high lumbar paralysis

A

Require high level bracing for standing and ambulation

High risk for hip subluxation/dislocation

19
Q

Orthotics for kids with Thoracic and High Lumbar paralysis

A
Early standing can use A frame
Swibel standers
HKAFOs
Reciprocating gait orthoses (RGOs)
Rolling walkers
Rorearm crutches
Swing through gait
20
Q

Orthotics for kids with Low Lumbar paralysis (L4/L5)

A
Strong hip flexors and adductors
Calcaneal valgus/varus deformities
Clubfoot deformity
RGOs
AFOs if trunk is controlled 
KARO if crouch is pressent
21
Q

Orthotics for kids with Sacral level paralysis

A

Most control of hip/knee
AFOs
Work on active trunk and LE alignment

22
Q

Hydromyelia

A

excess CSF collects in pockets down the spinal cord that created areas of pressure and necrosis of surrounding peripheral nerves
Causes Scoliosis

23
Q

Tethered Spinal Cord

A

Adhesions anchor spinal cord at site of lesion, cord is not free to slide upward and reposition
Excessive stretch causes metabolic changes and ischemia of the neural tissue

24
Q

Signs of Tethered spinal cord

A
rapidly progressive scoliosis
hypertonus at one or several sites in LE
changes in gait pattern
changes in urologic function
increased tone on PROM
asymmetric changes in MMT results
discomfort in back