Pathology
types/ deformities
deformities
interventions
Outcomes based on motor function
100

when does myelodysplasia/spina bifida occur

occurs during neurulation (28th day after conception) 

100

which type of spina bifida is a secondary neurulation defect that occurs from 28-32 days to 7 weeks of gestation, defect at L5-S1 from failure of vertebral arch to grow and fuse, only sign may be hemangioma dimple, lipoma, hair tuft

spina bifida occulta

100
what should be tested for sensory deficits? because of decreased safety sensation what is required?

test dermatomes to get an accurate baseline

document areas that are absent and decreased sensation for: light touch, pinprick, vibration, and thermal 

evaluate proprioception and kinesthetic 

decreased safety requires: education on checking water temperature and skin inspection/pressure relief techniques

100

which surgery is controversial and what are the requirements for it

hip surgery 

prerequisite for hip surgery in children with MM:

lesion level at or below L3, fixed a pelvic obliquity caused by unilateral subluxation, dislocation interferes with sitting or standing, contributes to scoliosis,skin care is unmanageable, painful hip dysplasia in ambulatory 


100

what are some interventions to improve function

strengthen weak muscles, increase endurance, increase efficiacy of performing tasks, protect weight-bearing joints, prolong mobility, work on age-appropriate developmental activities, work on activities that are problematic for the child, teach compensatory skills

200

is the main reason that spina bifida arises 

most arise from failure of closure of caudal neuropore; 80% occur in lumbar area 

200

which type of spina bifida is a sac with meninges that protrudes trough vertebral defect usually no paralysis

spina bifida aperta- meninglocele
200
what MSK deformites that are associated with spinal bifida can occur in the UE, trunk and LE?

UE: shoulder girdle overuse 

trunk: scoliosis (congenital or acquired), kyphosis, lordosis

LE: malalignment and contractures 

200

what are some posture assessment could we find in standing 

ankle pronation-calcaneal valgus

genu valgus

hip and knee flexion contractures

increased lumbar lordosis

200

what motor function is at the thoracic level, and what equipment could we use

intact innervation of: neck, upper limb, shoulder girdle, trunk (unless above T10)

weak lower abdominals, absent lower limb movement, decreased sitting balance, decreased respiratory function

Equipment: parapodium- for non functional ambulation, WC

300

what should pregnant women have in their diet to prevent spina bifida? what is the recommendation for how much they should take?

folic acid, they should consume 400 micrograms (0.4 mg) of folic acid daily-> higher recommendations of 4 mg from 3 months before pregnancy through first trimester for women with previous child with NTD

300

which type has a sac with spinal cord and/or nerve roots and meninges protrudes through vertebral defect, associated with nerve paralysis

spina bifida aperta- myelomeningocele

300

what is a chiari malformation and what are some symptoms

deformity of cerebellum, medulla and cervical spinal cord

posterior cerebellum herniates downward through foramen magnum 

symptoms: neck p!, balance problems, muscle weakness, numbness, difficulty swallowing, vomiting, HAs, poor or weak cry 

300

what is the minimum age for girls and boys when considering a spinal fusion

10-11 years old for girls 

12-13 years old for boys

300

what motor function and equipment could we see for a high lumbar (L1-L2) level? L3? 

L1-L2-> weak hip flexors, adductors, and rotators; potential for household ambulation; equipment: with UE support the use of KAFOs or RGOs; WC

L3-> strong hip flexion and adduction strength, potential for ambulation household and short community distances; equipment: assistive device, KAFOs, forearm crutches, WC

400

what are some common characteristics we could see in a child with spinal bifida

varyig degrees of muscle weakness, paralysis, loss of sensation in legs, and/or poor bladder and bowl control

some may have hydrocephalus

400

for motor paralysis what are 3 neuromuscular involvements that can happen

complete cord transection- manifest as normal function down to a particular lvl

incomplete lesions- mixed manifestations of spasticity and volitional control

skip lesions- more caudal segments are functioning despite the presence of one or more non-functioning segments interposed between the intact more cephalad spinal segments

400

why is skin breakdown important with children diagnoses MM 

skin breakdown occurs in 85-95% of all children with MM by the time they reach young adulthood

physical therapy is important for education and instruction on strategies for prevention of skin breakdown and proper cushion for a wheelchair 

400

what are some interventions we can perform for a child with spinal bifida

importance of maintaing joint ROM- perform without excessive force, to avoid fractures 

bed mobility, ADL function, transfer, pain management, avoid contractures (reduce the risk for skin breakdown and possible amputation), avoid surgery

400

what is motor function and equipment at L4 level? L5?

L4: strong ankle dorsiflexion, knee flexion and extension; potential for functional ambulation with wheelchair for long distances; equipment: may initially need KAFOs and a walker, AFOs, forearm crutches, WC 

L5: knee flexion strength, weak hip extension, hip abduction, plantarflexion; potential to be a functional ambulatory, may require a wheelchair during growth spurts, for long distances or on uneven surfaces; equipment: orthotics, upper limb support, WC

500

what are ways we can diagnosis it

maternal serum alpha fetoprotein screening

US in the 2nd trimester

Amniotic fluid analysis 

500

73% of children with MM have been reported to have what?

a latex allergy 

may also have allergies to kiwi, avocados and bananas 

500

what is tethered cord syndrome 

neuro disorder casued by tissue attachments that limit the movement of the spinal cord within the spinal column

these attachments cause an abnormal stretching of the spinal cord

20-50% of children with MM defects repaired shortly birth will requires surgery to untether the spinal cord

500

what is ambulation interventions

symmetric neutral joint alignment in sitting and standing

correct fitting assistive devices

orthoses that provide total contact 

500

what is motor functions and equipment for S1 level? S2, S2-S3?

S1: weak gastrocnemius/soleus, gluteus medius, gluteus maximus; potential for functional ambulation, equipment: orthotics may be used to improve alignment

S2, S2-S3: strong plantarflexors and gluteals, potential to be a functional ambulatory, orthotics may be needed to improve alignment