Spina Bifida Flashcards

1
Q

Spina Bifida Etiology and Diagnosis

A

Etiology

  • Folic acid deficiency, teratogens, family hx
  • obstetric care - C section - surg repair

Diagnosis

  • Fetal Ultrasound - 18 wks
  • Alphafetoprotein - blood test - 16wks
  • Amniocentesis - 20wks
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2
Q

Types of Spina Bifida and Severity

A
  1. Myelomeningocele
    • most severe - 2nd most common
    • vertebral arches dont close
    • open membranous sac contains CSF, meninges, SC and damaged below
  2. Meningocele
    • 2nd severe, least common
    • vert arches dont fuse
    • SC intact
    • neural elements covered
    • paresis, bowel and bladder
  3. SB Occulta
    • least severe, most common
    • vert arches dont fuse
    • no damage SC/nerves
    • dimpling/tuft of hair
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3
Q

SB Level Identification

A
  • post natal surgery 24-72 hours
  • motor level is assigned according to last intact nerve root found
  • determined by surgeon at time of reparative surgery

prenatal surgery = 19-25 weeks followed by cesarean section at 37 weeks gestation to reduce trauma to SC

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4
Q

Arnold Chiari CNS Abnormalities

A
  • primary cause of hydrocephalus
  • occurs 85% of time with SB
  • lower brain stem, cerebellum, 4th ventricle herniate through foramen magnum and impede flow of CNS
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5
Q

Symptoms Associated with Arnold Chiari

A
  • Stridor
  • apnea
  • GERD
  • vocal cord paralysis
  • difficulty swallowing
  • seizures
  • nystagmus
  • problems with feeding
  • ataxia
  • hypotonia
  • UE weakness/spasticity
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6
Q

Signs of Shunt Malfunction with Hydrocephalus (Infants and Toddlers)

A

Infants

  • bulging fontanelle
  • vomitting
  • changes in appetite
  • sunset sign of eyes
  • edema and redness along tract

Toddlers

  • vommiting
  • irritability
  • headache
  • Edema
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7
Q

Signs of Shunt Malfunction School Age Children

A
  • headache
  • lethargy
  • irritiability
  • edema/redness on tract
  • handwriting changes
  • high pitched crying
  • seizures
  • rapid growth of head circumference
  • thinning of skin over scalp
  • nystagmus (new)
  • vomiting
  • personality changes
  • changes in school performance
  • memory changes
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8
Q

Skeletal abnormalities associated with SB

A
  • scoliosis
  • deformity from muscle imbalance
  • club foot - talipes equinovarus
  • hip dislocation
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9
Q

Hydromyelia - Neurological Deterioration

A
  • accumulation of CSF in central canal of SC
  • signs: rapid progression of scoliosis, UE weakness, increased tone
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10
Q

Tethered Cord

A
  • adhesions form to anchor SC at original lesion site
  • Signs:
    • UTI or incontinence
    • leg/foot weakness; loss of nerve function
    • numbness
    • spasticity
    • leg or foot length discrepancy
    • foot deformity (claw toes)
    • spinal deformity scoliosis
    • pain/irritability
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11
Q

Frequently Related Problems with Spina Bifida

A
  • Laytex allergy
  • intelligence varied
  • poor STM
  • impaired hand/eye coordination
  • decreased receptive language skills
  • poor attention span
  • difficulty with organizational skills
  • poor problem solving skills
  • frequent hospitalizations affect social development
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12
Q

GOALS of PT WITH SB

A
  1. Establish motor level by MMT
  2. provide information to medical team about available LE movement
  3. provide instruction to family regarding positioning and handling to prevent deformity
  4. provide HEP for development
  5. Input regarding orthotic and mobility aids
  6. monitor patient for CNS deterioration
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13
Q

Focus of Treatment with Infant

A
  • age appropriate developmental skills
  • head/trunk control
  • postural reactions
  • mobility training
  • prone for UE strength
  • adaptive seating or standing (parapodium)
  • goal = upright standing
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14
Q

Focus of Treatment Preschool

A
  • functional upright mobility
  • orthotic management
  • orthopedic intervention
  • skin care
  • strengthening
  • adaptive training
  • skill acquisition
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15
Q

Focus of Treatment School Age

A
  • Energy expenditure
  • orthopedic intervention
  • orthotic management
  • home, school, community negotiation
  • skin care and pressure relief
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16
Q

Clinical Presentation

Level T6-T12

A

Muscle Function

  • upper trunk
  • abdominals
  • back
  • intercostals

2ndary impairments

  • kyphoscoliosis
  • contractures
  • hip abd/ER
  • club feet

Prognosis walking

  • SHORT DISTANCE AMB
  • TLSO
  • WC/standing frame
  • parapodium
  • RGO/Walker
17
Q

Clinical Presentation

Level L1-L3

A

Muscle function

  • hip flexors/adductors
  • possible quads

2ndary impairments

  • HFC
  • hip dislocation
  • Wind Swept Scoliosis?

Prognosis Walking

  • HOUSEHOLD AMBULATION
  • stander parapodium
  • RGO/Walker
  • HKAFO, KAFO, AFO
  • FA crutches/WC
18
Q

Clinical Presentation

Level L4-L5

A

Muscle Function

  • quads
  • glut med/min
  • hamstrings
  • AT, PT, peroneals

2ndary impairments

  • HFC
  • hip dislocation
  • lumbar lordosis
  • calcaneovarus

Prognosis walking

  • HOUSEHOLD or COMMUNITY
  • HKAFO, KAFO, AFO
  • crutches, cane, wheelchair
19
Q

Clinical Presentation

Level S1-S2

A

Muscle Function

  • quads
  • glut max
  • peroneals
  • gastroc
  • toe flexors

2ndary Impairments

  • Calcaneovarus
  • toe clawing
  • heel ulcers

Prognosis walking

  • COMMUNITY AMBULATION
  • AFO, SMO, FO
20
Q
A