Lecture 6 - Spina Bifida Flashcards

1
Q

What is spina bifida

A

Failure of the lamina to close during fetal development that occurs between 24-28 days gestation

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2
Q

What are 5 types of spina bifida

A
  1. Myelodysplasia: Range of defects in the formation of the spinal cord
  2. Spina Bifida Occulta: Vertebral defect without involvement of the spinal cord. They may have dimple, hairy tuft over defect
  3. Meningocele: Vertebral defect with protrusion of the meningeal sac without involvement of the spine
  4. Meningomyelocele: Herniation of the meningeal sac and neural elements (spinal cord, nerves)
    5.Anencephaly/Encephalocele: Cephalic end of the spinal cord that is usually incompatible with life
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3
Q

What does meningomyelocele impair

A

Loss of motor and sensory function below level of lesion (may not be complete and may be asymmetrical). Can cause neurogenic bladder and bowel

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4
Q

What are 6 comorbidities of meningomyelocele

A
  1. Hydrocephalus which is where accumulation of CSF in cerebral ventricles due to obstruction to flow. It is treated with a ventriculo-peritoneal (VP) shunt). Complications of the shunt can be obstruction, infection, mechanical failure and disconnections
    • Signs and Symptoms of shunt malfunction:
      ○Enlargement of the head
      ○Headache
      ○ Nausea
      ○Sunsetting eyes
      ○ Irritability
      ○ Seizures
      ○ Bulging of fontanelle (infants)
      ○Bulging/redness along shunt tubing
      ○Drowsiness
      ○ Poor appetite
  2. Arnold Chiari II Malformation: Downward displacement of the hindbrain (4th ventricle, cerebellum and brain stem) through the foramen magnum. It can be surgically treated with decompression if symptoms are problematic.
    * Signs and Symptoms:
    ○ Infants:
    ® Respiratory distress
    ® Stridor
    ® Apnea
    ® Arching of neck/back
    ® Difficulty feeding due to poor suck and swallow
    ® Weak cry
    ○ Children/Adolescent:
    ® Breathing difficulties
    ® Neck pain
    ® UE weakness/stiffness/sensory changes
    ® Poor balance/coordination
    ® Feeding difficulty
  3. Tethered Cord: Spinal cord gets stuck in the scar tissue/bony abnormalities at the site of the lesion. Symptoms appear during a growth spurt. Treated surgically if symptoms affect function.
    * Signs/Symptoms:
    ○ Changes in LE including spasticity, weakness, pain, sensory changes, new foot deformities
    ○ Worsening of gait pattern
    ○ Changes in bladder/bowel function
    ○ Rapidly developing spinal curve
  4. MSK Deformities:
    * Talipes equinovirus (clubbed feet): Midline defect
    * Dislocated hips: Due to lack of or imbalanced muscle function
    * Spine deformities: Kyphosis and scoliosis
  5. Latex Allergies
  6. Secondary Impairments:
    * Shunt complications
    * Skin breakdown
    * LE contractures
    * Osteoporosis leading to fractures
    * Obesity
    Renal Complications
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5
Q

What is the incidence of spina bifida

A
  • Highest in Hispanic women
    • Incidence is declining due to folic acid fortification
    • Risk factors include genetic predisposition, dietary deficiency in folic acid, valproic acid during early pregnancy, diabetes mellitus, and environmental factors
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6
Q

What is the treatment for spina bifida

A

Delivery through C-section and lesion is repaired within 24-hours after birth. There may be a VP shunt needed to control hydrocephalus.
- In-utero surgery is being done but is higher risk for mom and baby

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7
Q

Describe the lesion levels potentially impacted by spina bifida and what it impairs

A
  • Motor level is lowest functional level (grade 3 or higher)
    • May be asymmetrical and it may skip levels
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8
Q

What should a PT assessment include for spina bifida

A
  • Muscle strength
    • ROM
    • Sensation
    • Motor development/motor function
  • Equipment needs
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9
Q

What should PT treatment include for Spina Bifida

A
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10
Q

What are potential secondary impairments for CB based on Campbell et al.

A
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11
Q

What are recommendations for CB based on Campbell et al.

A
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12
Q

What is the importance of goal setting with CB

A
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13
Q

What is the importance of exercise for CB

A
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14
Q

What is important with transitioning children to adulthood for CB

A
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15
Q

What should be apart of the health care transition plan for Cerebral Palsy

A
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16
Q

What are some challenges of transitioning for CB

A
17
Q

Describe how lack of preparation can be a challenge for CB

A
18
Q

Describe how limited information and support can be a challenge for CB

A
19
Q

Describe how a lack of skills needed for adult roles can challenge CB

A
20
Q

How does disjointed adult services challenge CB

A
21
Q

What do we know about youth with CB

A
22
Q

What is being done for youth with CB to increase positiveness of transitioning (Part 1/2)

A
23
Q

What is being done for youth with CB to increase positiveness of transitioning (Part 2/2)

A
24
Q

Describe the shared management model

A
25
Q

Describe the transition planning framework

A