SCI, Scoliosis, CP Flashcards

1
Q

What is a spinal cord injury?

A

A spinal cord injury is caused by a complete or partial rupture of the spinal cord

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2
Q

What is paraplegia and how is it caused?

A
  • Paraplegia is loss of motor and sensory functions from arms and down
  • Can be complete - legs, abnomen, and chest
  • Incomplete - just legs
  • Caused by injury of thoracic level (complete) or lumbar level (complete or incomplete)
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3
Q

Symptoms of upper motor neuron lesion (in SCI)

A
  • No muscle atrophy
  • Positive Babinski
  • Hyperactive deep tendon reflexes
  • Hypertonia
  • Arm weakness
  • Spasticity, pain, sensory impairment, and autonomic impairment (ex. Bladder)
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4
Q

What are the different grades of SCI?

A
  • Complete which is no sensory or motor functions
  • Sensory incomplete where sensory functions still present but no motor functions
  • Motor incomplete where motor functions are still present but decreased
  • Normal which is normal functions but may have abnormalities of reflexes
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5
Q

What are the key points of assessments?

A

Sensory:

  • injury of C7 affects sensation of little finger dorsal surface
  • injury of L4 = medial melleoulus

Motor:

  • injury of C5 affects bicep brachii
  • injury of L4 affects dorsiflexion
  • injury of S1 plantarflexion

It is not black and white since multiple muscles and nerves work together

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6
Q

How is scoliosis defined?

A

It is a three-dimensional lateral deformity of the spine and trunk meaning that it is both curve and torque deformities

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7
Q

What are the types of scoliosis?

A

Functional = caused by factors outside spine

  • Different length of legs
  • Different pain in sides from ex. Lumbago sciatica

Structural = changes of the spine during development and growth

  • Congenital scoliosis = asymmetrical bone growth in in formation of spine
  • Degenerative scoliosis = degenerative changes of spine
  • Neuromuscular scoliosis = secondary to a neuromuscular condition (CP, SCI, atrophy)
  • Traumatic scoliosis (rare) = deformation may also be due to trauma
  • Idiopathic scoliosis = without any further explanation, most common and may be due to hormones affecting bone metabolism and is more common in females
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8
Q

How is the progression of scoliosis?

A
  • Youths are at highest risk of rapid progression especially for idiopathic
  • Adults with complete spinal growth will progress slower
  • The condition will get worse if you go untreated
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9
Q

Explain treatment options

A

Physiotherapy - self correction

  • Passive = correction driving positions of body with help of tools
  • Active = correction driving exercises without tools

Bracings - for curves over 25-45 Cobb

  • More you wear the better
  • Goal is to avoid surgical treatment and reach curve below 30 Cobb

Srugery - for curves over 45 Cobb

  • Maintain trunk balance
  • Prevent progression and deformities
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10
Q

What are the consequences of scoliosis?

A
  • Lung and heart problems in severe cases since ribcage is pushed against heart and lungs which may cause pain, nerve compression, and leakage of spinal fluid
  • There are also psychological consequences like low self-esteem and depression or anxiety due to physical limitations and abnormal appearance
  • Difficulties sleeping due to bracing
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11
Q

Name some tests that is used to diagnose scoliosis

A
  • Adam’s test: bend forward to measure torque of thorax with coliometer
  • Cobb’s test: determines severity of spinal curvature
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12
Q

Symptoms of scoliosis is…

A
  • Back pain going down to legs, shoulder pain
  • Uneven hips or shoulders
  • Fatigue in spine after sitting or standing
  • Trouble breathing
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13
Q

How is CP defined and what causes it?

A

A group of permanent neurological disorders that affects the motor functions.

Caused by a lesion of the brain before the age of 2 years old, and affects the brains plasticity (ability to form new neuron connections):

  • Intraventricular hemorrhage – bleeding into brain’s ventricles
  • Hypoxic injury/ischemic injury – restricted/complete disruption of oxygen supply to the brain
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14
Q

What are the classifications of CP?

A
  • Spastic (hypotonia first in babies) = most common and is defined as unbalanced/increase muscle tone causing stiff muscles
  • Dyskinetic:
    1. Dystonia = presented as sustained muscle contractions causing abnormal posture
    2. Dyskinesia = involuntary movements
  • Ataxic = disturbances in balance, coordination, and depth perception

Can be bi- or unilateral and is classified by dominant presentation of symptoms

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15
Q

Name some factors increasing risk of CP

A
  • Prenatal - before birth:
    1. High maternal age increase risk of thrombosis
    2. First time pregnancy increase risk of stroke
  • Maternal disease:
    1. Diabetes
    2. Anemia
    3. Hypertension
  • Trauma to brain as child (under 2 y/o)
  • Exposure to infectious disease at birth - urinary tract, STD
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16
Q

What are the symptoms of CP (Upper motor neuron lesion)?

A

Motor impairments affecting head, neck, trunk, and extremities:

  • Arm weakness, delayed motor development, oral impairments
  • Hyperactive deep tendon reflexes
  • Spasticity
  • Positive Babinski

Neurological impairments:

  • Sensory – vision and/or hearing
  • Cognitive and learning disabilities
  • Autonomic – incontinence
  • Seizure disorder
17
Q

Name some common consequences associated with CP

A
  • Joint dislocation, deformity, contracturs - Decreased mobility, osteoporosis, fractures
  • Crouched gait due to muscle weakness and spasticity
  • Sleeping problems due to intellectual and cognitive impairments
  • Mental health issues
18
Q

How do we treat CP and what is its goal?

A

Treatment should focus on management of symptoms, increase function, and prevent complications since there is no cure

  • Treat pain based on cause
  • Surgery for orthopedic complications
  • Rehabilitation to live with CP:
    1. Physical, speech, occupational, psychological therapy
    2. Orthotic devices
19
Q

How does the prognosis of CP look?

A
  • Limitations of function affecting daily life
  • Gross motor function that can only improve up to 7 years of age
  • Decreased mobility due to musculoskeletal disease which can get worse by age

depends on type of CP and the individual

20
Q

How to diagnose CP:

A

Thorough examination of symptoms and evaluation of function including:

  • Delayed motor development
    *ROM
  • Malalignments
  • Muscle tone and strength
  • Reflexes
  • Cognitive and sensory functions