cerebral palsy Flashcards

1
Q

Cerebral Palsy

A
  • A group of non-progressive, irreversible motor disorders caused by brain damage to an immature brain
  • This brain damage may occur in utero (from 2nd half of pregnancy onwards), during the birth process, or in early childhood (usually the first 3 years of life).
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2
Q

Etiology

A

Think hypoxia and ischemia

CP is usually due to hypoxia, which may occur via:

  • A very premature birth
  • Intrauterine virus (TORCH) or other infection/toxicity or source of brain damage
  • Ischemic insults
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3
Q

Hypoxia and ischemia – in utero causes

A

○ kink in the umbilical cord or the cord wrapping around the fetus’s neck

○ maldevelopment of the placenta

○ shock in the mother from an accident.

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4
Q

Postpartum hypoxia or ischemia

A

○ suppression of the respiratory centres b/c of overmedication of the mother;

or pneumonia, a collapsed lung or drowning of the infant

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5
Q

what causes Trauma to, or rupture of cerebral blood vessels

A

○ separation of the placenta

○ difficult or prolonged delivery

○ postpartum head injury from an accident or abuse

● The brain of a premature baby is particularly susceptible to hemorrhage.
● Strokes can occur as a result of dehydration.

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6
Q

Presentation

A

There is a very wide spectrum of presentations in CP

Some are very mild and would be noticed only by HCPs

Others are very profound and include significant disability

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7
Q

4 types of cerebral palsy

A
  1. Spastic
  2. Athetoid
  3. Ataxic
  4. Mixed
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8
Q

Spastic

A

increased tone; accounts for 75% of all cases (most common)

a. Monoplegia: 1 arm or leg
b. Diplegic: usually both legs, M/C of spastic form, fully ambulatory scissor gait
c. Hemiplegic: 1 side of body, usually most ambulatory
d. Quadriplegic: all 4 limbs

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9
Q

Athetoid

A

uncontrolled movement, slow & writhing, increase with intention & stops with sleep, has trouble holding themselves upright

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10
Q

Ataxic

A

poor coordination, least common, due to damage to cerebellum

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11
Q

Mixed

A

usually spastic & athetoid

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12
Q

Symptoms

A

● Not noticeable in early infancy - become more obvious as nervous system matures
○ Early signs are delayed milestones, persistence of primitive reflexes, in toddlers
not walking or forming sentences

● Spasticity – most common

● Athetoid movements – slow and writhing

● Choreiform – movements are quick, uncontrolled and without purpose; do not stop with sleep

● Ataxia – lack of coordination and clumsiness of movements; ataxia in the face causes grimacing

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13
Q

Classic gait pattern

A

“Scissors gait” due to adductor spasticity

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14
Q

Diagnosis (according to CDC)

A

● Developmental Monitoring
○ tracking child‘s growth & development over time

● Developmental Screening
○ Testing motor or movement delays, lacking milestones
○ Done at 9 months, 18 months, 24 or 30 months

● Developmental and Medical Evaluations
○ Goal is to diagnose specific type of disorder
○ Evaluation of movement/motor delays - mm tone, reflexes, posture
○ Related conditions like intellectual disability, seizures, vision, hearing, speech problems
○ MFI, CT, X-ray, electroencephalogram (EEG)

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15
Q

Treatment

A

● There is no cure

● Treatments such as physical and occupational therapy, speech therapy, drugs to control seizures, relax muscle spasms and alleviate pain

● Surgery to correct anatomical abnormalities or release tight muscles

● Braces and other orthotic devices

● Wheelchairs and rolling walkers

● Communication aids

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16
Q

Massage considerations

A
  • Communication
    Some people with CP are non-verbal or non-communicative. Establishing a method of communication via a carer is most important.

Yes / no / stop signal

  • Comfort
    Pillow and positioning (often in a wheelchair) for support and comfort
    May need to accommodate high amounts of salivary secretions