Cerebral Palsy (CP) Flashcards

1
Q

CNS vs PNS

A

CNS

  • UMN: cortical
  • other: basal ganglia, cerebellum
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2
Q

definition

A

a group of permanent disorders of the development of movement and posture, causing activity limitation, that are attributed to non-progressive disturbances that occurred in the developing fetal or infant brain

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3
Q

motor disorders are accompanied by

A

disturbances of sensation, perception, cognition, communication, and behavior by epilepsy, and secondary musculoskeletal problems

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4
Q

prevalance/incidence

A

8 year old children

3 in 1,000

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5
Q

pathogenesis/etiology

A
brain malformations
brain lesions
-white matter damage
-grey matter damage
-focal vascular insults
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6
Q

disease course

A

may be present at birth but not identified
0-2 y:atypical motor development identified, CP diagnosed
childhood:increase in motor function
after 8 y, high risk for decline in function due to inability to maintain function with growth and secondary musckuloskeletal conditions

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7
Q

clinical findings

A

spasticity (damage to cortex cortical spinal track)
inc reflex activity (damage to cortex cortical spinal track)
involuntary movements (basal ganglia injury)
insufficient force generation
atypical extensibility of muscles
impaired selective control of muscle activation (motor cortex or corticalspinal tract)
impaired anticipatory postural control

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8
Q

long-term consequences

A
25% experience mobility decline
84% significant pain
59% hip and back deformities
malnutrition/obesity
fatigue
OA
osteoporosis
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9
Q

classifications

A

movement abnormality resulting from common brain lesions
function using the Gross Motor Function Classification System
neuroanatomical findings

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10
Q

classifications-movement abnormality

A

pyramidal/spastic (97%)
-defects or damage to the motor cortex or corticospinal pathways
extrapyramidal (3%)
-damage to nerve cells/neural pathways in the basal ganglia or cerebellum

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11
Q

pyramidal/spastic

A

hemiplegia-involvement of UE and LE on one side of body
diplegia-LE more involved than UE
quadriplegia- involvement of all four extremities and trunk

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12
Q

extrapyramidal

A

ataxic

dyskinetic

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13
Q

ataxic

A

s/s: characterized by general instability of movement
function: GMFCS 4-5
brain areas affected: cerebellum
common MRI findings: MRI normal

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14
Q

dyskinetic

A

s/s: characterized by intermittent muscular tension of extremities/trunk and involuntary movement patterns,
function: GMFCS 4-5
brain areas affected: cortical-basal ganglia-thalamic loop
common MRI findings: gray matter injury

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15
Q

GMFCS

A
lvl 1: walks without restrictions
lvl 2: walks without AD
lvl 3: walks with AD
lvl 4: self-mobility with limitations
lvl 5: self-mobility severely limited
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16
Q

Prognosis based on GMFCS

A

lvls 3-5 decline with age

17
Q

classifications-malformations

A

abnormal proliferation
abnormal neuroblast migration
abnormal neocortical organization

18
Q

periventricular leukomalacia

A

involves necrosis of the white matter dorsal and lateral to the external angles of the lateral ventricles

19
Q

intraventricular hemorrhage

A

a hemorrhage of the germinal matrix which lines the ventricles, it also damages the white matter tracts

20
Q

spastic hemiplegic

A

s/s: inc tone/spasticity 1 side of body UE & LE
function:GMFCS 1-3
brain areas affected: motor cortex or white matter projections to and from the cortical sensorimotor areas
common MRI findings: focal vascular insult

21
Q

spastic diplegia

A

s/s: inc tone/spasticity LE>UE
function:GMFCS 1-3
brain areas affected: motor cortex or white matter projections to and from the cortical sensorimotor areas
common MRI findings: white matter injury

22
Q

spastic quadriplegic

A

s/s: inc tone/spasticity UE and LE
function:GMFCS 4-5
brain areas affected: motor cortex or white matter projections to and from the cortical sensorimotor areas
common MRI findings: gray matter injury

23
Q

diagnosis

A

medical history-birth defects, placental abnormalities, lesions during perinatal period, neonatal seizures, infections
clinical exams-atypical tone, reflexes, movement control, abnormal motor development
neuroimaging studies-MRI, cranial US

24
Q

medical management-maximize function and participation

A

foster autonomy, belonging, competence
child-active rehab: function
assistive technology

25
Q

medical management-minimize/prevent secondary impairments

A
spasticity management
musculoskeletal management
pain management
nutrition management
fitness programs
26
Q

key concepts

A

early identification is essential for optimal outcome
a clear differential diagnosis is required (if significant decline in function is noted, it is not likely CP and further diagnostic testing is required)
children diagnosed with CP need a body that lasts a lifetime