Cerebral Palsy (CP) Flashcards
CNS vs PNS
CNS
- UMN: cortical
- other: basal ganglia, cerebellum
definition
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
motor disorders are accompanied by
disturbances of sensation, perception, cognition, communication, and behavior by epilepsy, and secondary musculoskeletal problems
prevalance/incidence
8 year old children
3 in 1,000
pathogenesis/etiology
brain malformations brain lesions -white matter damage -grey matter damage -focal vascular insults
disease course
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
clinical findings
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
long-term consequences
25% experience mobility decline 84% significant pain 59% hip and back deformities malnutrition/obesity fatigue OA osteoporosis
classifications
movement abnormality resulting from common brain lesions
function using the Gross Motor Function Classification System
neuroanatomical findings
classifications-movement abnormality
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
pyramidal/spastic
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
extrapyramidal
ataxic
dyskinetic
ataxic
s/s: characterized by general instability of movement
function: GMFCS 4-5
brain areas affected: cerebellum
common MRI findings: MRI normal
dyskinetic
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
GMFCS
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
Prognosis based on GMFCS
lvls 3-5 decline with age
classifications-malformations
abnormal proliferation
abnormal neuroblast migration
abnormal neocortical organization
periventricular leukomalacia
involves necrosis of the white matter dorsal and lateral to the external angles of the lateral ventricles
intraventricular hemorrhage
a hemorrhage of the germinal matrix which lines the ventricles, it also damages the white matter tracts
spastic hemiplegic
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
spastic diplegia
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
spastic quadriplegic
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
diagnosis
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
medical management-maximize function and participation
foster autonomy, belonging, competence
child-active rehab: function
assistive technology
medical management-minimize/prevent secondary impairments
spasticity management musculoskeletal management pain management nutrition management fitness programs
key concepts
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