CP Flashcards
what is CP?
non-progressive brain injury that occurs before, during or after birth up to 3 years of age
UMNL resulting in motor abnormalities
wide range of involvement, mild to severe
cognitive skills also vary
difficult to diagnose in babies <4 months
what are major signs of CP?
slow motor development
retention of primitive reflexes
what are classifications of CP?
divided into several classifications each with typical patterns of movement
1- hypotonic 2-rigid 3-ataxic 4- fluctuating tone/athetoid/dystonic 5-spastic/hypertonic
describe hypotonic CP:
pattern of motor expression: whole body involvement
area of brain involvement: generalized
varying severity
describe rigid CP:
pattern of motor expression: whole body involvement
area of brain involvement: generalized
varying severity
describe ataxic CP:
pattern of motor expression: whole body involvement
area of brain involvement: extrapyramidal cerebellar
varying severity
describe fluctuating tone/athetoid/dystonic CP:
pattern of motor expression: whole body involvement
area of brain involvement: extrapyramidal basal ganglia
varying severity
describe spastic/hypertonic CP:
pattern of motor expression:
- monoplegia
- diplegia/paraplegia
area of brain involvement: pyramidal motor tracts
varying severity
describe mild severity for CP:
gross motor: independent walker
fine motor: unlimited function
IQ: >70
speech: >2 words
overall: independent function
describe moderate severity for CP:
gross motor: crawl or supported walk
fine motor: limited function
IQ: 50-70
speech: single words
overall: needs assistance
describe severe CP:
gross motor: no locomotion
fine motor: no function
IQ: <50
speech: severely impaired
overall: total care
what is spasticity?
motor disorder
velocity dependent increase in tonic stretch reflexes
hyper-excitability of the stretch reflex
exaggerated tendon jerks
one component of the UMNS
altered activity patterns of motor units occurring in response to sensory and central command signals which lead to co-contractions, mass movements, and abnormal postural control
what is the pathophysiology of spasticity?
Proposed theory:
- imbalance b/w excitatory and inhibitory impulses to the alpha motor neuron
- due to lack of descending inhibitory input to the alpha motor neuron
what are signs of UMNS?
positive signs:
- spasticity
- rigidity
- hyper-reflexia
- primitive reflexes
- clonus
negative signs:
- lack of strength
- lack of motor control
- lack of coordination
what are types of involuntary movement disorders?
dystonia
chorea
athetosis
choreoathetosis
ataxia
what is dystonia?
abnormal posturing, twisting or repetitive movements
what is chorea?
irregular dance-like movements
what is athetosis?
writhing, distal movements
what is choreoathetosis?
combo of both chorea and athetosis
what is ataxia?
flailing movements, wide-based gait
how is the ash worth scale of muscle tone scored?
1 = no increase in tone
2 = slight increase in tone
3 = marked increase in tone, but affected part(s) easily flexed
4 = considerable increase in tone: passive movement difficult
5 = affected part(s) rigid in flexion or extension
how is the modified ash worth scale of muscle tone scored?
0 = no increase in muscle tone
1 = slight increase in muscle tone, manifested by a catch and release or by min resistance at the end of ROM when the affect part(s) is moved into flexion or extension
1+ = slight increase in muscle tone, manifested by a catch, followed by min resistance throughout the remainder (less than half) of the ROM
2 = more marked increase in muscle tone through most of the ROM, but affected part(s) easily moved
3 = considerable increase in muscle tone, passive movement difficult
4 = affect part(s) rigid in flexion or extension
what is the modified tardieu scale??
consistent velocity stretch of muscle
standard positions for specific muscles
note point of resistance to max velocity stretch (R1)
note amount of muscle contracture or muscle length (R2)
relationship between R2-R1
what are the levels of the gross motor function classification system- expanded and revised (GMFCS- E&R)
Level I: walks w/out limitations
Level II: Walks with limitations
Level III: walks using a hand held mobility device
Level IV: self-mobility w/ limitations; may use power mobility
Level V: transported in a manual w/c