Peads CP Flashcards
Spastic CP brain involvement
Motor cortex
White matter projections to and from the sensory motor areas of the brain.
Athetoid CP brain involvement
Basal ganglia
Ataxic CP brain involvement
Cerebellar lesion
Distribution of CP
Monoplegia Diplegia Paraplegia Hemiplegia Quadriplegia
Types of CP
Spastic Athetoid Ataxic Hypotonia Mixed
GMFCS
Gross motor function classification system to classify the severity of CP
Cerebral palsy definition
Is a permanent but not unchanging neurodevelopmental condition which is caused by a defect or lesion to a single or multiple areas of the immature brain. This defect or lesion occurs in utero or during or shortly after birth and can cause motor impairments and possible sensory defects that is visible during early stages of infancy.
Musculoskeletal deformities of hemiplegia CP
Nearly all children with hemiplegia can walk independently
Underdeveloped affected side resulting in smaller limbs and leg shortening
Equinus of foot and ankle
Flexion of elbow wrist and fingers with addicted thumb are common deformities
Musculoskeletal deformities associated with diplegia (spastic)
- contracture in hipflexors, adductors and hamstrings. Internal rotation of the hip and femoral anteversion
- Most of them walk independently and deformities develop because they adapt a crouch walking pattern
- Knee hyperextension because of tight Achilles’ tendon
- Kyphosis because of tight hamstrings or hyper lordosis as a compensatory balance mechanism
Musculoskeletal deformities in quadriplegic cp
Dislocation of joints and experience spinal curvature
Hip subluxation or dislocation causes pain
Difficulty with postural control creating limitations for sitting walking hygiene and personal care considerations.
Therapist observation
Behaviour Attention span Understanding communication Position Postural control and allignment Sensory aspects Use of limbs and hands Locomotion Deformities
What is the difference between GMFCS and GMFM
GMFCS is used to classify the severity of Mobility in CP children
GMFM is used to evaluate a change that occur over time in the gross motor function of children with cerebral palsy
Principles of treatment: spasticity
Improve tone and facilitate movements
Use distal key points
Improve proximal stability
Provide equipment that facilitates proximal stability and improves function
Encourage self regulation adaption and self-correction.
Be aware of sensory problems
Antigravity activity
Treatment principles: athetoid
Slow firm handling- maintained posture that is aligned
Improve head trunk and limbs allignment to midline to prevent contractures and deformities and to enable eyes for communication and hands for function
Increase stability to maintain positions and alignment in positions and to enable functional activities with limbs
Create an environment that dampens the amount of stimulation
Improve use of arms for mobile weightbaring and sequencing
Improve eating and drinking skilles
Consider the child’s emotional and social needs as well as their physical
Principles of treatment : ataxia
Facilitate active and accurate adjustment to being moved
Work for quality of movement -improve grading by working on placing, holding, reversing directions all ranges
Regulate balance reactions
Obtain independent movement of limbs agains trunk
Mobile weight baring on arms
Treatments needs to be graded and emotionally supportive