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29 Cards in this Set

  • Front
  • Back
Cerebral palsy
a motor function disorder caused by a permanent nonprogressive brain defeat or lesion, characterized by a disruption in the volitional control of the posture and movement, produces atypical muscle tone and unusual ways of moving
co-activation: agonist and antagonist working at the same time
reciprocal innervations impaired when one part of muscles work while other doesn’t
Primary Impairments:
CNS damage occurs prenatally, perinatally, or within the first 2 years of age
Secondary Impairments:
-abnormal muscle tone
-muscle imbalance
-contractures
-weakness
-poor body alignment
- impaired initiation of movement
-repetition of atypical movement patterns
-impaired co-activation
Progression of atypical Movement Patterns;
-decreased ability to control co-activation of agonist/antagonist
-impaired reciprocal innervations of agonist and antagonist muscles
-development of compensations and atypical movement patterns
Prenatal Risk factors/causes: 70-80%
-genetic disorders
-maternal health factors
- teratogenic agents
Perinatal risk factors/causes:
-prenatal conditions
-premature detachment of placenta
- medical problems
-multiple births
- anoxia: lack of oxygen
-hypoxia: reduced amt of oxygen
Postnatal risk factors/causes;
-degenerative disorders
-infections
-alcohol/ drug intoxication during breastfeeding
-anoxic ischemic encephalopathy (damage to cells in CNS d/t inadequate oxygen)
Postural Mechanism:
-normal muscle tone
-normal postural tone
- integration of primitive reflex movement
-righting, equilibrium, and protective extension, reactions
-intentional, voluntary movement against the forces of gravity (movement purposeful with intention)
-ability to combine movement patterns in the performance of functional activities
Righting, equilibrium and protective reactions
when equilibrium doesn’t maintain or regain posture then protective reaction takes place)
-static posture
-dynamic posture
-balance reactions
-protective reactions
- righting reactions: ability to sense head isn’t aligned with trunk
Muscle tone:
-muscles resting stiffness
-the degree of tension of muscle fibers when muscle is at rest
Abnormal Muscle tone:
-Hypotonia: decreased muscle tone, floppy
-hypertonia: increased muscle tone, stiff
-fluctuating muscle tone: between hypo/hypertonia
Common problems of Motor development:
abnormal muscle tone
-persistance of primitive reflexes
-atypical righting, equilibrium, and protective reactions
-poor sensory processing
-joint hypermobility
-muscle weakness/ poor muscles co-contractions
-decreased exploration go environment
-delays in development of motor skills and adaptive functioning
Classification/ Distribution:
-involvement of Extremity:
-monoplegia (one limb)
-hemiplegia( one side)
-diplegia(UE wkness, LE severe wkness)
-paraplegia(LE body wkness)
-quadriplegia(all 4 limbs)
-tetraplegia (all 4 limbs +head/neck)
-Type of movement disorders:
-spastic
-dyskinetic
-ataxia
-Mixed
Spastic CP:
- quad/hemiplegia
-hypertonia and spasticity
- initiation of movement leads to increases in abnormal tone
Dyskinetic Cp:
-Athetosis: fluctuation of muscle tone low-high to normal (involuntary righting movements, increase and decrease tone)
-Choreoathestosis: constant fluctuation from high-low and jerky (jerky involuntary movement)
-Dystonia: sustained twisted postures triggered by movement ( twisting postures, absent at rest, present at movement)
Ataxic CP:
-Clumsy, with decreased balance and coordination
-decreased equilibrium reactions and lack of proximal stability
Mixed CP:
-comb of high and low tone
Functional Implications and Associated problems:
-muscle/bone
-contractures
-bone deformities
-joint dislocations/misalignment
-pain
-risk for skin breakdown
-decreased bone density
-pathological fxs
-cognition
-hearing
-speech and language, communication
-decreased speech production
-poor articulations
-decreased speech intelligibity
-dysarthria: hard time speaking clearly
-decreased receptive and expressive language skills
-sensory
visual , and hearing impairments and tactile, proprioceptive deficits
-UEs or hands
depend on type and distribution of abnormal tone
Vision
- stabismus (crossed eyes)
-exotropia (eye drifts temporal) one or both eyes turn OUTWARD
-esotropia (eyes drifts nasally) one or both eyes turn INWARD
-hypertropia (drifts up)
-hypotropia (drifts down)
-nystagmus (constant eye movement both eyes)
-physical and behavioral problems
-seizures
-compromised cardiac/ respiratory fx
-decreased endurance
- learned helpness
-social isolation
-undesirable social behaviors
OT interventions:
-engaging in occupations
-handling and positioning
-training in AT and AE
medical-based interventions:
-pharmacologic Txs
-orthopedic surgery
-immobilization during healing phase
Therapeutic Modalities:
-heat
-cryotherapy
-e stim
-robotics
-kinesio taping (to increase ROM)
-splinting.casting
Coactivation
Secondary to reciprocal innervations that means that two or more muscles are sent a message from the nervous system to become active or to contract/relax simultaneously
Co-contraction
Contraction of both the agonist and the antagonist to provide stability at a joint
Athetosis
A type of cerebral palsy characterized by involuntary writhing movements, particularly of the hands and feet; loss of ability to coordinate movement due to the fluctuation of muscle tone form abnormally low to abnormally high muscle writhing movements
Dystonia
Neurologic movement disorder, in which sustained muscle contractions result in twisting and/or repetitive movements and abnormal postures
Reciprocal innervation
The distribution of nerve supply to antagonistic muscles, which allows one muscle to be excited and contract while the other muscle is inhibited, thus relaxing the muscle(s); excitation of the agonist with inhibition of the antagonist thus allowing movement at a joint