Rehabilitation of Cerebral Palsy & Motor Delay

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REHABILITATION OF

CEREBRAL :PALSY &


MOTOR DELAY
BY

DR. ABDEL MOETY AFIFI


MD. Rheumatology & Rehabilitation
REHABILITATION OF C.P
CEREBRAL PALSY
Static encephalopathy(=non progressive) caused by an insult to the
immature brain

REHABILITATION:
The process of making the child w/ disability maximally able again through
the application of rehab principles & techniques.


REHABILITATION OF C.P
Principles of proper rehabilitation :
1. Proper evaluation ( individual treatment )
- to plan a therapy program.to assess progress.
- to add observation to the diagnostic picture.
2. Early treatment( increasing functional deficits w/
age as secondary effects of spasticity &other
primary problems
3. Team work ( global dysfunction )
EVALUATION OF CP CHILD
(A) Clinical evaluation
1. Functional : Postural control Mobility

Primitive reflexes Motor exam


2. Swallowing & dysphagia
3. Communication: Speech/ language Visual
Auditory Mentality
4. Chest 5. Urinary bladder 6. Bowel
7. Self -care activities (ADL) 8. psychosocial
EVALUATION OF CHILD
WITH CP.
(B) Imaging
1. Serial X-rays:
Hips (dislocation spastic adductors)
Th-L-Spine (scoliosis, hyperlordosis in spastic CP
kyphoscoliosis in floppy CP)
2. MRI or CT brain (progressive motor deficits ?
tumors, hydrocephalus
ASSESSMENT OF MILESTONES &
POSTURAL CONTROL
• Understanding normal development allows to adaptive
equipment to assist child in gaining increase the
interaction with the environment.
• Sitting balance at age 2 yrs. is an indicator of future
walking.
• Observe how much parental support given to child.
child own ability in postural stabilization.
collapse on one side of his body, twist to one
side, tilt & turn to one side.
EVALUATION OF PRIMITIVE
REFLEXES
• Can be used as indicator of ambulation
• Abnormal response for two of the following seven reflexes
by age 12 month has a poor prognosis for walking this are
Should be absent Should be present
ATNR parachute reaction
STNR foot placement
Moro response
Neck righting reflex
Extensory thrust
• Presence of Moro or ATNR, seizures, ability to sit at 12
month indicate ambulation by age of 6 yrs.
MOTOR EXAMINATION

GAIT
• Hemiplegia Toe walk
• Diplegia Bilateral equinovaras,
Knee flexed & in valgus
Scissoring
• Cerebellar Ataxic
MOTOR EXAMINATION
DEFORMITIES

• Hemiplegia : adducted arm, flexed elbow, wrist & fingers


equinus foot.
• Diplegia: adducted hip, flexed knee in valgus, bilateral EV
knee height discrepancy indicates hip dislocation.
• Quadriplegia: combination
scoliosis & hyperlordosis in spastic CP
kyphoscoliosis in hypotonic CP
MOTOR EXAMINATION
R.O.M.
• Degree by goniometry:
• Limited (= fixed deformity = ms. Contracture)
• Not limited (+ deformity = threatening deformity
= muscles imbalance)
ABNORMAL MOVEMENT
• Dystonia, ( cervical = spasmodic torticollis )
• Chorea & Athetosis
• Tremors
MOTOR EXAMINATION
MUSCLE TONE
• Spasticity ( = clasp knife ):
- generalized or focal
- grade 0 (non) - 4 (severe) [Ashworth scale]
• Rigidity ( = lead pipe )
• Hypotonia ( cerebellar )
• Combination : the predominant symptoms will
contribute to diagnostic type referred for treatment
MOTOR EXAMINATION
MUSCLE STRENGTH
Grade 0 = No contraction detected
1 = Flicker of contraction w/ no movement.
2 = Joint movement possible only with
gravity eliminated.
3 = Muscle contraction possible against
gravity without resistance.
4= Muscle contraction against gravity &
less than normal amount of resistance.
5 = Normal power against gravity and
resistance.
MOTOR EXAMINATION
MUSCLE STRENGTH
Values of muscles grading:
- To determine ambulation with or without brace
( grade 3 antigravity muscles can ambulate without brace
- Topographic classification for treatment plan
( strengthening exercise for weak muscles )
- Ex. must be low grade and non-fatiguing in ms.<3/5
-N.B (I) grade drops form muscle power following tendon
lengthening.
SWALLOWING STUDY
Values: - To facilitate appropriate position for safe, effective feeding
- To increase ability to self feed.
Methods:
1. Video fluoroscopic swallowing study
- Requires speech - pathologist & radiologist
- Patient is given liquid & various consistency of solid food
impregnated w/ baruim & folowed by X-ray until be sure safe
effective swallowing
2.Fiberoptic evaluation of swallowing ( FEES )
Transnasal endoscopy of hypopharynx to observe foodway &
airway before & after( but not during ) the moment of swallowing.
3. EMG, manometry, scintigraphy & U.S: less commonly use.
Assessment of speech
Speech problems :
• Dysarthria (oral motor control problems ) :
Spastic
Hypokinetic (ataxic )
Hyperkinetic (dystonia,chorea)
• Aphasia
• Language delay (brain pathology, MR, hearing
impairment )
VISUAL ASSESSMENT
• Problems: Strabismus ( imbalance in eye ms. )
Hemianopsia(in dense hemiplegi w/ MCA
occlusion)
Blindness ( anoxic cortical vision loss )
• Effects: 1. More motor delay 2. Language delay
3. Abnormal movements ( blindism )
4. More delayed postural mechanism
especially hypotonic CP
AUDIOLOGICAL EVALUATION
• Must be early so that important speech development period not
lost.
In infant (1-2 d. of birth):
Brain stem auditory evoked response (BAER):
Electrodes placed on the child & presenting a
stimulus picked up from a computerized system.
A specific wave form response is recorded from the brain stem
if stimulus is heard.
Otoacoustic emission testing (OAE):
Echo from hair cell of normally functioning cochlea
picked by a microphone placed in the middle ear & connected to
micro computer.(middle ear pathology is ruled out)
AUDIOLOGICAL
EVALUATION
• 6 months children:
Behavioral testing in sound treated room
• 2-3 years children :
Play audiometry done by presenting auditory
stimulus through loud speaker and associate the
sound with light or toy
CHEST EVALUATION

Vital Capacity is measured by spirometry


Ventilatory impairment may be caused by:
1. Rib cage abnormalities 2ry. to scoliosis &
hyperlordosis (spastic) or kyphoscoliosis (floppy)
2. Respiratory muscle dysfunction (spasticity or
hypotonic)
ASSESSMENT OF BLADDER
DYSFUNCTION
• Problems:
-incontinence,urgency,hesitancy (brain damage,motor
disability, impaired cognition )
-small capacity hypereflexic bladder
-detrusor sphincter dyssynergia
• Assessment :
-Renal function with serial determination of post-voidal
volume
-Cytometric evaluation with associated EMG
monitoring of pelvic floor muscle
ASSESSMENT OF BOWEL
DYSFUNCTION
• Problems :
-Fecal incontinence or defecation stress
( brain damage, motor disability, impaired
cognition,incoordination of anal sphincter
or pelvic floor muscle )
-Constipation : exaggerated by immobility
& inadequate fluid intake
• Assessment : anorectal manometry
SCOPE OF CP REHAB.
1. Neurodevelopmental training.
2. Motor facilitation approach.
3. Treatment of spasticity.
4. Rehab. of swallowing problems.
5. Rehab. of speech problems.
6. Rehab. of auditory problems.
7. Rehab. of visual problems.
8. Rehab. of chest problems.
9. Rehab. of urinary bladder & bowel problems.
10.Rehab. Of ADL &
11.Psychosocial rehab.
NEURODEVELOPMENTAL TRAINING
EQUIPMENT TRAINING
Criteria for selection:
1. to carry out tasks otherwise impossible with his ability.
2. appropriate support to participate in social & educational activities .
3. good alignment & correction of abnormal postures
4. adjust for child” growth, removal of support with increasing ability.
5. modification for different children in schools & clinics
6. provide additional motor experience in different posture
7. Comfort and protect joints & skin.
NEURODEVELOPMENTAL
TRAINING
Equipments varieties:
1. Wedges: Abductor W : prevent adduction deformities
2. Trumble form wedges & trumbles.

3. Large inflatable ball set


4.Crawlers:
-platforms on wheels or wedges on wheels
-A canavas sling under child” abdomen & supports
on casters, straps to hold thighs in flexion.
5. Sitters
NEURODEVELOPMENTAL
TRAINING
6. Apparatus for supporting standing
a) Prone or supine standers to encourage weight bearing & standing
b) Standing frames adjusting correct alignment:
-checked for height so that child does not grasp them w/ abnormal shoulder
hunching , excessive elbow flexion & radial deviation of wrist.
-supplied w/ strapping to correct flexed hip & knees
-feet held at right angles by a board &/or foot place.
c) Parallel bars

d) Mirrors
e) Stairs with bannisters: very in height.
f) Rumps, uneven ground, various floor services for gait training.
NEURODEVELOPMENTAL
TRAINING
7.Walking aids
Walkers
Crutches
Braces & Calipers:
Knee gaiters (polyethylene knee moulds) to keep
knee straight abduction parts to keep legs apart.
Elbow gaiters which keep elbow straight for
correct arm push & grasp of walkers.
MOTOR FACILITATION APPROACH

1. Bobath Method: inhibition of abnormal tone & posture of


released postural reflex while facilitating specific automatic
motor response (by special technique of handling) resulting in
performance of skilled voluntary movements.
2. Rood Method: Use of peripheral input of cutaneous sensory
stimuli (brushing, tapping, icing, heating, pressure, ms. stretch,
muscle contraction, joint approximation. or retraction)
Various nerves & sensory receptors are described & classified
into types ,location, effect, response, indication.
MOTOR FACILITATION APPROACH
3. Propioceptive Neuromuscular facilitation (Kabat & Knott)
Use of such mechanisms as maximum resistance , quick stretch &
spiral diagonal (mass) movements, sensory afferent stimuli (touch,
pressure, traction,compression & visual) to facilitate normal mov .
[special techniques: irradiation. stim. of reflexes,reversal(successive
induction), relaxation.].
4. Brunstrom Method ( hemiplegia): Produces motion by provoking
primitive movement pattern or synergitic pattern as follows :
-Reflex response used initially & later voluntary control
-Control of head & trunk by stim. of TNR, tonic labrinythine R
-Associated reaction : hyperextension of the thumb produces
relaxation of finger flexors.
MOTOR FACILITATION APPROACH
5. Motor relearning program of Carr & Shepherd:
functional training, practice, repitition, in the performance
of tasks & carry over those motor skills into functional
activities.
6. Forced use paradigm (= constraint - induced
movements therapy CIMT):
Non hemiplegic limb is restrained in a sling during 90% of
waking hrs. to force the patient to use the hemiplegic limb.
The minimum amount of motion in the paretic limb before
being enrolled into CIMT protocol is 20 of wrist extension
and 10 of extension of 2 fingers at MCP or IPJ.
TREATMENT OF SPASTICITY
Positioning
• Avoid prolong sitting (less hip & hamstring flexion )
• Prone lying at night (less hip flexion )
• Abduction wedge at night & in wheelchair (less hip
adduction)
• AFO splint
• Standing frame
• Molded thoracolumbar orthosis for early scoliosis or
kyphosis
• Total contact support incorporated into a contoured
TREATMENT OF SPASTICITY
Drugs
Indication : generalised spacticity to aid in mobility
Types :
1. Dantrolene Sodium (Dantrium):
Inhibits Ca release in excitation-contraction coupling
Used in cerebral form of spacticity Dose: 25- 200mg
2. Baclofen (Lioresal ) [ presynaptic inhibition ]
Used in spinal form of spasticity Dose :5-40mg
3. Diazepam (Valium) [postsynaptic inhibition]
Used in spinal form of spasticity Dose :2-30mg
TREATMENT OF SPASTICITY
PHYSIOTHERAPY

PHYSICAL AGENTS
Aim: a. Analgesia b. Ms. Relaxation c. Collagen extensibility
Modalities: 1) Ice 20mins.
2) Heat: Superficial : Dry: I.R. Moist: hot packs
Deep : S.W. U.S
ELECTRIC CURRENTS Aim: Ms. strengthening (galvanic & faradic) .
Analgesia ( TENS, IF)
EXERCISES For spasticity : Passive ROM Stretch (short ms.)
Strengthening (weak ms., antagonist),
resistive > 3/5
For hypotonia : Strengthening ( weak ms) Balance
For athetosis : Training to control simple joint motion
TREATMENT OF SPASTICITY
Nerve/ Motor Point Block

Indications Localized spasticity poorly responsive to drugs or PT,


interfering w/ mobility, bracing, hygiene & causing pain
Contraindication:
- Absolute: Allergy Infection Pregnancy
- Relative: Coagulopathy
Problems:
-Loss of motor function of injected ms.
-Return of spasticity ( axon sprouting )
TREATMENT OF SPASTICITY
Nerve/ Motor Point Block
Agents :
1- Botulinum toxin(Botox) [inhibits A.C at NMJ]
Used in motor point block of UL & LL
Antibodies are formed against it
2- Phenol [ produce coagulation of axon protein]
Used in nerve motor point block
Produces sensory dysesthesia.
3 - Alcohol [produce coagulation of axon protein]
Used in motor point > nerve block
Produces hyperaemia & transiant burning
TREATMENT OF SPASTICITY
INTRATHECAL BACLOFEN PUMP
Indications: ambulatory or non ambulatory child > 28lbs.w/ spastic
diplegia.
Method:
- Baclofen is delivered via pump implanted S.C.in abdominal wall
& surgically placed in subarachnoid space (CSF) close to its site
action ( receptors just 1mm under the surface of spinal cord )
- Start with intrathecal test dose via lumbar puncture to assess
baclofen effect over 6-8hs (1grade drops of spasticity)
. Advantage: avoid high dose of oral baclofen.
Risk: Infections e.g. meningitis, hypotonia & resp.problem
TREATMENT OF SPASTICIRY
SERIAL CASTING
Indications: focal contracture (especially elbows,
knees, ankles ).
Method:
• Limb is stretched then casted in a lengthened
position ( can be combined with blocks )
• Changed every few days or weeks to gradually
stretch contracted structures.
TREATMENT OF SPASTICITY
BRACES ( = CALIPERS = ORTHOSIS )
Aim: To correct deformity
To control athetosis
To obtain upright position
Types: AFO: For ankle instability w adequate Q > 3/5
Types: solid ( in ankle clonus )
Klenzak ankle joint w/spring(A,P)
w/ stop (A,P)
Accessories: varus strap valgus strap
KAFO: For correction of knee deform. & instab.
HKAFO: For ambulation w/ hip instability
. Shoe modification
TREATMENT OF SPASTICITY
ORTHOPAEDIC SURGERY
1. Spastic equinovarus foot: combination of:
a. Achillis tendon lengthening ( equinus def. )
b. Split anterior tibial transfer: Splitting TA tendon
medial half left attached to its origin
lateral half tunneled into 3rd cuneiform & cuboid
2. Tight hip adductor: Adductor tenotomy or derotational
osteotomy
( + surgical reduction )
3. Scoliosis: surgical correction in ambulatory child
w/ curvature > 45 & vital capacity < 35%
TREATMENT OF SPASTICITY

NEUROSURGERY
Dorsal Rhizotomy
- Ideal patient: young child (3-8 yrs.) w/ spastic diplegia
ambulatory w/ spastic gait.
- Method: - Surgical cutting of posterior (sensory) root to
decrease sensory input to spinal cord reducing
muscle tone (but decreases sensation)
- Must be followed by PT & OT
- Cutting anterior root produces atrophy &? ulcer
REHAB OF SWALLOWING
PROBLEMS
• Team: speech language specialist, OT, Dietary specialist.
• Items:
• Changes in posture & head position during feeding.
• Oral motor exercise for the tongue & lips to increase
strength,
ROM, velocity, percision.
• Use of thickened fluid & soft food in small boluse
• Use of alternative feeding routes e.g. nasogastric tube,
gastrotomy or jejunostomy tubes with severe aspiration or
caloric need.
REHAB OF SPEECH PROBLEMS

• Team : speech -language pathologist & nurse


• Items : 1- oral option : electrolarynx
2 - non oral options :
- simple hand writing
- gestures
- augmentative communication
device (simple alphabet & picture board

to sophosticated computer systems


3- treatment of hearing & visual problems
REHAB OF AUDITORY PROBLEMS
• Team: audiologist, speech therapist, OT
• Items:
Cochlear implants (for profoundly deaf):
to stimulate auditory nerve & provid awareness of sound
Hearing aid : - Do
not help purely central hearing loss. Used for
ttt of profound sensorineural hearing loss in infancy & early
childhood
REHAB OF AUDITORY
PROBLEMS
• Assistive listening device:
Voice amplifiers used with or in place of hearing aids.
Speaker microphone is connected to the listener’s head set or
hearing aid through a wire, FM radio waves or IR light.
The signal is amplified and background noise is not picked.
• Compensatory strategies:
Hand signs, lip reading, gestures, written communication,
speaking clearly at slow speed, visual fire alarms,
enrichment of visual & tactile
sensory environment,
protection of the child”s remaining hearing (use of ear plugs in
swimming, ototoxic drugs are avoided)
REHAB OF VISUAL PROBLEMS
• Training of postural reaction (large balls, rolls)

• Use of compensatory stimuli (auditory, tactile,


vestibular, propioceptive) for:.
-Training of motor function of child’s life e.g dressing,
feeding, bathing, roll over, creeping, crawling (listen to
sound, reach to sound, move to sound).
-Training of body image movements enjoyment (hand to
hand, hand to mouth, hand to body)
• Mother - child relationship ( kisses, touches, stroking,
talking to the baby) is important.
REHAB OF VISUAL

PROBLEMS
Use of vibrating toys, bells & playthings placed for his tummy
legs & similar ideas.
• Language development:
Important to talk & clearly label the body parts & to encourage
the child’s language.
• Visual enhancement (illumination, magnification, altered
contrast, glare reduction, expanders of visual field)
• Visual substitution: Recorded talking books,

Computer w/ vebral output,


Braille book.
REHAB. OF CHEST PROBLEMS

• Elimination of air way secretion by


manually assisted cough OR
mechanical insufflator or exsufflator.
• Respiratory ms. aid by manual force (breathing ex)
OR
mechanical ventillatory assistance(hypoxia)
• Mouth intermittent positive pressure ventillation
(IPPV) in late stages.
REHAB. OF U.B. PROBLEMS

Timed bladder emptying schedule


Regulation of fluid intake.
Use of diapers.
Adequate cleaning of perineum
Family education about transfer & dressing skill .

REHAB. OF BOWEL PROBLEMS


A timed toileting schedule for incontinence
Use of dietary fibers, adequate fluid intake, stool
softeners, supp., & enema for constipation
.
REHAB OF ADL
• Team : occupational therapist
• Items :
- provision of self help devices
- training in activities of ADL
- provision of creative interest
- training in suitable work
PSYCHOSOCIAL REHAB
• Team : psychiatrist + social specialist
• Items : - provision of recreational activities
e.g.- special olympics, athletic competition
- horse back riding programs

(recreational & therapeutic )


- computers ( for schools & recreation

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