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Rehabilitation of cerebral palsy
children
Dr. C. Kannan
1st Year Post Graduate
MD Pediatrics
MGMCRI
Cerebral palsy
CP has been defined as
 Non progressive injury to the immature
brain
 Leading to motor dysfunction
 Lesion is not progressive, but
 The clinical manifestations change over
time.
 Progressive disorders resembling CP
Type I Arginase deficiency
Sjögren – Larsson syndrome
Lesch - Nyhan syndrome
Chiari Type I malformation
Dandy - Walker syndrome
Angelman syndrome
 Nonprogressive disorders resembling CP
Mental retardation
Deprivation
Malnutrition
Non-motor handicaps (blindness)
Motor handicaps (spina bifida, myopathies)
Risk factors
Prenatal
 Prematurity (< 36 weeks)
 Low birth weight (less than 2500 g)
 Maternal epilepsy
 Infections (TORCH)
 Bleeding in the third trimester
 Severe toxemia,
 Eclampsia
 Multiple pregnancies
 Placental insufficiency
 Drug abuse and trauma
Perinatal
 Prolonged and difficult labor
 Premature rupture of membranes
 Presentation anomalies
 Vaginal bleeding at the time of labor
 Bradycardia and hypoxia
Postnatal
 CNS infection (encephalitis,
meningitis)
 Neonatal hyperbilirubinemia
 Head trauma
 Seizures and Coagulopathies
Clinical classification
Tone Lesion site
 Spastic Cortex
 Dyskinetic Basal ganglia
 Hypotonic/Ataxic Cerebellum
 Mixed Diffuse
Anatomical classification
Location Description
Hemiplegia Upper and lower extremity on one side of body
Diplegia Four extremities,
legs more affected than the arms
Quadriplegia Four extremities plus the trunk, neck and face
Triplegia Both lower extremities and one upper
extremity
Monoplegia One extremity (rare)
Double hemiplegia Four extremities, arms more affected than the
legs
Cp ppt (kannan)
Cp ppt (kannan)
Spastic CP
 Increase in the physiological resistance of muscle to passive
motion.
 It is part of the upper Motor neuron syndrome characterized with
Hyperreflexia
Clonus,
Extensor plantar responses and
Primitive reflexes
 Spastic CP is the most common form of CP.
 Approximately 70% to 80% of children with CP are spastic.
 Spastic CP is anatomically distributed into
Hemiplegia
Diplegia
Quadriplegia
Early signs of CP
Signs suggestive of CP in an infant
Abnormal behaviour
 Excessive docility or irritability
 Poor eye contact
 Poor sleep
Oromotor problems
 Frequent vomiting
 Poor sucking
 Tongue retraction
 Persistent bite Grimacing
Poor mobility
 Poor head control
 Hand preference before 2 years of age
 Abnormal tone
Early differential diagnosis in
developmental disability
Cerebral palsy Mental retardation
Risk factors Often present Mostly absent
Complaints Irritable, sleepless
baby
Easy baby
Milestones Delayed Delayed
Muscle tone Increased Normal or reduced
Primitive reflexes Persist Normal disappearance
Postural reflexes Delayed appearance Normal or Delayed
appearance
Focal signs Appear Absent
Neuromotor problems in CP
 Difficulty with flexing and extending
the body against gravity
 Sitting
 Functional ambulation
Impairments
Primary impairments (due to the brain lesion)
 Muscle tone (spasticity, dystonia)
 Balance
 Strength
 Selectivity
 Sensation
Secondary impairments
 Contractures (equinus, adduction)
 Deformities (scoliosis)
Tertiary impairments
 Adaptive mechanisms (knee hyperextension in stance)
Contractures and deformity
Common sites for
contracture
Upper extremity
 Pronator
 Wrist and finger flexor
 Thumb adductor
Lower extremity
 Hip adductor-flexor
 Knee flexor
 Ankle plantar flexor
Common sites for
deformity
Spine
 Scoliosis and kyphosis
Hip
 Subluxation, Dislocation
Femur & tibia
 Internal or external torsion
Foot
 Equinus, valgus and
varus.
Associated problems in CP
 Seizures
 Visual impairments
 Intellectual impairment
 Learning disabilities
 Hearing problems
 Communication problems
 Oromotor dysfunction
 Gastrointestinal problems and nutrition
 Teeth problems
 Respiratory dysfunction
 Bladder and bowel problems
 Social and emotional disturbances
Epileptic seizures
 Seizures affect about 30 to 50% of CP patients
 They are most Common in the
Quadriplegics and
Hemiplegics,
Patients with mental retardation
Postnatally acquired CP.
 Seizures most resistant to drug therapy occur in hemiplegics.
 Seizure frequency increases in the preschool period.
 Electroencephalograms are necessary for the diagnosis of
seizure disorder
Visual impairments seen in
CP
Pathology Clinical finding
Damage to the visual cortex Cortical blindness
Damage to the optic nerve Blindness
Loss of oculomotor control Loss of binocular vision
Refraction problems Myopia
Nutritional and oromotor issues
 Teeth problems
Dentin Primary or hyperbilirubinemia
Malocclusion Spasticity
Tooth decay Feeding, swallowing
problems
Gingival hyperplasia Antiepileptic drug use
 Causes of inadequate food intake
Difficulty chewing and swallowing
Hyperactive gag reflex
Spasticity of oropharyngeal muscles
Loss of selective control of oropharyngeal muscles
Gastroesophageal reflux
 Urinary problems
Enuresis
Frequency
Urgency
Urinary tract infections
Incontinence
 Causes of urinary problems
Poor cognition
Decreased mobility
Decreased communication skills
Neurogenic dysfunction
Psychosocial problems
 Extremely stressful for the family and the child when he
grows up.
 Stress leads from denial to anger, guilt and depression.
 Coping with the emotional burden of disability is easier if the
family has strong relationships, financial security, and
supportive members of the community.
 The child and the family need to find ways to connect to
each other.
 A healthy relationship between the mother and the child
forms the basis of future happiness.
 Prevention or appropriate treatment of associated
problems Improves the quality of life of the child and the
family.
Rehabilitation
 Rehabilitation is the name given to all
diagnostic and therapeutic procedures
 Which aim to develop maximum
physical social and vocational function
in a diseased or injured person
Goals of rehabilitationGoals Objectives of rehabilitation
Improve mobility Teach the child to use his remaining potential
Teach the child functional movement
Gain muscle strength
Prevent deformity Decrease spasticity
Improve joint alignment
Educate the parents To set reasonable expectations
Do the exercises at home
Teach daily living
skills
Have the child participate in daily living activities
Social integration Provide community and social support
Components of rehabilitation
 Physiotherapy
 Occupational therapy
 Bracing
 Assistive devices
 Adaptive technology
 Sports and recreation
 Environment modification
Rehabilitation planning
Example: Independent standing
 State the necessary time period
 Plan the methods to achieve this goal
 Evaluate the end state.
 Revise the treatment program
Therapy program
Age group Program
Infant Stimulating
Advanced postural equilibrium
Balance reactions for head and trunk
control
Toddler & pre-schooler Stretching the spastic muscles
Strengthening the weak ones
Promoting mobility
Adolescent Improving cardiovascular status
Principles of therapy
methods
 Support the development of multiple systems such as
Cognitive
Visual
Sensory
Musculoskeletal
 Involve play activities to ensure compliance
 Enhance social integration
 Involve the family
 Have fun
Gross Motor Function Classification
System
Class Goal of treatment
1- Walks independently, speed,
balance & coordination reduced.
Diminish energy expenditure
Decrease level of support
Improve appearance
2- Walks without assistive devices but
limitations present.
Diminish energy expenditure
Decrease level of support
Improve appearance
3- Walks with assistive devices Improve gait
Improve standing
4- Transported or uses powered
mobility
Decrease pain
Improve sitting & standing
5- Severely limited, dependent on
wheelchair.
Better positioning
Decrease pain
Improve hygiene
Conventional exercises
 Active and passive range of motion
 Stretching
 Strengthening
 Fitness
Neurofacilitation techniques
 Sensory input to the CNS produces reflex motor output.
 Various neurofacilitation techniques are based on this
basic principle.
 All of the techniques aim to normalize muscle tone
 To establish advanced postural reactions and to
facilitate normal movement patterns.
Vojta method of therapy
 18 points in the body –
crawling and reflex rolling.
 placing the child in particular positions and stimulation of the key
points in the body would enhance CNS development
 In this way the child is presumed to learn normal movement
patterns in place of abnormal motion.
 Applied by the primary caregiver at home at least 4-5 times daily
and stopped after a year if there is no improvement
Bobath neurodevelopmental
therapy
 This is the most commonly used therapy method in CP worldwide.
 It aims to
Normalize muscle tone
Inhibit abnormal primitive reflexes
Stimulate normal movement.
 It uses the idea of reflex inhibitory positions to decrease spasticity
and stimulation to promote the development of advanced postural
reactions.
 It is believed that through positioning and stimulation a
sense of normal movement will develop.
 To teach the mother how to position the child at home
during feeding and other activities.
 The baby is held in the antispastic position to prevent
contracture formation.
Occupational therapy
 OT aims to improve hand and upper extremity function in the child
through play and purposeful activity .
 There are defined systematic treatment methods for occupational
therapy.
 Sensory integration therapy aims to enhance the child’s ability to
organize and integrate sensory information.
 In response to sensory feedback, CNS perception and
execution functions may improve and the motor planning
capacity of the child may increase.
.
 Constraint induced movement therapy
Where the normal hand is constrained
Paralytic hand is forced to function
Useful in children with hemiplegia.
 Begin therapy toward one year of age when the child can
feed himself using a spoon and play with toys.
 Teach the child age appropriate self care activities such as
dressing, bathing and brushing teeth.
 Encourage the child to help with part of these activities even if
he is unable to perform them independently
play
 Always include play activities in the rehabilitation
program.
 Play improves mental capacity and provides
psychological satisfaction.
 Organized play can address specific gross and fine
motor problems
 This increases the child’s compliance with therapy.
 Riding a toy horse may improve
Weight shift over the pelvis
Swinging may improve sensation of movement.
Advantages of swimming
Normalizes muscle tone
Decreases rate of contracture
Strengthens muscles
Improves cardiovascular fitness
Improves walking
Horseback riding Improves
Head control
Trunk balance
Normalize muscle tone
Positive emotions
Self esteem
Recreational programs
 Arts and crafts
 Music
 Dancing
 Wheelchair dancing
 Drama,
 Camping
 Fishing
 Scuba diving
OTHERS
 Speech therapy
 Hearing aids and implants
 Drugs
Antispasmodics
Baclofen Diazepam
Clonidine Thizanidine
Dantroline Botulinum injections
Neoromuscular blockers
Proton pump inhibitors for GERD
Analgesics for pain
 Respiratory physiotherapy
Goals of brace
 Increase function
 Prevent deformity
 Keep joint in a functional position
 Stabilize the trunk and extremities
 Facilitate selective motor control
 Decrease spasticity
 Protect extremity from injury in the
postoperative phase
Braces in CP
 Ankle foot orthoses
 Knee-ankle foot orthoses
 Hip abduction orthoses
 Thoracolumbosacral orthoses
 Supramalleolar orthoses
 Foot orthoses
 Hand splints
Functions of the AFO
 Main function Keep the foot in a
plantigrade
position
 Stance phase Stable base of support
 Swing phase Prevent drop foot
 At night Prevent contracture
Spinal braces
 To slow the progression of deformity
 To delay surgery
 To allow skeletal growth
 To assist sitting balance
 To protect the surgical site from excessive loading
after surgery
Mobility aids
 Example
Standers
Walkers
Crutches
Canes
 Advantages of mobility aids
Develop balance
Decrease energy expenditure
Decrease loads on joints
Improve posture
Benefits of Standers
 Support erect posture
 Enable weight bearing
 Stretch muscles to prevent contractures
 Decrease muscle tone
 Improve head and trunk control
Goals of orthopaedic surgery
Goal Operate to achieve
Walking potential Functional
ambulation
Good hip and knee
extension Stable hips
Plantigrade stable feet
No walking
potential
Sitting balance Straight spine
Horizontal pelvis
Stable hips
Ortho surgeries in CP
Types of CP Surgical procedures most often performed
Quadriplegic Hip adductor flexor release
Osteotomy Spine fusion
Diplegic Hamstring-gastrocnemius lengthening
Hip adductor-flexor lengthening
Derotation osteotomy
Rectus femoris transfer
Hemiplegic Gastrocnemius lengthening
Split tibialis anterior & posterior transfer
Tibialis posterior lengthening
Message
 Enhance Familial bonding and support
 Therapy along with peers
 No aggressive therapy
 Don’t give false hopes
 Include sports and recreational activities
 Successful rehabilitation includes
Prevention of additional problems
Reduction of disability
Community integration.
 Rehabilitation is successful if
Child is happy
Parents are well adjusted
THANK YOU !!

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Cp ppt (kannan)

  • 1. Rehabilitation of cerebral palsy children Dr. C. Kannan 1st Year Post Graduate MD Pediatrics MGMCRI
  • 2. Cerebral palsy CP has been defined as  Non progressive injury to the immature brain  Leading to motor dysfunction  Lesion is not progressive, but  The clinical manifestations change over time.
  • 3.  Progressive disorders resembling CP Type I Arginase deficiency Sjögren – Larsson syndrome Lesch - Nyhan syndrome Chiari Type I malformation Dandy - Walker syndrome Angelman syndrome  Nonprogressive disorders resembling CP Mental retardation Deprivation Malnutrition Non-motor handicaps (blindness) Motor handicaps (spina bifida, myopathies)
  • 4. Risk factors Prenatal  Prematurity (< 36 weeks)  Low birth weight (less than 2500 g)  Maternal epilepsy  Infections (TORCH)  Bleeding in the third trimester  Severe toxemia,  Eclampsia  Multiple pregnancies  Placental insufficiency  Drug abuse and trauma Perinatal  Prolonged and difficult labor  Premature rupture of membranes  Presentation anomalies  Vaginal bleeding at the time of labor  Bradycardia and hypoxia Postnatal  CNS infection (encephalitis, meningitis)  Neonatal hyperbilirubinemia  Head trauma  Seizures and Coagulopathies
  • 5. Clinical classification Tone Lesion site  Spastic Cortex  Dyskinetic Basal ganglia  Hypotonic/Ataxic Cerebellum  Mixed Diffuse
  • 6. Anatomical classification Location Description Hemiplegia Upper and lower extremity on one side of body Diplegia Four extremities, legs more affected than the arms Quadriplegia Four extremities plus the trunk, neck and face Triplegia Both lower extremities and one upper extremity Monoplegia One extremity (rare) Double hemiplegia Four extremities, arms more affected than the legs
  • 9. Spastic CP  Increase in the physiological resistance of muscle to passive motion.  It is part of the upper Motor neuron syndrome characterized with Hyperreflexia Clonus, Extensor plantar responses and Primitive reflexes  Spastic CP is the most common form of CP.  Approximately 70% to 80% of children with CP are spastic.  Spastic CP is anatomically distributed into Hemiplegia Diplegia Quadriplegia
  • 10. Early signs of CP Signs suggestive of CP in an infant Abnormal behaviour  Excessive docility or irritability  Poor eye contact  Poor sleep Oromotor problems  Frequent vomiting  Poor sucking  Tongue retraction  Persistent bite Grimacing Poor mobility  Poor head control  Hand preference before 2 years of age  Abnormal tone
  • 11. Early differential diagnosis in developmental disability Cerebral palsy Mental retardation Risk factors Often present Mostly absent Complaints Irritable, sleepless baby Easy baby Milestones Delayed Delayed Muscle tone Increased Normal or reduced Primitive reflexes Persist Normal disappearance Postural reflexes Delayed appearance Normal or Delayed appearance Focal signs Appear Absent
  • 12. Neuromotor problems in CP  Difficulty with flexing and extending the body against gravity  Sitting  Functional ambulation
  • 13. Impairments Primary impairments (due to the brain lesion)  Muscle tone (spasticity, dystonia)  Balance  Strength  Selectivity  Sensation Secondary impairments  Contractures (equinus, adduction)  Deformities (scoliosis) Tertiary impairments  Adaptive mechanisms (knee hyperextension in stance)
  • 14. Contractures and deformity Common sites for contracture Upper extremity  Pronator  Wrist and finger flexor  Thumb adductor Lower extremity  Hip adductor-flexor  Knee flexor  Ankle plantar flexor Common sites for deformity Spine  Scoliosis and kyphosis Hip  Subluxation, Dislocation Femur & tibia  Internal or external torsion Foot  Equinus, valgus and varus.
  • 15. Associated problems in CP  Seizures  Visual impairments  Intellectual impairment  Learning disabilities  Hearing problems  Communication problems  Oromotor dysfunction  Gastrointestinal problems and nutrition  Teeth problems  Respiratory dysfunction  Bladder and bowel problems  Social and emotional disturbances
  • 16. Epileptic seizures  Seizures affect about 30 to 50% of CP patients  They are most Common in the Quadriplegics and Hemiplegics, Patients with mental retardation Postnatally acquired CP.  Seizures most resistant to drug therapy occur in hemiplegics.  Seizure frequency increases in the preschool period.  Electroencephalograms are necessary for the diagnosis of seizure disorder
  • 17. Visual impairments seen in CP Pathology Clinical finding Damage to the visual cortex Cortical blindness Damage to the optic nerve Blindness Loss of oculomotor control Loss of binocular vision Refraction problems Myopia
  • 18. Nutritional and oromotor issues  Teeth problems Dentin Primary or hyperbilirubinemia Malocclusion Spasticity Tooth decay Feeding, swallowing problems Gingival hyperplasia Antiepileptic drug use  Causes of inadequate food intake Difficulty chewing and swallowing Hyperactive gag reflex Spasticity of oropharyngeal muscles Loss of selective control of oropharyngeal muscles Gastroesophageal reflux
  • 19.  Urinary problems Enuresis Frequency Urgency Urinary tract infections Incontinence  Causes of urinary problems Poor cognition Decreased mobility Decreased communication skills Neurogenic dysfunction
  • 20. Psychosocial problems  Extremely stressful for the family and the child when he grows up.  Stress leads from denial to anger, guilt and depression.  Coping with the emotional burden of disability is easier if the family has strong relationships, financial security, and supportive members of the community.  The child and the family need to find ways to connect to each other.  A healthy relationship between the mother and the child forms the basis of future happiness.  Prevention or appropriate treatment of associated problems Improves the quality of life of the child and the family.
  • 21. Rehabilitation  Rehabilitation is the name given to all diagnostic and therapeutic procedures  Which aim to develop maximum physical social and vocational function in a diseased or injured person
  • 22. Goals of rehabilitationGoals Objectives of rehabilitation Improve mobility Teach the child to use his remaining potential Teach the child functional movement Gain muscle strength Prevent deformity Decrease spasticity Improve joint alignment Educate the parents To set reasonable expectations Do the exercises at home Teach daily living skills Have the child participate in daily living activities Social integration Provide community and social support
  • 23. Components of rehabilitation  Physiotherapy  Occupational therapy  Bracing  Assistive devices  Adaptive technology  Sports and recreation  Environment modification
  • 24. Rehabilitation planning Example: Independent standing  State the necessary time period  Plan the methods to achieve this goal  Evaluate the end state.  Revise the treatment program
  • 25. Therapy program Age group Program Infant Stimulating Advanced postural equilibrium Balance reactions for head and trunk control Toddler & pre-schooler Stretching the spastic muscles Strengthening the weak ones Promoting mobility Adolescent Improving cardiovascular status
  • 26. Principles of therapy methods  Support the development of multiple systems such as Cognitive Visual Sensory Musculoskeletal  Involve play activities to ensure compliance  Enhance social integration  Involve the family  Have fun
  • 27. Gross Motor Function Classification System Class Goal of treatment 1- Walks independently, speed, balance & coordination reduced. Diminish energy expenditure Decrease level of support Improve appearance 2- Walks without assistive devices but limitations present. Diminish energy expenditure Decrease level of support Improve appearance 3- Walks with assistive devices Improve gait Improve standing 4- Transported or uses powered mobility Decrease pain Improve sitting & standing 5- Severely limited, dependent on wheelchair. Better positioning Decrease pain Improve hygiene
  • 28. Conventional exercises  Active and passive range of motion  Stretching  Strengthening  Fitness
  • 29. Neurofacilitation techniques  Sensory input to the CNS produces reflex motor output.  Various neurofacilitation techniques are based on this basic principle.  All of the techniques aim to normalize muscle tone  To establish advanced postural reactions and to facilitate normal movement patterns.
  • 30. Vojta method of therapy  18 points in the body – crawling and reflex rolling.  placing the child in particular positions and stimulation of the key points in the body would enhance CNS development  In this way the child is presumed to learn normal movement patterns in place of abnormal motion.  Applied by the primary caregiver at home at least 4-5 times daily and stopped after a year if there is no improvement
  • 31. Bobath neurodevelopmental therapy  This is the most commonly used therapy method in CP worldwide.  It aims to Normalize muscle tone Inhibit abnormal primitive reflexes Stimulate normal movement.  It uses the idea of reflex inhibitory positions to decrease spasticity and stimulation to promote the development of advanced postural reactions.
  • 32.  It is believed that through positioning and stimulation a sense of normal movement will develop.  To teach the mother how to position the child at home during feeding and other activities.  The baby is held in the antispastic position to prevent contracture formation.
  • 33. Occupational therapy  OT aims to improve hand and upper extremity function in the child through play and purposeful activity .  There are defined systematic treatment methods for occupational therapy.  Sensory integration therapy aims to enhance the child’s ability to organize and integrate sensory information.  In response to sensory feedback, CNS perception and execution functions may improve and the motor planning capacity of the child may increase. .
  • 34.  Constraint induced movement therapy Where the normal hand is constrained Paralytic hand is forced to function Useful in children with hemiplegia.  Begin therapy toward one year of age when the child can feed himself using a spoon and play with toys.  Teach the child age appropriate self care activities such as dressing, bathing and brushing teeth.  Encourage the child to help with part of these activities even if he is unable to perform them independently
  • 35. play  Always include play activities in the rehabilitation program.  Play improves mental capacity and provides psychological satisfaction.  Organized play can address specific gross and fine motor problems  This increases the child’s compliance with therapy.  Riding a toy horse may improve Weight shift over the pelvis Swinging may improve sensation of movement.
  • 36. Advantages of swimming Normalizes muscle tone Decreases rate of contracture Strengthens muscles Improves cardiovascular fitness Improves walking Horseback riding Improves Head control Trunk balance Normalize muscle tone Positive emotions Self esteem
  • 37. Recreational programs  Arts and crafts  Music  Dancing  Wheelchair dancing  Drama,  Camping  Fishing  Scuba diving
  • 38. OTHERS  Speech therapy  Hearing aids and implants  Drugs Antispasmodics Baclofen Diazepam Clonidine Thizanidine Dantroline Botulinum injections Neoromuscular blockers Proton pump inhibitors for GERD Analgesics for pain  Respiratory physiotherapy
  • 39. Goals of brace  Increase function  Prevent deformity  Keep joint in a functional position  Stabilize the trunk and extremities  Facilitate selective motor control  Decrease spasticity  Protect extremity from injury in the postoperative phase
  • 40. Braces in CP  Ankle foot orthoses  Knee-ankle foot orthoses  Hip abduction orthoses  Thoracolumbosacral orthoses  Supramalleolar orthoses  Foot orthoses  Hand splints
  • 41. Functions of the AFO  Main function Keep the foot in a plantigrade position  Stance phase Stable base of support  Swing phase Prevent drop foot  At night Prevent contracture
  • 42. Spinal braces  To slow the progression of deformity  To delay surgery  To allow skeletal growth  To assist sitting balance  To protect the surgical site from excessive loading after surgery
  • 43. Mobility aids  Example Standers Walkers Crutches Canes  Advantages of mobility aids Develop balance Decrease energy expenditure Decrease loads on joints Improve posture
  • 44. Benefits of Standers  Support erect posture  Enable weight bearing  Stretch muscles to prevent contractures  Decrease muscle tone  Improve head and trunk control
  • 45. Goals of orthopaedic surgery Goal Operate to achieve Walking potential Functional ambulation Good hip and knee extension Stable hips Plantigrade stable feet No walking potential Sitting balance Straight spine Horizontal pelvis Stable hips
  • 46. Ortho surgeries in CP Types of CP Surgical procedures most often performed Quadriplegic Hip adductor flexor release Osteotomy Spine fusion Diplegic Hamstring-gastrocnemius lengthening Hip adductor-flexor lengthening Derotation osteotomy Rectus femoris transfer Hemiplegic Gastrocnemius lengthening Split tibialis anterior & posterior transfer Tibialis posterior lengthening
  • 47. Message  Enhance Familial bonding and support  Therapy along with peers  No aggressive therapy  Don’t give false hopes  Include sports and recreational activities  Successful rehabilitation includes Prevention of additional problems Reduction of disability Community integration.  Rehabilitation is successful if Child is happy Parents are well adjusted