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CEREBRAL PALSY DAY
Dr. Mansoor Alam
Consultant Developmental Specialist
Institute for Child Development, New Delhi
WORLD CEREBRAL PALSY DAY
 World Cerebral Palsy Day-6th October
 Indian National Cerebral Palsy-3rd October
CEREBRAL PALSY DAY
 World Cerebral Palsy Day is observed on October
6. Cerebral Palsy is a lifelong disability with no
known cure. The day celebrates lives of 17 million
people living with Cerebral Palsy, bringing people
living with cerebral palsy, their families, allies,
supporters and organisations across more than 100
countries together.
 In 2012, Cerebral Palsy Alliance created World
Cerebral Palsy Day on October 6. The day aims to
ensure that children and adults with cerebral palsy
have the same rights, access and opportunities as
rest of the world.
INDIAN CEREBRAL PALSY DAY
 3rd October, every year
 In remembrance of Dr Perin K Mulla Feroze, a lady
doctor from Mumbai.
CEREBRAL PALSY DAY
 There are many different ways you can spread
cerebral palsy awareness. One of the most popular ways
to show your support for National
Cerebral Palsy Month is to wear
the colour green
 Green is commonly associated with
new life, growth, and nourishment, which seems fitting
given the nature of cerebral palsy. Cerebral palsy
manifests in childhood, and is often the result of serious
birth injuries
THEME OF CP DAY-2023
 The theme for the day is #MillionsOfReasons – as
cerebral palsy affects more than 17 million people
worldwide, there are millions of reasons to support the
day and make your voice heard on October 6.
 World Cerebral Palsy Day is a movement of people with
cerebral palsy and their families, and the organisations
that support them, in more than 75 countries.
 The World Cerebral Palsy Day vision is to ensure that
children and adults with cerebral palsy have the same
rights, access and opportunities as anyone else in our
society.
TODAY…
 Quick facts about cerebral palsy (CP)
 Definition
 Causes of CP
 Risk factors
 Classification
 Diagnosis
 Assessments
 Treatment and Management
 F-words in CP Management
QUICK FACTS
 CP is the most common physical disability in childhood
CP occurs in approximately 1 in 400 live
Births worldwide
 It is caused by an injury to the developing
brain, which mostly happens before birth
 There is no single cause but researchers
have identified a number of factors that may
lead to the brain injury
 Babies can now be diagnosed as at ‘high
risk of CP’ at three months of age or even before
 There are many evidence-based interventions
for CP and new international clinical guidelines will soon
be available.
CEREBRAL PALSY
Cerebral palsy (CP) is a physical disability that affects
movement and posture
 CP is an umbrella term for a group of disorders that affects a
person’s ability to move
 CP is due to damage to the developing brain before, during or
after birth
 CP affects people in different ways. It can affect body
movement, muscle control, muscle coordination, muscle tone,
reflex, posture and balance.
 Although CP is a permanent life-long condition, some of these
signs of cerebral palsy can improve or worsen over time
 People who have CP may also have visual, learning, hearing,
speech, epilepsy and intellectual impairments.
THE CLINICAL PICTURE
OF A PERSON AS A WHOLE
DEFINITION
 Cerebral palsy describes a group of permanent disorders
of the development of movement and posture causing
activity limitation that are attributed to non-progressive
disturbances that occurred in the developing fetal or
infant brain.
DEFINITION
 The motor disorders of cerebral palsy are often
accompanied by disturbances of sensation,
perception, cognition, communication and behavior,
by epilepsy, and by secondary musculoskeletal
disorders”
CEREBRAL PALSY
Three part definition:
A disorder of movement and Posture caused by a non-progressive
Injury to the immature brain
Change in muscle tone and posture, both at rest and with voluntary
activity.
First year or two of life – included in most definitions
Upper age limit of post-natal brain insult- unclear
HISTORY
 Dr. Little was the first person who identified cerebral palsy. CP
was earlier known as little diseases
 It is not widely known that Sigmund Freud (1889) was the
leading European authority on CP of the late 19th Century. He
authored three Monographs on CP in the 1890’s.
 Freud was the first to point out that prematurity and birth
asphyxia might reflect a fetus already damaged in-utero
 Even less well known is that William Osler wrote the only
19th century monograph on CP published in the US
 Osler’s special interest was in clinical expression and brain
pathology
CP is classified in many ways to
understand and deal the condition
Based on the site of insult to the brain
Based on involvement of body parts
Based on severity of the damage to
the brain
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CLASSIFICATION / TYPES OF CP
Spastic Rigidity
Dyskinetic Floppy
Ataxia Mixed

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CLASSIFICATION
BASED ON SITE OF INSULT OF THE BRAIN
Quadriplegia
Triplegia
Diplegia
Hemiplegia
Monoplegia
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CLASSIFICATION
BASED ON INVOLVEMENT OF BODY PARTS
Mild
Moderate
Severe
Profound
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BASED ON SEVERITY OF THE CONDITION
Spastic hemiplegia CP
Spastic diplegia CP
Spastic quadriplegia CP
Spastic triplegia CP
Spastic monoplegia CP
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DIFFERENT FORMS OF CP
Dystonic CP
Athetoid CP
Ataxic CP
Hypotonic CP
Mixed CP
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DIFFERENT FORMS OF CP
ADVANCE CLASSIFICATION
Based on involvement of body parts
Bilateral CP
Bilateral Symmetrical CP
Bilateral Asymmetrical CP
Unilateral CP
Unilateral Symmetrical CP
Unilateral Asymmetrical CP
ADVANCE CLASSIFICATION
Based on Functional Ability
 Gross Motor Level- GMFCS (5 Functional Level)
 Mobility Level-FMS (5 Functional Level)
 Manual Ability Level-MACS (5 Functional Level)
 Visual Ability Level-VFCS (5 Functional Level)
 Communication Ability Level- CFCS (5 Functional Level)
 Feeding Ability Level- EDACS (5 Functional Level)
Lowest Ability to Highest Ability
 Level-5: Lowest Ability Level
 Level-1: Highest Ability Level
General Features
Infantile hemiplegia is a movement defect of one side of
the body only, either the right side or the left. The
disability is not always uniform. In the typical spastic
form in the older child, the following patterns are seen.
 The upper limb is held with the arm adducted and
internally rotated,
 The forearm flexed and pronated, the wrists flexed, and
the fingers flexed with the thumb pressed into the palm.
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CP SPASTIC HEMIPLEGIA
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CP SPASTIC HEMIPLEGIA
Symmetrical or near symmetrical involvement
the legs are more involved that the arms.
The hips knees and ankles may flex and the child
can sit in the tailor position on the base of his
spine.
The arms may be mildly, moderately or severely
affected.
Very mild cases of spastic diplegia may involve
the legs and feet only. There may be a tendency
to walk in planter flexion only.
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CP SPASTIC DIPLEGIA
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CEREBRAL PALSY SPASTIC DIPLEGIA
These children show asymmetrical involvement; and
the arms are more involved than the legs.
The arms may be mildly, moderately or severely
affected. If the arms are moderately affected, one
hand is better than the other because the child will
use one hand for play.
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CP SPASTIC TRIPLEGIA
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CEREBRAL PALSY SPASTIC TRIPLEGIA
These children show symmetrical or near symmetrical
involvement; and the arms are more involved than the
legs.
Both hands are severely involved and he finds
difficulty in feeding himself and playing with toys.
If a child with spastic quadriplegia is maintained in
one position for the greater part of the day,
particularly if it is a flexed posture, he may develop
flexion contracture in muscles and in the capsules of
joints. Severe deformities and joints dislocations can
result.
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CP SPASTIC QUADRIPLEGIA
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CP SPASTIC QUADRIPLEGIA
Dystonia is a movement disorder in which
involuntary sustained or intermittent muscle
contractions cause twisting and repetitive
movements, abnormal postures, or both.
Dystonia in cerebral palsy (CP) presents as
hypertonia, involuntary postures and movements, or a
combination
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CP DYSTONIA
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CEREBRAL PALSY DYSTONIA
Athetoid cerebral palsy is a type of cerebral
palsy characterized by athetosis, or uncontrolled
movements. This lack of control usually causes a
person with athetoid cerebral palsy to make erratic
movements, especially when the person is in motion.
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CP ATHETOSIS
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CEREBRAL PALSY ATHETOSIS
Ataxia is the least common form of cerebral
palsy. Ataxia means 'without order' or
'incoordination'. Ataxic movements are characterized
by clumsiness, imprecision, or instability. ...
Ataxia causes an interruption of muscle control in the
arms and legs, resulting in a lack of balance and
coordination.
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CP ATAXIA
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CEREBRAL PALSY ATAXIA
Hypotonia is diminished muscle tone. The infant or
child with hypotonic cerebral palsy appears floppy -
- like a rag doll.
In early infancy, hypotonia can be easily seen by the
inability of the infant to gain any head control when
pulled by the arms to a sitting position (this symptom
is often referred to as head lag).
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CP HYPOTONIA
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CEREBRAL PALSY HYPOTONIA
Rigidity – is not seen in cases of cerebral palsy
caused by prematurity; however it is a common
feature in cerebral palsy caused by anoxia, such as in
near drowning. Muscles that have rigidity feel heavy
and like “a lead pipe” when they are moved passively.
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CP RIGIDITY
Mixed cerebral palsy is a developmental disorder
caused by brain damage that takes place before,
during or shortly after birth. Those diagnosed
with mixed CP have damage to the motor control
centers in several parts of their brain.
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MIXED CP
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CEREBRAL PALSY MIXED
The exact cause is unknown but it is believed that
C.P occurs during pregnancy when the brain gets
damaged or is underdeveloped.
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CAUSES OF CEREBRAL PALSY
CAUSES OF CEREBRAL PALSY
Cerebral palsy (CP) is the result of a combination of events either
before, during, or after birth that can lead to an injury in a baby’s developing
brain
 There are multiple causes of CP –but a series
of ‘causal pathways’, i.e.
a sequence of events that combine to cause
or accelerate injury to the developing brain.
 About 45% of children diagnosed with CP
are born prematurely
 For most babies born at term with CP, the
cause remains unknown
 Only a small percentage of CP is due to
complications at birth (e.g. asphyxia or lack
of oxygen).
 Variety of perinatal, prenatal, and postnatal factors
contribute, either singly or multifactorily to CP.
 Commonly thought to be due to birth asphyxia; now
known to be due to existing prenatal brain
abnormalities.
 Premature delivery is the single most important
determinant of CP.
 In 24% of cases, no cause is found.
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CAUSES OF CEREBRAL PALSY
 Multifactorial but in most cases is unknown.
 Sometime Neuro-imaging may be entirely
normal.
 An increasing amount of literature suggests
a link between various prenatal, perinatal,
and postnatal factors and CP
 Prenatal factors play a significant role in the
etiology of CP.
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CAUSES OF CEREBRAL PALSY
• This disorder affects the Cerebrum. which
controls voluntary movement
• such as thinking and emotions.
• The cerebral motor cortex
• (at the back of the frontal lobe)
• is usually damaged also.
• Cerebral Palsy may occur due to the damage of
white matter (brain tissue).
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WHERE/HOW ?
RISK FACTORS
Risk factors do not cause CP. However, the
presence of some risk factors may lead to an
increased chance of a child being born with
CP.
Some risk factors for cerebral palsy have been
identified. These include:
 premature birth (less than 37 weeks)
 low birth weight (small for gestational age)
 blood clotting problems (thrombophilia)
 an inability of the placenta to provide the developing foetus with oxygen
and nutrients
 bacterial or viral infection of the mother, foetus or baby that directly or
indirectly attacks the infant’s central nervous system
 prolonged loss of oxygen during the pregnancy or birthing process, or
severe jaundice shortly after birth.
General
 Gestational Age < 32 weeks
 Birth Weight < 2500 Grams
Maternal History
 Mental Retardation
 Seizure disorder
 Hyperthyroidism
 Two or more fetal loss
 Sibling with motor deficits
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RISK FACTORS ASSOCIATED WITH CP
During Gestation
 Twin gestation
 Fetal growth retardation
 Third Trimester bleeding
 Premature Placental Separation
 Choionitis
 Increased urine protein excretion
 Low placental weight
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RISK FACTORS ASSOCIATED WITH CP
 Fetal Factors
 Abnormal fetal presentation
 Fetal malformation
 Fetal bradychardia
 Neonatal Seizures
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RISK FACTORS ASSOCIATED WITH CP
DIAGNOSIS
CP can sometimes be diagnosed early, so
interventions can start as soon as possible
Babies can now be assessed as being at ‘high risk of cerebral palsy’ as
early as 3-5 months of age.
The most sensitive tools are:
 General Movements Assessment in babies <20 weeks (corrected) - 95%
predictive
 Neuroimaging
 Hammersmith Infant Neurological Assessment (HINE) - 90% predictive
See CP: Diagnosis and Treatment poster at www.worldcpday.org
DIAGNOSIS (CONT)
 Diagnosis Making for CP
DIAGNOSIS (CONT)
 Assessing Motor Development
Assessing Motor Development
DIAGNOSIS (CONT)
 Neuroimaging
DIAGNOSIS MAKING
Cerebral Palsy is a complex disorder so diagnosis
making is always difficult. There is no specific test
which can confirm the presence of CP.
CP is diagnosed through observations, assessments
and clinical investigations.
DIAGNOSIS MAKING
Delayed milestones, mostly with gross motors and
fine motors
Persistence of primitive reflexes
No evidence of progressive disease / No loss of
milestones achieved previously
DIAGNOSIS MAKING
There is motor delay- variation by more than 50%
with abnormal movements and poor postural control
A child with CP may have a combination of
associated disorders such as Epilepsy, Visual deficits,
Hearing Deficits, Drooling, Feeding problems, Poor
Cognition, Poor speech, etc
DIAGNOSIS MAKING
 Observation and documentation ( Videography)of
the child while the child is in static, dynamic and
transitory postures during play, etc
 Documenting medical history starting from
pregnancy. Medical issues related to prenatal,
perinatal and postnatal to establish a good scientific
basis of the diagnosis
DIAGNOSIS MAKING
 Getting X-rays or Ultrasound (Skull / Hips / Spine),
 Getting MRI / CT scan of the Brain / Spine
 Getting EEG -to rule out epileptic syndrome
DIAGNOSIS MAKING
 Getting Blood Tests -to rule out other diseases
 Getting Chromosomal Study -to rule out genetic
disorder
 Getting Vision Test, Hearing Test, etc to have a
baseline
ASSOCIATED IMPAIRMENTS
 Children with CP may also have a range of physical
and cognitive impairments
 Children with CP always have some or the other
associated disorders
 In a recent study of 100 Children with CP, 34
associated disorders has been found.
 Lesser the number of comorbid conditions-
better the prognosis
ASSOCIATED DISORDERS
 All children with CP have some or the other associated
problems. There are three types of co morbidities have
been identified. The three co morbidity categories are
cocausal, complications, and co‐occurring.
 Cocausal: Disorders caused by the same injury to the
developing brain that caused CP (i.e. epilepsy and
cognitive impairment)
 Complications: Disorders that are complications of the
main CP condition (i.e. scoliosis and hip dislocation)
 Co‐occurring: Disorders not caused by the injury to the
developing brain, nor are complications of the main CP
condition
ASSOCIATED DISORDERS
In actual sense these associated factors are
considered the basis of prognosis (outcomes from the
treatment). Coping with these disabilities may be
even more of a challenge than coping with the motor
impairments of cerebral palsy. There is a common
saying “Lesser the number of associated
problems-more the chances of better future”.
EPILEPSY / SEIZURES / CONVULSIONS
 Children with CP can have focal / partial
seizures, generalized seizures, petit mal /
absence seizure, myoclonic seizure, tonic-
atonic seizure (drop attacks), etc

Management / Treatment Options
 Medicinal Treatments- Anti-epileptic Drugs
(AED) based on the types of seizure
 Neuro-surgery to remove the part of the brain
responsible for the seizures (lobotomy)
Vagus Nerve Stimulation
Ketogenic-a special diet, etc
VISUAL IMPAIRMENTS-EYE PROBLEMS
Children with CP may have cerebral visual
impairment (CVI), Eye Visual Impairment,
Strabismus, Poor visual acuity (Myopia or
Hypermetropia), Nystagmus, Lazy eye, etc
Treatment / Management options
Visual Aids-Spectacles
Eye Surgery
Vision therapy
HEARING IMPAIRMENTS / DEFICITS
Children with CP may have hearing loss (conductive
hearing loss, sensorineural hearing loss),etc
Treatment / Management Options
 Hearing aids
 Surgeries to correct malformation or injuries
 Cochlear implant
 Auditory Training, etc
SPEECH IMPAIRMENTS
Children with CP can have problems such as
aphasia, dyspraxia, dysprosody , dysarthria,
stuttering, dysphagia, resonance disorders, etc
Treatment / Management Options
 Use of Bliss Board
 Speech and language therapy, etc
FEEDING DISORDER
Very common problems in the form sucking
difficulties, swallowing difficulties, chewing difficulties,
drooling etc
Treatment / Management Options
 Combination therapy
 Nutritional modifications
 GERD is managed with medication
DROOLING-EXCESSIVE PRODUCTION OF
SALIVA (SIALORRHEA)
Drooling can be in the form of posterior drooling or
anterior drooling
Treatment / Management Options
1. Optimizing positions and conditions
2. Oro-motor and oro-sensory therapies
3. Behavioral therapies
4. Oral appliances
5. Anti-cholinergic agents
6. Botulinum toxin Injections
7. Surgical intervention
MENTAL RETARDATION-INTELLECTUAL DISABILITY-
LOW INTELLIGENCE-LOW COGNITION
33% children with CP may have low / subnormal
cognition or poor mental ability. They have average or
lower than average IQ.
Treatment / Management Options
 Medications
 Occupational therapy
 Cognitive therapy
 Special Education
 Vocational / Life Skills training
BLADDER RELATED ISSUES
Children with CP have urinary incontinence or
enuresis, Urinary infections, and indication issues
Treatment / Management Options
 Medicinal Management-
 Specialized Exercises- Kegel Exercises
 Toilet Training Program
BOWEL RELATED ISSUES
Incidence: 40% to 57% children with CP may have
bowel related issues
Treatment / Management Options
 Medications
 Physical therapy
CONSTIPATIONS
Incidence: Around 74% children with CP have
constipation
Treatment / Management Options
1. Encourage foods that contain fibres
2. Encourage a good intake of Fluids
3. Limit the period of idle sitting
4. Encourage to change posture regularly
5. Assist with medications to maintain good bowel
habit
DENTAL PROBLEMS
More than 50% children with CP have Dental
problems in the forms of, mal-alignment of the upper
and lower teeth, excessive gagging, gingivitis due to
seizure medications, etc
Treatment / Management Options
 Dental care
 Oral hygiene, etc
FAILURE TO THRIVE
Incidence: as many as 33% - 40% children with CP
may have failure to thrive situation
Failure to thrive is a condition which is considered in
children who are consistently underweight.
Management / Treatment Options
 Special Diet-Nutritional supplements
 Managing other medical conditions
OBESITY
There is worldwide tendency of increasing prevalence
of obesity in children.
Treatment / Management Options
 Diet Modification
 Weight reduction program
POOR MUSCLE GROWTH
Incidence: Very common in hemiplegic Cerebral
Palsy
Treatment / Management Options
 Nutritional supplements-Protein rich food
 Activity oriented exercises, etc
BREATHING PROBLEMS
Incidence: Children with cerebral palsy are very prone
to respiratory complications like upper respiratory
infections (URTI), aspiration, and pneumonia.
Breathing difficulties have been seen due to spinal
curvature (scoliosis)
Treatment / Management Options
 Symptomatic medications
 Breathing exercises
VISUAL -PERCEPTION IMPAIRMENTS /
PERCEPTUAL DISORDER
Incidence: About 50% Children with CP may have
visuo-perceptual disorders
Treatment / Management Options
 Ophthalmological support
 Vision therapy
 Occupational therapy
 Special education, etc
DELAYED MATURATION
Incidence: Very rare. Sometimes puberty begins
earlier but ends later in white children with CP,
compared with general population
Treatment / Management Options
 Symptomatic medical and surgical management
 Transitional Management
 Sex education, etc
ABNORMAL SENSATIONS-SENSORY LOSS
Incidence: Rare, mostly with hemiplegic CP
Treatment / Management Options
 Medications
 Physical therapy
 Occupational therapy, etc
SENSORY DYSFUNCTION
Incidence: Around 40% children may have sensory
dysfunction
Treatment / Management Options
 Sensory Integration therapy
HYDROCEPHALY (WATER IN THE BRAIN)
Incidence: Around 17.3%.
Treatment / Management Options
 Symptomatic medical management
 Need based surgical procedures, insertion of
shunt, Endoscopic third ventriculostomy,
MICROCEPHALY (SMALL SIZE HEAD)
Incidence: Lot children with cerebral palsy may have
Microcephaly. Around 26.5%
Treatment / Management Options
 Regular monitoring
 Surgery may be helpful if there is craniosynostosis
SKIN DISORDERS
Incidence: Skin infection and irritation is very common
in CP
Treatment / Management Options
 Symptomatic treatment
 Personal hygiene
 Skin care, etc
BEHAVIORAL ISSUES
Incidence: 1 in 4 children with CP have behavioral
disorders.
Treatment / Management Options
 Behavioral therapy-ABA, BMT, CBT, etc
 Medications
CONGENITAL HEART DISORDER
Incidence: Very rare. Commonly PDA
Treatment / Management Options
 Symptomatic medical and surgical treatments
HORMONAL IMBALANCE
Incidence: Poor growth or delayed puberty due to
multiple pituitary hormone deficiency hormone
deficiency (MPHD)
Treatment / Management Options
 Hormonal Therapy
SLEEP DISTURBANCE
Incidence: Difficulty in initiating and maintaining
sleep, sleep wake transition, sleep breathing
disorders, sleep bruxism, excessive day time
sleeping, nightmares and sleep talking , etc
Treatment / Management Options
 Modification environment like light system,
temperature and bedding used for the child
 Maintaining sleep diary and diet modification
 Medications, etc
PAIN
Incidence: Pain is very common with children with CP.
Adults are more prone to pain due to poor postures
and joint immobility
Treatment / Management Options
 Medications- Antispasmodic medications,
Anticholinergic drugs
 Botox Injection
 Muscle massage, acupuncture, ice packs and heat
therapy, hydrotherapy, and cognitive behavioral
therapy.
ISSUES WITH SECONDARY SEXUAL
CHARACTERS
Incidence: Very common with severely affected adults
Treatment / Management Options
 Sex education
 Behavior therapy
 Medications, etc
PSYCHOLOGICAL ISSUES
Incidence: Mental health and psychological
problems, in the forms of depression, anxiety and
conduct disorders, generally triggered by pain,
discomfort or sleep disturbances.
Treatment / Management Options
 Psychotherapy
 Medications
www.worldcpday
ASSOCIATED IMPAIRMENTS
Children with CP may also have a range of physical and
cognitive impairments
1 in 4
is unable to walk
1 in 4
is unable to talk
3 in 4
experience pain
1 in 4
has epilepsy
1 in 4
has a behaviour
problem
1 in 2
has an
intellectual
disability
1 in 10
has a severe
vision
impairment
1 in 4
has bladder
control problems
1 in 5
has a sleep
disorder
1 in 5
has saliva control
problems
Team Members
Family
Medical Management Team
Habilitation Service Providers
Life Cycle Approach
Birth to one year
One year to 3 years
Three years to 6 years
Six years to 13 years
Thirteen years to 18 years
Above 18 years
MANAGEMENT AND TREATMENT TEAM
Screening Team
Neonatologist
Child Specialist
Developmental Pediatrician
Medical Diagnosis Making and Medical Management Team
 Pediatric Neurologist
 Pediatric orthopedic Surgeon
 Pediatric Eye specialist
 Pediatric ENT Specialist
 Pediatric Cardiologist
 Pediatric Gastroenterologist

MULTIDISCIPLINARY MANAGEMENT TEAM
Pediatric Nephrologists
Genetic Specialist
Pediatric Dietitian-Nutritionist
Pediatric Endocrinologist
Pediatric Immunologist
Pediatric Physiatrist
Pediatric Plastic Surgeon
Pediatric Pulmonologist
MULTIDISCIPLINARY MANAGEMENT TEAM
Habilitation Team
 Neonatotherapist
 Early Intervention Specialist
 Developmental Therapy Specialist
 Pediatric physiotherapist
 Pediatric Occupational Therapist
 Special Educator
 Speech and language Pathologist
 Psychologist / Behavior Therapist
MULTIDISCIPLINARY MANAGEMENT
TEAM
Habilitation Team
 Pediatric Optometrist
 Pediatric Hearing Aids Technician
 Postural Aids Specialist
 Orthotician
 Mobility Aids Specialist
 Adaptive and assistive Aids Technician
 Apps and Games designers
MULTIDISCIPLINARY MANAGEMENT TEAM
MANAGEMENT APPROACHES
 Multidisciplinary
 Interdisciplinary
 Trans disciplinary
Thorough and accurate assessment of children with cerebral palsy by a
multidisciplinary team is essential to ensure chosen interventions meet
the child’s needs.
Most assessments measure a particular aspect of the child’s life. It can
be Physical, Communication, Social-emotional or cognition
The World Health Organization's International Classification of
Functioning, Disability and Health (ICF) has been used to guide
assessment.
The ICF domains include body function and structure, participation,
activity and personal and environmental factors.
ASSESSMENTS OF CEREBRAL PALSY
INTERNATIONAL CLASSIFICATION OF
FUNCTIONING, DISABILITY AND HEALTH
Standardized assessments and outcome
measures may be relevant to one or more
domains of the ICF.
A significant number of assessments are
available and it is often necessary to use a
combination of these.
ASSESSMENTS OF CEREBRAL PALSY
Selection of assessment tools should be based
on purpose, psychometrics and those most
relevant to the area/s of difficulty.
The functional ability classification scales
should be used to guide assessment and
intervention with all children diagnosed with
cerebral palsy to facilitate communication and
goal setting.
ASSESSMENTS OF CEREBRAL PALSY
 Communication
 ADL
 Mobility
 Ambulation
ICF MODEL OF INTERVENTION FOR HABILITATION
Further assessment should occur to ensure
realistic goal setting, provide a baseline for
intervention and for evaluation of intervention
programs.
ASSESSMENT GUIDELINES
 History and observation
 Assessment of reflexes and reactions
 Assessment of functional level and motor
development
 Assessment of muscle tone
 Assessment of muscle strength
ASSESSMENT PROTOCOLS
 Assessment of musculoskeletal system deformities
 Assessment of physical fitness
 Assessment of gait
 Assessment of balance
 Assessment of trunk impairment
ASSESSMENT PROTOCOLS
 Assessment of health-related quality of life
 Assessment of activities of daily life
 Assessments of upper extremity
 Cognition / Psychometric Assessments
 Speech and Communication Assessments
ASSESSMENT PROTOCOLS
Detailed information should be received from the
family or caretakers in all issues related to the
children including
 Family history
 Prenatal, natal and postnatal period
 Chronologic and corrected age
 Associated problems
 Developmental story
 Adaptive equipment used
 Intervention approaches applied
 Medication taken
 Family Profile
HISTORY AND OBSERVATION
 Observational analysis is crucial to determine
children’s functional skills, spontaneous motions
and motion strategies, and the underlying
fundamental problems. Thus, it can be decided in
which field detailed assessment needs to be carried
out.
 During observational analysis, children must be in a
setting they can be with their family, and they can
feel comfortable and safe.
HISTORY AND OBSERVATION
 There should be various toys and materials in the
setting to reveal the children’s capacity and to draw
their attention.
 The assessment room should not be crowded and
noisy . Video recordings during observation are
rather beneficial as well.
HISTORY AND OBSERVATION
 Observation of reflexes is important to illustrate the
severity of the influence in the nervous
system, and observation of balance and protective
reactions is important to support motor
developmental process.
 When these assessments are carried out, the
corrected age of the children should be considered.
It is known that primitive reflexes continue
insistently or disappear later than normal or never
occur in children with CP.
ASSESSMENT OF REFLEXES AND
REACTIONS
 It can be observed that symmetric tonic and
asymmetric tonic neck reflexes still continue in
adolescent stage in a case diagnosed with
dyskinetic-type CP.
 Insistence of these reflexes can complicate the
therapy. It may be necessary to make various
adaptations in the treatment program when the
primitive reflexes continue in advanced ages.
 At the same time, the assessment of protective
reactions is important for determining a treatment
program
ASSESSMENT OF REFLEXES AND
REACTIONS
 It is crucial to assess motor development, functional
skills, and activity limitations for determining the
current state of the children, and there are
frequently used test batteries for this purpose.
 Gross Motor Function Measurement (GMFM)
is a standardized measurement instrument
frequently used to measure the change in gross
motor function.
ASSESSMENT OF FUNCTIONAL LEVEL AND MOTOR
DEVELOPMENT
Gross Motor Function Classification System
(GMFCS)
The Gross Motor Function Classification System
(GMFCS) is a five level classification that describes
the gross motor function of children with cerebral
palsy on the basis of their self-initiated movement
with particular emphasis on sitting, walking, and
wheeled mobility.
FUNCTIONAL MOTOR ABILITY
GMFCS
(GMFCS) Levels
Level-I: Walk independently
Level-II: Walk independently with limitations
Level-III: Use assistive devices such as elbow crutches or
walking frames
Level-IV: Require a wheelchair but may have some form of
independent mobility such as a powered wheelchair or
may assist with transfers
Level-V: Require a wheelchair and are fully dependent in
their mobility
GROSS MOTOR FUNCTION CLASSIFICATION SYSTEM
The Functional Mobility Scale (FMS) has been
constructed to classify functional mobility in
children 4 to 18 years, taking into account a
range of assistive devices a child might use
over three distances: five meters (in and around
the home), 50 meters (in and around (School
/preschool) and 500 meters (in the community).
The FMS is sensitive to detect change after
Specialized interventions.
FUNCTIONAL MOBILITY SCALE (FMS)
FMS
ASSESSING UPPER LIMBS
Level-I: Handles objects easily
Level-II: Handles most objects but with reduced
speed and/or quality
Level-III: Has some difficulty and needs help to
modify or prepare activities
Level-IV: Handles a limited selection of easily
managed objects in adapted settings
Level-V: Does not handle objects
UPPER LIMB CLASSIFICATIONS
MANUAL ABILITY CLASSIFICATION SYSTEM (MACS)
MACS
 Communication is simply the act of transferring
information from one place, person or group to
another.
 Every communication involves (at least) one
sender, a message and a recipient. This may sound
simple, but communication is actually a very
complex subject.
COMMUNICATIONS
 Speech is human vocal communication using
language. Each language uses phonetic
combinations of vowel and consonants sounds that
form the sounds of its words
 Speech disorders affect a person's ability to
produce sounds that create words. ...
 Types of speech disorder include misarticulation,
apraxia, and dysarthria. There are many possible
causes of speech disorders, including muscles
weakness, brain injuries, degenerative diseases,
autism, and hearing loss.
SPEECH
SPEECH AND COMMUNICATION THERAPY
Level-I: Effective sender and/or receiver with familiar and
unfamiliar partners
Level-II: Effective but slower paced sender and/or receiver
with familiar and unfamiliar partners
Level-III: Effective sender and/or receiver with familiar
Partners
Level-IV: Inconsistent sender and/or receiver with familiar
partners
Level-V: Seldom effective sender and/or receiver even
with familiar partners
COMMUNICATION CLASSIFICATION
COMMUNICATION FUNCTION CLASSIFICATION SYSTEM-
CFCS
Level-I
An effective communicator in most situations
Can independently communicate a wide
variety of messages/topics to familiar and
unfamiliar people in most environments
FUNCTIONAL COMMUNICATION CLASSIFICATION SYSTEM
(FCCS)
Level-II
An effective communicator in most situations, but does need
some help
Can communicate a variety of messages/ topics to familiar
people but may experience some difficulties with unfamiliar
people/topics and environments and may need prompts, such
as, prompt questions, repetitions (to make themselves
understood) and loudness
An AAC user who requires assistance with set up,
and/or programming; and whose listener may need some
assistance with orientation/ interpretation of AAC strategies
FUNCTIONAL COMMUNICATION CLASSIFICATION SYSTEM
(FCCS)
Level-III
An effective communicator in some situations.
Can communicate a small range of messages/ topics to
most familiar people
Effective communicator with familiar people and
activities and in familiar settings about their needs and
wants, and things that are happening but require
assistance with unfamiliar people/topics and
environments
Relies on a familiar communication partner to interpret
AAC or speech attempts, and to prepare, set up and
support communication
FUNCTIONAL COMMUNICATION CLASSIFICATION SYSTEM
(FCCS)
Level-IV
Assistance is required in most situations, especially
with unfamiliar people and environments.
Communicates daily/routine needs and wants with
familiar people
Can initiate and attract attention but needs a familiar
person who is familiar with their routine, recent
/significant experiences and likes and dislikes, and to
interpret their communication
Responds to familiar voices, sounds and routines using
body movement, facial expression and vocalisation
FUNCTIONAL COMMUNICATION CLASSIFICATION SYSTEM
(FCCS)
Level-V
Communicates unintentionally with others, using
movement and behavior
Daily/routine needs and wants are interpreted
by familiar people from observation of the
individual’s emotional state, body movement
and behavior
Needs full assistance from a familiar person to
observe, interpret movements and behaviors,
anticipate, and problem solve based on their
experience, training and observation
FUNCTIONAL COMMUNICATION CLASSIFICATION SYSTEM
(FCCS)
 Academic Performance
 Adaptive Delay or Impairment
 Capacity to Learn/Learning Impairments
 Communication Level
 Emotional Status
 Health
 Intelligence
 Motor Abilities
 Social Ability
 Vision and Hearing
SPECIAL EDUCATION ASSESSMENT
 The assessments help to allocate the following
service and supports to accommodate, modify or
adapt a child’s needs:
 Program Modifications
 Related Services
 Special Accommodations
 Specially Designed Instruction
 Supplementary Aids
 Adapted Equipment
 Adapted Materials
 Assistive Technology
 Augmentative Communication Devices
SPECIAL EDUCATION ASSESSMENT
 The assessment of cognitive functioning is often
challenging in students with motor impairment because
the majority of tests require verbal and motor responses
 A careful consideration of the level of motor,
communication, and/or visual or visual perception
impairment in students with CP and motor impairments
can inform assessors on the choice of cognitive
assessment battery to use
 The use of Assistive Technology, together with
alternative response modes (e.g., partner assisted
scanning) is encouraged to enable access to
standardized cognitive assessment.
SPECIAL EDUCATION ASSESSMENT
For students with significant motor impairments for
whom standardized cognitive assessments are not
appropriate, the use of developmental scales, which
assess progress along a continuum rather than
providing comparative performance data with peers,
may be an appropriate alternative
SPECIAL EDUCATION ASSESSMENT
 For students with severe motor impairments, it is
important to conduct a functional skills assessment.
 A functional skills assessment targets the skills
needed in a given environment and activity, and
includes measures of social and adaptive
functioning with a focus on basic life skills.
 It focuses on practical independent living skills. It
also considers students’ functioning in their
environments, and examines the process of
learning and performance.
SPECIAL EDUCATION ASSESSMENT
 Based on the results of the assessment, intervention techniques
are implemented and evaluated on a regular basis
 The following test accommodations are helpful in supporting
students with significant motor impairments so as to obtain the
best responses during the assessment session
 Body positioning is of specific relevance to students with
significant motor impairments. Students should be positioned in a
way that facilitates the support of the trunk and independent use
of the arms and hands. This can be done via the use of an
Adaptive Seating System.
 Appropriate positioning can reduce pain, permit better fine motor
function, facilitate attention, reduce fatigue, and promote
improved social interaction, thereby optimizing performance.
SPECIAL EDUCATION ASSESSMENT
 Students should be allowed to use assistive
technology such as Augmentative and Alternative
Communication (AAC) devices to enhance their
functional communication.
 Information on the student’s communication style
and modality should be determined before
assessment. It may be helpful to involve the family,
caregivers and therapists who work closely with the
student to assist in understanding the student’s
responses.
SPECIAL EDUCATION ASSESSMENT
PLEASE REMEMBER-
TREATMENT AND MANAGEMENT
Treatment
Medicines / Drugs
Antispastic
Anti-Epileptic
Anti-drooling
GERD
Constipation
Chemodenervation
Phenol
Botox
TREATMENT AND MANAGEMENT
Orthopedic Surgery
STR
SEMLLARS
OSSCS
Ilizarov
Percutaneous
TREATMENT AND MANAGEMENT
Use of Implants
Use of Intrathecal Baclofen Pump
Use of Deep Brain Stimulation
Use of VP Shunt
Use of Neurosurgery
Selective Dorsal Rhizotomy
Gamma Knife Surgery
TREATMENT AND MANAGEMENT
Use of Regenerative Medicines
Hyperbaric Oxygen Therapy
Stem Cell Therapy
TREATMENT AND MANAGEMENT
Complementary and Alternative Medicines
Homeopathy
Unani
Ayurveda
Herbal
Acupuncture
Chinese Medicines
Acupressure
Magneto therapy
Nutritional Therapy
TREATMENT AND MANAGEMENT
Management
Habilitation and Rehabilitation Services
1. Infant Stimulation Therapy
2. Early Intervention
3. Play Therapy
4. Developmental Therapy
5. Physiotherapy
6. Occupational Therapy
7. Speech Therapy
8. Cognitive Therapy / Special Education
9. Behavioral Therapy
10. Assistive Technology
F-WORDS
THANK YOU ALL
For More Information, Please contact me at
Institute for Child Development
C-27, Malviya Nagar
New Delhi-110017
Landline Number: 011-41012124
Mobile / Whatsapp Number: 7838809241
Mail ID: helpicd@gmail.com
Website: www.icddelhi.org

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Cerebral Palsy Day-23.pptx

  • 1. CEREBRAL PALSY DAY Dr. Mansoor Alam Consultant Developmental Specialist Institute for Child Development, New Delhi
  • 2. WORLD CEREBRAL PALSY DAY  World Cerebral Palsy Day-6th October  Indian National Cerebral Palsy-3rd October
  • 3. CEREBRAL PALSY DAY  World Cerebral Palsy Day is observed on October 6. Cerebral Palsy is a lifelong disability with no known cure. The day celebrates lives of 17 million people living with Cerebral Palsy, bringing people living with cerebral palsy, their families, allies, supporters and organisations across more than 100 countries together.  In 2012, Cerebral Palsy Alliance created World Cerebral Palsy Day on October 6. The day aims to ensure that children and adults with cerebral palsy have the same rights, access and opportunities as rest of the world.
  • 4. INDIAN CEREBRAL PALSY DAY  3rd October, every year  In remembrance of Dr Perin K Mulla Feroze, a lady doctor from Mumbai.
  • 5. CEREBRAL PALSY DAY  There are many different ways you can spread cerebral palsy awareness. One of the most popular ways to show your support for National Cerebral Palsy Month is to wear the colour green  Green is commonly associated with new life, growth, and nourishment, which seems fitting given the nature of cerebral palsy. Cerebral palsy manifests in childhood, and is often the result of serious birth injuries
  • 6. THEME OF CP DAY-2023  The theme for the day is #MillionsOfReasons – as cerebral palsy affects more than 17 million people worldwide, there are millions of reasons to support the day and make your voice heard on October 6.  World Cerebral Palsy Day is a movement of people with cerebral palsy and their families, and the organisations that support them, in more than 75 countries.  The World Cerebral Palsy Day vision is to ensure that children and adults with cerebral palsy have the same rights, access and opportunities as anyone else in our society.
  • 7. TODAY…  Quick facts about cerebral palsy (CP)  Definition  Causes of CP  Risk factors  Classification  Diagnosis  Assessments  Treatment and Management  F-words in CP Management
  • 8. QUICK FACTS  CP is the most common physical disability in childhood CP occurs in approximately 1 in 400 live Births worldwide  It is caused by an injury to the developing brain, which mostly happens before birth  There is no single cause but researchers have identified a number of factors that may lead to the brain injury  Babies can now be diagnosed as at ‘high risk of CP’ at three months of age or even before  There are many evidence-based interventions for CP and new international clinical guidelines will soon be available.
  • 9. CEREBRAL PALSY Cerebral palsy (CP) is a physical disability that affects movement and posture  CP is an umbrella term for a group of disorders that affects a person’s ability to move  CP is due to damage to the developing brain before, during or after birth  CP affects people in different ways. It can affect body movement, muscle control, muscle coordination, muscle tone, reflex, posture and balance.  Although CP is a permanent life-long condition, some of these signs of cerebral palsy can improve or worsen over time  People who have CP may also have visual, learning, hearing, speech, epilepsy and intellectual impairments.
  • 10. THE CLINICAL PICTURE OF A PERSON AS A WHOLE
  • 11. DEFINITION  Cerebral palsy describes a group of permanent disorders of the development of movement and posture causing activity limitation that are attributed to non-progressive disturbances that occurred in the developing fetal or infant brain.
  • 12. DEFINITION  The motor disorders of cerebral palsy are often accompanied by disturbances of sensation, perception, cognition, communication and behavior, by epilepsy, and by secondary musculoskeletal disorders”
  • 13. CEREBRAL PALSY Three part definition: A disorder of movement and Posture caused by a non-progressive Injury to the immature brain Change in muscle tone and posture, both at rest and with voluntary activity. First year or two of life – included in most definitions Upper age limit of post-natal brain insult- unclear
  • 14. HISTORY  Dr. Little was the first person who identified cerebral palsy. CP was earlier known as little diseases  It is not widely known that Sigmund Freud (1889) was the leading European authority on CP of the late 19th Century. He authored three Monographs on CP in the 1890’s.  Freud was the first to point out that prematurity and birth asphyxia might reflect a fetus already damaged in-utero  Even less well known is that William Osler wrote the only 19th century monograph on CP published in the US  Osler’s special interest was in clinical expression and brain pathology
  • 15.
  • 16. CP is classified in many ways to understand and deal the condition Based on the site of insult to the brain Based on involvement of body parts Based on severity of the damage to the brain 10/6/2023 16 CLASSIFICATION / TYPES OF CP
  • 17. Spastic Rigidity Dyskinetic Floppy Ataxia Mixed  10/6/2023 17 CLASSIFICATION BASED ON SITE OF INSULT OF THE BRAIN
  • 20. Spastic hemiplegia CP Spastic diplegia CP Spastic quadriplegia CP Spastic triplegia CP Spastic monoplegia CP 10/6/2023 20 DIFFERENT FORMS OF CP
  • 21. Dystonic CP Athetoid CP Ataxic CP Hypotonic CP Mixed CP 10/6/2023 21 DIFFERENT FORMS OF CP
  • 22. ADVANCE CLASSIFICATION Based on involvement of body parts Bilateral CP Bilateral Symmetrical CP Bilateral Asymmetrical CP Unilateral CP Unilateral Symmetrical CP Unilateral Asymmetrical CP
  • 23. ADVANCE CLASSIFICATION Based on Functional Ability  Gross Motor Level- GMFCS (5 Functional Level)  Mobility Level-FMS (5 Functional Level)  Manual Ability Level-MACS (5 Functional Level)  Visual Ability Level-VFCS (5 Functional Level)  Communication Ability Level- CFCS (5 Functional Level)  Feeding Ability Level- EDACS (5 Functional Level) Lowest Ability to Highest Ability  Level-5: Lowest Ability Level  Level-1: Highest Ability Level
  • 24. General Features Infantile hemiplegia is a movement defect of one side of the body only, either the right side or the left. The disability is not always uniform. In the typical spastic form in the older child, the following patterns are seen.  The upper limb is held with the arm adducted and internally rotated,  The forearm flexed and pronated, the wrists flexed, and the fingers flexed with the thumb pressed into the palm. 10/6/2023 24 CP SPASTIC HEMIPLEGIA
  • 26. Symmetrical or near symmetrical involvement the legs are more involved that the arms. The hips knees and ankles may flex and the child can sit in the tailor position on the base of his spine. The arms may be mildly, moderately or severely affected. Very mild cases of spastic diplegia may involve the legs and feet only. There may be a tendency to walk in planter flexion only. 10/6/2023 26 CP SPASTIC DIPLEGIA
  • 28. These children show asymmetrical involvement; and the arms are more involved than the legs. The arms may be mildly, moderately or severely affected. If the arms are moderately affected, one hand is better than the other because the child will use one hand for play. 10/6/2023 28 CP SPASTIC TRIPLEGIA
  • 30. These children show symmetrical or near symmetrical involvement; and the arms are more involved than the legs. Both hands are severely involved and he finds difficulty in feeding himself and playing with toys. If a child with spastic quadriplegia is maintained in one position for the greater part of the day, particularly if it is a flexed posture, he may develop flexion contracture in muscles and in the capsules of joints. Severe deformities and joints dislocations can result. 10/6/2023 30 CP SPASTIC QUADRIPLEGIA
  • 32. Dystonia is a movement disorder in which involuntary sustained or intermittent muscle contractions cause twisting and repetitive movements, abnormal postures, or both. Dystonia in cerebral palsy (CP) presents as hypertonia, involuntary postures and movements, or a combination 10/6/2023 32 CP DYSTONIA
  • 34. Athetoid cerebral palsy is a type of cerebral palsy characterized by athetosis, or uncontrolled movements. This lack of control usually causes a person with athetoid cerebral palsy to make erratic movements, especially when the person is in motion. 10/6/2023 34 CP ATHETOSIS
  • 36. Ataxia is the least common form of cerebral palsy. Ataxia means 'without order' or 'incoordination'. Ataxic movements are characterized by clumsiness, imprecision, or instability. ... Ataxia causes an interruption of muscle control in the arms and legs, resulting in a lack of balance and coordination. 10/6/2023 36 CP ATAXIA
  • 38. Hypotonia is diminished muscle tone. The infant or child with hypotonic cerebral palsy appears floppy - - like a rag doll. In early infancy, hypotonia can be easily seen by the inability of the infant to gain any head control when pulled by the arms to a sitting position (this symptom is often referred to as head lag). 10/6/2023 38 CP HYPOTONIA
  • 40. Rigidity – is not seen in cases of cerebral palsy caused by prematurity; however it is a common feature in cerebral palsy caused by anoxia, such as in near drowning. Muscles that have rigidity feel heavy and like “a lead pipe” when they are moved passively. 10/6/2023 40 CP RIGIDITY
  • 41. Mixed cerebral palsy is a developmental disorder caused by brain damage that takes place before, during or shortly after birth. Those diagnosed with mixed CP have damage to the motor control centers in several parts of their brain. 10/6/2023 41 MIXED CP
  • 43. The exact cause is unknown but it is believed that C.P occurs during pregnancy when the brain gets damaged or is underdeveloped. 10/6/2023 43 CAUSES OF CEREBRAL PALSY
  • 44. CAUSES OF CEREBRAL PALSY Cerebral palsy (CP) is the result of a combination of events either before, during, or after birth that can lead to an injury in a baby’s developing brain  There are multiple causes of CP –but a series of ‘causal pathways’, i.e. a sequence of events that combine to cause or accelerate injury to the developing brain.  About 45% of children diagnosed with CP are born prematurely  For most babies born at term with CP, the cause remains unknown  Only a small percentage of CP is due to complications at birth (e.g. asphyxia or lack of oxygen).
  • 45.  Variety of perinatal, prenatal, and postnatal factors contribute, either singly or multifactorily to CP.  Commonly thought to be due to birth asphyxia; now known to be due to existing prenatal brain abnormalities.  Premature delivery is the single most important determinant of CP.  In 24% of cases, no cause is found. 10/6/2023 45 CAUSES OF CEREBRAL PALSY
  • 46.  Multifactorial but in most cases is unknown.  Sometime Neuro-imaging may be entirely normal.  An increasing amount of literature suggests a link between various prenatal, perinatal, and postnatal factors and CP  Prenatal factors play a significant role in the etiology of CP. 10/6/2023 46 CAUSES OF CEREBRAL PALSY
  • 47. • This disorder affects the Cerebrum. which controls voluntary movement • such as thinking and emotions. • The cerebral motor cortex • (at the back of the frontal lobe) • is usually damaged also. • Cerebral Palsy may occur due to the damage of white matter (brain tissue). 10/6/2023 47 WHERE/HOW ?
  • 48. RISK FACTORS Risk factors do not cause CP. However, the presence of some risk factors may lead to an increased chance of a child being born with CP. Some risk factors for cerebral palsy have been identified. These include:  premature birth (less than 37 weeks)  low birth weight (small for gestational age)  blood clotting problems (thrombophilia)  an inability of the placenta to provide the developing foetus with oxygen and nutrients  bacterial or viral infection of the mother, foetus or baby that directly or indirectly attacks the infant’s central nervous system  prolonged loss of oxygen during the pregnancy or birthing process, or severe jaundice shortly after birth.
  • 49. General  Gestational Age < 32 weeks  Birth Weight < 2500 Grams Maternal History  Mental Retardation  Seizure disorder  Hyperthyroidism  Two or more fetal loss  Sibling with motor deficits 10/6/2023 49 RISK FACTORS ASSOCIATED WITH CP
  • 50. During Gestation  Twin gestation  Fetal growth retardation  Third Trimester bleeding  Premature Placental Separation  Choionitis  Increased urine protein excretion  Low placental weight 10/6/2023 50 RISK FACTORS ASSOCIATED WITH CP
  • 51.  Fetal Factors  Abnormal fetal presentation  Fetal malformation  Fetal bradychardia  Neonatal Seizures 10/6/2023 51 RISK FACTORS ASSOCIATED WITH CP
  • 52. DIAGNOSIS CP can sometimes be diagnosed early, so interventions can start as soon as possible Babies can now be assessed as being at ‘high risk of cerebral palsy’ as early as 3-5 months of age. The most sensitive tools are:  General Movements Assessment in babies <20 weeks (corrected) - 95% predictive  Neuroimaging  Hammersmith Infant Neurological Assessment (HINE) - 90% predictive See CP: Diagnosis and Treatment poster at www.worldcpday.org
  • 54. DIAGNOSIS (CONT)  Assessing Motor Development Assessing Motor Development
  • 56. DIAGNOSIS MAKING Cerebral Palsy is a complex disorder so diagnosis making is always difficult. There is no specific test which can confirm the presence of CP. CP is diagnosed through observations, assessments and clinical investigations.
  • 57. DIAGNOSIS MAKING Delayed milestones, mostly with gross motors and fine motors Persistence of primitive reflexes No evidence of progressive disease / No loss of milestones achieved previously
  • 58. DIAGNOSIS MAKING There is motor delay- variation by more than 50% with abnormal movements and poor postural control A child with CP may have a combination of associated disorders such as Epilepsy, Visual deficits, Hearing Deficits, Drooling, Feeding problems, Poor Cognition, Poor speech, etc
  • 59. DIAGNOSIS MAKING  Observation and documentation ( Videography)of the child while the child is in static, dynamic and transitory postures during play, etc  Documenting medical history starting from pregnancy. Medical issues related to prenatal, perinatal and postnatal to establish a good scientific basis of the diagnosis
  • 60. DIAGNOSIS MAKING  Getting X-rays or Ultrasound (Skull / Hips / Spine),  Getting MRI / CT scan of the Brain / Spine  Getting EEG -to rule out epileptic syndrome
  • 61. DIAGNOSIS MAKING  Getting Blood Tests -to rule out other diseases  Getting Chromosomal Study -to rule out genetic disorder  Getting Vision Test, Hearing Test, etc to have a baseline
  • 62. ASSOCIATED IMPAIRMENTS  Children with CP may also have a range of physical and cognitive impairments  Children with CP always have some or the other associated disorders  In a recent study of 100 Children with CP, 34 associated disorders has been found.  Lesser the number of comorbid conditions- better the prognosis
  • 63. ASSOCIATED DISORDERS  All children with CP have some or the other associated problems. There are three types of co morbidities have been identified. The three co morbidity categories are cocausal, complications, and co‐occurring.  Cocausal: Disorders caused by the same injury to the developing brain that caused CP (i.e. epilepsy and cognitive impairment)  Complications: Disorders that are complications of the main CP condition (i.e. scoliosis and hip dislocation)  Co‐occurring: Disorders not caused by the injury to the developing brain, nor are complications of the main CP condition
  • 64. ASSOCIATED DISORDERS In actual sense these associated factors are considered the basis of prognosis (outcomes from the treatment). Coping with these disabilities may be even more of a challenge than coping with the motor impairments of cerebral palsy. There is a common saying “Lesser the number of associated problems-more the chances of better future”.
  • 65. EPILEPSY / SEIZURES / CONVULSIONS  Children with CP can have focal / partial seizures, generalized seizures, petit mal / absence seizure, myoclonic seizure, tonic- atonic seizure (drop attacks), etc  Management / Treatment Options  Medicinal Treatments- Anti-epileptic Drugs (AED) based on the types of seizure  Neuro-surgery to remove the part of the brain responsible for the seizures (lobotomy) Vagus Nerve Stimulation Ketogenic-a special diet, etc
  • 66. VISUAL IMPAIRMENTS-EYE PROBLEMS Children with CP may have cerebral visual impairment (CVI), Eye Visual Impairment, Strabismus, Poor visual acuity (Myopia or Hypermetropia), Nystagmus, Lazy eye, etc Treatment / Management options Visual Aids-Spectacles Eye Surgery Vision therapy
  • 67. HEARING IMPAIRMENTS / DEFICITS Children with CP may have hearing loss (conductive hearing loss, sensorineural hearing loss),etc Treatment / Management Options  Hearing aids  Surgeries to correct malformation or injuries  Cochlear implant  Auditory Training, etc
  • 68. SPEECH IMPAIRMENTS Children with CP can have problems such as aphasia, dyspraxia, dysprosody , dysarthria, stuttering, dysphagia, resonance disorders, etc Treatment / Management Options  Use of Bliss Board  Speech and language therapy, etc
  • 69. FEEDING DISORDER Very common problems in the form sucking difficulties, swallowing difficulties, chewing difficulties, drooling etc Treatment / Management Options  Combination therapy  Nutritional modifications  GERD is managed with medication
  • 70. DROOLING-EXCESSIVE PRODUCTION OF SALIVA (SIALORRHEA) Drooling can be in the form of posterior drooling or anterior drooling Treatment / Management Options 1. Optimizing positions and conditions 2. Oro-motor and oro-sensory therapies 3. Behavioral therapies 4. Oral appliances 5. Anti-cholinergic agents 6. Botulinum toxin Injections 7. Surgical intervention
  • 71. MENTAL RETARDATION-INTELLECTUAL DISABILITY- LOW INTELLIGENCE-LOW COGNITION 33% children with CP may have low / subnormal cognition or poor mental ability. They have average or lower than average IQ. Treatment / Management Options  Medications  Occupational therapy  Cognitive therapy  Special Education  Vocational / Life Skills training
  • 72. BLADDER RELATED ISSUES Children with CP have urinary incontinence or enuresis, Urinary infections, and indication issues Treatment / Management Options  Medicinal Management-  Specialized Exercises- Kegel Exercises  Toilet Training Program
  • 73. BOWEL RELATED ISSUES Incidence: 40% to 57% children with CP may have bowel related issues Treatment / Management Options  Medications  Physical therapy
  • 74. CONSTIPATIONS Incidence: Around 74% children with CP have constipation Treatment / Management Options 1. Encourage foods that contain fibres 2. Encourage a good intake of Fluids 3. Limit the period of idle sitting 4. Encourage to change posture regularly 5. Assist with medications to maintain good bowel habit
  • 75. DENTAL PROBLEMS More than 50% children with CP have Dental problems in the forms of, mal-alignment of the upper and lower teeth, excessive gagging, gingivitis due to seizure medications, etc Treatment / Management Options  Dental care  Oral hygiene, etc
  • 76. FAILURE TO THRIVE Incidence: as many as 33% - 40% children with CP may have failure to thrive situation Failure to thrive is a condition which is considered in children who are consistently underweight. Management / Treatment Options  Special Diet-Nutritional supplements  Managing other medical conditions
  • 77. OBESITY There is worldwide tendency of increasing prevalence of obesity in children. Treatment / Management Options  Diet Modification  Weight reduction program
  • 78. POOR MUSCLE GROWTH Incidence: Very common in hemiplegic Cerebral Palsy Treatment / Management Options  Nutritional supplements-Protein rich food  Activity oriented exercises, etc
  • 79. BREATHING PROBLEMS Incidence: Children with cerebral palsy are very prone to respiratory complications like upper respiratory infections (URTI), aspiration, and pneumonia. Breathing difficulties have been seen due to spinal curvature (scoliosis) Treatment / Management Options  Symptomatic medications  Breathing exercises
  • 80. VISUAL -PERCEPTION IMPAIRMENTS / PERCEPTUAL DISORDER Incidence: About 50% Children with CP may have visuo-perceptual disorders Treatment / Management Options  Ophthalmological support  Vision therapy  Occupational therapy  Special education, etc
  • 81. DELAYED MATURATION Incidence: Very rare. Sometimes puberty begins earlier but ends later in white children with CP, compared with general population Treatment / Management Options  Symptomatic medical and surgical management  Transitional Management  Sex education, etc
  • 82. ABNORMAL SENSATIONS-SENSORY LOSS Incidence: Rare, mostly with hemiplegic CP Treatment / Management Options  Medications  Physical therapy  Occupational therapy, etc
  • 83. SENSORY DYSFUNCTION Incidence: Around 40% children may have sensory dysfunction Treatment / Management Options  Sensory Integration therapy
  • 84. HYDROCEPHALY (WATER IN THE BRAIN) Incidence: Around 17.3%. Treatment / Management Options  Symptomatic medical management  Need based surgical procedures, insertion of shunt, Endoscopic third ventriculostomy,
  • 85. MICROCEPHALY (SMALL SIZE HEAD) Incidence: Lot children with cerebral palsy may have Microcephaly. Around 26.5% Treatment / Management Options  Regular monitoring  Surgery may be helpful if there is craniosynostosis
  • 86. SKIN DISORDERS Incidence: Skin infection and irritation is very common in CP Treatment / Management Options  Symptomatic treatment  Personal hygiene  Skin care, etc
  • 87. BEHAVIORAL ISSUES Incidence: 1 in 4 children with CP have behavioral disorders. Treatment / Management Options  Behavioral therapy-ABA, BMT, CBT, etc  Medications
  • 88. CONGENITAL HEART DISORDER Incidence: Very rare. Commonly PDA Treatment / Management Options  Symptomatic medical and surgical treatments
  • 89. HORMONAL IMBALANCE Incidence: Poor growth or delayed puberty due to multiple pituitary hormone deficiency hormone deficiency (MPHD) Treatment / Management Options  Hormonal Therapy
  • 90. SLEEP DISTURBANCE Incidence: Difficulty in initiating and maintaining sleep, sleep wake transition, sleep breathing disorders, sleep bruxism, excessive day time sleeping, nightmares and sleep talking , etc Treatment / Management Options  Modification environment like light system, temperature and bedding used for the child  Maintaining sleep diary and diet modification  Medications, etc
  • 91. PAIN Incidence: Pain is very common with children with CP. Adults are more prone to pain due to poor postures and joint immobility Treatment / Management Options  Medications- Antispasmodic medications, Anticholinergic drugs  Botox Injection  Muscle massage, acupuncture, ice packs and heat therapy, hydrotherapy, and cognitive behavioral therapy.
  • 92. ISSUES WITH SECONDARY SEXUAL CHARACTERS Incidence: Very common with severely affected adults Treatment / Management Options  Sex education  Behavior therapy  Medications, etc
  • 93. PSYCHOLOGICAL ISSUES Incidence: Mental health and psychological problems, in the forms of depression, anxiety and conduct disorders, generally triggered by pain, discomfort or sleep disturbances. Treatment / Management Options  Psychotherapy  Medications
  • 94. www.worldcpday ASSOCIATED IMPAIRMENTS Children with CP may also have a range of physical and cognitive impairments 1 in 4 is unable to walk 1 in 4 is unable to talk 3 in 4 experience pain 1 in 4 has epilepsy 1 in 4 has a behaviour problem 1 in 2 has an intellectual disability 1 in 10 has a severe vision impairment 1 in 4 has bladder control problems 1 in 5 has a sleep disorder 1 in 5 has saliva control problems
  • 95. Team Members Family Medical Management Team Habilitation Service Providers Life Cycle Approach Birth to one year One year to 3 years Three years to 6 years Six years to 13 years Thirteen years to 18 years Above 18 years MANAGEMENT AND TREATMENT TEAM
  • 96. Screening Team Neonatologist Child Specialist Developmental Pediatrician Medical Diagnosis Making and Medical Management Team  Pediatric Neurologist  Pediatric orthopedic Surgeon  Pediatric Eye specialist  Pediatric ENT Specialist  Pediatric Cardiologist  Pediatric Gastroenterologist  MULTIDISCIPLINARY MANAGEMENT TEAM
  • 97. Pediatric Nephrologists Genetic Specialist Pediatric Dietitian-Nutritionist Pediatric Endocrinologist Pediatric Immunologist Pediatric Physiatrist Pediatric Plastic Surgeon Pediatric Pulmonologist MULTIDISCIPLINARY MANAGEMENT TEAM
  • 98. Habilitation Team  Neonatotherapist  Early Intervention Specialist  Developmental Therapy Specialist  Pediatric physiotherapist  Pediatric Occupational Therapist  Special Educator  Speech and language Pathologist  Psychologist / Behavior Therapist MULTIDISCIPLINARY MANAGEMENT TEAM
  • 99. Habilitation Team  Pediatric Optometrist  Pediatric Hearing Aids Technician  Postural Aids Specialist  Orthotician  Mobility Aids Specialist  Adaptive and assistive Aids Technician  Apps and Games designers MULTIDISCIPLINARY MANAGEMENT TEAM
  • 100. MANAGEMENT APPROACHES  Multidisciplinary  Interdisciplinary  Trans disciplinary
  • 101. Thorough and accurate assessment of children with cerebral palsy by a multidisciplinary team is essential to ensure chosen interventions meet the child’s needs. Most assessments measure a particular aspect of the child’s life. It can be Physical, Communication, Social-emotional or cognition The World Health Organization's International Classification of Functioning, Disability and Health (ICF) has been used to guide assessment. The ICF domains include body function and structure, participation, activity and personal and environmental factors. ASSESSMENTS OF CEREBRAL PALSY
  • 103. Standardized assessments and outcome measures may be relevant to one or more domains of the ICF. A significant number of assessments are available and it is often necessary to use a combination of these. ASSESSMENTS OF CEREBRAL PALSY
  • 104. Selection of assessment tools should be based on purpose, psychometrics and those most relevant to the area/s of difficulty. The functional ability classification scales should be used to guide assessment and intervention with all children diagnosed with cerebral palsy to facilitate communication and goal setting. ASSESSMENTS OF CEREBRAL PALSY
  • 105.  Communication  ADL  Mobility  Ambulation ICF MODEL OF INTERVENTION FOR HABILITATION
  • 106. Further assessment should occur to ensure realistic goal setting, provide a baseline for intervention and for evaluation of intervention programs. ASSESSMENT GUIDELINES
  • 107.  History and observation  Assessment of reflexes and reactions  Assessment of functional level and motor development  Assessment of muscle tone  Assessment of muscle strength ASSESSMENT PROTOCOLS
  • 108.  Assessment of musculoskeletal system deformities  Assessment of physical fitness  Assessment of gait  Assessment of balance  Assessment of trunk impairment ASSESSMENT PROTOCOLS
  • 109.  Assessment of health-related quality of life  Assessment of activities of daily life  Assessments of upper extremity  Cognition / Psychometric Assessments  Speech and Communication Assessments ASSESSMENT PROTOCOLS
  • 110. Detailed information should be received from the family or caretakers in all issues related to the children including  Family history  Prenatal, natal and postnatal period  Chronologic and corrected age  Associated problems  Developmental story  Adaptive equipment used  Intervention approaches applied  Medication taken  Family Profile HISTORY AND OBSERVATION
  • 111.  Observational analysis is crucial to determine children’s functional skills, spontaneous motions and motion strategies, and the underlying fundamental problems. Thus, it can be decided in which field detailed assessment needs to be carried out.  During observational analysis, children must be in a setting they can be with their family, and they can feel comfortable and safe. HISTORY AND OBSERVATION
  • 112.  There should be various toys and materials in the setting to reveal the children’s capacity and to draw their attention.  The assessment room should not be crowded and noisy . Video recordings during observation are rather beneficial as well. HISTORY AND OBSERVATION
  • 113.  Observation of reflexes is important to illustrate the severity of the influence in the nervous system, and observation of balance and protective reactions is important to support motor developmental process.  When these assessments are carried out, the corrected age of the children should be considered. It is known that primitive reflexes continue insistently or disappear later than normal or never occur in children with CP. ASSESSMENT OF REFLEXES AND REACTIONS
  • 114.  It can be observed that symmetric tonic and asymmetric tonic neck reflexes still continue in adolescent stage in a case diagnosed with dyskinetic-type CP.  Insistence of these reflexes can complicate the therapy. It may be necessary to make various adaptations in the treatment program when the primitive reflexes continue in advanced ages.  At the same time, the assessment of protective reactions is important for determining a treatment program ASSESSMENT OF REFLEXES AND REACTIONS
  • 115.  It is crucial to assess motor development, functional skills, and activity limitations for determining the current state of the children, and there are frequently used test batteries for this purpose.  Gross Motor Function Measurement (GMFM) is a standardized measurement instrument frequently used to measure the change in gross motor function. ASSESSMENT OF FUNCTIONAL LEVEL AND MOTOR DEVELOPMENT
  • 116. Gross Motor Function Classification System (GMFCS) The Gross Motor Function Classification System (GMFCS) is a five level classification that describes the gross motor function of children with cerebral palsy on the basis of their self-initiated movement with particular emphasis on sitting, walking, and wheeled mobility. FUNCTIONAL MOTOR ABILITY
  • 117. GMFCS
  • 118. (GMFCS) Levels Level-I: Walk independently Level-II: Walk independently with limitations Level-III: Use assistive devices such as elbow crutches or walking frames Level-IV: Require a wheelchair but may have some form of independent mobility such as a powered wheelchair or may assist with transfers Level-V: Require a wheelchair and are fully dependent in their mobility GROSS MOTOR FUNCTION CLASSIFICATION SYSTEM
  • 119. The Functional Mobility Scale (FMS) has been constructed to classify functional mobility in children 4 to 18 years, taking into account a range of assistive devices a child might use over three distances: five meters (in and around the home), 50 meters (in and around (School /preschool) and 500 meters (in the community). The FMS is sensitive to detect change after Specialized interventions. FUNCTIONAL MOBILITY SCALE (FMS)
  • 120. FMS
  • 122. Level-I: Handles objects easily Level-II: Handles most objects but with reduced speed and/or quality Level-III: Has some difficulty and needs help to modify or prepare activities Level-IV: Handles a limited selection of easily managed objects in adapted settings Level-V: Does not handle objects UPPER LIMB CLASSIFICATIONS MANUAL ABILITY CLASSIFICATION SYSTEM (MACS)
  • 123. MACS
  • 124.  Communication is simply the act of transferring information from one place, person or group to another.  Every communication involves (at least) one sender, a message and a recipient. This may sound simple, but communication is actually a very complex subject. COMMUNICATIONS
  • 125.  Speech is human vocal communication using language. Each language uses phonetic combinations of vowel and consonants sounds that form the sounds of its words  Speech disorders affect a person's ability to produce sounds that create words. ...  Types of speech disorder include misarticulation, apraxia, and dysarthria. There are many possible causes of speech disorders, including muscles weakness, brain injuries, degenerative diseases, autism, and hearing loss. SPEECH
  • 127. Level-I: Effective sender and/or receiver with familiar and unfamiliar partners Level-II: Effective but slower paced sender and/or receiver with familiar and unfamiliar partners Level-III: Effective sender and/or receiver with familiar Partners Level-IV: Inconsistent sender and/or receiver with familiar partners Level-V: Seldom effective sender and/or receiver even with familiar partners COMMUNICATION CLASSIFICATION COMMUNICATION FUNCTION CLASSIFICATION SYSTEM- CFCS
  • 128. Level-I An effective communicator in most situations Can independently communicate a wide variety of messages/topics to familiar and unfamiliar people in most environments FUNCTIONAL COMMUNICATION CLASSIFICATION SYSTEM (FCCS)
  • 129. Level-II An effective communicator in most situations, but does need some help Can communicate a variety of messages/ topics to familiar people but may experience some difficulties with unfamiliar people/topics and environments and may need prompts, such as, prompt questions, repetitions (to make themselves understood) and loudness An AAC user who requires assistance with set up, and/or programming; and whose listener may need some assistance with orientation/ interpretation of AAC strategies FUNCTIONAL COMMUNICATION CLASSIFICATION SYSTEM (FCCS)
  • 130. Level-III An effective communicator in some situations. Can communicate a small range of messages/ topics to most familiar people Effective communicator with familiar people and activities and in familiar settings about their needs and wants, and things that are happening but require assistance with unfamiliar people/topics and environments Relies on a familiar communication partner to interpret AAC or speech attempts, and to prepare, set up and support communication FUNCTIONAL COMMUNICATION CLASSIFICATION SYSTEM (FCCS)
  • 131. Level-IV Assistance is required in most situations, especially with unfamiliar people and environments. Communicates daily/routine needs and wants with familiar people Can initiate and attract attention but needs a familiar person who is familiar with their routine, recent /significant experiences and likes and dislikes, and to interpret their communication Responds to familiar voices, sounds and routines using body movement, facial expression and vocalisation FUNCTIONAL COMMUNICATION CLASSIFICATION SYSTEM (FCCS)
  • 132. Level-V Communicates unintentionally with others, using movement and behavior Daily/routine needs and wants are interpreted by familiar people from observation of the individual’s emotional state, body movement and behavior Needs full assistance from a familiar person to observe, interpret movements and behaviors, anticipate, and problem solve based on their experience, training and observation FUNCTIONAL COMMUNICATION CLASSIFICATION SYSTEM (FCCS)
  • 133.  Academic Performance  Adaptive Delay or Impairment  Capacity to Learn/Learning Impairments  Communication Level  Emotional Status  Health  Intelligence  Motor Abilities  Social Ability  Vision and Hearing SPECIAL EDUCATION ASSESSMENT
  • 134.  The assessments help to allocate the following service and supports to accommodate, modify or adapt a child’s needs:  Program Modifications  Related Services  Special Accommodations  Specially Designed Instruction  Supplementary Aids  Adapted Equipment  Adapted Materials  Assistive Technology  Augmentative Communication Devices SPECIAL EDUCATION ASSESSMENT
  • 135.  The assessment of cognitive functioning is often challenging in students with motor impairment because the majority of tests require verbal and motor responses  A careful consideration of the level of motor, communication, and/or visual or visual perception impairment in students with CP and motor impairments can inform assessors on the choice of cognitive assessment battery to use  The use of Assistive Technology, together with alternative response modes (e.g., partner assisted scanning) is encouraged to enable access to standardized cognitive assessment. SPECIAL EDUCATION ASSESSMENT
  • 136. For students with significant motor impairments for whom standardized cognitive assessments are not appropriate, the use of developmental scales, which assess progress along a continuum rather than providing comparative performance data with peers, may be an appropriate alternative SPECIAL EDUCATION ASSESSMENT
  • 137.  For students with severe motor impairments, it is important to conduct a functional skills assessment.  A functional skills assessment targets the skills needed in a given environment and activity, and includes measures of social and adaptive functioning with a focus on basic life skills.  It focuses on practical independent living skills. It also considers students’ functioning in their environments, and examines the process of learning and performance. SPECIAL EDUCATION ASSESSMENT
  • 138.  Based on the results of the assessment, intervention techniques are implemented and evaluated on a regular basis  The following test accommodations are helpful in supporting students with significant motor impairments so as to obtain the best responses during the assessment session  Body positioning is of specific relevance to students with significant motor impairments. Students should be positioned in a way that facilitates the support of the trunk and independent use of the arms and hands. This can be done via the use of an Adaptive Seating System.  Appropriate positioning can reduce pain, permit better fine motor function, facilitate attention, reduce fatigue, and promote improved social interaction, thereby optimizing performance. SPECIAL EDUCATION ASSESSMENT
  • 139.  Students should be allowed to use assistive technology such as Augmentative and Alternative Communication (AAC) devices to enhance their functional communication.  Information on the student’s communication style and modality should be determined before assessment. It may be helpful to involve the family, caregivers and therapists who work closely with the student to assist in understanding the student’s responses. SPECIAL EDUCATION ASSESSMENT
  • 141. TREATMENT AND MANAGEMENT Treatment Medicines / Drugs Antispastic Anti-Epileptic Anti-drooling GERD Constipation Chemodenervation Phenol Botox
  • 142. TREATMENT AND MANAGEMENT Orthopedic Surgery STR SEMLLARS OSSCS Ilizarov Percutaneous
  • 143. TREATMENT AND MANAGEMENT Use of Implants Use of Intrathecal Baclofen Pump Use of Deep Brain Stimulation Use of VP Shunt Use of Neurosurgery Selective Dorsal Rhizotomy Gamma Knife Surgery
  • 144. TREATMENT AND MANAGEMENT Use of Regenerative Medicines Hyperbaric Oxygen Therapy Stem Cell Therapy
  • 145. TREATMENT AND MANAGEMENT Complementary and Alternative Medicines Homeopathy Unani Ayurveda Herbal Acupuncture Chinese Medicines Acupressure Magneto therapy Nutritional Therapy
  • 146. TREATMENT AND MANAGEMENT Management Habilitation and Rehabilitation Services 1. Infant Stimulation Therapy 2. Early Intervention 3. Play Therapy 4. Developmental Therapy 5. Physiotherapy 6. Occupational Therapy 7. Speech Therapy 8. Cognitive Therapy / Special Education 9. Behavioral Therapy 10. Assistive Technology
  • 148. THANK YOU ALL For More Information, Please contact me at Institute for Child Development C-27, Malviya Nagar New Delhi-110017 Landline Number: 011-41012124 Mobile / Whatsapp Number: 7838809241 Mail ID: helpicd@gmail.com Website: www.icddelhi.org