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
 PRESENTATION BY:
 SYLVIA E. SELASSIE, RD, LD
CEREBRAL PALSY

 Brief history
 Cerebral palsy overview
 Types of cerebral palsy
 Assessment and diagnosis
 Treatment regimen
 Definition of terms
 References
CONTENT

 In 1860s, referred to as ‘cerebral Paralysis’ or ‘Little’s
Disease’
 After a first medical descriptions by an English
surgeon- William John Little(1810-1894)
BRIEF HISTORY

 “Cerebral”- Latin Cerebrum
 Affected part of the brain
 “Palsy”- Para-beyond
-lysis- loosening
 Lack of muscle control
CEREBRAL PALSY

 A motor function disorder
 Due to permanent, non-progressive brain lesion
 Present at birth or shortly thereafter(Mosby, 2006)
 Non-curable, life-long condition
 Damage doesn’t worsen
 May be congenital or acquired
CEREBRAL PALSY

 A heterogeneous group of movement disorders
 An umbrella term
 Not a single diagnosis

 Balance
 Posture
 Movements
CEREBRAL PALSY
EFFECTS

 An insult or injury to the brain
 Fixed, static lesion(s)
 In single or multiple areas of the motor centers of the
brain
 Early in CNS development
ETIOLOGY

 Development Malformations
 The brain fails to develop correctly
 Neurological damage
 Can occur before, during or after delivery
 Rh incompatibility, illness, severe lack of oxygen
ETIOLOGY

 Severe deprivation of oxygen or blood flow to the
brain
 hypoxic-ischemic encephalopathy or intrapartal
asphyxia
MAJOR NOTED CAUSE

 Prematurity
 Blood-type incompatibility
 Placental insufficiency;
 Maternal infection that includes German measles
 other viral diseases
 Neonatal jaundice
 Anoxia at birth
 Bacterial infections of the mother, fetus, or infant that
affect the central nervous system
Causative agents

 ACCORDING TO NEUROLOGIC DEFICITS
 Based on: extent of brain damage and area of the brain
damage
 Each type involves the way a person moves
TYPES OF CEREBRAL
PALSY

1. Pyramidal
-originates from the motor areas of the cerebral cortex
2. Extrapyramidal
- basal ganglia and cerebellum
3. Mixed
MAIN TYPES

 MAIN TYPES:
 PYRAMIDAL : 1. Spastic CP
 Extrapyramidal: 2. Athethoid CP
3. Ataxic CP
 Mixed : 4. Spastic & Athethoid CP
ACCORDING TO TYPE
OF MOVEMENTS

 -Plegia/paresis-paralyzed or weak
 Paraplegia
 Diplegia
 Hemiplegia
 Quadriplegia
 Monoplegia- one limb(extremely rare)
 Triplegia- three limbs(extremely rare)
ACCORDING TO AFFECTED LIMBS:

 MILD- 20% of cases
 MODERATE- 50%; require self help for assisting their
impaired ambulation capacity
 SEVERE- 30%; total incapacitation and bedridden
ACCORDING TO
DEGREE OF SEVERITY

 Hypotonia
 Hypertonia
 Dystonia
ACCORDING TO MUSCLE TONE
ABNORMALITIES

SYMPTOMS



 Poor ability to concentrate
 Unusual tenseness
 Irritability
BEHAVIOURAL
SYMPTOMS

PROBLEMS OF
CEREBRAL PALSY

 Physical evaluation
 MRI, CT Scan
 Laboratory and radiologic work up
 Assessment tools: growth curve monitoring, MUAC,
height and length, Peabody Development Motor
Skills
DIAGNOSIS


 Interview
 A. history taking: involves all predisposition factors
such as
 Risk factors
 Psychosocial factors
 Family adaptation
 B. child’s health history: often admitted to hospitals
for corrective surgeries and other complications.
Subjective

 Respiratory status
 Motor function
 Presence of fever
 Feeding and weight loss
 Any changes in physical state
 Medical regimen

Objective -Physical
Examination

 Crucial for children with Cerebral palsy
 Early identification, multidisciplinary care and
support
 Nonphysical: proper nutrition and personal care
Treatment

 Botox, Intrathecal, Baclofen
 Controls muscle spasms and seizures
 Glycopyrrolate- controls drooling
 Pamidronate- may help with osteoporosis
Pharmacologic
treatment

 To loosen joints
 Relieve muscle tightness
 Straightening of different twists or unusual
curvatures of leg muscles
 Improve the ability to sit, stand and walk.
Surgery

Note

 Physical aids: orthosis, braces and splints;
positioning devices; walkers, special scooters,
wheelchairs
 Special Education
 Rehabilitation services- speech and occupational
therapies
 Family services- professional

 Spastic CP: Increased muscle tone, persistent infant
reflexes, increased deep tendon reflexes in one of
three patterns: hemiplegia (arm and leg on one side
of the body), diplegia (involving the lower
extremities), and
 quadriplegia (all four extremities and may include
the trunk, head, and neck)
 Dyskinetic CP: Abnormalities in muscle tone that
affect the entire body; includes athetoid CP, which
includes uncontrolled and continuous involuntary
movements
Definition of terms

 Mixed CP: A condition in which both athetosis and
spasticity are present
 Ataxic CP: Abnormalities of voluntary movement
and balance such as unsteady gait
 Athetoid dyskinetic CP: Normal intelligence but
difficulty walking, sitting, speaking clearly
 Pyramidal: one of the carpal bone
 Athetosis: series of involuntary writhing movements
of the limbs

 Krause chapter 45
 Ida Sherri L. Cerebral palsy
 Capone G, et al: Down syndrome. In Ekvall SW,
Ekvall VK, editors: Pediatric nutrition in chronic disease
and developmental disorders, New York, 2005, Oxford
University Press
 Stevenson RD: Use of segmental measures to
estimate stature in children with cerebral palsy, Arch
Paediatr Adolesc Med 149:658,2005.
References

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Diet and disease-CEREBRAL PALSY

  • 1.
  • 2.   PRESENTATION BY:  SYLVIA E. SELASSIE, RD, LD CEREBRAL PALSY
  • 3.   Brief history  Cerebral palsy overview  Types of cerebral palsy  Assessment and diagnosis  Treatment regimen  Definition of terms  References CONTENT
  • 4.   In 1860s, referred to as ‘cerebral Paralysis’ or ‘Little’s Disease’  After a first medical descriptions by an English surgeon- William John Little(1810-1894) BRIEF HISTORY
  • 5.   “Cerebral”- Latin Cerebrum  Affected part of the brain  “Palsy”- Para-beyond -lysis- loosening  Lack of muscle control CEREBRAL PALSY
  • 6.   A motor function disorder  Due to permanent, non-progressive brain lesion  Present at birth or shortly thereafter(Mosby, 2006)  Non-curable, life-long condition  Damage doesn’t worsen  May be congenital or acquired CEREBRAL PALSY
  • 7.   A heterogeneous group of movement disorders  An umbrella term  Not a single diagnosis
  • 8.   Balance  Posture  Movements CEREBRAL PALSY EFFECTS
  • 9.   An insult or injury to the brain  Fixed, static lesion(s)  In single or multiple areas of the motor centers of the brain  Early in CNS development ETIOLOGY
  • 10.   Development Malformations  The brain fails to develop correctly  Neurological damage  Can occur before, during or after delivery  Rh incompatibility, illness, severe lack of oxygen ETIOLOGY
  • 11.   Severe deprivation of oxygen or blood flow to the brain  hypoxic-ischemic encephalopathy or intrapartal asphyxia MAJOR NOTED CAUSE
  • 12.   Prematurity  Blood-type incompatibility  Placental insufficiency;  Maternal infection that includes German measles  other viral diseases  Neonatal jaundice  Anoxia at birth  Bacterial infections of the mother, fetus, or infant that affect the central nervous system Causative agents
  • 13.   ACCORDING TO NEUROLOGIC DEFICITS  Based on: extent of brain damage and area of the brain damage  Each type involves the way a person moves TYPES OF CEREBRAL PALSY
  • 14.  1. Pyramidal -originates from the motor areas of the cerebral cortex 2. Extrapyramidal - basal ganglia and cerebellum 3. Mixed MAIN TYPES
  • 15.   MAIN TYPES:  PYRAMIDAL : 1. Spastic CP  Extrapyramidal: 2. Athethoid CP 3. Ataxic CP  Mixed : 4. Spastic & Athethoid CP ACCORDING TO TYPE OF MOVEMENTS
  • 16.   -Plegia/paresis-paralyzed or weak  Paraplegia  Diplegia  Hemiplegia  Quadriplegia  Monoplegia- one limb(extremely rare)  Triplegia- three limbs(extremely rare) ACCORDING TO AFFECTED LIMBS:
  • 17.   MILD- 20% of cases  MODERATE- 50%; require self help for assisting their impaired ambulation capacity  SEVERE- 30%; total incapacitation and bedridden ACCORDING TO DEGREE OF SEVERITY
  • 18.   Hypotonia  Hypertonia  Dystonia ACCORDING TO MUSCLE TONE ABNORMALITIES
  • 20.
  • 21.
  • 22.   Poor ability to concentrate  Unusual tenseness  Irritability BEHAVIOURAL SYMPTOMS
  • 24.   Physical evaluation  MRI, CT Scan  Laboratory and radiologic work up  Assessment tools: growth curve monitoring, MUAC, height and length, Peabody Development Motor Skills DIAGNOSIS
  • 25.
  • 26.   Interview  A. history taking: involves all predisposition factors such as  Risk factors  Psychosocial factors  Family adaptation  B. child’s health history: often admitted to hospitals for corrective surgeries and other complications. Subjective
  • 27.   Respiratory status  Motor function  Presence of fever  Feeding and weight loss  Any changes in physical state  Medical regimen
  • 29.   Crucial for children with Cerebral palsy  Early identification, multidisciplinary care and support  Nonphysical: proper nutrition and personal care Treatment
  • 30.   Botox, Intrathecal, Baclofen  Controls muscle spasms and seizures  Glycopyrrolate- controls drooling  Pamidronate- may help with osteoporosis Pharmacologic treatment
  • 31.   To loosen joints  Relieve muscle tightness  Straightening of different twists or unusual curvatures of leg muscles  Improve the ability to sit, stand and walk. Surgery
  • 33.   Physical aids: orthosis, braces and splints; positioning devices; walkers, special scooters, wheelchairs  Special Education  Rehabilitation services- speech and occupational therapies  Family services- professional
  • 34.   Spastic CP: Increased muscle tone, persistent infant reflexes, increased deep tendon reflexes in one of three patterns: hemiplegia (arm and leg on one side of the body), diplegia (involving the lower extremities), and  quadriplegia (all four extremities and may include the trunk, head, and neck)  Dyskinetic CP: Abnormalities in muscle tone that affect the entire body; includes athetoid CP, which includes uncontrolled and continuous involuntary movements Definition of terms
  • 35.   Mixed CP: A condition in which both athetosis and spasticity are present  Ataxic CP: Abnormalities of voluntary movement and balance such as unsteady gait  Athetoid dyskinetic CP: Normal intelligence but difficulty walking, sitting, speaking clearly  Pyramidal: one of the carpal bone  Athetosis: series of involuntary writhing movements of the limbs
  • 36.   Krause chapter 45  Ida Sherri L. Cerebral palsy  Capone G, et al: Down syndrome. In Ekvall SW, Ekvall VK, editors: Pediatric nutrition in chronic disease and developmental disorders, New York, 2005, Oxford University Press  Stevenson RD: Use of segmental measures to estimate stature in children with cerebral palsy, Arch Paediatr Adolesc Med 149:658,2005. References

Notas del editor

  1. Cerebral Palsy Cerebral palsy results from damage to the structures of the cerebral cortex, cerebellum, and spinal cord. It is characterized by atypical muscle tone and poor coordination among muscle groups which results in postural abnormalities and structural deformities.
  2. Unknown in many instances
  3. A moderate disability child has normal life expectancy and most can lead a relatively independent life