Cerebral Palsy - doc meg`s hideout

advertisement

CEREBRAL PALSY

Dr. Meg-angela Christi Amores

Cerebral Palsy (CP)

 diagnostic term used to describe a group of motor syndromes

 resulting from disorders of early brain development

 often associated with epilepsy and abnormalities of speech, vision, and intellect

 selective vulnerability of the brain's motor systems

Epidemiology and Etiology

 the most common and costly form of chronic motor disability that begins in childhood

 prevalence of 2/1000

80% of cases – antenatal factors causing abnormal brain development

<10% - had evidence of intrapartum asphyxia

High prevalence in low birth weight infants due to intracerebral hemorrhage

Etiology

 congenital anomalies external to the central nervous system

Intrauterine exposure to maternal infection (e.g., chorioamnionitis, inflammation of placental membranes, umbilical cord inflammation, foulsmelling amniotic fluid, maternal sepsis, temperature greater than 38°C during labor, and urinary tract infection)

Periventricular leukomalacia

Clinical manifestations - syndromes

Spastic hemiplegia

 arm is often more involved than the leg

 difficulty in hand manipulation is obvious by 1 yr old

Walking delayed until 18-24 mo

 growth arrest, particularly in the hand and thumbnail

1/3 have seizure disorder

25% have cognitive abnormalities including mental retardation

MRI : Focal cerebral infarction

Clinical manifestations - syndromes

Spastic diplegia

 bilateral spasticity of the legs greater than in the arms

 often noted when an affected infant begins to crawl

 tends to drag the legs behind as a rudder (commando crawl)

 scissoring posture of the lower extremities

Walking is significantly delayed

Excellent prognosis for normal cognition

Minimal seizures

MRI: periventricular leukomalacia

Clinical manifestations – syndromes

Spastic quadriplegia

Most severe form

 marked motor impairment of all extremities

 high association with mental retardation and seizures

 speech and visual abnormalities

MRI: severe PVL and multicystic cortical encephalomalacia

Clinical manifestations – syndromes

Athetoid CP

 also called choreoathetoid or extrapyramidal CP

 characteristically hypotonic with poor head control and marked head lag

Feeding may be difficult, and tongue thrust and drooling

Speech is typically affected

Diagnosis

 thorough history and physical examination should preclude a progressive disorder of the CNS

MRI scan of the brain is generally indicated to determine the location and extent of structural lesions

 tests of hearing and visual function

Treatment

 team of physicians from various specialties, as well as occupational and physical therapists, speech pathologists, social workers, educators, and developmental psychologists

 no proof that physical or occupational therapy prevents development of CP

 evidence shows that therapy optimizes the development of an abnormal child

Treatment

 spastic diplegia

 assistance of adaptive equipment, such as walkers, poles, and standing frames

Quadriplegia

 motorized wheelchairs, special feeding devices, modified typewriters, and customized seating arrangements

Treatment

Communication skills

Bliss symbols, talking typewriters, and specially adapted computers including artificial intelligence computers

Drugs for spasticity:

 dantrolene sodium, the benzodiazepines, and baclofen

Download