Cerebral Palsy Flashcards
Definition: cerebral palsy
- non-progressive central motor impairment syndrome due to insult to or anomaly of the immature CNS
Aetiology of cerebral palsy
• Prenatal events (75% of all cases) ○ Malformations ○ Vascular ○ Infective (TORCH infections, esp T1 and T2) ○ Genetic ○ Metabolic (iodine deficiency) ○ Toxic
• Perinatal events (15%)
○ Problems during labour and delivery (e.g. obstructed labour, APH, cord prolapse)
○ Neonatal problems (e.g. hypoglycaemia, untreated jaundice)
○ Prematurity (low BW risk factor)
• Postnatal causes (10%) ○ Infectionse.g. encephalopathy ○ Injuries ○ CVA ○ ABI < 2 years
Classify cerebral palsy by motor disorder
• Spastic cerebral palsy (70%)
○ Increased muscle tone, reflexes and clonus, with characteristic clasp-knife quality
○ Underlying weakness
○ Pyramidal tract
• Dyskinetic/athetoid cerebral palsy
○ Dystonia: sustained muscle contractions that frequently cause twisting or repetitive movements
○ Atheosis: slow, writhing movememnts involving distal parts of limbs
○ Chorea: rapid, jerky, involuntary movements
○ Basal ganglia
• Ataxic cerebral palsy ○ Fine tremor ○ Poor balance ○ Poor coordination ○ Cerebellum
Classify cerebral palsy by topographical distribution
• Diplegia
○ Predominant problem in lower limbs
○ Most children have normal intelligence
• Spastic hemiplegia
○ Normal intelligence
○ Epilepsy in 50-70%
○ Visual deficits
• Spastic quadriplegia ○ Intellectual disability ○ Epilepsy ○ Visual impairment ○ Poor trunk control and oromotor difficulties
Classify cerebral palsy by motor disorder severity
Gross Motor Function Classification System (GMFCS):
- I: speed, balance, co-ordination impaired, gross motor ok
- II: limitations on uneven surfaces, inclines, crowds, need railing on stairs
- III: assistive mobility device walking, wheelchair if long distances
- IV: walker for short distances, wheelchair elsewhere
- V: wheelchair for all settings
Clinical features of cerebral palsy
- Developmental issues
- Delayed motor milestones (especially in learning to sit, stand and walk)
- in utero, antenatal and post-natal Hx: Premature?
- Exposure Hx
- Genetic Hx - Motor disorder
• Development of asymmetrical movement patternse.g. chorea
• Abnormal muscle tone (esp. spasticity, hypotonia)
3. Consequences of motor disorder ○ Drooling ○ Incontinence ○ Undescended testes ○ Orthopaedic problemse.g. dislocation ○ Spasticity ○ Deformity, contracture
- Associated disabilities
○ Visual problems (strabismus, refractive errors, VF defects, cortical visual impairments) - 40%
○ Hearing deficits
○ Communication disorders
○ Epilepsy - 50%
○ Cognitive impairments (ID, learning problems, perceptual deficits) - Mx issues
• Management problems (e.g. feeding difficulties, behavioural abnormalities such as unexplained irritability)
Who might be part of the MDT for Mx of cerebral palsy?
- Medical input
- Physiotherapy
- OT
- Speech pathologists
- Orthotists
- Social work
- Psychologist
- Special education teachers
- Dentist