Cerebral palsy Flashcards

1
Q

Risk factors for cerebral palsy

A
  • CP = abnormality of movement and posture, causing activity limitation attributed to non-progressive disturbances that occured in the developing fetal or infant brain.
  • 2 in 1000 births
  • brain injuries occuring up to 2 years of age
  • after this = acquired brain injury
  • Antenatal (80%)
    • risk factors: IUGR, prematurity, twin births, African ethnicity, maternal age > 35 years
    • ​vascular occlusion
    • cortical migration disorders
    • structural maldevelopment of the brain
    • genetic deletions
    • genetic syndromes
    • congenital infection
  • Perinatal
    • hypoxic-ischaemic injury (10%)
      • preterm infants at risk of PVL and IVH
  • Postnatal (10%)
    • meningitis
    • encephalitis
    • encephalopathy
    • head trauma- non-accidental/ accidental injury
    • symptomatic hypoglycaemia
    • hydrocephalus
    • hyperbilirubinaemia
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2
Q

Distinguish the different types of CP

A
  • spastic (90%)
    • damage to UMN
    • hypertonia
    • hyperreflexia
      • hemiplegia
        • upper or lower leg and arm (arm more affected)
        • tip toe walking
        • present age 4-12 m
        • if stroke cause- hemianopia on same side
      • quadriplegia
        • all 4 limb involvement
        • poor head control
        • seizures, microcephaly, severe ID
        • history of HIE
      • diplegia
        • all 4 limb involvement but legs worse
        • abnormal
        • pre-maturity and PV brain damage
  • dyskinetic (6%)
    • ​involuntary, uncontrolled movements (chorea, athetosis, dystonia)
    • poor trunk control
    • floppy
    • delayed motor deviation
    • abnormal movements owards 12m
    • extrapyramidal lesion (BG)
    • kernicterus, HIE
  • ataxic (4%)
    • ​hypotonic CP
    • if acquired cerebellum injury- ipsilateral side
    • early
      • trunk and limb hypotonia
      • poor balance
      • delayed motor developments
    • late
      • inco-ordinate movements
      • intention tremor
      • ataxic gate
  • mixed pattern can occur
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3
Q

Clinical presentation of CP

A
  • abnormal limb and/ or trunk posture and tone in infancy with delayed motor milestones
  • slowing of head growth
  • feeding difficulties
  • oromotor inco-ordination
  • slow feeding
  • gagging
  • vomiting
  • abnormal gait
  • risk of visual/ hearing/ learning difficulties, speech, epilepsy, nutrition and psychiatric impairments
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4
Q

Treatment of CP

A
  • MDT: paediatrician, physiotherapist, OT, SALT, clinical psychologist, specialist health visitor, socia worker, parent support groups
  • Posture and movement
    • physio
    • strengthening exercises
    • orthotics
    • botox
    • surgery
  • Communication
    • SALT- feeding, laguage development, AAC aids- Makaton sign language, Bliss symbol boards, voice synthesisers
  • Medical
    • seizure control (anti-epileptics)
    • constipation (laxtives)
    • malnutrition
    • spasm control (baclofen pumps)
  • Ortho/ neurosurgical
    • sclolisis corrections
    • tendon lengthening
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