Cerebral Palsy

Definition

Cerebral Palsy (CP) is a non-progressive brain injury causing neuromuscular imbalance and upper motor neuron disease, typically presenting before the age of 2.


Risk Factors

  • Prematurity
  • Anoxic birth trauma
  • TORCH infections (toxoplasmosis, syphilis, rubella, cytomegalovirus, herpes)
  • Other third-trimester disturbances or intrauterine issues

Classification

Type Characteristics
Spastic Muscle imbalance and contractures, eventually causing bone deformity and arthrosis. Most common and treatable surgically.
Athetoid Dystonia and involuntary movements.
Ataxic Predominantly cerebellar symptoms.
Geography Characteristics
Quadriplegia All limbs involved, low IQ, severe spasticity, unable to walk.
Diplegia Primarily lower limbs, possible normal intelligence, most able to walk.
Hemiparesis Unilateral involvement, most eventually able to walk.

GMFCS - Gross Motor Function Classification System

Level Functional Description
GMFCS 1 Walks, jumps, runs, climbs; minor balance/speed issues.
GMFCS 2 Walks with stair rail support; difficulty on uneven surfaces.
GMFCS 3 Walks with aid; self-propels wheelchair.
GMFCS 4 Occasional frame walking; primarily wheelchair-dependent.
GMFCS 5 Cannot support head independently; requires wheelchair assistance.

Future Functional Estimation

Poor prognostic indicators include: - Retention of two or more primitive reflexes at 1 year (e.g., Moro and Parachute reflexes). - Inability to sit by 5 years or walk by 8 years.


Treatment Principles

  • Multidisciplinary Approach: Includes PT and OT.
  • Surgery: Generally deferred until after age 3, aiming to restore function and relieve pain.
  • Treatment Ladder:
    • MDT: Physio, OT for ADL support, speech therapy.
    • Splinting/Serial Casting and Bracing.
    • Medications:
      • Baclofen: GABA receptor agonist for muscle relaxation.
      • Botulinum Toxin (Botox): Temporary muscle relaxation.
Surgery Type Description
Dorsal Rhizotomy Cutting of dorsal rootlets (L1-S1) to reduce spasticity.
Soft Tissue Releases Includes tendon transfers, osteotomy, and fusion for structural corrections.

Treatment of Commonly Affected Areas

Spine

  • Deformity: Primarily scoliosis, sometimes kyphosis.
  • Management: Posterior and long fusion including pelvis, anterior fusion if needed.

Hips

  • Hip Subluxation/Dislocation: Common in non-ambulatory, GMFCS level 5 children.
  • Management: Includes adductor tenotomy, iliopsoas release, VDRO, or Dega osteotomy based on age and migration percentage.

Feet

  • Planovalgus/Equinovalgus Foot: Common in spastic diplegia, treated with calcaneal lengthening osteotomy and peroneus brevis lengthening.
  • Equinovarus Foot: Common in spastic hemiparesis, managed with SPLAT transfer, TA/TP transfer, and Achilles lengthening if needed.

Knee

  • Crouch Gait: Often due to hamstring contractures, managed through gait analysis, bracing, and hamstring release if necessary.

Upper Limb

  • Shoulder Adduction/Internal Rotation: Often requires Botox or release if affecting ADLs.
  • Hand and Wrist Deformities: Managed with OT, physio, tendon transfers, or fusion where needed.

Prognostic Indicators and Surgical Outcomes

Outcomes depend on flexibility, patient aims, pain, and severity of joint or skeletal arthrosis. Non-surgical management includes splints and orthoses, while surgical interventions aim to correct structural deformities to maximize function and comfort.

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