Children’s Orthopaedics - Complex Needs Flashcards

1
Q

What is the criteria for an under 19 to be defined as having complex exceptional needs (CEN)?

A

•Severe impairment in at least 4 categories + enteral/ parenteral feeding
OR
•Severe impairment in at least 2 categories + ventilation/CPAP
AND
•Impairments are sustained for more than 6 months and ongoing

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2
Q

What are the categories of impairment?

A
  • Learning and mental functions
  • Communication
  • Motor skills
  • Self care
  • Hearing
  • Vision
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3
Q

Give some examples of complex need disorders with orthopaedic involvement

A
  • Cerebral Palsy
  • Spina Bifida
  • Muscular Dystrophy
  • Arthrogryposis
  • Neurofibromatosis
  • Syndromes – Downs, Turners etc.
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4
Q

What is cerebral palsy?

A

A permanent and non-progressive motor disorder due to brain damage before birth or during the first 2 years of life

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5
Q

What is the incidence of CP?

A

2/1000

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6
Q

What are the prenatal causes of CP?

A
  • Placental insufficiency
  • Toxaemia
  • Smoking
  • Alcohol
  • Drugs
  • Infection e.g. toxoplasmosis, rubella, CMS and HSV II (TORCH)
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7
Q

What are the perinatal causes of CP?

A
  • Prematurity - most common
  • Anoxic injuries
  • Infections
  • Kernicterus (caused by high levels of bilirubin in blood)
  • Haemolytic disease of new born
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8
Q

What are the postnatal causes of CP?

A
  • Infection - CMV, rubella

* Head trauma

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9
Q

What are the physiological classifications of CP?

A
  • Spastic - pyramidal system, motor cortex
  • Athetoid - extrapyramidal system, basal ganglia
  • Ataxia - cerebellum and brainstem
  • Mixed - combination of spasticity and athetosis
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10
Q

What are the anatomical classifications of CP?

A
  • Monoplegia - one limb involved
  • Hemiplegia - one side of the body
  • Diplegia - lower limbs
  • Quadriplegia - total body involvement
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11
Q

What is GMFCS for CP?

A

Gross Motor Function Classification System fo CP

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12
Q

What are the levels described by GMFCS?

A

•LEVEL I - Walks without Limitations
•LEVEL II - Walks with Limitations
•LEVEL III - Walks Using a Hand-Held Mobility Device
•LEVEL IV - Self-Mobility with Limitations (May Use Powered Mobility)
LEVEL V - Transported in a Manual Wheelchair

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13
Q

What are the disabilities experienced by CP sufferers?

A
  • Spasticity
  • Lack of voluntary limb control
  • Weakness
  • Poor co-ordination
  • Impaired senses (Hearing, Vision, Taste, Touch etc)
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14
Q

What can happen as a result of CP?

A
  1. Dynamic contractures
  2. Fixed muscle contractures
  3. Joint subluxation/dislocation
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15
Q

What are dynamic contractures?

A
  • Increased muscle tone and hyper-reflexia
  • No fixed deformity of joints
  • Deformity can be overcome
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16
Q

What are fixed muscle contractures?

A
  • Persistent spasticity and contracture
  • Shortened muscle tendon units
  • Deformity cannot be overcome
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17
Q

What is joint subluxation/dislocation?

A

•Secondary bone changes/ joint degeneration

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18
Q

What are the orthopaedic priorities in CP?

A
  • Maintain sitting balance
  • Improve/maintain standing posture
  • Optimise gait
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19
Q

How is gait analysed in CP?

A
  • Observation
  • Video
  • 3D instrumented analysis
  • ±EMG, energy expenditure
20
Q

What is measured in a gait lab?

A
  • Joint movement
  • Force distribution through feet
  • Timing of cycle
21
Q

How are hips affected by CP?

A
  • Hips are normal at birth
  • Hip displacement in 1/3 by maturity
  • Likelihood of displacement proportional to GMFCS
  • Dislocated hips are often painful
  • Dislocated hips upset sitting posture
  • Early surgical intervention leads to better long term outcome
22
Q

What are the non-operative interventions used to treat posture in CP?

A
  • Physiotherapy

* Seating

23
Q

What are the non-operative interventions used to treat spasticity in CP?

A
  • Generalised - baclofen oral (anti-spasmodic), diazepam

* Localised - baclofen (intra-thecae pump), botox

24
Q

How is deformity in CP managed surgically?

A

•Soft tissue release

  • adductors
  • hamstrings

•Bony realignment

  • varus derotaion osteotomy (prevents hip dislocation)
  • pelvic osteotomy
25
What are the pros of surgical intervention?
* Reduced risk dislocation * Reduced risk pain * Better seating
26
What are the cons of surgical intervention?
* Not all would have gone on to dislocate | * BIG surgery
27
What is club foot also known as?
Talipes equinovarus
28
What is the epidemiology of talipes equinovarus?
* Most common congenital deformity * 1 to 2 in 1000 live births (variable) * 3 Male : 1 Female * 50% bilateral * Risk for 2nd child 1 in 35
29
What is the aetiology of talipes equinovarus?
``` •Pressure theories -Oligohydramnios -Abnormal fetal position -Unstretched uterus •Placental insufficiency •Constriction bands •Toxin •Temperature •Infective pathogen (enterovirus) •Drugs •EM radiation •Chromosomal abnormality •Sex-linked •Single dominant •Single recessive •Polygenic MULTIFACTORIAL ```
30
How well can talipes equinovarus be diagnosed prenatally?
* 60% of cases may be identified by ultra-sound * 50% may have defects in other systems * No relationship to ‘stiffness’ of feet
31
How is talipes equinovarus traditionally treated?
``` •Strapping (positional talipes only) •Serial casting •Dennis Browne Boots •Surgery -Postero-medial release -Ilizarov frame ```
32
What are the anatomical terms used in club foot?
``` •Cavus •Adductus (midfoot) •Varus (hindfoot) •Equinus (hindfoot) CAVE ```
33
How is equines corrected?
•Percutaneous tenotomy of Achilles tendon - 90% will need this
34
What are the outcomes of club foot?
* 95% of club feet successfully treated * 45 year results show that feet are mobile, pain free and plantigrade * Results reproduced at major centres around the world * Level 1 RCT evidence * Majority of recurrences due to failure of compliance with splints
35
What is scoliosis?
Any deviation in coronal plane
36
What degree of deviation is of clinical significance?
>10 degrees
37
What are the 2 broad classes of scoliosis?
* Non-structural = due to extrinsic cause – a leg length discrepancy, a hip problem etc. Resolves when causal factor is addressed. * Structural scoliosis = abnormal rotation of the vertebrae and is an intrinsic spinal problem. It has a propensity to progress.
38
How is scoliosis categorised by aetiology?
•Congenital (vertebral formation abnormalities) •Idiopathic •Neuromuscular •Others: -post traumatic, degenerative, infective, syndromic etc.
39
How is scoliosis categorised by age at presentation?
* Infantile (<3y) * Juvenile (3-10y) * Adolescent (>10y)
40
How is scoliosis categorised by region of spine primarily affected?
* Thoracic * Lumbar * Thoracolumbar * Double
41
What are the clinical signs of scoliosis?
* Inspect posterior torso - structural scoliosis will look worse when bent forward into flexion * Abnormal neurology or pain should be noted
42
What investigations are used for scoliosis?
•AP Erect Whole spine +/- Lateral (Tilting films to assess flexibility) •MRI *Cord abnormalities - Tethering, syrinx, diastematomyelia *Vertebral anomalies - Failures of formation and segmentation *Tumours
43
Why is early diagnosis important in scoliosis?
* Cardiorespiratory compromise * Pain from rib/pelvic abutment * Seating issues * Surgical challenge * Neuromuscluar causes are at high risk of progression
44
How is scoliosis managed non-surgically?
``` BRACING •Needs to be worn 23/24 hours to work •Delays progression of curve •Custom made •Usually used to delay surgery while spine growing ```
45
How is scoliosis managed surgically?
``` •Complex and extensive •Surgical approaches: -Anterior -Posterior -Both •Wake up test (Traditional) •Intra-operative spinal cord monitoring ```
46
What are the surgical complications for scoliosis?
``` •Nerve root damage •Cord traction injury •Vascular injury •Degenerative changes later •Problems of growth: -Growing rods -Changing rods -Crankshaft phenomenon ```