paeds - ortho Flashcards

1
Q

developmental dysplasia of hip DDH

A
  • Abnormal development of hip joint
  • Spectrum
  • Dysplasia, subluxation and possible dislocation (low & high)
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2
Q

developmental dysplasia of hip epidemiology

A
  • Most common orthopaedic disorder in neonates
  • Incidence of dislocation 1.4/1000 births
  • Clinical instability 2.3/100
  • Ultrasound abnormal 8/100
  • More common in females 6:1
  • Most common in left hip
  • Bilateral 20%
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3
Q

Causes of developmental dysplasia of hip

A

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  • First born
  • Unstretched uterus & tight abdominal muscles
  • Female
    Estrogens released by fetus
  • Footling breech
  • Family History
    One parent = 12%
  • Oligohydramnios
  • Neonatal hip instability
    20-60% spontaneously resolve
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4
Q

features hip dysplasia in neonate

A
  • Relaxed child
  • Ortolani’s sign = delicate ‘clunk’ of entry
  • Barlow’s sign = adduction ‘clunk’ of exit
  • Hip may remain reducible
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5
Q

features hip dysplasia in older child

A
  • Asymmetric groin folds
  • Limited abduction
  • Galeazzi sign
  • Klisic’s sign = GT - ASIS
  • Nelaton’s line = ischial tuberosity - ASIS
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6
Q

hip dysplasia screening programs in UK, Europe, SA

A
  • UK
    – Clinical assessment and ultrasound for high risk cases
    – Concerns re high incidence of late presenting / missed cases dt poorly trained staff
  • Europe – Universal ultrasound screening
  • SA CHB and CMJ – Officially clinical screening
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7
Q

DDH radiographic diagnosis

A
  1. X-rays not used in the newborn
    * Ossification femoral head @ 4-6months
  2. Ultrasound diagnosis
    * Static
    * Dynamic
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8
Q

DDH Rx - birth- 6 months

A
  • Pavlik Harness : Hip flexion → docks; hip abduction → locates
  • Weekly adjustments

= With treatment, > 75% stabilize

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9
Q

DDH Rx - 7 - 18 months

A

closed reduction
* Under anaesthesia & intraoperative screening
* Confirm reduction – arthrogram, Xray, MRI, CT
* Hip spica = 12 weeks
* Batchelor cast = 12 weeks

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10
Q

DDH Rx - >18 months

A
  • Open reduction
  • Extensive surgical release of contracted soft tissue & clearing of potential hip joint
  • Hip spica + Batchelor cast = 12 weeks
  • Femoral osteotomies useful if under tension
  • Pelvic osteotomies to augment coverage
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11
Q

DDH Rx - open reduction approach

A

iliofemoral approach
- critically exposes the capsule laterally, anteriorly & medially

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12
Q

DDH Rx - open reduction age limit

A
  • bilateral: </= 6y/o
  • unilateral: </= 8y/o
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13
Q

DDH - Rx complications

A
  • Re-dislocation (Reported < 5%, probably higher)
  • Avascular necrosis should be < 10%
    • Femoral head compression
    • Vessel injury to medial femoral circumflex artery
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14
Q

Perthes’ Disease what is it

A
  • Idiopathic avascular necrosis of femoral head in children
  • Focal disruption of blood supply
  • Generalised disorder (osteochondrosis)
  • 1 in 10 000 children
  • 5:1 M:F
  • 4-8 years old
  • Bilateral in 12%
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15
Q

Perthes’ Disease presentation

A

History
* Insidious onset of pain (knee, hip, groin)
* Limp

Examination
* Antalgic, Trendelenburg gait
* Quads & calf wasting
* Limited hip abduction and internal rotation

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16
Q

Perthes’ disease JHB Rx protocol

A

No lateral subluxation <8 yrs old
* Symptomatic management: limited weightbearing, analgesia, maintain ROM with physiotherapy

Lateral subluxation <8 yrs old → arthrogram
* Spherical, containable → Salter
* Aspherical / non-containable → Chiari

Child 8yrs or older, Catterall 3 or 4

17
Q

clubfoot epidemiology

A
  • 1:1000 live births
  • CAVE
  • Idiopathic
  • Teratologic
  • MMC, arthrogryposis
  • Gold standard = Ponseti method
18
Q

Ponseti Rx

A
  • Weekly manipulation & casting
  • Once foot abducts to 60 degrees : TA tenotomy, 3 weeks in cast
  • Foot abduction brace 3 months full time, then at night till 4 years
  • Importance of parental counselling
  • Initial success over 90%
  • Recurrence requires repeat casting / surgery