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SUMMARY
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Legg-Calve-Perthes Disease is an idiopathic avascular necrosis of the proximal femoral epiphysis in children.
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Diagnosis can be suspected with hip radiographs. MRI may be required for diagnosis of occult or early disease.
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Treatment is typically observation in children less than 8 years of age, and femoral and/or pelvic osteotomy in children greater than 8 years of age.
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EPIDEMIOLOGY
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Incidence
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affects 1 in 10,000 children
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Demographics
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4-8 years is most common age of presentation
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male to female ratio is 5:1
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higher incidence in urban areas
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socioeconomic class
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higher among lower socioeconomic class
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latitude
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higher incidence in high latitude (low incidence around equator)
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race
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Caucasian > East Asian and African American
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Anatomic location
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bilateral in 12%
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asymmetrical, asynchronous involvement
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rarely at the same stage of disease
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symmetrical involvement suggests MED (multiple epiphyseal dysplasia)
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Risk factors
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positive family history
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low birth weight
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abnormal birth presentation
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second hand smoke
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Asian, Inuit, and Central European decent
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ETIOLOGY
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Pathophysiology
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osteonecrosis occurs secondary to disruption of blood supply to femoral head
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followed by revascularization with subsequent resorption and later collapse
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creeping substitution provides pathway for remodeling after collapse
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proposed mechanisms
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possible association with abnormal clotting factors (Protein S and Protein C deficiencies)
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controversial etiology
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thrombophilia has been reported to be present in 50% of patients
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up to 75% of affected patients have some form of coagulopathy
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repeated subclinical trauma and mechanical overload lead to bone collapse and repair (multiple-infarction theory)
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damages result from epiphyseal bone resorption, collapse, and the effect of subsequent repair during the course of disease
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maternal / passive smoking aggravates
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Associated conditions
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associated with ADHD in 33% of cases
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bone age is delayed in 89% of patients
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CLASSIFICATION
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Lateral Pillar Classification
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has best agreement and is most predictive
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determined during fragmentation stage
- usually occurs 6 months after the onset of symptoms
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based on the height of the lateral pillar of the capital femoral epiphysis on AP imaging of the pelvis
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designed to provide prognostic information
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limitation is that final classification is not possible at initial presentation due to the fact that the patient needs to have entered into the fragmentation stage radiographically
- usually occurs 6 months after the onset of symptoms
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Waldenstrom classification
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Stages of Legg-Calves-Perthes (Waldenström)
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Initial
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Infarction produces a smaller, sclerotic epiphysis with medial joint space widening
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Radiographs may remain occult for 3 to 6 months
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Fragmentation
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Begins with presence of subchondral lucent line (cresent sign)
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Femoral head appears to fragment or dissolve
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Result of revascularization process with bone resorption producing collapse with subsequent patchy density and lucencies
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Hip related symptoms are most prevalent
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Lateral pillar classification based on this stage Can last from 6m to 2y
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Reossification
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Ossific nucleus undergoes reossification with new bone appearing as necrotic bone is resorbed
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May last up to 18m
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Healing or remodeling
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Femoral head remodels until skeletal maturity
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Begins once ossific nucleus is completely reossified; trabecular patterns return
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Catteral Calssification
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Emphasizes extent of head involvement and outcome (see groups below)
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Applied during fragmentation stage when the necrotic segment is demarcated from the viable portion
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Catterall also described head
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At-risk signs that are associated with poor outcomes
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Gage sign (V-shaped radiolucency in the lateral portion of the epiphysis and/or adjacent metaphysis)
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Calcification lateral to the epiphysis
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Metaphyseal cyst
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Lateral subluxation of the femoral head
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Horizontal proximal femoral physis
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Salter-Thompson Calssification
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Stulberg classification
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Gold standard for rating residual femoral head deformity and joint congruence
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Recent studies show poor interobserver and intraobserver reliability
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PRESENTATION
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Symptoms
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insidious onset
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may cause painless limp
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intermittent hip, knee, groin or thigh pain
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Physical exam
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hip stiffness
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loss of internal rotation and abduction
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gait disturbance
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antalgic limp
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Trendelenburg gait (head collapse leads to decreased tension of abductors)
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limb length discrepancy is a late finding
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hip adduction contracture can exacerbate the apparent LLD
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IMAGING
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Radiographs
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AP of pelvis and frog leg laterals
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critical in diagnosis and prognosis
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early findings include
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medial joint space widening (earliest) from less ossification of head
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measured between teardrop and ossification center
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irregularity of femoral head ossification
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decreased size of ossification center
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sclerotic appearance
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cresent sign (represents a subchondral fracture)
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Bone scan
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can confirm suspected case of LCPD
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decreased uptake (cold lesion) can predate changes on radiographs
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provides information on extent of femoral head involvement
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MRI
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early diagnosis revealing alterations in the capital femoral epiphysis and physis
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more sensitive than radiograph
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Perfusion studies predict maximum extent of lateral pillar involvement
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Arthrogram
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a dynamic arthrogram can demonstrate coverage and containment of the femoral head
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STUDIES
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Histology
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femoral epiphysis and physis exhibit areas of disorganized cartilage with areas of hypercellularity and fibrillation
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DIFFERENTIAL
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Radiographic differential diagnosis
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infecitious etiology
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septic arthritis, osteomyelitis, pericapsular pyomyositis
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transient synovitis
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multiple epiphyseal dysplasia (MED)
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spondyloepiphyseal dysplasia (SED)
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sickle cell disease
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Gaucher disease
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hypothyroidism
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Meyers dysplasia
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TREATMENT
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Goals
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resolution of symptoms
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NSAIDs, traction, crutches
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restoration of range of motion
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physical therapy (may exacerbate symptoms), muscle lengthenings, Petrie casting
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containment of hip
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improve range of motion, bracing, proximal femoral osteotomy, pelvic osteotomy
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ensure that femoral head is well seated in acetabulum
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Nonoperative
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observation alone, activity restriction (non-weightbearing), and physical therapy (ROM exercises)
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indications
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children < 8 years of age (bone age <6 years)
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young patients typically do not benefit from surgery
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lateral pillar A involvement
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technique
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activity restriction and protected weight-bearing during earlier stages until reossification is complete
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main goals of treatment are to keep the femoral head contained and maintain good motion
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containment limits deformity and minimizes loss of sphericity
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lessen subsequent degenerative changes
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bracing and casting for containment have not been found to be beneficial in a large, prospective study
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all patients require periodic clinical and radiographic followup until completion of disease process
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outcomes
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good outcomes correlate with a spherical femoral head
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60% do not require operative intervention
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good outcomes associated with lateral pillar A and Catterall I groups
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Operative
- femoral and/or pelvic osteotomy
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indications
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children > 8 years of age, especially lateral pillar B and B/C
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technique
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proximal femoral varus osteotomy
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to provide containment
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pelvic osteotomy
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Salter or triple innominate osteotomy
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Shelf arthroplasty may be performed to prevent lateral subluxation and resultant lateral epiphyseal overgrowth
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outcomes
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children with lateral pillar A and those with B under 8 years did well regardless of treatment
- large recent studies show improved outcomes with surgery for lateral pillar B and B/C in children > 8 years (bone age >6 years)
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studies sugggest earlier surgery before femoral head deformity develops may be best
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poor outcome for lateral pillar C regardless of treatment
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valgus and/or shelf osteotomies
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indications
- hinge abduction
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lateral extrusion of the capital femoral epiphysis producing a painful hinge effect on the lateral acetabulum during abduction
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- hinge abduction
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abduction-extension osteotomy
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reposition the hinge segment away from the acetabular margin
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correct shortening from fixed adduction
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improve abductor mechanism by improving abductor muscle contractile length
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Shelf or Chiari osteotomies are also considered when the femoral head is no longer containable
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hip arthroscopy
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emerging treatment modality for mechanical abnormalities in the setting of healed LCPD
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femoroacetabular impingement
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hip arthrodiastasis
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indications
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controversial indications and outcomes
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technique
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hip distraction via external fixation
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- femoral and/or pelvic osteotomy
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TECHNIQUE
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Proximal Femoral Varus Osteotomy (VRDO)
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indications
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extrusion in early stages of LCPD
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technique
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reposition femoral head into acetabulum for containment purposes
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COMPLICATIONS
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Femoral head deformity
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coxa magna
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widened femoral head
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coxa plana
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flattened femoral head
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important prognostic factor
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Stulberg classification
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Lateral hip subluxation (extrusion)
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associated with poor prognosis
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can lead to hinge abduction
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Premature physeal arrest
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trochanteric overgrowth
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coxa breva
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shortened femoral neck
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leg length discrepancy
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typically mild
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Acetabular dysplasia
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poor development secondary to deformed femoral head
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can alter hip congruency
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Labral injury
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secondary to femoral head deformity
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femoroacetabular impingement
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Osteochondritis dissecans
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can lead to loose fragments
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- Degenerative arthritis
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Stulberg I and most Stulberg II hips perform well for the lifetime of the patient
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PROGNOSIS
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Important prognostic variables
- younger age (bone age) < 6 years at presentation is most important good prognostic indicator
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sphericity of femoral head and congruency at skeletal maturity (Stulberg classification)
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lateral pillar classification
- younger age (bone age) < 6 years at presentation is most important good prognostic indicator
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Variables of poor prognosis
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female sex
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decreased hip abduction (adduction contracture)
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heavy patient
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longer duration from onset to completion of healing
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stiffness with progressive loss of ROM
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Catterall "head at risk" signs (see under classification)
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Natural history
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long-term studies suggest that most patients do well until fifth or sixth decade of life
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approximately 1/2 of patients develop premature osteoarthritis secondary to an aspherical femoral head
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Self-limiting process
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variable course to final healing from initial ischemic event
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can take 2-5 years to resolve
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Differentiated from adult osteonecrosis by its ability to heal and remodel
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