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Farah Adibah Kasmin
     2008402312
   Formerly known as congenital dislocation of the hip
   Comprise a spectrum of disorder:
    1. Dislocation during neonatal period
    2. Subluxation or partial displacement
    3. Shallow acetabulum without actual displacement


   5-20 per 1000 live births
   Re-examination 3 weeks after birth , the incidence : 1-2 per
    1000 infants
   Girls>boys, 7:1
   Left hip> right hip
   1:5 cases - bilateral
• Generalized joint laxity
  Genetic      • Shallow acetabula

               • High level of maternal estrogen,
Hormonal         progesterone and relaxin in the last few
 changes         weeks of pregnancy aggravate
                 ligamentous laxity in infant

Intrauterine   • esp. breech position with extended legs ->
malposition      dislocation


               • Who swaddle their babies & carry them
 Postnatal       with fully extended hips n knees >
  factors        compare to person who carry babies
                 astride their backs with hips abducted
In the neonate:
 Every newborn child should be

   examine for sign of hip instability esp:
   - FHx of congenital hip instability, breech
   presentation

Special tests:
 Ortolani’s test

 Barlow’s test
   Late features:
       Asymmetry, a clicking hip or difficulty in applying
        napkin
       Unilateral dislocation- skin creases look
        asymmetrical, short leg, internally rotated
       Bilateral dislocation- wide perineal gap, abduction is
        limited
       Walking is delayed
       Gait: limp or Trendelanburg gait
   hip dislocation
     Hilgenreiner's line
         horizontal line through
           right and left triradiate
           cartilage
         femoral head
           ossification should be
           inferior to this line
     Perkin's line
         line perpendicular line
           to Hilgenreiner's
           through point at lateral
           margin of acetabulum
         femoral head
           ossification should be
           medial to this line
     Shenton's line
         arc along inferior
           border of femoral neck
           and inferior edge of
           superior pubic ramus
         arc line should be
           continuous
   hip dyplasia
     acetabular index - angle formed
       by a line drawn from point on
       triradiate cartilage to point on
       lateral margin of
       acetabulum (normal is < 30 deg.)



    Von Rosen’s lines- the hip abducted
      45degree.The femoral shaft should
      pointed into acetabula
   Plain X rays




        Normal     Dislocated hip
   The first 3-6 month of age
     Double napkin or an abduction pillow for 1st 6weeks
     Re-examined
     Persistent instability  abduction splintage until hip
      is stable
     Follow up- until the child walking


   Splintage:
    - hold the hip 100 degree flexed and abducted
    - allow some movement in the splint
Persistent dislocation: 6month to 6 years
 Closed reduction

 Splintage

 Open reduction



After the age 6 years
Unilateral dislocation- operative reduction
Bilateral dislocation- Symmetrical, less notifiable
     - Greater risk for surgical intervention
     - avoid operation unless pain and deformity is
     unusually severe
   Displacement of the proximal femoral epiphysis
   aka epiphysiolysis
   Most common hip pain in adolescence
   M > F->3:2
   M: 12 - 16 y/o, F: 10 - 15 y/o
   Bilateral: 17 – 50% of cases
   Risk factors include:
     Obesity
     Hx of radiation therapy to femoral head
      region
     Endocrine disorders (e.g. hypothyroidism
      and osteodystrophy of chronic renal
      failure)
     Positive family history of SUFE/SCFE
      (autosomal dominant)
     African American
1.   History:

    Pain       - Hip or groin pain (most common)
                - Reffered pain: ant part of thigh and knee
    Limp

 2. Physical examination

    Trendelenburg gait
    Leg is externally rotated
    1-2cm short
    Limitation of abduction and internal rotation
SUFE Grading
Management

Non weight bearing and rest

Surgical: Percutaneous in-situ
stabilization/fixation

Complications
   Avascular necrosis of femoral head (10-15%)
   Acute cartilage necrosis/chondrolysis (7-10%)
   Deformity
   Secondary osteoarthritis (~90%)
   Slip progression (1-2% of single screw fixation)
   Hip stiffness
   Painful hip disorder of childhood characterized by
    necrosis of the femoral head
   Incidence: 1 in 10 000
   Boys>girls , 4x as often as girls
   Usually 4-8 years old

                                      Femoral head supplied
                                      by:
                                      •Mataphyseal vessels
                                      •Lateral epiphyseal
                                      vessels
                                      •Scanty vessels
•Bone death
          •Part of the bony femoral head dies, stop enlarge
Stage 1

          •Revascularization and repair
          •New blood vessel enter the necrotic area and new bone is laid down on the

Stage 2    dead trabeculae




          •Distortion and remodelling
          •Epiphysis is damaged and the growth at the head and neck will be distorted
          •Epiphysis ends up flattened (‘coxa plana’) but enlarged (‘coxa magna’)
Stage 3   •The femoral head is incompletely covered by the acetabulum.
   Complaint of pain and start to limp
   Little wasting of muscles in the upper thigh
   Joint is irritable
       All movements are diminished
       Extremely painful
   The child is not seen till later
       Limited abduction and internal rotation
   X- ray

       Earliest changes – increased density of the bony epiphysis
        and apparent widening of the joint space

       Followed by - flattening, fragmentation and lateral
        displacement of the epiphysis, with rarefaction and
        broadening of the metaphysis.
   Symptomatic tx:
       Pain control
       Gentle exercise to maintain movement
   Containment
   Operative reconstruction
Transient synovitis is the most common cause of
acute hip pain
aged 3-10 years.
Boys >> Girls
The disease causes arthralgia and arthritis
secondary to a transient inflammation of the
synovium of the hip.

Usually it is a diagnoses of exclusion, once
trauma and infection are ruled out
Symptoms
                            Signs-

-   Most commonly:          -Hold the hip in flexion
    Unilateral hip or       with slight abduction
    groin pain              and external rotation.
-    Limp.                  - mild restriction of
                            abduction and internal
-   50% patient has         rotation, but 1/3
    recent history of an    demonstrate no
    URTI                    limitation of motion.
-    Usually afebrile or    - The hip may be tender
    have a mildly           and painful even with
    elevated                passive movement.
    temperature.            - The most sensitive test
                            :the log roll
-   Very young
    children -> crying at
    night.
Investigatios
   Usually to rule out other diagnoses.
   WBC, ESR and CRP are usually elevated in septic
    arthritis.
   XRay: can exclude bony lesions.
   Ultrasound- may show a joint effusion



Management
   Apply heat and massage
   .Non-steroidal anti-inflammatory drugs (NSAIDs).
   Advise bedrest until pain dissapear and the effusion
    resolves

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Paediatric Orthopaedic

  • 1. Farah Adibah Kasmin 2008402312
  • 2. Formerly known as congenital dislocation of the hip  Comprise a spectrum of disorder: 1. Dislocation during neonatal period 2. Subluxation or partial displacement 3. Shallow acetabulum without actual displacement  5-20 per 1000 live births  Re-examination 3 weeks after birth , the incidence : 1-2 per 1000 infants  Girls>boys, 7:1  Left hip> right hip  1:5 cases - bilateral
  • 3. • Generalized joint laxity Genetic • Shallow acetabula • High level of maternal estrogen, Hormonal progesterone and relaxin in the last few changes weeks of pregnancy aggravate ligamentous laxity in infant Intrauterine • esp. breech position with extended legs -> malposition dislocation • Who swaddle their babies & carry them Postnatal with fully extended hips n knees > factors compare to person who carry babies astride their backs with hips abducted
  • 4. In the neonate:  Every newborn child should be examine for sign of hip instability esp: - FHx of congenital hip instability, breech presentation Special tests:  Ortolani’s test  Barlow’s test
  • 5. Late features:  Asymmetry, a clicking hip or difficulty in applying napkin  Unilateral dislocation- skin creases look asymmetrical, short leg, internally rotated  Bilateral dislocation- wide perineal gap, abduction is limited  Walking is delayed  Gait: limp or Trendelanburg gait
  • 6. hip dislocation  Hilgenreiner's line  horizontal line through right and left triradiate cartilage  femoral head ossification should be inferior to this line  Perkin's line  line perpendicular line to Hilgenreiner's through point at lateral margin of acetabulum  femoral head ossification should be medial to this line  Shenton's line  arc along inferior border of femoral neck and inferior edge of superior pubic ramus  arc line should be continuous
  • 7. hip dyplasia  acetabular index - angle formed by a line drawn from point on triradiate cartilage to point on lateral margin of acetabulum (normal is < 30 deg.) Von Rosen’s lines- the hip abducted 45degree.The femoral shaft should pointed into acetabula
  • 8. Plain X rays Normal Dislocated hip
  • 9. The first 3-6 month of age  Double napkin or an abduction pillow for 1st 6weeks  Re-examined  Persistent instability  abduction splintage until hip is stable  Follow up- until the child walking  Splintage: - hold the hip 100 degree flexed and abducted - allow some movement in the splint
  • 10. Persistent dislocation: 6month to 6 years  Closed reduction  Splintage  Open reduction After the age 6 years Unilateral dislocation- operative reduction Bilateral dislocation- Symmetrical, less notifiable - Greater risk for surgical intervention - avoid operation unless pain and deformity is unusually severe
  • 11. Displacement of the proximal femoral epiphysis  aka epiphysiolysis  Most common hip pain in adolescence  M > F->3:2  M: 12 - 16 y/o, F: 10 - 15 y/o  Bilateral: 17 – 50% of cases
  • 12. Risk factors include:  Obesity  Hx of radiation therapy to femoral head region  Endocrine disorders (e.g. hypothyroidism and osteodystrophy of chronic renal failure)  Positive family history of SUFE/SCFE (autosomal dominant)  African American
  • 13. 1. History:  Pain - Hip or groin pain (most common) - Reffered pain: ant part of thigh and knee  Limp 2. Physical examination  Trendelenburg gait  Leg is externally rotated  1-2cm short  Limitation of abduction and internal rotation
  • 14.
  • 16. Management Non weight bearing and rest Surgical: Percutaneous in-situ stabilization/fixation Complications  Avascular necrosis of femoral head (10-15%)  Acute cartilage necrosis/chondrolysis (7-10%)  Deformity  Secondary osteoarthritis (~90%)  Slip progression (1-2% of single screw fixation)  Hip stiffness
  • 17. Painful hip disorder of childhood characterized by necrosis of the femoral head  Incidence: 1 in 10 000  Boys>girls , 4x as often as girls  Usually 4-8 years old Femoral head supplied by: •Mataphyseal vessels •Lateral epiphyseal vessels •Scanty vessels
  • 18. •Bone death •Part of the bony femoral head dies, stop enlarge Stage 1 •Revascularization and repair •New blood vessel enter the necrotic area and new bone is laid down on the Stage 2 dead trabeculae •Distortion and remodelling •Epiphysis is damaged and the growth at the head and neck will be distorted •Epiphysis ends up flattened (‘coxa plana’) but enlarged (‘coxa magna’) Stage 3 •The femoral head is incompletely covered by the acetabulum.
  • 19. Complaint of pain and start to limp  Little wasting of muscles in the upper thigh  Joint is irritable  All movements are diminished  Extremely painful  The child is not seen till later  Limited abduction and internal rotation
  • 20. X- ray  Earliest changes – increased density of the bony epiphysis and apparent widening of the joint space  Followed by - flattening, fragmentation and lateral displacement of the epiphysis, with rarefaction and broadening of the metaphysis.
  • 21. Symptomatic tx:  Pain control  Gentle exercise to maintain movement  Containment  Operative reconstruction
  • 22. Transient synovitis is the most common cause of acute hip pain aged 3-10 years. Boys >> Girls The disease causes arthralgia and arthritis secondary to a transient inflammation of the synovium of the hip. Usually it is a diagnoses of exclusion, once trauma and infection are ruled out
  • 23. Symptoms Signs- - Most commonly: -Hold the hip in flexion Unilateral hip or with slight abduction groin pain and external rotation. - Limp. - mild restriction of abduction and internal - 50% patient has rotation, but 1/3 recent history of an demonstrate no URTI limitation of motion. - Usually afebrile or - The hip may be tender have a mildly and painful even with elevated passive movement. temperature. - The most sensitive test :the log roll - Very young children -> crying at night.
  • 24. Investigatios  Usually to rule out other diagnoses.  WBC, ESR and CRP are usually elevated in septic arthritis.  XRay: can exclude bony lesions.  Ultrasound- may show a joint effusion Management  Apply heat and massage  .Non-steroidal anti-inflammatory drugs (NSAIDs).  Advise bedrest until pain dissapear and the effusion resolves

Notes de l'éditeur

  1. Ortolani- Baby thigh held with thumbs medially and finger resting on greater trochanter , flexed 90dgree and abducted the hipIf abduction stop halfway, no jerk of entry irreducible dislocationBarlow- thumb in the groin, gasping upper thigh , make the femoral head in n out of acetabulum during abduct and adduct
  2. Xray usually dificult to evaluate bcoz the acetabulum and femoral head are largely cartilaginous, therefore not visible on Xray before
  3. Hip that unstable at birth 80-90% will stabilized spontaneously in 2-3w