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Department of Orthopaedics
       AFMC, Pune
         PG SEMINAR


 DEVELOPMENTAL DYSPLASIA
         OF HIP

                      Maj Rohit Vikas
                      Resident
CDH/ DDH
Instability of the hip in the newborn

Includes
           Dislocatable hips
           Acetabular dysplasia
           Subluxation of femoral head
           Dislocated Femoral head

As the child grows it may
          Progress to dislocation or poor acetabular
          coverage
          Secondary changes develop in head and
          acetabulum

Process is not restricted to congenital abnormalities
of the hip, and includes some hips that were normal
at birth and subsequently became abnormal.
DEVELOPMENTAL DYSPLASIA
        OF HIP


        DEFINITIONS
Which is an Unstable Hip?


Positive Barlow/ Ortolani Tests

Clinically stable but abnormal USG

Acetabular Index

Lateral displacement of femoral
beak in relation to Perkin’s line
What is Dysplasia?


Radiographic finding

Increased obliquity of acetabulum

Loss of acetabular concavity

Intact Shenton line
What is Subluxation?


Femoral head not fully in contact
with acetabulum

Widened Teardrop – femoral head
distance

Reduced CE angle

Break in Shenton line

Dysplastic changes in acetabulum
What is Dislocation?


Femoral head not in contact with
acetabulum

Dysplastic changes in acetabulum
Teratologic / Antenatal Dislocations

Fixed dislocation at birth with limited range of motion at hip

During gestation the hip is at risk of dislocation

          during the 12th week when the lower limb rotates medially,

          during the 18th week as the hip muscles develop.

Dislocations during these developmental stages are termed teratologic and are
the result of congenital abnormal neuromuscular development.

Treatment unsuccessful

Open Reduction at 6 months of age
Secondary Hip Dysplasia


Strictly, DDH applies to idiopathic hip dysplasia

Secondary Hip dysplasia

          Neurological conditions
                   Myelomeningocele
                   Cerebral palsy

          Connective tissue diseases
                   Ehlers-Danlos syndrome

          Myopathic disorders
                  Arthrogryposis multiplex congenita.
DEVELOPMENTAL DYSPLASIA
        OF HIP


     ETIOPATHOGENESIS
INCIDENCE
                                                Breech delivery


                                                Frank Breech
                                                20% incidence
                                                of DDH




Left hip > Bilateral > Right hip


                                                Complete or
Lowry, et al, showed that breech infants        footling breech
delivered by elective caesarean section (pre-   lower incidence
labor) had a lower incidence of DDH than        of DDH (2%)
those breech babies delivered vaginally
ASSOCIATED CONDITIONS


Other positional abnormalities including:

         Torticollis (20%)
         Metatarsus adductus (10%)
         Positional club foot
         Congenital Knee dislocation
THEORIES




Mechanical factors
Hormone induced ligamentous laxity
Primary acetabular dysplasia
Genetic inheritance
DEVELOPMENTAL DYSPLASIA
        OF HIP


 CLINICAL DETECTION OF DDH

     BIRTH TO 6 MONTHS
Asymmetrical Thigh Folds




            Indicative of Abnormal hips
            Also seen in infants with normal hips


            Widened perineum
            Prominent Greater trochanter
Galeazzi’s / Allis sign




                         Limited Abduction



           In bilateral hip abnormality, asymmetry may not
           be a feature
Ortolani’s sign
      (Ortolani 1937, 1976).




      Hold the knees and abduct the hip while lifting
      up on the greater trochanter

      A positive test is feeling the dislocated hip
      clunk into the acetabulum
Barlow’s Provocative Test
           (Barlow,1962)




           Adduct and push posteriorly on the hip

           A positive test is feeling the hip push out of the
           acetabulum
Klisic sign in bilateral DDH


    The Ortolani and Barlow manoeuvres are the mainstay of clinical diagnosis in
    the first months of life



Even in the best hands physical examination can fail to detect DDH, and after 3 months
of age the Ortolani and Barlow tests become negative due to progressive soft tissue
contractures.
DEVELOPMENTAL DYSPLASIA
        OF HIP


 CLINICAL DETECTION OF DDH

        OLDER CHILD
Abduction becomes more limited which is particularly noticeable when there is
unilateral disease.

Femoral shortening (positive Galeazzi test) may be apparent but this can be difficult
to appreciate with bilateral disease.

Ambulatory children will have a Trendelenburg gait in addition to limited hip
abduction

Trendelenburg sign

Telescopy positive

Exaggerated lumbar lordosis
DEVELOPMENTAL DYSPLASIA
        OF HIP


      NATURAL HISTORY
What happens to a Dysplastic hip without subluxation ?




Usually become painful

Degenerative Arthritis over time

Often subluxate as degeneration progresses

Hips with Acetabular index > 35 will likely require hip replacement later

If these hips are well reduced after primary treatment of DDH, with a greater
than normal CE angle, risk of Degenerative arthritis decreases
What happens to a Subluxated hip?




Always lead to symptomatic degenerative arthritis

Rapid progression

Severe subluxation – symptoms in 2nd decade
Moderate subluxation – in 3rd to 4th decade
Mild subluxation – in 5th to 6th decade
What happens to a completely dislocated hip?




Symptoms much later than a subluxated hip

May never become painful

False acetabulum




                                            False acetabulum
Consequences of Persistent Dysplasia

Abnormal gait
Restricted abduction
Reduced strength
Increased rate of degenerative joint disease.

Outcome of untreated unilateral DDH is less favorable compared with bilateral
disease
        Limb length discrepancy,
        Asymmetrical movement, strength
        Ipsilateral valgus knee.

Degenerative joint disease tends to present earlier in subluxated hips than in
dysplastic hips without subluxation
Natural History

Over the age of 6 months spontaneous resolution of dysplasia is unlikely

Usually more aggressive treatment is required compared with younger children.

Older children tend to have more advanced changes in the soft tissues and bony
structures.

Changes in acetabulum
         Ossification is delayed
         Shallow,
         Anteverted
         Deficient anterolaterally.

Changes in Femoral Head
         Delayed ossification
         Exaggerated femoral anteversion.
Natural History




A 16y /F with longstanding “missed” left DDH.
The left femoral head articulates with a neo-acetabulum in the iliac bone.
The left femoral shaft is reduced in diameter and there is wasting of the thigh muscles
Natural History
Natural History
DEVELOPMENTAL DYSPLASIA
        OF HIP


      PLAIN RADIOLOGY
Normal Hip




                                     Perkins’ line
acetabular
index


                                 Hilgenreiner’s line




             Shenton’s line
Normal Hip
         Acetabular index

         Angle between the acetabulum
         and hilgenreiner’s line

         It should be < 30 degrees in a
         newborn




         Center-edge angle of Wiberg

         Cannot be measured until the ossific
         nucleus appears

         Normal is > 10 degrees in children 6-
         13 yrs
DDH




      Ossification centre
      Head of femur
      2 and 7 months
DDH

      8 month /F with left DDH.

      Left acetabulum is shallow and the
      hip is dislocated.

      Left proximal femoral ossification
      centre is small compared with the
      normal right side.

      The normal right acetabulum has a
      central depression and well-defined
      lateral edge.

      The acetabular teardrop is
      developing on the right but not on
      the dysplastic left side
DEVELOPMENTAL DYSPLASIA
        OF HIP


        ULTRASOUND
L




                                                                                            β
                                                                         Iliac Wing                 Femoral Head
                                                                                            α

                                                                                                T

                                                                          Bony
Diagram showing hip anatomy on standard coronal US plane and lines        Acetabular
used to evaluate hip dysplasia using the Graf method.                     roof


Femoral head (FH) is centred over the hypoechoic triradiate cartilage
(T). The promontory is at the junction of the iliac wing (IL) and the
bony acetabular roof (A). L, labrum.
The alpha angle reflects the depth of the bony acetabular roof and is    Standard coronal ultrasound of the normal
formed by the intersection of the baseline (BL) and acetabular roof      infant hip joint. The promontory is sharply
line (AL). In a normal mature hip the alpha angle is greater than 60°.
                                                                         defined and the bony acetabular roof is
The beta angle reflects cartilaginous coverage and is formed by the      steep. The ossification centre for the femoral
intersection of the baseline with the labral line (LL). A normal beta    head has not yet developed
angle is less than 55°
SONOGRAPHIC CLASSIFICATION
DEVELOPMENTAL DYSPLASIA
        OF HIP


      ARTHROGRAPHY
Not routinely performed

Either performed before surgery or intraoperatively.

Goal of arthrography in DDH is to demonstrate the position of the femoral head with
respect to other joint structures both at rest and during reduction or stress manoeuvres

It also outlines any deformities or obstructions to concentric reduction
           Inverted limbus,
           Capsular constriction,
           Pulvinar Hypertrophy
           Hypertrophied ligamentum teres
Arthrogram, made after
fifteen days of overhead
traction, showing the hip
to be reduced. A square-
shaped limbus (arrow) at
the superior pole of the
epiphysis and marked
capsular distension are
evident.
DEVELOPMENTAL DYSPLASIA
        OF HIP


  COMPUTED TOMOGRAPHY
Two main indications for CT in DDH:

To document hip reduction post-
operatively if a child is placed in a spica
cast

Pre-operative planning in severely
dysplastic hips that require corrective
procedures.

                                              Axial CT scan following open reduction of the left hip.

                                              The left femoral metaphysis is not aligned with the
                                              acetabulum and the femoral head is displaced
                                              posteriorly.
                                              The spica cast was removed and patient underwent
                                              further manipulation under anaesthesia to achieve
                                              successful reduction
DEVELOPMENTAL DYSPLASIA
        OF HIP


           MRI
Distinct advantages over both CT and arthrography in pre-operative imaging in
patients with DDH.

Ability to differentiate between different types of soft tissue which enables
visualisation of unossified cartilage, ligaments, fat, muscle and fluid including those soft
tissues that present an obstruction to concentric reduction such as pulvinar, the labrum
and joint capsule.

Lack of ionising radiation

MR imaging is more time-consuming than CT or arthrography.

In newborns and infants sedation may be required, except if patents are in a spica cast
since this limits movement.

The main disadvantages of MR imaging is increased cost and limited availability
DEVELOPMENTAL DYSPLASIA
        OF HIP


         SCREENING
General Examination


-Plagiocephaly,

-Sternomastoid Tumour (Torticollis),

-Feet for any congenital deformity
Hip Examination


Barlow’s test (<3-4 months of age)
Ortolani’s test (<3-4 months of age)
Limitation of Abduction
Leg length discrepancy (Galleazi test)
Asymmetry of thigh folds
Limp in a walking child
Radiology

Children <6 months - Ultrasound using Graf
    classification system

   Class   Alpha angle        Description
   I       >60                Normal
   II      60-43              Immature/Dysplastic
   III     <43                Subluxed/Dislocated
   IV      Unmeasurable       Dislocated




Children >6 months - Xrays.
Criteria for Screening

Clinical Screening for all neonates for Hip Instability.
Careful screening for infants with risk factors:
   Family history of DDH
   Breech
   Torticollis
   Metatarsus adductus
   Oligohydomnios

Screening with USG
    Controversial

    As per AAP guidelines
          Female infants delivered breech
          Family history of DDH +
DEVELOPMENTAL DYSPLASIA
        OF HIP


         TREATMENT

     BIRTH – 6 MONTHS
DEVELOPMENTAL DYSPLASIA
        OF HIP


      PAVLIK HARNESS
Indications

All Dislocated hip that can be reduced (Ortolani’s sign)
          Start harness at the time of diagnosis

Hips that are located but can be subluxated (Barlow’s sign)
          Some may spontaneously stabilize, some may dislocate.
          Re-examine after few weeks before starting treatment

Hips that are normal on clinical examination but abnormal on USG
          Close observation
          Repeat USG at 6 weeks of age
          Abnormal hips treated
          Graf II hips more likely to improve without treatment than Graf III/ IV hips

Irreducible hips
          Likely to fail treatment if initial coverage was < 20%
Application
Flexion – 120°
Hyper flexion
          Femoral nerve palsy
          Inferior dislocation of head
Inadequate flexion < 90°
          Fails to reduce hip
Abduction by gravity
                                                           1



                                                   4
                                                       3



                                                       2
Follow Up
Weekly Follow up during harness treatment
Change size after 3-4 weeks

USG at 3-4 weeks
          If unreduced – discontinue treatment
                      Examine under anaesthesia
                      Arthrogram for cause of instability
          If hip reduced but can be dislocated
                      Continue harness for 3-6 more weeks

After 6 weeks of harness – USG with child out of harness.
          If reduced head – Wean/ discontinue harness

X rays at 3-4 months
X rays at 1 yr

Annual Follow up

Follow up till skeletal maturity
           (Late asymmetric epiphyseal closure – valgus femoral head and reduced coverage
           Acetabular dysplasia in 20%)
Problems in Harness

If reduction not achieved with harness in 3 – 4 weeks then discontinue harness and
other treatment started.

PAVLIK DISEASE
         Prolonged positioning of dislocated hip in flexion and abduction
         Dysplasia increased - Flattening of posterior acetabulum
         Open reduction needed

Femoral nerve palsy
DEVELOPMENTAL DYSPLASIA
        OF HIP


        TREATMENT

      6 – 18 MONTHS
Goal of Treatment
Obtain and maintain reduction without damaging femoral head

                 Closed Reduction
                 Open Reduction



Problems

   Risk of Avascular Necrosis

   Growth potential of acetabulum declines with age (and hence remodelling
   potential)
Role of Pre Reduction Traction

Reduced risk of Avascular Necrosis
         30% without Traction
         15% with prereduction traction
         < 5% in Human position
         (flexion 90 and mild abduction)

Reduced need for Open reduction

Portable Home Traction
         for 2 – 3 weeks
Role of Pre Reduction Traction




              Bryant’s Traction
Closed Reduction
Gentle positioning
Determine Stability – Wider Zones of Safety
Adductor Tenotomy


Increases the Zones of Safety by allowing wider range of abduction
Hip Spica Cast
  Flexion > 90

  Abduction 30 – 40 acceptable as long as
  further abduction possible

  Slight internal rotation (10 – 15)
Hip Spica Cast




Intraop radiograph
Confirm reduction – USG/ CT Scan
MRI – reduction and vascular status of head can both be assessed

Remove cast after 6 weeks under anesthesia
Assess stability through moderate range of motion/ do not dislocate.
Xray AP pelvis to confirm reduction
Reapply second cast for 6 weeks.

Third cast/ Abduction splinting
          Usually applied for 6 more weeks and discontinue immobilization
Obstacles to Reduction


•   Extra- articular
     – Iliopsoas tendon
     – adductors

•   Intra-articular
     – inverted hypertrophic labrum
     – tranverse acetabular ligament
     – pulvinar, ligamentum teres
     – constricted anteromedial capsule espec in late cases

•   neolimbus is not an obstacle to reduction and represents epiphyseal cartilage
    that must not be removed as this impairs acetabular development
Open Reduction +/- Capsulorrhaphy

For unstable hips
Widened joint space


Approaches
Medial Approch                     v/s   Anterior approach

Minimum dissection                       Better exposure
Obstructions approached directly         Capsulorrhaphy can be performed

Limited exposure
Medial femoral Cx Artery

< 1 yr of age                            in older children
Open Reduction + Femoral Shortening
            If there is excessive pressure on femoral head when it is reduced



Consider in a dislocated hip in > 2 yrs age

To correct excessive anteversion

To place femoral head into Varus position

Intertrochanteric/ Subtrochanteric
osteotomy
Open Reduction + Innominate Osteotomy
                           If there is need for added coverage


Assess need:

Hip in extension – neutral rotation –
abduction

If > 30% head visible then innominate
osteotomy required

Innominate osteotomy in > 18 months.
        Salter / Pemberton

Consider femoral shortening for
excessive pressure on head
DEVELOPMENTAL DYSPLASIA
        OF HIP


         TREATMENT

      18 – 36 MONTHS
Open Reduction


Evaluate stability of hip during open reduction


Assess need for added coverage
         Salter/ Pemberton pelvic osteotomy

For Children > 3 yrs, usually an acetabular procedure is needed to cover femoral
head adequately
Varus Derotational Femoral Osteotomy
DEVELOPMENTAL DYSPLASIA
        OF HIP


        TREATMENT

        3 – 8 YEARS
Problems


Proximal head location
Contracted muscles

Femoral shortening required, greater shortening required for higher dislocations

Primary acetabular repositioning osteotomy often needed
         Salter/ Pemberton

In > 3 yr, an acetabular procedure needed to adequately cover the head
Open Reduction


Upper age for Successful Reduction

Unilateral dislocations
         Open reduction should be attempted till 9 – 10 yrs of age
         Gait asymmetry

Bilateral dislocations
          Upto 8 yrs
          Increased complication if both hips reduced
          Natural outcome of untreated B/L Dislocation better than results of treatment
PELVIC OSTEOTOMIES
Simple osteotomies that Reposition the Acetabulum
   Salter Innominate Ostetomy
   Pemberton’s Acetabuloplasty
   Dega Osteotomy

Complex Osteotomies that Reposition the Acetabulum
   Steel osteotomy
   Tonnis Osteotomy
   Ganz Osteotomy

Spherical Acetabular osteotomy

Osteotomies that Augment the Acetabulum
   Chiari Osteotomy
   Shelf Procedures
          Staheli Slotted Acetabular Augmentation
PELVIC OSTEOTOMIES
Salter Innominate Osteotomy

Prerequisite – concentrically reduced hip

Acetabular dysplasia
Failure of acetabular index to improve within 2 yrs after
reduction
Persistent dysplasia after 5 yrs of age

Likely hood of Degenerative osteoarthritis high

For 2 – 9 yrs of age
(< 2 yrs – not enough iliac wings that are thick enough to
support bone graft,
> 9 yrs – acetabular fragment not adequately mobilized.

Improves Acetabular index by avg 10°.
Salter Innominate Osteotomy
Salter Innominate Osteotomy
Pemberton’s Acetabuloplasty


Improves anterior and lateral coverage of femoral head

Stable osteotomy, does not require Internal Fixation

Hinges through triradiate cartilage, reduces the volume
of acetabulum

Contraindicated if acetabulum is small relative to femoral
head.

Complication
         Closure of triradiate cartilage (very rare)
         Damage to acetabular growth areas if
         osteotomy too close to acetabulum
Pemberton’s Acetabuloplasty
Pemberton’s Acetabuloplasty



                    6-year-old child underwent
                    open reduction with
                    capsular placation, femoral
                    shortening, and a pelvic
                    (Pemberton) osteotomy.
Dega Osteotomy

Increases acetabular coverage anteriorly, centrally and posteriorly.

Placement of wedges determine the areas of coverage to be improved
Dega Osteotomy




Residual acetabular
dysplasia on right
side.
Steel Triple Osteotomy


Osteotomies through ilium and both pubic rami.

Increases anterolateral coverage
(More than Salter)
Chiari Osteotomy

Used when other procedures cannot
achieve a concentric reduction of hip.

Controlled fracture through ilium with
medial displacement of acetabular
fragment and the intact hip capsule
under the ilium.

Over time the hip capsule converts into
fibrocartilage and becomes the new
acetabular coverage.

A Salvage surgery
Chiari Osteotomy
Shelf Operations
Slotted Acetabular
Augmentation (Staheli)
Staheli Acetabular Augmentation
DEVELOPMENTAL DYSPLASIA
        OF HIP


        TREATMENT

        > 8 YEARS
If Femoral head cannot be repositioned distally to the level of Acetabulum
         Palliative Salvage Surgeries
         Rarely, Femoral shortening + Pelvic Osteotomy

Degenerative Arthritic Painful Hip
        Total Hip Replacement

Role of Arthrodesis
          Rarely used now for old unreduced dislocations
          Contraindicated in bilateral dislocations

Bilateral Dislocations
          Leave hip unreduced
          Later do THR

Reduced hip but painful acetabular dysplasia
        Pelvic osteotomy
DEVELOPMENTAL DYSPLASIA
        OF HIP


      COMPLICATIONS
Complications



Avascular Necrosis of Femoral Head

Trochanteric overgrowth

Inadequate Reduction and Redislocation

Residual Acetabular Dysplasia

Acetabular dysplasia Presenting late
Avascular Necrosis
THANK YOU

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DDH

  • 1. Department of Orthopaedics AFMC, Pune PG SEMINAR DEVELOPMENTAL DYSPLASIA OF HIP Maj Rohit Vikas Resident
  • 2. CDH/ DDH Instability of the hip in the newborn Includes Dislocatable hips Acetabular dysplasia Subluxation of femoral head Dislocated Femoral head As the child grows it may Progress to dislocation or poor acetabular coverage Secondary changes develop in head and acetabulum Process is not restricted to congenital abnormalities of the hip, and includes some hips that were normal at birth and subsequently became abnormal.
  • 3. DEVELOPMENTAL DYSPLASIA OF HIP DEFINITIONS
  • 4. Which is an Unstable Hip? Positive Barlow/ Ortolani Tests Clinically stable but abnormal USG Acetabular Index Lateral displacement of femoral beak in relation to Perkin’s line
  • 5. What is Dysplasia? Radiographic finding Increased obliquity of acetabulum Loss of acetabular concavity Intact Shenton line
  • 6. What is Subluxation? Femoral head not fully in contact with acetabulum Widened Teardrop – femoral head distance Reduced CE angle Break in Shenton line Dysplastic changes in acetabulum
  • 7. What is Dislocation? Femoral head not in contact with acetabulum Dysplastic changes in acetabulum
  • 8. Teratologic / Antenatal Dislocations Fixed dislocation at birth with limited range of motion at hip During gestation the hip is at risk of dislocation during the 12th week when the lower limb rotates medially, during the 18th week as the hip muscles develop. Dislocations during these developmental stages are termed teratologic and are the result of congenital abnormal neuromuscular development. Treatment unsuccessful Open Reduction at 6 months of age
  • 9. Secondary Hip Dysplasia Strictly, DDH applies to idiopathic hip dysplasia Secondary Hip dysplasia Neurological conditions Myelomeningocele Cerebral palsy Connective tissue diseases Ehlers-Danlos syndrome Myopathic disorders Arthrogryposis multiplex congenita.
  • 10. DEVELOPMENTAL DYSPLASIA OF HIP ETIOPATHOGENESIS
  • 11. INCIDENCE Breech delivery Frank Breech 20% incidence of DDH Left hip > Bilateral > Right hip Complete or Lowry, et al, showed that breech infants footling breech delivered by elective caesarean section (pre- lower incidence labor) had a lower incidence of DDH than of DDH (2%) those breech babies delivered vaginally
  • 12. ASSOCIATED CONDITIONS Other positional abnormalities including: Torticollis (20%) Metatarsus adductus (10%) Positional club foot Congenital Knee dislocation
  • 13. THEORIES Mechanical factors Hormone induced ligamentous laxity Primary acetabular dysplasia Genetic inheritance
  • 14. DEVELOPMENTAL DYSPLASIA OF HIP CLINICAL DETECTION OF DDH BIRTH TO 6 MONTHS
  • 15. Asymmetrical Thigh Folds Indicative of Abnormal hips Also seen in infants with normal hips Widened perineum Prominent Greater trochanter
  • 16. Galeazzi’s / Allis sign Limited Abduction In bilateral hip abnormality, asymmetry may not be a feature
  • 17. Ortolani’s sign (Ortolani 1937, 1976). Hold the knees and abduct the hip while lifting up on the greater trochanter A positive test is feeling the dislocated hip clunk into the acetabulum
  • 18. Barlow’s Provocative Test (Barlow,1962) Adduct and push posteriorly on the hip A positive test is feeling the hip push out of the acetabulum
  • 19. Klisic sign in bilateral DDH The Ortolani and Barlow manoeuvres are the mainstay of clinical diagnosis in the first months of life Even in the best hands physical examination can fail to detect DDH, and after 3 months of age the Ortolani and Barlow tests become negative due to progressive soft tissue contractures.
  • 20. DEVELOPMENTAL DYSPLASIA OF HIP CLINICAL DETECTION OF DDH OLDER CHILD
  • 21. Abduction becomes more limited which is particularly noticeable when there is unilateral disease. Femoral shortening (positive Galeazzi test) may be apparent but this can be difficult to appreciate with bilateral disease. Ambulatory children will have a Trendelenburg gait in addition to limited hip abduction Trendelenburg sign Telescopy positive Exaggerated lumbar lordosis
  • 22. DEVELOPMENTAL DYSPLASIA OF HIP NATURAL HISTORY
  • 23. What happens to a Dysplastic hip without subluxation ? Usually become painful Degenerative Arthritis over time Often subluxate as degeneration progresses Hips with Acetabular index > 35 will likely require hip replacement later If these hips are well reduced after primary treatment of DDH, with a greater than normal CE angle, risk of Degenerative arthritis decreases
  • 24. What happens to a Subluxated hip? Always lead to symptomatic degenerative arthritis Rapid progression Severe subluxation – symptoms in 2nd decade Moderate subluxation – in 3rd to 4th decade Mild subluxation – in 5th to 6th decade
  • 25. What happens to a completely dislocated hip? Symptoms much later than a subluxated hip May never become painful False acetabulum False acetabulum
  • 26. Consequences of Persistent Dysplasia Abnormal gait Restricted abduction Reduced strength Increased rate of degenerative joint disease. Outcome of untreated unilateral DDH is less favorable compared with bilateral disease Limb length discrepancy, Asymmetrical movement, strength Ipsilateral valgus knee. Degenerative joint disease tends to present earlier in subluxated hips than in dysplastic hips without subluxation
  • 27. Natural History Over the age of 6 months spontaneous resolution of dysplasia is unlikely Usually more aggressive treatment is required compared with younger children. Older children tend to have more advanced changes in the soft tissues and bony structures. Changes in acetabulum Ossification is delayed Shallow, Anteverted Deficient anterolaterally. Changes in Femoral Head Delayed ossification Exaggerated femoral anteversion.
  • 28. Natural History A 16y /F with longstanding “missed” left DDH. The left femoral head articulates with a neo-acetabulum in the iliac bone. The left femoral shaft is reduced in diameter and there is wasting of the thigh muscles
  • 31. DEVELOPMENTAL DYSPLASIA OF HIP PLAIN RADIOLOGY
  • 32. Normal Hip Perkins’ line acetabular index Hilgenreiner’s line Shenton’s line
  • 33. Normal Hip Acetabular index Angle between the acetabulum and hilgenreiner’s line It should be < 30 degrees in a newborn Center-edge angle of Wiberg Cannot be measured until the ossific nucleus appears Normal is > 10 degrees in children 6- 13 yrs
  • 34. DDH Ossification centre Head of femur 2 and 7 months
  • 35. DDH 8 month /F with left DDH. Left acetabulum is shallow and the hip is dislocated. Left proximal femoral ossification centre is small compared with the normal right side. The normal right acetabulum has a central depression and well-defined lateral edge. The acetabular teardrop is developing on the right but not on the dysplastic left side
  • 36. DEVELOPMENTAL DYSPLASIA OF HIP ULTRASOUND
  • 37. L β Iliac Wing Femoral Head α T Bony Diagram showing hip anatomy on standard coronal US plane and lines Acetabular used to evaluate hip dysplasia using the Graf method. roof Femoral head (FH) is centred over the hypoechoic triradiate cartilage (T). The promontory is at the junction of the iliac wing (IL) and the bony acetabular roof (A). L, labrum. The alpha angle reflects the depth of the bony acetabular roof and is Standard coronal ultrasound of the normal formed by the intersection of the baseline (BL) and acetabular roof infant hip joint. The promontory is sharply line (AL). In a normal mature hip the alpha angle is greater than 60°. defined and the bony acetabular roof is The beta angle reflects cartilaginous coverage and is formed by the steep. The ossification centre for the femoral intersection of the baseline with the labral line (LL). A normal beta head has not yet developed angle is less than 55°
  • 39. DEVELOPMENTAL DYSPLASIA OF HIP ARTHROGRAPHY
  • 40. Not routinely performed Either performed before surgery or intraoperatively. Goal of arthrography in DDH is to demonstrate the position of the femoral head with respect to other joint structures both at rest and during reduction or stress manoeuvres It also outlines any deformities or obstructions to concentric reduction Inverted limbus, Capsular constriction, Pulvinar Hypertrophy Hypertrophied ligamentum teres
  • 41. Arthrogram, made after fifteen days of overhead traction, showing the hip to be reduced. A square- shaped limbus (arrow) at the superior pole of the epiphysis and marked capsular distension are evident.
  • 42. DEVELOPMENTAL DYSPLASIA OF HIP COMPUTED TOMOGRAPHY
  • 43. Two main indications for CT in DDH: To document hip reduction post- operatively if a child is placed in a spica cast Pre-operative planning in severely dysplastic hips that require corrective procedures. Axial CT scan following open reduction of the left hip. The left femoral metaphysis is not aligned with the acetabulum and the femoral head is displaced posteriorly. The spica cast was removed and patient underwent further manipulation under anaesthesia to achieve successful reduction
  • 45. Distinct advantages over both CT and arthrography in pre-operative imaging in patients with DDH. Ability to differentiate between different types of soft tissue which enables visualisation of unossified cartilage, ligaments, fat, muscle and fluid including those soft tissues that present an obstruction to concentric reduction such as pulvinar, the labrum and joint capsule. Lack of ionising radiation MR imaging is more time-consuming than CT or arthrography. In newborns and infants sedation may be required, except if patents are in a spica cast since this limits movement. The main disadvantages of MR imaging is increased cost and limited availability
  • 46. DEVELOPMENTAL DYSPLASIA OF HIP SCREENING
  • 47. General Examination -Plagiocephaly, -Sternomastoid Tumour (Torticollis), -Feet for any congenital deformity
  • 48. Hip Examination Barlow’s test (<3-4 months of age) Ortolani’s test (<3-4 months of age) Limitation of Abduction Leg length discrepancy (Galleazi test) Asymmetry of thigh folds Limp in a walking child
  • 49. Radiology Children <6 months - Ultrasound using Graf classification system Class Alpha angle Description I >60 Normal II 60-43 Immature/Dysplastic III <43 Subluxed/Dislocated IV Unmeasurable Dislocated Children >6 months - Xrays.
  • 50. Criteria for Screening Clinical Screening for all neonates for Hip Instability. Careful screening for infants with risk factors: Family history of DDH Breech Torticollis Metatarsus adductus Oligohydomnios Screening with USG Controversial As per AAP guidelines Female infants delivered breech Family history of DDH +
  • 51. DEVELOPMENTAL DYSPLASIA OF HIP TREATMENT BIRTH – 6 MONTHS
  • 52. DEVELOPMENTAL DYSPLASIA OF HIP PAVLIK HARNESS
  • 53. Indications All Dislocated hip that can be reduced (Ortolani’s sign) Start harness at the time of diagnosis Hips that are located but can be subluxated (Barlow’s sign) Some may spontaneously stabilize, some may dislocate. Re-examine after few weeks before starting treatment Hips that are normal on clinical examination but abnormal on USG Close observation Repeat USG at 6 weeks of age Abnormal hips treated Graf II hips more likely to improve without treatment than Graf III/ IV hips Irreducible hips Likely to fail treatment if initial coverage was < 20%
  • 54. Application Flexion – 120° Hyper flexion Femoral nerve palsy Inferior dislocation of head Inadequate flexion < 90° Fails to reduce hip Abduction by gravity 1 4 3 2
  • 55. Follow Up Weekly Follow up during harness treatment Change size after 3-4 weeks USG at 3-4 weeks If unreduced – discontinue treatment Examine under anaesthesia Arthrogram for cause of instability If hip reduced but can be dislocated Continue harness for 3-6 more weeks After 6 weeks of harness – USG with child out of harness. If reduced head – Wean/ discontinue harness X rays at 3-4 months X rays at 1 yr Annual Follow up Follow up till skeletal maturity (Late asymmetric epiphyseal closure – valgus femoral head and reduced coverage Acetabular dysplasia in 20%)
  • 56. Problems in Harness If reduction not achieved with harness in 3 – 4 weeks then discontinue harness and other treatment started. PAVLIK DISEASE Prolonged positioning of dislocated hip in flexion and abduction Dysplasia increased - Flattening of posterior acetabulum Open reduction needed Femoral nerve palsy
  • 57. DEVELOPMENTAL DYSPLASIA OF HIP TREATMENT 6 – 18 MONTHS
  • 58. Goal of Treatment Obtain and maintain reduction without damaging femoral head Closed Reduction Open Reduction Problems Risk of Avascular Necrosis Growth potential of acetabulum declines with age (and hence remodelling potential)
  • 59. Role of Pre Reduction Traction Reduced risk of Avascular Necrosis 30% without Traction 15% with prereduction traction < 5% in Human position (flexion 90 and mild abduction) Reduced need for Open reduction Portable Home Traction for 2 – 3 weeks
  • 60. Role of Pre Reduction Traction Bryant’s Traction
  • 61. Closed Reduction Gentle positioning Determine Stability – Wider Zones of Safety
  • 62. Adductor Tenotomy Increases the Zones of Safety by allowing wider range of abduction
  • 63. Hip Spica Cast Flexion > 90 Abduction 30 – 40 acceptable as long as further abduction possible Slight internal rotation (10 – 15)
  • 64. Hip Spica Cast Intraop radiograph Confirm reduction – USG/ CT Scan MRI – reduction and vascular status of head can both be assessed Remove cast after 6 weeks under anesthesia Assess stability through moderate range of motion/ do not dislocate. Xray AP pelvis to confirm reduction Reapply second cast for 6 weeks. Third cast/ Abduction splinting Usually applied for 6 more weeks and discontinue immobilization
  • 65. Obstacles to Reduction • Extra- articular – Iliopsoas tendon – adductors • Intra-articular – inverted hypertrophic labrum – tranverse acetabular ligament – pulvinar, ligamentum teres – constricted anteromedial capsule espec in late cases • neolimbus is not an obstacle to reduction and represents epiphyseal cartilage that must not be removed as this impairs acetabular development
  • 66. Open Reduction +/- Capsulorrhaphy For unstable hips Widened joint space Approaches Medial Approch v/s Anterior approach Minimum dissection Better exposure Obstructions approached directly Capsulorrhaphy can be performed Limited exposure Medial femoral Cx Artery < 1 yr of age in older children
  • 67. Open Reduction + Femoral Shortening If there is excessive pressure on femoral head when it is reduced Consider in a dislocated hip in > 2 yrs age To correct excessive anteversion To place femoral head into Varus position Intertrochanteric/ Subtrochanteric osteotomy
  • 68. Open Reduction + Innominate Osteotomy If there is need for added coverage Assess need: Hip in extension – neutral rotation – abduction If > 30% head visible then innominate osteotomy required Innominate osteotomy in > 18 months. Salter / Pemberton Consider femoral shortening for excessive pressure on head
  • 69. DEVELOPMENTAL DYSPLASIA OF HIP TREATMENT 18 – 36 MONTHS
  • 70. Open Reduction Evaluate stability of hip during open reduction Assess need for added coverage Salter/ Pemberton pelvic osteotomy For Children > 3 yrs, usually an acetabular procedure is needed to cover femoral head adequately
  • 72. DEVELOPMENTAL DYSPLASIA OF HIP TREATMENT 3 – 8 YEARS
  • 73. Problems Proximal head location Contracted muscles Femoral shortening required, greater shortening required for higher dislocations Primary acetabular repositioning osteotomy often needed Salter/ Pemberton In > 3 yr, an acetabular procedure needed to adequately cover the head
  • 74. Open Reduction Upper age for Successful Reduction Unilateral dislocations Open reduction should be attempted till 9 – 10 yrs of age Gait asymmetry Bilateral dislocations Upto 8 yrs Increased complication if both hips reduced Natural outcome of untreated B/L Dislocation better than results of treatment
  • 75. PELVIC OSTEOTOMIES Simple osteotomies that Reposition the Acetabulum Salter Innominate Ostetomy Pemberton’s Acetabuloplasty Dega Osteotomy Complex Osteotomies that Reposition the Acetabulum Steel osteotomy Tonnis Osteotomy Ganz Osteotomy Spherical Acetabular osteotomy Osteotomies that Augment the Acetabulum Chiari Osteotomy Shelf Procedures Staheli Slotted Acetabular Augmentation
  • 77. Salter Innominate Osteotomy Prerequisite – concentrically reduced hip Acetabular dysplasia Failure of acetabular index to improve within 2 yrs after reduction Persistent dysplasia after 5 yrs of age Likely hood of Degenerative osteoarthritis high For 2 – 9 yrs of age (< 2 yrs – not enough iliac wings that are thick enough to support bone graft, > 9 yrs – acetabular fragment not adequately mobilized. Improves Acetabular index by avg 10°.
  • 80. Pemberton’s Acetabuloplasty Improves anterior and lateral coverage of femoral head Stable osteotomy, does not require Internal Fixation Hinges through triradiate cartilage, reduces the volume of acetabulum Contraindicated if acetabulum is small relative to femoral head. Complication Closure of triradiate cartilage (very rare) Damage to acetabular growth areas if osteotomy too close to acetabulum
  • 82. Pemberton’s Acetabuloplasty 6-year-old child underwent open reduction with capsular placation, femoral shortening, and a pelvic (Pemberton) osteotomy.
  • 83. Dega Osteotomy Increases acetabular coverage anteriorly, centrally and posteriorly. Placement of wedges determine the areas of coverage to be improved
  • 85. Steel Triple Osteotomy Osteotomies through ilium and both pubic rami. Increases anterolateral coverage (More than Salter)
  • 86. Chiari Osteotomy Used when other procedures cannot achieve a concentric reduction of hip. Controlled fracture through ilium with medial displacement of acetabular fragment and the intact hip capsule under the ilium. Over time the hip capsule converts into fibrocartilage and becomes the new acetabular coverage. A Salvage surgery
  • 90. DEVELOPMENTAL DYSPLASIA OF HIP TREATMENT > 8 YEARS
  • 91. If Femoral head cannot be repositioned distally to the level of Acetabulum Palliative Salvage Surgeries Rarely, Femoral shortening + Pelvic Osteotomy Degenerative Arthritic Painful Hip Total Hip Replacement Role of Arthrodesis Rarely used now for old unreduced dislocations Contraindicated in bilateral dislocations Bilateral Dislocations Leave hip unreduced Later do THR Reduced hip but painful acetabular dysplasia Pelvic osteotomy
  • 92. DEVELOPMENTAL DYSPLASIA OF HIP COMPLICATIONS
  • 93. Complications Avascular Necrosis of Femoral Head Trochanteric overgrowth Inadequate Reduction and Redislocation Residual Acetabular Dysplasia Acetabular dysplasia Presenting late