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Local revision copy · not clinical advice

Combined Paed

Topic 16 · slides 494–510 · 17 slides · 124 questions
17 slides
▸ Slide 494 · Combined - PaedCombined Paed · 2 questions expand
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slide 494
Question list
Q1-Q22 questions — tap to reveal all answerslist
  1. What does the paediatric combined session cover?
  2. Which paediatric orthopaedic conditions are examinable in this section?
Answers · Q & A
Q1.What does the paediatric combined session cover?
  • Not covered in the speaker notes
Q2.Which paediatric orthopaedic conditions are examinable in this section?
  • Not covered in the speaker notes
▸ Slide 495 · HipCombined Paed · 2 questions expand
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slide 495
Question list
Q1-Q22 questions — tap to reveal all answerslist
  1. What are the common paediatric hip conditions?
  2. How is the paediatric hip assessed clinically?
Answers · Q & A
Q1.What are the common paediatric hip conditions?
  • Not covered in the speaker notes
Q2.How is the paediatric hip assessed clinically?
  • Not covered in the speaker notes
▸ Slide 496 · Overall treatment principle:Combined Paed · 11 questions expand
slide 496
Question list
Q1-Q1111 questions — tap to reveal all answerslist
  1. What is the overall treatment principle for DDH by age?
  2. What are the risk factors and history features of DDH?
  3. How do Ortolani and Barlow tests differ?
  4. What is Klisic sign?
  5. What is the evidence on universal ultrasound screening for DDH?
  6. What are the reported test performances in DDH?
  7. What clinical signs in the photographs suggest DDH?
  8. What associated conditions are seen with DDH?
  9. How is a subluxable or dislocated hip managed in the first weeks of life?
  10. What is the proposed aetiology of DDH?
  11. What are the Wilson and Jungner (1968) criteria for a screening programme?
Answers · Q & A
Q1.What is the overall treatment principle for DDH by age?
  • < 6 months: Pavlik harness
  • Teratogenic irreducible: CR + arthrogram at 4 months
  • 6-18 months or < 6 months failing Pavlik: arthrogram + closed reduction or open reduction
  • > 18 months: open reduction +/- secondary femoral and acetabular procedures
Q2.What are the risk factors and history features of DDH?
  • Family history, first born, female, breech, oligohydramnios, twin
Q3.How do Ortolani and Barlow tests differ?
  • Ortolani: tests whether the hip is reducible, by elevation and abduction of the flexed femur
  • Barlow: tests whether the hip is subluxable, by adduction and depression of the flexed femur
Q4.What is Klisic sign?
  • Connect greater trochanter to ASIS
  • Normal if the line points at or above the umbilicus
Q5.What is the evidence on universal ultrasound screening for DDH?
  • Low sensitivity (89%) and poor PPV (62%) leading to overdiagnosis and overtreatment
  • Does not meet the WHO/Wilson and Jungner criteria for universal screening
  • 2002 JBJS Norwegian group: universal missed 1 case, selective missed 5, no significant difference
  • 2009 JBJS international hip dysplasia institute study: selective screening most cost effective
Q6.What are the reported test performances in DDH?
  • USG (static and dynamic): sensitivity/specificity ~90%
  • Ortolani/Barlow: sensitivity 70%, specificity 100% in experienced hands
Q7.What clinical signs in the photographs suggest DDH?
  • Asymmetrical proximal skin crease
  • Limited abduction of the left thigh
  • Galeazzi test shows left femur shortening
  • These findings raise suspicion of DDH
Q8.What associated conditions are seen with DDH?
  • Torticollis, congenital recurvatum/knee dislocation
  • Calcaneovalgus feet, clubfoot, metatarsus adductus
  • Older child: waddling gait with hyperlordosis of the lumbar spine
Q9.How is a subluxable or dislocated hip managed in the first weeks of life?
  • Subluxable <2week can be physiological: double napkin
  • Dislocated and reducible, or subluxable > 2 weeks: Pavlik harness
  • Dislocated and not reducible: can still try PH x 1 mth
Q10.What is the proposed aetiology of DDH?
  • Genetic
  • Mechanical: breech + knee in extension (strong hamstring action on hip)
  • Maternal hormone: ligament laxity, especially in the female fetus
  • More common over the left side
Q11.What are the Wilson and Jungner (1968) criteria for a screening programme?
  • Disease: important health issue, high enough prevalence, natural history known, early treatment better
  • Test: accepted by patient, high sensitivity, available facilities, cost effective
  • Population: accepted and effective treatment; willing to undergo further evaluation/treatment
  • USG screening for DDH has low sensitivity (89%) and poor PPV (62%), causing overdiagnosis
▸ Slide 497 · What is the use of USG?Combined Paed · 5 questions expand
slide 497
Question list
Q1-Q55 questions — tap to reveal all answerslist
  1. What is the use of ultrasound in DDH?
  2. How do you interpret a hip ultrasound?
  3. What is the alpha angle and its normal value?
  4. What is the beta angle and its normal value?
  5. What is the Graf ultrasound classification?
Answers · Q & A
Q1.What is the use of ultrasound in DDH?
  • Confirm reduction
  • Baseline of alpha and beta angles
  • Perform within 2 weeks of starting Pavlik harness
Q2.How do you interpret a hip ultrasound?
  • Identify landmarks: ilium, bony acetabulum, labrum, femoral head
  • Confirm concentric reduction
  • Assess coverage: > 50% in vs < 50% in; labrum pointing upwards vs inwards
  • Measure alpha and beta angles
Q3.What is the alpha angle and its normal value?
  • Angle between the ilium and bony acetabulum
  • Normal > 60 degrees
Q4.What is the beta angle and its normal value?
  • Angle between the ilium and labrum
  • Normal < 55 degrees
Q5.What is the Graf ultrasound classification?
  • I: alpha > 60
  • II: alpha 43-60 (ABCD), C = critical zone hip, D = decentered (beta > 77)
  • III: alpha < 43
  • IV: alpha < 43 + interposed labrum
  • Harcke = dynamic USG measurement
▸ Slide 498 · GrafCombined Paed · 3 questions expand
slide 498
Question list
Q1-Q33 questions — tap to reveal all answerslist
  1. On static USG, how is the alpha angle used to guide DDH treatment?
  2. What are the two angles measured on static ultrasound?
  3. What is dynamic USG (Harcke)?
Answers · Q & A
Q1.On static USG, how is the alpha angle used to guide DDH treatment?
  • I: > 60 normal, no treatment needed
  • IIA and IIB: 50-59
  • < 3 months: follow up with USG
  • > 3 months: Pavlik harness
  • IIC: < 50: start Pavlik harness
Q2.What are the two angles measured on static ultrasound?
  • Alpha angle and beta angle
  • They represent femoral head coverage
Q3.What is dynamic USG (Harcke)?
  • Dynamic ultrasound technique
  • Visualises the Barlow test
▸ Slide 499 · What is Pavlik harness?Combined Paed · 13 questions expand
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slide 499
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Q1-Q1313 questions — tap to reveal all answerslist
  1. What is a Pavlik harness and when is it used?
  2. What are the indications for a Pavlik harness?
  3. Describe the parts and application of the Pavlik harness.
  4. What advice is given to parents on the Pavlik harness?
  5. What is the timing of follow-up and ultrasound in Pavlik harness treatment?
  6. What are the complications of Pavlik harness treatment?
  7. What is the aim of treatment with a Pavlik harness?
  8. What is the application sequence of the Pavlik harness?
  9. What is assessed at follow-up during Pavlik harness treatment?
  10. What are the risk factors for Pavlik harness failure?
  11. What is the Pavlik harness success rate and the supporting study?
  12. What is Pavlik harness disease?
  13. What are the human and frog positions in an abduction brace?
Answers · Q & A
Q1.What is a Pavlik harness and when is it used?
  • Dynamic corrective orthosis maintaining flexion and preventing adduction to keep the hip reduced for dynamic remodelling
  • Use up to 6 months old
  • 90% success in < 3 month old presentation
  • Other abduction brace: von Rosen splint
Q2.What are the indications for a Pavlik harness?
  • Ortolani positive
  • Barlow positive at 6 weeks
  • Fracture femur
Q3.Describe the parts and application of the Pavlik harness.
  • Chest strap at nipple line (can place hand in between)
  • Shoulder straps at anterior axillary line
  • Stirrup at popliteal fossa (not too distal or else knee hyperflexion)
  • AM strap maintains 100 degrees flexion, along anterior axillary line
  • PL strap prevents adduction; knees able to come together but not touch
Q4.What advice is given to parents on the Pavlik harness?
  • Tighten till markers; keep two sets, one for washing
  • Assess kicking of leg and upper limb movement (brachial plexus)
  • Change napkin in the harness; sponge bath and dry completely
  • No self adjustment; regular P&O and ortho follow-up
Q5.What is the timing of follow-up and ultrasound in Pavlik harness treatment?
  • Continue until hip stable clinically and radiologically (~6 weeks) + 6 weeks
  • USG: within 2 weeks of starting, at the end of the 1st 6 weeks, and before stopping the harness
Q6.What are the complications of Pavlik harness treatment?
  • Failure of reduction: inferior dislocation (too much flexion), Pavlik harness disease (splintage in incongruent reduction > 1mth)
  • AVN (too much abduction) ~2.4%
  • Femoral nerve palsy (too much flexion) ~2.5%; if persisting beyond 3 days, probability of success only 30%
  • Murnaghan JBJS 2011: adjust or temporarily suspend, do not completely abandon the harness
Q7.What is the aim of treatment with a Pavlik harness?
  • Maintain a stable concentric reduction
  • Promote normal growth of the femoral head and acetabulum
Q8.What is the application sequence of the Pavlik harness?
  • Supine; fasten the chest strap first
  • Fasten the shoulder straps to keep the chest strap at the nipple line
  • Feet into the stirrups one by one
  • Fasten AM strap to flex the hip
  • PL strap last
Q9.What is assessed at follow-up during Pavlik harness treatment?
  • Confirm concentric reduction clinically and radiologically
  • Adjust size and tension (mainly chest strap and PL strap)
  • Compliance
  • Complications: loss of reduction, nerve palsy
Q10.What are the risk factors for Pavlik harness failure?
  • Graf type IV or radiographically dislocated hips
  • Treatment after 3 months of age; non-visible ossific nucleus at start
  • Prolonged duration of treatment; significant adductor contracture
  • Bilateral disease, low alpha angle, femoral head coverage < 20%
  • Initial irreducibility, advanced age, poor parental compliance
  • Larger patients are also at risk
Q11.What is the Pavlik harness success rate and the supporting study?
  • 85-95% (Omeroglu, Turkey, CORR 2016)
  • 90% success in presentation < 3 months old
Q12.What is Pavlik harness disease?
  • Hip not reduced in the harness causing superior acetabular erosion
  • Occurs with splintage in incongruent reduction > 1mth
Q13.What are the human and frog positions in an abduction brace?
  • Human position: 95 deg flexion, 45 deg abduction
  • Frog position: extreme flexion and abduction
▸ Slide 500 · Presentation 6-18mthsCombined Paed · 9 questions expand
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Q1-Q99 questions — tap to reveal all answerslist
  1. Describe the X-ray measurements used in DDH at 6-18 months.
  2. What is the Tonnis grading of DDH?
  3. What is the treatment sequence for DDH presenting at 6-18 months?
  4. How is a hip spica cast applied?
  5. What examination findings are relevant in late-presenting DDH?
  6. What acetabular morphology should be assessed on the DDH X-ray?
  7. What is the caution when measuring acetabular angles?
  8. What history should be revisited in late-presenting DDH?
  9. What additional X-ray view is needed in DDH?
Answers · Q & A
Q1.Describe the X-ray measurements used in DDH at 6-18 months.
  • Hilgenreiner's line: horizontal line through superior edge of triradiate cartilage
  • Perkin's line: perpendicular to Hilgenreiner's line at lateral acetabular roof
  • Quadrants and Shenton's line
  • Acetabular index: < 2 yo < 30 deg, > 2 yo < 20 deg (take < 25 deg)
Q2.What is the Tonnis grading of DDH?
  • I: below SL margin of acetabulum (SMA), medial to Perkin's line
  • II: below SMA line, lateral to Perkin's line
  • III: at the level of the SMA line
  • IV: above the SMA line
Q3.What is the treatment sequence for DDH presenting at 6-18 months?
  • GA, gentle closed reduction with flexion, traction, abduction
  • Determine Ramsey safety zone (cut off 40 degrees)
  • Adductor tenotomy first to reduce intracapsular pressure
  • Arthrogram, +/- open reduction, hip spica cast
  • Postop CT to assess AP congruency
Q4.How is a hip spica cast applied?
  • Spica table; folded towel over anterior chest
  • Stockinette over torso, cotton/gore-tex wrap, felt over bony prominences
  • Apply in human position: 100 flexion 50 degree abduction
  • 6 weeks, then another 6 weeks in human position, then removable abduction brace for 6 weeks
Q5.What examination findings are relevant in late-presenting DDH?
  • Asymmetric groin crease, LLD, Galeazzi test
  • Barlow and Ortolani not relevant at this age
  • Examine for packaging disorders: torticollis, clubfoot, metatarsus adductus
  • Look for neuromuscular conditions e.g. spina bifida, arthrogryposis, CP
  • Document NV status
Q6.What acetabular morphology should be assessed on the DDH X-ray?
  • Tear drop morphology (internal and external acetabular wall)
  • Acetabular index varies with age: < 2 yo < 30 deg, > 2 yo < 20 deg (take < 25 deg)
  • Small femoral ossification centre
Q7.What is the caution when measuring acetabular angles?
  • Do not mix up acetabular angle (of Sharp) and acetabular index
  • AA = adult whole acetabulum, ~45 degrees
  • AI = measured from Hilgenreiner's line, ~25 degrees
Q8.What history should be revisited in late-presenting DDH?
  • Birth history and breech presentation
  • First born child, family history
  • Other perinatal complications
Q9.What additional X-ray view is needed in DDH?
  • Von Rosen views
▸ Slide 501 · IHDI classification XR for DDHCombined Paed · 2 questions expand
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Q1-Q22 questions — tap to reveal all answerslist
  1. What is the IHDI classification used for in DDH?
  2. What are the grades of the IHDI X-ray classification for DDH?
Answers · Q & A
Q1.What is the IHDI classification used for in DDH?
  • Not covered in the speaker notes
Q2.What are the grades of the IHDI X-ray classification for DDH?
  • Not covered in the speaker notes
▸ Slide 502 · Use of arthrogramCombined Paed · 7 questions expand
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slide 502
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Q1-Q77 questions — tap to reveal all answerslist
  1. What is the use of an arthrogram in DDH?
  2. How is an arthrogram performed?
  3. What structures can obscure reduction?
  4. What is the safe zone?
  5. When can a closed reduction be accepted and casted?
  6. What additional procedures may be required during reduction, and what are the risks?
  7. What two factors determine hip positioning in the spica cast?
Answers · Q & A
Q1.What is the use of an arthrogram in DDH?
  • Assess congruency of reduction
  • Define obstacles to reduction
  • Delineate optimal position for immobilization
Q2.How is an arthrogram performed?
  • GA, supine, with X-ray control
  • Closed reduction first
  • Medial sub adductor approach, aiming for ipsilateral scapula
  • 22 gauge needle; inject normal saline and look for back flow, then dye to confirm position
  • Image at dislocated and reduced positions
  • Risks: cartilage damage, injection into growth plate, vessel injury
Q3.What structures can obscure reduction?
  • Intracapsular superior: inverted labrum, neolimbus
  • Intracapsular central: pulvinar, ligamentum teres
  • Intracapsular inferior: transverse acetabular ligament, constricted capsule
  • Extracapsular: tight iliopsoas, tight adductor
Q4.What is the safe zone?
  • Difference (in degrees) between the angle of maximal hip abduction (causes AVN) and the hip adduction at which the femoral head dislocates, with hip examined in 90 deg flexion
  • Safety cone lies within 15-20 degree of maximal ROM and dislocation range; satisfactory if at least 40 degrees
Q5.When can a closed reduction be accepted and casted?
  • Successful reduction with <7mm medial pooling
  • Check range with stable reduction
  • Congruent reduction with safety zone larger than 40 deg
  • Hip spica cast + 1 axial cut CT to rule out posterior dislocation
  • Otherwise, open reduction
Q6.What additional procedures may be required during reduction, and what are the risks?
  • Adductor tenotomy if post-reduction safe zone is narrow
  • Psoas tendon release if the hip tends to sublux as it is extended below 90 degrees
  • Risk: injury to the anterior division of the obturator nerve
Q7.What two factors determine hip positioning in the spica cast?
  • Average hip movement in the spica is 15 degrees, so keep the hip ~20 degrees away from the line of dislocation
  • Risk of AVN increases at maximum ROM, so stay 20 degrees inside the maximum ROM
▸ Slide 503 · Normal arthrogramCombined Paed · 3 questions expand
slide 503
Question list
Q1-Q33 questions — tap to reveal all answerslist
  1. What are the abnormal arthrogram findings in DDH?
  2. What does absence of the rose thorn sign indicate?
  3. What is done after a successful reduction on arthrogram?
Answers · Q & A
Q1.What are the abnormal arthrogram findings in DDH?
  • Medial pooling > 7 mm
  • Hourglass constriction of capsule by tight iliopsoas
  • Hypertrophied ligamentum teres (head linear defect)
  • Pulvinar fat and transverse acetabular ligament
  • Inverted labrum (absent rose thorn sign)
Q2.What does absence of the rose thorn sign indicate?
  • Inverted labrum
Q3.What is done after a successful reduction on arthrogram?
  • Spica cast
  • Confirm with single cut CT
  • Change cast every 6 weeks x 3 months
▸ Slide 504 · Open reductionCombined Paed · 8 questions expand
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Q1-Q88 questions — tap to reveal all answerslist
  1. What are the indications for an anterior open reduction?
  2. What are the advantages and disadvantages of the anterior approach?
  3. What are the key steps of the anterior approach?
  4. What are the advantages and disadvantages of the medial approach?
  5. What are the dissection planes of the medial approach?
  6. What structures are at risk in the medial approach?
  7. How is the medial approach performed?
  8. What is the innervation of the medial compartment of the thigh?
Answers · Q & A
Q1.What are the indications for an anterior open reduction?
  • High and chronic dislocations with femoral head stuck to ilium (> 1-1.5 yo)
  • Perform capsulorrhaphy for very unstable hips
  • Plan acetabuloplasty
Q2.What are the advantages and disadvantages of the anterior approach?
  • Advantages: good exposure, can do capsulorrhaphy, can reduce highly dislocated hip
  • Disadvantages: large wound, more bleeding
  • Iliac crest apophysis and hip abductors at risk
  • Lateral cutaneous femoral nerve at risk
Q3.What are the key steps of the anterior approach?
  • Bikini incision
  • Plane between sartorius and TFL (protect LCFN)
  • Plane between rectus and gluteus medius
  • Detach and tag straight and reflected heads of rectus
  • Psoas tendon lengthening at the pelvic brim, T capsulotomy, excise intra-articular obstacles
  • +/- femoral osteotomy, then capsulorrhaphy
Q4.What are the advantages and disadvantages of the medial approach?
  • Advantages: small wound, less bleeding; can deal with iliopsoas and transverse acetabular ligament; avoids stripping iliac apophysis/abductors; adductor tenotomy through same incision
  • Disadvantages: risk to medial circumflex femoral artery -> AVN
  • Cannot perform capsulorrhaphy
  • Obturator nerve injury
  • Not for open reduction within 6 months
Q5.What are the dissection planes of the medial approach?
  • Weinstein: between NVB and pectineus (landmark = anterior obturator nerve; best to reach labrum)
  • Ludloff: between pectineus and adductor brevis
  • Ferguson: between gracilis and adductor longus, then AM, AB
Q6.What structures are at risk in the medial approach?
  • Obturator nerve (anterior branch between adductor longus and brevis -> adductor contracture)
  • Medial circumflex femoral artery (direct vision when performing tenotomy)
  • External pudendal artery and femoral vessels
Q7.How is the medial approach performed?
  • GA, supine, affected limb in abduction, flexion and external rotation
  • Landmark: 3 cm below the pubic tubercle (attachment of adductor longus)
  • Incision: longitudinal just below the pubic tubercle along adductor longus
  • Palpate the lesser tuberosity
Q8.What is the innervation of the medial compartment of the thigh?
  • Adductor magnus: posterior branch of obturator nerve + tibial nerve
  • Other adductors (longus, brevis, gracilis): anterior branch of obturator nerve
▸ Slide 505 · Presented >18mthsCombined Paed · 6 questions expand
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slide 505
Question list
Q1-Q66 questions — tap to reveal all answerslist
  1. Describe the X-ray findings in DDH presenting after 18 months.
  2. What is the aim of treatment in late-presenting DDH?
  3. Why is an anterior approach chosen for late-presenting DDH?
  4. When do you choose a femoral vs acetabular osteotomy?
  5. What is the choice of osteotomy by age?
  6. How do you decide the osteotomy intra-operatively?
Answers · Q & A
Q1.Describe the X-ray findings in DDH presenting after 18 months.
  • Dislocated left hip
  • Small femoral epiphysis and increased neck-shaft angle
  • Poorly formed tear drop and ill-defined acetabular margins
  • Shenton's line broken
  • Further imaging: von Rosen views to check reducibility
Q2.What is the aim of treatment in late-presenting DDH?
  • Stable, congruent, concentric reduction without too much tension
  • Painless hip with good ROM
  • Prevent complications
Q3.Why is an anterior approach chosen for late-presenting DDH?
  • Better exposure
  • Can do capsulorrhaphy and pelvic osteotomy
  • Avoids injury to the medial circumflex femoral artery
  • Can attack intra-articular obstacles to relocation
  • Precautions: iliac apophysis, abductor stripping, more bleeding
Q4.When do you choose a femoral vs acetabular osteotomy?
  • Femoral osteotomy (VDRO +/- shortening) if reduction maintained in internal rotation and abduction
  • Acetabular osteotomy if reduction maintained in flexion
Q5.What is the choice of osteotomy by age?
  • 2-10 yrs: redirection (Salter, triple); reshape (Pemberton for AL deficiency)
  • 10-14 yrs: open triradiate cartilage -> triple; closed triradiate -> Ganz
  • > 14 yrs: Chiari/shelf as no remodelling
  • +/- shortening in > 3 yo (contracted soft tissue -> increased tension on head -> AVN)
Q6.How do you decide the osteotomy intra-operatively?
  • Find a stable position of the hip intra-op
  • Stable in abduction + IR -> VDRO
  • Stable in flexion -> Salter
  • Stable in flexion + abduction + IR -> pelvic + femoral osteotomy
  • Double acetabulum due to erosion -> Pemberton
▸ Slide 506 · Complication of treatmentCombined Paed · 4 questions expand
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Question list
Q1-Q44 questions — tap to reveal all answerslist
  1. What are Salter's criteria for AVN in DDH?
  2. What is the Kalamchi and McEwen classification of AVN?
  3. What is the risk of AVN by treatment?
  4. What is the differential diagnosis of AVN in DDH?
Answers · Q & A
Q1.What are Salter's criteria for AVN in DDH?
  • Any one of the following:
  • Failure of formation or growth of ossific nucleus 1 year after reduction
  • Broad metaphysis
  • Increased density and fragmentation of the head
  • Residual deformity after ossification
Q2.What is the Kalamchi and McEwen classification of AVN?
  • 1: mild with delayed ossification
  • 2: lateral, valgus deformity
  • 3: central, shortening
  • 4: complete, varus deformity
Q3.What is the risk of AVN by treatment?
  • Pavlik harness: 1-5%
  • Closed reduction + hip spica: 10%
  • Open reduction: up to 30%
Q4.What is the differential diagnosis of AVN in DDH?
  • MED
  • Perthes
  • Infection
  • DDH with AVN
  • PFFD
▸ Slide 507 · Xray showing pelvis of skeletally immature patient with abnormalities over left Combined Paed · 18 questions expand
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Question list
Q1-Q1818 questions — tap to reveal all answerslist
  1. What are the X-ray signs of SCFE?
  2. What are the signs of chronic SCFE?
  3. How is SCFE classified?
  4. What is the management and in-situ pinning technique for SCFE?
  5. When is contralateral (prophylactic) pinning considered?
  6. What is looked for at follow-up after SCFE?
  7. What is the definition of SCFE?
  8. What history points are important in SCFE?
  9. What is Drehmann's sign?
  10. What is the Southwick angle classification?
  11. Which X-ray view is used in SCFE depending on stability?
  12. What is the natural history of untreated SCFE?
  13. What radiological markers aid the decision for prophylactic pinning?
  14. What is the rehabilitation after SCFE pinning?
  15. How does SCFE present and what deformity results?
  16. What is the role of capsulotomy in unstable SCFE?
  17. What does the 2017 J O&T meta-analysis compare for severe slip?
  18. Which SCFE management decisions remain controversial?
Answers · Q & A
Q1.What are the X-ray signs of SCFE?
  • Klein's line (Trethowan's sign)
  • Widened physis with decreased epiphyseal height
  • Increased distance between the teardrop and femoral neck metaphysis
  • Metaphyseal blanch sign of Steel
  • Carpenter's sign (less overlap of metaphysis with posterior acetabular wall)
Q2.What are the signs of chronic SCFE?
  • Metaphysis smooth and sclerotic with callus formation
  • Metaphysis widens (coxa magna)
Q3.How is SCFE classified?
  • Chronicity: pre-slip, acute, chronic, acute-on-chronic (no bearing on prognosis)
  • Stability (Loder): stable vs unstable (< 10% vs 50% AVN)
  • Severity: Southwick angle on frog view; Wilson grade on AP view
  • Wilson: I < 33%, II 33-50%, III > 50% of slip over physis
Q4.What is the management and in-situ pinning technique for SCFE?
  • Aim: prevent further slip, promote physeal closure, prevent complications
  • Unstable = O&T emergency: aim at preventing further slippage and allow physis to fuse in 6hrs; in-situ pinning; stable also pinned, less urgent
  • also say whether go for prophylactic pin
  • GA, X-ray guidance, supine on traction table; no traction or forceful manipulation
  • Triangulation for entry point; one pin center-center, perpendicular to physis, crossing by at least 4 threads
  • 6.5 mm cannulated titanium partially threaded screw with reverse cutting flutes; avoid multiple punctures -> chondrolysis
Q5.When is contralateral (prophylactic) pinning considered?
  • Young < 10 yo (open triradiate cartilage)
  • Systemic disease: hypothyroid, GH deficiency, hypogonadism, renal failure
  • Obese/ retroverted neck
  • ? Lost to follow-up
  • 22% contralateral slip in 18 months
Q6.What is looked for at follow-up after SCFE?
  • Fixation of the pathological side; early: recurrent slippage, chondrolysis
  • Late: AVN, OA, FAI
  • Contralateral side
  • Follow up until epiphyseal closure
  • Pain + stiffness: rule out infection; chondrolysis if joint space < 3 mm
  • Chondrolysis risk factors: manipulation, immobilization, hardware through head
Q7.What is the definition of SCFE?
  • Disorder of the proximal femoral physis leading to slippage of the epiphysis relative to the femoral neck
Q8.What history points are important in SCFE?
  • Timing (chronicity); able to walk at all (stability)
  • Preexisting illness/risk factors: hypothyroidism, GH deficiency, hypogonadism, renal failure
  • Symptoms on the other side (20% bilateral, 80% chronic)
Q9.What is Drehmann's sign?
  • In chronic SCFE: obligatory external rotation with flexion
  • See if patient can stand; check the position of the limb
Q10.What is the Southwick angle classification?
  • Measured on frog view: line perpendicular to the base of the epiphysis vs line along the shaft, compared with the contralateral side
  • Categories: < 30, 30-60, > 60
  • If bilateral, subtract 12 degrees from the corresponding lateral epiphyseal shaft angle
Q11.Which X-ray view is used in SCFE depending on stability?
  • Frog lateral if stable
  • Cross-table if unstable
Q12.What is the natural history of untreated SCFE?
  • Weinstein CORR 1996: 28 untreated patients
  • Increasing displacement over time
  • Degree of displacement is proportional to the risk of OA
Q13.What radiological markers aid the decision for prophylactic pinning?
  • Posterior slope angle (>14deg – 83% risk)
  • Modified Oxford bone age (Popejoy 2012 JPO): score femoral head, LT, ilium, GT, triradiate cartilage
  • Score range 16-26; < 18 = 85-97% risk; 20 = 5%; > 21 = 0-1%
Q14.What is the rehabilitation after SCFE pinning?
  • Stable: weight bear
  • Unstable: non-weight bearing
Q15.How does SCFE present and what deformity results?
  • May present with knee pain due to radiation by the obturator nerve
  • Deformity: extension, external rotation, varus
  • Loss of flexion, internal rotation, abduction
  • CAM-type FAI and accelerated osteoarthritis from anterior impingement
Q16.What is the role of capsulotomy in unstable SCFE?
  • 10. Capsulotomy: theoretical benefit, no strong evidence
  • Dodwell JPO 2019 meta-analysis: no statistically significant decrease in odds of AVN
  • Still recommend routine capsulotomy for all unstable SCFE - adds little and may minimise devastating insult to the femoral head
Q17.What does the 2017 J O&T meta-analysis compare for severe slip?
  • Surgical dislocation (Modified Dunn): 3% AVN but better patient satisfaction
  • In-situ pinning: 1.5% AVN and lower satisfaction
Q18.Which SCFE management decisions remain controversial?
  • Timing of operation
  • Pinning of the contralateral hip
▸ Slide 508 · Any other options for unstable severe slip?Combined Paed · 6 questions expand
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Question list
Q1-Q66 questions — tap to reveal all answerslist
  1. Any other options for unstable severe slip?
  2. When is the Modified Dunn procedure for unstable severe slip performed?
  3. What are the steps of the Modified Dunn approach for severe slip?
  4. What is the AVN risk of this procedure?
  5. What is the anatomical basis of the Modified Dunn procedure?
  6. How is the slip fixed after surgical dislocation?
Answers · Q & A
Q1.Any other options for unstable severe slip?
  • Modified Dunn procedure
Q2.When is the Modified Dunn procedure for unstable severe slip performed?
  • Done in the elective setting
Q3.What are the steps of the Modified Dunn approach for severe slip?
  • Gibson interval (gluteus medius / gluteus maximus)
  • Trochanteric flip osteotomy
  • Z capsulotomy (from troch ridge to acetabulum along neck of femur, distal anterior towards calcar, parallel towards posterior)
  • Cut ligamentum teres -> ER + adduction -> anterior dislocation
Q4.What is the AVN risk of this procedure?
  • AVN up to 25% in inexp hands
Q5.What is the anatomical basis of the Modified Dunn procedure?
  • The MFCA is protected by obturator externus
  • Avoid obturator externus during the approach
Q6.How is the slip fixed after surgical dislocation?
  • Reduction and fixation with multiple pins
▸ Slide 509 · Xray pelvis of skeletally immature patient with left hip pathologyCombined Paed · 17 questions 1 check expand
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Q1-Q1717 questions — tap to reveal all answerslist
  1. Describe the radiographic findings in this case.
  2. What is the Waldenstrom classification and what are the differential diagnoses?
  3. What are the clinical and radiological at-risk signs in Perthes disease?
  4. What is the aim of treatment in Perthes disease and what is the natural history?
  5. What is the lateral pillar classification and how does it guide management?
  6. What is the blood supply to the femoral head by age?
  7. What further investigations are needed in suspected Perthes disease?
  8. What is the etiology of Perthes disease?
  9. What are the operative containment options in Perthes disease and their problems?
  10. What are the prerequisites for surgical containment in Perthes disease?
  11. Take me through the surgical steps of proximal femoral varus osteotomy.
  12. What is the postoperative care and follow-up after Perthes surgery?
  13. What other problems occur in Perthes disease?
  14. What is the advantage of surgical containment according to B Joseph?
  15. What were the limitations of Herring's study?
  16. What did Benjamin Joseph's study recommend for containment?
  17. What are the limitations of non-operative containment with casts?
Answers · Q & A
Q1.Describe the radiographic findings in this case.
  • Flattened, irregular, fragmented left proximal femoral epiphysis with lateral extrusion
  • Cystic changes over the metaphyseal area and lucency over the lateral epiphysis, consistent with Gage sign
  • Widened medial joint space
  • Contralateral hip not involved (10% bilateral, never same time)
  • Working diagnosis: Perthes disease, in the fragmentation phase
Q2.What is the Waldenstrom classification and what are the differential diagnoses?
  • Waldenstrom stages: initial, fragmentation, reossification, remodelling
  • This case is in the fragmentation phase
  • Unilateral Ddx: septic arthritis, Meyer's disease, MED
  • Bilateral Ddx: hypothyroidism, lipid storage disease, Meyer's dysplasia, MED, sickle cell
  • History/PE focus: Age, gender, body built, onset of symptoms, at-risk signs (FOOBS), r/o Ddx, ROM
Q3.What are the clinical and radiological at-risk signs in Perthes disease?
  • Clinical at-risk signs (FOOBS): female, old, obese, bilateral, stiff
  • Catterall sign: hip flexion with obligatory external rotation
  • Radiological (Catterall): Gage sign (inverted V lucency lateral to the epiphysis)
  • Horizontal physis and lateral subluxation of the femoral head
  • Calcification lateral to the epiphysis and metaphyseal cyst
Q4.What is the aim of treatment in Perthes disease and what is the natural history?
  • Pain control (rest, analgesics)
  • Maintain ROM (physio, temporary NWB)
  • Contain the hip during the critical period of biologic plasticity during creeping substitution so the head remodels with less incongruity
  • Containment position: abduction and internal rotation
  • Natural history: We know from the classic Iowa study with a 50yr FU that 40% need arthroplasty if left untreated. Counsel patient regarding containment. Still has a possibility of future OA
  • Non-operative containment options: observation, activity restriction, NWB + ROM exercise (abd + IR), Petrie cast, A-frame
Q5.What is the lateral pillar classification and how does it guide management?
  • Based on AP X-ray, comparing both sides (Herring); lateral pillar 25%, central 50%, medial 20-35%
  • A = normal height; B = > 50%; B/C = exactly 50% or very narrow lateral pillar >50% of original height / very little ossification but > 50%; C = < 50%
  • Herring study (2004 JBJS): A and B < 8 yo do well regardless; B and B/C > 8 yo improve with surgery; B/C < 8 and C poor regardless of treatment; no significant effect regardless of treatment in those <8yo
  • For this case (lateral pillar B or B/C, > 8 yo): surgical containment improves outcome
  • Surgical containment: proximal femoral VDRO (at most 20deg) or ROWO +/- pelvic osteotomy
  • Outcome at maturity by Stulberg classification: I normal, II spherical congruent, III mushroom congruent, IV flat congruent, V incongruent
Q6.What is the blood supply to the femoral head by age?
  • < 4 yo: equal contribution by MFCA and LFCA
  • 4-10 yo: LFCA regresses and supplies metaphysis only
  • 10-14 yo: increased contribution from ligamentum teres
  • > 14 yo: anastomosis between the three systems
Q7.What further investigations are needed in suspected Perthes disease?
  • WBC (infection), lipid (storage disorder), ESR, CRP
  • Bone profile (tumour), TSH (hypothyroid), peripheral smear (sickel cell)
  • XR frog-leg lateral; +/- USG, aspiration if infection suspected
Q8.What is the etiology of Perthes disease?
  • Anatomical
  • Hydrostatic pressure
  • Thrombophilic
Q9.What are the operative containment options in Perthes disease and their problems?
  • Proximal femoral VDRO (at most 20deg) or ROWO - problems: short limb and Trendelenburg gait
  • Pelvic osteotomy - re-directional (Salter): potential lengthening increases pressure on the head -> AVN
  • Combination with femoral osteotomy increases coverage by 20%
  • Shelf to prevent lateral subluxation/no longer containable; Chiari
  • Valgus osteotomy for hinged abduction (reposition hinge, correct shortening, improve abductor function)
Q10.What are the prerequisites for surgical containment in Perthes disease?
  • Prerequisites include timing: fragmentation phase
  • Containable: good range on examination
  • > XR – spherical and congruent reduction, containable upon abduction XR/ intraop arthrogram
Q11.Take me through the surgical steps of proximal femoral varus osteotomy.
  • Preop plan the amount of varisation; GA; adductor release if tight
  • Lateral subvastus approach; elevate periosteum
  • Paediatric proximal locking plate: 3.5 mm if < 35 kg, 5 mm if > 35 kg
  • Jig angle = plate angle + desired varisation; fix plate proximally then remove it
  • Mark rotation, use 2 K-wires above and below the osteotomy, osteotomy with oscillating saw
  • Fix plate proximally then distally; Add some internal rotation or extension for better containment
Q12.What is the postoperative care and follow-up after Perthes surgery?
  • NWB walking, HKO
  • Follow up until maturity
Q13.What other problems occur in Perthes disease?
  • LLD, Trendelenburg
  • Pain: labral tear, loose body, hinged abduction, FAI
Q14.What is the advantage of surgical containment according to B Joseph?
  • The patient will go through the fragmentation phase faster
Q15.What were the limitations of Herring's study?
  • Based on AP view only
  • 7/12 had surgery before reliable classification
  • 1/3 needed upgrade; only 4% in group A on final grading
  • Difficult in bilateral disease
Q16.What did Benjamin Joseph's study recommend for containment?
  • Factors: age at onset, femoral head extrusion (> 20% Reimer migration index), ROM
  • Containment ASAP if: >= 8 yo with extrusion and reduced ROM (restore motion with traction/abduction cast for 6 weeks first)
  • < 8 yo with extrusion
  • < 8 yo: femoral osteotomy (more remodelling, less Trendelenburg later)
  • >= 8 yo: acetabular osteotomy (less shortening)
Q17.What are the limitations of non-operative containment with casts?
  • Petrie cast / A-frame must be worn for 6 months to 1 year
  • Problem: cannot guarantee abduction
Fact check

Classic Iowa study with 50-year follow-up shows 40% of untreated Perthes disease need arthroplasty — outdated/overstated — The 40% figure comes from a selected historical Iowa cohort (McAndrew & Weinstein, mean 47.7 years follow-up: 15/37 hips). A modern nonoperative cohort (Oslo, mean 48 years) reported only 19% THA, so 40% should not be quoted as the universal natural history. — medium confidence — source

▸ Slide 510 · AP Xray pelvis of skeletally immature patientCombined Paed · 8 questions expand
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Q1-Q88 questions — tap to reveal all answerslist
  1. Describe the X-ray findings of developmental coxa vara.
  2. What are the causes of coxa vara?
  3. What are the clinical features of coxa vara?
  4. What is the prognosis by HE angle and when is surgery indicated?
  5. What is the pathomechanics of coxa vara?
  6. What is the diagnosis and inheritance of developmental coxa vara?
  7. What history is relevant in coxa vara?
  8. What preoperative planning is needed before VDRO for coxa vara?
Answers · Q & A
Q1.Describe the X-ray findings of developmental coxa vara.
  • Bilateral coxa vara deformity
  • Vertical physis with increased HE angle (> 25 abnormal)
  • Decreased neck shaft ankle (<125 abnormal)
  • Coxa breva
  • Fairbank triangle: Inverted Y shape lucency in inferior femoral neck (ossification defect)
  • Acetabulum and tear drop normal
Q2.What are the causes of coxa vara?
  • Acquired: Perthes, chronic SCFE, trauma, infection
  • Developmental
  • Dysplasia: MED, SED, OI
  • Metabolic: cretinism
  • Congenital: PFFD; bilateral in 30-50%
Q3.What are the clinical features of coxa vara?
  • Trendelenburg gait
  • LLD and high riding greater trochanter
  • Excessive lumbar lordosis
  • Restricted hip ROM
Q4.What is the prognosis by HE angle and when is surgery indicated?
  • < 45: 20% resolve
  • 45-60: uncertain
  • > 60: will progress
  • VDRO if HE > 60 and NSA < 110 (subtrochanteric if < 3 yo, intertrochanteric if > 3 yo)
  • Goal: overcorrect NSA, correct LLD and version, restore abductor tension; aim HE < 30
Q5.What is the pathomechanics of coxa vara?
  • Decreased neck-shaft angle with an ossification defect in the inferior femoral neck
  • -> vertical physis
  • -> increased shearing force
Q6.What is the diagnosis and inheritance of developmental coxa vara?
  • Developmental coxa vara
  • No clear genetic inheritance
  • Bilateral in 30-50%
Q7.What history is relevant in coxa vara?
  • Previous hip trauma or infection
  • Associated skeletal abnormalities
  • Perinatal history and family history
Q8.What preoperative planning is needed before VDRO for coxa vara?
  • CT PRE OP for associated deformities: coxa breva, femoral retroversion, acetabular dysplasia, GT overgrowth
  • Lateral approach, protect physis and periosteum
  • Goal: overcorrect NSA, correct LLD, correct version, restore abductor tension; aim HE < 30