T&O: Paediatric Hip Pain Flashcards Preview

Year 3 - Junior surgery > T&O: Paediatric Hip Pain > Flashcards

Flashcards in T&O: Paediatric Hip Pain Deck (17)
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1
Q

What are the 4 main causes of paediatric hip pain? What age ranges an gender do they usually affect?

A
  1. Transient synovitis (3-8 yrs), more common in males
  2. Septic arthritis (0-6 yrs)
  3. Slipped capital femoral epiphysis (10-17 yrs), more common in obese M
  4. Perthes disease (4-7 yrs), M:F = 5:1
2
Q

What is transient synovitis?

A

Inflammation of the synovium of the hip joint capsule. Self-limiting. Exact cause unknown but may be associated with URI.

3
Q

What is septic arthritis? What is the most common causative organism?

A

Intra-articular infection as a result of trauma, recent instrumentation of joint or haematogenous seeding.
S. aureus is most common organism.

4
Q

How would you clinically differentiate between septic arthritis and transient synovitis?

A

Have similar early symptoms with spontaneous onset of hip, groin or thigh pain.

Pain

  • TS: usually mild, allowing weight bearing, absent at rest
  • SA: severe, prevents weight bearing

Fever

  • TS: absent to mild, systemically well
  • SA: high, appears ill, irritable

ROM

  • TS: restricted abduction
  • SA: rests in external rotation, refuse movement

Labs

  • TS: CRP <20
  • SA: WBC >12,000, ESR >40
5
Q

How are transient synovitis and septic arthritis diagnosed?

A

TS: diagnosis of exclusion
- USS often shows fluid inside joint capsule (Fabella sign)

SA: arthrocentesis
- shows raised WBCs and lactate
- perform gram stain and culture
(Treatment should not be delayed for the results of culture but should be based on Gram stain and polarising microscopy (exclude crystal arthropathy) results)

6
Q

What is the management for transient synovitis and septic arthritis?

A

TS: rest, analgesia and NSAIDs

SA: surgical drainage and lavage of joint, and high-dose IV antibiotics

7
Q

What is the prognosis of transient synovitis an septic arthritis?

A

TS: usually resolves within 7-10 days. Recurrence rate is 4-17%, mostly within 1st 6mths.

SA: 90% recovery with treatment, but if unrecognised and untreated can cause:

  • irreversible joint damage within 48hrs of infection onset due to proteolytic enzymes of WBCs that flood infected synovial space
  • osteonecrosis due to effuson and increased intra-articular pressure compromising blood circulation
8
Q

What is Perthes disease? How does it present?

A

Idiopathic osteonecrosis of femoral epiphysis seen in children.

Most children present with atraumatic hip pain or limp. Blood tests typically normal.

9
Q

Describe the 4 stages of Perthes disease.

A
  1. Disruption of blood supply to femoral head, causing necrosis (several mths).
  2. Fragmentation of femoral head, with replacement of dead bone by soft woven bone (1-2 yrs).
  3. Reossification with stronger cortical bone (several yrs).
  4. Healing/completed bone growth.
10
Q

Describe the management options for Perthes disease.

A

Goal of treatment is to relieve pain, protect shape of femoral head and restore normal hip movement, preventing early onset arthritis.

Conservative:

  • observation
  • NSAIDs
  • limiting activity
  • physiotherapy
  • casting and bracing (Petrie casts)

Surgical (>8yrs, >50% femoral head damage, unsuccessful conservative therapy):
- osteotomy - cut and reposition femur to replace femoral head within acetabulum

11
Q

What is SCFE? Name 3 risk factors. How does it present?

A

Relatively common condition affecting the physis of the proximal femur – type I Salter-Harris epiphyseal fracture due to repeated trauma on background of mechanical and probably hormonal predisposing factors.

Risk factors:

  • male
  • afro-carribean
  • obesity

Pts present with hip pain progressing to a limp and even leg length discrepancy.

12
Q

What is the management for SCFE?

A

surgical pinning +/- prophylactic pinning of contralateral side

13
Q

Name 4 possible complications for SCFE.

A
  1. long term degenerative OA (90%)
  2. AVN (10-15%)
  3. chondrolysis (10%) - acute cartilage necrosis
  4. deformity/leg length discrepancy
14
Q

What is developmental dysplasia of the hip? Name 3 risk factors.

A

Aberrant development of hip joint, usually occuring from ligamentous laxity and abnormal presentation in utero. Affects 1-3% newborns.

Risk factors:

  • female gender (1:8)
  • breech presentation
  • oligohydramnios
15
Q

How is DDH diagnosed?

A

USS prior to ossification of proximal femoral epiphysis, X-ray after

16
Q

Describe the management of DDH.

A
  • <6mths: Pavlik harness
  • older children: closed reduction
  • older Pts or unsuccessful closed reduction: open reduction
17
Q

What is the main long-term complication of DDH?

A

premature degenerative joint disease requiring joint replacement