MSK Flashcards
Which JIA has a particularly poor prognosis?
RhF +ve polyarthritis
Which JIA is more common in boys than girls?
Ethesitis-related arthritis
DDx for limp in children
Traumatic/mechanical
- Scoliosis
- Fracture
- SUFE
- Sprain/contusion
- Leg length discrepancy
Inflammatory
- JIA
- Transient synovitis
- Osgood Schlatter’s
Vacular
- Perthe’s
Infectious
- Osteomyelitis
- Septic arthritis
- Reactive arthritis
Malignancy
- Osteoma
- Ewing’s sarcoma
Neuromuscular
- CP
- Musculr dystrophy
- Peripheral neuropathy
Metabolic
- Ricket’s
Traumatic/mechanical causes of limp
- Scoliosis
- Fracture
- SUFE
- Sprain/contusion
- Leg length discrepancy
Infectious causes of limp/joint pain
- Osteomyelitis
- Septic arthritis
- Reactive arthritis
Inflammatory causes of limp/joint pain
- JIA
- Transient Synovitis
- Osgood-Schlatter’s
- Reiter’s
- Lupus
- Ank spond
Vacular causes of limp/joint pain
Perthe’s (AVN)
Three “severities” of DDH
Dysplasia, subluxation, dislocation
When is DDH normally picked up?
NIPE - in Barlow/Ortolani manoeuvres
Which manoeuvres are used to assess DDH?
Barlow and Ortolani
Signs of DDH
Asymmetry of skin folds around buttocks and hips. Limited abduction. One leg may be shorter than the other
What is DDH
Developmental dysplasia of the hip - ball and socket joint is not formed completely
What happens in most cases of DDH
Resolves spontaneously by 3-6 weeks
Mx DDH
R/f for ORTHOPAEDIC OPINION
1) Observation - use USS if under 6 months, XR after
2) >6mos. Place in Pavlik harness/splint up to 6mos. Keeps hip flexed and abducted.
3) Surgery if conservative measures have failed - with spica casting
Which infants are at highest risk of DDH? How should they be monitored?
Breech
FHx
- Monitored with USS at 6/52
Which imaging modality is best in assessing DDH?
USS < 6months
XR > 6mos
Mx of fractures
Consider safeguarding
Pain management - PO ibuprofen/paracetamol. IV opioids
Immobilisation
Mx distal radius #
Manipulation
K-wire fixation if fracture off-ended
Mx of femoral shaft #
ADMIT
Orthopaedic management
0-6 mos: Pavlik’s harness, Gallow’s traction
2-18mos: Gallow’s traction
1-6yrs: straight leg skin traction, hip spica cast
6-12yrs: elastic intramedullary nail
11yrs+: elastic intramedullary nail, end caps, ridid intramedullary nails, submuscular plating
Signs/symptoms of SUFE
Acute onset hip/groin pain/referred knee pain
Restricted abduction and internal rotation
- Legs presents as slightly shorter and externally rotated
Commonest age of presentation SUFE
Adolescents (10-15 years)
Pathophysiology of SUFE
Posterior-inferior slippage after fracture through the growth plate
What is a SUFE?
Slipped upper femoral epiphysis - a fracture through the growth plate in the femoral head
Posterior-inferior slippage
Patients at higher risk of SUFE
Boys
Obesity
Metabolic abnormalities - hypoCa, hypothyroid, hypogonad
What views should be requested in SUFE XR?
AP
Frog lateral
Mx of SUFE
Surgical repair - screw fixation
Age of presentation Perthe’s
5-10 years
What is Perthes?
AVN of capital femoral epiphysis of femoral head due to interruption of the blood supply, followwd by revascularisation and ossification over 18-36 months
Signs/symptoms of Perthes
Insidious limp, hip pain
Referred knee pain
What percentage of Perthes is bilateral
10-20%
Ix requested in suspected Perthes
AP
Frog lateral
(+MRI/bone scan)
Findings on XR Perthes
Increased density in femoral head
Fragmented/irregular femoral head
Widening of joint space
Most important factor in Perthes prognosis?
Early diagnosis - if 1/2 femoral head affected, bed rest and traction
If >1/2 affected, plaster/calipers to keep femoral head close to acetabulum to use as mould for reossification
Mx for Perthes
Supportive care (analgesia, ice packs, etc.)
Continued activity
Physical therapy - stretching and strengthening of quads and hamstrings
Surgical treatment if fail to resond to conservative measures
Commonest chronic inflammatory joint disease in children/adolescents
JIA
What is JIA?
Juvenile idiopathic arthritis - persistent joint swelling for more than 6 weeks before 16 years old. Absence of an infecive cause.
How many subtypes of JIA? exist? Give examples
7 Poly (>4 joints) Oligo (<4 joints) Systemic (if ever presents with rash) RhF/B27 tissue subtypes
What percentage of JIA diagnoses are distinct from RhA in adulthood?
95%