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  • Poster presentation
  • Open Access

Knee disease in juvenile idiopathic arthritis (JIA): correlation between clinical and ultrasonographic findings

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Pediatric Rheumatology20086 (Suppl 1) :P95

  • Published:


  • Steroid
  • Clinical Assessment
  • Knee Joint
  • Clinical Finding
  • Recurrent Disease


There is increasing evidence that ultrasound (US) scanning is more accurate than clinical examination in detecting effusions in adults. We wished to compare clinical and ultrasonographic findings in knee joints of children with JIA.


We are undertaking a five year prospective study of children with newly diagnosed JIA who have knee involvement. Review is three monthly with clinical assessment and US of knee(s) at each visit. Knee swelling is graded 0–4. US scans were performed by an experienced rheumatologist MR using a Sonosite 180 Plus (L38 5–10 MHZ linear transducer) or Esaote MyLab25 scanner (LA523E 7.5–12 MHZ linear transducer). The scans have been scored independently by 2 observers unaware of the clinical findings (graded 0–3).


48 children have been recruited and to date, 25 have been followed for 2 years. To date 124 scans have been scored for effusions and synovial hypertrophy. There was good correlation between clinical and US scores r = 0.7. In 78 clinically normal knees, 50 had normal US scans, 21 had mild effusions and 7 had moderate effusions. Of the 18 patients with oligoarticular disease, synovial hypertrophy was more marked in the 9 patients who required repeat IA steroid injections.


There was good correlation between clinical and US findings. However 36% of clinically normal knees had evidence of effusion on ultrasound suggesting that ultrasound is indeed more accurate and may be of value in determining disease classification. Detection of disease activity by US, in particular synovial hypertrophy may prove a useful indicator for recurrent disease.

Authors’ Affiliations

Rheumatology, Musgrave Park Hospital, Belfast, UK
Musculoskeletal Research Group, Queen's University, Belfast, UK


© McCarron et al; licensee BioMed Central Ltd. 2008

This article is published under license to BioMed Central Ltd.