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Arthritis in children: comparison of clinical and biological characteristics of septic arthritis and juvenile idiopathic arthritis
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  1. Camille Aupiais1,2,3,
  2. Romain Basmaci3,4,5,
  3. Brice Ilharreborde3,6,
  4. Audrey Blachier7,
  5. Marie Desmarest8,
  6. Chantal Job-Deslandre9,10,
  7. Albert Faye2,3,4,
  8. Stéphane Bonacorsi3,5,11,
  9. Corinne Alberti1,2,3,
  10. Mathie Lorrot2,3,4
  1. 1Unité d’Epidémiologie Clinique, AP-HP, Hôpital Robert Debré, Paris, France
  2. 2Inserm, U1123, ECEVE and CIC-EC 1426, Paris, France
  3. 3Univ Denis Diderot Paris 7, Sorbonne Paris Cité, Paris, France
  4. 4Service de Pédiatrie Générale, AP-HP, Hôpital Robert Debré, Paris, France
  5. 5Inserm, UMR1137, Infection, Antimicrobials, Modelling, Evolution (IAME), Paris, France
  6. 6Service d'Orthopédie Pédiatrique, AP-HP, Hôpital Robert Debré, Paris, France
  7. 7Département Informatique Médicale, Hôpital Robert Debré (APHP), Paris, France
  8. 8Service d'Accueil des Urgences Pédiatriques, AP-HP, Hôpital Robert Debré, Paris, France
  9. 9Service de Rhumatologie, AP-HP, Hôpital Cochin, Paris, France
  10. 10Université René Descartes Paris 5, Paris, France
  11. 11Service de Microbiologie, AP-HP, Hôpital Robert Debré, Paris, France
  1. Correspondence to Dr Camille Aupiais, Unité d'Epidémiologie clinique, Hôpital Robert Debré (APHP), 48 boulevard Sérurier, Paris 75935, Cedex 19, France; camille.aupiais{at}rdb.aphp.fr

Abstract

Aim Childhood arthritis arises from several causes. The aim of this observational study is to compare the clinical and biological features and short-term outcome of different types of arthritis because they have different treatment and prognoses.

Methods Children <16 years of age hospitalised in a French tertiary care centre for a first episode of arthritis lasting for less than 6 weeks who underwent joint aspiration were retrospectively included. We performed non-parametrical tests to compare groups (septic arthritis (SA), juvenile idiopathic arthritis (JIA) and arthritis with no definitive diagnosis). The time before apyrexia or C reactive protein (CRP) <10 mg/L was analysed using the Kaplan-Meier method.

Results We studied 125 children with a sex ratio (M/F) of 1.1 and a median age of 2.2 years (range 0.3 to 14.6). SA was associated with a lower age at onset (1.5 years, IQR 1.2–3.0 vs 3.6 years, IQR 2.2–5.6), shorter duration of symptoms before diagnosis (2 days, IQR 1–4 vs 7 days, IQR 1–19) and higher synovial white blood cell count (147 cells ×103/mm3, IQR 71–227, vs 51 cells ×103/mm3, IQR 12–113), than JIA. Apyrexia occurred later in children with JIA (40% after 2 days, 95% CI 17% to 75%) than children with SA (82%, 95% CI 68% to 92%), as did CRP<10 mg/L (18% at 7 days, 95% CI 6.3% to 29.6% vs 82.1%, 95% CI 76.1% to 89.7%, p=0.01).

Conclusions There were no sufficiently reliable predictors for differentiating between SA and JIA at onset. The outcomes were different; JIA should be considered in cases of poor disease evolution after antibiotic treatment and joint aspiration.

  • Arthritis, Infectious
  • Arthritis, Juvenile
  • Child
  • Diagnosis, differential

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