Abstract
Juvenile idiopathic arthritis (JIA) is a group of heterogeneous conditions characterised by chronic inflammatory arthritis in children (<16 years), persisting for longer than 6 weeks, with no known cause. The current International League of Associations for Rheumatology (ILAR) classification has 7 subtypes: (1) systemic (sJIA), (2) oligoarticular (oJIA), (3) polyarticular (pJIA) Rheumatoid factor-negative, (4) polyarticular (pJIA) Rheumatoid factor-positive, (5) enthesitis-related (ERA), (6) psoriatic (PsA), (7) undifferentiated. Considerable advances have been made in the past two decades with the advent of the 'biologic' agents (especially Tumour Necrosis Factor-α inhibitors) but also with better use of earlier disease-modifying treatments. It is hoped that management paradigms for the different arthritides translate into better outcomes and fewer long-term sequelae, including the requirements for surgery. With more modern treatments, hip surgery is rarely required in the child, though contracture release and synovectomy can be useful. The hip is commonly affected later in the course of the disease, and arthroplasty is often required as a young adult. Nevertheless, for joint destruction, arthroplasty can be a vital treatment even in the child. The surgical approach to pediatric patients requires consideration of anatomical differences, drug therapy and future arthroplasty implant failure.
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Huntley, J.S., Young, P.S., Patil, S. (2019). Juvenile Idiopathic Arthritis and the Hip. In: Alshryda, S., Howard, J., Huntley, J., Schoenecker, J. (eds) The Pediatric and Adolescent Hip. Springer, Cham. https://doi.org/10.1007/978-3-030-12003-0_13
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