Inflammatory Arthritis Flashcards
Rheumatic disorders
Juvenile Idiopathic Arthritis
Dermatomyositis
Systemic lupus erythematosus
Juvenile Idiopathic Arthritis
Arthritis in one or more joints for 6 weeks after excluding other causes
3 main types - classification by onset over first 6 months
Systemic (previously Still’s disease)
Mainly <5years Primarily knees, wrist, ankles and tarsals Symmetrical RF negative High daily spiking fever Salmon-pink rash Lymphadenopathy and hepatosplenomegaly Arthralgia, malaise and myalgia Inflammation of pleura and serosal membranes Often no arthritis at presentation One-third have progressive course Worst prognosis at younger age
Polyarticular RF negative
All ages
All joints sparing MCPs
Symmetrical
Limitation of the motion of the neck and temperomandibular joints
Good prognosis but disease may be prolonged
Polyarticular RF positive
Mainly females over 8 years Small joints of hand and feet Hip and knee affected early Symmetrical Rheumatoid nodules over pressure points May be a systemic vasculitis Funtional prognosis poor
Oligoarticular
Girls - more than four joints, after 6 months - poorer prognosis)
Investigations
FBC - anaemia in systemic disease Acute-phase reactants elevated RF - classification ANA - classification Xrays - soft tissue swelling early; bony erosion and loss of joint space late
Management
MDT
Physio: optimize joint mobility, prevent deformity, increase muscle strength
NSAIDs - pain control and inflammation suppression
Oligo: NSAIDS and/or glucocorticoid injections, escalation to methotrexate and then a THF-alpha inhibitor
Poly: as oligo with further escalation to second TNF-alpha inhibitor
Systemic: glucocorticoids with escalation to interleukin-1 receptor agonists