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What is RA?
A Chronic, systemic inflammatory disease, characterised by symmetrical joint involvement which is typically erosive/destructive.
hallmark feature: persistent symmetric polyarthritis (synovitis)
Recap on the anatomy and physiology Function of JOINTS: To allow articulation between two or more bones and secondarily to permit movement by contraction of opposing muscles.
Etiology
Pathophysiology
Antigen Environmental agent, infectious agent
Genetic Susceptibility
HLA-DR4 HLA-DQ HLA- DP
Activates B lymphocytes
Pathophysiology
T cells stimulates synovial macrophage and fibroblast
Activates B lymphocytes
Joint injury
Pannus formation Joint destruction Cartilage fibrosis Ankylosis
INTERLEUKIN 1
IL-1 is a potent stimulator of synoviocytes, chondrocytes and osteoblasts (Figure 1).
IL-1 is a proinflammatory cytokine that amplifies and perpetuates the disease process in RA
Clinical Manifestations
1. arthritis
Associated with low fever
Fatigue
Morning stiffness Joint soft, warm to touch
Clinical Manifestations
2. extra-articular features
Clinical Manifestations
3. Associated syndromes (possible complications)
(a) Sjgrens syndrome-salivary gland inflammation and keratoconjunctivitis (b) Feltys syndrome-profound neutropenia, thrombocytopenia and splenomegaly (C) Pulmonary involvement-(pleuritis, interstitial pneumonitis, alveolitis and intrapulmonary rheumatoid nodules) (d) Cardiac involvement-pericarditis
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Diagnnostic criteria
1. Morning stiffness lasting more than 1 hour 2. Arthritis of 3 or more joint areas. 3. Arthritis of the hand joints 4. Symetric arthritis 5. Rheumatoid nodules over extensor surface or bony prominences. 6. Serum rheumatoid factor. 7. Radiologic changes.
Types of JIA
Nursing Diagnosis:
1. Acute Pain r/t inflammation & swelling 2. Fatigue r/t increased metabolic rate 3. Impaired physical mobility r/t decreased range of motion 4. Disturbed body image r/t physical & psychological changes