RA is a systemic autoimmune inflammatory disease.
It is characterized by symmetric and chronic destructive synovitis, which is the inflammation of the synovial membrane lining joints.
Define RA: Understand the nature of RA and its systemic effects.
Epidemiology and Risk Factors: Discuss prevalence and contributing factors.
Pathogenesis: Identify how RA develops in the body.
Clinical Presentation: Review signs and symptoms associated with RA.
Diagnostic Criteria: Understand the necessary criteria for RA diagnosis.
Treatment Algorithm: Examine pharmacologic and non-pharmacologic treatment methods.
Typically affects small joints: proximal interphalangeal, metacarpophalangeal joints, wrists, and ankles.
More significant affectation of:
Proximal interphalangeal and metatarsophalangeal joints.
Cervical spine joints.
Hips are less commonly involved.
Ulnar deviation: due to collateral ligament rupture at MCP joints.
Swan neck deformity: caused by rupture of the volar plate at PIP joints.
Boutonnière deformity: due to rupture of the central extensor of fingers.
Additional symptoms may include muscle wasting and tendon rupture.
RA is believed to be triggered by an autoimmune response, typically involving exposure to unknown arthritogenic antigens in genetically predisposed individuals.
Key processes:
Activation of CD4+ T cells and production of inflammatory mediators leading to joint destruction.
Cytokines like TNF and IL-1 stimulate inflammatory processes damaging synovial tissues and bone.
Cytokines (e.g., TNF, IL-1):
Produced by macrophages and activated synovial lining.
Lead to joint damage by promoting inflammation and activating osteoclasts.
Hyperplastic synovium rich in inflammatory cells invades joint surfaces, leading to cartilage destruction and bone erosion.
Release of IL-1 and growth factors from the pannus promotes joint degeneration.
Individuals must meet four of the seven criteria:
Morning stiffness for at least one hour for six weeks.
Soft tissue swelling (arthritis) in three or more joints for at least six weeks.
Swelling in specific joints (e.g., proximal interphalangeal) for six weeks.
Symmetrical joint involvement for six weeks.
Presence of subcutaneous nodules.
Positive test for rheumatoid factor.
Radiographic features showing erosion or periarticular osteopenia in hand/wrist joints.
Early RA: Less than 6 months of symptoms.
Established RA: Symptoms present for at least 6 months.
DMARDs (Disease-Modifying Antirheumatic Drugs): Methotrexate is the preferred first-line treatment due to its rapid onset.
Biologics: TNF inhibitors (Etanercept, Infliximab etc.) are administered for moderately to severely active RA.
Glucocorticoids: Used as adjunct therapy to manage inflammation.
Physical Therapies: Exercise and physiotherapy are essential for joint function.
Dietary Interventions: Nutritional support can help manage symptoms.
Regularly monitor disease activity using validated tools such as the Disease Activity Scale (DAS).
Assess and manage potential adverse effects of treatments, particularly for DMARDs and biologics.