SPOTTERS MEDICINE

 

RHEUMATOID ARTHRITIS 





🔹 Definition:

Rheumatoid arthritis is a chronic, systemic autoimmune disease that primarily affects synovial joints, causing symmetrical, inflammatory polyarthritis and progressive joint destruction.


🔹 Etiology:

  • Autoimmune response
  • Genetic predisposition – HLA-DR4, HLA-DR1
  • Environmental triggers (e.g., smoking, infections)

🔹 Pathogenesis:

  • Autoantibodies like Rheumatoid Factor (RF) and anti-CCP target synovium
  • Chronic synovitis → pannus formation → cartilage destruction → joint deformity
  • Inflammatory cytokines: TNF-α, IL-1, IL-6 involved

🔹 Clinical Features:

  • Symmetrical joint pain, swelling, morning stiffness >1 hour
  • Common joints: MCP, PIP, wrists, knees, ankles
  • Extra-articular features:
    • Rheumatoid nodules
    • Fatigue, anemia
    • Vasculitis, pleuritis, pericarditis
    • Eye involvement (scleritis, keratoconjunctivitis)

🔹 Deformities (late stage):

  • Swan neck deformity
  • Boutonnière deformity
  • Ulnar deviation
  • Z deformity of thumb

🔹 Diagnosis:

  • Clinical criteria (ACR/EULAR)
  • Rheumatoid Factor (RF) – positive in 70–80%
  • Anti-CCP antibodies – more specific
  • Elevated ESR, CRP
  • X-ray: joint space narrowing, erosions, osteopenia

🔹 Differential Diagnosis:

  • Osteoarthritis
  • SLE
  • Psoriatic arthritis
  • Viral arthritis (e.g., parvovirus)

🔹 Treatment:

Symptomatic Relief:

  • NSAIDs (e.g., diclofenac, ibuprofen)
  • Low-dose corticosteroids

Disease-Modifying Anti-Rheumatic Drugs (DMARDs):

  • Methotrexate (first-line)
  • Sulfasalazine, Leflunomide, Hydroxychloroquine

Biologics:

  • Anti-TNF agents: Etanercept, Infliximab
  • IL-6 inhibitors: Tocilizumab
  • Others: Rituximab, Abatacept

Non-Pharmacological:

  • Physiotherapy, occupational therapy
  • Joint protection, splints

Surgery:

  • Joint replacement in severe deformity

🔹 Complications:

  • Joint destruction and disability
  • Rheumatoid vasculitis
  • Felty’s syndrome (RA + splenomegaly + neutropenia)
  • Osteoporosis, amyloidosis

🔹 Prognosis:

  • Variable; early diagnosis and treatment with DMARDs improves outcome
  • Progressive disability if untreated

DR.C.GANESAN M.D.,

PROFESSOR OF MEDICINE

 

 

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