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Rheumatoid Arthritis Systemic chronic inflammatory disease Mainly affects synovial joints

Rheumatoid Arthritis Systemic chronic inflammatory disease Mainly affects synovial joints Variable expression Prevalence about 3% Worldwide distribution Female:male ratio 3:1 Peak age of onset: 25-50 years. Rheumatoid Arthritis. Unknown etiology Genetics Environmental

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Rheumatoid Arthritis Systemic chronic inflammatory disease Mainly affects synovial joints

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  1. Rheumatoid Arthritis Systemic chronic inflammatory disease Mainly affects synovial joints Variable expression Prevalence about 3% Worldwide distribution Female:male ratio 3:1 Peak age of onset: 25-50 years

  2. Rheumatoid Arthritis • Unknown etiology • Genetics • Environmental • Possible infectious component • Autoimmune disorder

  3. THE PATHOLOGY OF RA • Serositis 1. Synovitis Joints Tendon sheaths Bursae • Nodules • Vasculitis

  4. Signs and Symptoms • Joint inflammation • Tender, warm swollen joints • Symmetrical pattern • Pain and stiffness • Symptoms in other parts of the body • Nodules • Anemia • Fatigue, occasional fever, malaise

  5. JOINT INVOLVEMENT ON PRESENTATION OF RA Polyarticular 75% Monoarticular 25% Small joints Knee 50% of hands and feet 60% Large joints 30% Shoulder } Wrist } Large and Hip } 50% Small joints 10% Ankle } Elbow }

  6. Articular features seen in the Rheumatoid Hand WRIST:PIPs: Synovitis Synovitis Prominent ulnar styloid Fixed flexion or extension Subluxation and collapse of deformities carpus (Swan neck or boutonniere Radial deviation deformity) MCPs: THUMBS: Synovitis Synovitis Ulnar deviation ‘Z’ deformity Subluxation

  7. Joint Destruction

  8. Extra-articular manifestations • General • fever, lymphadenopathy, weight loss, fatigue • Dermatologic • palmar erythema, nodules, vasculitis • Ocular • episcleritis/scleritis, scleromalacia perforans, choroid and retinal nodules

  9. Extra-articular manifestations • Cardiac • pericarditis, myocarditis, coronary vasculitis, nodules on valves • Neuromuscular • entrapment neuropathy, peripheral neuropathy, mononeuritis multiplex • Hematologic • Felty’s syndrome, large granular lymphocyte syndrome, lymphomas

  10. Extra-articular manifestations • Pulmonary • pleuritis, nodules, interstitial lung disease, bronchiolitis obliterans, arteritis, effusions • Others • Sjogren’s syndrome, amyloidosis

  11. Investigations: • Hematology : CBC , ESR • Biochemistry : LFT , Renal profile • Serology : RF , Anti-CCP • Radiography : Joints , Spines ,Chest

  12. Treatment Goals • Relieve pain • Reduce inflammation • Prevent/slow joint damage • Improve functioning and quality of life

  13. Treatment Approaches • Lifestyle modifications • Rest • Physical and occupational therapy • Medications • Surgery

  14. Rationale for the Early Treatment of R.A. • •Erosions develop early in the disease course • •Destruction is irreversible • •Disease activity is strongly associated with joint destruction later in the disease course • •Early treatment can slow down radiographic progress • •Disease activity must be suppressed maximally in its early stages to prevent destruction and preserve function

  15. Drug Treatments • Nonsteroidal anti-inflammatory drugs (NSAIDs) • Disease-modifying antirheumatic drugs (DMARDs) • Biologic response modifiers • Corticosteroids

  16. Traditional NSAIDs Aspirin Ibuprofen Ketoprofen Naproxen COX-2 Inhibitors Celecoxib Rofecoxib Nonsteroidal Anti-Inflammatory Drugs (NSAIDs)

  17. Nonsteroidal Anti-Inflammatory Drugs (NSAIDs) • To relieve pain and inflammation • Use in combination with a DMARD • Gastrointestinal side effects

  18. Hydroxychloroquine Sulfasalazine Methotrexate Leflunomide Gold Azathioprine Disease-Modifying Antirheumatic Drugs (DMARDs)

  19. Disease-Modifying Antirheumatic Drugs (DMARDs) • Control symptoms • No immediate analgesic effects • Can delay progression of the disease (prevent/slow joint and cartilage damage and destruction) • Effects generally not seen until a few weeks to months

  20. DMARDs • hydroxychloroquine • mild non-erosive disease • combinations • 200 mg bid • eye exams

  21. DMARDs • Sulfasalazine • 1 gm bid - tid • CBC, LFTs • onset 1 - 2 months • Methotrexate • most commonly used drug • fast acting (4-6 weeks) • po, SQ - weekly • CBC, LFTs

  22. DMARDs • IM Gold • slow onset (3-6 months) • weekly then monthly injections • CBC, UA before each injection • Oral Gold • less effective • slow acting (4-6 months) • daily • CBC, UA

  23. Biologic Response Modifiers • Etanercept • Infliximab • Anakinra

  24. Biologic Response Modifiers • Etanercept and infliximab target tumor necrosis factor alpha (TNF-) • Anakinra targets interleukin-1 receptor

  25. OSTEOARTHRITIS

  26. MULTIFACTORAL ETIOLOGY OF OA ● Joint instability ● Age ● Hormonal factors ● Trauma ● Altered biochemistry ● Inflammation ● Genetic predisposition ● ? Others

  27. SYMPTOMS AND SIGNS OF OA • Pain – worse on use of joint • Stiffness – mild after immobility • Loss of movement • Pain on movement/restricted range • Tenderness (articular or periarticular) • Bony swelling • Soft tissue swelling • Joint crepitus

  28. RADIOLOGICAL FEATURES OF OA • Narrowing of joint space • Osteophytosis • Altered bone contour • Bone sclerosis and cysts • Periarticular calcification • Soft-tissue swelling

  29. MANAGEMENT OF OSTEOARTHTITIS Confirm diagnosis Initial Therapy : Pysiotherapy Wt loss Local therapy Paracetamol

  30. MANAGEMENTOFOSTEOARTHTITIScont • Second-line approach: NSAIDS Intra-articular therapy: steroids,hyalurinate Opioids ?glucosamines Arthroscopy Surgery

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