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Rheumatic Disorders Overview

Rheumatic Disorders: Introduction

  • Prevalence: Most common disabling musculoskeletal disorder in the U.S. with about 46 million affected.
  • Demographics: Increasing age is a major factor; nearly 2/3 of adults with arthritis are aged 18-64 years.
  • Types of Disorders:
    • Local Disorders:
    • Osteoarthritis
    • Infectious arthritis (e.g., Lyme disease)
    • Systemic Disorders:
    • Immune-mediated conditions (e.g., rheumatoid arthritis)
    • Post-infectious joint issues
    • Joint dysfunction secondary to other diseases (e.g., psoriatic arthritis, gout)

Local Disorders of Joint Function: Osteoarthritis

  • Definition: Most common arthritis globally; degenerative disorder associated with aging and repetitive stress.
  • Characteristics:
    • Loss of articular cartilage
    • Calcification of cartilage
    • Bone spur formation
    • Primarily affects weight-bearing joints.

Etiology of Osteoarthritis

  • Factors that increase wear and tear:
    • Obesity: Increases stress on joints.
    • Joint Trauma: Previous injuries can predispose.
    • Congenital Disorders: Structural malformations.
    • Lifestyle and Occupation: High-stress activities on joints.
    • Genetic Factors: Hereditary predispositions.
    • Hormonal Changes: Particularly in postmenopausal women.

Pathogenesis of Osteoarthritis

  • Initial Injury:
    • Chondrocytes release enzymes that promote breakdown, leading to collagen fatigue.
    • Resulting in microfractures.
  • Progressive Damage:
    • Structural damage leads to osteophyte (bone spur) formation, synovial inflammation, joint effusion, and loss of proteoglycan and collagen matrix.

Clinical Manifestations of Osteoarthritis

  • Symptoms include:
    • Localized joint pain
    • Crepitus (grating sensation) with movement
    • Morning stiffness
    • Bony enlargements (e.g., Heberden and Bouchard nodes)

Radiologic Changes in Osteoarthritis

  • Findings:
    • Bony proliferation at joint margins.
    • Asymmetric narrowing of joint spaces.
    • Subchondral bone sclerosis.
    • Joint malalignment and cyst formation.

Treatment of Osteoarthritis

  • Goals: Decrease joint stress, manage pain, and protect against further trauma.
  • Medications:
    • Acetaminophen and NSAIDs (e.g., COX-2 inhibitors like Celebrex)
    • Intra-articular injections of hyaluronan
    • Physical therapy to improve function
    • Surgery as a last resort.

Systemic Disorders of Joint Function: Rheumatoid Arthritis

  • Overview: Autoimmune inflammatory disease affecting synovial membranes, cartilage, and surrounding structures.
  • Demographics: Primarily affects women and peaks between ages 40-50.
  • Cause: Unknown; linked to abnormal autoimmune responses potentially triggered by infections in predisposed individuals.

Pathogenesis of Rheumatoid Arthritis

  • Initial Phase: Immune response appears localized in synovial tissue with activation of B cells, T cells, and macrophages.
  • Inflammatory Phase: Immune mediators escalate inflammation, leading to the formation of a pannus that destroys cartilage.
  • Destruction Phase: Ongoing inflammation results in joint subluxations and deformities.

Clinical Manifestations of Rheumatoid Arthritis

  • Symptoms:
    • Bilateral symmetric polyarthritis mainly in smaller joints
    • Malaise and fatigue
    • Swelling, particularly in hands, wrists, knees, and feet.
    • Characteristic hand deformities (e.g., swan-neck and boutonniere deformities).

Other Clinical Manifestations

  • Cardiac Issues: Pericarditis, myocarditis, mitral valve disease.
  • Pulmonary Issues: Pleuritis, pulmonary effusion.
  • Ophthalmic Issues: Scleritis, particularly associated with Sjögren's syndrome.

Diagnosis of Rheumatoid Arthritis

  • Criteria: According to guidelines, requires:
    • At least one swollen joint
    • No alternative diagnosis explaining the swelling
    • Minimum score of 6 on the diagnostic criteria scale.

Treatment of Rheumatoid Arthritis

  • Goals: Manage symptoms, prevent joint damage, maintain function.
  • Medications:
    • NSAIDs, corticosteroids, and disease-modifying antirheumatic drugs (DMARDs)
    • Biological agents targeting TNF-α and IL-1
    • Tyrosine kinase inhibitors (oral).

Joint Dysfunction Secondary to Other Diseases

  • Common Conditions: Diabetes, hemophilia, and metabolic disorders associated with chronic diseases.
  • Gout:
    • Characterized by hyperuricemia and deposition of uric acid crystals in joints.
    • Common in middle-aged men and postmenopausal women.

Clinical Manifestations of Gout

  • Phases:
    • Asymptomatic Hyperuricemia: Elevated urate levels with no clinical signs.
    • Acute Gouty Arthritis: Involves warm, red, and tender joints, most commonly the great toe.
    • Intercritical Gout: Intervals between acute attacks without symptoms.
    • Chronic Tophaceous Gout: Development of tophi and possible joint deformities after 10 years.

Diagnosis and Treatment of Gout

  • Diagnosis: Joint fluid analysis, serum uric acid levels, imaging tests.
  • Treatment: Colchicine for acute attacks, NSAIDs, and medications to correct hyperuricemia.

Summary

  • Rheumatic disorders encompass a range of conditions affecting joint function, with specific local (e.g., osteoarthritis) and systemic (e.g., rheumatoid arthritis) implications, involving complex pathophysiological processes necessitating comprehensive management strategies.