Systemic Lupus Erythematosus (SLE)
Overview
- Chronic inflammatory disorder of connective tissue causing widespread inflammation and tissue damage.
- Different from discoid lupus which primarily affects the skin.
- Autoimmune disorder resulting in production of antinuclear antibodies (ANA).
- Affects skin, lungs, kidneys, and heart with periods of exacerbations and remissions.
Risk Factors
- More common in women.
- Onset typically between ages 20 and 40.
- Higher risk in African Americans, Asians, and Native Americans.
Signs and Symptoms
- Fatigue and joint pain.
- Fever.
- Butterfly rash across the face (hallmark symptom).
- Raynaud’s phenomenon: vasospasms leading to pale, numb, and cold fingers.
- Anemia and pericarditis (inflammation of heart membrane).
- Lymphadenopathy (enlarged lymph nodes).
Diagnosis
- Positive ANA titer.
- Decreased serum complement (C3 and C4).
- Decreased red blood cells, white blood cells, and platelet counts.
- Increased BUN and creatinine if kidneys are involved.
Treatment
- NSAIDs for pain and inflammation.
- Immunosuppressants like prednisone and methotrexate.
- Hydroxychloroquine, also used for malaria, is effective.
- Topical steroid cream for facial rash.
Nursing Care
- Monitor for complications like renal failure.
- Essential teaching points:
- Avoid UV and sun exposure to prevent skin damage.
- Prevent infection by avoiding sick people and taking protective measures.
- Take frequent rest periods to manage fatigue.
Next topic to be discussed in series: Scleroderma.