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Their treatment recommendations are based on evidence-based data, clinical expertise, and patient-reported outcomes and preferences, with those highlighted as “strong” summarized here along with good practice statements for treatment.
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Key learnings |
Glucocorticoid exposure should be minimized (e.g. tapering prednisone from ≥5 mg/day to ≤5 mg/day within 6 months in patients with stable, controlled SLE), hydroxychloroquine used routinely unless contraindicated, and conventional or biologic immunosuppressive therapies introduced early. |
Patients with SLE should be diagnosed and treated promptly, with the severity of disease activity guiding the intensity and choice of therapy; when multiple organ systems are involved, therapy should be directed toward all manifestations while prioritizing areas of irreversible damage. |
Organ- or life-threatening SLE should be treated urgently with aggressive therapy such as high-dose glucocorticoid and immunosuppressive therapy; combination therapies should be considered, guided by the patient’s clinical condition and preference. |
All treatment decisions should be individualized and involve shared decision-making between patients, rheumatologists, and relevant specialists. |
Abbreviations: ACR, American College of Rheumatology; SLE, systemic lupus erythematosus.
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