SLEDAI-2K for SLE Disease Activity
Systemic Lupus Erythematosus Disease Activity Index 2000. 24-item weighted score measuring disease activity across 9 organ systems in the preceding 10 days.
Score interpretation
SLEDAI-2K = 0: No disease activity. Remission.
→ Continue maintenance therapy. Consider slow taper of immunosuppressants if sustained remission > 6–12 months. 3–6 monthly rheumatology review. Monitor: BP, urine PCR, FBC, renal function, anti-dsDNA, complement.
SLEDAI-2K 1–5: mild disease activity (Mosca & Bombardieri 2006).
→ Continue or optimise hydroxychloroquine (adults: up to 5 mg/kg/day). Low-dose prednisolone for symptomatic control. Children: use a children's formulary. Rheumatology review in 4–8 weeks. Monitor renal function and urine PCR.
SLEDAI-2K 6–10: moderate disease activity. Escalation of therapy warranted.
→ Adults: prednisolone 0.5 mg/kg/day; add/optimise immunosuppressant: azathioprine (2 mg/kg/day) or mycophenolate mofetil (2–3 g/day). Children: use a children's formulary. Rheumatology review in 2–4 weeks. Check anti-dsDNA, complement, renal function.
SLEDAI-2K 11–19: high disease activity.
→ Urgent rheumatology review. Adults: IV methylprednisolone 500mg–1g/day × 3 days for severe flare; prednisolone 1 mg/kg/day oral. Children: use a children's formulary. Cyclophosphamide IV (Euro-Lupus protocol) for severe nephritis or CNS involvement. Belimumab or voclosporin for renal disease. Rituximab for refractory disease. Nephrology referral for lupus nephritis ≥ Class III/IV.
SLEDAI-2K ≥ 20: very high disease activity — organ- or life-threatening flare.
→ Urgent rheumatology review. Adults: IV methylprednisolone 500mg–1g/day × 3 days for severe flare; prednisolone 1 mg/kg/day oral. Children: use a children's formulary. Cyclophosphamide IV (Euro-Lupus protocol) for severe nephritis or CNS involvement. Belimumab or voclosporin for renal disease. Rituximab for refractory disease. Nephrology referral for lupus nephritis ≥ Class III/IV.
Interpretation bands for the SLEDAI-2K. Apply clinical judgement and local guidance.
References
- Bombardier C, Gladman DD, Urowitz MB, et al. Derivation of the SLEDAI. A disease activity index for lupus patients. Arthritis Rheum. 1992;35(6):630–640.
- Gladman DD, Ibañez D, Urowitz MB. Systemic lupus erythematosus disease activity index 2000. J Rheumatol. 2002;29(2):288–291.
- Mosca M, Bombardieri S. Assessing remission in systemic lupus erythematosus. Clin Exp Rheumatol. 2006;24(6 Suppl 43):S99–S104.
Related
Curated clinical cross-links plus same-class fallbacks.
- Obinutuzumab (Anti-CD20 — Lupus Nephritis) · Glycoengineered Type II Anti-CD20 Monoclonal Antibody
- Hydroxychloroquine · Antimalarial — Lupus / Dermatoses
- Belimumab (Cutaneous Lupus) · BLyS/BAFF Inhibitor (Anti-B-Lymphocyte Stimulator)
- Natalizumab · Disease-Modifying Therapy — MS (Anti-VLA-4 Monoclonal Antibody)
- Cyclophosphamide (Nephrology) · ANCA Vasculitis / Lupus Nephritis
- Belimumab (Lupus Nephritis) · Lupus Nephritis
- Cutaneous Lupus Erythematosus · BAD; EULAR
- Osteoporosis / Fragility Fracture · NOGG 2021; NICE NG147; NG224
- Arteritic AION (Giant Cell Arteritis) · RCOphth; BSR
- Osteoarthritis Hip / Knee Management · NICE NG226 (2022)
- Lupus Nephritis · EULAR/ERA-EDTA 2019; KDIGO 2024
- Rheumatoid Arthritis Management · NICE CG79 2018 / EULAR 2022
Decision support only — verify against a current formulary, NICE, or your local guideline before clinical use.