4.7 Article

Definition and initial validation of a Lupus Low Disease Activity State (LLDAS)

期刊

ANNALS OF THE RHEUMATIC DISEASES
卷 75, 期 9, 页码 1615-1621

出版社

BMJ PUBLISHING GROUP
DOI: 10.1136/annrheumdis-2015-207726

关键词

Systemic Lupus Erythematosus; Disease Activity; Outcomes research

资金

  1. Arthritis Australia
  2. David Bickart Clinician Research Fellowship from the University of Melbourne Faculty of Medicine, Dentistry and Health Sciences
  3. NHMRC Research Fellowship [APP1071735]
  4. Arthritis and Osteoporosis Victoria
  5. GlaxoSmithKline, UK
  6. UCB Biopharma SPRL, Belgium

向作者/读者索取更多资源

Aims Treating to low disease activity is routine in rheumatoid arthritis, but no comparable goal has been defined for systemic lupus erythematosus (SLE). We sought to define and validate a Lupus Low Disease Activity State (LLDAS). Methods A consensus definition of LLDAS was generated using Delphi and nominal group techniques. Criterion validity was determined by measuring the ability of LLDAS attainment, in a single-centre SLE cohort, to predict non-accrual of irreversible organ damage, measured using the Systemic Lupus International Collaborating Clinics Damage Index (SDI). Results Consensus methodology led to the following definition of LLDAS: (1) SLE Disease Activity Index (SLEDAI)-2K 4, with no activity in major organ systems (renal, central nervous system (CNS), cardiopulmonary, vasculitis, fever) and no haemolytic anaemia or gastrointestinal activity; (2) no new lupus disease activity compared with the previous assessment; (3) a Safety of Estrogens in Lupus Erythematosus National Assessment (SELENA)-SLEDAI physician global assessment (scale 0-3) 1; (4) a current prednisolone (or equivalent) dose 7.5mg daily; and (5) well tolerated standard maintenance doses of immunosuppressive drugs and approved biological agents. Achievement of LLDAS was determined in 191 patients followed for a mean of 3.9years. Patients who spent greater than 50% of their observed time in LLDAS had significantly reduced organ damage accrual compared with patients who spent less than 50% of their time in LLDAS (p=0.0007) and were significantly less likely to have an increase in SDI of 1 (relative risk 0.47, 95% CI 0.28 to 0.79, p=0.005). Conclusions A definition of LLDAS has been generated, and preliminary validation demonstrates its attainment to be associated with improved outcomes in SLE.

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