Lupus & antiphospholipid syndrome

Assessment and personalised advice for fatigue in systemic lupus erythematosus using an innovative digital tool: the Lupus Expert system for the Assessment of Fatigue (LEAF) study

RMD OpenPublished Cross-sectional study

Authors' conclusion

Fatigue is commonly severe in SLE, and associated with insomnia, pain, fibromyalgia and active disease according to patients' perspective. Our study shows the usefulness of an automated digital tool to manage fatigue in SLE.

Study context

Population
Participants with systemic lupus erythematosus (SLE) using the LEAF digital tool, May–November 2022 (95.2% women, median age 43yo, IQR 34–51)
Participants
1,250 participants
Outcome
Usefulness of an automated digital tool (LEAF) to manage fatigue in SLE
Methodological detailsdigital tool, completely automated, validated patient-reported instruments
  • Digital tool
  • Completely automated
  • Validated patient-reported instruments

Main finding

As reported in the abstract

Significant fatigue (Functional Assessment of Chronic Illness Therapy-Fatigue <34)

78.9%

Found LEAF helpful

93.2%

Would recommend LEAF to another patient with SLE

92.3%

Observational data: associations, not effects.

Further findings

Fatigue vs no significant fatigue, univariate analysis

More likely women
P = 0.01
Perceived disease as more active
P < 0.0001
Higher pain
P < 0.0001
Higher anxiety
P < 0.0001
Higher depression
P < 0.0001
Higher insomnia
P < 0.0001
Higher stress
P < 0.0001
More likely to screen for fibromyalgia
P < 0.0001
  • Univariate analysis

Parameters independently associated with fatigue, multivariable analysis

Insomnia
P = 0.0003
Pain
P = 0.002
Fibromyalgia
P = 0.008
Self-reported active SLE
P = 0.02
Stress
P = 0.045
  • Multivariable analysis

Original publication

Assessment and personalised advice for fatigue in systemic lupus erythematosus using an innovative digital tool: the Lupus Expert system for the Assessment of Fatigue (LEAF) study. RMD Open. Published 6 December 2023. doi:10.1136/rmdopen-2023-003476

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