Evidence map›Paper›PMID 42414039›Full record

ArticleLupus science & medicine2026

Qualitative interview study in patients with SLE to assess patient perception of fatigue and skin-related symptoms.

Joseph F Merola, Victoria P Werth, Jiyoon C Choi, Brandon Becker, Teresa Edwards, Coburn Hobar, Samantha Pomponi, Laurie Eliason, Vibeke Strand

Abstract read
In one paragraph

Article in Lupus science & medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Joseph F MerolaDepartment of Medicine and Rheumatology, UT Southwestern Medical Center, Dallas, Texas, USA Joseph.Merola@utsouthwestern.edu.
Victoria P WerthDepartment of Dermatology, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania, USA.ORCID 0000-0003-3030-5369
Jiyoon C ChoiBristol Myers Squibb, Princeton, New Jersey, USA.
Brandon BeckerBristol Myers Squibb, Princeton, New Jersey, USA.
Teresa EdwardsRTI International, Research Triangle Park, North Carolina, USA.
Coburn HobarBristol Myers Squibb, Princeton, New Jersey, USA.
Samantha PomponiBristol Myers Squibb, Princeton, New Jersey, USA.
Laurie EliasonBristol Myers Squibb, Princeton, New Jersey, USA.
Vibeke StrandDivision of Immunology and Rheumatology, Stanford University School of Medicine, Palo Alto, California, USA.ORCID 0000-0003-4978-4072

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveSLE is a chronic autoimmune disorder with a range of symptoms. While these are broadly reported in the literature, the symptom impact of SLE on patient health-related quality of life is less well documented. This qualitative interview study aimed to understand the nature and importance of skin symptoms, evaluate the content validity of the Functional Assessment of Chronic Illness Therapy-Fatigue (FACIT-Fatigue) scale in SLE and assess what constitutes meaningful change in SLE-associated fatigue and skin symptoms.

methodsIn August 2023, 60 min individual interviews were conducted virtually with 18 adults in the USA who self-reported a diagnosis of SLE and reported experiencing SLE-related fatigue within the prior 30 days. 17 participants also reported experiencing SLE-related skin symptoms. Participants described their experiences with these symptoms and their perceptions of the smallest meaningful improvement using their own words and using the Patient Global Impression of Severity (PGIS) and Patient Global Impression of Change (PGIC) scales. Cognitive debriefing was conducted to evaluate content validity of the 13-item FACIT-Fatigue scale (V.4) for SLE-related fatigue.

resultsOf the 18 participants interviewed (mean age 51.7 years (range 33-67 years)), 17 were female and nine were white. All participants acknowledged that all items of the FACIT-Fatigue scale were relevant to SLE-related fatigue and most could comprehend and answer all items without difficulty. 13 participants indicated that a one-point improvement in fatigue on the PGIS would be meaningful. All participants with skin symptoms understood the skin-specific PGIS and PGIC items without difficulty. A one-point improvement on the PGIS and 'a little better/moderately better' on the PGIC represented meaningful improvements in skin symptoms by most participants.

conclusionThese results support the use of the FACIT-Fatigue scale in SLE trials and suggest that even minimal improvements in fatigue and skin symptoms are meaningful to patients.

Indexed as

FatigueLupus Erythematosus, SystemicQuality of LifeAdultAgedFemaleHumansInterviews as TopicMaleMiddle AgedPerceptionQualitative ResearchReproducibility of ResultsSeverity of Illness IndexSymptom BurdenAutoimmune DiseasesFatigueLupus Erythematosus, SystemicPatient Reported Outcome MeasuresQualitative research

Identifiers

PMID42414039
PMCPMC13343079

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.