Evidence map›Paper›PMID 39608865›Full record

ArticleRMD open2024

Performance of the EULAR Systemic sclerosis Impact of Disease (ScleroID) questionnaire as a patient-reported outcome measure for patients with diffuse systemic sclerosis.

Rucsandra Dobrota, Alexandru Garaiman, Kim Fligelstone, Ann Tyrrell Kennedy, Annelise Roennow, Yannick Allanore, Patricia E Carreira, László Czirják, Chris Denton, Roger Hesselstrand and 11 more

Abstract readMulticenter Study
In one paragraph

Article in RMD open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

1 citing paper in PubMed.

  1. Article
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

21 authors.

Rucsandra DobrotaDepartment of Rheumatology, University Hospital Zurich, Zurich, Switzerland.ORCID 0000-0001-9819-7574
Alexandru GaraimanDepartment of Rheumatology, University Hospital Zurich, Zurich, Switzerland.
Kim FligelstoneFederation of European Scleroderma Associations (FESCA), London, UK.
Ann Tyrrell KennedyFederation of European Scleroderma Associations (FESCA), Tournai, Belgium.
Annelise RoennowFederation of European Scleroderma Associations (FESCA), Aalborg, Denmark.
Yannick AllanoreDepartment of Rheumatology A, Universite Paris Descartes, APHP and Cochin Hospital, Paris, France.ORCID 0000-0002-6149-0002
Patricia E CarreiraDepartment of Rheumatology, Hospital Universitario Doce de Octubre, Madrid, Spain.ORCID 0000-0001-8279-3806
László CzirjákDepartment of Rheumatology and Immunology, Medical School, University of Pécs, Pécs, Hungary.
Chris DentonCentre for Rheumatology, University College London, London, UK.
Roger HesselstrandDepartment of Rheumatology, Lund University, Lund, Sweden.
Gunnel SandqvistDepartment of Rheumatology, Lund University, Lund, Sweden.
Otylia Kowal-BieleckaRheumatology and Internal Medicine, Medical University of Bialystok, Bialystok, Poland.
Cosimo BruniDepartment of Rheumatology, University Hospital Zurich, Zurich, Switzerland.ORCID 0000-0003-2813-2083
Marco Matucci-CerinicDepartment of Experimental and Clinical Medicine, Division of Rheumatology AOUC, University of Florence, Florence, Italy.
Carina MihaiDepartment of Rheumatology, University Hospital Zurich, Zurich, Switzerland.ORCID 0000-0002-8627-8817
Ana Maria GhergheDepartment of Internal Medicine and Rheumatology, Carol Davila University of Medicine and Pharmacy, Cantacuzino Hospital, Bucharest, Romania.
Ulf Mueller-LadnerDepartment of Rheumatology and Clinical Immunology, Justus Liebig University Giessen, Campus Kerckhoff, Bad Nauheim, Germany.
Tore KvienCenter for Treatment of Rheumatic and Musculoskeletal Diseases (REMEDY), Diakonhjemmet Hospital, Oslo, Norway.
Turid HeibergRegional Research Support, Oslo University Hospital, Oslo, Norway.
Oliver DistlerDepartment of Rheumatology, University Hospital Zurich, Zurich, Switzerland.ORCID 0000-0002-0546-8310
Mike Oliver BeckerDepartment of Rheumatology, University Hospital Zurich, Zurich, Switzerland MikeOliver.Becker@usz.ch.ORCID 0000-0001-9102-3088

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveSystemic sclerosis Impact of Disease (ScleroID) is the first comprehensive patient-reported outcome measure (PROM) specifically developed for systemic sclerosis (SSc). We investigated the performance of ScleroID in patients with diffuse cutaneous SSc (dcSSc), as a prerequisite for its use in randomised controlled trials (RCTs) testing potentially disease-modifying drugs.

methodsAll patients with dcSSc from the large, multicentric, ScleroID cohort were included. SSc-Health Assessment Questionnaire (HAQ), EuroQol-5 Dimensions and 36-item Short Form Health Survey (SF-36) were used as comparators. The study includes a longitudinal arm with a reliability visit at 7±3 days and a 12 months follow-up visit. The performance of ScleroID in dcSSc was assessed according to the Outcome Measures in Rheumatology filter.

resultsIn total, 152 dcSSc patients were analysed (29% male, median age 54 years). ScleroID reflected well the disease impact of dcSSc, showing a good construct validity with high Spearman's correlation coefficients with comparators (SSc-HAQ, 0.79, 95% CI (0.69, 0.86); HAQ-Disability Index, 0.72 95% CI (0.60, 0.80); SF-36 physical score, -0.69 95% CI (-0.77, -0.60)). The internal consistency was strong (Cronbach's alpha 0.87, split-half reliability coefficient 0.88).In the longitudinal arm, 44 patients had a reliability visit and 113 had a follow-up visit, of whom 19/113 (17%) reported a significant change (11 improved, 8 worsened). ScleroID showed a good consistency and discriminative ability with excellent test-retest reliability (intraclass correlation coefficient 0.89, 95% CI (0.84, 0.92)) and moderate sensitivity to change (standardised response mean -0.63 in the improved subgroup and 0.48 in the worsened subgroup), but superior to the comparators.

conclusionThe European Alliance of Associations for Rheumatology (EULAR) ScleroID performs well for patients with dcSSc. This supports its inclusion and regular assessment as PROM in RCTs.

Indexed as

Patient Reported Outcome MeasuresQuality of LifeScleroderma, DiffuseAdultAgedFemaleHumansMaleMiddle AgedReproducibility of ResultsScleroderma, SystemicSeverity of Illness IndexSurveys and QuestionnairesConnective Tissue DiseasesHealth-Related Quality Of LifePatient Reported Outcome MeasuresScleroderma, Systemic

Identifiers

PMID39608865
PMCPMC11603699

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Registered trials

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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.