Domains and outcome measures for the assessment of limited cutaneous systemic sclerosis: an international collaborative scoping review

Author:

Lescoat Alain1234ORCID,Sandler Robert D5ORCID,Zimmermann François2,Roofeh David34,Hughes Michael5,Pauling John D6,Murphy Susan L478ORCID,Chen Yen T478ORCID,Townsend Whitney 9,Buch Maya H1011ORCID,Khanna Dinesh34

Affiliation:

1. Univ Rennes, CHU Rennes, Inserm, EHESP, Irset (Institut de Recherche en Santé, Environnement et Travail) – UMR_S 1085

2. Department of Internal Medicine and Clinical Immunology, Rennes University Hospital , Rennes, France

3. Department of Internal Medicine, Division of Rheumatology

4. Department of Internal Medicine, Scleroderma Program, University of Michigan , Ann Arbor, MI, USA

5. Department of Rheumatology, Royal Hallamshire Hospital, Sheffield Teaching Hospitals NHS Foundation Trust , Sheffield

6. Department of Pharmacy and Pharmacology, Royal National Hospital for Rheumatic Diseases, Royal United Hospitals , Bath, UK

7. Department of Physical Medicine & Rehabilitation, University of Michigan

8. VA Ann Arbor Healthcare System, Geriatric Research Education and Clinical Center, GRECC

9. Taubman Health Sciences Library, University of Michigan , Ann Arbor, MI, USA

10. Department of Rheumatology, Centre for Musculoskeletal Research, School of Biological Sciences, Faculty of Biology, Medicine & Health, University of Manchester

11. NIHR Manchester Biomedical Research Centre, Manchester Academic Health Science Centre, Manchester University Foundation Trust , Manchester, UK

Abstract

Abstract Objectives The aim of this study was to comprehensively identify instruments within relevant domains employed to assess lcSSc since the endorsement of its consensus definition in 1988. The overall objective is to inform the creation of a Combined Response Index for Scleroderma Trials Assessing lcSSc (CRISTAL). Methods MEDLINE and Embase were searched using terms selected to comprehensively retrieve titles and abstracts mentioning both lcSSc and dcSSc, along with those only mentioning lcSSc, SSc sine scleroderma, limited SSc and/or CREST/CRST. Because our initial assessment of the literature revealed that very few studies included only lcSSc subjects, we also assessed literature that included both cutaneous subsets. A total of 3964 titles and abstracts were screened by two reviewers, and 270 articles were selected for data extraction. Results We identified 27 domains encompassing 459 instruments. Instruments from ‘Skin involvement’, ‘Pulmonary involvement’ and ‘Health-related quality of life and general functioning’ were the most frequently retrieved. Among the 15 most represented instruments announced as primary end points in efficacy or effectiveness studies, 7 were clinician-reported outcomes (ROs), 7 were patient ROs, and one was a performance outcome (6 min-walk test). The mean proportion of lcSSc patients in studies of lcSSc, including studies that mention both lcSSc and dcSSc, was 56.4%, demonstrating that this subset is underrepresented in the literature, given that the prevalence of lcSSc ranges from 60% to 80% in national registries and international cohorts. Conclusion This scoping literature review provides a comprehensive identification of domains and outcomes used to assess lcSSc. Our results also highlight that lcSSc is underrepresented in the literature.

Funder

Scleroderma Raynaud UK

World Scleroderma Foundation

Scleroderma Clinical Trials Consortium

French network of the University Hospitals HUGO

Rennes University Hospital

University of Michigan’s Advanced Rehabilitation Research Training Program in Community Living and Participation

National Institute of Disability

Independent Living, and Rehabilitation Research, Administration for Community Living

National Institutes of Health

National Institute of Arthritis and Musculoskeletal and Skin Diseases T32

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

Reference43 articles.

1. Systemic sclerosis;Denton;Lancet,2017

2. Synovial involvement assessed by power Doppler ultra-sonography in systemic sclerosis: results of a cross-sectional study;Lescoat;Rheumatology (Oxford),2018

3. Scleroderma (systemic sclerosis): classification, subsets and pathogenesis;LeRoy;J. Rheumatol,1988

4. The nosology of systemic sclerosis: how lessons from the past offer new challenges in reframing an idiopathic rheumatological disorder;Lescoat;Lancet Rheumatol,2019

5. Limited cutaneous systemic sclerosis: the unfairly neglected subset;Allanore;J Scleroderma Relat Disord,2016

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