Preliminary criteria for the very early diagnosis of systemic sclerosis: results of a Delphi Consensus Study from EULAR Scleroderma Trials and Research Group
Objective To identify a core set of preliminary items considered as important for the very early diagnosis of systemic sclerosis (SSc). Methods A list of items provided by European League Against Rheumatism (EULAR) Scleroderma Trial and Research(EUSTAR) centres were subjected to a Delphi exercise am...
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Published in | Annals of the rheumatic diseases Vol. 70; no. 3; pp. 476 - 481 |
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Main Authors | , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
BMJ Publishing Group Ltd and European League Against Rheumatism
01.03.2011
BMJ Publishing Group Elsevier Limited |
Subjects | |
Online Access | Get full text |
ISSN | 0003-4967 1468-2060 1468-2060 |
DOI | 10.1136/ard.2010.136929 |
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Abstract | Objective To identify a core set of preliminary items considered as important for the very early diagnosis of systemic sclerosis (SSc). Methods A list of items provided by European League Against Rheumatism (EULAR) Scleroderma Trial and Research(EUSTAR) centres were subjected to a Delphi exercise among 110 experts in the field of SSc. In round 1, experts were asked to choose the items they considered as the most important for the very early diagnosis of SSc. In round 2, experts were asked to reconsider the items accepted after the first stage. In round 3, the clinical relevance of selected items and their importance as measures that would lead to an early referral process were rated using appropriateness scores. Results Physicians from 85 EUSTAR centres participated in the study and provided an initial list of 121 items. After three Delphi rounds, the steering committee, with input from external experts, collapsed the 121 items into three domains containing seven items, developed as follows: skin domain (puffy fingers/puffy swollen digits turning into sclerodactily); vascular domain (Raynaud's phenomenon, abnormal capillaroscopy with scleroderma pattern) and laboratory domain (antinuclear, anticentromere and antitopoisomerase-I antibodies). Finally, the whole assembly of EUSTAR centres ratified with a majority vote the results in a final face-to-face meeting. Conclusion The three Delphi rounds allowed us to identify the items considered by experts as necessary for the very early diagnosis of SSc. The validation of these items to establish diagnostic criteria is currently ongoing in a prospective observational cohort. |
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AbstractList | Objective To identify a core set of preliminary items considered as important for the very early diagnosis of systemic sclerosis (SSc). Methods A list of items provided by European League Against Rheumatism (EULAR) Scleroderma Trial and Research(EUSTAR) centres were subjected to a Delphi exercise among 110 experts in the field of SSc. In round 1, experts were asked to choose the items they considered as the most important for the very early diagnosis of SSc. In round 2, experts were asked to reconsider the items accepted after the first stage. In round 3, the clinical relevance of selected items and their importance as measures that would lead to an early referral process were rated using appropriateness scores. Results Physicians from 85 EUSTAR centres participated in the study and provided an initial list of 121 items. After three Delphi rounds, the steering committee, with input from external experts, collapsed the 121 items into three domains containing seven items, developed as follows: skin domain (puffy fingers/puffy swollen digits turning into sclerodactily); vascular domain (Raynaud's phenomenon, abnormal capillaroscopy with scleroderma pattern) and laboratory domain (antinuclear, anticentromere and antitopoisomerase-I antibodies). Finally, the whole assembly of EUSTAR centres ratified with a majority vote the results in a final face-to-face meeting. Conclusion The three Delphi rounds allowed us to identify the items considered by experts as necessary for the very early diagnosis of SSc. The validation of these items to establish diagnostic criteria is currently ongoing in a prospective observational cohort. To identify a core set of preliminary items considered as important for the very early diagnosis of systemic sclerosis (SSc).OBJECTIVETo identify a core set of preliminary items considered as important for the very early diagnosis of systemic sclerosis (SSc).A list of items provided by European League Against Rheumatism (EULAR) Scleroderma Trial and Research(EUSTAR) centres were subjected to a Delphi exercise among 110 experts in the field of SSc. In round 1, experts were asked to choose the items they considered as the most important for the very early diagnosis of SSc. In round 2, experts were asked to reconsider the items accepted after the first stage. In round 3, the clinical relevance of selected items and their importance as measures that would lead to an early referral process were rated using appropriateness scores.METHODSA list of items provided by European League Against Rheumatism (EULAR) Scleroderma Trial and Research(EUSTAR) centres were subjected to a Delphi exercise among 110 experts in the field of SSc. In round 1, experts were asked to choose the items they considered as the most important for the very early diagnosis of SSc. In round 2, experts were asked to reconsider the items accepted after the first stage. In round 3, the clinical relevance of selected items and their importance as measures that would lead to an early referral process were rated using appropriateness scores.Physicians from 85 EUSTAR centres participated in the study and provided an initial list of 121 items. After three Delphi rounds, the steering committee, with input from external experts, collapsed the 121 items into three domains containing seven items, developed as follows: skin domain (puffy fingers/puffy swollen digits turning into sclerodactily); vascular domain (Raynaud's phenomenon, abnormal capillaroscopy with scleroderma pattern) and laboratory domain (antinuclear, anticentromere and antitopoisomerase-I antibodies). Finally, the whole assembly of EUSTAR centres ratified with a majority vote the results in a final face-to-face meeting.RESULTSPhysicians from 85 EUSTAR centres participated in the study and provided an initial list of 121 items. After three Delphi rounds, the steering committee, with input from external experts, collapsed the 121 items into three domains containing seven items, developed as follows: skin domain (puffy fingers/puffy swollen digits turning into sclerodactily); vascular domain (Raynaud's phenomenon, abnormal capillaroscopy with scleroderma pattern) and laboratory domain (antinuclear, anticentromere and antitopoisomerase-I antibodies). Finally, the whole assembly of EUSTAR centres ratified with a majority vote the results in a final face-to-face meeting.The three Delphi rounds allowed us to identify the items considered by experts as necessary for the very early diagnosis of SSc. The validation of these items to establish diagnostic criteria is currently ongoing in a prospective observational cohort.CONCLUSIONThe three Delphi rounds allowed us to identify the items considered by experts as necessary for the very early diagnosis of SSc. The validation of these items to establish diagnostic criteria is currently ongoing in a prospective observational cohort. To identify a core set of preliminary items considered as important for the very early diagnosis of systemic sclerosis (SSc). A list of items provided by European League Against Rheumatism (EULAR) Scleroderma Trial and Research(EUSTAR) centres were subjected to a Delphi exercise among 110 experts in the field of SSc. In round 1, experts were asked to choose the items they considered as the most important for the very early diagnosis of SSc. In round 2, experts were asked to reconsider the items accepted after the first stage. In round 3, the clinical relevance of selected items and their importance as measures that would lead to an early referral process were rated using appropriateness scores. Physicians from 85 EUSTAR centres participated in the study and provided an initial list of 121 items. After three Delphi rounds, the steering committee, with input from external experts, collapsed the 121 items into three domains containing seven items, developed as follows: skin domain (puffy fingers/puffy swollen digits turning into sclerodactily); vascular domain (Raynaud's phenomenon, abnormal capillaroscopy with scleroderma pattern) and laboratory domain (antinuclear, anticentromere and antitopoisomerase-I antibodies). Finally, the whole assembly of EUSTAR centres ratified with a majority vote the results in a final face-to-face meeting. The three Delphi rounds allowed us to identify the items considered by experts as necessary for the very early diagnosis of SSc. The validation of these items to establish diagnostic criteria is currently ongoing in a prospective observational cohort. |
Author | Randone, S Bellando Furst, DE Czirjak, L Tarner, IH Walker, UA Miniati, I Valentini, G Tyndall, A Müller-Ladner, U Riccieri, V Avouac, J Distler, O Muller, C Matucci-Cerinic, M Smith, V Allanore, Y Cutolo, M Fransen, J |
Author_xml | – sequence: 1 givenname: J surname: Avouac fullname: Avouac, J email: javouac@me.com organization: Rheumatology A Department, Paris Descartes University, Cochin Hospital, Paris, France – sequence: 2 givenname: J surname: Fransen fullname: Fransen, J email: javouac@me.com organization: Department of Rheumatology, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands – sequence: 3 givenname: UA surname: Walker fullname: Walker, UA email: javouac@me.com organization: Department of Rheumatology, Basel University, Basel, Switzerland – sequence: 4 givenname: V surname: Riccieri fullname: Riccieri, V email: javouac@me.com organization: Sapienza University of Rome, Medical Clinic and Therapy Department, Rome, Italy – sequence: 5 givenname: V surname: Smith fullname: Smith, V email: javouac@me.com organization: Department of Rheumatology, Ghent University Hospital, Ghent, Belgium – sequence: 6 givenname: C surname: Muller fullname: Muller, C email: javouac@me.com organization: Hospital de Clínicas da Universidade Federal do Paraná, Curitiba, Brazil – sequence: 7 givenname: I surname: Miniati fullname: Miniati, I email: javouac@me.com organization: Department of Medicine, Section of Rheumatology, University of Florence, Florence, Italy – sequence: 8 givenname: IH surname: Tarner fullname: Tarner, IH email: javouac@me.com organization: Department of Internal Medicine and Rheumatology, Justus-Liebig-University of Giessen, Kerckhoff-Klinik, Bad Nauheim, Germany – sequence: 9 givenname: S Bellando surname: Randone fullname: Randone, S Bellando email: javouac@me.com organization: Hospital de Clínicas da Universidade Federal do Paraná, Curitiba, Brazil – sequence: 10 givenname: M surname: Cutolo fullname: Cutolo, M email: javouac@me.com organization: Department of Internal Medicine, Research Laboratory and Academic Unit of Clinical Rheumatology, University of Genova, Genova, Italy – sequence: 11 givenname: Y surname: Allanore fullname: Allanore, Y email: javouac@me.com organization: Rheumatology A Department, Paris Descartes University, Cochin Hospital, Paris, France – sequence: 12 givenname: O surname: Distler fullname: Distler, O email: javouac@me.com organization: Department of Rheumatology, University Hospital Zurich, Zurich, Switzerland – sequence: 13 givenname: G surname: Valentini fullname: Valentini, G email: javouac@me.com organization: Rheumatology Section, Department of Clinical and Experimental Medicine, Second University of Naples, Naples, Italy – sequence: 14 givenname: L surname: Czirjak fullname: Czirjak, L email: javouac@me.com organization: Department of Rheumatology, University of Pécs, Pecs, Hungary – sequence: 15 givenname: U surname: Müller-Ladner fullname: Müller-Ladner, U email: javouac@me.com organization: Department of Internal Medicine and Rheumatology, Justus-Liebig-University of Giessen, Kerckhoff-Klinik, Bad Nauheim, Germany – sequence: 16 givenname: DE surname: Furst fullname: Furst, DE email: javouac@me.com organization: Division of Rheumatology, Department of Medicine, David Geffen School at UCLA, Los Angeles, California, USA – sequence: 17 givenname: A surname: Tyndall fullname: Tyndall, A email: javouac@me.com organization: Department of Rheumatology, Basel University, Basel, Switzerland – sequence: 18 givenname: M surname: Matucci-Cerinic fullname: Matucci-Cerinic, M email: javouac@me.com organization: Department of Medicine, Section of Rheumatology, University of Florence, Florence, Italy |
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References | Weiner, Hildebrandt, Senécal 1991; 34 Allanore, Avouac, Wipff 2007; 8 Matucci-Cerinic, Allanore, Czirják 2009; 68 Jones, Hunter 1995; 311 LeRoy, Medsger 2001; 28 Taylor 2005; 64 Zochling, van der Heijde, Burgos-Vargas 2006; 65 1980; 23 Lonzetti, Joyal, Raynauld 2001; 44 Denton, Black, Korn 1996; 347 Koenig, Joyal, Fritzler 2008; 58 Khanna, Hays, Park 2007; 57 Khanna, Lovell, Giannini 2008; 67 LeRoy, Black, Fleischmajer 1988; 15 Hudson, Taillefer, Steele 2007; 25 1981; 31 Koenig (10.1136/ard.2010.136929_bib11) 2008; 58 Taylor (10.1136/ard.2010.136929_bib15) 2005; 64 LeRoy (10.1136/ard.2010.136929_bib3) 1988; 15 Jones (10.1136/ard.2010.136929_bib8) 1995; 311 (10.1136/ard.2010.136929_bib2) 1981; 31 Lonzetti (10.1136/ard.2010.136929_bib4) 2001; 44 Denton (10.1136/ard.2010.136929_bib10) 1996; 347 Hudson (10.1136/ard.2010.136929_bib5) 2007; 25 Weiner (10.1136/ard.2010.136929_bib7) 1991; 34 Khanna (10.1136/ard.2010.136929_bib14) 2007; 57 Khanna (10.1136/ard.2010.136929_bib12) 2008; 67 Subcommittee for scleroderma criteria of the American Rheumatism Association Diagnostic and Therapeutic Criteria Committee (10.1136/ard.2010.136929_bib16) 1980; 23 LeRoy (10.1136/ard.2010.136929_bib6) 2001; 28 Allanore (10.1136/ard.2010.136929_bib1) 2007; 8 Zochling (10.1136/ard.2010.136929_bib13) 2006; 65 Matucci-Cerinic (10.1136/ard.2010.136929_bib9) 2009; 68 |
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It is time to cut the Gordian knot and develop a prevention or rescue strategy publication-title: Ann Rheum Dis doi: 10.1136/ard.2008.106302 – volume: 65 start-page: 442 year: 2006 ident: 10.1136/ard.2010.136929_bib13 article-title: ASAS/EULAR recommendations for the management of ankylosing spondylitis publication-title: Ann Rheum Dis doi: 10.1136/ard.2005.041137 – volume: 8 start-page: 607 year: 2007 ident: 10.1136/ard.2010.136929_bib1 article-title: New therapeutic strategies in the management of systemic sclerosis publication-title: Expert Opin Pharmacother doi: 10.1517/14656566.8.5.607 – volume: 58 start-page: 3902 year: 2008 ident: 10.1136/ard.2010.136929_bib11 article-title: Autoantibodies and microvascular damage are independent predictive factors for the progression of Raynaud's phenomenon to systemic sclerosis: a twenty-year prospective study of 586 patients, with validation of proposed criteria for early systemic sclerosis publication-title: Arthritis Rheum doi: 10.1002/art.24038 – volume: 34 start-page: 68 year: 1991 ident: 10.1136/ard.2010.136929_bib7 article-title: Prognostic significance of anticentromere antibodies and anti-topoisomerase I antibodies in Raynaud's disease. A prospective study publication-title: Arthritis Rheum doi: 10.1002/art.1780340111 – volume: 28 start-page: 1573 year: 2001 ident: 10.1136/ard.2010.136929_bib6 article-title: Criteria for the classification of early systemic sclerosis publication-title: J Rheumatol – volume: 25 start-page: 754 year: 2007 ident: 10.1136/ard.2010.136929_bib5 article-title: Improving the sensitivity of the American College of Rheumatology classification criteria for systemic sclerosis publication-title: Clin Exp Rheumatol |
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SubjectTerms | Antibodies, Antinuclear - blood Biological and medical sciences Classification Delphi Technique Diagnosis, Differential Diseases of the osteoarticular system Early Diagnosis Edema - etiology Experts Fingers Humans Medical research Medical sciences Microscopic Angioscopy Mortality Raynaud disease Raynaud Disease - etiology Response rates Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis Scleroderma Scleroderma, Systemic - complications Scleroderma, Systemic - diagnosis Scleroderma, Systemic - immunology Skin Diseases - etiology Studies |
Title | Preliminary criteria for the very early diagnosis of systemic sclerosis: results of a Delphi Consensus Study from EULAR Scleroderma Trials and Research Group |
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