Construct validity and reliability of the Assessment of Systemic Sclerosis-Associated Raynaud's Phenomenon (ASRAP) questionnaire

被引:5
|
作者
Pauling, John D. [1 ,2 ,3 ]
Yu, Lan [4 ]
Frech, Tracy M. [5 ]
Herrick, Ariane L. [6 ,7 ,8 ]
Hummers, Laura K. [9 ]
Shah, Ami A. [9 ]
Denton, Christopher P. [10 ]
Saketkoo, Lesley Ann [11 ]
Withey, Jane [3 ]
Khanna, Dinesh [12 ,13 ]
Domsic, Robyn T. [14 ]
机构
[1] North Bristol NHS Trust, Dept Rheumatol, Bristol, England
[2] Univ Bristol, Bristol Med Sch, Musculoskeletal Res Unit, Translat Hlth Sci, Bristol, England
[3] Royal United Hosp NHS Fdn Trust, Royal Natl Hosp Rheumat Dis part, Dept Rheumatol, Bath, England
[4] Univ Pittsburgh, Dept Med, Philadelphia, PA USA
[5] Vanderbilt Univ, Nashville, TN USA
[6] Univ Manchester, Manchester Acad, Northern Care Alliance NHS Fdn Trust, Hlth Sci Ctr, Manchester, England
[7] Manchester Acad, NIHR Manchester Biomed Res Ctr, Cent Manchester NHS Fdn Trust, Hlth Sci Ctr, Manchester, England
[8] Salford Royal NHS Fdn Trust, Dept Rheumatol, Salford, England
[9] Johns Hopkins Univ, Dept Rheumatol, Sch Med, Baltimore, MD USA
[10] Royal Free Hosp, Ctr Rheumatol & Connect Tissue Dis, London, England
[11] Univ Tulane, Dept Rheumatol, Med Ctr, New Orleans, LA USA
[12] Univ Michigan, Scleroderma Program, Ann Arbor, MI USA
[13] Univ Michigan, Div Rheumatol, Ann Arbor, MI USA
[14] Univ Pittsburgh, Div Rheumatol & Clin Immunol, Pittsburgh, PA USA
关键词
SSc; RP; patient-reported outcome instrument; clinical trial; validation; PHENOMENON SECONDARY; ORAL ILOPROST; METAANALYSIS; MULTICENTER;
D O I
10.1093/rheumatology/kead371
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: Assessment of construct validity and reliability of a novel patient-reported outcome (PRO) instrument for assessing the severity and impact of RP in SSc. Methods: An international multicentre study validation study of the 27-item Assessment of Systemic Sclerosis-Associated Raynaud's Phenomenon (ASRAP) and 10-item short-form (ASRAP-SF) questionnaires. The relationship between ASRAP questionnaires and demographics, clinical phenotype and legacy instruments for assessing SSc-RP severity, disability and pain was assessed. Repeatability was evaluated at 1 week. Anchor-based statements of health status facilitated assessment of ASRAP thresholds of meaning. Results: A total of 420 SSc subjects were enrolled. There was good correlation between ASRAP (and ASRAP-SF) with RP visual analogue scale (VAS) and Scleroderma Health Assessment Questionnaire RP VAS (rho range 0.648-0.727, P < 0.001). Correlation with diary-based assessment of SSc-RP attack frequency and duration was lower (rho range 0.258-0.504, P < 0.001). ASRAP questionnaires had good correlation with instruments for assessing disability, hand function, pain and global health assessment (rho range 0.427-0.575, P < 0.001). Significantly higher ASRAP scores were identified in smokers, patients with active digital ulceration (DU), previous history of DU and calcinosis (P < 0.05 for all comparisons). There was excellent repeatability at 1 week among patients with stable SSc-RP symptoms (intra-class coefficients of 0.891 and 0.848, P < 0.001). Patient-acceptable symptom state thresholds for ASRAP and ASRAP-SF were 45.34 and 45.77, respectively. A preliminary Minimally Important Clinical Difference threshold of 4.17 (95% CI 0.53, 7.81, P 1/4 0.029) was estimated. Conclusion: ASRAP and ASRAP-SF questionnaires are valid and reliable novel PRO instruments for assessing the severity and impact of SSc-RP.
引用
收藏
页码:1281 / 1290
页数:10
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