TY - JOUR
T1 - Performance of the Patient-Reported Outcomes Measurement Information System-29 in scleroderma
T2 - A Scleroderma Patient-centered Intervention Network Cohort Study
AU - on behalf of the SPIN Investigators
AU - Kwakkenbos, Linda
AU - Thombs, Brett D.
AU - Khanna, Dinesh
AU - Carrier, Marie Eve
AU - Baron, Murray
AU - Furst, Daniel E.
AU - Gottesman, Karen
AU - Van Den Hoogen, Frank
AU - Malcarne, Vanessa L.
AU - Mayes, Maureen D.
AU - Mouthon, Luc
AU - Nielson, Warren R.
AU - Poiraudeau, Serge
AU - Riggs, Robert
AU - Sauvé, Maureen
AU - Wigley, Fredrick
AU - Hudson, Marie
AU - Bartlett, Susan J.
N1 - Funding Information:
Disclosure statement: W.R.N. has acted as a consultant for the CIHR. D.E.F. has consulted for and received research grants from AbbVie, Actelion, Amgen, Corbus, Cytori, NIH, Novartis, Pfizer and Roche/Genetech. D.K. was funded by NIH/NIAMS K24 AR063120 and was a PROMIS investigator under NIH/NIAMS U01 AR057936A. All other authors have declared no conflicts of interest.
Funding Information:
SPIN is funded by a Canadian Institutes of Health Research (CIHR) Emerging Team Grant for Rare Diseases (PI, B.D.T.; TR3-119192). In addition to CIHR funding, SPIN has received institutional contributions from the Lady Davis Institute for Medical Research of the Jewish General Hospital, Montréal, Canada and from McGill University, Montréal, Canada. SPIN has also received support from the Scleroderma Society of Ontario, the Scleroderma Society of Canada and Sclérodermie Québec. The funding that SPIN has received was for establishing the SPIN Cohort and developing a series of eHealth interventions. Dr L.K. was supported by a CIHR Banting Postdoctoral Fellowship. Dr B.D.T. was supported by an Investigator Salary Award from the Arthritis Society. Dr D.K. was supported by the NIH/National Institute of Arthritis and Musculoskeletal and Skin diseases (NIAMS) K24 AR063120. A full list of the SPIN investigators is available in the SPIN investigators section of the Supplementary Data, available at Rheumatology Online.
Publisher Copyright:
© The Author 2017. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved.
PY - 2017/8/1
Y1 - 2017/8/1
N2 - Objective. The Patient-Reported Outcomes Measurement Information System (PROMIS)-29 assesses seven health-related quality of life domains plus pain intensity. The objective was to examine PROMIS-29v 2 validity and explore clinical associations in patients with SSc. Methods. English-speaking SSc patients in the Scleroderma Patient-centered Intervention Network Cohort from 26 sites in Canada, the USA and the UK completed the PROMIS-29v 2 between July 2014 and November 2015. Enrolling physicians provided medical data. To examine convergent validity, hypotheses on the direction and magnitude of correlations with legacy measures were tested. For clinical associations, t-tests were conducted for dichotomous variables and PROMIS-29v 2 domain scores. Effect sizes (ESs) were labelled as small (<0.25), small to moderate (0.25-0.45), moderate (0.46-0.55), moderate to large (0.56-0.75) and large (>0.75).Results. There were 696 patients (87% female), mean (s.d.) disease duration 11.6 (8.7) years, 57% with limited cutaneous subtype. Validity indices were consistent with seven of nine hypotheses (|r| =0.51-0.87, P < 0.001), with minor divergence for two hypotheses. Gastrointestinal involvement was associated with significantly worse outcomes for all eight PROMIS-29v 2 domains (moderate or moderate to large ES in six of eight). Presence of joint contractures was associated with significant decrements in seven domains (small or small to moderate ESs). Skin thickening, diffuse cutaneous subtype and presence of overlap syndromes were significantly associated (small or small to moderate ESs) with five or six domains. Conclusion. This study further establishes the validity of the PROMIS-29v2 in SSc and underlines the importance of gastrointestinal symptoms and joint contractures in reduced health-related quality of life.
AB - Objective. The Patient-Reported Outcomes Measurement Information System (PROMIS)-29 assesses seven health-related quality of life domains plus pain intensity. The objective was to examine PROMIS-29v 2 validity and explore clinical associations in patients with SSc. Methods. English-speaking SSc patients in the Scleroderma Patient-centered Intervention Network Cohort from 26 sites in Canada, the USA and the UK completed the PROMIS-29v 2 between July 2014 and November 2015. Enrolling physicians provided medical data. To examine convergent validity, hypotheses on the direction and magnitude of correlations with legacy measures were tested. For clinical associations, t-tests were conducted for dichotomous variables and PROMIS-29v 2 domain scores. Effect sizes (ESs) were labelled as small (<0.25), small to moderate (0.25-0.45), moderate (0.46-0.55), moderate to large (0.56-0.75) and large (>0.75).Results. There were 696 patients (87% female), mean (s.d.) disease duration 11.6 (8.7) years, 57% with limited cutaneous subtype. Validity indices were consistent with seven of nine hypotheses (|r| =0.51-0.87, P < 0.001), with minor divergence for two hypotheses. Gastrointestinal involvement was associated with significantly worse outcomes for all eight PROMIS-29v 2 domains (moderate or moderate to large ES in six of eight). Presence of joint contractures was associated with significant decrements in seven domains (small or small to moderate ESs). Skin thickening, diffuse cutaneous subtype and presence of overlap syndromes were significantly associated (small or small to moderate ESs) with five or six domains. Conclusion. This study further establishes the validity of the PROMIS-29v2 in SSc and underlines the importance of gastrointestinal symptoms and joint contractures in reduced health-related quality of life.
KW - Clinical
KW - PROMIS
KW - Quality of life
KW - Systemic sclerosis
KW - Validation
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UR - http://www.scopus.com/inward/citedby.url?scp=85028315835&partnerID=8YFLogxK
U2 - 10.1093/rheumatology/kex055
DO - 10.1093/rheumatology/kex055
M3 - Article
C2 - 28431140
AN - SCOPUS:85028315835
SN - 1462-0324
VL - 56
SP - 1302
EP - 1311
JO - Rheumatology and Rehabilitation
JF - Rheumatology and Rehabilitation
IS - 8
ER -