Literature DB >> 35169058

PROMIS Provides a Broader Overview of Health-related Quality of Life Than the ESSPRI in Evaluation of Sjögren Syndrome.

Dana D DiRenzo1, Susan Robinson1, Clifton O Bingham1, Alan N Baer1, Thomas Grader-Beck1.   

Abstract

OBJECTIVE: Sjögren syndrome (SS) has a significant impact on health-related quality of life (HRQOL). We sought to evaluate how the Patient Reported Outcome Measurement Information System (PROMIS) domains in SS may supplement the European League Against Rheumatism (EULAR) Sjögren Syndrome Patient Reported Index (ESSPRI).
METHODS: A cross-sectional evaluation was performed on consecutive adult patients during visits to an SS clinic between March 2018 and February 2020. Each patient completed PROMIS short forms related to HRQOL and the ESSPRI, and had a clinical assessment. Patients were either classified as SS by 2016 American College of Rheumatology (ACR)/EULAR criteria, or as "sicca not otherwise specified (NOS)" and used as a comparison group. Univariable and multivariable linear regression models were used to evaluate predictors of PROMIS fatigue (-F), pain interference (-PI), and ability to participate in social roles and activities (-APS).
RESULTS: Two hundred twenty-seven patients with SS and 85 with sicca NOS were included and did not differ in ESSPRI domains; 26% of the SS and 20% of the sicca NOS group had concurrent autoimmune disease. In SS, PROMIS-PI, PROMIS-F, and PROMIS physical function were at least one-half SD worse than US population normative values. PROMIS-PI (r = 0.73) and PROMIS-F (r = 0.80) were highly correlated with ESSPRI pain and fatigue subdomains. Fatigue and pain interference, but not dryness or mood disturbance, were the strongest predictors of social participation in multivariable analysis.
CONCLUSION: In our SS cohort, PROMIS instruments identified a high disease burden of pain interference, fatigue, and physical function. PROMIS-F strongly predicted PROMIS-APS. PROMIS-PI and PROMIS-F scores correlated highly with their respective ESSPRI domains. PROMIS instruments should be considered to identify relevant HRQOL patterns in SS.
Copyright © 2022 The Journal of Rheumatology.

Entities:  

Keywords:  ESSPRI; PROMIS; Sjögren syndrome; fatigue; health-related quality of life

Mesh:

Year:  2022        PMID: 35169058      PMCID: PMC9522433          DOI: 10.3899/jrheum.210633

Source DB:  PubMed          Journal:  J Rheumatol        ISSN: 0315-162X            Impact factor:   5.346


  17 in total

1.  Health-related quality of life and costs in Sjögren's syndrome.

Authors:  Samira T Miyamoto; Valéria Valim; Benjamin A Fisher
Journal:  Rheumatology (Oxford)       Date:  2019-02-15       Impact factor: 7.580

2.  Statistics corner: A guide to appropriate use of correlation coefficient in medical research.

Authors:  M M Mukaka
Journal:  Malawi Med J       Date:  2012-09       Impact factor: 0.875

3.  The Patient-Reported Outcomes Measurement Information System (PROMIS) developed and tested its first wave of adult self-reported health outcome item banks: 2005-2008.

Authors:  David Cella; William Riley; Arthur Stone; Nan Rothrock; Bryce Reeve; Susan Yount; Dagmar Amtmann; Rita Bode; Daniel Buysse; Seung Choi; Karon Cook; Robert Devellis; Darren DeWalt; James F Fries; Richard Gershon; Elizabeth A Hahn; Jin-Shei Lai; Paul Pilkonis; Dennis Revicki; Matthias Rose; Kevin Weinfurt; Ron Hays
Journal:  J Clin Epidemiol       Date:  2010-08-04       Impact factor: 6.437

Review 4.  Primary Sjögren's Syndrome.

Authors:  Xavier Mariette; Lindsey A Criswell
Journal:  N Engl J Med       Date:  2018-03-08       Impact factor: 91.245

5.  Patient-reported outcomes in primary Sjogren's syndrome: comparison of the long and short versions of the Profile of Fatigue and Discomfort--Sicca Symptoms Inventory.

Authors:  S J Bowman; J Hamburger; A Richards; R J Barry; S Rauz
Journal:  Rheumatology (Oxford)       Date:  2008-12-11       Impact factor: 7.580

6.  Sicca symptoms are associated with similar fatigue, anxiety, depression, and quality-of-life impairments in patients with and without primary Sjögren's syndrome.

Authors:  Morgane Milin; Divi Cornec; Myriam Chastaing; Veronique Griner; Sofian Berrouiguet; Emmanuel Nowak; Thierry Marhadour; Alain Saraux; Valérie Devauchelle-Pensec
Journal:  Joint Bone Spine       Date:  2016-01-13       Impact factor: 4.929

7.  2016 American College of Rheumatology/European League Against Rheumatism Classification Criteria for Primary Sjögren's Syndrome: A Consensus and Data-Driven Methodology Involving Three International Patient Cohorts.

Authors:  Caroline H Shiboski; Stephen C Shiboski; Raphaèle Seror; Lindsey A Criswell; Marc Labetoulle; Thomas M Lietman; Astrid Rasmussen; Hal Scofield; Claudio Vitali; Simon J Bowman; Xavier Mariette
Journal:  Arthritis Rheumatol       Date:  2016-10-26       Impact factor: 10.995

8.  Anxiety impacts rheumatoid arthritis symptoms and health-related quality of life even at low levels.

Authors:  Dana D DiRenzo; Ethan T Craig; Clifton O Bingham Iii; Susan J Bartlett
Journal:  Clin Exp Rheumatol       Date:  2020-03-05       Impact factor: 4.473

9.  Health-related quality of life and depression among participants in the Sjögren's International Collaborative Clinical Alliance registry.

Authors:  Annie Chou; John A Gonzales; Troy E Daniels; Lindsey A Criswell; Stephen C Shiboski; Caroline H Shiboski
Journal:  RMD Open       Date:  2017-09-26

Review 10.  Minimal important change (MIC): a conceptual clarification and systematic review of MIC estimates of PROMIS measures.

Authors:  Caroline B Terwee; John Devin Peipert; Robert Chapman; Jin-Shei Lai; Berend Terluin; David Cella; Philip Griffith; Lidwine B Mokkink
Journal:  Qual Life Res       Date:  2021-07-10       Impact factor: 4.147

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