Literature DB >> 28412708

Validity and Reliability of Patient Reported Outcomes Measurement Information System Computerized Adaptive Tests in Systemic Lupus Erythematosus.

Shanthini Kasturi1,2, Jackie Szymonifka3,4, Jayme C Burket1,2, Jessica R Berman1,2, Kyriakos A Kirou1,2, Alana B Levine1,2, Lisa R Sammaritano1,2, Lisa A Mandl1,2.   

Abstract

OBJECTIVE: The aims of this study were to assess the construct validity and the test-retest reliability of Patient Reported Outcomes Measurement Information System (PROMIS) computerized adaptive tests (CAT) in patients with systemic lupus erythematosus (SLE).
METHODS: Adults with SLE completed the Medical Outcomes Study Short Form-36, LupusQoL-US version ("legacy instruments"), and 14 selected PROMIS CAT. Using Spearman correlations, PROMIS CAT were compared with similar domains measured with legacy instruments. CAT were also correlated with the Safety of Estrogens in Lupus Erythematosus National Assessment-Systemic Lupus Erythematosus Disease Activity Index (SELENA-SLEDAI) disease activity and the Systemic Lupus International Collaborating Clinics/American College of Rheumatology Damage Index (SDI) scores. Test-retest reliability was evaluated using ICC.
RESULTS: There were 204 outpatients with SLE enrolled in the study and 162 completed a retest. PROMIS CAT showed good performance characteristics and moderate to strong correlations with similar domains in the 2 legacy instruments (r = -0.49 to 0.86, p < 0.001). However, correlations between PROMIS CAT and the SELENA-SLEDAI disease activity and SDI were generally weak and statistically insignificant. PROMIS CAT test-retest ICC were good to excellent, ranging from 0.72 to 0.88.
CONCLUSION: To our knowledge, these data are the first to show that PROMIS CAT are valid and reliable for many SLE-relevant domains. Importantly, PROMIS scores did not correlate well with physician-derived measures. This disconnect between objective signs and symptoms and the subjective patient disease experience underscores the crucial need to integrate patient-reported outcomes into clinical care to ensure optimal disease management.

Entities:  

Keywords:  PATIENT OUTCOME ASSESSMENT; QUALITY OF LIFE; SYSTEMIC LUPUS ERYTHEMATOSUS; VALIDATION STUDY

Mesh:

Year:  2017        PMID: 28412708     DOI: 10.3899/jrheum.161202

Source DB:  PubMed          Journal:  J Rheumatol        ISSN: 0315-162X            Impact factor:   4.666


  13 in total

1.  Systemic lupus erythematosus: The promise of PROMIS - is it ready for prime time in SLE?

Authors:  Meenakshi Jolly; Patricia Katz
Journal:  Nat Rev Rheumatol       Date:  2017-06-22       Impact factor: 20.543

Review 2.  Anxiety and Mood Disorders in Systemic Lupus Erythematosus: Current Insights and Future Directions.

Authors:  Annaliese Tisseverasinghe; Christine Peschken; Carol Hitchon
Journal:  Curr Rheumatol Rep       Date:  2018-11-12       Impact factor: 4.592

3.  Psychometric Evaluation of the National Institutes of Health Patient-Reported Outcomes Measurement Information System in a Multiracial, Multiethnic Systemic Lupus Erythematosus Cohort.

Authors:  Patricia Katz; Jinoos Yazdany; Laura Trupin; Stephanie Rush; Charles G Helmick; Louise B Murphy; Cristina Lanata; Lindsey A Criswell; Maria Dall'Era
Journal:  Arthritis Care Res (Hoboken)       Date:  2019-11-05       Impact factor: 4.794

4.  Feasibility, Validity, and Reliability of the 10-item Patient Reported Outcomes Measurement Information System Global Health Short Form in Outpatients with Systemic Lupus Erythematosus.

Authors:  Shanthini Kasturi; Jackie Szymonifka; Jayme C Burket; Jessica R Berman; Kyriakos A Kirou; Alana B Levine; Lisa R Sammaritano; Lisa A Mandl
Journal:  J Rheumatol       Date:  2018-02-01       Impact factor: 4.666

Review 5.  Measuring and monitoring health-related quality of life responsiveness in systemic lupus erythematosus patients: current perspectives.

Authors:  Jamal Mikdashi
Journal:  Patient Relat Outcome Meas       Date:  2018-10-04

6.  Development and content validity of the Lupus Foundation of America rapid evaluation of activity in lupus (LFA-REAL™): a patient-reported outcome measure for lupus disease activity.

Authors:  Anca D Askanase; R Paola Daly; Miya Okado; Kayla Neville; Avery Pong; Leslie M Hanrahan; Joan T Merrill
Journal:  Health Qual Life Outcomes       Date:  2019-06-07       Impact factor: 3.186

7.  Evaluating quality of life tools in North American patients with erythropoietic protoporphyria and X-linked protoporphyria.

Authors:  Hetanshi Naik; Jessica R Overbey; Robert J Desnick; Karl E Anderson; D Montgomery Bissell; Joseph Bloomer; Herbert L Bonkovsky; John D Phillips; Bruce Wang; Ashwani Singal; Manisha Balwani
Journal:  JIMD Rep       Date:  2019-09-14

8.  Electronic patient-reported outcome measures using mobile health technology in rheumatology: A scoping review.

Authors:  Jaclyn Shelton; Sierra Casey; Nathan Puhl; Jeanette Buckingham; Elaine Yacyshyn
Journal:  PLoS One       Date:  2021-07-22       Impact factor: 3.240

9.  Major Depression and Adverse Patient-Reported Outcomes in Systemic Lupus Erythematosus: Results From a Prospective Longitudinal Cohort.

Authors:  Brett Dietz; Patricia Katz; Maria Dall'Era; Louise B Murphy; Cristina Lanata; Laura Trupin; Lindsey A Criswell; Jinoos Yazdany
Journal:  Arthritis Care Res (Hoboken)       Date:  2020-12-06       Impact factor: 5.178

10.  Patient-reported outcome measures for use in clinical trials of SLE: a review.

Authors:  Zara Izadi; Julie Gandrup; Patricia P Katz; Jinoos Yazdany
Journal:  Lupus Sci Med       Date:  2018-08-21
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