Literature DB >> 28320078

Comparison of the Sensitivity to Change of the 36-Item Short Form Health Survey and the Lupus Quality of Life Measure Using Various Definitions of Minimum Clinically Important Differences in Patients With Active Systemic Lupus Erythematosus.

Stephanie G Nantes1, Vibeke Strand2, Jiandong Su3, Zahi Touma3.   

Abstract

OBJECTIVE: The Medical Outcomes Study Short Form 36 (SF-36) and Lupus Quality of Life (LupusQoL) are health-related quality of life questionnaires used in systemic lupus erythematosus (SLE). We first determined the hypothesis-testing construct validity of the SF-36 and LupusQoL against disease activity in patients with active SLE and then compared the sensitivity to change of SF-36 and LupusQoL domains according to different definitions of minimum clinically important differences (MCIDs) for improvement and worsening in the current cohort.
METHODS: Seventy-eight clinically active SLE patients concurrently completed both questionnaires at their baseline and followup visits. Questionnaire domain scores were correlated with the SLE Disease Activity Index 2000 (SLEDAI-2K) and evaluated for floor/ceiling effects. The sensitivity to change of domains in each questionnaire was analyzed first, according to the various MCID definitions and, second, by clinically meaningful changes in disease activity. The magnitudes of change in each domain score between the baseline and followup visit were evaluated using standardized response means.
RESULTS: In the 78 patients, the mean ± SD SLEDAI-2K scores were 9.7 ± 4.8 at baseline and 8.8 ± 5.1 at followup. SF-36/LupusQoL domain scores did not correlate with disease activity. The SF-36 showed floor effects, and ceiling effects were evident in both questionnaires. All domains of both questionnaires showed sensitivity to change over time. Specific domains that reflected worsening or improvement differed according to differing MCID definitions.
CONCLUSION: In SLE patients with active disease, both the SF-36 and LupusQoL are sensitive to change, reflecting both improvement and worsening. More importantly, the LupusQoL SLE-specific domains (planning, burden to others, body image, and intimate relationships) were largely responsive to change.
© 2017, American College of Rheumatology.

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Year:  2017        PMID: 28320078     DOI: 10.1002/acr.23240

Source DB:  PubMed          Journal:  Arthritis Care Res (Hoboken)        ISSN: 2151-464X            Impact factor:   4.794


  13 in total

1.  Patient-Reported Outcomes Predict Mortality in Lupus.

Authors:  Desiree R Azizoddin; Meenakshi Jolly; Shilpa Arora; Ed Yelin; Patricia Katz
Journal:  Arthritis Care Res (Hoboken)       Date:  2019-07-13       Impact factor: 4.794

2.  Efficacy of three-dimensional guide plate technique guided sacral 2 alar iliac screws fixation in patients with degenerative kyphoscoliosis.

Authors:  Liqiang Cui; Shuangquan Gong; Shiming Xie; Lei Zhang; Wusi Peng
Journal:  Am J Transl Res       Date:  2021-05-15       Impact factor: 4.060

3.  Measurement properties of selected patient-reported outcome measures for use in randomised controlled trials in patients with systemic lupus erythematosus: a systematic review.

Authors:  Vibeke Strand; Lee S Simon; Alexa Simon Meara; Zahi Touma
Journal:  Lupus Sci Med       Date:  2020-06

Review 4.  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

5.  Effectiveness of Mindfulness-based Relapse Prevention on Quality of Life and Craving in Methadone-treated Patients: A Randomized Clinical Trial.

Authors:  Mehdi Yaghubi; Fatemeh Zargar
Journal:  Addict Health       Date:  2018-10

6.  Long-Term Impact of Belimumab on Health-Related Quality of Life and Fatigue in Patients With Systemic Lupus Erythematosus: Six Years of Treatment.

Authors:  Vibeke Strand; Pamela Berry; Xiwu Lin; Yumi Asukai; Rajesh Punwaney; Sulabha Ramachandran
Journal:  Arthritis Care Res (Hoboken)       Date:  2019-04-29       Impact factor: 4.794

Review 7.  Antiphospholipid Syndrome Alliance for Clinical Trials and International Networking (APS ACTION): 10-Year Update.

Authors:  Doruk Erkan; Savino Sciascia; Maria Laura Bertolaccini; Hannah Cohen
Journal:  Curr Rheumatol Rep       Date:  2021-05-01       Impact factor: 4.592

8.  Validity and reliability of patient reported outcomes measurement information system computerized adaptive tests in systemic lupus erythematous.

Authors:  Mitra Moazzami; Patricia Katz; Dennisse Bonilla; Lisa Engel; Jiandong Su; Pooneh Akhavan; Nicole Anderson; Oshrat E Tayer-Shifman; Dorcas Beaton; Zahi Touma
Journal:  Lupus       Date:  2021-11-19       Impact factor: 2.911

9.  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

10.  What Does It Mean to Be a British Isles Lupus Assessment Group-Based Composite Lupus Assessment Responder? Post Hoc Analysis of Two Phase III Trials.

Authors:  Richard Furie; Eric F Morand; Ian N Bruce; David Isenberg; Ronald van Vollenhoven; Gabriel Abreu; Lilia Pineda; Raj Tummala
Journal:  Arthritis Rheumatol       Date:  2021-09-22       Impact factor: 10.995

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