Development of the Systemic Lupus Erythematosus Steroid Questionnaire (SSQ): a novel patient-reported outcome tool to assess the impact of oral steroid treatment

被引:17
作者
Mathias, Susan D. [1 ]
Berry, Pamela [2 ]
De Vries, Jane [3 ]
Askanase, Anca [4 ]
Pascoe, Katie [3 ]
Colwell, Hilary H. [1 ]
Chang, David J. [5 ]
机构
[1] Hlth Outcomes Solut, POB 2343, Winter Pk, FL 32790 USA
[2] GSK, King Of Prussia, PA USA
[3] GSK, London, England
[4] Columbia Univ, Med Ctr, New York, NY USA
[5] GSK, Philadelphia, PA USA
来源
HEALTH AND QUALITY OF LIFE OUTCOMES | 2017年 / 15卷
关键词
Patient-reported outcomes; Oral steroids; Systemic lupus erythematosus; Impact; Steroid burden; ORGAN DAMAGE;
D O I
10.1186/s12955-017-0609-9
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Background: Oral glucocorticoids (steroids) are the mainstay of treatment for systemic lupus erythematosus (SLE), but their use is often associated with short-and long-term side effects. Following a literature review and discussions with patients with SLE, clinicians, and payers, a need was identified for a comprehensive SLE-specific tool that can be used to evaluate the side effects and benefits of steroids over time from a patient perspective. The objective of this study was to develop a patient-reported outcome (PRO) measure to assess general impact (baseline burden), benefits, side effects, and impacts associated with the use of oral steroids in patients with SLE. Methods: A qualitative research protocol was developed in which adults with SLE currently receiving or who had received steroids in the past year were recruited from six US rheumatology practices to participate in concept elicitation (CE) interviews. The SLE Steroid Questionnaire (SSQ) was developed based on CE interview results and clinical input. Cognitive debriefing interviews with a second group of patients with SLE evaluated the content, clarity, and relevance of the items. The SSQ was refined using patient feedback, clinician review, and a translatability assessment. The protocol received central independent review board approval. Results: Thirty-three patients (52% moderate disease severity; 58% currently receiving steroids, mean dose 8.7 mg/day) completed CE interviews. Patients reported benefits, side effects, and impacts from steroids. The refined SSQ contains 50 items assessing steroid dose/duration (4 items), general impact (baseline burden; 19 items), benefits (7 items), work/productivity (3 items), side effects (10 items), emotions (6 items), and overall satisfaction (1 item). Conclusion: The SSQ is a unique PRO, developed using robust scientific methodology in accordance with the Food and Drug Administration PRO Guidance. It was designed to comprehensively assess the patient experience with steroid therapy and better understand the benefits and burden of steroids for patients with SLE.
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页数:9
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共 47 条
  • [31] Measurement properties of selected patient-reported outcome measures for use in randomised controlled trials in patients with systemic lupus erythematosus: a systematic review
    Strand, Vibeke
    Simon, Lee S.
    Meara, Alexa Simon
    Touma, Zahi
    [J]. LUPUS SCIENCE & MEDICINE, 2020, 7 (01):
  • [32] IMPACT OF PATIENT-REPORTED DISEASE ACTIVITY ON HEALTH-RELATED QUALITY OF LIFE (HRQOL) IN SYSTEMIC LUPUS ERYTHEMATOSUS (SLE) PATIENTS. DATA FROM THE ALMENARA LUPUS COHORT
    Ugarte-Gil, M. F.
    Gamboa Cardenas, R. V.
    Pimentel-Quiroz, V.
    Reategui Sokolova, C.
    Elera-Fitzcarrald, C.
    Alfaro Lozano, J.
    Pastor Asurza, C.
    Rodriguez Bellido, Z.
    Perich Campos, R.
    Alarcon, G. S.
    [J]. ANNALS OF THE RHEUMATIC DISEASES, 2023, 82 : 1485 - 1485
  • [33] Development and psychometric validation of a patient-reported outcome measure of recurrent urinary tract infection impact: the Recurrent UTI Impact Questionnaire
    Newlands, Abigail F.
    Roberts, Lindsey
    Maxwell, Kayleigh
    Kramer, Melissa
    Price, Jessica L.
    Finlay, Katherine A.
    [J]. QUALITY OF LIFE RESEARCH, 2023, 32 (06) : 1745 - 1758
  • [34] Development and psychometric validation of a patient-reported outcome measure of recurrent urinary tract infection impact: the Recurrent UTI Impact Questionnaire
    Abigail F. Newlands
    Lindsey Roberts
    Kayleigh Maxwell
    Melissa Kramer
    Jessica L. Price
    Katherine A. Finlay
    [J]. Quality of Life Research, 2023, 32 : 1745 - 1758
  • [35] Validation of a novel patient reported tool to assess the impact of treatment in erythropoietic protoporphyria: the EPP-QoL
    G. Biolcati
    S. Hanneken
    E. I. Minder
    N. J. Neumann
    J. H. P. Wilson
    P. J. Wolgen
    D. J. Wright
    A. J. Lloyd
    [J]. Journal of Patient-Reported Outcomes, 5
  • [36] Validation of a novel patient reported tool to assess the impact of treatment in erythropoietic protoporphyria: the EPP-QoL
    Biolcatti, G.
    Hanneken, S.
    Minder, E., I
    Neumann, N. J.
    Wilson, J. H. P.
    Wolgen, P. J.
    Wright, D. J.
    Lloyd, A. J.
    [J]. JOURNAL OF PATIENT-REPORTED OUTCOMES, 2021, 5 (01)
  • [37] Comparing longitudinal patient-reported outcome measures between Swedish patients with recent-onset systemic lupus erythematosus and early rheumatoid arthritis
    Rebecca Heijke
    Mathilda Björk
    Ingrid Thyberg
    Alf Kastbom
    Laura McDonald
    Christopher Sjöwall
    [J]. Clinical Rheumatology, 2022, 41 : 1561 - 1568
  • [38] Comparing longitudinal patient-reported outcome measures between Swedish patients with recent-onset systemic lupus erythematosus and early rheumatoid arthritis
    Heijke, Rebecca
    Bjork, Mathilda
    Thyberg, Ingrid
    Kastbom, Alf
    McDonald, Laura
    Sjowall, Christopher
    [J]. CLINICAL RHEUMATOLOGY, 2022, 41 (05) : 1561 - 1568
  • [39] An Investigation into the Scale and Impact of Self-Reported Foot Problems Associated with Systemic Lupus Erythematosus: A Study Protocol and Survey Questionnaire Development
    Williams, Anita Ellen
    Cherry, Lindsey
    Blake, Alison
    Alcacer-Pitarch, Begonya
    Edwards, Christopher
    Hopkinson, Neil
    Vital, Edward
    Teh, Lee-Suan
    [J]. MUSCULOSKELETAL CARE, 2016, 14 (02) : 110 - 115
  • [40] Anifrolumab treatment improves patient-reported quality of life and decreases disease activity and corticosteroid use in patients with systemic lupus erythematosus: A qualitative study in Denmark
    Troldborg, Anne
    Remkus, Lauren
    Eek, Daniel
    Deleuran, Bent
    [J]. LUPUS, 2024, 33 (09) : 962 - 973