Development and Validation of the FSIQ-RMS: A New Patient-Reported Questionnaire to Assess Symptoms and Impacts of Fatigue in Relapsing Multiple Sclerosis

被引:31
作者
Hudgens, Stacie [1 ]
Schuler, Rene [2 ]
Stokes, Jonathan [3 ]
Eremenco, Sonya [4 ]
Hunsche, Elke [5 ]
Leist, Thomas P. [6 ]
机构
[1] Clin Outcomes Solut, 1790 East River Rd,Suite 205, Tucson, AZ 85718 USA
[2] Actelion, Global Market Access & Pricing, Singapore, Singapore
[3] Adelphi Values, Patient Ctr Outcomes, Boston, MA USA
[4] Evidera, Outcomes Res, Bethesda, MD USA
[5] Actelion, Global Market Access & Pricing, Allschwil, Switzerland
[6] Thomas Jefferson Univ, Comprehens Multiple Sclerosis Ctr, Philadelphia, PA 19107 USA
关键词
fatigue; patient-reported outcome; relapsing multiple sclerosis; symptoms; RASCH ANALYSIS; SEVERITY SCALE; DISABILITY;
D O I
10.1016/j.jval.2018.11.007
中图分类号
F [经济];
学科分类号
02 ;
摘要
Objectives: A new patient-reported outcome (PRO) instrument to measure fatigue symptoms and impacts in relapsing multiple sclerosis (RMS) was developed in a qualitative stage, followed by psychometric validation and migration from paper to an electronic format. Methods: Adult patients with relapsing-remitting multiple sclerosis (RRMS) were interviewed to elicit fatigue-related symptoms and impacts. A draft questionnaire was debriefed in cognitive interviews with further RRMS patients, and revised. Content confirmation interviews were conducted with patients with progressiverelapsing multiple sclerosis (PRMS) and relapsing secondaryprogressive multiple sclerosis (RSPMS). Psychometric analyses used data from adult patients with different RMS subtypes and matched non-RMS controls in a multicenter, observational study. After item reduction, the final instrument was migrated to a smartphone (eDiary) and usability was confirmed in interviews with additional adult RMS patients. Results: The qualitative stage included 37 RRMS, 5 PRMS, and 5 RSPMS patients. Saturation of concepts was reached during concept elicitation. Cognitive interviews confirmed that participants understood the instructions, items, and response options of the instrument-named FSIQ-RMS-as intended. Psychometric validation included 164 RMS and 74 control patients. Internal consistency and test-retest reliability were demonstrated. The symptoms domain discriminated along the RMS symptom-severity continuum and between patients and controls. Patients were able to attribute fatiguerelated symptoms to RMS. Usability and conceptual equivalence of the eDiary were confirmed (n = 10 participants). Conclusions: With 7 symptom items and 13 impact items (in 3 impacts subdomains: physical, cognitive and emotional, and coping) after item reduction, the FSIQ-RMS is a comprehensive, valid, and reliable measure of fatigue-related symptoms and impacts in RMS patients.
引用
收藏
页码:453 / 466
页数:14
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