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Quantifying the patient's perspective in neuromyelitis optica spectrum disorder: Psychometric properties of the SymptoMScreen questionnaire

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dc.contributor.author Meca-Lallana, José-E
dc.contributor.author Maurino, Jorge
dc.contributor.author Pérez-Miralles, Francisco
dc.contributor.author Forero, Lucía
dc.contributor.author Sepulveda, María
dc.contributor.author Calles, Carmen
dc.contributor.author Martínez-Gines, María-L
dc.contributor.author González-Suárez, Ines
dc.contributor.author Boyero, Sabas
dc.contributor.author Romero-Pinel, Lucía
dc.contributor.author Sempere, Ángel-P
dc.contributor.author Meca-Lallana, Virginia
dc.contributor.author Querol, Luis
dc.contributor.author Costa-Frossard, Lucienne
dc.contributor.author Prefasi, Daniel
dc.contributor.author Gómez-Ballesteros, Rocio
dc.contributor.author Ballesteros, Javier
dc.date.accessioned 2025-11-20T12:48:56Z
dc.date.available 2025-11-20T12:48:56Z
dc.date.issued 2021-07
dc.identifier.citation Meca-Lallana JE, Maurino J, Pérez-Miralles F, Forero L, Sepúlveda M, Calles C, et al. Quantifying the patient´s perspective in neuromyelitis optica spectrum disorder: Psychometric properties of the SymptoMScreen questionnaire. Moccia M, editor. PLoS ONE. 29 de julio de 2021;16(7):e0255317.
dc.identifier.issn 1932-6203
dc.identifier.uri https://sms.carm.es/ricsmur/handle/123456789/21779
dc.description.abstract BACKGROUND: The assessment of self-reported outcomes in neuromyelitis optica spectrum disorder (NMOSD) is limited by the lack of validated disease-specific measures. The SymptoMScreen (SyMS) is a patient-reported questionnaire for measuring symptom severity in different domains affected by multiple sclerosis (MS), but has not been thoroughly evaluated in NMOSD. The aim of this study was to assess the psychometric properties of the SyMS in a sample of patients with NMOSD. METHODS: A non-interventional, cross-sectional study in adult subjects with NMOSD (Wingerchuk 2015 criteria) was conducted at 13 neuroimmunology clinics applying the SyMS. A non-parametric item response theory procedure, Mokken analysis, was performed to assess the underlying dimensional structure and scalability of items and overall questionnaire. All analyses were performed with R (v4.0.3) using the mokken library. RESULTS: A total of 70 patients were studied (mean age: 47.5 ± 15 years, 80% female, mean Expanded Disability Status Scale score: 3.0 [interquartile range 1.5, 4.5]). Symptom severity was low (median SyMS score: 19.0 [interquartile range 10.0, 32.0]). The SyMS showed a robust internal reliability (Cronbach's alpha: 0.90 [95% confidence interval 0.86, 0.93]) and behaved as a unidimensional scale with all items showing scalability coefficients > 0.30. The overall SyMS scalability was 0.45 conforming to a medium scale according to Mokken's criteria. Fatigue and body pain were the domains with the highest scalability coefficients. The SyMS was associated with disability (rho: 0.586), and physical and psychological quality of life (rho: 0.856 and 0.696, respectively). CONCLUSIONS: The SyMS shows appropriate psychometric characteristics and may constitute a valuable and easy-to-implement option to measure symptom severity in patients with NMOSD.
dc.language.iso eng
dc.publisher PUBLIC LIBRARY SCIENCE
dc.rights Atribución-NoComercial-SinDerivadas 3.0 España
dc.rights.uri http://creativecommons.org/licenses/by-nc-nd/3.0/es/ *
dc.subject.mesh Humans
dc.subject.mesh Neuromyelitis Optica/psychology/diagnosis
dc.subject.mesh Female
dc.subject.mesh Male
dc.subject.mesh Middle Aged
dc.subject.mesh Psychometrics/methods
dc.subject.mesh Adult
dc.subject.mesh Surveys and Questionnaires
dc.subject.mesh Cross-Sectional Studies
dc.subject.mesh Severity of Illness Index
dc.subject.mesh Self Report
dc.subject.mesh Quality of Life
dc.subject.mesh Patient Reported Outcome Measures
dc.title Quantifying the patient's perspective in neuromyelitis optica spectrum disorder: Psychometric properties of the SymptoMScreen questionnaire
dc.type info:eu-repo/semantics/article
dc.identifier.pmid 34324586
dc.relation.publisherversion https://dx.plos.org/10.1371/journal.pone.0255317
dc.identifier.doi 10.1371/journal.pone.0255317
dc.journal.title Plos One


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