Identificador persistente para citar o vincular este elemento: https://accedacris.ulpgc.es/handle/10553/143902
Campo DC Valoridioma
dc.contributor.authorRodríguez-Sánchez, Ariadnaen_US
dc.contributor.authorRodríguez Suárez, Claudio Albertoen_US
dc.contributor.authorDíaz González, Candelaria Merceden_US
dc.contributor.authorGonzález De La Torre, Héctoren_US
dc.date.accessioned2025-07-28T12:30:40Z-
dc.date.available2025-07-28T12:30:40Z-
dc.date.issued2025en_US
dc.identifier.issn2168-8184en_US
dc.identifier.urihttps://accedacris.ulpgc.es/handle/10553/143902-
dc.description.abstractBackground Behçet’s syndrome (BS) is a systemic autoimmune disease, classified among the vasculitides, with an unknown etiology. It significantly impacts the quality of life of those affected. Healthcare professionals must understand the characteristics of this syndrome to provide comprehensive care. Objectives The main objective of this study is to synthesize qualitative evidence on BS, and explore the life experiences of a person living with this condition, through a biographical-narrative account to inform clinical and psychosocial care strategies. Methods A two-phase study was conducted. Phase 1 involved a qualitative systematic review, including studies in English and Spanish, without restrictions on publication year. A search was conducted in the Medline, Web of Science, and Scopus databases. Themes and sub-themes were extracted to develop the interview guide. In Phase 2, a semi-structured interview was conducted with a woman diagnosed with BS, employing a biographical-narrative design. The interview was recorded, transcribed, and coded, and themes and sub-themes were identified using ATLAS.ti software (version 25.0.1; ATLAS.ti Scientific Software Development GmbH, Berlin, Germany). Results The themes (n = 3) and sub-themes (n = 7) identified in the interview were: coping and adaptation strategies (self-care and seeking support), interactions with the healthcare system (medical care and health education), and the experience of living with the disease (emotional well-being, physical discomfort, and vulnerability). Conclusions Qualitative literature on BS is limited and focused on adults, revealing gaps in care and psychosocial support. The testimonial collected highlights the everyday barriers faced by individuals with BS, and identifies key areas for clinical and psychosocial intervention. Further multidisciplinary qualitative research is recommended to improve diagnosis, treatment, and comprehensive support.en_US
dc.languageengen_US
dc.relation.ispartofCureusen_US
dc.sourceCureus, [ISSN 2168-8184], v. 17 (7), e88891, (Julio 2025)en_US
dc.subject32 Ciencias médicasen_US
dc.subject3201 Ciencias clínicasen_US
dc.subject3212 Salud públicaen_US
dc.subject.otherAutoimmune diseasesen_US
dc.subject.otherBehçet syndromeen_US
dc.subject.otherBiographies as topicen_US
dc.subject.otherQualitative researchen_US
dc.subject.otherReview literature as topicen_US
dc.titleExploring the Patient Experience in Behçet’s Syndrome: A Two-Phase Qualitative Study Using a Biographical-Narrative Approachen_US
dc.typeArticleen_US
dc.identifier.doi10.7759/cureus.88891en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.utils.revisionen_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.esciESCI-
dc.description.miaricds4,6-
item.grantfulltextopen-
item.fulltextCon texto completo-
crisitem.author.deptDepartamento de Enfermería-
crisitem.author.deptGIR IUIBS: Nutrición-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptDepartamento de Enfermería-
crisitem.author.deptDepartamento de Enfermería-
crisitem.author.orcid0000-0001-6226-7374-
crisitem.author.orcid0000-0003-1797-4752-
crisitem.author.orcid0000-0003-1774-4260-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.fullNameRodríguez Suárez, Claudio Alberto-
crisitem.author.fullNameDíaz González, Candelaria Merced-
crisitem.author.fullNameGonzález De La Torre, Héctor-
Colección:Artículos
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