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dc.contributor.authorRamos Alejos Pita, Carmen
dc.contributor.authorArias Santiago, Salvador Antonio 
dc.contributor.authorMolina Leyva, Alejandro 
dc.date.accessioned2020-11-11T11:52:54Z
dc.date.available2020-11-11T11:52:54Z
dc.date.issued2020-08-18
dc.identifier.citationRamos-Alejos-Pita, C.; Arias-Santiago, S.; Molina-Leyva, A. Quality of Life in Cohabitants of Patients with Hidradenitis Suppurativa: A Cross-sectional Study. Int. J. Environ. Res. Public Health 2020, 17, 6000. [doi:10.3390/ijerph17166000]es_ES
dc.identifier.urihttp://hdl.handle.net/10481/64204
dc.descriptionThe following are available online at http://www.mdpi.com/1660-4601/17/16/6000/s1, Table S1: Sociodemographic variables of patients and cohabitants; Table S2: Clinical variables of patients with hidradenitis suppurativa.es_ES
dc.description.abstractHidradenitis suppurativa (HS) is a chronic inflammatory disease that impairs patients’ physical and mental health. However, few studies have considered the consequences of HS on cohabitants. The aims of this study were to explore the impact of HS on the quality of life (QOL) of cohabitants and to assess potentially associated factors. A cross-sectional study was conducted and patients with HS and their cohabitants were invited to participate. Validated questionnaires were used to measure QOL, anxiety and depression, type D personality and sexual dysfunction. The clinical variables of patients and the demographic characteristics of cohabitants were also collected. Twenty-seven patients and 27 cohabitants were included for analysis. Patients and cohabitants presented significant QOL impairment. A direct association was found between the Dermatology Life Quality Index (DLQI) and the Familiar Dermatology Life Quality Index (FDLQI). DLQI scores were associated with the presence of negative affectivity, a trait typical of type D personality, as well as with cohabitants’ anxiety. FDLQI scores were associated with cohabitant anxiety and patient depression. Hidradenitis suppurativa damages quality of life in patients and cohabitants. Identifying potential psychological factors could help us to recognize at-risk patients and apply personalized treatments for them and their environment.es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.rightsAtribución 3.0 España*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.subjectHidradenitis suppurativaes_ES
dc.subjectQuality of life es_ES
dc.subjectCohabitantses_ES
dc.subjectSecondary impactes_ES
dc.titleQuality of Life in Cohabitants of Patients with Hidradenitis Suppurativa: A Cross-sectional Studyes_ES
dc.typejournal articlees_ES
dc.rights.accessRightsopen accesses_ES
dc.identifier.doi10.3390/ijerph17166000
dc.type.hasVersionVoRes_ES


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