Please use this identifier to cite or link to this item: https://repositorio.usj.es/handle/123456789/952

Full metadata record
DC FieldValueLanguage
dc.contributor.authorKrajewski, Piotr K.-
dc.contributor.authorMarron, Servando E.-
dc.contributor.authorGómez-Barrera, Manuel-
dc.contributor.authorTomas-Aragones, Lucia-
dc.contributor.authorGilaberte-Calzada, Yolanda-
dc.contributor.authorSzepietowski, Jacek C-
dc.date.accessioned2023-08-01T08:58:39Z-
dc.date.available2023-08-01T08:58:39Z-
dc.date.issued2021-11-22-
dc.identifier.citationKrajewski, P.K.; Marrón, S.E.; Gomez-Barrera, M.; Tomas-Aragones, L.; Gilaberte-Calzada, Y.; Szepietowski, J.C. The Use of HSQoL-24 in an Assessment of Quality-of-Life Impairment among Hidradenitis Suppurativa Patients: First Look at Real-Life Data. J. Clin. Med. 2021, 10, 5446. https://doi.org/10.3390/jcm10225446en_US
dc.identifier.issn2077-0383en_US
dc.identifier.urihttps://repositorio.usj.es/handle/123456789/952-
dc.description.abstractHidradenitis suppurativa (HS) is a chronic inflammatory skin disorder with well-documented effects on patients’ quality of life (QoL). The aim of this study was to evaluate the QoL of patients with HS via the use of a newly developed questionnaire: Hidradenitis Suppurativa Quality of Life-24 (HSQoL-24). This study was performed on a population of 342 HS patients. Their QoL was assessed via the HSQoL-24 questionnaire. The perceived impairment of QoL due to HS in the studied group was considered to be serious (mean HSQoL-24 score: 58.3 _ 21.0 points). Women tended to experience a significantly higher impact from the disease than men (61.6 _ 19.2 points vs. 51.1 _ 23.1 points, p < 0.001). The HS severity had an effect on the perceived QoL, with statistically significant differences being evident between the self-assessed HS severity groups. The level of QoL impairment correlated positively with the number of affected body areas (r = 0.285, p < 0.001) and the duration of the disease (r = 0.173, p = 0.001), while the patients’ age at disease onset correlated negatively with the HSQoL-24 global score (r = -0.182, p = 0.001). Patients living in their family house scored higher than other groups. The least affected were patients who lived alone. The study shows that the HSQoL-24 questionnaire is a reliable, HS-specific tool for measuring the QoL among patients with HS in real-life clinical settings.en_US
dc.format.extent9 p.en_US
dc.format.mimetypeapplication/pdfen_US
dc.language.isoengen_US
dc.publisherMDPIen_US
dc.relationThe study was founded with the Research Grant from Wroclaw Medical University (number: SUB.C260.21.011).en_US
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectHidradenitis suppurativaen_US
dc.subjectQuality of lifeen_US
dc.subjectHSQoL-24en_US
dc.subjectBurdenen_US
dc.titleThe Use of HSQoL-24 in an Assessment of Quality-of-LifeImpairment among Hidradenitis Suppurativa Patients: FirstLook at Real-Life Dataen_US
dc.typejournal articlees_ES
dc.identifier.doihttps://doi.org/10.3390/jcm10225446en_US
dc.rights.accessRightsopen accesses_ES
Appears in Collections:Artículos de revistas

Files in This Item:
File Description SizeFormat 
The Use of HSQoL-24 in an Assessment of Quality-of-Life.pdf240,02 kBAdobe PDFThumbnail
View/Open


This item is licensed under a Creative Commons License Creative Commons