The psychosocial burden of hidradenitis suppurativa: the patients' perspectives
Resumen: We designed a qualitative study to interview 12 patients with Hidradenitis Suppurativa. This was done by means of a semistructured interview. Questions on quality of life, the impact of their skin disease on family, friends, work, intimate relationships, treatments, etc. were asked. Patients consented to be interviewed and to be video taped to facilitate the transcription of the interviews. The interviews lasted between 30 and 60 minutes and were carried out by a psychologist and a social worker. The dermatologist had previously seen the patients and filled in a form with the Hurley Stage, years of evolution and treatment...
Idioma: Inglés
Año: 2017
Publicado en: ACTA DERMATO-VENEREOLOGICA 97, 7 (2017), PP46 [892]
ISSN: 0001-5555

Originalmente disponible en: Texto completo de la revista

Factor impacto JCR: 3.127 (2017)
Categ. JCR: DERMATOLOGY rank: 12 / 63 = 0.19 (2017) - Q1 - T1
Factor impacto SCIMAGO: 1.089 - Medicine (miscellaneous) (Q1) - Dermatology (Q1)

Tipo y forma: Article (Published version)
Área (Departamento): Área Psicolog.Evolut.Educac (Dpto. Psicología y Sociología)

Creative Commons You must give appropriate credit, provide a link to the license, and indicate if changes were made. You may do so in any reasonable manner, but not in any way that suggests the licensor endorses you or your use. You may not use the material for commercial purposes.


Exportado de SIDERAL (2020-11-05-08:19:45)


Visitas y descargas

Este artículo se encuentra en las siguientes colecciones:
Articles > Artículos por área > Psicología Evolutiva y de la Educación



 Record created 2018-03-23, last modified 2020-11-05


Versión publicada:
 PDF
Rate this document:

Rate this document:
1
2
3
 
(Not yet reviewed)