Illness Experiences in Women with Oral Dryness as a Result of Sjögren’s Syndrome: The Patient Point of View

dc.creatorRojas Alcayaga, Gonzalo
dc.creatorHerrera Ronda, Andrea
dc.creatorEspinoza Santander, Iris
dc.creatorBustos Reydet, Claudia Tanya
dc.creatorRíos Erazo, Matías
dc.creatorWurmann Kiblisky, Pamela Andrea
dc.creatorSabugo Siraqyan, María Francisca
dc.creatorGeenen, Rinie
dc.date.accessioned2018-03-06T16:03:31Z
dc.date.available2018-03-06T16:03:31Z
dc.date.created2018-03-06T16:03:31Z
dc.date.issued2016-04
dc.identifierMusculoskelet. Care 14 (2016) 233–242 © 2016 John Wiley & Sons, Ltd.
dc.identifier1557-0681
dc.identifier10.1002/msc.1134
dc.identifierhttps://repositorio.uchile.cl/handle/2250/146722
dc.description.abstractSjögren’s syndrome and the associated dryness can have multiple consequences. The aim of the presentqualitative study was to give an in-depth account of the life experiences of women with primary Sjögren’ssyndrome (pSS) and health-related behaviours, and to summarize these experiences in an integrated model. Methods: Twelve women diagnosed with pSS who regularly attended the Hospital of the University of Chile participated in detailed interviews. The data were analysed using qualitative methods based on the principles of grounded theory.
dc.languageen
dc.publisherWiley Online Library
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
dc.sourceMusculoskelet
dc.subjectoral dryness
dc.subjecthealth experiences
dc.subjectSjögren’s Syndrome
dc.titleIllness Experiences in Women with Oral Dryness as a Result of Sjögren’s Syndrome: The Patient Point of View
dc.typeArtículo de revista


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