Experience of adults with cystic fi brosis: a perspective based on social phenomenology

dc.contributor.authorOliveira, Deise Moura de
dc.contributor.authorCordeiro, Samara Macedo
dc.contributor.authorJesus, Maria Cristina Pinto de
dc.contributor.authorTavares, Renata Evangelista
dc.contributor.authorMerighi, Miriam Aparecida Barbosa
dc.date.accessioned2019-03-20T11:55:31Z
dc.date.available2019-03-20T11:55:31Z
dc.date.issued2018-12
dc.description.abstractTo understand the experience of adults living with cystic fibrosis. A qualitative study based on the social phenomenology by Alfred Schütz, carried out with 12 adults interviewed in 2016. The statements were analyzed and organized into concrete categories. The following categories were evidenced: “The biopsychosocial impact of the disease on daily life”, “Social prejudice as a generator of embarrassment”, “Coping strategies” and “Fear, uncertainties and the desire to carry out life projects”. The understanding of the experience lived by adults with cystic fibrosis allowed unveiling intersubjective aspects experienced by this public that should be considered by health professionals in the care of this group. It is up to the professionals involved in assisting these people to develop care strategies aimed at completeness, respect for the world of meanings of each individual, their life history, and intersubjectivity that is specially built in the relationship between professionals and people with cystic fibrosis.en
dc.description.abstractComprender la experiencia de personas adultas que conviven con la fibrosis quística.Estudio cualitativo fundamentado en la fenomenología social de Alfred Schütz, realizado con 12 adultos entrevistados en 2016. Los testimonios fueron analizados y organizados en categorías concretas.Fueron evidenciadas las categorías: “Impacto biopsicosocial de la enfermedad en el día a día”, “Preconcepto social como generador de bochorno”, “Estrategias de enfrentamiento” y “Miedo, incertidumbres y deseos de realizar proyectos de vida”.La comprensión de la experiencia atravesada por adultos con fibrosis quística permitió develar aspectos intersubjetivos experimentados por ese grupo, que deben considerar los profesionales de salud para su cuidado. Corresponde a los profesionales involucrados en la atención de estas personas elaborar estrategias de atención que apunten a la integralidad, el respeto al mundo de significaciones de cada uno, su historia de vida y la intersubjetividad especialmente construida en la relación profesional/persona con fibrosos quística.es
dc.formatpdfpt-BR
dc.identifier.issn19840446
dc.identifier.urihttp://dx.doi.org/10.1590/0034-7167-2017-0749
dc.identifier.urihttp://www.locus.ufv.br/handle/123456789/24002
dc.language.isoengpt-BR
dc.publisherRevista Brasileira de Enfermagempt-BR
dc.relation.ispartofseriesVolume 71, Number 06, Pages 2891- 2898, December 2018pt-BR
dc.rightsOpen Accesspt-BR
dc.subjectCystic fibrosispt-BR
dc.subjectAdultpt-BR
dc.subjectEmotionspt-BR
dc.subjectNursingpt-BR
dc.subjectQualitative researchpt-BR
dc.subjectFibrose císticapt-BR
dc.subjectAdultopt-BR
dc.subjectEmoçõespt-BR
dc.subjectEnfermagempt-BR
dc.subjectPesquisa qualitativapt-BR
dc.subjectFibrosis quísticapt-BR
dc.subjectAdultopt-BR
dc.subjectEmocionespt-BR
dc.subjectEnfermeríapt-BR
dc.subjectInvestigación cualitativapt-BR
dc.titleExperience of adults with cystic fi brosis: a perspective based on social phenomenologyen
dc.typeArtigopt-BR

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