dc.contributorUniversidade Estadual Paulista (Unesp)
dc.contributorUniversidade de São Paulo (USP)
dc.date.accessioned2014-05-27T11:28:34Z
dc.date.accessioned2022-10-05T18:44:32Z
dc.date.available2014-05-27T11:28:34Z
dc.date.available2022-10-05T18:44:32Z
dc.date.created2014-05-27T11:28:34Z
dc.date.issued2013-03-01
dc.identifierHeart and Lung: Journal of Acute and Critical Care, v. 42, n. 2, p. 120-125, 2013.
dc.identifier0147-9563
dc.identifier1527-3288
dc.identifierhttp://hdl.handle.net/11449/74664
dc.identifier10.1016/j.hrtlng.2012.09.006
dc.identifierWOS:000316035900008
dc.identifier2-s2.0-84875248440
dc.identifier1432728078910527
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3923616
dc.description.abstractObjective: To understand the experience of primary caregivers of heart transplant recipients. Methods: A phenomenological approach was used to understand the caregivers' experience of caring for a heart transplant patient. In-depth interviews were conducted with 11 caregivers, in a Brazilian hospital, from December 2008 to March 2009. Results: Following the transplant, caregivers' lives change drastically; their priority becomes providing care for their relative. Despite successful transplant results, the uncertainty about future remains, generating permanent distress. Anxiety is exacerbated by familial or economic problems and, consequently, many participants turn to their local communities for support. Some caregivers learn from the experience and plan return to regular activities. Others feel helpless, unable to overcome personal losses and difficulties. Conclusions: Nurses are ideally placed to lead the way by providing family-centered support and education for caregivers of heart recipients. Listening to the concerns of family caregivers seems to be an essential aspect of effective interventions. © 2013 Elsevier Inc.
dc.languageeng
dc.relationHeart and Lung: Journal of Acute and Critical Care
dc.relation1.730
dc.relation0,757
dc.rightsAcesso restrito
dc.sourceScopus
dc.subjectFamily caregivers
dc.subjectHeart transplantation
dc.subjectLived experience
dc.subjectNursing
dc.subjectPhenomenology
dc.subjectadult
dc.subjectanxiety
dc.subjectBrazil
dc.subjectcaregiver
dc.subjectclinical article
dc.subjecteconomic aspect
dc.subjectfemale
dc.subjectgraft recipient
dc.subjectheart transplantation
dc.subjecthuman
dc.subjectmale
dc.subjectnurse
dc.subjectpatient care
dc.subjectpriority journal
dc.subjectquality of life
dc.subjectsocial support
dc.subjectAdaptation, Psychological
dc.subjectAdult
dc.subjectCaregivers
dc.subjectCommunity Networks
dc.subjectCost of Illness
dc.subjectEmotions
dc.subjectFemale
dc.subjectHealth Education
dc.subjectHeart Transplantation
dc.subjectHumans
dc.subjectLife Change Events
dc.subjectMale
dc.subjectMiddle Aged
dc.subjectQualitative Research
dc.subjectSocial Support
dc.subjectStress, Psychological
dc.subjectUncertainty
dc.titleCaring for heart transplant recipients: The lived experience of primary caregivers
dc.typeArtigo


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