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Parents’ hope in perinatal and neonatal palliative care: a scoping review

dc.contributor.authorSilveira, Aline Oliveira
dc.contributor.authorWernet, Monika
dc.contributor.authorFranco, Larissa Fernandes
dc.contributor.authorDias, Patrícia Luciana Moreira
dc.contributor.authorCharepe, Zaida
dc.date.accessioned2024-01-03T13:04:26Z
dc.date.available2024-01-03T13:04:26Z
dc.date.issued2023-12
dc.description.abstractBackground: The diagnosis of a life-limiting condition of a child in the perinatal or neonatal period is a threat to parental hopes. Hope is an interactional and multidimensional construct, and in palliative care, it is a determinant of quality of life, survival, acceptance and peaceful death. Objective: To map scientific evidence on parents’ hope in perinatal and neonatal palliative care contexts. Method: a scoping review theoretically grounded on Dufault and Martocchio’s Framework, following the Joanna Briggs Institute methodological recommendations. Searches were performed until May 2023 in the MEDLINE, CINAHL and PsycINFO databases. The searches returned 1341 studies. Results: Eligible papers included 27 studies, most of which were carried out in the United States under a phenomenological or literature review approach. The centrality of women’s perspectives in the context of pregnancy and perinatal palliative care was identified. The parental hope experience is articulated in dealing with the uncertainty of information and diagnosis, an approach to which interaction with health professionals is a determinant and potentially distressful element. Hope was identified as one of the determinants of coping and, consequently, linked to autonomy and parenthood. Cognitive and affiliative dimensions were the hope dimensions that predominated in the results, which corresponded to the parents’ ability to formulate realistic goals and meaningful interpersonal relationships, respectively. Conclusion: Hope is a force capable of guiding parents along the path of uncertainties experienced through the diagnosis of a condition that compromises their child’s life. Health professionals can manage the family’s hope by establishing sensitive therapeutic relationships that focus on the dimension of hope. The need for advanced research and intervention in parental and family hope are some of the points made in this study. Protocol registration: https://osf.io/u9xr5/.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.doi10.1186/s12904-023-01324-zpt_PT
dc.identifier.eid85179925360
dc.identifier.issn1472-684X
dc.identifier.pmid38110974
dc.identifier.urihttp://hdl.handle.net/10400.14/43456
dc.identifier.wos001126926500001
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectFamilypt_PT
dc.subjectHopept_PT
dc.subjectNeonatalpt_PT
dc.subjectPalliative carept_PT
dc.subjectPerinatalpt_PT
dc.titleParents’ hope in perinatal and neonatal palliative care: a scoping reviewpt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.issue1pt_PT
oaire.citation.titleBMC Palliative Carept_PT
oaire.citation.volume22pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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