Understanding clinicians’ perspectives on end-of-life dreams and visions. An international survey

dc.contributor.authorHamza Habib, Muhammad
dc.contributor.authorFontanesi, Laura
dc.contributor.authorMotiwala, Zainab Yusufali
dc.contributor.authorCöltekin, Arzu
dc.contributor.authorMisra, Sidharth
dc.contributor.authorMacLullich, Alasdair
dc.contributor.authorVinay, Rasita
dc.contributor.authorHertler, Caroline
dc.contributor.authorBlum, David
dc.contributor.authorSingler, Katrin
dc.contributor.authorSimões, Catarina
dc.contributor.authorFrisardi, Vincenza
dc.contributor.authorBoccardi, Virginia
dc.contributor.authorBellelli, Giuseppe
dc.contributor.authorKoca, Meltem
dc.contributor.authorKerr, Christopher W.
dc.contributor.authorJones, Christopher A.
dc.contributor.authorPeng-Keller, Simon
dc.contributor.authorSchlögl, Mathias
dc.date.accessioned2026-07-27T09:26:50Z
dc.date.issued2026
dc.description.abstractBackground: End-of-life dreams and visions (ELDVs) are vivid, often subjective experiences that occur during the dying process. Even though the patient and family experiences of ELDVs are well documented, there is limited knowledge regarding the perspectives, preparedness, and perceived needs of health care professionals. ELDVs also remain insufficiently addressed in clinical care. Objective: To describe how frequently clinicians encounter ELDVs, perceived preparedness/training, and approaches to clinician and family education and communication. Methods: We conducted a survey to explore health care professional’s perspectives and experiences surrounding ELDVs. The Checklist for Reporting Results of internet E-Surveys was followed. Our survey included 30 items across 7 sections. Professionals that take care of patients with serious or terminal illness were eligible for the study. We utilized a structured multimodal dissemination to achieve maximum diversity in participants. Results: Briefly, 247 participants were eligible for analysis. Frequent encounters for ELDVs were reported by participants. Participants perceived positive effects on patients more frequently than negative effects (W = 446.0, p < 0.001, r = 0.64). Clinical challenges were rated differently across categories (χ 2 = 160.97, p < 0.001, Kendall’s W = 0.13). The most commonly endorsed clinical challenges were lack of institutional protocols and lack of standardized diagnostic criteria, both rated significantly higher than all other challenges (Bonferroni-corrected Wilcoxon tests: All p < 0.001). Participants endorsed multidisciplinary involvement and formal policy implementation. Conclusion: ELDVs are common, but clinicians feel underprepared to respond to them. There is a need for structured training and institutional protocols. Future studies should include patients and their families and analyze how their experiences are shaped by physician responses.
dc.identifier.doi10.1177/10966218261463311
dc.identifier.issn1096-6218
dc.identifier.issn1557-7740
dc.identifier.urihttps://irf.fhnw.ch/handle/11645/57578
dc.language.isoen
dc.publisherMary Ann Liebert
dc.relation.ispartofJournal of Palliative Medicine
dc.rights.uri
dc.subject.ddc360 - Soziale Probleme, Sozialdienste, Versicherungen
dc.titleUnderstanding clinicians’ perspectives on end-of-life dreams and visions. An international survey
dc.type01A - Beitrag in wissenschaftlicher Zeitschrift
dspace.entity.typePublication
fhnw.InventedHereYes
fhnw.ReviewTypepeer-reviewed
fhnw.oastatus.auroraVersion: Accepted *** Embargo: None *** Licence: None *** URL: https://v2.sherpa.ac.uk/id/publication/1466
fhnw.openAccessCategoryClosed
fhnw.pagination10966218261463311-10966218261463311
fhnw.publicationStatePublished
fhnw.targetcollection7bd9def6-c3d0-4b0d-b3ed-5ee99f1e1df8
relation.isAuthorOfPublication01ecfa9e-7c0e-497e-9237-71425ddff983
relation.isAuthorOfPublication4aca25a6-2eac-45d3-8cfa-0bbb4912383d
relation.isAuthorOfPublication.latestForDiscovery01ecfa9e-7c0e-497e-9237-71425ddff983
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