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dc.creatorVan-der-Elst, M. (M.)-
dc.creatorPayne, S. (Sheila)-
dc.creatorArantzamendi-Solabarrieta, M. (María)-
dc.creatorPreston, N. (Nancy)-
dc.creatorHasselaar, J. (Jeroen)-
dc.creatorCenteno, C. (Carlos)-
dc.creatorBelar, A. (Alazne)-
dc.creatorJaspers, B. (Birgit)-
dc.creatorBrunsch, H. (Holger)-
dc.creatorSurges, S. M. (Séverine M.)-
dc.creatorAdile, C. (Claudio)-
dc.creatorMenten, J. (Johan)-
dc.date.accessioned2023-02-13T10:52:03Z-
dc.date.available2023-02-13T10:52:03Z-
dc.date.issued2022-
dc.identifier.citationVan-der-Elst, M. (M.); Payne, S. (Sheila); Arantzamendi-Solabarrieta, M. (María); et al. "An analysis of the experiences of bereaved relatives and health care providers following palliative sedation: a study protocol for a qualitative international multicenter case study". BMC Palliative Care. 21, 2022, 227es
dc.identifier.issn1472-684X-
dc.identifier.urihttps://hdl.handle.net/10171/65404-
dc.description.abstractBackground: Patients at the end-of-life may experience refractory symptoms of which pain, delirium, vomiting and dyspnea are the most frequent. Palliative sedation can be considered a last resort option to alleviate one or more refractory symptoms. There are only a limited number of (qualitative) studies exploring the experiences of relatives of sedated patients and their health care professionals (HCPs). The aims of this study protocol are: 1) to elicit the experiences of bereaved relatives and health care professionals of patients treated with palliative sedation and 2) to explore the understanding of the decision-making process to start palliative sedation across care settings in 5 European countries. Methods: This study protocol is part of the larger HORIZON 2020 Palliative Sedation project. Organisational case study methodology will be used to guide the study design. In total, 50 cases will be conducted in fve European countries (10 per country). A case involves a semi-structured interview with a relative and an HCP closely involved in the care of a deceased patient who received some type of palliative sedation at the end-of-life. Relatives and health care professionals of deceased patients participating in a linked observational cohort study of sedated patients cared for in hospital wards, palliative care units and hospices will be recruited. The data will be analyzed using a framework analysis approach. The frst full case will be analyzed by all researchers after being translated into English using a preprepared code book. Afterwards, bimonthly meetings will be organized to coordinate the data analysis. Discussion: The study aims to have a better understanding of the experiences of relatives and professional caregivers regarding palliative sedation and this within diferent settings and countries. Some limitations are: 1) the sensitivity of the topic may deter some relatives from participation, 2) since the data collection and analysis will be performed by at least 5 diferent researchers in 5 countries, some diferences may occur which possibly makes it difcult to compare cases, but using a rigorous methodology will minimize this risk.es_ES
dc.description.sponsorship‘Palliative Sedation’ is funded by the Horizon 2020 Framework Program of the European Union under Grant Agreement nº No. 825700. The Funder had no role in the development of the protocol.es_ES
dc.language.isospaes_ES
dc.relationinfo:eu-repo/grantAgreement/EC/H2020/825700/EUes_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.subjectPalliative sedationes_ES
dc.subjectRefractory symptomses_ES
dc.subjectQualitative researches_ES
dc.subjectCase studyes_ES
dc.subjectRelativeses_ES
dc.subjectHealth caregiveres_ES
dc.subjectStudy protocoles_ES
dc.titleAn analysis of the experiences of bereaved relatives and health care providers following palliative sedation: a study protocol for a qualitative international multicenter case studyes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.identifier.doi10.1186/s12904-022-01117-w-
dadun.citation.publicationNameBMC Palliative Carees_ES
dadun.citation.startingPage227es_ES
dadun.citation.volume21es_ES
dc.identifier.pmid36550539-

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