Please use this identifier to cite or link to this item: https://doi.org/10.1186/s12904-022-01071-7
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dc.titleA systematic review defining non-beneficial and inappropriate end-of-life treatment in patients with non-cancer diagnoses: theoretical development for multi-stakeholder intervention design in acute care settings
dc.contributor.authorLo, Jamie Jay-May
dc.contributor.authorGraves, Nicholas
dc.contributor.authorChee, Joyce Huimin
dc.contributor.authorHildon, Zoe Jane-Lara
dc.date.accessioned2023-05-31T03:09:28Z
dc.date.available2023-05-31T03:09:28Z
dc.date.issued2022-11-09
dc.identifier.citationLo, Jamie Jay-May, Graves, Nicholas, Chee, Joyce Huimin, Hildon, Zoe Jane-Lara (2022-11-09). A systematic review defining non-beneficial and inappropriate end-of-life treatment in patients with non-cancer diagnoses: theoretical development for multi-stakeholder intervention design in acute care settings. BMC PALLIATIVE CARE 21 (1). ScholarBank@NUS Repository. https://doi.org/10.1186/s12904-022-01071-7
dc.identifier.issn1472-684X
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/241386
dc.description.abstractBackground: Non-beneficial treatment is closely tied to inappropriate treatment at the end-of-life. Understanding the interplay between how and why these situations arise in acute care settings according to the various stakeholders is pivotal to informing decision-making and best practice at end-of-life. Aim: To define and understand determinants of non-beneficial and inappropriate treatments for patients with a non-cancer diagnosis, in acute care settings at the end-of-life. Design: Systematic review of peer-reviewed studies focusing on the above and conducted in upper-middle- and high-income countries. A narrative synthesis was undertaken, guided by Realist principles. Data sources: Cochrane; PubMed; Scopus; Embase; CINAHL; and Web of Science. Results: Sixty-six studies (32 qualitative, 28 quantitative, and 6 mixed-methods) were included after screening 4,754 papers. Non-beneficial treatment was largely defined as when the burden of treatment outweighs any benefit to the patient. Inappropriate treatment at the end-of-life was similar to this, but additionally accounted for patient and family preferences. Contexts in which outcomes related to non-beneficial treatment and/or inappropriate treatment occurred were described as veiled by uncertainty, driven by organizational culture, and limited by profiles and characteristics of involved stakeholders. Mechanisms relating to ‘Motivation to Address Conflict & Seek Agreement’ helped to lessen uncertainty around decision-making. Establishing agreement was reliant on ‘Valuing Clear Communication and Sharing of Information’. Reaching consensus was dependent on ‘Choices around Timing & Documenting of end-of-life Decisions’. Conclusion: A framework mapping determinants of non-beneficial and inappropriate end-of-life treatment is developed and proposed to be potentially transferable to diverse contexts. Future studies should test and update the framework as an implementation tool. Trial registration: PROSPERO Protocol CRD42021214137.
dc.language.isoen
dc.publisherBMC
dc.sourceElements
dc.subjectNon-beneficial treatment
dc.subjectEnd-of-life care
dc.subjectInappropriate treatment
dc.subjectMedical futility
dc.subjectRealist approach
dc.typeReview
dc.date.updated2023-05-31T01:33:47Z
dc.contributor.departmentDEAN'S OFFICE (DUKE-NUS MEDICAL SCHOOL)
dc.contributor.departmentSAW SWEE HOCK SCHOOL OF PUBLIC HEALTH
dc.description.doi10.1186/s12904-022-01071-7
dc.description.sourcetitleBMC PALLIATIVE CARE
dc.description.volume21
dc.description.issue1
dc.published.statePublished
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