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The “good death”: An integrative literature review
Abstract
OBJECTIVE: The "good death" is a dynamic concept and has evolved over time to become a "revivalist" good death: a planned, peaceful, and dignified death, at home, surrounded by family members. As the "good death" continues to evolve, the key questions are: How do cultural perceptions of death and dying change? What are the forces that shape Western attitudes and beliefs around death and dying? And how does the "good death" discourse frame the dying experience in contemporary society? The purpose of this manuscript is to describe the underlying discourse in the literature on the "good death" in Western societies. METHOD: An integrative literature review of data from experimental and nonexperimental sources in PubMed, CINAHL, PsychINFO, and SocINDEX of 39 articles from 1992 to 2014. RESULTS: Four main themes emerged from reviewing 39 articles on the "good death": (1) the "good death" as control, (2) the wrong "good death," (3) the threatened "good death," and (4) the denial of dying. SIGNIFICANCE OF RESULTS: Evolving in response to prominent social attitudes and values, the contemporary "good death" is a powerful, constraining discourse that limits spontaneity and encourages one way to die. Social, political, and demographic changes now threaten the stability of the "good death"; dying is framed as an increasingly negative or even unnecessary process, thus marginalizing the positive aspects of dying and rendering dying absent, invisible.
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These ideals might not represent all patients' understandings of a 'good death'.
“however, these ideals might not represent all patients’ understandings of a ‘good death’ [18].”
From General practitioners’ experiences of emergency care and treatment planning in England: a focus group study (2021) · cites this paper as [18]
Patients are sometimes pressured into making decisions that correspond with these Western ideals.
“Patients are sometimes pressured into making decisions that correspond with these Western ideals [18]”
From General practitioners’ experiences of emergency care and treatment planning in England: a focus group study (2021) · cites this paper as [18]
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Metadata
- Authors
- Cottrell, L., & Duggleby, W.
- Affiliations
- University of Alberta (CA)
- Corresponding author
- Cottrell, Laura
- Venue
- Palliative and Supportive Care
- Publisher
- Cambridge University Press (CUP)
- Published
- 2016-01-06
- Volume
- 14
- Issue
- 6
- Pages
- 686-712
- ISSN
- 1478-9515 (ISSN-L)
- 1478-9523
- OpenAlex
- W2233774516
- Cited by
- 183
- References
- 49
- Citations by year
- 2026: 25 · 2025: 21 · 2024: 24 · 2023: 23 · 2022: 23 · 2021: 24 · 2020: 13 · 2019: 11 · 2018: 13 · 2017: 3 · 2016: 3
- FWCI
- 1.49
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Palliative & Supportive Care (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Palliative Care and End-of-Life Issues
- Social Sciences › Anthropology › Death, Funerary Practices, and Mourning
- Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Palliative and Oncologic Care
- Keywords
- good death, dying, death and dying, home death, family-centered care, end-of-life care
- MeSH terms
- Attitude to Death, Cultural Characteristics, Humans, Palliative Care, Right to Die
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