Evidence map›Paper›PMID 33959886›Full record

ArticleMedicine, health care, and philosophy2021

Dying as an issue of public concern: cultural scripts on palliative care in Sweden.

Axel Agren, Ann-Charlotte Nedlund, Elisabet Cedersund, Barbro Krevers

Abstract read
In one paragraph

Article in Medicine, health care, and philosophy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Policy Narratives on Palliative Care in Sweden 1974-2018.Health care analysis : HCA : journal of health philosophy and policy · 2023
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Axel AgrenDepartment of Health, Medicine and Caring Sciences (HMV), Linköping University, Linköping, Sweden. axel.agren@liu.se.ORCID http://orcid.org/0000-0003-2891-646X
Ann-Charlotte NedlundDepartment of Health, Medicine and Caring Sciences (HMV), Linköping University, Linköping, Sweden.ORCID http://orcid.org/0000-0003-0204-4536
Elisabet CedersundDepartment of Culture and Society (IKOS), Linköping University, Campus Norrköping, Sweden.ORCID http://orcid.org/0000-0002-1443-5895
Barbro KreversDepartment of Health, Medicine and Caring Sciences (HMV), Linköping University, Linköping, Sweden.ORCID http://orcid.org/0000-0003-3678-2932

Funding

FORTE 2017-01187
6 · The paper itself

Abstract

In Sweden, palliative care has, over the past decades, been object to policies and guidelines with focus on how to achieve "good palliative care". The aim of this study has been to analyse how experts make sense of the development and the current state of palliative care. Departing from this aim, focus has been on identifying how personal experiences of 'the self' are intertwined with culturally available meta-level concepts and how experts contribute to construct new scripts on palliative care. Twelve qualitative interviews were conducted. Four scripts were identified after analysing the empirical material: 1. script of paths towards working within palliative care; 2. script of desirable and deterrent reference points; 3. script of tensions between improvement and bureaucracy; and 4. script of low status and uncertain definitions. The findings of this study illustrate how experts in complex ways intertwine experiences of 'the self' with meta-levels concepts in order to make sense of the field of palliative care. The participants did not endorse one "right way" of "good" deaths. Instead, palliative care was considered to be located in a complex state where the historical development, consisting of both desirable ideals, death denials and lack of guidelines, and more recent developments of strives towards universal concepts, "improvement" and increased bureaucracy altogether played a significant role for how palliative care has developed and is organised and conducted today.

Indexed as

Palliative CareHumansQualitative ResearchSwedenCultural scriptsPalliative carePolicymakingQualitative interviews

Identifiers

PMID33959886
PMCPMC8557170

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.