Evidence map›Paper›PMID 17975729›Full record

ArticleHealth care analysis : HCA : journal of health philosophy and policy2008

Advocating mandatory patient 'autonomy' in healthcare: adverse reactions and side effects.

Myfanwy Davies, Glyn Elwyn

Abstract read
PubMed Publisher
In one paragraph

Article in Health care analysis : HCA : journal of health philosophy and policy, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Doctors as Appointed Fiduciaries: A Supplemental Model for Medical Decision-Making.Cambridge quarterly of healthcare ethics : CQ : the international journal of healthcare ethics committees · 2022
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. "What would you recommend doctor?"-Discourse analysis of a moment of dissonance when sharing decisions in clinical consultations.Health expectations : an international journal of public participation in health care and health policy · 2019
    Article
  10. Article
  11. Article
  12. Article
  13. Governance mechanisms in the physician-patient relationship: a literature review and conceptual framework.Health expectations : an international journal of public participation in health care and health policy · 2013
    Review
  14. Article
  15. Power and powerlessness: GPs' narratives about lifestyle counselling.The British journal of general practice : the journal of the Royal College of General Practitioners · 2012
    Article
  16. Article
  17. Article
  18. Review
  19. 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

2 authors.

Myfanwy DaviesDepartment of Primary Care and Public Health, Cardiff University, Neuadd Meirionnydd, Heath Park, Cardiff CF14 4XN, UK. daviesmm@cardiff.ac.uk
Glyn Elwyn

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Promoting patient autonomy has become a key imperative in health service encounters. We will examine the potential negative effects of over-promoting patient autonomy and consider the impact on patient access, their experience and the provision of equitable services by focusing on an extreme manifestation of this trend, i.e. calls for patient involvement in health care decision making to be mandatory. Advocates of mandatory autonomy hold that patients have a duty to themselves, to society and to the medical system to make decisions on their health care independently. Models of mandatory autonomy may be contrasted to those of optional autonomy that seek to ascertain patients' decisional preferences and to understand wider limitations on their freedom to choose. Where choice as decisional responsibility becomes mandatory it ceases to promote agency and where autonomous choice is understood as an individualistic practice it will contribute to the cultural dominance of Western values. Moreover, taking a view that principlist ethics needs to take account of the social and cultural contexts of individual lives, we argue that if mandatory autonomy were to be over-emphasised as part of an ongoing move towards patient choice in UK National Health Service (NHS), educated and affluent people would be more able to exercise choices at the expense of people who are experienced in asserting preferences and who have the resources to make use of choices. We will argue that the promotion of autonomy needs to be tempered by steps to enable less powerful social, cultural and economic groups to contribute to decision making and to support individuals who may feel abandoned by having decisional responsibility transferred to them. Until constraints on individual choice can be understood and addressed, we advocate the model of optional autonomy used in shared decision making and make recommendations for practice, policy, education and research.

Indexed as

Patient ParticipationPatient RightsPersonal AutonomyChoice BehaviorDelivery of Health CareDrug-Related Side Effects and Adverse ReactionsHumansModels, TheoreticalPhysician-Patient RelationsTreatment Outcome

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.