Evidence map›Paper›PMID 21838833›Full record

ArticleHealth expectations : an international journal of public participation in health care and health policy2013

Same description, different values. How service users and providers define patient and public involvement in health care.

Marit By Rise, Marit Solbjør, Mariela C Lara, Heidi Westerlund, Hilde Grimstad, Aslak Steinsbekk

Abstract read
In one paragraph

Article in Health expectations : an international journal of public participation in health care and health policy, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 2 pooled it
–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

37 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Trial
  5. Article
  6. Article
  7. Challenges in using patient involvement principles in substance use treatment.International journal of qualitative studies on health and well-being · 2023
    Article
  8. Article
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  11. Conceptualizing patient participation in psychiatry: A survey describing the voice of patients in outpatient care.Health expectations : an international journal of public participation in health care and health policy · 2021
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  12. Review
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  14. Beneficial self-management support and user involvement in Healthy Life Centres-A qualitative interview study in persons afflicted by overweight or obesity.Health expectations : an international journal of public participation in health care and health policy · 2020
    Article
  15. Article
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  19. Respect, trust and continuity: A qualitative study exploring service users' experience of involvement at a Healthy Life Centre in Norway.Health expectations : an international journal of public participation in health care and health policy · 2019
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  20. 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

6 authors.

Marit By RiseDepartment of Public Health and General Practice, Norwegian University of Science and Technology, Trondheim, Norway. marit.b.rise@ntnu.no
Marit Solbjør
Mariela C Lara
Heidi Westerlund
Hilde Grimstad
Aslak Steinsbekk

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPatient and public involvement in health care is important, but the existing definitions of the concept do not integrate the stakeholders' own perceptions.

objectiveTo investigate and compare service users' and service providers' own definitions of patient and public involvement and their implications. DESIGN, SETTING AND

participantsQualitative study with mainly individual in-depth semi-structured interviews conducted between June 2007 and June 2009. Data were analysed using a grounded theory approach.

resultsA total of 20 patients, 13 public representatives and 44 health service providers/managers in both somatic and mental health care were interviewed. A common definition of patient and public involvement emerged: It is founded on mutual respect, carried out through dialogue aiming at achieving shared decision making. Nevertheless, users and providers assigned different values to the core aspects: Respect was imperative for service users and implied for providers, dialogue was a way to gain respect for service users and to achieve good outcome for providers, and both worried that the other party wanted to make sole decisions.

conclusionsUsers and providers need to consider that although they have a common definition of involvement in health care, they assign different values to its aspects. Increasing and improving patient and public involvement therefore requires knowledge on and dialogue between the parties about these differences.

Indexed as

Community ParticipationPatient ParticipationDecision MakingDelivery of Health CareHealth Facility AdministratorsHealth PersonnelHumansInterviews as TopicNorwayPersonhoodQualitative Researchconsumer participationdecision makingpatient-centred carepatient participationprofessional-patient relations

Identifiers

PMID21838833
PMCPMC5060665

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.