Evidence map›Paper›PMID 30014364›Full record

ArticleJournal of bioethical inquiry2018

One For All, All For One? Collective Representation in Healthcare Policy.

Karin Jongsma, Nitzan Rimon-Zarfaty, Aviad Raz, Silke Schicktanz

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of bioethical inquiry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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.

Karin JongsmaDepartment for Medical Ethics and History of Medicine, University Medical Center, Humboldtallee 36, 37073, Goettingen, Germany. Karin.Jongsma@medizin.uni-goettingen.de.
Nitzan Rimon-ZarfatyDepartment for Medical Ethics and History of Medicine, University Medical Center, Humboldtallee 36, 37073, Goettingen, Germany.
Aviad RazDepartment of Sociology and Anthropology, Ben-Gurion University of The Negev, Beersheba, Israel.
Silke SchicktanzDepartment for Medical Ethics and History of Medicine, University Medical Center, Humboldtallee 36, 37073, Goettingen, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Healthcare collectives, such as patient organizations, advocacy groups, disability organizations, professional associations, industry advocates, social movements, and health consumer organizations have been increasingly involved in healthcare policymaking. Such collectives are based on the idea that individual interests can be aggregated into collective interests by participation, deliberation, and representation. The topic of collectivity in healthcare, more specifically collective representation, has only rarely been addressed in (Western) bioethics. This symposium, entitled: "Collective Representation in Healthcare Policy" of the Journal of Bioethical Inquiry draws attention to this understudied topic from a variety of disciplines, within a variety of socio-cultural contexts. We draw attention to important ethical, cultural, and social questions, and into the practices, justifications for, and implications of collective representation of patients in healthcare policy.

Indexed as

Bioethical IssuesBioethicsCommunity ParticipationHealth PolicyOrganizationsPatient AdvocacyPolicy MakingHumansPatient Participation

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.