Evidence map›Paper›PMID 34951093›Full record

ArticleHealth expectations : an international journal of public participation in health care and health policy2022

Expectations of a new opt-out system of consent for deceased organ donation in England: A qualitative interview study.

Pippa K Bailey, Hannah Lyons, Fergus J Caskey, Yoav Ben-Shlomo, Mohammed Al-Talib, Adarsh Babu, Lucy E Selman

Open access · goldAbstract read
In one paragraph

Article in Health expectations : an international journal of public participation in health care and health policy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 32% of its field
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

1 citing paper in PubMed, 16 citations in OpenAlex.

  1. Expectations of a new opt-out system of consent for deceased organ donation in England: A qualitative interview study.Health expectations : an international journal of public participation in health care and health policy · 2022
    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

7 authors at 4 institutions in 1 country.

Pippa K BaileyDepartment of Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.ORCID 0000-0003-2323-1082
Hannah LyonsDepartment of Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
Fergus J CaskeyDepartment of Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
Yoav Ben-ShlomoDepartment of Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
Mohammed Al-TalibDepartment of Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
Adarsh BabuDepartment of Renal Medicine, Gloucestershire Royal Hospital, Gloucestershire Hospitals NHS Foundation Trust, Gloucester, UK.
Lucy E SelmanDepartment of Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
North Bristol NHS Trust · GBUniversity of Bristol · GBGloucestershire Hospitals NHS Foundation Trust · GBUniversity of Leeds · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

introductionIn 2020 England moved to an opt-out deceased donation law. We aimed to investigate the views of a mixed stakeholder group comprising people with kidney disease, family members and healthcare practitioners towards the change in legislation. We investigated the expected impacts of the new legislation on deceased-donor and living-donor transplantation, and views on media campaigns regarding the law change.

methodsWe undertook in-depth qualitative interviews with people with kidney disease (n = 13), their family members (n = 4) and healthcare practitioners (n = 15). Purposive sampling was used to ensure diversity for patients and healthcare practitioners. Family members were recruited through snowball sampling and posters. Interviews were audio-recorded and transcribed verbatim. Transcripts were analysed using thematic analysis.

resultsThree themes with six subthemes were identified: (i) Expectations of impact (Hopeful patients; Cautious healthcare professionals), (ii) Living-donor transplantation (Divergent views; Unchanged clinical recommendations), (iii) Media campaigns (Single message; Highlighting recipient benefits). Patients expected the law change would result in more deceased-donor transplant opportunities.

conclusionsClinicians should ensure patients and families are aware of the current evidence regarding the impact of opt-out consent: expectations of an increased likelihood of receiving a deceased-donor transplant are not currently supported by the evidence. This may help to prevent a decline in living-donor transplantation seen in other countries with similar legislation. Media campaigns should include a focus on the impact of organ receipt. PATIENT OR PUBLIC CONTRIBUTION: Two patient representatives from the Kidney Disease Health Integration Team, Primrose Granville and Soumeya Bouacida, contributed to the content and design of the study documents.

Indexed as

MotivationTissue and Organ ProcurementEnglandHumansInformed ConsentLiving DonorsQualitative ResearchTissue Donorsdeceased donationopt-out laworgan donationqualitative interviewstransplantation

Identifiers

PMID34951093
PMCPMC8957744
OpenAlexW4200497888

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.