Learning from stakeholders to inform good practice guidance on consent to research in intensive care units: a mixed-methods study.

Adult intensive & critical care ETHICS (see Medical Ethics) INTENSIVE & CRITICAL CARE QUALITATIVE RESEARCH

Journal

BMJ open
ISSN: 2044-6055
Titre abrégé: BMJ Open
Pays: England
ID NLM: 101552874

Informations de publication

Date de publication:
14 11 2022
Historique:
entrez: 14 11 2022
pubmed: 15 11 2022
medline: 18 11 2022
Statut: epublish

Résumé

Obtaining informed consent from patients in intensive care units (ICUs) prior to enrolment in a study is practically and ethically complex. Decisions about the participation of critically ill patients in research often involve substitute decision makers (SDMs), such as a patient's relatives or doctors. We explored the perspectives of different stakeholder groups towards these consent procedures. Mixed-methods study comprising surveys completed by ICU patients, their relatives and healthcare practitioners in 14 English ICUs, followed by qualitative interviews with a subset of survey participants. Empirical bioethics informed the analysis and synthesis of the data. Survey data were analysed using descriptive statistics of Likert responses, and analysis of interview data was informed by thematic reflective approaches. Analysis included 1409 survey responses (ICU patients n=333, relatives n=488, healthcare practitioners n=588) and 60 interviews (ICU patients n=13, relatives n=30, healthcare practitioners n=17). Most agreed with relatives acting as SDMs based on the perception that relatives often know the patient well enough to reflect their views. While the practice of doctors serving as SDMs was supported by most survey respondents, a quarter (25%) disagreed. Views were more positive at interview and shifted markedly depending on particularities of the study. Participants also wanted reassurance that patient care was prioritised over research recruitment. Findings lend support for adaptations to consent procedures, including collaborative decision-making to correct misunderstandings of the implications of research for that patient. This empirical evidence is used to develop good practice guidance that is to be published separately. Participants largely supported existing consent procedures, but their perspectives on these consent procedures depended on their perceptions of what the research involved and the safeguards in place. Findings point to the importance of explaining clearly what safeguards are in place to protect the patient.

Identifiants

pubmed: 36375987
pii: bmjopen-2022-066149
doi: 10.1136/bmjopen-2022-066149
pmc: PMC9664286
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e066149

Informations de copyright

© Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

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Auteurs

Katie Paddock (K)

Department of Childhood, Youth and Education Studies, Manchester Metropolitan University, Manchester, UK k.paddock@mmu.ac.uk.
Department of Public Health, Policy and Systems, University of Liverpool, Liverpool, UK.

Kerry Woolfall (K)

Department of Public Health, Policy and Systems, University of Liverpool, Liverpool, UK.

Anna Kearney (A)

Department of Public Health, Policy and Systems, University of Liverpool, Liverpool, UK.

Natalie Pattison (N)

East and North Hertfordshire National Health Service Trust, Hertfordshire, UK.
School of Health and Social Work, University of Hertfordshire, Hatfield, UK.

Lucy Frith (L)

Centre for Social Ethics and Policy, The University of Manchester, Manchester, UK.

Carrol Gamble (C)

Department of Biostatistics, University of Liverpool, Liverpool, UK.

Ingeborg Welters (I)

Department of Critical Care, Liverpool University Hospitals NHS Foundation Trust, Liverpool, UK.
Institute of Life Course and Medical Sciences, University of Liverpool, Liverpool, UK.

John Trinder (J)

Ulster Hospital, Belfast, South Eastern Health & Social Services Trust, Belfast, Ireland.

Bridget Young (B)

Department of Public Health, Policy and Systems, University of Liverpool, Liverpool, UK.

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