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A comprehensive systematic review of stakeholder attitudes to alternatives to prospective informed consent in paediatric acute care research
BACKGROUND: A challenge of performing research in the paediatric emergency and acute care setting is obtaining valid prospective informed consent from parents. The ethical issues are complex, and it is important to consider the perspective of participants, health care workers and researchers on rese...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245534/ https://www.ncbi.nlm.nih.gov/pubmed/30453948 http://dx.doi.org/10.1186/s12910-018-0327-9 |
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author | Furyk, Jeremy McBain-Rigg, Kris Renison, Bronia Watt, Kerrianne Franklin, Richard Emeto, Theophilus I. Ray, Robin A. Babl, Franz E. Dalziel, Stuart |
author_facet | Furyk, Jeremy McBain-Rigg, Kris Renison, Bronia Watt, Kerrianne Franklin, Richard Emeto, Theophilus I. Ray, Robin A. Babl, Franz E. Dalziel, Stuart |
author_sort | Furyk, Jeremy |
collection | PubMed |
description | BACKGROUND: A challenge of performing research in the paediatric emergency and acute care setting is obtaining valid prospective informed consent from parents. The ethical issues are complex, and it is important to consider the perspective of participants, health care workers and researchers on research without prospective informed consent while planning this type of research. METHODS: We performed a systematic review according to PRISMA guidelines, of empirical evidence relating to the process, experiences and acceptability of alternatives to prospective informed consent, in the paediatric emergency or acute care setting. Major medical databases and grey sources were searched and results were screened and assessed against eligibility criteria by 2 authors, and full text articles of relevant studies obtained. Data were extracted onto data collection forms and imported into data management software for analysis. RESULTS: Thirteen studies were included in the review consisting of nine full text articles and four abstracts. Given the heterogeneity of the methods, results could not be quantitatively combined for meta-analysis, and qualitative results are presented in narrative form, according to themes identified from the data. Major themes include capacity of parents to provide informed consent, feasibility of informed consent, support for alternatives to informed consent, process issues, modified consent process, child death, and community consultation. CONCLUSION: Our review demonstrated that children, their families, and health care staff recognise the requirement for research without prior consent, and are generally supportive of enrolling children in such research with the provisions of limiting risk, and informing parents as soon as possible. Australian data and perspectives of children are lacking and represent important knowledge gaps. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12910-018-0327-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6245534 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-62455342018-11-26 A comprehensive systematic review of stakeholder attitudes to alternatives to prospective informed consent in paediatric acute care research Furyk, Jeremy McBain-Rigg, Kris Renison, Bronia Watt, Kerrianne Franklin, Richard Emeto, Theophilus I. Ray, Robin A. Babl, Franz E. Dalziel, Stuart BMC Med Ethics Research Article BACKGROUND: A challenge of performing research in the paediatric emergency and acute care setting is obtaining valid prospective informed consent from parents. The ethical issues are complex, and it is important to consider the perspective of participants, health care workers and researchers on research without prospective informed consent while planning this type of research. METHODS: We performed a systematic review according to PRISMA guidelines, of empirical evidence relating to the process, experiences and acceptability of alternatives to prospective informed consent, in the paediatric emergency or acute care setting. Major medical databases and grey sources were searched and results were screened and assessed against eligibility criteria by 2 authors, and full text articles of relevant studies obtained. Data were extracted onto data collection forms and imported into data management software for analysis. RESULTS: Thirteen studies were included in the review consisting of nine full text articles and four abstracts. Given the heterogeneity of the methods, results could not be quantitatively combined for meta-analysis, and qualitative results are presented in narrative form, according to themes identified from the data. Major themes include capacity of parents to provide informed consent, feasibility of informed consent, support for alternatives to informed consent, process issues, modified consent process, child death, and community consultation. CONCLUSION: Our review demonstrated that children, their families, and health care staff recognise the requirement for research without prior consent, and are generally supportive of enrolling children in such research with the provisions of limiting risk, and informing parents as soon as possible. Australian data and perspectives of children are lacking and represent important knowledge gaps. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12910-018-0327-9) contains supplementary material, which is available to authorized users. BioMed Central 2018-11-20 /pmc/articles/PMC6245534/ /pubmed/30453948 http://dx.doi.org/10.1186/s12910-018-0327-9 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Furyk, Jeremy McBain-Rigg, Kris Renison, Bronia Watt, Kerrianne Franklin, Richard Emeto, Theophilus I. Ray, Robin A. Babl, Franz E. Dalziel, Stuart A comprehensive systematic review of stakeholder attitudes to alternatives to prospective informed consent in paediatric acute care research |
title | A comprehensive systematic review of stakeholder attitudes to alternatives to prospective informed consent in paediatric acute care research |
title_full | A comprehensive systematic review of stakeholder attitudes to alternatives to prospective informed consent in paediatric acute care research |
title_fullStr | A comprehensive systematic review of stakeholder attitudes to alternatives to prospective informed consent in paediatric acute care research |
title_full_unstemmed | A comprehensive systematic review of stakeholder attitudes to alternatives to prospective informed consent in paediatric acute care research |
title_short | A comprehensive systematic review of stakeholder attitudes to alternatives to prospective informed consent in paediatric acute care research |
title_sort | comprehensive systematic review of stakeholder attitudes to alternatives to prospective informed consent in paediatric acute care research |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245534/ https://www.ncbi.nlm.nih.gov/pubmed/30453948 http://dx.doi.org/10.1186/s12910-018-0327-9 |
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