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The use of personal health information outside the circle of care: consent preferences of patients from an academic health care institution
BACKGROUND: Immense volumes of personal health information (PHI) are required to realize the anticipated benefits of artificial intelligence in clinical medicine. To maintain public trust in medical research, consent policies must evolve to reflect contemporary patient preferences. METHODS: Patients...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7992944/ https://www.ncbi.nlm.nih.gov/pubmed/33761938 http://dx.doi.org/10.1186/s12910-021-00598-3 |
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author | Tosoni, Sarah Voruganti, Indu Lajkosz, Katherine Habal, Flavio Murphy, Patricia Wong, Rebecca K. S. Willison, Donald Virtanen, Carl Heesters, Ann Liu, Fei-Fei |
author_facet | Tosoni, Sarah Voruganti, Indu Lajkosz, Katherine Habal, Flavio Murphy, Patricia Wong, Rebecca K. S. Willison, Donald Virtanen, Carl Heesters, Ann Liu, Fei-Fei |
author_sort | Tosoni, Sarah |
collection | PubMed |
description | BACKGROUND: Immense volumes of personal health information (PHI) are required to realize the anticipated benefits of artificial intelligence in clinical medicine. To maintain public trust in medical research, consent policies must evolve to reflect contemporary patient preferences. METHODS: Patients were invited to complete a 27-item survey focusing on: (a) broad versus specific consent; (b) opt-in versus opt-out approaches; (c) comfort level sharing with different recipients; (d) attitudes towards commercialization; and (e) options to track PHI use and study results. RESULTS: 222 participants were included in the analysis; 83% were comfortable sharing PHI with researchers at their own hospital, although younger patients (≤ 49 years) were more uncomfortable than older patients (50 + years; 13% versus 2% uncomfortable, p < 0.05). While 56% of patients preferred broad consent, 38% preferred specific consent; 6% preferred not sharing at all. The majority of patients (63%) preferred to be asked for permission before entry into a contact pool. Again, this trend was more pronounced for younger patients (≤ 49 years: 76%). Approximately half of patients were uncomfortable sharing PHI with commercial enterprises (51% uncomfortable, 27% comfortable, 22% neutral). Most patients preferred to track PHI usage (61%), with the highest proportion once again reported by the youngest patients (≤ 49 years: 71%). A majority of patients also wished to be notified regarding study results (70%). CONCLUSIONS: While most patients were willing to share their PHI with researchers within their own institution, many preferred a transparent and reciprocal consent process. These data also suggest a generational shift, wherein younger patients preferred more specific consent options. Modernizing consent policies to reflect increased autonomy is crucial in fostering sustained public engagement with medical research. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12910-021-00598-3. |
format | Online Article Text |
id | pubmed-7992944 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-79929442021-03-25 The use of personal health information outside the circle of care: consent preferences of patients from an academic health care institution Tosoni, Sarah Voruganti, Indu Lajkosz, Katherine Habal, Flavio Murphy, Patricia Wong, Rebecca K. S. Willison, Donald Virtanen, Carl Heesters, Ann Liu, Fei-Fei BMC Med Ethics Research Article BACKGROUND: Immense volumes of personal health information (PHI) are required to realize the anticipated benefits of artificial intelligence in clinical medicine. To maintain public trust in medical research, consent policies must evolve to reflect contemporary patient preferences. METHODS: Patients were invited to complete a 27-item survey focusing on: (a) broad versus specific consent; (b) opt-in versus opt-out approaches; (c) comfort level sharing with different recipients; (d) attitudes towards commercialization; and (e) options to track PHI use and study results. RESULTS: 222 participants were included in the analysis; 83% were comfortable sharing PHI with researchers at their own hospital, although younger patients (≤ 49 years) were more uncomfortable than older patients (50 + years; 13% versus 2% uncomfortable, p < 0.05). While 56% of patients preferred broad consent, 38% preferred specific consent; 6% preferred not sharing at all. The majority of patients (63%) preferred to be asked for permission before entry into a contact pool. Again, this trend was more pronounced for younger patients (≤ 49 years: 76%). Approximately half of patients were uncomfortable sharing PHI with commercial enterprises (51% uncomfortable, 27% comfortable, 22% neutral). Most patients preferred to track PHI usage (61%), with the highest proportion once again reported by the youngest patients (≤ 49 years: 71%). A majority of patients also wished to be notified regarding study results (70%). CONCLUSIONS: While most patients were willing to share their PHI with researchers within their own institution, many preferred a transparent and reciprocal consent process. These data also suggest a generational shift, wherein younger patients preferred more specific consent options. Modernizing consent policies to reflect increased autonomy is crucial in fostering sustained public engagement with medical research. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12910-021-00598-3. BioMed Central 2021-03-24 /pmc/articles/PMC7992944/ /pubmed/33761938 http://dx.doi.org/10.1186/s12910-021-00598-3 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data. |
spellingShingle | Research Article Tosoni, Sarah Voruganti, Indu Lajkosz, Katherine Habal, Flavio Murphy, Patricia Wong, Rebecca K. S. Willison, Donald Virtanen, Carl Heesters, Ann Liu, Fei-Fei The use of personal health information outside the circle of care: consent preferences of patients from an academic health care institution |
title | The use of personal health information outside the circle of care: consent preferences of patients from an academic health care institution |
title_full | The use of personal health information outside the circle of care: consent preferences of patients from an academic health care institution |
title_fullStr | The use of personal health information outside the circle of care: consent preferences of patients from an academic health care institution |
title_full_unstemmed | The use of personal health information outside the circle of care: consent preferences of patients from an academic health care institution |
title_short | The use of personal health information outside the circle of care: consent preferences of patients from an academic health care institution |
title_sort | use of personal health information outside the circle of care: consent preferences of patients from an academic health care institution |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7992944/ https://www.ncbi.nlm.nih.gov/pubmed/33761938 http://dx.doi.org/10.1186/s12910-021-00598-3 |
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