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Secondary research use of personal medical data: patient attitudes towards data donation
BACKGROUND: The SARS-CoV-2 pandemic has highlighted once more the great need for comprehensive access to, and uncomplicated use of, pre-existing patient data for medical research. Enabling secondary research-use of patient-data is a prerequisite for the efficient and sustainable promotion of transla...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8672332/ https://www.ncbi.nlm.nih.gov/pubmed/34911502 http://dx.doi.org/10.1186/s12910-021-00728-x |
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author | Richter, Gesine Borzikowsky, Christoph Hoyer, Bimba Franziska Laudes, Matthias Krawczak, Michael |
author_facet | Richter, Gesine Borzikowsky, Christoph Hoyer, Bimba Franziska Laudes, Matthias Krawczak, Michael |
author_sort | Richter, Gesine |
collection | PubMed |
description | BACKGROUND: The SARS-CoV-2 pandemic has highlighted once more the great need for comprehensive access to, and uncomplicated use of, pre-existing patient data for medical research. Enabling secondary research-use of patient-data is a prerequisite for the efficient and sustainable promotion of translation and personalisation in medicine, and for the advancement of public-health. However, balancing the legitimate interests of scientists in broad and unrestricted data-access and the demand for individual autonomy, privacy and social justice is a great challenge for patient-based medical research. METHODS: We therefore conducted two questionnaire-based surveys among North-German outpatients (n = 650) to determine their attitude towards data-donation for medical research, implemented as an opt-out-process. RESULTS: We observed a high level of acceptance (75.0%), the most powerful predictor of a positive attitude towards data-donation was the conviction that every citizen has a duty to contribute to the improvement of medical research (> 80% of participants approving data-donation). Interestingly, patients distinguished sharply between research inside and outside the EU, despite a general awareness that universities and public research institutions cooperate with commercial companies, willingness to allow use of donated data by the latter was very low (7.1% to 29.1%, depending upon location of company). The most popular measures among interviewees to counteract reservations against commercial data-use were regulation by law (61.4%), stipulating in the process that data are not sold or resold (84.6%). A majority requested control of both the use (46.8%) and the protection (41.5%) of the data by independent bodies. CONCLUSIONS: In conclusion, data-donation for medical research, implemented as a combination of legal entitlement and easy-to-exercise-right to opt-out, was found to be widely supported by German patients and therefore warrants further consideration for a transposition into national law. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12910-021-00728-x. |
format | Online Article Text |
id | pubmed-8672332 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-86723322021-12-15 Secondary research use of personal medical data: patient attitudes towards data donation Richter, Gesine Borzikowsky, Christoph Hoyer, Bimba Franziska Laudes, Matthias Krawczak, Michael BMC Med Ethics Research BACKGROUND: The SARS-CoV-2 pandemic has highlighted once more the great need for comprehensive access to, and uncomplicated use of, pre-existing patient data for medical research. Enabling secondary research-use of patient-data is a prerequisite for the efficient and sustainable promotion of translation and personalisation in medicine, and for the advancement of public-health. However, balancing the legitimate interests of scientists in broad and unrestricted data-access and the demand for individual autonomy, privacy and social justice is a great challenge for patient-based medical research. METHODS: We therefore conducted two questionnaire-based surveys among North-German outpatients (n = 650) to determine their attitude towards data-donation for medical research, implemented as an opt-out-process. RESULTS: We observed a high level of acceptance (75.0%), the most powerful predictor of a positive attitude towards data-donation was the conviction that every citizen has a duty to contribute to the improvement of medical research (> 80% of participants approving data-donation). Interestingly, patients distinguished sharply between research inside and outside the EU, despite a general awareness that universities and public research institutions cooperate with commercial companies, willingness to allow use of donated data by the latter was very low (7.1% to 29.1%, depending upon location of company). The most popular measures among interviewees to counteract reservations against commercial data-use were regulation by law (61.4%), stipulating in the process that data are not sold or resold (84.6%). A majority requested control of both the use (46.8%) and the protection (41.5%) of the data by independent bodies. CONCLUSIONS: In conclusion, data-donation for medical research, implemented as a combination of legal entitlement and easy-to-exercise-right to opt-out, was found to be widely supported by German patients and therefore warrants further consideration for a transposition into national law. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12910-021-00728-x. BioMed Central 2021-12-15 /pmc/articles/PMC8672332/ /pubmed/34911502 http://dx.doi.org/10.1186/s12910-021-00728-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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 Richter, Gesine Borzikowsky, Christoph Hoyer, Bimba Franziska Laudes, Matthias Krawczak, Michael Secondary research use of personal medical data: patient attitudes towards data donation |
title | Secondary research use of personal medical data: patient attitudes towards data donation |
title_full | Secondary research use of personal medical data: patient attitudes towards data donation |
title_fullStr | Secondary research use of personal medical data: patient attitudes towards data donation |
title_full_unstemmed | Secondary research use of personal medical data: patient attitudes towards data donation |
title_short | Secondary research use of personal medical data: patient attitudes towards data donation |
title_sort | secondary research use of personal medical data: patient attitudes towards data donation |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8672332/ https://www.ncbi.nlm.nih.gov/pubmed/34911502 http://dx.doi.org/10.1186/s12910-021-00728-x |
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