Literature DB >> 30357557

Enabling Posthumous Medical Data Donation: An Appeal for the Ethical Utilisation of Personal Health Data.

Jenny Krutzinna1, Mariarosaria Taddeo2,3, Luciano Floridi2,3.   

Abstract

This article argues that personal medical data should be made available for scientific research, by enabling and encouraging individuals to donate their medical records once deceased, similar to the way in which they can already donate organs or bodies. This research is part of a project on posthumous medical data donation developed by the Digital Ethics Lab at the Oxford Internet Institute at the University of Oxford. Ten arguments are provided to support the need to foster posthumous medical data donation. Two major risks are also identified-harm to others, and lack of control over the use of data-which could follow from unregulated donation of medical data. The argument that record-based medical research should proceed without the need to secure informed consent is rejected, and instead a voluntary and participatory approach to using personal medical data should be followed. The analysis concludes by stressing the need to develop an ethical code for data donation to minimise the risks, and offers five foundational principles for ethical medical data donation suggested as a draft code.

Keywords:  Data donation; Data philanthropy; Ethical code; Medical data ethics

Mesh:

Year:  2018        PMID: 30357557     DOI: 10.1007/s11948-018-0067-8

Source DB:  PubMed          Journal:  Sci Eng Ethics        ISSN: 1353-3452            Impact factor:   3.525


  14 in total

1.  Can Broad Consent be Informed Consent?

Authors:  Mark Sheehan
Journal:  Public Health Ethics       Date:  2011-08-03       Impact factor: 1.940

2.  Data donation after death.

Authors:  David M Shaw; Julianne V Gross; Thomas C Erren
Journal:  Lancet       Date:  2015-07-25       Impact factor: 79.321

3.  Scientific research is a moral duty.

Authors:  John Harris
Journal:  J Med Ethics       Date:  2005-04       Impact factor: 2.903

4.  Data philanthropy and the design of the infraethics for information societies.

Authors:  Mariarosaria Taddeo
Journal:  Philos Trans A Math Phys Eng Sci       Date:  2016-12-28       Impact factor: 4.226

5.  Data donation after death: A proposal to prevent the waste of medical research data.

Authors:  David M Shaw; Juliane V Gross; Thomas C Erren
Journal:  EMBO Rep       Date:  2015-12-10       Impact factor: 8.807

6.  Are disruptive innovators in GP provision strengthening or weakening the NHS?

Authors:  Rebecca Rosen
Journal:  BMJ       Date:  2017-11-29

7.  Donors' attitudes towards body donation for dissection.

Authors:  R Richardson; B Hurwitz
Journal:  Lancet       Date:  1995-07-29       Impact factor: 79.321

8.  Public preferences for electronic health data storage, access, and sharing - evidence from a pan-European survey.

Authors:  Sunil Patil; Hui Lu; Catherine L Saunders; Dimitris Potoglou; Neil Robinson
Journal:  J Am Med Inform Assoc       Date:  2016-04-23       Impact factor: 4.497

9.  Facilitating the ethical use of health data for the benefit of society: electronic health records, consent and the duty of easy rescue.

Authors:  Sebastian Porsdam Mann; Julian Savulescu; Barbara J Sahakian
Journal:  Philos Trans A Math Phys Eng Sci       Date:  2016-12-28       Impact factor: 4.226

10.  Ethical sharing of health data in online platforms - which values should be considered?

Authors:  Brígida Riso; Aaro Tupasela; Danya F Vears; Heike Felzmann; Julian Cockbain; Michele Loi; Nana C H Kongsholm; Silvia Zullo; Vojin Rakic
Journal:  Life Sci Soc Policy       Date:  2017-08-21
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  4 in total

Review 1.  Special Section on Ethics in Health Informatics.

Authors:  Carolyn Petersen; Vignesh Subbian
Journal:  Yearb Med Inform       Date:  2020-08-21

2.  Present value of future health data: ethics of data collection and use.

Authors:  Ann Dulhanty
Journal:  Bull World Health Organ       Date:  2020-12-15       Impact factor: 9.408

3.  Contextual Exceptionalism After Death: An Information Ethics Approach to Post-Mortem Privacy in Health Data Research.

Authors:  Marieke A R Bak; Dick L Willems
Journal:  Sci Eng Ethics       Date:  2022-08-03       Impact factor: 3.777

4.  Secondary research use of personal medical data: attitudes from patient and population surveys in The Netherlands and Germany.

Authors:  Gesine Richter; Christoph Borzikowsky; Wiebke Lesch; Sebastian C Semler; Eline M Bunnik; Alena Buyx; Michael Krawczak
Journal:  Eur J Hum Genet       Date:  2020-10-01       Impact factor: 5.351

  4 in total

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