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David Magnus

Stanford University
  •  Home
  •  Publications
    88
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    9

 More details
  • Stanford University
    Department of Philosophy
    Unknown
Stanford, California, United States of America
  • All publications (88)
  •  116
    Allocation of Opportunities to Participate in Clinical Trials during the Covid‐19 Pandemic and Other Public Health Emergencies
    with Kayte Spector-Bagdady, Holly Fernandez Lynch, Barbara E. Bierer, Luke Gelinas, Sara Chandros Hull, Michelle N. Meyer, Richard R. Sharp, Jeremy Sugarman, Benjamin S. Wilfond, Ruqaiijah Yearby, and Seema Mohapatra
    Hastings Center Report 52 (1): 51-58. 2021.
    Hastings Center Report, Volume 52, Issue 1, Page 51-58, January/February 2022.
    Biomedical Ethics
  •  154
    Digital Contact Tracing, Privacy, and Public Health
    with Nicole Martinez-Martin, Sarah Wieten, and Mildred K. Cho
    Hastings Center Report 50 (3): 43-46. 2020.
    Digital contact tracing, in combination with widespread testing, has been a focal point for many plans to “reopen” economies while containing the spread of Covid‐19. Most digital contact tracing projects in the United States and Europe have prioritized privacy protections in the form of local storage of data on smartphones and the deidentification of information. However, in the prioritization of privacy in this narrow form, there is not sufficient attention given to weighing ethical trade‐offs …Read more
    Digital contact tracing, in combination with widespread testing, has been a focal point for many plans to “reopen” economies while containing the spread of Covid‐19. Most digital contact tracing projects in the United States and Europe have prioritized privacy protections in the form of local storage of data on smartphones and the deidentification of information. However, in the prioritization of privacy in this narrow form, there is not sufficient attention given to weighing ethical trade‐offs within the context of a public health pandemic or to the need to evaluate safety and effectiveness of software‐based technology applied to public health.
    Biomedical Ethics
  •  54
    The Limits of Individualism: Potential Societal Harms from the EAP for Convalescent Plasma
    American Journal of Bioethics 20 (9): 1-3. 2020.
    Volume 20, Issue 9, September 2020, Page 1-3.
    Biomedical Ethics
  •  43
    Dimensions of Research-Participant Interaction: Engagement is Not a Replacement for Consent
    with Emily Shearer and Nicole Martinez
    Journal of Law, Medicine and Ethics 48 (1): 183-184. 2020.
    Biomedical EthicsScientific Research Ethics
  •  54
    Using Implementation Science to Enact Specific Ethical Norms: The Case of Code Status Policy
    with Emily Shearer
    American Journal of Bioethics 20 (4): 6-7. 2020.
    Volume 20, Issue 4, May 2020, Page 6-7.
    Biomedical Ethics
  •  42
    Frontiers in Bioethics
    American Journal of Bioethics 20 (1): 1-2. 2020.
    Biomedical Ethics
  •  71
    Response to Commentaries: When “Everyday Language” Contributes to Miscommunication in Serious Illness
    with Jason N. Batten and Bonnie O. Wong
    Cambridge Quarterly of Healthcare Ethics 28 (3): 433-438. 2019.
    Biomedical Ethics
  •  63
    Introduction: Through the Lens of Linguistic Theory
    with Jason N. Batten
    Cambridge Quarterly of Healthcare Ethics 28 (3): 392-393. 2019.
    Biomedical Ethics
  •  87
    Citizen Science and Gamification
    with Karola V. Kreitmair
    Hastings Center Report 49 (2): 40-46. 2019.
    According to the mainstream conception of research involving human participants, researchers have been trained scientists acting within institutions and have been the individuals doing the studying, while participants, who are nonscientist members of the public, have been the individuals being studied. The relationship between the public and scientists is evolving, however, giving rise to several new concepts, including crowdsourcing and citizen science. In addition, the practice of gamification…Read more
    According to the mainstream conception of research involving human participants, researchers have been trained scientists acting within institutions and have been the individuals doing the studying, while participants, who are nonscientist members of the public, have been the individuals being studied. The relationship between the public and scientists is evolving, however, giving rise to several new concepts, including crowdsourcing and citizen science. In addition, the practice of gamification has been applied to research protocols. The role of gamified, crowdsourced citizen scientist is new in the domain of scientific research and does not fit into the existing taxonomy of researchers and participants. We delineate and explicate this role and show that, while traditional roles are governed by well‐established norms and regulations, individuals engaged in gamified, crowdsourced citizen science—gamers—fall through the cracks of research protections and regulations. We consider the issues this raises, including exploitation and the absence of responsibility and accountability. Finally, we offer suggestions for how the current lack of appropriate norms may be rectified.
    Biomedical Ethics
  •  99
    A Defense of the Dead Donor Rule
    Hastings Center Report 48 (6): 36-38. 2018.
    Discussion of the “dead donor rule” is challenging because it implicates views about a wide range of issues, including whether and when patients are appropriately declared dead, the validity of the doctrine of double effect, and the moral difference between or equivalence of active euthanasia and withdrawal of life‐sustaining treatment. The DDR will be defined here as the prohibition against removal of organs necessary for the life of the patient—that is, the prohibition of intentionally ending …Read more
    Discussion of the “dead donor rule” is challenging because it implicates views about a wide range of issues, including whether and when patients are appropriately declared dead, the validity of the doctrine of double effect, and the moral difference between or equivalence of active euthanasia and withdrawal of life‐sustaining treatment. The DDR will be defined here as the prohibition against removal of organs necessary for the life of the patient—that is, the prohibition of intentionally ending the life of a patient through organ removal. At a minimum, it is difficult not to see the DDR as grounded in a set of laws, norms, values, and practices that are firmly entrenched and have a great deal of philosophical, religious, and legal support. Obviously, the primary argument against the DDR is that it is highly desirable that we continue to procure organs for transplantation, combined with the belief that those from whom we often and possibly typically procure organs are not “really” dead. If donors are not really dead, then we are left with a dilemma: either we abandon organ procurement, or we abandon the DDR. Such a move should be taken only if the way we currently delineate the dead (those from whom it is acceptable to remove organs) cannot be maintained or defended. I will suggest that this is not the case.
    Biomedical Ethics
  •  59
    The One Health Approach to Zoonotic Emerging Infectious Diseases
    with Ariadne Nichol
    American Journal of Bioethics 18 (10): 1-2. 2018.
    Biomedical Ethics
  •  98
    We Convey More Than We (Literally) Say
    with Jason N. Batten, Bonnie O. Wong, and William F. Hanks
    American Journal of Bioethics 18 (9): 1-3. 2018.
    Biomedical Ethics
  •  97
    Managing Expectations: Delivering the Worst News in the Best Way?
    with Alyssa M. Burgart
    American Journal of Bioethics 18 (1): 1-2. 2018.
    Biomedical Ethics
  •  48
    The Potential Harms and Benefits from Research on Medical Practices
    with Benjamin S. Wilfond
    Hastings Center Report 45 (3): 5-6. 2015.
    A commentary on “SUPPORT and the Ethics of Study Implementation: Lessons for Comparative Effectiveness Research from the Trial of Oxygen Therapy for Premature Babies,” by John D. Lantos and Chris Feudtner, in the January‐February 2015 issue.
    Biomedical Ethics
  •  57
    Organizational Needs Versus Ethics Committee Practice
    American Journal of Bioethics 9 (4): 1-2. 2009.
    No abstract
    Biomedical EthicsPublic Health, Misc
  •  96
    Clinical Ethics Consultation: A Need for Evidence
    American Journal of Bioethics 15 (1): 1-2. 2015.
    Biomedical EthicsMedical Ethics
  •  132
    Can Informed Consent Go Too Far? Balancing Consent and Public Benefit in Research
    with Lauren C. Milner
    American Journal of Bioethics 13 (4). 2013.
    (2013). Can Informed Consent Go Too Far? Balancing Consent and Public Benefit in Research. The American Journal of Bioethics: Vol. 13, No. 4, pp. 1-2. doi: 10.1080/15265161.2013.778645
    Biomedical EthicsInformed Consent in Medicine
  •  105
    A Commentary on Oocyte Donation for Stem Cell Research in South Korea
    with Mildred K. Cho
    American Journal of Bioethics 6 (1). 2006.
    No abstract
    Stem Cell Research
  •  45
    100th Issue Anniversary Editorial
    American Journal of Bioethics 13 (1): 1-2. 2013.
    No abstract
    Biomedical Ethics
  •  125
    Genomic Contraindications for Heart Transplantation
    with Danton S. Char, Gabriel Lázaro-Muñoz, Aliessa Barnes, Michael J. Deem, and John D. Lantos
    Pediatrics 139 (4). 2017.
    Organ TransplantationDisability RightsInformed Consent in MedicineBeneficence in Medical Ethics
  •  83
    Professional Judgment and Justice: Equal Respect for the Professional Judgment of Critical-Care Physicians
    with Norm Rizk
    American Journal of Bioethics 16 (1): 1-2. 2016.
    Biomedical Ethics
  •  45
    Finding the Right Tools for Assessing Quality of Clinical Ethics Consultation
    American Journal of Bioethics 16 (3): 1-2. 2016.
    Biomedical EthicsMedical Ethics
  •  142
    Can the Dead Donor Rule be Resuscitated?
    with Simone Lucia Vernez
    American Journal of Bioethics 11 (8): 1-1. 2011.
    The American Journal of Bioethics, Volume 11, Issue 8, Page 1, August 2011
    Biomedical EthicsMedical Ethics
  •  67
    Beyond the IRB: Local Service Versus Global Oversight
    with Molly Havard
    American Journal of Bioethics 11 (5): 1-2. 2011.
    Biomedical EthicsMedical Ethics
  •  72
    The Proper Locus of Professionalization: The Individual or the Institutions?
    with Bela Fishbeyn
    American Journal of Bioethics 15 (5): 1-2. 2015.
    Biomedical Ethics
  •  64
    Innocent Fun or “Microslavery”?
    with Hayden Harvey, Molly Havard, Mildred K. Cho, and Ingmar H. Riedel-Kruse
    Hastings Center Report 44 (6): 38-46. 2014.
    In 2011, Ingmar Riedel‐Kruse's bioengineering laboratory at Stanford University publicized an application that uses paramecia for what the researchers termed “biotic games.” These games make use of living organisms, computer programs, and lab equipment to implement games like Pong, Pac‐man, and soccer. Gamesand related activities are often considered nonserious or trivial, whereas life, biological systems, and science are treated very seriously in moral analysis and public perception. The manipu…Read more
    In 2011, Ingmar Riedel‐Kruse's bioengineering laboratory at Stanford University publicized an application that uses paramecia for what the researchers termed “biotic games.” These games make use of living organisms, computer programs, and lab equipment to implement games like Pong, Pac‐man, and soccer. Gamesand related activities are often considered nonserious or trivial, whereas life, biological systems, and science are treated very seriously in moral analysis and public perception. The manipulation of living matter frequently engenders at least some controversy in the marketplace of ideas, and using living things in games is no exception. Some of the objections lodged against biotic games have appeared in the ethics literature on similar topics; however, the addition of an entertainment element introduces some objections distinct from those about similar cases, as the online comments vividly illustrate. We aim to explore and address the objections in this paper, using the comments to organize and launch the discussion. In scientific work, there is typically a presumption of some prospect of translation and application of generated knowledge for public benefit. In the case of biotic games, these applications are not self‐evident. Because of this, a serious analysis of the justifications, limitations, and features of biotic games is warranted. To this end, we outline key ethical limits that ought to be placed on these activities as well as the obligations that these activities generate for researchers, other professionals, and lay people who design, implement, use, and play them.
    Biomedical Ethics
  •  98
    The concept of genetic disease
    In Arthur L. Caplan, James J. McCartney & Dominic A. Sisti (eds.), Health, Disease, and Illness: Concepts in Medicine, Georgetown University Press. pp. 233--42. 2004.
    The Concept of Disease
  •  95
    Overthrowing the Tyranny of the Journal Impact Factor
    American Journal of Bioethics 13 (7): 1-2. 2013.
    No abstract
    Biomedical EthicsPsychopathology
  •  64
    Causal stories
    Behavioral and Brain Sciences 13 (4): 744-744. 1990.
    Philosophy of Cognitive ScienceAspects of ConsciousnessPhilosophy of Psychology
  •  97
    Duty-Free: The Non-Obligatory Nature of Preimplantation Genetic Diagnosis
    with Lauren C. Sayres
    American Journal of Bioethics 12 (4): 1-2. 2012.
    The American Journal of Bioethics, Volume 12, Issue 4, Page 1-2, April 2012
    Reproductive EthicsHuman Genetic Modification
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