Events Archive

Past events

Friday, April 6, 2018 - 12:15pm to 1:30pm

3-100 Mayo, U of M East Bank Campus

Climate Justice: A Bioethics Perspective

Speaker:  Andrew Jameton, PhD
Affiliate Faculty, Center for Bioethics, UMN; Professor Emeritus, College of Public Health University of Nebraska Medical Center

The background to justice in bioethics revolves around fair access to costly health care resources. Meanwhile, social movements emphasize economic, racial, and identity inequalities within the United States. The demands of climate change add conceptions of justice: environmental justice, intra-specific justice, global inequality, differential responsibility for climate change, and generational justice. How are we to sort out these different emphases? Meanwhile, the rate of climate change is accelerating, and 27 years of negotiations has yielded no actual reduction in global greenhouse gas emissions. While we argue, inevitable misery is mounting up unjustly for young people and future generations.

Nneka Sederstrom
Friday, November 10, 2017 - 12:15pm to 1:30pm

3-100 Mayo, U of M East Bank Campus

The Girl with the DNR Tattoo
Presented by: Nneka Sederstrom, PhD, MPH, MA, FCCP, FCCM
Director, Clinical Ethics Department, Children's Hospital and Clinics of Minnesota and Affiliate Faculty, Center for Bioethics

What truly is a patient's right to self-determine? Can an advance directive take any form? This talk will look at the complexities of autonomous decision making and end of life through the eyes of a young adult expressing her wishes in the form of a tattoo.

Jerome Singh
Friday, September 15, 2017 - 12:15pm to 1:30pm

2-690 Moos Tower, U of M East Bank Campus

Vector-Borne Diseases and Gene Drive
 Jerome Singh, BA, LLB, LLM, PhD, MHSc, Nelson R. Mandela School of Medicine, University of KwaZulu-Natal (UKZN); Joint Center for Bioethics, University of Toronto

Prof. Singh provides Ethical, Legal, Social Issues (ELSI) support to the Gates Foundation and its partners on gene drive research and its applications. In short, using a promising new technology called CRISPR/Cas9 to do targeted genome editing on mosquitos so that they produce male offspring (thus driving the species to extinction and, in the process, eliminating the spread of a disease), scientists will soon be field-testing these GM mosquitos in various settings. As you can imagine, this technology raises several ELSI issues 

  • Do we have the moral right to alter ecosystems? 
  • How do we deal with non-consensual communities or individuals in a field trial context, how do we engage with communities regarding this technology?
  • How do deal with reparations if a field trial goes wrong, etc.   
Jochen Vollmann
Friday, July 21, 2017 - 12:45pm to 2:00pm

5-125 Moos Tower, U of M East Bank campus

Palliative Care Exceptionalism? A Broader Perspective on End of Life Care and Modern Medicine

Presented by:  Jochen Vollmann, MD, PhD
Professor, Medical Ethics, Director, Institute for Medical Ethics and History of Medicine, and President, Center for Medical Ethics, Ruhr University Bochum, Germany

Palliative care is an innovative and growing field focussing on life-threatening illness and on the relief of suffering by means of early identification and impeccable assessment and treatment of pain and other problems, physical, psychosocial and spiritual. In this “holistic” approach palliative care differs from science based modern medicine and shows similarities to other “holistic” approaches to the patient as a subject as well as to pre-modern medicine. Professor Vollmann discusses from his ongoing research palliative care exceptionalism and a broader perspective on end of life care and modern medicine and its’ consequences for future health care.

Seminars are free and open to the public.

Jon Merz, MBA, JD, PhD
Thursday, June 29, 2017 - 12:15pm to 1:30pm

2-520 Moos Tower, U of M East Bank Campus

Is There a Legal Privilege to Waive Consent for Research?

Presented by: Jon Merz, MBA, JD, PhD
Medical Ethics and Health Policy, Perelman School of Medicine, University of Pennsylvania

Waivers of informed consent for research participation are permitted under the Common Rule as well as the Exception from Informed Consent (EFIC) for emergency research rule. We examine waivers as embodiments of legal privilege, which permit actors to violate legal norms in furtherance of greater social goods. The emergency privilege, which allows a caregiver to provide emergency medical care to an incompetent victim of an accident, is the clearest example. But fundamental to the privilege to acting without consent is the presumption that reasonable persons in the patients' position would agree, if capable, and that no evidence exists that the particular patient would not agree. An assessment of what is known about participation and refusal rates in research show that the presumption with respect to standard care is not applicable to research. This suggests that, while researchers may assert the social utility of their studies are high enough to justify waivers,there is reason to suspect that many who would be enrolled under a waiver of consent would not want to be enrolled.Our analysis suggests that waivers should be rare, IRBs and researchers must explicitly address study acceptability, and it should be incumbent upon researchers to establish by clear, sound evidence that proposed studies would be acceptable in the community at large and the target population.

Seminars are free and open to the public.

Emma Bedor talk
Thursday, May 4, 2017 - 12:15pm to 1:30pm

The Digital Mental Health Industry: New Problems, New Solutions, New Practices

Presented by:  Emma Bedor Hiland, PhD Candidate
Department of Communication Studies, University of Minnesota

As our day-to-day lives are increasingly reliant upon (and enmeshed with) digital platforms, it is not surprising that the ways we address and manage our health generally, and mental health in particular, are increasingly digitized as well. Our culture’s generally favorable attitude toward digital solutions for everyday problems has led to the emergence of a digital mental health industry, which includes smartphone applications (“apps”) and telemental health services.

New and largely unregulated, the digital mental health industry presents its toolsets as affordable and a cost and time-effective alternative to many of the problems and barriers associated with the treatment of mental illness: clinician and specialist scarcity, treatment unaffordability, and the geographic remoteness of rural patients. Through a combination of fieldwork and interview analysis, this research addresses these claims and the future of the industry, with findings that are relevant to medical practitioners, technologists, researchers, mental health advocates and activists, and others whose work explores the connections between technology and medicine.

Deborah E. Laxon
Friday, March 10, 2017 - 12:15pm to 1:30pm

Life Support: When is Enough, Enough?

Speaker: Deborah Day Laxson
Founder of the Health Care Agent Literacy Project and author of the award winning book The Gray Zone: When Life Support No Longer Supports Life."

How does a non-medically trained individual respond when life support no longer supports life? Using her own real life example, Deborah brings the audience on her journey as she learned to navigate the complexities of the medical world in order to honor her husband’s choices regarding medical care at end-of-life.


Friday, February 10, 2017 - 12:15pm to 1:30pm

Bioethics and the Crisis of Global Ecology

Speaker: Steven Miles, MD
Professor and Maas Family Endowed Chair in Bioethics, Center for Bioethics; and
Department of Medicine, University of Minnesota Medical School

A disappearing arctic ice cap. Rising oceans. Once in a century floods are occurring annually, even as deserts expand. Plastic and chemicals cover the seas and lands. Pollinating bees are disappearing as agriculture defends the chemicals that kill them. Tropical diseases are migrating north into temperate zones that are warming to greet new species of mosquitos. Some say we are living in an “Anthropocene Epoch” where humans rather than natural forces are transforming the planet. Does bioethics have anything useful to say? Dr. Miles will explore the history and future directions for bioethics. This talk is based on a collaboration with Susan Craddock, PhD. 

Friday, October 14, 2016 - 12:15pm to 1:30pm

Center for Bioethics Seminar


Don Brunnquelll

Don Brunquell, PhD, LP
Affiliate Faculty, Center for Bioethics

Christopher Michaelson

Christopher Michaelson, PhD
David A. and Barbara Koch Distinguished Professor of Business Ethics and Social Responsibility
Associate Professor, Ethics & Business Law
University of St. Thomas, Opus College of Business

“Moral hazard” is a term familiar in economics and business ethics that illuminates why rational parties sometimes choose decisions with bad moral outcomes without necessarily intending to behave selfishly or immorally. The term is not generally used in medical ethics. Decision makers such as parents and physicians generally do not use the concept or the word in evaluating ethical dilemmas. They may not even be aware of the precise nature of the moral hazard problem they are experiencing, beyond a general concern for the patient’s seemingly excessive burden. Our seminar will bring the language and logic of moral hazard to pediatrics. The concept reminds us that decision makers in this context are often not the primary party affected by their decisions. It appraises the full scope of risk at issue when decision makers decide on behalf of others and leads us to separate, respect, and prioritize the interests of affected parties. 

Friday, September 30, 2016 - 12:15pm to 1:30pm

5-125 Moos Tower

Center for Bioethics Seminar Series


Prof. Mary Faith Marshall, University of Virginia                                

Mary Faith Marshall, PhD, FCCM
Emily Davie and Joseph S. Kornfeld Professor of Biomedical Ethics, University of Virginia

Prof. Elizabeth Epstein, University of Virginia

Beth Epstein, PhD, RN
Associate Professor, Chair, Department of Acute and Specialty Care, 
University of Virginia School of Nursing

Healthcare professionals, hospital administrators, and clinical ethics consultants are increasingly aware of the existence of moral distress in the workplace and the potentially damaging long-term effects of burnout, moral distancing, and intent to leave a position or profession. Studies indicate that 15-20% of physicians and nurses are considering leaving their positions due to moral distress. Strategies to address moral distress are needed but few have been proposed. Such strategies are necessarily different from those used in clinical ethics consultation where the objective is to resolve a patient-focused problem. In morally distressing situations, the problems are often at the unit, team, and/or organizational level; solutions require interprofessional collaborative effort and buy-in at different levels of the organization. 

Professors Brunnquell and Michaelson have argued for the deleterious effects of moral hazard in the clinical setting. Moral hazard occurs when those who are empowered to parse risk and fashion responses to it are not those who suffer its burdens. It involves a power differential between the decision maker and the decision bearer. The presenting problem in most situations that occasion moral distress is a real or perceived power imbalance. Professors Marshall and Epstein argue that moral distress is inherently occasioned by moral hazard (not vice-versa) and that moral hazard is, indeed, a background condition for moral distress. 

They will discuss the relationship between moral distress and moral hazard, and show how building an interprofessional Moral Distress Consult Service is one strategy to address morally distressing (and thus morally hazardous) situations in the health care setting.