Saturday, June 17, 2017

California Uniform Determination of Death Act - Constitutional Challenge

The family of Israel Stinson continues its lawsuit asking a federal court to declare that the California Uniform Determination of Death Act is unconstitutional.

In late May, the State of California filed a motion to dismiss the family's third amended complaint.  The State focuses heavily on the fact that the CUDDA does not tell physicians how to determine death. Nor does the CUDDA tell physicians to stop organ-sustaining treatment once death is declared.  Therefore, the State argues that CUDDA did not cause Israel any harm, and the family is suing the wrong party.

The U.S. District Court for the Eastern District of California will hear the motion to dismiss later this summer.  Meanwhile, in the Jahi McMath case, the Alameda County Superior Court will hold key hearings on motions for bifurcation and summary adjudication this summer.  

Friday, June 16, 2017

Thursday, June 15, 2017

Advance Care Planning and End of Life (ACPEL) Conference

The program for the 2017 Advance Care Planning and End of Life (ACPEL) Conference in Banff is now available.

Pre-Conference Sessions (Part 1)
Session 1: CRIO 
1. How do people with disabilities perceive advance care planning - Robin Gray, University of Calgary

2. Differences in survey methodology of two Advance Care Planning survey polls conducted in Alberta, Canada - Sunita Ghosh, Alberta Health Services-CancerControl

3. Efficacy of Advance Care Planning and Goals of Care Designations Discussions: A Randomized Controlled Trial and Video Intervention - Maureen Douglas, University of Alberta
  
4. Identification of indicators to monitor successful implementation of Advance Care Planning policies: a modified Delphi study - Patricia Biondo, University of Calgary

5. The economics of advance care planning, Konrad Fassbender, University of Alberta; Covenant Health

Session 2: Health Care Consent, Advance Care Planning, and Goals of Care: The Challenge to Get It Right in Ontario

Health Care Consent, Advance Care Planning, and Goals of Care: The Challenge to Get It Right in Ontario - Tara Walton, Ontario Palliative Care Network Secretariat

Session 3: How to Invite Clinicians to Initiate ACP

1. How to Invite Clinicians to Initiate ACP to Residents, Patients, and Family Carers? - Luc Deliens  
  
2. Development of a complex intervention to support the initiation of advance care planning by general practitioners in patients at risk of deteriorating or dying: a phase 0-1 study - Aline De Vleminck, Free University of Brussels & Ghent University

Pre-Conference Sessions (Part 2)

Session 1: Faith Based Workshop

Inviting the voice of Spirituality within the conversation of Advanced Care Planning - Thomas Butler, Bon Secours Health System Inc.

Session 2: Respecting Choices and Advance Care Planning    

1. Leadership Matters: Engaging and Sustaining ACP Leadership Support - Stephanie Anderson, Respecting Choices

2. Implementing Respecting Choices Within A Midwestern Quaternary Healthcare Delivery System - Iris Boettcher, Spectrum Health

3. The role of social workers in facilitating ACP conversations - Kathleen Ziemba, Respecting Choices

4. Interprofessional Collaboration: A team approach to assure person-centered decision making and enduring conversations - Kathleen Ziemba, Respecting Choices 
  
5. Advance Care Planning and Tomorrow's Clinicians - Karen Petersen, Honoring Choices Minnesota

Session 3: Improving the Content of ACP Conversations
  
Content and documentation of facilitated advance care planning (ACP) conversations: How can they be improved to make a relevant impact on clinical decision making? - Jürgen in der Schmitten, Institute of General Practice, Medical Faculty of the University of Duesseldorf, Georg Marckmann

Opening Keynote

The Power of Collaboration Over Competition in Achieving Person-Centred Conversations
Linda Briggs, MSN, MA, RN, Director, Program Development and Research, Respecting Choices, A Division of C-TAC Innovations

Plenary Session
  
Are Patients “Competent” to Participate in ACP/GCDs?
Daren Heyland, MD, MSc, FRCPC, Director, Clinical Evaluation Research Unit, Kingston General Hospital

Session 1: Setting-Specific (Part 1)
   
1. Influence of an ACP intervention on documentation of end-of-life issues – a cluster randomized clinical trial - Trygve Johannes Lereim Sævareid, University of Oslo
   
2. Advance care Planning and concrete (palliative) emergency planning: The ACP-NOPA project - Barbara Loupatatzis, University Hospital Zurich
   
3. Improving advance care planning and end of life care in Acute and Community Hospitals, using the Gold Standards Framework Hospital Programme – findings from the accredited teams - Keri Thomas, The National GSF Centre in End of Life Care UK
   
4. Improving communication about goals of care with hospitalized patients who have serious illness: a Canadian, multi-centre program of research - Marilyn Swinton, McMaster University

Session 2: Ethical Issues        
   
1. Advance care planning and patient autonomy in cancer: A qualitative study of doctor’s perspectives - Stephanie Johnson, The University of Sydney
  
2. Putting the cart before the horse: is there a right time to start ACP? - Sumytra Menon, National University of Singapore
   
3. Advance directives by proxy in German nursing homes: prevalence, formats, contents, and ethical justification - Jürgen in der Schmitten, Institute of General Practice, Medical Faculty of the University of Duesseldorf

Session 3: Prepare Workshop
Rebecca Sudore, MD, Professor, UCSF School of Medicine

Panel Session: Successful Strategies to Engage Clinicians and Administrators 

Concurrent Sessions

Session 1: Setting-Specific Questions (Part 2)
  
1. ‘Going for Gold’- Achieving top quality end of life care in GP Practices and mainstreaming Advance Care Planning (ACP)  discussions - findings from the first 10 GSF Accredited GP practices - Keri Thomas, The National GSF Centre in End of Life Care UK

2. “What is the one thing that makes it very hard to talk to your family doctor about end-of-life medical treatments?” Examining patient barriers to talking about Advance Care Planning (ACP) with Family Physicians - Amy Tan, University of Calgary
  
3. Advance Care Planning in the acute hospital setting - lessons learnt from the MAPS trial - Tanja Krones, University Hospital Zurich

4. General practitioners’ experiences with timely end-of-life discussions. An interview study, Scientific Institute for Quality of Heathcare (IQ healthcare) - Anne Wichmann, Radboud University Medical Center

Session 2: Nudging: The Notion of choice architechture and whether it has a place in shared decision making  
Pat Tadel, Respecting Choices

Session 3: Improving communication about goals of care with hospitalized patients who have serious illness: A Canadian, Multi-centre program of research  
John You

Plenary Sessions

ACP in the Netherlands
Agnes van der Heide, MD, PhD, Professor of Decision Making and Care at the End of Life  

Serious Illness Conversations
Rachelle Bernacki, MD, MS, Associate Director, Serious Illness Care Program, Ariadne Labs

Plenary Session

 Evolution of advance care planning in Federal, Provincial and Regional Canada – Three levels of engagement, education and research
Jessica Simon, MD, FRCPC, Division Head, Palliative Medicine, University of Calgary

Concurrent Sessions
 Session 1: Health Care System

1. Definition and recommendations for optimal advance care planning: an international consensus - Judith Rietjens, Erasmus Medical Centre

2. Evaluating uptake of a system-wide program of advance care planning and goals of care designations - Eric Wasylenko, Health Quality Council of Alberta

3. Healthcare System Interactions Influence Advance Care Planning in Developed Countries - Hillary Lum, University of Colorado School of Medicine and VA Eastern Colorado Geriatric Research Education and Clinical Center (GRECC)
   
4. When, where, and who is appropriate to have Advance Care Planning conversation with our patients? - Seiko Izumi, Oregon Health & Science University         

5. An integration of Legislation and policy. How advance care planning and Goals of Care Designation works in Alberta - Alexandra Kushliak, Alberta Health Services

 Session 2: Change Management (Part 1)      

1. Introducing advance care planning in Norwegian nursing homes: an effectiveness-implementation randomized clinical hybrid trial (2013-2017) - Irene Aasmul, University of Bergen 
  
2. Sustaining Advance Care Planning in a New World -  Cari Borenko, Fraser Health 

3. An Advance Care Planning Volunteer Service, Exploring ACP Prevalence in the Community - Linda Nolte, Advance Care Planning Australia
  
4. Assessing the effectiveness of an Alberta Health Services-led Advance Care Planning change management intervention to improve team process and patient oriented outcomes for cardiac patients across four clinical contexts - Marta Shaw, University of Calgary

Session 3: Serious Illness Conversations Guide Workshop
  
Rachelle Bernacki, MD, MS, Professor, Harvard Medical School

Concurrent Sessions
Session 1: Patient-Specific Questions (Part 2)

1. “Confronting but we need to live in the real world”: an interview study of patient and caregiver perspectives on advance care planning in CKD - Marcus Sellars, Kolling Institute, Northern Clinical School, Faculty of Medicine, The University of Sydney, Australia

 2. Health care professionals’ experiences with conducting advance care planning conversations in oncology: an international focus group study - Marieke Zwakman, University Medical Center Utrecht

3. Efficacy of the PREPARE website to engage patients in advance care planning in primary care and cancer outpatient care: a prospective study - Neha Arora, McMaster University
   
4. Co-designing ACP resources with the Korean Community in New Zealand - Shona Muir, Auckland District Health Board & the New Zealand ACP Cooperative
   
5. Advance care planning in adolescents with life-threatening illness: Dispelling myths and misconceptions - Jennifer Needle, University of Minnesota
  
Session 2: Change Management (part 2)   

1. Co-designing the New Zealand ACP Plan and Guide - Shona Muir, Auckland District Health Board & the New Zealand ACP Cooperative

2. A Preliminary Analysis of the Role of Systematic Advance Care Planning in Reducing Potentially Avoidable Hospitalizations of Nursing Home Residents - Susan Hickman, Indiana University

3. The role of social workers in facilitating ACP conversations - Kathleen Ziemba, Respecting Choices
   
4. Advance Care Planning: National Prevalence in General Practice, Aged Care and Hospital-Interim Findings/Protocol - Linda Nolte, Advance Care Planning Australia

Session 3: Enhancing ACP Community Capacity in Canada

1. Enhancing ACP Community Capacity in Canada, Sharon Baxter & Chad Hammond

2. Serious Illness Conversation Program Initiative in a Canadian Provincial Setting - Elizabeth Beddard-Huber, BC Centre for Palliative Care

Session 4: Legal Issues Workshop & Meeting (3.5 hours - 30 minute Break) 
  
1. Health & Legal Sector Collaboration to Support Advance Care Planning, Nola Ries

2. Can one size fit all?, Bernadette Richards, University of Adelaide

Plenary Sessions

Nationwide implementation of ACP in German long-term care institutions: Struggling for a consistent quality standard

Georg Marckmann, MPH, Institut für Ethik, Geschichte und Theorie der Medizin, Ludwig-Maximilians-Universität München

Advance Care Planning in Australia: the past, the present and looking towards the future       

Karen Detering, MD, Respiratory Physician & Clinical Ethicist, Respecting Patients Choices Program, Austin Health  

Making Sense of Birth, Life & Death
Louis Hugo Francescutti, MD, PhD, MPH, FRCPC, FACPM, CCFP, FACP (Hon), ICD-D, Physician & Storyteller

Plenary Session
Title TBD
Rebecca Sudore, MD, Professor, UCSF School of Medicine     

Concurrent Sessions
Session 1: Research Methods

1. Using a novel mixed-method approach to study communication during treatment decision making - Kristen Pecanac, William S Middleton Memorial Veterans Hospital
  
2. A Leadership Guide to Implementing Advance Care Planning Programs - Stephanie Anderson, Respecting Choices, a division of C-TAC Innovations

3. Passing out of place: Adolescent and young adult preferences for where they die meet a different reality - Chad Hammond, Canadian Hospice Palliative Care Association 
  
4. What’s Important to Me? Acceptability and potential utility of a novel values clarification tool to facilitate person-centred conversations about goals of care - Anna Consoli, University of Calgary - W21C

 Session 2: Education      
  
1. Identifying best practices for volunteers and lay health navigators to enhance advance care planning, Hillary Lum, University of Colorado School of Medicine and VA Eastern Colorado Geriatric Research Education and Clinical Center (GRECC)

2. Facilitating Goals of Care and Care Planning Discussions at End of Life:  Customized Training for Oncology Fellows - Sarah Thirlwell, Moffitt Cancer Center

3. ACP Conversation communication strategies and their impact - Leigh Manson, National ACP Cooperative

4. Development and Achievement of Education for Implementing End-of-Life Discussion (E-FIELD) project - a nationwide ACP project in Japan - Yoshiyuki Kizawa, Kobe University School of Medicine

Session 3: Patient-Specific Questions (Part 2)

1. Advance Care Planning (ACP) in patients with incurable cancer: a randomised controlled trial of a nurse led intervention, Stephanie Johnson, The University of Sydney
  
2. Uptake, impact and cost-effectiveness of a nurse-led facilitated advance care planning intervention: A randomised controlled trial among patients with severe respiratory disease, Craig Sinclair, University of Western Australia

3. Presentation Matters in Advance Care Planning and Goals of Care Conversations, Shannon Cunningham, Alberta Innovate
  
4. Congruence in Treatment Preferences Decreases Suffering among Adolescents Living with HIV/AIDS through Facilitated Advance Care Planning Conversations, Maureen Lyon, Children's National Health System; The George Washington University School of Medicine and Health Sciences
  
Session 4: Workshop: Advance Care Planning. Whose Job?

1. Advance Care Planning. Whose Job? - Josie Dixon, Assistant Professororial Research Fellow, PSSRU, LSE

2. Examining the use of a guideline for ACP-conversations in nursing homes - Lisbeth Thoresen, University of Oslo 

Wednesday, June 14, 2017

Decision-making on Withholding or Withdrawing Life Support in the ICU: A Worldwide Perspective

A new study in Chest documents the characteristics of intensive care unit (ICU) patients with a decision to withhold/withdraw life-sustaining treatment, including the types of supportive treatments used, patterns of organ dysfunction, and international differences, including gross national income.

The authors conclude: "There is considerable worldwide variability in decisions to withhold/withdraw life-sustaining treatments. Interestingly, almost one-third of patients with a decision to withhold/withdraw life-sustaining treatment left the hospital alive."

Among the more specific findings:  "The percentage of ICU non-survivors from North American ICUs in whom a decision was made during the ICU stay to limit life-sustaining treatment was 76%. In 1998, a study in 110 US institutions reported that 10% of 5,910 patients who died in the ICU had life-support withheld and 38% had life-support withdrawn.14 This observation suggests that the proportion of ICU patients who die after a decision to limit life-sustaining therapy may have increased in North America in recent years."

2nd International Conference on End-of-Life Law, Ethics, Policy, and Practice

Check out this remarkable collection of concurrent sessions coming up at the 2nd International Conference on End-of-Life Law, Ethics, Policy, and Practice (ICEL) in Halifax.

The Ethics of POLST
Lloyd Steffen

The Perils of POLST
Jean Abbott

Advanced Directives and Advanced Care Planning
Peter Saul

“Rock, Paper, Scissors” – Ideologies of End of Life Care for Older People in Hospital
Laura Green

The Cultural Construction of End of Life Issues in Biomedicing: Anthropological Perspectives
Betty Wolder Levin

Caregiver Perspectives of Palliative and End of Life Care for Individuals at End-Stage Dementia in Newfoundland and Labrador: A Qualitative 
Phenomenological Perspective
Barbara Mason

End of Life Regulation and Recent Evolutions in France
Veronique Fournier

To Live and Let Die. Withholding and Withdrawing Life Sustaining Treatment in Argentina: From Therapeutic to Judicial Obstinacy
Maria Ciruzzi

When and How I Shan’t Live: Refusing Life-Prolonging Medical Treatment and Article 8 ECHR
Isra Black

Divorcing Mercy Killing from Euthanasia
Bryanna Moore

The Shift Away from Suicide Talk: Incorporating Voices of Experience
Phoebe Friesen

Elderly Who are Ready to Give Up on Life and the Right to Autonomy
Michelle Habets

Dutch GP’s Views on Good Dying and Euthanasia
Katja ten Cate

Medical Aid in Dying in New York State: Physician Attitudes and Impact of Framing Bias
Brendan Parent

Physicians’ Perceptions of Aid in Dying in Vermont
Ari Kirshenbaum

A New American Threat to Open Discussion of End-of-Life Issues
Robert Rivas

Demedicalised Assistance in Suicide
Martijn Hagens

The Human Rights Implications of the Blanket Ban on Assisted Suicide in England and Wales
Stevie Martin

A Year in Review: The Who, When, Why and How of Requests for Medical Aid in Dying in Quebec
Lori Seller and Veronique Fraser

Medical Aid in Dying: An Update from Québec
Michelle Giroux

Regulating MAiD: The Medical Regulatory Perspective
Andréa Foti

Patients with Parkinson’s Disease, Caregivers’, and Healthcare Providers’ Perspectives on Advance Care Planning on End-of-Life Care
Kim Jameson

‘You’re Going to Die. How Would You Like to?’ Timing Discussions of End-of Life Treatment Preferences
Jaklin Eliott

Advance Care Planning in Australia: Aspirational or Practical?
Bernadette Richards

Palliative Care Including Euthanasia. Responses to Fundamental Criticisms of the Flemish-Belgian Model of Integral End-of-Life Care
Jan L. Bernheim

Fine Lines and Dr. Syme: Intention, Palliation and Death Causation in Regulation and Law
Malcolm Parker

Mapping Out the Implementation of Bill C-14 on Health Care Providers
Rafael Wainer and Jennifer Kryworuchko

Australian Doctors’ Legal Compliance in Relation to Decisions About Withholding or Withdrawing Life-Sustaining Medical Treatment
Ben White

Not “Worth” It? Doctors’ Perceptions of the Role of Resources in Futility Determinations
Eliana Close

Withdrawing Life-Prolonging Treatment from Patients in Vegetative or Minimally Conscious States in England and Wales
Celia Kitzinger

A Comparative Analysis of Voluntariness in the Netherlands and Oregon Physician Assisted Dying Laws
Michaela Okninski

Voluntary Assisted Dying: The Proposed Framework for Victoria, Australia
Deborah Lawson

Should Assisted Dying Require the Consent of a High Court Judge?
Penney Lewis

Conceivability of Performing Euthanasia in Cases of Psychiatric Disease, Dementia or Being Tired of Living
Kirsten Evenblij

What Characterises Complex Euthanasia Consultations?: Experiences of SCEN-Physicians
Roeline Pasman

Euthanasia for People with Psychiatric Disorders or Dementia in Belgium: Analysis of Officially Reported Cases
Sigrid Dierickx

Ethical Issues: MAiD and its Provision in Rural and Remote Settings
Fiona McDonald and Christy Simpson

Challenges in End-of-Life Care and Medical Assistance in Dying: Towards a Relational Ethics Approach
Patricia (Paddy) Rodney

Developing and Implementing a Medical Assistance in Dying Curriculum in a Family Medicine Residency Program
Susan MacDonald

Updating the Evidence about Physician-Assisted Dying and the Impact on Vulnerable Groups (Panel)
Margaret Battin, Bregje D. Onwuteaka-Philipsen, and Agnes van der Heide

Twenty Years of Experience with Physician Assisted Death in Oregon
Linda Ganzini

Advance Decisions to Refuse Treatment: Explaining Low Uptake in England and Wales
Sue Wilkinson

The Notion of Advance Directives: Headway or Hazard?
Jean Abbott and Megan Prescott

Should Medical Input be Required in Completion of Advance Care Directives?
Deborah Lawson

A Grey Area Between Palliative Sedation and Euthanasia
Veerle van de Wetering

An International Perspective on Patient Preferences in the Decision-Making of Continuous Sedation Until Death
Agnes van der Heide

The Evolving Role of Palliative Sedation in the Era of MAiD
Blair Henry

Carter vs. Rasouli – Why was One Supreme Court Decision Right and the Other Wrong?
James Downar

Conversations About CPR – Professional Judgement or Autonomy?
James East

Medical Futility Dispute Resolution Options in the United States: Law and Ethics Fundamentals
Thaddeus Pope

Medical Aid in Dying for Mature Minors: Re-Interpreting the Problem of Decisional Capacity
Kathryn Morrison

The Under-Examined End-of-Life Option: Hastening Death by Voluntary Stopping Eating and Drinking (VSED)
Thaddeus Pope

Experiences of Psychiatrists with (Granting) Requests for Euthanasia in Patients with Psychiatric Diseases
Kirsten Evenblij

Consensus View on Assisted Dying for Dementia: A Delphi Study on Key Issues and Concerns
Aida Dehkhoda

Expert Views on Developments in the Practice of Physician-Assisted Dying in the Netherlands
Marianne Snijdewind

Reframing Hope: A Rehabilitation Perspective on End-of-Life Care (Panel)
Preya Tarsney, Debjani Mukherjee, Gayle Spill, and Andy Kondrat

Medically Assisted Deaths on Vancouver Island – The First Year
Stefanie Green

Experiences of Patients and Their Support People with Medical Assistance in Dying in Canada
Ellen Wiebe

Reasons for Requesting Medical Assistance in Dying (MAiD) in Canada
Ellen Wiebe

Against Advance Directives for MAiD
Hilary Young

Advance Directives Requesting Euthanasia in the Netherlands
Liselotte Postma

Euthanasia in Advanced Dementia: The Use of Advance Directives
Suzanne van de Vathorst

Trying and Dying: Are Some Wishes Better?
Oliver Kim

End of Life Care at the Beginning of Life
Kimberly Mutcherson

The Research Protocol of a Post-Mortem Survey on End-of-Life Decisions
Laure Dombrecht

The Influence of Doctors in the Australian Assisted Dying Debate
Jodhi Rutherford

The Politics Behind the Law on Assisted Dying
Adam McCann

Attitudes of Doctors on the Role of Law in End-of-Life Medical Practice: Empirical Findings from Australia
Lindy Wilmott

Organ Donation in the Context of MAiD: Ethics, Law and Policy
Jennifer Chandler

Euthanasia by Organ Donation
Michael Shapiro

Organ Donation and Assisted Death: Are there Special Ethics Considerations?
Eric Wasylenko

Considering MAiD in Severe, Refractory Mental Illness
Justine Dembo

Are Concerns about Irremediableness, Vulnerability, or Competence Sufficient to Justify Excluding Psychiatric Patients from MAiD?
William Rooney

Psychiatrists’ Views on Physician-Assisted Suicide and Psychiatric Patients: A Qualitative Study
Rosalie Pronk

End-of-Life Issues in Canadian Prisons (Panel)
Adelina Iftene, Crystal Dieleman, David Champagne, and Ivan Zinger

Medical Assistance in Dying (MAiD) – Early Experiences and Practical Considerations in Nova Scotia
(Panel) Gordon Gubitz, Tim Holland, Janice Chisholm, Lianne Yoshida, and Robyn MacQuarrie on behalf of the Nova Scotia MAiD Providers

Charlie Gard - A Different Kind of Medical Futility Conflict - No Transfer Allowed

Before the UK Supreme Court, attorneys for the
Great Ormond Street Hospital argued that the Charlie Gard case is not unique.  On the one hand, they are correct.  British courts have adjudicated dozens of medical futility conflicts, many of them involving children.  On the other hand, the GOSH lawyers are incorrect.  This case has two distinguishing features.

First, Charlie's parents argue that the best interest standard is the wrong standard to apply in these cases.  The scope of parental rights is broad and they contend that a best interest test is not sufficiently respectful of parental rights.  Instead, Gard's parents argue that parents may make any decision for a child, so long as it does not cause "significant harm."  Of course, they are forced to make this argument, because the appellate courts will defer to the trial court's judgment that the treatment at hand is not in Charlie's best interest.  Charlie's parents must make a legal argument that the judge applied the wrong standard.

Second, this case denied Charlie transfer to a willing and available provider.  This is remarkable.  In most medical futility conflicts, the hospital simply wants the court to give it permission to stop life-sustaining treatment.  Clinicians at the treating hospital do not want to administer the interventions the parents or surrogate want. But clinicians at the treating hospital normally do not seek to prevent other clinicians at other facilities from providing the disputed treatment. Normally, if there is another willing provider, then transfer of the patient is the preferred method of dispute resolution.

Here, Charlie's parents argue that the hospital is treating him like "a prisoner."  After all, Charlie's parents are not asking GOSH clinicians to administer treatment contrary to their professional norms or personal consciences.  Instead, they want to take Charlie to a US provider at their own expense.

Still, the denial of transfer seems correct, if the best interest decision is correct. Given that judicial determination, it seems outside the scope of parental authority to provide the disputed treatment anywhere. Transfer is a dispute resolution mechanism that might have been successfully deployed before the matter reached the court. But now the court has already adjudicated the best interest question.  

On the other hand, there was a similar situation, several years ago, in the Joseph Maraachli case from Canada.  Several courts had ruled that his parents were not acting in his best interests. Nevertheless, Joseph's parents were still able to transfer him to the United States.

Monday, June 12, 2017

Legal Briefing: Unwanted Cesareans and Obstetric Violence

In my latest legal briefing for the Journal of Clinical Ethics, I discuss "Legal Briefing: Unwanted Cesareans and Obstetric Violence."

A capacitated pregnant woman has a nearly unqualified right to refuse a cesarean section. Her right to say “no” takes precedence over clinicians’ preferences and even over clinicians’ concerns about fetal health. Leading medical societies, human rights organizations, and appellate courts have all endorsed this principle. Nevertheless, clinicians continue to limit reproductive liberty by forcing and coercing women to have unwanted cesareans. This “Legal Briefing” reviews recent court cases involving this type of obstetric violence. I have organized these court cases into the following six categories:
1.   Epidemic of Unwanted Cesareans
2.   Court-Ordered Cesareans
3.   Physician-Coerced Cesareans
4.   Physician-Ordered Cesareans
5.   Cesareans for Incapacitated Patients
6.   Cesareans for Patients in a Vegetative State or Who Are Brain Dead

Legal Briefing: Unwanted Cesareans and Obstetric Violence
Thaddeus Mason Pope, The Journal of Clinical Ethics 28, no. 2 (Summer 2017): 163-73.

Vanderbilt Children's Hospital Removes Life Support over Parents' Objections

Steffen Rivenburg Jr. was born in October 2016 with a congenital heart defect. In February 2017, because his parents had missed several medical appointments, the Tennessee Department of Child Services took custody.  But during that time, Steffen became quite ill.

Steffen was admitted to Vanderbilt Children's Hospital where he had several heart surgeries and was placed on ECMO.  He needed a heart transplant, but was too sick to be eligible. Determining it was in Steffen's best interest, Vanderbilt planned to withdraw life-sustaining treatment.

On May 30, Steffen's parents obtained a court injunction mandating Vanderbilt to continue treatment until June 6.  The Montgomery County, Tennessee Juvenile Court later denied the parents' request for an extension.  Vanderbilt discontinued life-sustaining treatment on June 8.

In some states, like Ohio, temporary guardians may not consent to withdrawing life-sustaining treatment unless there has been a termination of parental rights.  In other states, like Delaware, temporary guardians may consent to withdrawing life-sustaining treatment if that is in the child's best interest.  

Sunday, June 11, 2017

In re Charlie Gard - UK Supreme Court Judgment (video)

Here is a video from Thursday, June 8, 2017 of the UK Supreme Court issuing its judgment in the Charlie Gard case.  (PDF copies of judgments from all three levels of UK courts are here.)

The court upheld the two lower court decisions that it would not be in Charlie's best interest to pursue experimental treatment in the United States.  The case is now pending before the European Court of Human Rights.



Texas Special Legislative Session to Narrow DNR Orders

Last week, Texas Governor Greg Abbott announced a legislative special session that will begin on July 18th, 2017.

Among the items included on the special session call is "strengthening patient protections relating to do-not-resuscitate orders." This is presumably a reference to H.B. 2063 supported by Texas Right to Life.