- Residency Requirements for Medical Aid in Dying
- Identity Theft, Deep Brain Stimulation, and the Primacy of Post‐trial Obligations
- Ethical Challenges of Advances in Vaccine Delivery Technologies
- Care or Complicity? Medical Personnel in Prisons
- A Coeditors’ Note
- Challenging Disability Discrimination in the Clinical Use of PDMP Algorithms
- Digital Humans to Combat Loneliness and Social Isolation: Ethics Concerns and Policy Recommendations
- Hidden Ethical Challenges in Health Data Infrastructure
- Brain Pioneers and Moral Entanglement: An Argument for Post‐trial Responsibilities in Neural‐Device Trials
- Neuroscience and Society: Supporting and Unsettling Public Engagement
- Related Developments and Debates in Canada: Time Line and Publications
- Selected Publications Relevant to Topics Explored in This Special Report, with a Focus on the United States
- Choice in the Context of Dementia: Emerging Issues for Health Care Practice in Aging Societies
- Opening the Door: Rethinking “Difficult Conversations” about Living and Dying with Dementia
- What Makes a Better Life for People Facing Dementia? Toward Dementia‐Friendly Health and Social Policy, Medical Care, and Community Support in the United States
- Guiding the Future: Rethinking the Role of Advance Directives in the Care of People with Dementia
- Too Soon or Too Late: Rethinking the Significance of Six Months When Dementia Is a Primary Diagnosis
- When People Facing Dementia Choose to Hasten Death: The Landscape of Current Ethical, Legal, Medical, and Social Considerations in the United States
- Shared Problems
- Feminist Bioethics: Moving Forward in Coalition
- Clinician Moral Distress: Toward an Ethics of Agent‐Regret
- Forgotten and without Protections: Older Adults in Prison Settings
- Making the World Safer and Fairer in Pandemics
- The Problem Is Not (Merely) Mass Incarceration: Incarceration as a Bioethical Crisis and Abolition as a Moral Obligation
- Preventing Another Fifty Years of Mass Incarceration: How Bioethics Can Help
- Big Mistake: Knowing and Doing Better in Patient Engagement
- Issue Information and About the Cover Art
- Fifty Years of U.S. Mass Incarceration and What It Means for Bioethics
- Lockdowns, Bioethics, and the Public: Policy‐Making in a Liberal Democracy
- Dependence
- A Path Forward—and Outward: Repositioning Bioethics to Face Future Challenges
- Past: Imperfect; Future: Tense
- Can I Hold That Thought for You? Dementia and Shared Relational Agency
- The Pitfalls of Genomic Data Diversity
- Cultivating Peace and Health at Community Health Centers
- Hope and Exploitation in Commercial Provision of Assisted Reproductive Technologies
- Demonstrating Trustworthiness to Patients in Data‐Driven Health Care
- Trust in Health Care and Science: Toward Common Ground on Key Concepts
- About The Hastings, the American Board of Internal Medicine Foundation, and the Cover Art
- Community‐Based Organizations as Trusted Messengers in Health
- Securing the Trustworthiness of the FDA to Build Public Trust in Vaccines
- “You have to trust yourself”: The Overlooked Role of Self‐Trust in Coping with Chronic Illness
- Climates of Distrust in Medicine
- Betraying, Earning, or Justifying Trust in Health Organizations
- The Public Performativity of Trust
- When Mistakes Multiply: How Inadequate Responses to Medical Mishaps Erode Trust in American Medicine
- What Patient‐Experience Data Reveal about Trust
- Physician Perspectives on Building Trust with Patients
- When Artists Go to Work: On the Ethics of Engaging the Arts in Public Health
- Regaining Trust in Public Health and Biomedical Science following Covid: The Role of Scientists
- The Sociotechnical Construction of Distrust during the Covid‐19 Pandemic
- Trust in Crises and Crises of Trust
- Editors’ Statement on the Responsible Use of Generative AI Technologies in Scholarly Journal Publishing
- Why the Gene Was (Mis)Placed at the Center of American Health Policy
- Telemedicine and Healing Relationships
- Love Is Good, but Does It Have Teeth?
- Tyler Tate replies
- Risk‐Sensitive Assessment of Decision‐Making Capacity: A Comprehensive Defense
- The Moral Difference between Faces & FaceTime
- Rethinking the Ethics of the Covid‐19 Pandemic Lockdowns
- The Moral Value of Telemedicine to the Physician‐Patient Relationship
- Facing Progress with Pragmatism: Telemedicine and Family Medicine
- Global Efforts to Protect Healthy Volunteers
- Smuggled Doughnuts and Forbidden Fried Chicken: Addressing Tensions around Family and Food Restrictions in Hospitals
- Expanding Boundaries
- Home Care in America: The Urgent Challenge of Putting Ethical Care into Practice
- Gender‐Affirming Care for Cisgender People
- Dementia and Concurrent Consent to Sexual Relations
- Examining the Ethics and Impacts of Laws Restricting Transgender Youth‐Athlete Participation
- Dementia, Sex, and Consent: Beyond the Uncomplicated Cases
- Centering Home Care in Bioethics Scholarship, Education, and Practice
- Recalibrating Bioethics for the Reality of Interdependence: The Challenge of Collective‐Impact Problems
- Bioethics and War
- The Business of Medicine Fails Many American Patients
- Dignity and the Founding Myth of Bioethics
- Legal Discrepancies and Expectations of Women: Abortion, Fetal Therapy, and NICU Care
- Love Your Patient as Yourself: On Reviving the Broken Heart of American Medical Ethics
- Refusal of Representation in Advance Care Planning: A Case‐Inspired Ethical Analysis
- Cruzan after Dobbs: What Remains of the Constitutional Right to Refuse Treatment?
- To Understand Inequity, Bioethics Needs to Sort Things Out
- Bioethics’ Conceptual Tool Kit
- Wrestling with Public Input on an Ethical Analysis of Scientific Research
- Wrestling with Social and Behavioral Genomics: Risks, Potential Benefits, and Ethical Responsibility
- An Ambitious Goal: A Grounded, Informed, and Compelling Theological Bioethics
- In Defense of Openness—Genetic Knowledge and Gamete Donation
- Vulnerability, Autonomy, and the Living Organ Donor
- Public Health at the Kitchen Table: Lessons from the Home HIV Test’s Long Road to Approval
- Distressed Work: Chronic Imperatives and Distress in Covid‐19 Critical Care
- Expanding Paid Sick Leave Laws: The Public Health Imperative
- Mapping the Moral Terrain of Clinical Deception
- Deception, Pain, and Placebo: Applying the Brummett‐Salter Deception Framework
- Justifying Clinical Deception: Some Amendments to Brummett and Salter
- The Problem of Clinical Deception and Why We Cannot Begin in the Middle
- The Obligation of Engagement
- Deception and Distress
- Henri Wijsbek and Thomas Nys Respond
- On Psychological Continuity and Dementia
- Louisiana’s “Medically Futile” Unborn Child List: Ethical Lessons at the Post‐Dobbs Intersection of Reproductive and Disability Justice
- Complex Decisions
- Locked In
- Stories and Shame in Front‐Line Medicine
- Issue Information (About the Cover Art)
- Care beyond Covid
- An Ecostructural Lens for Health Ethics
- Protecting Health after Dobbs
- Exploring the Ethics of the Parental Role in Parent‐Clinician Conflict
- Raising the Dead? Limits of CPR and Harms of Defensive Practices
- Deciding with Others: Interdependent Decision‐Making
- Rethinking Decision Quality: Measures, Meaning, and Bioethics
- Clarifying the Ethics and Oversight of Chimeric Research
- Human, Nonhuman, and Chimeric Research: Considering Old Issues with New Research
- Threats to Benefits: Assessing Knowledge Production in Nonhuman Models of Human Neuropsychiatric Disorders
- How Chimeric Animal Research Impacts Animal Welfare: A Conversation with Animal Welfare Experts
- A Conversation with Chimeric Animal Researchers
- About The Hastings Center, the Department of Bioethics at Case Western Reserve University, and the Cover Art
- Composite Animals: Then and Now
- Moral Status and the Oversight of Research Involving Chimeric Animals
- Not Just for Nurses
- Maybe We Should Try the Precautionary Principle?
- Zoonoses and Animal Culling: The Need for One Health Policy
- Burdening Others
- U.S. Lawsuit Claims Federal Law Can Require Emergency Abortions
- Xenotransplantation Clinical Trials and the Need for Community Engagement
- To Assess Technologies, Bioethicists Must Take Off Their Blinkers
- Thinking about Moral Progress
- Choosing to Die
- On the Authority of Advance Euthanasia Directives for People with Severe Dementia: Reflections on a Dutch Case
- Reevaluating the Ethical Issues in Porcine‐to‐Human Heart Xenotransplantation
- Errors in Converting Principles to Protocols: Where the Bioethics of U.S. Covid‐19 Vaccine Allocation Went Wrong
- Disability, Bioethics, and the Problem of Prejudice
- Ethics Big and Small, Thinking Fast and Slow
- Rethinking Theory in Bioethics
- Carbon Emissions from Overuse of U.S. Health Care: Medical and Ethical Problems
- The Microethics of Communication in Health Care: A New Framework for the Fast Thinking of Everyday Clinical Encounters
- Reproductive Embryo Editing: Attending to Justice
- Ethics of a Mandatory Waiting Period for Female Sterilization
- Do Health Care Organizations Have Legitimate Responsibilities beyond the Delivery of Health Care? Insights from Citizenship Theory
- Mask Mandates and Dilemmas of Disability Difference
- Ourselves, with Dementia
- Bioethics in Community Health
- What Happened to Consent? Rationalizing Its Breaches
- Learning Health Systems, Informed Consent, and Respect for Persons
- Compulsory Research in Learning Health Care: Against a Minimal Risk Limit
- Toward Meeting the Obligation of Respect for Persons in Pragmatic Clinical Trials
- Setting Risk Limits and Ensuring Fairness in Learning Health Care
- Necessity, Rights, and Rationing in Compulsory Research
- Covid‐19: Medical Decisions, Mandates, and High‐Risk Minors
- Learning Health Care and the Obligation to Participate in Research
- Facilitating Ukrainian Refugees’ Continued Participation in Clinical Trials
- DEI Is Not Enough
- Envisioning Solidarity
- If Not Now, Then When? Taking Disability Seriously in Bioethics
- The Right Recognition of Rights
- Public Trust and Medical Ethics
- Ethics and Structure
- New Findings on Unconsented Intimate Exams Suggest Racial Bias and Gender Parity
- Before The Birth of Bioethics: James M. Gustafson at Yale
- Industry Technicians Embedded in Clinical Teams: Impacts on Medical Knowledge
- Handle with Care: The WHO Report on Human Genome Editing
- The Bioethics of Built Space: Health Care Architecture as a Medical Intervention
- The Case for Ethical Efficiency: A System That Has Run Out of Time
- The UN Challenge to Guardianship and Surrogate Decision‐Making
- Looking Closely at Health Inequities
- Earning Mistrust through Fake Compromises and Broken Promises
- Is Trust Enough? Anti‐Black Racism and the Perception of Black Vaccine “Hesitancy”
- Anti‐Black Racism as a Chronic Condition
- About the Cover Art and Artist
- Anti‐Black Racism and Power: Centering Black Scholars to Achieve Health Equity
- Testimonies and Healing: Anti‐oppressive Research with Black Women and the Implications for Compassionate Ethical Care
- Womanist Ethics as a Contribution to Bioethics
- Addressing Anti‐Black Racism in Bioethics: Responding to the Call
- Black and Waiting: Bioethics and Care during the Covid‐19 Pandemic
- Herstory as an Important Force in Bioethics
- Colonial Geographies, Black Geographies, and Bioethics
- Speaking Volumes: The Encyclopedia of Bioethics and Racism
- Toward Critical Bioethics Studies: Black Feminist Insights for a Field “Reckoning” with Anti‐Black Racism
- About The Hastings, The Greenwall Foundation, and the Cover Art
- A Call for Solidarity in Bioethics: Confronting Anti‐Black Racism Together
- From a Reckoning to Racial Concordance: A Strategy to Protect Black Mothers, Children, and Infants
- Black Feminist Bioethics: Centering Community to Ask Better Questions
- Latinx Bioethics: Toward a Braver, Broader, and More Just Bioethics
- Racism, Not Race: A Physician Perspective on Anti‐Black Racism in America
- Bioethics Rooted in Justice: Community‐Expert Reflections
- Holding Them Accountable: Organizational Commitments to Ending Systemic Anti‐Black Racism in Medicine and Public Health
- On the Shoulders of Giants: A Reckoning with Social Justice
- Now You Are Part of the Solution: Bioethicists’ Contribution in Addressing Racialized Health Inequity
- Trust Also Means Centering Black Women’s Reproductive Health Narratives
- Authenticity and Clinical Decision‐Making
- The Bleak Future of Reproductive Rights for Queer Indians
- Death in a Cold Climate: Medical Aid in Dying in Vermont
- Risk Trade‐Offs and Equitable Decision‐Making in the Covid‐19 Pandemic
- On Ethicists and Their Diets
- The Surrogation of Surrogacy: The Perils and Pitfalls of Epistemic Authority
- “We have nothing left to bury.”
- Pediatric Authenticity: Hiding in Plain Sight
- Consent for Intimate Exams on Unconscious Patients: Sharpening Legislative Efforts
- Advance Directives: The Principle of Determining Authenticity
- Bioethics for Journalists
- Disability Affirmative Action Requirements for the U.S. HHS and Academic Medical Centers
- Resisting Transhumanist Fantasies
- The Market in Noninvasive Prenatal Tests and the Message to Consumers: Exploring Responsibility
- Allocation of Opportunities to Participate in Clinical Trials during the Covid‐19 Pandemic and Other Public Health Emergencies
- Deficits of Public Deliberation in U.S. Oversight for Gene Edited Organisms
- Deliberative Public Consultation via Deliberative Polling: Criteria and Methods
- Giving Voice to the Voiceless in Environmental Gene Editing
- Public Deliberation about Gene Editing in the Wild
- Envisioning Complex Futures: Collective Narratives and Reasoning in Deliberations over Gene Editing in the Wild
- Empowering Indigenous Knowledge in Deliberations on Gene Editing in the Wild
- Genetic Control in Historical Perspective: The Legacy of India’s Genetic Control of Mosquitoes Unit
- Restructuring Deliberation Using a Cultural Theory Lens
- Narratives in Public Deliberation: Empowering Gene Editing Debate with Storytelling
- The Decision Phases Framework for Public Engagement: Engaging Stakeholders about Gene Editing in the Wild
- About The Hastings Center and the Cover Art
- Regulating Gene Editing in the Wild: Building Regulatory Capacity to Incorporate Deliberative Democracy
- Does Gene Editing in the Wild Require Broad Public Deliberation?
- Virginia A. Brown replies
- Removing a Disabled Person from Her Treasured Independent Living
- A Developing Timeline for Bioethics
- Living Out a Life’s Meaning
- Health Justice and Rawls’s Theory at Fifty: Will New Thinking about Health and Inequality Influence the Most Influential Account of Justice?
- Justice, Bioethics, and Covid‐19
- ICU Care in a Pandemic
- A “Surprise” Health Policy Legislative Victory
- John Rawls, Godfather of Bioethics
- Govind Persad replies
- Considering People with Dementia and Their Caregivers in Covid‐19 Lockdowns
- Divided Loyalties: Fire and ICE
- Social Equality in an Alternate World
- Covid‐19, Free Exercise, and the Changing Constitution
- Pediatric Off‐Label Use of Covid‐19 Vaccines: Ethical and Legal Considerations
- Covid Vaccine Mandates and Religious Accommodation in Employment
- “Am I safe?”
- The University of California Crisis Standards of Care: Public Reasoning for Socially Responsible Medicine
- Values across Ages
- Disability Access and Digital Platforms
- Ventilator Allocation Protocols: Sophisticated Bioethics for an Unworkable Strategy
- The Crisis in Standards of Care
- Centering Social Justice for Covid‐19 Resources and Research
- Life‐Years & Rationing in the Covid‐19 Pandemic: A Critical Analysis
- Crisis Standards of Care—More Than Just a Thought Experiment?
- Against Exclusive Survivalism: Preventing Lost Life and Protecting the Disadvantaged in Resource Allocation
- Lessons from Biomedical Innovation during World War II
- Structural Inequities, Fair Opportunity, and the Allocation of Scarce ICU Resources
- The Vaccination Cold War
- Material Insecurity, Racial Capitalism, and Public Health
- Mind the Gaps: Ethical and Epistemic Issues in the Digital Mental Health Response to Covid‐19
- Genomic Testing, Unexpected Consanguinity, and Adolescent Parents
- The Center’s Highest Award
- A Realpolitik for Presidential Health: A Psychiatrist’s Perspective
- Hope to the End
- Activism and Bioethics: Taking a Stand on Things That Matter
- Why Clinical Ethicists Are Not Activists
- Antiracist Activism in Clinical Ethics: What’s Stopping Us?
- Equal Access to Organ Transplantation for People with Disabilities
- Opioid Treatment Agreements and Patient Accountability
- Care Ethics versus the CARES Act
- Activism and the Clinical Ethicist
- Essential Reading for Bioethicists in the Anthropocene Era
- It Is Time to Abandon the Dogma That Brain Death Is Biological Death
- Ethicists and Activists
- Regulating AI in Health Care: The Challenges of Informed User Engagement
- Alzheimer’s and Aducanumab: Unjust Profits and False Hopes
- Justice through a Wide‐Angle Lens
- Gene Editing: How Can You Ask “Whether” If You Don’t Know “How”?
- Ending One’s Life in Advance
- In the Name of Racial Justice: Why Bioethics Should Care about Environmental Toxins
- Reciprocity and Liability Protections during the Covid‐19 Pandemic
- What Has Covid‐19 Exposed in Bioethics? Four Myths
- Centering across the Center
- Out of Africa: A Solidarity‐Based Approach to Vaccine Allocation
- Legal and Ethical Issues in the Report Heritable Human Genome Editing
- Public Engagement and the Social Risks of Science
- Variations on Consent
- Prioritizing the Prevention of Early Deaths during Covid‐19
- Teneille Brown, Leslie Francis, and James Tabery respond
- Antiracist Praxis in Public Health: A Call for Ethical Reflections
- Public Attitudes toward Consent When Research Is Integrated into Care—Any “Ought” from All the “Is”?
- The Consent Continuum: A New Model of Consent, Assent, and Nondissent for Primary Care
- In This Together: Navigating Ethical Challenges Posed by Family Clustering during the Covid‐19 Pandemic
- The Limited Value of Dementia‐Specific Advance Directives
- History and Bioethics
- What Do Genomics Studies Really Mean? A New Resource
- Coming to Terms with the Black Box Problem: How to Justify AI Systems in Health Care
- Does a Public Health Crisis Justify More Research with Incarcerated People?
- Checking in with Neuroethics
- Digital Health Care Disparities
- Heart and Soul
- Can Clinical Empathy Survive? Distress, Burnout, and Malignant Duty in the Age of Covid‐19
- Weighted Lotteries and the Allocation of Scarce Medications for Covid‐19
- A Heart without Life: Artificial Organs and the Lived Body
- Rethinking Human Embryo Research Policies
- Congee for the Soul
- When Following the Rules Feels Wrong
- Residential Segregation and Publicly Spirited Democracy
- About The Hastings Center and Knight Foundation
- Civic Learning, Science, and Structural Racism
- Civic Learning When the Facts Are Politicized: How Values Shape Facts, and What to Do about It
- White Privilege, White Poverty: Reckoning with Class and Race in America
- Civic Learning for a Democracy in Crisis
- Redoing the Demos
- Recommendations for Better Civic Learning: Building and Rebuilding Democracy
- The Vanishing Square: Civic Learning in the Internet Age
- Does the Civic Renewal Movement Have a Future?
- Can Our Schools Help Us Preserve Democracy? Special Challenges at a Time of Shifting Norms
- Creative Democracy—the Task Still before Us
- Trust: The Need for Public Understanding of How Science Works
- A Leap of Faith: Is There a Formula for “Trustworthy” AI?
- Getting to the Truth: Ethics, Trust, and Triage in the United States versus Europe during the Covid‐19 Pandemic
- When Is Age Choosing Ageist Discrimination?
- The Social Risks of Science
- Realizing Present and Future Promise of DIY Biology and Medicine through a Trust Architecture
- Human Genome Editing and a Global Socio‐bioethics Approach
- Surrogates, Chaos, and the Inadequacy of Autonomy
- Structural Injustices in Our Nonideal World
- Listening to Scientists—and Each Other
- Health Research and Social Justice Philosophy
- Manuscript Reviewers 2020
- Prescription Requirements and Patient Autonomy: Considering an Over‐the‐Counter Default
- Living Donors and the Issue of “Informed Consent”
- A Small‐Town Heart
- OK, Boomer, MD: The Rights of Aging Physicians and the Health of Our Communities
- Third Parties
- Can Genetic Nondiscrimination Laws Save Lives?
- The Emerging Hazard of AI‐Related Health Care Discrimination
- Genetic Data Aren’t So Special: Causes and Implications of Reidentification
- Words Matter
- A Matter of Justice: “Fat” Is Not Necessarily a Bad Word
- Your Father’s a Fighter; Your Daughter’s a Vegetable: A Critical Analysis of the Use of Metaphor in Clinical Practice
- Restricting Reasons: A New Battleground in Abortion Regulation
- A Man of Vision: Daniel Callahan on the Nasty Problem and the Noxious Brew
- Between Crisis and Convention: How Should We Address Contingency?
- On “Not Recommending” ECMO
- The Golden Rule
- Some Lives Matter: The Dirty Little Secret of the U.S. Health Care System
- Can We Do without Respect and Justice in Animal Research Ethics?
- “Reproductive Negligence”: A Necessary and Sufficient Remedy?
- Considering the Role of Transparency in Health and Health Care
- Remembering Hospice
- Bioethics and Addiction
- Toward Fair and Humane Pain Policy
- What We’re Not Talking about When We Talk about Addiction
- Patients Left Behind: Ethical Challenges in Caring for Indirect Victims of the Covid‐19 Pandemic
- Solving the Opioid Crisis Isn’t Just a Public Health Challenge—It’s a Bioethics Challenge
- The Ethical Limits of Children’s Participation in Clinical Research
- A Futile Use of Futility
- A Pandemic Diary
- Dueling Definitions of Abortifacient: How Cultural, Political, and Religious Values Affect Language in the Contraception Debate
- Rethinking Ethical Categories in the Age of Technology
- Rethinking the Importance of the Individual within a Community of Data
- Does Solidarity Require “All of Us” to Participate in Genomics Research?
- Why and How Bioethics Must Turn toward Justice: A Modest Proposal
- About The Special Report
- We Have Seen the Mutants—and They Are Us: Gifts and Burdens of a Genetic Diagnosis
- Excavating the Personal Genome: The Good Biocitizen in the Age of Precision Health
- Provoking Bad Biocitizenship
- Disability and the Damaging Master Narrative of an Open Future
- Conceptualizing Race in the Genomic Age
- Coding the Self: The Infopolitics and Biopolitics of Genetic Sciences
- Health for Whom? Bioethics and the Challenge of Justice for Genomic Medicine
- Reading in the Postgenomic Age: On Contemporary Literature and the Good Bionarrative Citizen
- Editors and Authors
- The Ethics of Everyday Life in the Midst of a Pandemic
- Recognizing Moral Injury: Toward Legal Intervention for Physician Burnout
- Covid‐19: Exposing the Lack of Evidence‐Based Practice in Medicine
- 62,406 and Counting
- The Future of Bioethics: It Shouldn’t Take a Pandemic
- Learning from a Pandemic
- Black Lives in a Pandemic: Implications of Systemic Injustice for End‐of‐Life Care
- Doubt, Disorientation, and Death in the Plague Time
- Communities Matter
- Ventilators, Guidelines, Judgment, and Trust
- Duties toward Patients with Psychiatric Illness
- Employment‐Based, For‐Profit Health Care in a Pandemic
- Avoiding Ineffective End‐of‐Life Care: A Lesson from Triage?
- The Pandemic: Lessons for Bioethics?
- What Could “Fair Allocation” during the Covid‐19 Crisis Possibly Mean in Sub‐Saharan Africa?
- Pandemics, Protocols, and the Plague of Athens: Insights from Thucydides
- Realigning Pakistan’s Bioethics Center during Covid‐19
- Digital Contact Tracing, Privacy, and Public Health
- Walls
- The Hang Up
- A Strategy to Prevent and Control Zoonoses?
- Learning from Covid
- Rethinking “Elective” Procedures for Women’s Reproduction during Covid‐19
- Planetary Ethics: Russell Train and Richard Nixon at the Creation
- Dying during Covid‐19
- Global Disparity and Solidarity in a Pandemic
- Older Adults and Covid‐19: The Most Vulnerable, the Hardest Hit
- Interdependent Citizens: The Ethics of Care in Pandemic Recovery
- Our Next Pandemic Ethics Challenge? Allocating “Normal” Health Care Services
- Reassessing the Three Rs?
- Vulnerable Children in a Dual Epidemic
- Disability Rights as a Necessary Framework for Crisis Standards of Care and the Future of Health Care
- AI Surveillance during Pandemics: Ethical Implementation Imperatives
- Vaccine Rationing and the Urgency of Social Justice in the Covid‐19 Response
- Covid‐19: Ethical Challenges for Nurses
- Experiencing Community in a Covid Surge
- Health Inequalities
- Sharona Hoffman Replies
- The Legal Challenge of Abortion Stigma—and Government Restrictions on the Practice of Medicine
- Reasonable Persons, Autonomous Persons, and Lady Hale: Determining a Standard for Risk Disclosure
- All People
- Scarcity in the Covid‐19 Pandemic
- Budgets versus Bans: How U.S. Law Restricts Germline Gene Editing
- Plus ça change: Renée Fox and the Sociology of Organ Replacement Therapy
- Kevin Mintz and David Wasserman Reply
- The New Wallet Biopsy and Involuntary Patient Transfers Abroad: How Physicians Can Help Protect Patients
- Health Care Surrogacy Laws Do Not Adequately Address the Needs of Minors
- African Conceptions of Age‐Based Moral Standing: Anchoring Values to Regional Realities
- Chinese Bioethicists Speak Out on Covid‐19, and Others Follow
- A Demanding Ethics of Care
- Green Bioethics and Hope
- Physician Burnout and the Americans with Disabilities Act
- Responding to Covid‐19: How to Navigate a Public Health Emergency Legally and Ethically
- Should Institutions Disclose the Names of Employees with Covid‐19?
- Responding to COVID‐19: How to Navigate a Public Health Emergency Legally and Ethically
- Julian J. Koplin Replies
- “Do we have to replace the balloon pump when it fails?”
- Trust, Risk, and Race in American Medicine
- High Hopes for “Deep Medicine”? AI, Economics, and the Future of Care
- Earning Patient Trust: More Than a Question of Signaling
- Trust in American Medicine: A Call to Action for Health Care Professionals
- Hans Jonas and the Ethics of Human Subjects Research
- The United Kingdom Revisits Its Surrogacy Law
- The Business of Certification
- Chimeras and the Problem of Other Minds
- Caring for People with Disabilities: An Ethics of Respect
- Equity Care
- Pediatric Drug Labeling and Imperfect Information
- Patient Welfare and Trust
- Precision (Mis)Education
- Medically Assisted Dying and Suicide: How Are They Different, and How Are They Similar?
- Medical Crowdfunding for Unproven Medical Treatments: Should Gofundme Become a Gatekeeper?
- Sugar, Taxes, & Choice
- Not Whether but How: Considerations on the Ethics of Telling Patients’ Stories
- Can the Case Report Withstand Ethical Scrutiny?
- Physician Burnout Calls for Legal Intervention
- Toward the Polyphonic Case
- Why Won’t My Patient Act Like a Jerk?
- Dementia and the Death Penalty
- Unhealthy Partnerships and Public Health: Breaking Free of Industry
- Between a Rock and a Hard Place: The Collective Good at a Time of Medical Narcissism
- Surgeon General’s Warning: Gender Is Bad for Your Health
- Storytelling
- Getting Close
- MANUSCRIPT REVIEWERS 2019
- What Medical Students Teach: The Healing Skill of Being a Team Player
- Dan Callahan’s Press Clips
- Daniel Callahan and the Vocation of Bioethics
- Developing, Administering, and Scoring the Healthcare Ethics Consultant Certification Examination
- Healing Relationships
- Of Slide Rules and Stethoscopes: AI and the Future of Doctoring
- Admiring Dan’s Creation
- Callahanian Bioethics
- California Takes the Lead on Data Privacy Law
- A Champion for the Unestablished
- Crossing Boundaries
- Human‐Animal Chimeras, “Human” Cognitive Capacities, and Moral Status
- Disability, Technology, and Flourishing
- Animals with Human Cells in Their Brains: Implications for Research
- The Moral Status of Human‐Animal Chimeras with Human Brain Cells
- Human‐Animal Chimeras: The Moral Insignificance of Uniquely Human Capacities
- Clinical Trial Portfolios: A Critical Oversight in Human Research Ethics, Drug Regulation, and Policy
- Homeless, Ill, and Psychiatrically Complex: The Grueling Carousel of Cassandra Lee
- When No One Notices: Disorders of Consciousness and the Chronic Vegetative State
- Bystander Ethics and Good Samaritanism: A Paradox for Learning Health Organizations
- Patient as Gift
- Out of the Freezer and into the Policy Fire: Quandaries in Reproductive Cryopreservation
- Of Drowning Children and Doubtful Analogies
- Ostriches and Obligations: Ethical Challenges Facing Research on Usual Care
- Thinking Together
- The Tyranny of Hope
- A Last Gift
- Daniel Callahan (1930–2019)
- The Harms of a Penal Colony
- The Haves, the Have‐nots, and the Will‐nots
- The Relational Potential Standard: Rethinking the Ethical Justification for Life‐Sustaining Treatment for Children with Profound Cognitive Disabilities
- A Reluctant Critic: Why Gynecologic Surgery Needs Reform
- Heritable Genome Editing in a Global Context: National and International Policy Challenges
- Choice Architecture
- Beecher Reconsidered
- The Stress Test
- Capacity and Relationship
- Relational Potential versus the Parent‐Child Relationship
- Dying with Dignity; Living with Laws (and Ethics)
- The Experts Are Not Enough
- Embracing Asymmetry and Humility in the Face of Disability
- Asylum, Refuge, and Justice in Health
- The Implications of Genetic and Other Biological Explanations for Thinking about Mental Disorders
- About The Hastings Center and the Columbia University Center for Research on Ethical, Legal & Social Implications of Psychiatric, Neurologic & Behavioral Genetics
- On What We Have Learned and Still Need to Learn about the Psychosocial Impacts of Genetic Testing
- Genomic Essentialism: Its Provenance and Trajectory as an Anticipatory Ethical Concern
- Making Sense of Genetics: The Problem of Essentialism
- Assessing the Psychological Impact of Genetic Susceptibility Testing
- Laypeople Are Strategic Essentialists, Not Genetic Essentialists
- The Psychological Well‐being of Pregnant Women Undergoing Prenatal Testing and Screening: A Narrative Literature Review
- Psychosocial Effects of Multigene Panel Testing in the Context of Cancer Genomics
- Qualitative Research on Expanded Prenatal and Newborn Screening: Robust but Marginalized
- Actions and Uncertainty: How Prenatally Diagnosed Variants of Uncertain Significance Become Actionable
- What Is the Psychosocial Impact of Providing Genetic and Genomic Health Information to Individuals? An Overview of Systematic Reviews
- The Social Science Blues
- Controlling Measles through Politics and Policy
- Empathetic Practice: The Struggle and Virtue of Empathizing with a Patient’s Suffering
- Changing the Question
- Citizen Science and Gamification
- The Critical Role of Medical Institutions in Expanding Access to Investigational Interventions
- Federal Right to Try: Where Is It Going?
- Medical School: The Wrong Applicant Pool?
- Conscience and Religious Freedom Division Marks Its First Anniversary with Action
- Achieving Meaningful Access to Medicaid
- Better Guidance for Surrogates
- Annual Award for an Essay by an Early‐Career Scholar
- Danielle M. Wenner Replies
- Rawls and Social Value in Research
- Capacity for Preferences and Pediatric Assent: Implications for Pediatric Practice
- Deep Ethical Learning: Taking the Interplay of Human and Artificial Intelligence Seriously
- Social Media, E‐Health, and Medical Ethics
- Welcoming the “Intel‐ethicist”
- Fighting Novel Diseases amidst Humanitarian Crises
- Artificial Intelligence and Black‐Box Medical Decisions: Accuracy versus Explainability
- Ethical Use of Social Media Data: Beyond the Clinical Context
- Capacity for Preferences and Pediatric Assent Implications for Pediatric Practice
- The Strange Tale of Three Identical Strangers: Cinematic Lessons in Bioethics
- An Ethical Obligation for Bioethicists to Utilize Social Media
- Requests for PAD and the Assessment of Capacity
- Pregnant Women Can Finally Expect Better
- North of Home: Obligations to Families of Undocumented Patients
- Could We Be Marsupials? Very Premature Babies and Artificial Wombs
- Editorial Trends
- IRB Becomes E&HR
- The Social Value Requirement in Research: From the Transactional to the Basic Structure Model of Stakeholder Obligations
- Work Requirements That Don’t Work
- Medical Aid in Dying: Bioethics as Sideshow
- Rereading Frankenstein: What If Victor Frankenstein Had Actually Been Evil?
- Difficulties with Applying a Strong Social Value Requirement to Clinical Research
- Research Information for Reasonable People
- Unexpected Creatures: Procreative Liberty and the Frankenstein Ballet
- Locating the Source(s) of the Social Value Requirement(s)
- On Cute Monkeys and Repulsive Monsters
- Wrestling with the Monster: Frankenstein and Organ Transplantation
- Of Monsters and Men
- Who Are You?
- Poverty: Not a Justification for Banning Physician‐Assisted Death
- Who Deserves Access to Care in Children’s Hospitals?
- 2018 Manuscript Reviewers
- Imposing Death: Religious Witness on Brain Death
- Respecting Choice in Definitions of Death
- Brain Death and the Law: Hard Cases and Legal Challenges
- The Public’s Right to Accurate and Transparent Information about Brain Death and Organ Transplantation
- Lessons from the Case of Jahi McMath
- Brain Death: A Conclusion in Search of a Justification
- A Path Not Taken: Beecher, Brain Death, and the Aims of Medicine
- Brain Death at Fifty: Exploring Consensus, Controversy, and Contexts
- The Other Animal of Transplant’s Future
- A Conceptual Justification for Brain Death
- Would a Reasonable Person Now Accept the 1968 Harvard Brain Death Report? A Short History of Brain Death
- Beecher Dépassé: Fifty Years of Determining Death, Legally
- About The Hastings Center and the Center for Bioethics at Harvard Medical School
- DCDD Donors Are Not Dead
- Uncontrolled DCD: When Should We Stop Trying to Save the Patient and Focus on Saving the Organs?
- Revisiting Death: Implicit Bias and the Case of Jahi McMath
- Death: An Evolving, Normative Concept
- Conceptual Issues in DCDD Donor Death Determination
- Bodies in Transition: Ethics in Xenotransplantation Research
- Rethinking Brain Death as a Legal Fiction: Is the Terminology the Problem?
- The Dead Donor Rule as Policy Indoctrination
- The Case of Jahi McMath: A Neurologist’s View
- A Defense of the Dead Donor Rule
- Justifying Conscience Clauses
- Patient‐Engaged Research: Choosing the “Right” Patients to Avoid Pitfalls
- Amyloid in the Brain, Alzheimer’s on the Mind
- Disentangling Conscience Protections
- Whom to Engage in Patient‐Engaged Research? Reflection on Selection
- How Bioethics Can Shape Artificial Intelligence and Machine Learning
- Crossing U.S. Borders While Pregnant: An Increasingly Complex Reality
- When Societal Structural Issues Become Patient Problems: The Role of Clinical Ethics Consultation
- At the Borders of Bioethics
- Solidarity: Careful What We Wish For
- A Medical Pedagogy of Mutual Suffering
- Investing in Parenthood
- Evidence and Human Genome Editing
- Defining Life and Regulating Reproductive Choice
- Population Aging and the Sustainability of the Welfare State
- “Tho’ much is taken, much abides”: A Good Life within Dementia
- About the Special Report
- Improving Long‐Term Care by Finally Respecting Home‐Care Aides
- What Can Thinking Like a Gerontologist Bring to Bioethics?
- Solidarity and Care Coming of Age: New Reasons in the Politics of Social Welfare Policy
- Becoming Good Citizens of Aging Societies
- Aging: Drawing a Map for the Future
- Precarious Aging: Insecurity and Risk in Late Life
- Realizing and Maintaining Capabilities: Late Life as a Social Project
- Taking a Systems Approach to Chronic Illness in Old Age
- Age‐Friendly Initiatives, Social Inequalities, and Spatial Justice
- Co‐creating Environments: Empowering Elders and Strengthening Communities through Design
- Housing, the Built Environment, and the Good Life
- How Do We Fund Flourishing? Maybe Not through Health Care
- The Extended Body: On Aging, Disability, and Well‐being
- Advance Directives for Refusing Life‐Sustaining Treatment in Dementia
- On Talking Together about Ordinary Abortion
- Are Obese Children Abused Children?
- Learning from Me Too
- On Avoiding Deep Dementia
- When Voluntary Stopping of Eating and Drinking in Advanced Dementia Is No Longer Voluntary
- Caring for Patients with Substance Use Disorders: Addressing a Missed Opportunity in the Hospital
- An Open Letter to Norman Cantor Regarding Dementia and Physician‐Assisted Suicide
- Advance Directives and Discrimination against People with Dementia
- Discriminatory Demands by Patients
- Proposed Regulations Favor Providers’ Conscience Rights over Patients’ Rights
- The Next Wave in Health Care Priority Setting
- Bigger, Faster, Stronger, More Ethical
- Advance Directives and Dementia
- Defining Misprescribing to Inform Prescription Opioid Policy
- Using Newborn Sequencing to Advance Understanding of the Natural History of Disease
- About the University of California, San Francisco, Program in Bioethics
- Authors
- Eugenics Redux: “Reproductive Benefit” as a Rationale for Newborn Screening
- Sequencing Newborns: A Call for Nuanced Use of Genomic Technologies
- What Genomic Sequencing Can Offer Universal Newborn Screening Programs
- About The Hastings Center
- A New Era, New Strategies: Education and Communication Strategies to Manage Greater Access to Genomic Information
- Are Parents Really Obligated to Learn as Much as Possible about Their Children’s Genomes?
- Whose Odyssey Is It? Family‐Centered Care in the Genomic Era
- My Diagnostic Odyssey—A Call to Expand Access to Genomic Testing for the Next Generation
- Single‐Gene Sequencing in Newborn Screening: Success, Challenge, Hope
- The Legal Dimensions of Genomic Sequencing in Newborn Screening
- Commercial Interests, the Technological Imperative, and Advocates: Three Forces Driving Genomic Sequencing in Newborns
- Families’ Experiences with Newborn Screening: A Critical Source of Evidence
- Lessons for Sequencing from the Addition of Severe Combined Immunodeficiency to Newborn Screening Panels
- The Human Being in Full
- Returning Incidental Findings in Low‐Resource Settings: A Case of Rescue?
- GINA at Ten and the Future of Genetic Nondiscrimination Law
- Personalized Medicine Is the Postgenomic Condition
- A note—and a call—from the weeds
- Only in Silence
- Change without Change? Assessing Medicare Reimbursement for Advance Care Planning
- Genetic Information, the Principle of Rescue, and Special Obligations
- Rescue via Genetic Findings
- In the Balance: Weighing Preferences of Decisionally Incapacitated Patients
- You Can’t Always Get (or Give) What You Want: Preferences and Their Limits
- Genetic Privacy, Disease Prevention, and the Principle of Rescue
- Groundhog Day for Medical Artificial Intelligence
- Capacity for Preferences: Respecting Patients with Compromised Decision‐Making
- Incidental Findings in Low‐Resource Settings
- Illness as a Crisis of Meaning
- Progress: Its Glories and Pitfalls
- The Right to Know: A Revised Standard for Reporting Incidental Findings
- Financial Conflicts of Interest at FDA Drug Advisory Committee Meetings
- Organ Transplantation and the Uniform Anatomical Gift Act: A Fifty‐Year Perspective
- Abortion Bans, Doctors, and the Criminalization of Patients
- Mass Shootings, Mental Illness, and Gun Control
- One Ventilator Too Few?
- Fetal Medicine and the Pregnant Woman
- Bioethics and Science
- Genome “Surgery”?
- Can Rationing through Inconvenience Be Ethical?
- Manuscript Reviewers 2017
- Raising the Stakes for Nondiscrimination Protections in the ACA
- Tackling Obesity and Disease: The Culprit Is Sugar; the Response Is Legal Regulation
- Market Language, Moral Language
- Time Is Ethics
- The Intimate Responsibility of Surrogate Decision-Making
- The Different Moral Bases of Patient and Surrogate Decision-Making
- Patient Care to Public Health to Synthetic Biology
- Bioethics as care work
- On Nudging Health
- It’s All Relative
- Community Engagement and Field Trials of Genetically Modified Insects and Animals
- Rationing Care through Collaboration and Shared Values
- Being Better Bodies
- The Real-World Ethics of Adaptive-Design Clinical Trials
- Real-World Evidence, Public Participation, and the FDA
- “What’s in a name?” CAR-T Gene Therapy
- Contemplating Resectability
- Public Health Autonomy: A Critical Reappraisal
- The Sticky Standard of Care
- Stemming the Standard-of-Care SPRAWL
- Global bioethics
- Delegating Informed Consent
- Ending DACA Has Pragmatic and Ethical Implications for U.S. Health Care
- Social Practices
- The Morality of Health Care Reform: Liberal and Conservative Views and the Space between Them
- ERRATUM
- A Modern, Rational Jeremiad
- Standards of Care in Global Health: Identifying the Right Question
- Mitochondrial Replacement Techniques, Scientific Tourism, and the Global Politics of Science
- CRISPR Becomes Clearer
- Physician-Assisted Death and Severe, Treatment-Resistant Depression
- Urgently Creating the Better in Global Health
- The Case for Resource Sensitivity: Why It Is Ethical to Provide Cheaper, Less Effective Treatments in Global Health
- field notes
- Despairing about Health Disparities
- When Public Health Becomes Politicized
- Empty Spaces
- Charlie Gard and the Limits of Parental Authority
- The Pluralism of Coherent Approaches to Global Health
- Rough Justice
- Are Transplant Recipients Human Subjects When Research Is Conducted on Organ Donors?
- Patients as Rights Holders
- On Legalizing Physician-Assisted Death for Dementia
- The art of the cover
- Artificial Wombs and Abortion Rights
- Conservationism and Bioethic
- Shared Decision-Making in Pediatrics: Honoring Multiple Voices
- A Failure to Be Candid
- Looking Back at the Ethical Tangles of Pediatric AIDS
- The Precision Medicine Nation
- How Long a Life Is Enough Life?
- Genomic Justice and Imagined Communities
- It’s “the End of Sex” As We Know It, and I Feel … a Little Nervous
- Trump’s Abortion-Promoting Aid Policy
- Expanding the Horizon of Our Obligations in the Clinician-Patient Relationship
- Decision-Making for an Incapacitated Pregnant Patient
- “Please amputate my child’s arms”
- Flu, Floods, and Fire: Ethical Public Health Preparedness
- From the Foundation Up
- Foreign Relations
- Reconciling Patient Safety and Epistemic Humility: An Ethical Use of Opioid Treatment Plans
- Regulating Research with Biospecimens under the Revised Common Rule
- Crowdsourcing the Moral Limits of Human Gene Editing?
- Closed Financial Loops: When They Happen in Government, They’re Called Corruption; in Medicine, They’re Just a Footnote
- Toward Public Bioethics?
- How to Rethink the Fourteen-Day Rule
- The Anatomy of Research Scandals
- Research with Pregnant Women: New Insights on Legal Decision-Making
- Opioid Treatment Agreements Repurposed—But Who Monitors the Monitors?
- Defending Opioid Treatment Agreements: Disclosure, Not Promises
- Rethinking Reprogenetics
- Implementing California’s Law on Assisted Dying
- The Clue
- Space for the Prisoner’s Point of View
- Best Evidence Aside: Why Trump’s Executive Order Makes America Less Healthy
- Bioethics and “Rightness”
- Managing Opioid Withdrawal for Hospital Patients in Custody
- Reprioritizing Research Activity for the Post-Antibiotic Era: Ethical, Legal, and Social Considerations
- Authenticity, Best Interest, and Clinical Nudging
- Coercion and Access to Health Care
- Enrolling in Clinical Research While Incarcerated: What Influences Participants’ Decisions?
- Facts, values, and journalism
- Bioethics and Populism: How Should Our Field Respond?
- Toward an Ethically Sensitive Implementation of Noninvasive Prenatal Screening in the Global Context
- Justifying Clinical Nudges