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Rebecca Dresser

Biographic Data

ID7169209
NAMERebecca Dresser
GIVEN NAMESRebecca
FAMILY NAMEDresser
SIGNATUREDRESSER R
AFFILIATIONSWashington University in St. Louis
VERIFIEDNo
TOTAL WORKS68
TOTAL CITATIONS0
AUTHOR COUNT68
EDITOR COUNT0
FIRST PUBLICATION YEAR1980
LATEST PUBLICATION YEAR2026
H-INDEX0
  • Banning Gender‐Affirming Treatment for Minors: The Supreme Court Speaks

    Open Access•Rebecca Dresser•ARTICLE•The Hastings Center Report•2026

    In United States v. Skrmetti, the U.S. Supreme Court considered the constitutionality of a Tennessee law prohibiting certain medical procedures for the treatment of minors with gender dysphoria. A majority of the justices agreed that the law failed to violate the U.S. Constitution's equal protection provision. Because the law failed to distinguish among patients on the basis of sex, they said, it required only a rational basis to survive constitu…

  • Food and Drug Administration v. Alliance for Hippocratic Medicine: How Conscience Protections Preserved Mifepristone Access

    Open Access•Rebecca Dresser•ARTICLE•The Hastings Center Report•2025

    People in the bioethics field generally agree that clinicians should have reasonable freedom to practice according to their moral and religious convictions. But this general position leaves room for debate over how much freedom objecting clinicians ought to have. Some commentators contend that exemptions from criminal, civil, and professional consequences for conscientious refusals to provide care impose too many burdens on patients, colleagues, …

  • Residency Requirements for Medical Aid in Dying

    Open Access•Rebecca Dresser•ARTICLE•The Hastings Center Report•2024

    In 1997, when Oregon became the first U.S. jurisdiction authorizing medical aid in dying (MAID), its law included a requirement that patients be legal residents of the state. Other U.S. jurisdictions legalizing MAID followed Oregon in adopting residency requirements. Recent litigation challenges the legality, as well as the justification, for such requirements. Facing such challenges, Oregon and Vermont eliminated their MAID residency requirement…

  • Medical choices and changing selves

    Rebecca Dresser•ARTICLE•Journal of Medical Ethics•2023

  • Cruzan after Dobbs: What Remains of the Constitutional Right to Refuse Treatment

    Open Access•Rebecca Dresser•ARTICLE•The Hastings Center Report•2023

    In 2022, the U.S. Supreme Court removed constitutional protection from the individual's right to end a pregnancy. In Dobbs v. Jackson Women's Health Organization , the Court invalidated previous rulings protecting that right as part of the individual liberty and privacy interests embedded in the U.S. Constitution. Now, many observers are speculating about the fate of other rights founded on those interests. The Dobbs ruling conflicts with the Cou…

  • Ourselves, with Dementia

    Open Access•Rebecca Dresser•ARTICLE•The Hastings Center Report•2022

    Fear of dementia leads some people to demand an opportunity to choose death over life with the illness. They want the power to make advance euthanasia directives and to refuse hand feeding at some point in the dementia process. But the choices we make in advance aren't always suited to the people we become. Experts and family members say people with dementia often adapt, becoming content with their lives. People should care about their future sel…

  • The UN Challenge to Guardianship and Surrogate Decision‐Making

    Open Access•Rebecca Dresser•ARTICLE•The Hastings Center Report•2022

    In 2006, the United Nations issued the Convention on the Rights of Persons with Disabilities. The Convention, together with an accompanying commentary, urges governments to abandon laws authorizing guardianship and substitute decision‐making for people with intellectual disabilities and to replace them with supportive decision‐making laws that give all individuals the freedom to make choices reflecting their “will and preferences.” Although criti…

  • The Limited Value of Dementia‐Specific Advance Directives

    Open Access•Rebecca Dresser•ARTICLE•The Hastings Center Report•2021

    Many people are worried about developing dementia, fearing the losses and burdens that accompany the condition. Dementia‐specific advance directives are intended to address dementia's progressive effects, allowing individuals to express their treatment preferences for different stages of the condition. But enthusiasm for dementia‐specific advance directives should be tempered by recognition of the legal, ethical, and practical issues they raise. …

  • Dementia and the Death Penalty

    Open Access•Rebecca Dresser•ARTICLE•The Hastings Center Report•2019

    During its 2018–2019 term, the United States Supreme Court considered the constitutionality of executing a prisoner with dementia. In Madison v. Alabama, the Court ruled that, in certain circumstances, executing a prisoner with dementia violates the Eighth Amendment’s ban on cruel and unusual punishment. Vernon Madison was sentenced to death for killing a police officer in 1985. After many years on Alabama’s death row, he had a series of strokes …

  • Advance Directives and Discrimination against People with Dementia

    Open Access•Rebecca Dresser•ARTICLE•The Hastings Center Report•2018

    In the article “On Avoiding Deep Dementia,” Norman Cantor defends a position that I suspect many readers share. In my years writing and speaking on advance directives and dementia, I've found that most people support one of two positions. They are convinced either that advance choices should control the treatment dementia patients receive or that the welfare of a person with dementia should sometimes take priority over earlier choices. As Cantor …

  • Research Information for Reasonable People

    Open Access•Rebecca Dresser•ARTICLE•The Hastings Center Report•2018

    In 2017, federal officials issued a revised version of the Common Rule, the federal regulations that govern much of the human subject research conducted in the United States. Two provisions on information disclosure have reportedly provoked confusion among researchers and people responsible for research oversight. These provisions incorporate the familiar and foundational legal concept known as the reasonable person standard, applying this to res…

  • Experimentation without Representation

    Open Access•Rebecca Dresser•ARTICLE•IRB Ethics and Human Research•2018

  • On Legalizing Physician‐Assisted Death for Dementia

    Open Access•Rebecca Dresser•ARTICLE•The Hastings Center Report•2017

    Last November, soon after Colorado became the latest state to authorize physician‐assisted suicide, National Public Radio's The Diane Rehm Show devoted a segment to legalization of “physician assistance in dying,” a label that refers to both physician‐assisted suicide and voluntary active euthanasia. Although the segment initially focused on PAD in the context of terminal illness in general, it wasn't long before PAD's potential application to de…

  • Inclusion, Access, and Civility in Public Bioethics

    Open Access•Rebecca Dresser•ARTICLE•The Hastings Center Report•2017

    I could tell many war stories about my experience serving on the President's Council on Bioethics—one of the most controversial national bioethics commissions so far—but I want to focus instead on how the experience influenced my views on bioethics, politics, and the potential contributions of national commissions. The executive order that established the Council directed it to consider policy questions, but it spoke primarily of providing a foru…

  • Silent Partners

    Rebecca Dresser•BOOK•Silent Partners•2016

    Scientists and ethicists often speak of subjects as partners in research, but the reality is quite different. Experienced subjects are rarely appointed to the committees that create guidelines for ethical research or the committees that review individual studies to determine whether they meet ethical and regulatory standards. Yet experienced research subjects can make valuable contributions to research ethics. People who have been in studies know…

  • Embedded Ethics in Developing-Country Research

    Rebecca Dresser•BOOK•Silent Partners•2016

    This chapter considers subject inclusion in multinational studies. Many studies are initiated and financed by wealthy countries but are conducted in low-income countries. Community engagement and participatory research have a long history in developing-country research. Over the years, there has been impressive progress in including experienced subjects and other community members in research activities and in integrating research staff into comm…

  • Participants as Partners in Genetic Research: Human Subjects and Research Ethics

    Rebecca Dresser•BOOK•Silent Partners•2016

    This chapter focuses on subject-centered developments in genetic research. Modern genetic research requires scientists to collect, store, and study DNA samples and health information from thousands of people. In the past, researchers have been allowed to use DNA samples and information without consent. Researchers have not been required to explain study results to subjects, nor have they been required to compensate people who contribute samples a…

  • Medicare and Advance Planning: The Importance of Context

    Open Access•Rebecca Dresser•ARTICLE•The Hastings Center Report•2016

    In January 2016, a long‐delayed Medicare change took effect. The Medicare program will now reimburse doctors for time they spend talking with patients about end‐of‐life care. This is the move that Sarah Palin and other Affordable Care Act critics said would authorize government “death panels” to decide whether older Americans should live or die. Today virtually no one buys into Palin's death panel rhetoric. But many people do think the Medicare c…

  • “Right to Try” Laws: The Gap between Experts and Advocates

    Open Access•Rebecca Dresser•ARTICLE•The Hastings Center Report•2015

    The year 2014 brought a new development in the bioethics “laboratory of the states.” Five states adopted “right to try” laws intended to promote terminally ill patients' access to investigational drugs. Many more state legislatures are now considering such laws. The campaign for right to try laws is the latest move in an ongoing effort to give seriously ill patients access to drugs whose safety and effectiveness remain largely unknown. Although s…

  • Toward a Humane Death with Dementia

    Open Access•Rebecca Dresser•ARTICLE•The Hastings Center Report•2014

    In this issue, Paul Menzel and M. Colette Chandler‐Cramer propose a novel advance directive. Besides giving competent people the opportunity to refuse future life‐prolonging medical interventions, they say, advance directives should give people the opportunity to refuse ordinary food and water if they later experience severe dementia . This proposal is both appealing and unsettling. It is appealing because it offers some relief to people seeking …

  • Drugs and the Death Penalty

    Open Access•Rebecca Dresser•ARTICLE•The Hastings Center Report•2014

    In October 2013, Missouri officials abandoned a plan to execute a convicted murderer using a novel method—an injection of propofol. The name of this drug became a household word after propofol played a role in singer Michael Jackson's death, but this has been a popular therapeutic drug for many years. Clinicians use it in intensive care, surgery, and common procedures like colonoscopy. After deciding to halt the execution, Missouri governor Jay N…

  • Drug Compounding, Drug Safety, and the First Amendment

    Open Access•Rebecca Dresser•ARTICLE•The Hastings Center Report•2013

    In September 2012, news broke of a developing drug disaster in the United States. Health authorities had linked a fungal meningitis outbreak to a contaminated steroid made by a company called the New England Compounding Center. The contaminated steroid was a compounded drug that had not been approved by the Food and Drug Administration, differing from three others that had been approved in that it lacked preservatives present in those agents. Fac…

  • A Status Elevation for Great Apes

    Open Access•Rebecca Dresser•ARTICLE•The Hastings Center Report•2012

  • The Varieties of Consent

    Open Access•Rebecca Dresser•ARTICLE•The Hastings Center Report•2011

  • Bioethics and Cancer: When the Professional Becomes Personal

    Open Access•Rebecca Dresser•ARTICLE•The Hastings Center Report•2011

Next

No prominent works on this page.

  • "On Weinstein's "Patient Attitudes toward Mental Hospitalization: A Review of Quantitative Research

    Marilyn J Essex, Marilyn Essex et al.•ARTICLE•Journal of Health and Social…•1980

    Marilyn Essex, Sue Estroff, Steven Kane, Sara McLanahan, Jim Robbins, Rebecca Dresser, Ronald Diamond, On Weinstein's "Patient Attitudes toward Mental Hospitalization: A Review of Quantitative Research", Journal of Health and Social Behavior, Vol. 21, No. 4 (Dec., 1980), pp. 393-396

  • Deception Research and the HHS Final Regulations

    Rebecca Dresser, Rebecca S Dresser•ARTICLE•IRB Ethics and Human Research•1981

  • Case Studies: Saying 'No' to Electroshock

    Richard Sherlock, Richard K Sherlock et al.•ARTICLE•The Hastings Center Report•1982

  • Morality, Law and ECT

    Efrem Nulman, Rebecca Dresser•ARTICLE•The Hastings Center Report•1983

  • Bound to Treatment: The Ulysses Contract

    Rebecca Dresser•ARTICLE•The Hastings Center Report•1984

    Several commentators have proposed a novel legal mechanism, the\n"Ulysses contract" or "voluntary commitment contract," to permit mental\npatients with recurrent treatable disorders to consent in advance to treatment\nwhich they might reject at a time when their cognitive abilities are impaired. \nDresser discusses the legal ramifications of precommitment, the implications\nof basing consent on a patient's past rather than current wishes, problem…

  • The DES Disaster and Other Hazards

    Rebecca Dresser, Roberta J Apfel et al.•ARTICLE•The Hastings Center Report•1985

    Book reviewed in this article: To Do No Harm: DES and the Dilemmas of Modern Medicine. By Roberta J. Apfel and Susan M. Fisher

  • Wanted Single, White Male for Medical Research

    Rebecca Dresser•ARTICLE•The Hastings Center Report•1992

    How did white males come to be the prototype of the human research\nsubject? Whether misplaced chivalry or tacit assumption of a human norm, the\nexclusion of women and nonwhite minorities is a glaring moral mistake

  • The Public Context of Private Medical Decisions

    Rebecca Dresser•ARTICLE•The Hastings Center Report•1994

    Normative standards powerfully affect the course of our lives. They guide our everyday behavior--how we drive, how we teach our students, how we respond to strangers and intimates. Our expectations about others rely on these standards as well. We assume the actions of people we encounter will fall within a range of appropriate conduct. So much do we take this for granted that we notice it only in the rare instances when our expectations are in er…

  • The Incompetent Patient on the Slippery Slope

    Rebecca Dresser, P J Whitehouse•ARTICLE•The Hastings Center Report•1994

    Most patients suffering from progressive dementia have thoughts, emotions, perspectives, and perceptions of a world of experience. Decisions about life-sustaining treatment should incorporate a principled approach to evaluating what life is like for these patients

  • Advance Directives Implications for Policy

    Rebecca Dresser•ARTICLE•The Hastings Center Report•1994

    One mark of a maturing discipline is its members' willingness to expose the field's accepted wisdom to scrutiny and challenge. In any applied field, such scrutiny must include consideration of whether accepted theoretical principles are well-suited to real life conditions. We in bioethics are fortunate to have many colleagues eager to explore the practical dimensions of various theoretical viewpoints. One of their most popular subjects has been t…

  • Dworkin on Dementia: Elegant Theory, Questionable Policy

    Rebecca Dresser•ARTICLE•The Hastings Center Report•1995

    When patients have progressive and incurable dementia, should their\nadvance directives always be followed? Contra Dworkin, Dresser argues that\nwhen patients remain able to enjoy and participate in their lives, directives\nto hasten death should sometimes be disregarded

  • Long-Term Contraceptives in the Criminal Justice System

    Rebecca Dresser•ARTICLE•The Hastings Center Report•1995

    Contraceptive Sentencing: A Proposal -- One way to reconcile the\ncompeting concerns about potential abuses and possible benefits of\ncontraceptive sentencing would be to adopt the following principle: whenever\nlong-acting contraceptives are proposed as a probation condition, judges must\nalso present to the defendant at least one nonincarcerative alternative\nsentence. If the defendant was convicted of an offense that would not\nordinarily call…

  • At Law: Still Troubled: In re Martin

    Rebecca Dresser•ARTICLE•The Hastings Center Report•1996

    After many years of discussion and debate, decisions on life-sustaining treatment for incompetent patients continue to pose profound ethical and policy questions. A controversial Michigan Supreme Court decision issued last August highlights four major unresolved issues. First, how specific must a patient's prior remarks be to provide and convincing of the individual's preferences on a current treatment question? Second, should competent persons b…

  • At Law: Giving Scientists Their Due The Imanishi-Kari Decision

    Rebecca Dresser•ARTICLE•The Hastings Center Report•1997

    After ten years of investigation and controversy, the case against Dr. Thereza Imanishi-Kari has finally been resolved. Imanishi-Kari, an immunologist, was accused of scientific misconduct in 1986. After the fifth inquiry into the case, a Department of Health and Human Services (DHHS) appeals panel concluded in June 1996 that the evidence against Imanishi-Kari was insufficient prove that she had intentionally and deliberately fabricated and falsi…

  • At Law: Scientists in the Sunshine

    Rebecca Dresser•ARTICLE•The Hastings Center Report•1997

    Thanks to a recent federal appellate court decision, the National Academy of Sciences (NAS) may soon conducting much of its business in public. In January 1997, the U.S. Court of Appeals for the D.C. Circuit held that the Federal Advisory Committee Act (FACA)[1] applied to one of the academy's committees, based on the court's reading of the statute and a 1989 Supreme Court decision interpreting this legislation. Animal legal Defense Fund, Inc. v.…

  • At Law: Time for New Rules on Human Subjects Research

    Rebecca Dresser•ARTICLE•The Hastings Center Report•1998

    An era of relative contentment with the federal rules on human subjects research appears to have ended. Beginning with the 1995 Final Report of the Advisory Committee on Human Radiation Experiments,[1] a growing array of federal officials and advisory groups have raised concerns about the state of human studies oversight. The latest assessment and the most detailed to date comes from the Department of Health and Human Services Inspector General, …

  • Case Study: An Alert and Incompetent Self The Irrelevance of Advance Directives

    Rebecca Dresser, Alan B Astrow•ARTICLE•The Hastings Center Report•1998

    A seventy-three-year-old woman with a history of emphysema and manic depression was admitted to the hospital with shortness of breath. She was treated with steroids but developed progressive respiratory failure and psychosis. She was intubated and transferred to the intensive care unit where she was found to have a blood clot in her lung. She was treated with a blood-thinning agent and had a major blood episode. She remained confused, presumably …

  • At Law: Setting Priorities for Science Support

    Rebecca Dresser•ARTICLE•The Hastings Center Report•1998

  • The Incompetent Self: Metamorphosis of a Person

    Sarah M Dietz, Sarah-Vaughan Brakman et al.•ARTICLE•The Hastings Center Report•1998

  • The Human Use of Animals: Case Studies in Ethical Choice

    F Barbara Orlans, Tom L Beauchamp et al.•BOOK•The human use of animals•1998

    "The first set of case studies on animal use, this volume offers a thorough, up-to-date exploration of the moral issues related to animal welfare. Its main purpose is to examine how far it is ethically justifiable to harm animals in order to benefit mankind. An excellent introduction provides a framework for the cases and sets the background of philosophical and moral concepts underlying the subject." "The Human Use of Animals will be welcomed by…

  • At Law: Surfing for Studies Clinical Trials on the Internet

    Rebecca Dresser•ARTICLE•The Hastings Center Report•1999

  • At Law: Science in the Courtroom A New Approach

    Rebecca Dresser•ARTICLE•The Hastings Center Report•1999

    Judges, legislators, policymakers and often base decisions concerning health risks on evidence and testimony from scientists, physicians, and other experts. Unfortunately, the quality of this information can be questionable and its implications unclear. How are nonscientists to determine which expert presentations provide the strongest basis for law and policy? The controversy over the safety of silicone gel breast implants exemplifies what can g…

  • At Law: Accountability in Science and Government: Is Access the Answer

    Rebecca Dresser•ARTICLE•The Hastings Center Report•2000

    Last year, scientific and academic organizations were immersed in efforts to minimize the negative impact of a new federal law. The new law increases public access to data produced in federally funded research projects. Supporters portray it as a good reform, but the research community believes the measure is seriously flawed. The Provision and Its Interpretation The controversial legislation instructs the Office of Management and Budget to hold …

  • At Law: Regulating Assisted Reproduction

    Rebecca Dresser•ARTICLE•The Hastings Center Report•2000

    As the twentieth century comes to a close, this country's laissez-faire approach to assisted reproduction is under attack. References to the Wild West of infertility treatment are common. With each high-profile incident --advertisements offering huge sums to Ivy League students providing eggs for infertile couples, the release of new statistics on multiple births to women undergoing infertility treatment, gametes and embryos accidentally or inten…

  • At Law: Procreation and Punishment

    Rebecca Dresser•ARTICLE•The Hastings Center Report•2001

    This article highlights the case of David Oakley convicted in the Wisconsin Supreme Court for intentionally failing to financially support his nine children. Oakley was sentenced by Judge Jon Wilcox to 3 years of imprisonment followed by 5 years of probation during which he was prohibited from having more children unless he could demonstrates the ability to support them and his current children. Wilcox concluded that Oakleys probation was reasona…

Political science (43 works) · Law (40 works) · Psychology (40 works) · Ethics in medical practice (19 works) · Medicine (19 works) · Computer Science (16 works) · Ethics and Legal Issues in Pediatric Healthcare (13 works) · Palliative Care and End-of-Life Issues (12 works) · Sociology (12 works) · Ethics in Clinical Research (10 works)

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