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  1. Rescuing Informed Consent: How the new “Key Information” and “Reasonable Person” Provisions in the Revised U.S. Common Rule open the door to long Overdue Informed Consent Disclosure Improvements and why we need to walk Through that door.Mark Yarborough - 2020 - Science and Engineering Ethics 26 (3):1423-1443.
    There is substantial published evidence showing that countless people enroll each year in ethically deficient clinical trials. Many of the trials are problematic because the quality of the science used to justify their launch may not be sufficiently vetted while many other trials may lack requisite social value. This poses the question: why do people volunteer for them? The answer resides in large part in the fact that informed consent practices have historically masked, rather than disclosed, the information that would (...)
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  • Faith, Hope And (No) Clarity.Barry Lyons - 2016 - Journal of Medical Ethics 42 (8):520-521.
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  • Treatability Statements in Serious Illness: The Gap Between What is Said and What is Heard.Jason N. Batten, Bonnie O. Wong, William F. Hanks & David C. Magnus - 2019 - Cambridge Quarterly of Healthcare Ethics 28 (3):394-404.
    :Empirical work has shown that patients and physicians have markedly divergent understandings of treatability statements in the context of serious illness. Patients often understand treatability statements as conveying good news for prognosis and quality of life. In contrast, physicians often do not intend treatability statements to convey improvement in prognosis or quality of life, but merely that a treatment is available. Similarly, patients often understand treatability statements as conveying encouragement to hope and pursue further treatment, though this may not be (...)
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