24 found
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  1.  19
    Comprehension and Choice Under the Revised Common Rule: Improving Informed Consent by Offering Reasons Why Some Enroll in Research and Others Do Not.Benjamin S. Wilfond, Seema K. Shah, Kathryn M. Porter & Stephanie A. Kraft - 2017 - American Journal of Bioethics 17 (7):53-55.
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  2.  25
    A Narrative Review of the Empirical Evidence on Public Attitudes on Brain Death and Vital Organ Transplantation: The Need for Better Data to Inform Policy.Seema K. Shah, Kenneth Kasper & Franklin G. Miller - 2015 - Journal of Medical Ethics 41 (4):291-296.
  3.  4
    Reframing Recruitment: Evaluating Framing in Authorization for Research Contact Programs.Candace D. Speight, Charlie Gregor, Yi-An Ko, Stephanie A. Kraft, Andrea R. Mitchell, Nyiramugisha K. Niyibizi, Bradley G. Phillips, Kathryn M. Porter, Seema K. Shah, Jeremy Sugarman, Benjamin S. Wilfond & Neal W. Dickert - forthcoming - AJOB Empirical Bioethics:1-12.
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  4.  47
    What Does the Duty to Warn Require?Seema K. Shah, Sara Chandros Hull, Michael A. Spinner, Benjamin E. Berkman, Lauren A. Sanchez, Ruquyyah Abdul-Karim, Amy P. Hsu, Reginald Claypool & Steven M. Holland - 2013 - American Journal of Bioethics 13 (10):62 - 63.
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  5.  10
    Rethinking Brain Death as a Legal Fiction: Is the Terminology the Problem?Seema K. Shah - 2018 - Hastings Center Report 48 (S4):S49-S52.
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  6.  24
    Examining the Ethics of Clinical Use of Unproven Interventions Outside of Clinical Trials During the Ebola Epidemic.Seema K. Shah, David Wendler & Marion Danis - 2015 - American Journal of Bioethics 15 (4):11-16.
    The recent Ebola outbreak in West Africa began in the spring of 2014 and has since caused the deaths of over 6,000 people. Since there are no approved treatments or prevention modalities specifically targeted at Ebola Virus Disease , debate has focused on whether unproven interventions should be offered to Ebola patients outside of clinical trials. Those engaged in the debate have responded rapidly to a complex and evolving crisis, however, and this debate has not provided much opportunity for in-depth (...)
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  7.  7
    Bridging the Researcher-Participant Gap: A Research Agenda to Build Effective Research Relationships.Stephanie A. Kraft, Devan M. Duenas, Hannah Lewis & Seema K. Shah - 2020 - American Journal of Bioethics 20 (5):31-33.
    Volume 20, Issue 5, June 2020, Page 31-33.
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  8.  8
    The Role of Community Engagement in Addressing Bystander Risks in Research: The Case of a Zika Virus Controlled Human Infection Study.Seema K. Shah, Franklin Miller & Holly Fernandez Lynch - 2020 - Bioethics 34 (9):883-892.
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  9.  8
    Ethics of Controlled Human Infection Studies: Past, Present and Future.Seema K. Shah & Annette Rid - 2020 - Bioethics 34 (8):745-748.
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  10.  3
    Demonstrating ‘Respect for Persons’ in Clinical Research: Findings From Qualitative Interviews with Diverse Genomics Research Participants.Stephanie A. Kraft, Erin Rothwell, Seema K. Shah, Devan M. Duenas, Hannah Lewis, Kristin Muessig, Douglas J. Opel, Katrina A. B. Goddard & Benjamin S. Wilfond - forthcoming - Journal of Medical Ethics:medethics-2020-106440.
    The ethical principle of ‘respect for persons’ in clinical research has traditionally focused on protecting individuals’ autonomy rights, but respect for participants also includes broader, although less well understood, ethical obligations to regard individuals’ rights, needs, interests and feelings. However, there is little empirical evidence about how to effectively convey respect to potential and current participants. To fill this gap, we conducted exploratory, qualitative interviews with participants in a clinical genomics implementation study. We interviewed 40 participants in English or Spanish (...)
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  11.  11
    Substantiating the Social Value Requirement for Research: An Introduction.Annette Rid & Seema K. Shah - 2017 - Bioethics 31 (2):72-76.
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  12.  7
    Informed Consent for Controlled Human Infection Studies in Low‐ and Middle‐Income Countries: Ethical Challenges and Proposed Solutions.Vina Vaswani, Abha Saxena, Seema K. Shah, Ricardo Palacios & Annette Rid - 2020 - Bioethics 34 (8):809-818.
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  13.  27
    Outsourcing Ethical Obligations: Should the Revised Common Rule Address the Responsibilities of Investigators and Sponsors?Seema K. Shah - 2013 - Journal of Law, Medicine and Ethics 41 (2):397-410.
    The Common Rule creates a division of moral labor in research. It implies that investigators and sponsors can outsource their ethical obligations to IRBs and participants, thereby fostering a culture of compliance, rather than one of responsibility. The proposed revisions to the Common Rule are likely to exacerbate this problem. To harness the expressive power of the law, I propose the Common Rule be revised to include the ethical responsibilities of investigators and sponsors.
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  14.  6
    Outsourcing Ethical Obligations: Should the Revised Common Rule Address the Responsibilities of Investigators and Sponsors?Seema K. Shah - 2013 - Journal of Law, Medicine and Ethics 41 (2):397-410.
    Imagine a study in which HIV-infected pregnant women are given antiretroviral treatment to determine how effectively it will prevent HIV transmission during childbirth. Each mother’s involvement in this study ends with the birth of her child, at which time her access to antiretrovirals provided by the study also ceases. At the outset of the study, the investigator and sponsor agree that after the child’s birth, they will refer mothers who require treatment for their HIV to a national program that provides (...)
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  15.  7
    Reexamining the Categorical Exclusion of Pediatric Participants From Controlled Human Infection Trials.Sean C. Murphy, Devan M. Duenas, Thomas L. Richie & Seema K. Shah - 2020 - Bioethics 34 (8):785-796.
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  16.  4
    Should Social Value Obligations Be Local or Global?Rahul Nayak & Seema K. Shah - 2017 - Bioethics 31 (2):116-127.
    According to prominent bioethics scholars and international guidelines, researchers and sponsors have obligations to ensure that the products of their research are reasonably available to research participants and their communities. In other words, the claim is that research is unethical unless it has local social value. In this article, we argue that the existing conception of reasonable availability should be replaced with a social value obligation that extends to the global poor. To the extent the social value requirement has been (...)
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  17.  13
    Towards Identifying an Upper Limit of Risk: A Persistent Area of Controversy in Research Ethics.Erin T. Paquette & Seema K. Shah - 2020 - Perspectives in Biology and Medicine 63 (2):327-345.
    A core tenet of research ethics is that risks assumed by research participants are reasonable, balanced, and minimized in relation to benefit to the individual and to society. It is also generally accepted that people who cannot give their own informed consent ought only to be exposed to low risks in research, unless there is a compensating potential for direct benefit.However, there is no consensus on whether individuals should be able to voluntarily consent to high net risk in research—or, in (...)
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  18.  5
    Improving Care for Suicidal Patients While Protecting Human Subjects: Addressing Ethical Challenges in Mental Health Research Involving Emergency Medical Services Providers.Kathryn M. Porter, Seema K. Shah & Christopher R. DeCou - 2019 - American Journal of Bioethics 19 (10):99-101.
    Volume 19, Issue 10, October 2019, Page 99-101.
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  19.  14
    Advancing Independent Adolescent Consent for Participation in HIV Prevention Research.Seema K. Shah, Susannah M. Allison, Bill G. Kapogiannis, Roberta Black, Liza Dawson & Emily Erbelding - 2018 - Journal of Medical Ethics 44 (7):431-433.
    In many regions around the world, those at highest risk for acquiring HIV are young adults and adolescents. Young men who have sex with men in the USA are the group at greatest risk for HIV acquisition, particularly if they are part of a racial or ethnic minority group.1 Adolescent girls and young women have the highest incidence rates of any demographic subgroup in sub-Saharan Africa.2 To reverse the global AIDS pandemic’s toll on these high-risk groups, it is important to (...)
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  20.  15
    Conflicts Between Regulations and Ethical Principles: Resolving Ambiguity in Favor of the Ethically Preferable Outcome.Seema K. Shah & Kathryn Porter - 2018 - American Journal of Bioethics 18 (4):93-94.
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  21.  22
    How Lethal Injection Reform Constitutes Impermissible Research on Prisoners.Seema K. Shah - manuscript
    This essay exposes how recent attempts at lethal injection reform have involved unethical and illegal research on prisoners. States are varying the doses and types of drugs used, developing methods designed for non-medical professionals to administer medical procedures, and gathering data or making provisions for the gathering of data to learn from executions gone wrong. When individual prisoners are executed under these conditions, states are conducting research on them. Conducting research or experimentation on prisoners in the process of reform is (...)
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  22.  6
    HIV Remission in Neonates: Ethical and Human Rights Considerations.Seema K. Shah & Benjamin S. Wilfond - 2015 - Perspectives in Biology and Medicine 58 (3):341-343.
    A published case report of an infant who inadvertently developed remission of HIV viral expression has prompted research to determine if this observation is reproducible and can offer a potentially novel clinical approach to inducing sustained viral remission of HIV.Typically HIV-infected mothers receive antiretroviral therapy before delivery and infants receive between one and three drugs at “low doses” for prevention. In the case report, the mother delivered before she could receive ART. The infant was placed on a three-drug approach with (...)
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  23.  9
    The Role of Community Engagement in Novel HIV Research in Infants.Seema K. Shah & Benjamin S. Wilfond - 2015 - Perspectives in Biology and Medicine 58 (3):344-347.
    The proposed study would be a single-arm interventional trial in a community where HIV is endemic. The proposed observational design can provide confirmatory data for the initial clinical observation, data that would be necessary before considering whether a randomized controlled trial is appropriate. A previous ethical analysis has argued for conducting such a study in a country with limited resources and with higher HIV prevalence, and to recruit those with the highest risk of transmission. The primary rationale was to address (...)
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  24.  14
    When to Start Paediatric Testing of the Adult HIV Cure Research Agenda?Seema K. Shah - 2017 - Journal of Medical Ethics 43 (2):82-86.
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