Is the conceptualisation of trust in NHS’ code of conduct for artificial intelligence problematic?

By Soogeun S Lee. In 2018, the UK government published a Code of Conduct, hereafter the Code, for using artificial intelligence (AI) technologies in the NHS. The Code contains ten principles that outline a gold-standard of ethical conduct of AI developers and implementers within the NHS. Considering the importance of trust in traditional medical practice, […]

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Who should get to choose their surrogates?

By Mark Christopher Navin, Jason Adam Wasserman, Devan Stahl, and Tom Tomlinson, Clinical ethics consultants regularly witness something like the following progression: A patient is determined to lack decision-making capacity (DMC). In the absence of an Advanced Care Planning document that names a surrogate decision maker (e.g. a Durable Power of Attorney for Health Care), […]

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Discrimination on the basis of vaccination status (is inherently wrong)

By Michael Kowalik. The worldwide spread of SARS-CoV-2 has re-invigorated the debate about the ethical permissibility of vaccine mandates and immunity certification. Public attitudes towards this complex issue are nevertheless dominated by fear, half-truths and ungrounded value-judgements, limiting the scope of rational deliberation in favour of ideological partisanship. My paper, ‘Ethics of Vaccine Refusal’, is […]

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Self-experimentation with vaccines

By Jonathan Pugh, Dominic Wilkinson and Julian Savulescu. A group of citizen scientists has launched a non-profit, non-commercial organisation named ‘RaDVaC’, which aims to rapidly develop, produce, and self-administer an intranasally delivered COVID-19 vaccine. As an open source project, a white paper detailing RaDVaC’s vaccine rationale, design, materials, protocols, and testing is freely available online. […]

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In defence of social egg freezing

By Thomas Søbirk Petersen. In my latest JME article I defend social egg-freezing. Social egg freezing (or ‘non-medical egg freezing’) is, roughly speaking, the process whereby healthy women freeze their eggs to preserve their future fertility for reasons that have nothing directly to do with medical issues. However, some feminist bioethicists worry that women’s legal […]

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How to ethically conduct research with Black populations at the intersection of COVID-19 and Black lives matter

By Natasha Crooks, Geri Donenberg, Alicia Matthews. For months now, we have been asking ourselves if it is appropriate to engage populations in research who are disproportionately impacted by COVID-19 and continuously being murdered by institutions (i.e., government, police, hospitals) that are supposed to be protecting them. The current societal context suggests Black lives are […]

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Who’s responsible for informing relatives about genetic risk?

By Kalle Grill and Anna Rosén. It is established practice in many countries that healthcare professionals encourage patients to share relevant risk information with genetic relatives. We mostly endorse this practice but question a normative assumption that typically underpins it. Both practitioners and academics in the field are in general agreement that: It is desirable […]

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Dialyzing the discourse: a response to Rohrig and Manheim

By Hayden P. Nix and Charles Weijer In a recent blog post, we sought to answer the narrow question: is altruistic kidney donation sufficiently analogous to participation in a SARS-CoV-2 challenge study to justify the risks of SARS-CoV-2 challenge studies? We argued that three morally relevant differences (the risk of adverse effects, the availability of […]

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