Name:
Medical Effective Altruism, ...
Embargo:
2025-03-11
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167.5Kb
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PDF
Description:
Final Accepted Manuscript
Author
Quigley, TravisAffiliation
Department of Philosophy, University of ArizonaIssue Date
2024-03-11
Metadata
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WileyCitation
Quigley, T. (2024). Why restrict medical effective altruism? Bioethics, 38, 452–459. https://doi.org/10.1111/bioe.13279Journal
BioethicsRights
© 2024 John Wiley & Sons Ltd.Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
In a challenge trial, research subjects are purposefully exposed to some pathogen in a controlled setting, in order to test the efficacy of a vaccine or other experimental treatment. This is an example of medical effective altruism (MEA), where individuals volunteer to risk harms for the public good. Many bioethicists rejected challenge trials in the context of Covid-19 vaccine research on ethical grounds. After considering various grounds of this objection, I conclude that the crucial question is how much harm research subjects can permissibly risk. But we lack a satisfying way of making this judgment that does not appeal simply to the intuitions of doctors or bioethicists. I consider one recent and structurally plausible approach to critically evaluating the harm question. Alex London defends a social consistency test for research risks: we should compare the risks undertaken by research subjects to relevantly similar risks which are accepted in other spheres of society. I argue there is no good reason not to consider volunteer military service as a relevant social comparison. This implies there is essentially no cap on acceptable risks on the social consistency rationale. In short, if soldiers can be heroes, why can't research volunteers?.Note
12 month embargo; 11 March 2024ISSN
0269-9702EISSN
1467-8519Version
Final accepted manuscriptae974a485f413a2113503eed53cd6c53
10.1111/bioe.13279