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  1. Avoidance of nocebo effects by coincident naming of treatment benefits during the medical interview for informed consent—Evidence from dynamometry.Nina Zech, Matthias Schrödinger & Ernil Hansen - 2022 - Frontiers in Psychology 13.
    IntroductionIn the context of giving risk information for obtaining informed consent, it is not easy to comply with the ethical principle of “primum nihil nocere.” Carelessness, ignorance of nocebo effects and a misunderstood striving for legal certainty can lead doctors to comprehensive and brutal risk information. It is known that talking about risks and side effects can even trigger those and result in distress and nonadherence to medication or therapy.MethodsRecently, we have reported on significant clinically relevant effects of verbal and (...)
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  • Patient attitudes towards side effect information: An important foundation for the ethical discussion of the nocebo effect of informed consent.Mette Sieg & Lene Vase - forthcoming - Clinical Ethics:147775092210773.
    A growing body of evidence suggests that the informed consent process, in which patients are warned about potential side effects of a treatment, can trigger a nocebo effect where expectations about side effects increase side effect occurrence. This has sparked an ethical debate about how much information patients ought to receive before a treatment while trying to balance the moral principles of patient autonomy and nonmaleficence. In keeping with the principle of patient autonomy, the opinion of patients themselves in relation (...)
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  • Nonmaleficence, Nondisclosure, and Nocebo: Response to Open Peer Commentaries.John T. Fortunato, Jason Adam Wasserman & Daniel Londyn Menkes - 2017 - American Journal of Bioethics 17 (7):4-5.
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