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Ethical and Social Considerations for Increasing Use of DTC Neurotechnologies

机译:用于增加DTC神经技术的伦理和社会考虑因素

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In her article, Kreitmair (2019) identifies eight ethical dimensions to address with respect to direct-to-consumer (DTC) neurotechnologies to ensure they contribute to human flourishing. Here we expand on three important points for further reflection. USE OF DTC NEUROTECHNOLOGIES FOR SELF-TREATMENT: First, Kreitmair seems to suggest that DTC neurotechnologies are not classified as medical devices under Food and Drug Administration (FDA) law. The author supports this claim, in part, by stating, "DTC neurotechnologies are ones that consumers decide whether to buy, not ones that are prescribed to them or monitored by physicians" (155). However, assuming a DTC neurotechnology can achieve outcomes like decreasing stress or improving cognition, it would presumably do so by affecting brain function and, potentially, brain structure. Given that the FDA's definition (FDA 2018) of a medical device includes any device "intended to affect the structure or any function of the body of man or other animals and which does not achieve its ... purpose through chemical action," such a device would be considered "medical" even if not prescribed by a clinician.
机译:在她的文章中,KreitMair(2019)确定了八个道德尺寸,以解决直接消费者(DTC)神经技术,以确保它们有助于人类繁荣。在这里,我们扩展了三个重要点以获得进一步的反思。使用DTC神经技术进行自我治疗:首先,KreitMair似乎表明DTC神经技术在食品和药物管理局(FDA)法下没有被归类为医疗设备。提交人支持这一索赔,部分通过陈述,“DTC神经技术是消费者决定购买的,而不是由医生监督的人决定购买,而不是由医生监督的人(155)。然而,假设DTC神经技术能够达到降低压力或改善认知的结果,这将通过影响脑功能和潜在的脑结构来实现这么做。鉴于医疗装置的FDA定义(FDA 2018)包括任何设备“旨在影响人体或其他动物身体的结构或任何功能,并且通过化学作用,不会达到其...目的”这样的即使没有由临床医生规定的设备也将被视为“医疗”。

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