Abstract
The term placebo is widely used to indicate a perceived health-related improvement following administration of a treatment lacking a therapeutically acknowledged active component. For a long time placebo response meaning “I shall please” or “I shall be acceptable or pleasing” was something of a mystery, at best linked to but not altogether explicable within the clinical encounter. Attempts at explanation tended to be psychological, based on the probability that response to a placebo was a consequence of the patient’s own expectation of benefit, confidence, and trust in the practitioner or unawareness of the “dummy” nature of treatment. What was lacking was a scientific theory and detailed understanding of the underlying psychology, and more importantly knowledge of just how a patient’s thoughts and beliefs might result in biochemical and cellular changes which mimic some of those caused by medicinal drugs. Recent research has begun to unravel important aspects of the phenomenon.
The ethical implications of placebo use either in clinical practice or as a baseline comparator in clinical trials turn on important aspects of duty of care toward patients, autonomy, informed consent, and trust.
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Further Readings
Enck, P., et al. (2013). The placebo response in medicine: Minimize, maximize or personalize? Nature Reviews. Drug Discovery, 12(3), 191–204.
Miller, F., & Kaptchuk, T. (2008). The power of context: Reconceptualizing the placebo effect. Journal of the Royal Society of Medicine, 101(5), 222–225.
Miller, F., et al. (Eds.). (2013). The placebo: A reader. Baltimore: Johns Hopkins University Press.
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Badcott, D. (2015). Placebo. In: ten Have, H. (eds) Encyclopedia of Global Bioethics. Springer, Cham. https://doi.org/10.1007/978-3-319-05544-2_339-1
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DOI: https://doi.org/10.1007/978-3-319-05544-2_339-1
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