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How Should Physicians Help Patients Understand Unknowns of Nanoparticle-Based Medicines?
Nancy M P King1, Christine E Bishop2
1A professor in the Department of Social Sciences and Health Policy as well as in the Institute for Regenerative Medicine at the Wake Forest School of Medicine in Winston-Salem, North Carolina, and the co-director of the Center for Bioethics, Health, and Society and the graduate program in bioethics at Wake Forest University in Winston-Salem, North Carolina.
Abstract:
When a patient wants to enroll in a clinical trial to gain early access to an apparently promising but unproven intervention, her physician should clarify differences between participating in research and receiving treatment to help her avoid therapeutic misconception, make a thoughtful decision, and consider relevant clinical and ethical details. These include a patient's disease and treatment experiences, needs, interests, values, the design and phase of the trial, and the nature of the intervention being studied. When an unproven intervention is a nanodrug, a physician's role is especially difficult, because though nanomedicine might offer real benefits, it can also pose unexpected or even unprecedented harms. Thus, a physician should help a patient explore possible outcomes while promoting realism, countering hype, and preserving hope.
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