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Seniors covered by BlueCross BlueShield of Tennessee's Medicare Advantage plan are guided through the end-of-life (EOL) processes and are being empowered with the education, resources, and assistance they need to make their own decisions about what kind of care they want to receive at the end of life.
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Can the informed consent process actually provide too much information? That's the contention of HIV researcher Susan Allen, MD, MPH, DTM&H, director of the Rwanda Zambia HIV Research Group, based at Emory University in Atlanta, who points to a recent study she tried to conduct in Zambia of participants' knowledge about contraceptive options.
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The new edition of a widely used human subjects protection curriculum has an increased emphasis on community engagement and the importance of ongoing informed consent, says one of its developers.
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Acute stroke trials pose unique ethical challenges to researchers. Stroke interventions are extremely time-sensitive, meaning that decisions about treatment and research participation often must be made quickly.
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The blurring lines between personal and professional relationships between physicians and patients have raised multiple ethical and legal concerns for the healthcare field.
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