The way in which the results of community-based participatory research are presented is extremely important, both for reasons of justice and cultural sensitivity and to ensure that they not unnecessarily badly received.
By failing to follow informed consent protocols and regulations, a researcher engaging in CBPR may inflict permanent harm on the participating community and chill future research among disadvantaged populations.
The differences between CBPR and traditional research have been enumerated, but how to overcome them is still up for discussion, collaboration with community members is advocated, and examples are given.
A hospital shares responsibility for system failures that result in harm to a patient in its care. A fully functional computerized physician order-entry (CPOE) system should be able to prevent “copy and paste” medication errors from harming patients.
Laura N. Gitlin, PhD and Nancy A. Hodgson, PhD, RN
As a matter of medical ethics, physicians must address the health care needs of and be advocates for family caregivers of their patients with dementia.
AMA J Ethics. 2016; 18(12):1171-1181. doi:
10.1001/journalofethics.2016.18.12.ecas1-1612.
Medical specialty boards improve the quality and safety of health care, but they can overreach, and their board members express disapproval of board action by petition and through legal action.
AMA J Ethics. 2015; 17(3):193-198. doi:
10.1001/journalofethics.2015.17.3.spec1-1503.