Black and Hispanic/Latinx adults report experiencing discrimination when seeking health care at higher rates than white adults, which raises the question: How might these reported experiences adversely affect health care? More
This qualitative study examines both negative and positive attitudes expressed by physicians about patients in electronic medical records. More
The latest Covid-19 surge felt extra personal as more and more of my patients' names were appearing in my email's 'postmortem' folder. More
Many people with intellectual and developmental disabilities receive substandard and even harmful healthcare. Tragically, they die preventable, premature deaths, including from extraordinarily high rates of suicide and accidents. More
Covid-19 made virtual medicine a popular investment. But patients should beware. More
Informed consent is fundamental to the ethical and legal doctrines respecting research participants’ voluntary participation in clinical research, enshrined in such documents as the 1947 Nuremberg Code; reaffirmed in the 1964 Declaration of Helsinki, revised in 1975, and the 1978 Belmont Report; and codified in the United States in the 1981 Common Rule, revised in 2018 and implemented in 2019. More
As the pandemic brings long-standing health disparities into sharper view, community health workers are being asked to help the public health response. More
As the nation copes with Covid-19, it sorely needs a plan to allow family visits to and communication with hospitalized loved ones. More
A nudge based on artificial intelligence helps cancer doctors start conversations with their dying patients about their end-of-life wishes. More
Perspective from The New England Journal of Medicine — #WhiteCoatsForBlackLives — Addressing Physicians’ Complicity in Criminalizing Communities More