Lack of ethical, legal, and clinical consensus about best practice sometimes combines with a poor clinical evidence base.

For many physicians, lack of understanding about brain death leads to confusion and muddles interactions with patients’ loved ones at the end of life.

Since 1995, the American Academy of Neurology has provided guidelines for brain death determination, but nationwide adherence to these guidelines has been incomplete.

Lobbying, maintaining diagnostic skill, participating in national societies, and contributing to robust discourse can influence practice and policy.

Criteria in statutes and tests used to diagnose brain death don’t always jibe, and this can undermine public trust in death pronouncements.

Dr Ariane Lewis discusses how we can navigate uncertainty and ambiguity about brain death by understanding clinical criteria for brain death determination and how our approaches to death are culturally and socially situated.

Recent popular interest in Henrietta Lacks has prompted interest in better engaging AA nurses and communities.

Amendments to the Common Rule and Health Insurance Portability and Accountability Act (HIPAA) raise questions about broad consent and sale of health data.

More cesarean deliveries among Black and Hispanic women in the United States has long demonstrated racial inequity in obstetrical care.

Patients writing daily journal briefs about work-related activities and pain can help clinicians help them.