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

Long-acting injectables powerfully augment HIV care, but broad acceptance and uptake could be compromised by what we know about experiences with antipsychotics.

Fostering transgender patients’ sense of agency should be a clinical and ethical priority.

This charcoal gesture drawing, inspired by a mid-adolescent nonbinary patient, investigates a caregiver’s and patient’s journey from despair to hope.

Priorities far beyond generating morbidity or mortality data are needed to improve patients’ experiences, innovate metrics, and advance surgical palliation as a field.

Researchers and scholars should co-develop research with Indigenous peoples to ensure respect for culture, language, and ways of knowing.

Patients leaving against medical advice draw attention to intersections of tort law, federal and state regulations, and clinical ethics.

The best interests of a pregnant psychotic patient can be served by determining her decision making capacity and using surrogate decision making if needed.

Nudges can improve patient outcomes, but decisions need to be made about where they fit in the flow of health service delivery.