This article argues that inequitable access to interventions capable of dramatically extending human lifespans would undermine individual and collective upkeep of civic virtue.

This commentary offers best-practice recommendations about informed consent processes and patient-clinician relationship formation.

Since health care organizations’ widespread adoption of electronic health records, clinicians’ notes about patients’ care have become longer and more cumbersome.

Electronic health records are now critical in day-to-day health care operations.

This commentary on a case canvasses federal and organizational rules applicable to health recordkeeping and “open notes.”

Electronic health records can be hard for people with a range of disabilities to access, which demands ethical and legal attention.

Electronic health records offer immediate access to a broad swath of health information and data that patients are often not prepared to interpret or review.

Announcement that the AMA Journal of Ethics will cease publishing new content after December 2025.

Electronic health records have fundamentally changed how health care is given and received, and not always for the better.

The UDN seeks to advance diagnostic science and to facilitate accurate diagnoses of individual patient-participants’ “medical mysteries.”