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

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

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

This comic prompts viewers and readers to consider conditions under which sharing raw clinical data with patients promotes better care.

Brett Feldman joins Ethics Talk to discuss the evolution of electronic health records in street health care practice.

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

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.

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

Coded data from patients’ health records are used in epidemiological research about incidence or prevalence of disease, drug safety monitoring, or long-term cohort tracking.

Dr Shelli L. Feder joins Ethics Talk to discuss her article, coauthored with Dr Kathleen M. Akgün: “Whom Should We Regard as Responsible for Health Record Inaccuracies That Hinder Population-Based Fact Finding?”