The study of health law tends to focus on industry and public policy concerns, such as quality, cost, and access. Typically neglected is the core experience of patients being ill and seeking care. Our belief that law relating to patient care should better take into account what it means to be a patient led us to convene a group of ethics and legal scholars for a two-day conference in April 2010 to consider what a more patient-centered approach to health law and ethics would mean. This report identifies the areas in which participating scholars appeared to reach some consensus on this subject over the course of the conference, as well as issues about which there was disagreement or hesitation, and questions for future debate. The final version will be published in a forthcoming issue of the Wake Forest Law Review, along with other essays by conference participants relating to patient-centered health law.

Citation
Mark A. Hall & Lois Shepherd, Patient-Centered Law and Ethics, 45 Wake Forest Law Review, 1427–1452 (2010).