What is the Origin of Patient Data Ownership?

This principle has gained prominence with the advent of electronic health records and large-scale data aggregation, rooted in established patient privacy rights and legislation like the Health Insurance Portability and Accountability Act (HIPAA). It is a response to the increasing value and transferability of health data in the digital age.

What is the Mechanism of Patient Data Ownership?

Operationalizing data ownership requires secure, interoperable digital platforms that provide patients with direct, unmediated access to their complete clinical record. Furthermore, it relies on regulatory frameworks that mandate explicit, informed consent for any secondary use of the data, ensuring that the patient retains ultimate control over who accesses their sensitive health information and for what purpose.

Patient Data Ownership

Meaning

Patient Data Ownership is the ethical and legal principle affirming that an individual possesses the exclusive right to control, access, modify, and determine the use and sharing of all their personal health information. This encompasses a broad spectrum of clinical data, including laboratory test results, physician notes, diagnostic images, and genomic sequencing information. This concept is fundamental to patient autonomy and is a cornerstone of modern digital health governance.