Digital Policies for Patient Consents: The Thorny (and General) Technical Challenges

Abstract

To protect patient privacy, release of patient records must be in accordance with patient consents to share clinical data, either explicitly or from a government default. Explicit consents allow a patient to customize the balance between confidentiality versus sharing. However, the system of request-specific paper consent forms already acts as sand in the gears of data exchange[GSK], and will become far more bothersome as data sharing becomes nationwide, and progress on electronic health records gradually automates data extraction and transmission. Our project is architecting and prototyping key elements of a system to elicit and manage consents. All of a patients consent rules are to be managed in one place, editable over the web, and accessible by authorized record holders; the user interface will help the patient manage their consent rules. Then when an information request is received, it will put the appropriate set of rules on the record holders screen, in human-readable and automation-friendly forms.

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Document Details

Document Type
Technical Report
Publication Date
Jan 01, 2011
Accession Number
AD1108605

Entities

People

  • Arnon Rosenthal

Organizations

  • MITRE Corporation

Tags

DTIC Thesaurus Topics

  • Accuracy
  • Automation
  • Computer Access Control
  • Corporations
  • Drug Therapy
  • Extraction
  • Filters
  • Filtration
  • Governments
  • Guarantees
  • Health
  • Health Services
  • Infectious Diseases
  • Information Exchange
  • Information Systems
  • Measurement
  • Medical Personnel
  • Mental Health
  • Multiple Access
  • Natural Languages
  • Physicians
  • Product Prototyping
  • Public Health
  • Standards
  • Therapy
  • User Interface
  • Vocabulary

Readers

  • Database Systems and Applications
  • Government and Public Administration Law.
  • Women's Health and Cancer Risk Research: African American Women and Pregnancy Outcomes.

Technology Areas

  • Microelectronics