A national data infrastructure for patient-centered outcomes research

Author:

Dymek Christine1,Gingold Janelle1,Shanbhag Avinash2,Fridsma Doug23,Yong Pierre L1

Affiliation:

1. Office of the Assistant Secretary for Planning & Evaluation, US Department of Health & Human Services, 200 Independence Ave SW, Washington, DC 20201, USA

2. Office of the National Coordinator for Health Information Technology, US Department of Health & Human Services, 200 Independence Ave SW, Washington, DC 20201, USA

3. AMIA, 4720 Montgomery Lane, Suite 500, Bethesda, MD 20814, USA, previously Office of the National Coordinator for Health Information Technology

Abstract

Concerted efforts are underway to improve healthcare decision-making through patient-centered outcomes research. These efforts are supported by the Patient-Centered Outcomes Research Trust Fund, which was established within the Patient Protection and Affordable Care Act. This article focuses on describing national data infrastructure efforts that support patient-centered outcomes research. A national data infrastructure has the potential to decrease research costs and improve research throughput. We describe early and current efforts that demonstrated this potential, how the national effort is utilizing the lessons learned from these predecessor efforts and remaining challenges.

Publisher

Future Medicine Ltd

Subject

Health Policy

Reference31 articles.

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3. Role of practice-based research networks in comparative effectiveness research

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