The 2021 Office of the Secretary Patient-Centered Outcomes Research Trust Fund (OS PCORTF) Annual Report Executive Summary and Full Report highlights the accomplishments of 34 multi-agency projects to build data capacity and support the mission of HHS to advance science and improve knowledge about the comparative effectiveness of health care interventions.
Division of Health Care Quality and Outcomes (HQO)
The Division of Health Care Quality and Outcomes (HQO) is responsible for analysis, coordination, research, and evaluation of policies related to health care quality and outcomes. HQO’s responsibilities include long-range planning, data development and analysis, program oversight, analysis of regulations and legislation, review and conduct of research and evaluation activities, and information dissemination. Relevant topic areas include:
- Quality measures;
- Value-based purchasing;
- Public reporting; and
- Comparative effectiveness research (CER) and patient-centered outcomes research and associated data infrastructure and information technology.
Reports
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Scoping Review Report: Data Elements for Research on the Role of Social Determinants of Health in Coronavirus Disease 2019 Infection and Outcomes in the U.S.
The rapid emergence of the novel Coronavirus Disease 2019 (COVID-19) pandemic spurred national concerns about the social determinants of health (SDOH) as risk factors for infection and their potential to negatively impact health outcomes.
ASPE Issue Brief
National Survey Trends in Telehealth Use in 2021: Disparities in Utilization and Audio vs. Video Services
Telehealth services expanded rapidly during the COVID-19 pandemic. Using data from the Census Bureau’s Household Pulse Survey (HPS) in 2021, this Issue Brief analyzes national trends in telehealth utilization across all payers and examines how use of video-enabled vs. audio-only telehealth services differ across patient populations.
Report
Considerations for Building Federal Data Capacity for Patient-Centered Outcomes Research Related to Intellectual and Developmental Disabilities
This report describes the current state of Patient-Centered Outcomes Research (PCOR) data infrastructure resources related to Intellectual and Developmental Disabilities (ID/DD), highlights data issues in the ID/DD research landscape that require more research, and identifies opportunities to enhance data infrastructure to improve PCOR for ID/DD.
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Report
Federal Data for Conducting Patient-Centered Outcomes Research on Economic Outcomes
The objective of this report is to assess the current landscape of federal and federally funded health care data relevant to PCOR and economic analysis to identify gaps for data stewards, researchers, and future collection efforts.
Report
Research Data Networks and Patient-Centered Outcomes Research Trends and Opportunities: Scan and Interviews with Key Informants
This report focuses on research networks that engage in or support research on patient-centered outcomes. The report was produced as part of the strategic planning process for the Office of the Secretary Patient-Centered Outcomes Research Trust Fund portfolio.
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