Doing some policy research? Need some background materials? You've come to the right place.
Note: Documents in the library are organized by issue area — and PDFs require Adobe Reader (free download/upgrade available).
Health information technology (health IT) can enable the access, engagement and partnership that individuals and families need for better care coordination and better health. In 2016, the Consumer Partnership for eHealth (CPeH) successfully integrated person-centered health IT into new national initiatives designed to transform the way care is delivered and shift the emphasis from quantity of health services to quality and value.
Under the Medicare Access and CHIP Reauthorization Act of 2015 (MACRA), the new Quality Payment Program (QPP) will bring the biggest change in Medicare reimbursement in decades. It offers a critical opportunity to drive health system transformation that results in authentic patient- and family-centered care.
This fact sheet outlines how health information technology supports patients and family caregivers (revised version).
The Consumer Partnership for eHealth comments on ONC's Request for Information regarding Assessing Interoperability for MACRA, or the Medicare Access and CHIP Reauthorization Act.
This webinar presentation reviews health information technology in the context of the Medicare Access and CHIP Reauthorization Act.
Hearing on Opportunities and Challenges in Advancing Health Information Technology, U.S. House of Representatives Committee on Oversight and Government Reform, Subcommittee on Information Technology and Subcommittee on Health Care, Benefits, and Administrative Rules
The National Partnership for Women & Families shares the principle that to achieve open, connected health care for our communities, we all have the responsibility to take action. To further these goals, we commit to the following principles to advance interoperability among health information systems enabling appropriate and secure movement of data, which are foundational to the success of delivery system reform.
The Consumer Partnership for eHealth (CPeH) and the undersigned 24 organizations and individuals submit these formal comments on the finalized requirements for Stage 2 modifications and Stage 3 of the Meaningful Use program.
The National Partnership for Women & Families appreciates the opportunity to offer comments on the proposed rule on Medicaid and Children's Health Insurance Program (CHIP) Programs; Medicaid Managed Care, CHIP Delivered in Managed Care, Medicaid and CHIP Comprehensive Quality Strategies, and Revisions Related to Third Party Liability.
When the Centers for Medicare & Medicaid Services proposed a significant retreat in key patient-engagement provisions of the Meaningful Use EHR Incentive Program on April 10, the National Partnership for Women & Families informed people across the United States of the proposed amendments. Over 5,000 people, from every state and territory, sent letters urging CMS not to reverse these requirements.
Testimony of Christine Bechtel, Advisor, National Partnership for Women & Families. Submitted to the U.S. Senate Health, Education, Labor & Pensions Committee Hearing on Health Information Exchange - A Path Toward Improving Quality and Value for Patients
The Consumer Partnership for eHealth's (CPeH) comments on the proposed 2015 Edition Health Information Technology Criteria delivered to Dr. Karen DeSalvo, National Coordinator for Health Information Technology, U.S. Department of Health and Human Services.
The Consumer Partnership for e-Health's (CPeH) comments on the proposed requirements for Stage 3 of Meaningful Use delivered to Andy Slavitt, Acting Administrator, Centers for Medicare & Medicaid Services, U.S. Department of Health and Human Services.
The Consumer Partnership for eHealth's (CPeH) Comments on the draft Shared Nationwide Interoperability Roadmap delivered to Dr. Karen DeSalvo, National Coordinator for Health Information Technology, U.S. Department of Health and Human Services.
Nearly every stakeholder recognizes that greater patient centeredness and patient engagement are essential to the “Triple Aim” of federal health reform: improving care, improving health and reducing cost.
A growing number of consumers are embracing electronic health records (EHRs), and the significant boost in online access to health information is increasing patient engagement in their care. In the last year, more than four in five patients with online access to their health records (86 percent) used their online records at least once – and more than half (55 percent) used them three or more times a year. Those are among the findings from a study released by the National Partnership for Women & Families.
Presentation: Mark Savage, Director of Health IT Policy and Programs, National Partnership, Audio Press Briefing, December 10, 2014
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