The Patient-Centered Coordinated Care Program, an initiative of the New York City-based Commonwealth Fund is accepting Letters of Inquiry (LOI) for projects designed to improve the quality of primary healthcare in the U.S.
The program makes grants to:
- Collect and dissemination information on patients and their healthcare experiences and provide information on physician office systems and practices that are associated with high-quality patient-centered care
- Assist primary care practices with the adoption of practices, models, and tools to help practices become more patient-centered with the ability to coordinate more closely with hospitals, specialists, and other public and private healthcare providers in their communities
- Develop policies to encourage patient and family-centered care in medical homes
The Commonwealth Fund is going to support projects in several areas to make medical homes more successful and to enable resource sharing. One of the future directions is to integrate the medical home with the medical neighborhood. The plan is going to support efforts to understand how medical homes can integrate and partner with the other providers in their community. This can include integrating with specialists, hospitals, and mental healthcare providers in both safety-net and commercial settings.
For more information, go to www.commonwealthfund.org.
Each year, telemedicine provides secure video links to help thousands of Virginians access specialty care not available in their home communities. The University of Virginia (UVA) network serves more than 85 telemedicine locations enabling thousands of Virginians each year to access UVA physicians in more than 40 specialties without traveling to Charlottesville where the university is located.
To make it easier for residents of Southside Virginia and other rural localities to receive specialty care not readily available locally, a new state grant for $270,000 has been awarded to help patients and healthcare workers access specialists through telemedicine. (more…)
The Department of Vermont Health Access (DVHA) the state’s largest insurer in terms of dollars spent and the second largest in terms of covered lives, manages Medicaid, SCHIP, and other publicly funded health coverage programs in the state. In addition, DVHA is responsible for Vermont’s Blueprint for Health, for HIT strategic planning, coordination, oversight, and to implement the health benefit exchange. (more…)
At the recent HIMSS Annual Conference held March 3-7 in New Orleans, researchers from the Regenstrief Institute discussed and demonstrated how the Open Health Information Exchange (OpenHIE) operates in Rwanda.
OpenHIE an open source HIE using a community approach, was developed by the Regenstrief Institute, Jembi Health Systems, and Instedd. These partners initially came together to improve the national health infrastructure in Rwanda with support from the U.S. President’s Emergency Plan for AIDS Relief.
To accomplish the mission, the group collaborated with the Rwandan Ministry of Health on the Rwanda Health Enterprise Architecture (RHEA) project initially supported by the Rockefeller Foundation and the International Development Research Center.
The National Minority Quality Forum (The Forum) is working with its National Health Index (NHI) and Microsoft Corporation to launch the National Clinical Trial Network (NCTN). It is expected that the network will be available in the fourth quarter of 2013 to address the issues of recruitment and diversity in conducting clinical trials. This collaboration will enable NCTN to provide a comprehensive database of clinical trial options to providers.
The Forum is a Washington D.C. based not-for-profit, non-partisan, independent research and education organization dedicated to improving the quality of healthcare available for all populations.
“It’s our view big data will change the way we conduct clinical trials moving forward. What makes the NCTN platform unique is it will provide an interactive, communications portal linking researchers to practicing physicians whose diversity of patients may be candidates for clinical trials,” reports Gary Puckrein, President and CEO of the National Minority Quality Forum. “Being able to quickly link the broader community of medical researchers, practicing physicians, tertiary care centers, and allied health professionals together, we can expedite discovery and translational research.”