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Partners in ESRD Care

Many stakeholders complement the ESRD QIP’s efforts to improve the quality of dialysis care provided to beneficiaries with ESRD. Some of those entities are highlighted in the following non-comprehensive list. Additional stakeholders are referenced on many of these websites.

ESRD Center on CMS.gov
The ESRD Center is a repository for technical information about the ESRD billing and payment processes, Conditions for Coverage, and other topics.
www.cms.gov/Center/Special-Topic/End-Stage-Renal-Disease-ESRD-Center.html?redirect=/center/esrd.asp


The National Forum of ESRD Networks
The Forum of ESRD Networks is a nonprofit organization that advocates on behalf of its membership, and coordinates projects and activities of mutual interests to ESRD Networks. All eighteen ESRD Networks are members of the forum, which facilitates the flow of information and advances a national quality agenda with CMS and other renal organizations.
http://www.esrdnetworks.org/


The ESRD National Coordinating Center
Eighteen ESRD Network Organizations, organized regionally, serve as liaisons between the federal government and providers of ESRD services. The ESRD National Coordinating Center (NCC) provides support and coordination at the national level for the Medicare ESRD Network Program under contract with CMS. The NCC supports improvement in the three core goals of the program (better care for the individual through beneficiary- and family-centered care; better health for the ESRD population; and reduced costs of ESRD care by improving care.
www.esrdncc.org


Dialysis Facility Compare
Dialysis Facility Compare (DFC) is a Medicare service that helps beneficiaries, caregivers, and others find detailed information about Medicare-certified dialysis facilities. Individuals can compare the services and the quality of care that facilities provide; the website also has other resources for patients and family members who want to learn more about chronic kidney disease and dialysis.
www.medicare.gov/dialysisfacilitycompare


National Healthcare Safety Network
The Center for Disease Control and Prevention’s (CDC) National Healthcare Safety Network (NHSN) is the nation’s most widely used healthcare-associated infection (HAI) tracking system, providing data needed to identify problem areas, measure progress of prevention efforts, and ultimately eliminated HAIs. In addition, NHSN allows healthcare facilities to track blood-safety errors and important healthcare process measures, such as the influenza-vaccine status of healthcare personnel and adherence rates for infection control. NHSN functions as an important data source for ESRD QIP performance measures.
www.cdc.gov/nhsn


The CDC also offers an excellent resource on the patient’s role in his or her own safety from acquiring an HAI.
http://www.cdc.gov/HAI/patientSafety/patient-safety.html

Another excellent CDC resource involves patient safety when receiving dialysis treatment.
http://www.cdc.gov/dialysis/patient/index.html


CROWNWeb
Consolidated Renal Operations in a Web-enabled Network (CROWN) is a Web-based data-collection system mandated by CMS to enable dialysis facilities to meet portions of the Conditions for Coverage for ESRD Dialysis Facilities. CROWNWeb helps the renal community transition from a legacy paper-based data-collection method to an electronic “always on” format. The system is designed to help improve patient care efforts by reducing the time it takes CMS to produce clinical performance results. CROWNWeb functions as an important data source for ESRD QIP performance measures.
www.mycrownweb.org


In-Center Hemodialysis CAHPS Survey
The In-Center Hemodialysis (ICH) Consumer Assessment of Healthcare Providers and Systems (CAHPS) is designed to measure, collect, and publicly report the experiences of people receiving ICH care from Medicare-certified dialysis facilities. The survey is an element of evaluating facility performance as an ESRD QIP reporting measure.
https://ichcahps.org


United States Renal Data Service
The United States Renal Data Service (USRDS) is a national data system that collects, analyzes, and distributes information about ESRD in the United States. Six central goals define the mission of the USRDS: to characterize the ESRD population; to describe the prevalence and incidence of ESRD along with trends in mortality and disease rates; to investigate relationships among patient demographics, treatment modalities, and morbidity; to report the costs of ESRD treatments and total burden of the ESRD program in the United States; to identify new areas for special renal studies and support investigator-initiated research; and to provide data sets and samples of national data to support research by the Special Studies Centers.
www.usrds.org


Dialysis Outcomes and Practice Patters Study Program
The Dialysis Outcomes and Practice Patters Study (DOPPS) program is a collection of studies designed to identify best practices for treating patients with chronic kidney failure. DOPPS helps researches identify practices and other modifiable characteristics that improve patient lives. DOPPS projects are coordinated by Arbor Research Collaborative for Health.
www.dopps.org


National Quality Forum
The National Quality Forum (NQF) is a nonprofit, nonpartisan, membership-based organization that works to catalyze improvements in healthcare. NQF convenes working groups to foster quality improvement in the public and private sectors alike; endorses consensus standards for performance measurement, including for treating patients with ESRD; ensures that consistent, high-quality performance information is publicly available; and seeks real-time feedback to ensure that measures are meaningful and accurate. NQF endorsement is the “gold standard” for healthcare quality; such measures are evidence-based and valid.
www.qualityforum.org


United Network for Organ Sharing
The purpose of United Network for Organ Sharing (UNOS) is to promote long, healthy, and productive lives for persons with organ failure by promoting maximized organ supply, effective and safe care, and equitable organ allocation and access to transplantation. It seeks to advance organ availability and transplantation by uniting and supporting its communities for the benefit of patients through education, technology, and policy development.
www.unos.org


Children’s Organ Transplant Association
The Children’s Organ Transplant Association (COTA) helps children and young adults who need a life-saving organ, bone marrow, cord blood, or stem cell transplant by providing fundraising assistance and family support. It also works with any patient who needs a transplant due to a genetic disease such as cystic fibrosis or sickle cell anemia.
www.cota.org

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