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Audiences

Patients and Families  Patients and Families

The Scientific Registry of Transplant Recipients (the SRTR) provides useful information about transplant outcomes and transplant programs for patients and their families. While much of our work focuses on statistical research that helps shape organ allocation policy and health care practices, we also report statistics for patients. These include outcomes concerning patients on the waiting list and those who receive transplants. Patients and families can also learn how these statistics differ from one transplant program to the next.


Transplant Community and Policy Makers  Transplant Community and Policy Makers

The primary mission of the SRTR is to support the transplant community — in particular, transplant professionals and policymakers — with analyses to aid in the development of organ allocation and other policies. More generally, the SRTR strives to advance medical care by providing evidence about treatments and outcomes. This research takes the form of reports to policymaking committees, as well as publication and presentation of our research in the medical literature and scientific meetings. In addition to these national-level studies, we also perform analyses specific to each transplant program and organ procurement organization (OPO) in the United States.


Researchers  Researchers

The SRTR works to support and collaborate with the community of researchers interested in transplantation issues. Typically, the research audience of the SRTR includes public health services researchers, biostatisticians, and transplant clinicians.
2010 Annual Report
Transplant Data
Contact the SRTR
914 South 8th Street Suite S-206 Minneapolis, MN 55404
Tel: (877) 970-SRTR
Fax: (612) 347-5878
Email Us

The SRTR is administered by the Chronic Disease Research Group of the Minneapolis Medical Research Foundation,
with oversight and funding from the Health Resources and Services Administration.
Citation Advice