2012 National Healthcare Quality and Disparities Reports
Data Sources—National Institutes of Health
U.S. Department of Health and Human Services, National Institutes of Health (NIH), National Cancer Institute (NCI), Division of Cancer Control and Population Sciences, Surveillance Research Program, Surveillance Systems Branch.
The SEER Program is an authoritative source of information on cancer incidence and survival in the United States. SEER currently collects and publishes cancer incidence and survival data from population-based cancer registries covering approximately 28% of the U.S. population.
Geographic areas were selected for inclusion in the SEER Program based on their ability to operate and maintain a high-quality population-based cancer reporting system and for their epidemiologically significant population subgroups.
The SEER Program registries routinely collect data on patients with cancer diagnoses among residents of various geographic coverage areas.
Patient demographic information, primary tumor site, morphology, stage at diagnosis, first course of treatment, and vital status.
U.S. population. The population data used in calculating cancer rates are obtained periodically from the Census Bureau.
Age, sex, race, year of diagnosis, and geographic areas.
National and States with registries.
The SEER*Stat statistical software package provides a convenient, intuitive mechanism for the analysis of SEER and other cancer-related databases. Cancer incidence rates used for the NHQR and NHDR were generated using SEER*Stat and were adjusted to the 2000 U.S. standard population by 5-year age groups.
Agency home page: http://www.cancer.gov.
Data system home page: http://www.seer.cancer.gov.
Altekruse SF, Kosary CL, Krapcho M, et al., eds. SEER cancer statistics review, 1975-2007. Based on November 2009 SEER data submission, posted to the SEER Web site, 2010. Bethesda, MD: National Cancer Institute. Available at: http://seer.cancer.gov/csr/1975_2007/.
U.S. Department of Health and Human Services, National Institutes of Health (NIH), National Institute of Diabetes and Digestive and Kidney Disease (NIDDK) in collaboration with the U.S. Department of Health and Human Services, Centers for Medicare & Medicaid Services (CMS).
USRDS is a national data system that collects, analyzes, and distributes information about end stage renal disease (ESRD) in the United States. It includes continuous mandated reporting from physicians who treat ESRD. The major source of ESRD patient information for USRDS is the CMS Renal Beneficiary and Utilization System (REBUS)/Program Management and Medical Information System (PMMIS) database. The REBUS/PMMIS database contains demographic, diagnostic, and treatment history information for all Medicare beneficiaries with ESRD. The database has been expanded to include non-Medicare patients.
These CMS-supplied data are supplemented by data from the Social Security Administration, U.S. Department of Veterans Affairs facilities, U.S. Census Bureau, local and national ESRD provider databases, and international ESRD registries. Patient-specific data are compiled from medical records, as well as data on medical providers and treatment facilities.
Date of onset of ESRD, treatment modality, causes of death, patient survival, hospitalization, cost and cost-effectiveness, and institutional providers of ESRD treatment. Special surveys cover behavioral risk factors (for example, alcohol and tobacco use), preventive health measures, health status, activity limitations, and health care access and utilization.
Gender, age, income, education, race, and ethnicity.
Continuously since 1988.
National, State, and county.
Agency home page: http://www.niddk.nih.gov.
Data system home page: http://www.usrds.org.
U.S. Renal Data System. USRDS 2008 annual data report: atlas of chronic kidney disease and end-stage renal disease in the United States. Bethesda, MD: National Institute of Diabetes and Digestive and Kidney Diseases; 2008. More information is available at: http://www.usrds.org/research.htm.