An Introduction to the Healthcare Cost and Utilization Project (HCUP): A Resource for Medical Librarians
April 23rd at ECRI Institute
HCUP databases can be used to identify, track, and analyze national trends in health care utilization, access, charges, quality, and outcomes — on a nationwide and state-specific databases. (See “About HCUP” at the end of article.)
April 23, 1-4 PM
ECRI Institute Auditorium,
www.ecri.org
To register, email jderichemond@gmail.com
Course outline
Introduction to HCUP Resources (60 minutes)
Overview of healthcare administrative data
Introduction to the 5 main types of HCUP databases
Benefits and limitations of HCUP databases
Discussion about the use of HCUP in medical and health services research
Example Publications Using HCUP (30 minutes)
Review of the wide range of publications that HCUP data have supported, including selected peer-reviewed articles, AHRQ-produced documents, and congressionally-mandated reports.
Break (15 minutes)
HCUPnet – free online tool for retrieving data (45 minutes)
Demonstration of the HCUP free querying tool
(Note: this section of the course will be very interactive)
Other HCUP-related Tools and Resources (30 minutes)
Discussion of healthcare software tools that can be applied to HCUP data to enhance the value of the data
Instruction on where librarians can access detailed documentation about HCUP resources
Detailed overview of the HCUP User Support Website
About HCUP
The Healthcare Cost and Utilization Project (HCUP, pronounced “H-Cup”) is a family of health care databases and related software tools and products developed through a Federal-State-Industry partnership and sponsored by the Agency for Healthcare Research and Quality (AHRQ). HCUP databases bring together the data collection efforts of State data organizations, hospital associations, private data organizations, and the Federal government to create a national information resource of patient-level health care data (HCUP Partners). HCUP includes the largest collection of longitudinal hospital care data in the United States, with all-payer, encounter-level information beginning in 1988. These databases enable research on a broad range of health policy issues, including cost and quality of health services, medical practice patterns, access to health care programs, and outcomes of treatments at the national, State, and local market levels.



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