Annual Reports on the Exchange of Medical Information and Sharing Medical Resources, Fiscal Year 1980
Author: United States. Veterans Administration
Publisher:
Published: 1981
Total Pages: 144
ISBN-13:
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Author: United States. Veterans Administration
Publisher:
Published: 1981
Total Pages: 144
ISBN-13:
DOWNLOAD EBOOKAuthor: United States. Veterans Administration
Publisher:
Published: 1976
Total Pages: 132
ISBN-13:
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Publisher:
Published: 1977
Total Pages: 168
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DOWNLOAD EBOOKAuthor: National Library of Medicine (U.S.)
Publisher:
Published: 1979
Total Pages:
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DOWNLOAD EBOOKFirst multi-year cumulation covers six years: 1965-70.
Author: National Library of Medicine (U.S.)
Publisher:
Published: 1984
Total Pages: 1516
ISBN-13:
DOWNLOAD EBOOKA keyword listing of serial titles currently received by the National Library of Medicine.
Author: United States. Superintendent of Documents
Publisher:
Published: 1968
Total Pages: 1220
ISBN-13:
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Publisher:
Published: 1969
Total Pages:
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Publisher:
Published: 1980
Total Pages: 1234
ISBN-13:
DOWNLOAD EBOOKAuthor: United States. Veterans Administration
Publisher:
Published: 1979
Total Pages: 32
ISBN-13:
DOWNLOAD EBOOKAuthor: Agency for Healthcare Research and Quality/AHRQ
Publisher: Government Printing Office
Published: 2014-04-01
Total Pages: 385
ISBN-13: 1587634333
DOWNLOAD EBOOKThis User’s Guide is intended to support the design, implementation, analysis, interpretation, and quality evaluation of registries created to increase understanding of patient outcomes. For the purposes of this guide, a patient registry is an organized system that uses observational study methods to collect uniform data (clinical and other) to evaluate specified outcomes for a population defined by a particular disease, condition, or exposure, and that serves one or more predetermined scientific, clinical, or policy purposes. A registry database is a file (or files) derived from the registry. Although registries can serve many purposes, this guide focuses on registries created for one or more of the following purposes: to describe the natural history of disease, to determine clinical effectiveness or cost-effectiveness of health care products and services, to measure or monitor safety and harm, and/or to measure quality of care. Registries are classified according to how their populations are defined. For example, product registries include patients who have been exposed to biopharmaceutical products or medical devices. Health services registries consist of patients who have had a common procedure, clinical encounter, or hospitalization. Disease or condition registries are defined by patients having the same diagnosis, such as cystic fibrosis or heart failure. The User’s Guide was created by researchers affiliated with AHRQ’s Effective Health Care Program, particularly those who participated in AHRQ’s DEcIDE (Developing Evidence to Inform Decisions About Effectiveness) program. Chapters were subject to multiple internal and external independent reviews.