Medicaid-medicare Common Data Initiative
Author: United States. Health Care Financing Administration
Publisher:
Published: 1994
Total Pages:
ISBN-13:
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Author: United States. Health Care Financing Administration
Publisher:
Published: 1994
Total Pages:
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Publisher:
Published: 1983
Total Pages: 188
ISBN-13:
DOWNLOAD EBOOKWith 1990: Includes trends for medicare enrollees and Medicaid recipients, Medicare and Medicaid expenditures, and the use of and expenditures for hospital inpatient and physicians services in both programs. Also includes a listing of Medicare carriers and intermediaries, as well as Medicaid agencies and fiscal agents.
Author: United States. Medicaid Bureau. Division of Analysis and Evaluation
Publisher:
Published: 1977
Total Pages: 36
ISBN-13:
DOWNLOAD EBOOKAuthor: United States. Physician Payment Review Commission
Publisher:
Published: 1997
Total Pages: 548
ISBN-13:
DOWNLOAD EBOOKAuthor: United States. Social and Rehabilitation Service
Publisher:
Published: 1975
Total Pages: 460
ISBN-13:
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Publisher:
Published: 1995
Total Pages: 1040
ISBN-13:
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Publisher:
Published: 1995
Total Pages: 1032
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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.
Author: Medicaid/Medicare Management Institute (U.S.)
Publisher:
Published: 1980
Total Pages: 112
ISBN-13:
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