Author: Robert H. MuggePublisher:
ISBN:
Category : Health planning
Languages : en
Pages : 28
Book Description
Guidelines for Conducting an Inventory of State Data Sources for Health Planners
Author: Robert H. MuggePublisher:
ISBN:
Category : Health planning
Languages : en
Pages : 28
Book Description
GUIDELINES FOR CONDUCTING AN INVENTORY OF STATE DATA SOURCES FOR HEALTH PLANNERS.
Author: United States Public Health ServicePublisher:
ISBN:
Category :
Languages : en
Pages :
Book Description
Guidelines for Conducting and Inventory of State Data Sources for Health Planners
Author: National Center for Health Statistics (U.S.)Publisher:
ISBN:
Category : Health planning
Languages : en
Pages : 8
Book Description
Guidelines for the Acquisition and Use of Data Under Public Law 93-641
Author: United States. Bureau of Health Planning and Resources DevelopmentPublisher:
ISBN:
Category : Health planning
Languages : en
Pages : 200
Book Description
Health Planning Information Series
Author: Resources in Education
Author: Catalog of Health Resources Administration Publications
Author: United States. Health Resources AdministrationPublisher:
ISBN:
Category : Health planning
Languages : en
Pages : 94
Book Description
Catalog of Publications
Author: United States. Health Resources AdministrationPublisher:
ISBN:
Category : Health planning
Languages : en
Pages : 84
Book Description
Monthly Catalog of United States Government Publications
Author: United States. Superintendent of DocumentsPublisher:
ISBN:
Category : Government publications
Languages : en
Pages : 1092
Book Description
February issue includes Appendix entitled Directory of United States Government periodicals and subscription publications; September issue includes List of depository libraries; June and December issues include semiannual index
Registries for Evaluating Patient Outcomes
Author: Agency for Healthcare Research and Quality/AHRQPublisher: Government Printing Office
ISBN: 1587634333
Category : Medical
Languages : en
Pages : 385
Book Description
This 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.