Author: Publisher:
ISBN:
Category :
Languages : en
Pages : 294
Book Description
Aggregate Hospital Discharge Data Summary
Author: Aggregate Hospital Discharge Data for California
Author: Publisher:
ISBN:
Category : Costs and cost analysis
Languages : en
Pages : 546
Book Description
Uniform Hospital Discharge Data
Author: United States. National Committee on Vital and Health StatisticsPublisher:
ISBN:
Category : Government publications
Languages : en
Pages : 36
Book Description
National Hospital Discharge Survey
Author: Publisher:
ISBN:
Category : Hospital utilization
Languages : en
Pages : 212
Book Description
Aggregate hospital discharge data for California. 1982 | publ. Apr. 1984
Author: Individual Hospital Discharge Data Summary (IHDDS)
Author: Aggregate Hospital Discharge Data for California
Author: Publisher:
ISBN:
Category : Hospital utilization
Languages : en
Pages : 1026
Book Description
1999 National Hospital Discharge Survey
Author: Edward J. SondikNational Hospital Discharge Survey
Author: Publisher:
ISBN:
Category : Hospital utilization
Languages : en
Pages : 208
Book Description
Registries for Evaluating Patient Outcomes
Author: Agency for Healthcare Research and Quality/AHRQPublisher: Government Printing Office
ISBN: 1587634333
Category : Medical
Languages : en
Pages : 396
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.