Author: United States. Office of Revenue Sharing
Publisher:
ISBN:
Category : Intergovernmental fiscal relations
Languages : en
Pages : 468
Book Description
Initial Data Elements
Final Data Elements, Entitlement Periods 1, 2 & 3
Author:
Publisher:
ISBN:
Category : Intergovernmental fiscal relations
Languages : en
Pages : 468
Book Description
Publisher:
ISBN:
Category : Intergovernmental fiscal relations
Languages : en
Pages : 468
Book Description
Final State & Local Data Elements
Author:
Publisher:
ISBN:
Category : Revenue sharing
Languages : en
Pages : 540
Book Description
Publisher:
ISBN:
Category : Revenue sharing
Languages : en
Pages : 540
Book Description
Data Elements, Entitlement Period
Author: United States. Department of the Treasury
Publisher:
ISBN:
Category :
Languages : en
Pages : 890
Book Description
Publisher:
ISBN:
Category :
Languages : en
Pages : 890
Book Description
Registries for Evaluating Patient Outcomes
Author: Agency for Healthcare Research and Quality/AHRQ
Publisher: 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.
Publisher: 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.
Data Elements
Author:
Publisher:
ISBN:
Category : Intergovernmental fiscal relations
Languages : en
Pages : 420
Book Description
Publisher:
ISBN:
Category : Intergovernmental fiscal relations
Languages : en
Pages : 420
Book Description
Federal Register
Author:
Publisher:
ISBN:
Category : Delegated legislation
Languages : en
Pages : 412
Book Description
Publisher:
ISBN:
Category : Delegated legislation
Languages : en
Pages : 412
Book Description
Enterprise Information Systems
Author: Joaquim Filipe
Publisher: Springer Nature
ISBN: 3031647556
Category :
Languages : en
Pages : 296
Book Description
Publisher: Springer Nature
ISBN: 3031647556
Category :
Languages : en
Pages : 296
Book Description
Publications Related to Payments Under the State and Local Fiscal Assistance Act of 1972 (revenue Sharing)
Author: United States. Office of Revenue Sharing
Publisher:
ISBN:
Category : Intergovernmental fiscal relations
Languages : en
Pages : 1228
Book Description
Publisher:
ISBN:
Category : Intergovernmental fiscal relations
Languages : en
Pages : 1228
Book Description
Allocations
Author:
Publisher:
ISBN:
Category : Revenue sharing
Languages : en
Pages : 460
Book Description
Publisher:
ISBN:
Category : Revenue sharing
Languages : en
Pages : 460
Book Description