Author: AMEC Earth and Environmental
Publisher:
ISBN:
Category :
Languages : en
Pages :
Book Description
Final Report with Addendum to Address Comments Received
Addendum to the December 31, 1999 Final Report
Author: California. Task Force on Trial Court Employees
Publisher:
ISBN:
Category : Court administration
Languages : en
Pages :
Book Description
Publisher:
ISBN:
Category : Court administration
Languages : en
Pages :
Book Description
Addendum to FIAT Final Report 715
Final Report and Recommendations
Author: Maryland. Task Force on Health Care Access and Reimbursement
Publisher:
ISBN:
Category : Health insurance
Languages : en
Pages :
Book Description
Publisher:
ISBN:
Category : Health insurance
Languages : en
Pages :
Book Description
Mist Final Report Volume 11
Revised Final Remedial Investigation Addendum Report for Operable Units 4, 8, and 9. Volume II, (Appendices A Through H), Part 2
Author:
Publisher:
ISBN:
Category :
Languages : en
Pages : 911
Book Description
Report contains Appendices A through H, Volume 2, (Part 2). Addendum reports for Operable units 4, 8 and 9.
Publisher:
ISBN:
Category :
Languages : en
Pages : 911
Book Description
Report contains Appendices A through H, Volume 2, (Part 2). Addendum reports for Operable units 4, 8 and 9.
Addendum to the Draft Final Report Reflecting Comments from the March 22 Meeting of the Task Force
Author: Connecticut. Task Force on State Tax Revenue
Publisher:
ISBN:
Category : Corporations
Languages : en
Pages : 52
Book Description
Publisher:
ISBN:
Category : Corporations
Languages : en
Pages : 52
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.
MIST Final Report
Addendum II to the Final Remedial Investigation Report
Author: Philip Services Corporation
Publisher:
ISBN:
Category : Georgetown (Seattle, Wash.)
Languages : en
Pages :
Book Description
Publisher:
ISBN:
Category : Georgetown (Seattle, Wash.)
Languages : en
Pages :
Book Description