Author: Publisher:
ISBN:
Category :
Languages : en
Pages :
Book Description
Francoise Bresnahan. February 15 (legislative Day, February 8), 1954. -- Ordered to be Printed
Author: Report
Author: United States. Congress SenatePublisher:
ISBN:
Category : United States
Languages : en
Pages : 2732
Book Description
Francoise O. McMahon. August 2 (legislative Day, July 2), 1954. -- Ordered to be Printed
Author: Julie Nicola Frangou. February 15 (legislative Day, February 8), 1954. -- Ordered to be Printed
Author: Suzanne Jacquet. February 24 (legislative Day, February 8), 1954. -- Ordered to be Printed
Author: Gertrude Rena Carlson. February 24 (legislative Day, February 8), 1954. -- Ordered to be Printed
Author: Sofia B. Panagoulopoulos Kanell. February 24 (legislative Day, February 8), 1954. -- Ordered to be Printed
Author: Sister Marie Therese De Galzain. February 24 (legislative Day, February 8), 1954. -- Ordered to be Printed
Author: Productivity Measurement and Analysis
Author: OECDPublisher: OECD Publishing
ISBN: 9264044612
Category :
Languages : en
Pages : 556
Book Description
Presents the proceedings of two workshops on productivity measurement and analysis, which brought together representatives of statistical offices, central banks and other officials involved with the analysis and measurement of productivity at aggregate and industry levels.
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.