Outcomes Research Resource Guide
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Author | : |
Publisher | : American Medical Association Press |
Total Pages | : 164 |
Release | : 1997 |
Genre | : Medical |
ISBN | : 9780899709079 |
This latest edition of the Outcomes Research Resource Guide provides detailed information regarding the outcomes research activities of nearly 150 physician organizations and other groups. A one-stop resource, it contains the most comprehensive information about sponsoring organizations and contact names, type of intervention measured, physician involvement, methodology, and sponsor goals and interests. Principles of Outcomes Research from AMA policy is also included.
Author | : American Medical Association. Department of Practice Parameters |
Publisher | : |
Total Pages | : 0 |
Release | : 1996 |
Genre | : Medicine |
ISBN | : 9780899708584 |
Author | : Agency for Healthcare Research and Quality/AHRQ |
Publisher | : Government Printing Office |
Total Pages | : 385 |
Release | : 2014-04-01 |
Genre | : Medical |
ISBN | : 1587634333 |
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.
Author | : |
Publisher | : American Medical Association Press |
Total Pages | : 0 |
Release | : 1997 |
Genre | : Outcome assessment (Medical care) |
ISBN | : 9780899709079 |
This latest edition of the Outcomes Research Resource Guide provides detailed information regarding the outcomes research activities of nearly 150 physician organizations and other groups. A one-stop resource, it contains the most comprehensive information about sponsoring organizations and contact names, type of intervention measured, physician involvement, methodology, and sponsor goals and interests. Principles of Outcomes Research from AMA policy is also included.
Author | : Robert Kane |
Publisher | : Jones & Bartlett Learning |
Total Pages | : 369 |
Release | : 2011 |
Genre | : Medical |
ISBN | : 0763786772 |
Health Sciences & Professions
Author | : University Hospital (Denver, Colo.). Department of Professional Resources |
Publisher | : |
Total Pages | : 125 |
Release | : 2000 |
Genre | : |
ISBN | : |
Author | : |
Publisher | : |
Total Pages | : 852 |
Release | : 1997 |
Genre | : Medical care |
ISBN | : |
Author | : Robert L. Kane |
Publisher | : Jones & Bartlett Publishers |
Total Pages | : 369 |
Release | : 2010-08-25 |
Genre | : Medical |
ISBN | : 1449619851 |
Conducting Health Outcomes Research serves as the definitive guide to successful investigation of health care outcomes and the key resource for ensuring quality care. As consumer, insurer and government demands for quality health care increase, the field of research required to measure such quality stands to grow exponentially. Conducting Health Outcomes Research brings together the practical, actionable information needed to conduct research on health outcomes, with the goal of measuring the quality of the care being delivered. The book details the methodology for performing successful research in this growing field: from formulating models, choosing study design, measuring and gathering data to assessing and presenting results. Important Notice: The digital edition of this book is missing some of the images or content found in the physical edition.
Author | : |
Publisher | : |
Total Pages | : 800 |
Release | : 1996-01-01 |
Genre | : Medical |
ISBN | : 9781881393665 |
Author | : Maralee T. Youngs |
Publisher | : |
Total Pages | : 753 |
Release | : 1996-01-01 |
Genre | : Medical |
ISBN | : 9781881393436 |