Medicaid Eligibility Quality Control: Sampling methods
Author: United States. Social and Rehabilitation Service
Publisher:
Published: 1975
Total Pages: 34
ISBN-13:
DOWNLOAD EBOOKRead and Download eBook Full
Author: United States. Social and Rehabilitation Service
Publisher:
Published: 1975
Total Pages: 34
ISBN-13:
DOWNLOAD EBOOKAuthor: United States. Social and Rehabilitation Service
Publisher:
Published: 1975
Total Pages: 164
ISBN-13:
DOWNLOAD EBOOKAuthor: United States. Social and Rehabilitation Service
Publisher:
Published: 1975
Total Pages: 26
ISBN-13:
DOWNLOAD EBOOKAuthor: United States. Social and Rehabilitation Service
Publisher:
Published: 1975
Total Pages: 46
ISBN-13:
DOWNLOAD EBOOKAuthor: United States. Social and Rehabilitation Service
Publisher:
Published: 1975
Total Pages: 132
ISBN-13:
DOWNLOAD EBOOKAuthor: United States. Social and Rehabilitation Service
Publisher:
Published: 1975
Total Pages: 70
ISBN-13:
DOWNLOAD EBOOKAuthor: United States. Social and Rehabilitation Service
Publisher:
Published: 1975
Total Pages: 240
ISBN-13:
DOWNLOAD EBOOKAuthor: Institute of Medicine
Publisher: National Academies Press
Published: 1986-02-01
Total Pages: 432
ISBN-13: 0309036461
DOWNLOAD EBOOKAs more people live longer, the need for quality long-term care for the elderly will increase dramatically. This volume examines the current system of nursing home regulations, and proposes an overhaul to better provide for those confined to such facilities. It determines the need for regulations, and concludes that the present regulatory system is inadequate, stating that what is needed is not more regulation, but better regulation. This long-anticipated study provides a wealth of useful background information, in-depth study, and discussion for nursing home administrators, students, and teachers in the health care field; professionals involved in caring for the elderly; and geriatric specialists.
Author: United States. Department of Health and Human Services
Publisher:
Published: 1988
Total Pages: 362
ISBN-13:
DOWNLOAD EBOOKAuthor: Agency for Healthcare Research and Quality/AHRQ
Publisher: Government Printing Office
Published: 2014-04-01
Total Pages: 385
ISBN-13: 1587634333
DOWNLOAD EBOOKThis 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.