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Author: United States. Alcohol, Drug Abuse, and Mental Health Administration
Publisher:
ISBN:
Category : Alcoholism
Languages : en
Pages : 100
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Book Description
Author: United States. Alcohol, Drug Abuse, and Mental Health Administration
Publisher:
ISBN:
Category : Alcoholism
Languages : en
Pages : 100
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Book Description
Author:
Publisher:
ISBN:
Category :
Languages : en
Pages : 87
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Author:
Publisher:
ISBN:
Category :
Languages : en
Pages : 0
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![National Center for Health Statistics [a Guide]. PDF](https://books.google.com/books/content/images/frontcover/hnfP5u17O2IC?fife=w80-h100)
Author: National Center for Health Statistics (U.S.)
Publisher:
ISBN:
Category : Health services administration
Languages : en
Pages : 24
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Author: United States. National Committee on Vital and Health Statistics
Publisher:
ISBN:
Category :
Languages : en
Pages : 36
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Report year ends June 30.
Author: Bruce B. Cohen
Publisher:
ISBN:
Category : Automatic data collection systems
Languages : en
Pages : 88
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Author: Haroutune K. Armenian
Publisher: Oxford University Press, USA
ISBN: 9780195093599
Category : Medical
Languages : en
Pages : 300
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Book Description
What is the relevance of epidemiology to decision making in the health services? If our ability to launch large-scale experimental studies of health services is limited, what are some alternative approaches to study design? How can we best make use of routinely collected data from health information systems? How can we best synthesize information to make more reasonable inferences? Epidemiology and Health Services is different from other books in the field. Many books and specialized publications have presented a comprehensive picture of epidemiologic methods, but they have not shown in a systematic way how these methods apply to health services. This book fills the gap, and goes even further by analyzing the strengths and limitations of epidemiologic methods in the context of health care delivery, and discussing approaches for making pertinent inferences in actual cases. The book addresses the needs of a broad spectrum of health professionals. It will help health service administrators, managers and other professionals design and conduct evaluative and intervention research on the delivery of health services. It will also give epidemiology and public health students a wider perspective on the various applications of the discipline.
Author: National Research Council
Publisher: National Academies Press
ISBN: 0309075823
Category : Medical
Languages : en
Pages : 94
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Book Description
The Committee on National Statistics (CNSTAT) convened a workshop on November 4-5, 1999, to identify new directions for health statistics and the implications for health data of changes in the health arena faced by DHHS; state and local health departments; the consumers, developers, and providers of health care products and services; and other health policy makers. Changes in our understanding of health, in health care (managed care, Medicaid, Medicare), in welfare reform, in federal-state relations, in the availability of administrative data, in advanced genetic data, in information technology, in confidentiality issues, and in data integration are examples of recent developments that may play a significant role for DHHS in making future policy decisions.
Author: Agency for Healthcare Research and Quality/AHRQ
Publisher: Government Printing Office
ISBN: 1587634333
Category : Medical
Languages : en
Pages : 385
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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.
Author: Institute of Medicine
Publisher: National Academies Press
ISBN: 0309212197
Category : Medical
Languages : en
Pages : 200
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Book Description
Chronic diseases are common and costly, yet they are also among the most preventable health problems. Comprehensive and accurate disease surveillance systems are needed to implement successful efforts which will reduce the burden of chronic diseases on the U.S. population. A number of sources of surveillance data-including population surveys, cohort studies, disease registries, administrative health data, and vital statistics-contribute critical information about chronic disease. But no central surveillance system provides the information needed to analyze how chronic disease impacts the U.S. population, to identify public health priorities, or to track the progress of preventive efforts. A Nationwide Framework for Surveillance of Cardiovascular and Chronic Lung Diseases outlines a conceptual framework for building a national chronic disease surveillance system focused primarily on cardiovascular and chronic lung diseases. This system should be capable of providing data on disparities in incidence and prevalence of the diseases by race, ethnicity, socioeconomic status, and geographic region, along with data on disease risk factors, clinical care delivery, and functional health outcomes. This coordinated surveillance system is needed to integrate and expand existing information across the multiple levels of decision making in order to generate actionable, timely knowledge for a range of stakeholders at the local, state or regional, and national levels. The recommendations presented in A Nationwide Framework for Surveillance of Cardiovascular and Chronic Lung Diseases focus on data collection, resource allocation, monitoring activities, and implementation. The report also recommends that systems evolve along with new knowledge about emerging risk factors, advancing technologies, and new understanding of the basis for disease. This report will inform decision-making among federal health agencies, especially the Department of Health and Human Services; public health and clinical practitioners; non-governmental organizations; and policy makers, among others.
