Author: National Center for Health Statistics (U.S.)
Publisher:
ISBN:
Category : Death
Languages : en
Pages : 144
Book Description
Medical Examiners' and Coroners' Handbook on Death Registration and Fetal Death Reporting
Author: National Center for Health Statistics (U.S.)
Publisher:
ISBN:
Category : Death
Languages : en
Pages : 144
Book Description
Publisher:
ISBN:
Category : Death
Languages : en
Pages : 144
Book Description
Funeral Directors' Handbook on Death Registration and Fetal Death Reporting
Author: National Center for Health Statistics (U.S.)
Publisher:
ISBN:
Category : Death certificates
Languages : en
Pages : 60
Book Description
Publisher:
ISBN:
Category : Death certificates
Languages : en
Pages : 60
Book Description
Physicians' Handbook on Medical Certification of Death
Author:
Publisher:
ISBN:
Category : Death
Languages : en
Pages : 44
Book Description
Publisher:
ISBN:
Category : Death
Languages : en
Pages : 44
Book Description
Hospital Handbook on Birth Registration and Fetal Death Reporting
Author: National Center for Health Statistics (U.S.)
Publisher:
ISBN:
Category : Birth certificates
Languages : en
Pages : 56
Book Description
Publisher:
ISBN:
Category : Birth certificates
Languages : en
Pages : 56
Book Description
Safe Abortion
Author: World Health Organization
Publisher: World Health Organization
ISBN: 9241590343
Category : Medical
Languages : en
Pages : 107
Book Description
At a UN General Assembly Special Session in 1999, governments recognised unsafe abortion as a major public health concern, and pledged their commitment to reduce the need for abortion through expanded and improved family planning services, as well as ensure abortion services should be safe and accessible. This technical and policy guidance provides a comprehensive overview of the many actions that can be taken in health systems to ensure that women have access to good quality abortion services as allowed by law.
Publisher: World Health Organization
ISBN: 9241590343
Category : Medical
Languages : en
Pages : 107
Book Description
At a UN General Assembly Special Session in 1999, governments recognised unsafe abortion as a major public health concern, and pledged their commitment to reduce the need for abortion through expanded and improved family planning services, as well as ensure abortion services should be safe and accessible. This technical and policy guidance provides a comprehensive overview of the many actions that can be taken in health systems to ensure that women have access to good quality abortion services as allowed by law.
Handbook on the Reporting of Induced Termination of Pregnancy
Author: National Center for Health Statistics (U.S.)
Publisher:
ISBN:
Category : Abortion
Languages : en
Pages : 28
Book Description
Publisher:
ISBN:
Category : Abortion
Languages : en
Pages : 28
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.
Principles and Recommendations for a Vital Statistics System, Revision 3
Author: United Nations. Statistical Office
Publisher:
ISBN:
Category : Mathematics
Languages : en
Pages : 242
Book Description
The publication is an international standard on the design and operation of an efficient and accurate vital statistics system at national level. It provides guidelines on collection, compiling and disseminating vital statistics. More specifically it contains (a) basic principles for a vital statistics system; (b) uses of vital statistics and civil registration records; (c) topics to be covered in a vital statistics system; (d) sources of vital statistics and how they function; (e) quality assurance in the vital statistics system and (f) strategies in improving civil registration and vital statistics systems in countries. It also informs policy makers and the general public on the importance of vital statistics and hence further improving the vital statistics system.
Publisher:
ISBN:
Category : Mathematics
Languages : en
Pages : 242
Book Description
The publication is an international standard on the design and operation of an efficient and accurate vital statistics system at national level. It provides guidelines on collection, compiling and disseminating vital statistics. More specifically it contains (a) basic principles for a vital statistics system; (b) uses of vital statistics and civil registration records; (c) topics to be covered in a vital statistics system; (d) sources of vital statistics and how they function; (e) quality assurance in the vital statistics system and (f) strategies in improving civil registration and vital statistics systems in countries. It also informs policy makers and the general public on the importance of vital statistics and hence further improving the vital statistics system.
U.S. Vital Statistics System
Author: Alice M. Hetzel
Publisher:
ISBN:
Category : Statistics, Vital
Languages : en
Pages : 74
Book Description
Publisher:
ISBN:
Category : Statistics, Vital
Languages : en
Pages : 74
Book Description
Handbook on Marriage Registration
Author:
Publisher:
ISBN:
Category : Marriage
Languages : en
Pages : 32
Book Description
Publisher:
ISBN:
Category : Marriage
Languages : en
Pages : 32
Book Description