Author: Canadian Institute for Health Information
Publisher:
ISBN: 9781896389349
Category : Communication in medicine
Languages : en
Pages :
Book Description
Health Data Sharing in Canada : a Resource Guide
Author: Canadian Institute for Health Information
Publisher:
ISBN: 9781896389349
Category : Communication in medicine
Languages : en
Pages :
Book Description
Publisher:
ISBN: 9781896389349
Category : Communication in medicine
Languages : en
Pages :
Book Description
Resource Guide to Digital Health in Canada
Author:
Publisher:
ISBN:
Category : Information storage and retrieval systems
Languages : en
Pages : 0
Book Description
"Presenting the new Resource Guide to Digital Health in Canada - a comprehensive overview of the health informatics body of knowledge and the Canadian digital health ecosystem. Building on the CPHIMS-CA Canadian Health Informatics Review and Reference Guide, the new Resource Guide examines both the traditional and emerging challenges and opportunities that digital health professionals face today. The new Resource Guide includes updates to existing topic areas (The Canadian Health System, Clinical Health Services, Analysis and Evaluation, Organizational and Behavioural Management, Information Management, and Information Technology) plus four new content areas: Innovation, Business Intelligence, Health Information Technology and Applications, and Health Analytics."--Provided by publisher.
Publisher:
ISBN:
Category : Information storage and retrieval systems
Languages : en
Pages : 0
Book Description
"Presenting the new Resource Guide to Digital Health in Canada - a comprehensive overview of the health informatics body of knowledge and the Canadian digital health ecosystem. Building on the CPHIMS-CA Canadian Health Informatics Review and Reference Guide, the new Resource Guide examines both the traditional and emerging challenges and opportunities that digital health professionals face today. The new Resource Guide includes updates to existing topic areas (The Canadian Health System, Clinical Health Services, Analysis and Evaluation, Organizational and Behavioural Management, Information Management, and Information Technology) plus four new content areas: Innovation, Business Intelligence, Health Information Technology and Applications, and Health Analytics."--Provided by publisher.
Guide to the De-Identification of Personal Health Information
Author: Khaled El Emam
Publisher: CRC Press
ISBN: 1466579080
Category : Business & Economics
Languages : en
Pages : 413
Book Description
Offering compelling practical and legal reasons why de-identification should be one of the main approaches to protecting patients' privacy, the Guide to the De-Identification of Personal Health Information outlines a proven, risk-based methodology for the de-identification of sensitive health information. It situates and contextualizes this risk-ba
Publisher: CRC Press
ISBN: 1466579080
Category : Business & Economics
Languages : en
Pages : 413
Book Description
Offering compelling practical and legal reasons why de-identification should be one of the main approaches to protecting patients' privacy, the Guide to the De-Identification of Personal Health Information outlines a proven, risk-based methodology for the de-identification of sensitive health information. It situates and contextualizes this risk-ba
The Reference Guide to Data Sources
Author: Julia Bauder
Publisher: American Library Association
ISBN: 0838912273
Category : Computers
Languages : en
Pages : 183
Book Description
This concise sourcebook takes the guesswork out of locating the best sources of data, a process more important than ever as the data landscape grows increasingly cluttered. Much of the most frequently used data can be found free online, and this book shows readers how to look for it with the assistance of user-friendly tools. This thoroughly annotated guide will be a boon to library staff at public libraries, high school libraries, academic libraries, and other research institutions, with concentrated coverage of Data sources for frequently researched subjects such as agriculture, the earth sciences, economics, energy, political science, transportation, and many more The basics of data reference along with an overview of the most useful sources, focusing on free online sources of reliable statistics like government agencies and NGOs Statistical datasets, and how to understand and make use of them How to use article databases, WorldCat, and subject experts to find data Methods for citing data Survey Documentation and Analysis (SDA) software This guide cuts through the data jargon to help librarians and researchers find exactly what they're looking for.
Publisher: American Library Association
ISBN: 0838912273
Category : Computers
Languages : en
Pages : 183
Book Description
This concise sourcebook takes the guesswork out of locating the best sources of data, a process more important than ever as the data landscape grows increasingly cluttered. Much of the most frequently used data can be found free online, and this book shows readers how to look for it with the assistance of user-friendly tools. This thoroughly annotated guide will be a boon to library staff at public libraries, high school libraries, academic libraries, and other research institutions, with concentrated coverage of Data sources for frequently researched subjects such as agriculture, the earth sciences, economics, energy, political science, transportation, and many more The basics of data reference along with an overview of the most useful sources, focusing on free online sources of reliable statistics like government agencies and NGOs Statistical datasets, and how to understand and make use of them How to use article databases, WorldCat, and subject experts to find data Methods for citing data Survey Documentation and Analysis (SDA) software This guide cuts through the data jargon to help librarians and researchers find exactly what they're looking for.
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.
Current Catalog
Author: National Library of Medicine (U.S.)
Publisher:
ISBN:
Category : Medicine
Languages : en
Pages : 1728
Book Description
First multi-year cumulation covers six years: 1965-70.
Publisher:
ISBN:
Category : Medicine
Languages : en
Pages : 1728
Book Description
First multi-year cumulation covers six years: 1965-70.
Chronic Illness in Canada
Author: Joseph Osuji
Publisher: Jones & Bartlett Publishers
ISBN: 1449681948
Category : Medical
Languages : en
Pages : 593
Book Description
Adapted from our best-selling text, Chronic Illness: Impact and Intervention, Eighth Edition by Pamala D. Larsen and Ilene Morof Lubkin, this text includes recent definitions and models of care aimed towards chronic disease management (CDM) currently used in Canada. Canadian and global perspectives on chronic illness management are addressed throughout the text, and chapters on the role of primary health care in chronic care, family nursing, global health, and chronic illness are included to address the needs of nursing curriculum standards in Canada. Key Features *Chapter on complementary therapies within a Canadian health context *Every chapter is updated to include Canadian content and an emphasis on global healthcare *Contains theoretical and practical perspectives to address the continuing emergence of chronic illness in Canada and the world
Publisher: Jones & Bartlett Publishers
ISBN: 1449681948
Category : Medical
Languages : en
Pages : 593
Book Description
Adapted from our best-selling text, Chronic Illness: Impact and Intervention, Eighth Edition by Pamala D. Larsen and Ilene Morof Lubkin, this text includes recent definitions and models of care aimed towards chronic disease management (CDM) currently used in Canada. Canadian and global perspectives on chronic illness management are addressed throughout the text, and chapters on the role of primary health care in chronic care, family nursing, global health, and chronic illness are included to address the needs of nursing curriculum standards in Canada. Key Features *Chapter on complementary therapies within a Canadian health context *Every chapter is updated to include Canadian content and an emphasis on global healthcare *Contains theoretical and practical perspectives to address the continuing emergence of chronic illness in Canada and the world
Resources in Education
Author:
Publisher:
ISBN:
Category : Education
Languages : en
Pages : 748
Book Description
Publisher:
ISBN:
Category : Education
Languages : en
Pages : 748
Book Description
Nursing Foundations
Author: Beverly Witter Du Gas
Publisher: Scarborough, Ont. : Prentice Hall Canada
ISBN: 9780138995270
Category : Medical
Languages : en
Pages : 1438
Book Description
Publisher: Scarborough, Ont. : Prentice Hall Canada
ISBN: 9780138995270
Category : Medical
Languages : en
Pages : 1438
Book Description
MEDINFO 2007
Author: K.A. Kuhn
Publisher: IOS Press
ISBN: 1607502666
Category : Computers
Languages : en
Pages : 1532
Book Description
The theme of Medinfo2007 is “Building Sustainable Health Systems”. Particular foci are health challenges for the developing and developed world, the social and political context of healthcare, safe and effective healthcare, and the difficult task of building and maintaining complex health information systems. Sustainable health information systems are those that can meet today’s needs without compromising the needs of future generations. To build a global knowledge society, there needs to be an increased cooperation between science and technology and access to high-quality knowledge and information. The papers presented are refereed and from all over the world. They reflect the breadth and depth of the field of biomedical and health informatics, covering topics such as; health information systems, knowledge and data management, education, standards, consumer health and human factors, emerging technologies, sustainability, organizational and economic issues, genomics, and image and signal processing. As this volume carries such a wide collection, it will be of great interest to anyone engaged in biomedical and health informatics research and application.
Publisher: IOS Press
ISBN: 1607502666
Category : Computers
Languages : en
Pages : 1532
Book Description
The theme of Medinfo2007 is “Building Sustainable Health Systems”. Particular foci are health challenges for the developing and developed world, the social and political context of healthcare, safe and effective healthcare, and the difficult task of building and maintaining complex health information systems. Sustainable health information systems are those that can meet today’s needs without compromising the needs of future generations. To build a global knowledge society, there needs to be an increased cooperation between science and technology and access to high-quality knowledge and information. The papers presented are refereed and from all over the world. They reflect the breadth and depth of the field of biomedical and health informatics, covering topics such as; health information systems, knowledge and data management, education, standards, consumer health and human factors, emerging technologies, sustainability, organizational and economic issues, genomics, and image and signal processing. As this volume carries such a wide collection, it will be of great interest to anyone engaged in biomedical and health informatics research and application.