A Nordic survey to monitor citizens use and experience with eHealth PDF Download

Author: Eriksen, Jeppe
Publisher: Nordic Council of Ministers
ISBN: 928937697X
Category : Medical
Languages : en
Pages : 328

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Book Description
Available online: https://pub.norden.org/temanord2023-541/ The Nordic eHealth Research Network (NeRN) conducted a comprehensive survey study across Denmark, Finland, Iceland, Norway, and Sweden to gauge Nordic citizens' experiences, usage patterns, and attitudes regarding digital healthcare systems. Employing a cross-sectional design, the study aims to furnish policymakers and decision-makers with quantitative data that can inform evidence-based policies in the realm of digital healthcare. Consequently, the study's outcomes enable cross-country comparisons, facilitating targeted interventions and policies. Various stakeholders, including patient associations, professional bodies, interest groups, healthcare practitioners, and citizens, can leverage these research-driven insights.

Author: Rissanen, Riikka
Publisher: Nordic Council of Ministers
ISBN: 9289377054
Category : Computers
Languages : en
Pages : 106

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Book Description
Available online: https://pub.norden.org/temanord2023-542/ The Handbook of cross-border data exchange is part of the project ‘World’s smoothest cross-border mobility and daily life through digitalisation’, with a broader objective of streamlining the daily life and mobility of citizens and companies across borders by facilitating the exchange of data between authorities in the Nordic and Baltic countries. The handbook is collects the lessons learned in cross-border data exchange in the fields of studying and using healthservices in another Nordic and Baltic country, and in the use of Nordic and Baltic legal databases. The aim is to provide the reader with insights and ideas for future development by pinpointing identified networks, interesting initiatives, and potential funding mechanisms, as well as highlighting case examples that could be utilised in the development of cross-border collaboration.

Author: Nøhr, Christian
Publisher: Nordic Council of Ministers
ISBN: 9289365242
Category : Political Science
Languages : en
Pages : 95

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Book Description
Online publication: https://pub.norden.org/temanord2020-505/ Abstract [en] The Nordic eHealth Research Network (NeRN) was established by the Nordic Council of Ministers (NCM) eHealth group in 2012. The objective was to develop, test, and evaluate a common set of indicators for monitoring eHealth in the Nordic countries, Greenland, Faroe Islands and Aaland, for use to support the development of Nordic welfare.The results of the network’s first three mandate periods were published in the Nordic Council of Ministers reports. Links can be found on the NeRN web page: https://thl.fi/en/web/thlfi-en/research-and-expertwork/projects-and-programmes/nordic-ehealth-research-network-nern This publication reports the outcomes of the fourth mandate period focusing on five tasks: 1 New analysis of eHealth policies in the Nordic countries. 2 Updating common indicators in accordance with emerging new policy goals. 3 Developing a Nordic model survey to monitor citizen views on eHealth. 4 Cyber security in the Nordic Countries. 5 Personas for users of indicators of eHealth availability, use and outcome in the Nordic countries.

Author: Hyppönen, Hannele
Publisher: Nordic Council of Ministers
ISBN: 928934976X
Category : Business & Economics
Languages : en
Pages : 87

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Book Description
This report proposes a long-term management of earlier NeRN work to be utilized also in the European and OECD context, and indicators on patients and citizens' use and experiences of eHealth services. An update to prior eHealth policy analysis shows an increase on governance and stakeholder involvement in all countries. The existing NeRN indicators form a good basis for continued monitoring. Common eHealth indicators from citizens’ point of view are needed. Current Nordic citizen surveys offer a good basis for this. Decisions on governance of eHealth benchmarking work and of collaboration between several different reporting organisations are required for long-term maagement on eHealth benchmarking. With very similar eHealth policy goals, the EU, WHO, and OECD should join forces in defining common indicators to be collected nationally and reported internationally (e.g. by Eurostat).

Author: A. Ugon
Publisher: IOS Press
ISBN: 1614998523
Category : Medical
Languages : en
Pages : 996

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Book Description
The domain of eHealth faces ongoing challenges to deliver 21st century healthcare. Digitalization, capacity building and user engagement with truly interdisciplinary and cross-domain collaboration are just a few of the areas which must be addressed. This book presents 190 full papers from the Medical Informatics Europe (MIE 2018) conference, held in Gothenburg, Sweden, in April 2018. The MIE conferences aim to enable close interaction and networking between an international audience of academics, health professionals, patients and industry partners. The title of this year’s conference is: Building Continents of Knowledge in Oceans of Data – The Future of Co-Created eHealth, and contributions cover a broad range of topics related to the digitalization of healthcare, citizen participation, data science, and changing health systems, addressed from the perspectives of citizens, patients and their families, healthcare professionals, service providers, developers and policy makers. The second part of the title in particular has attracted a large number of papers describing strategies to create, evaluate, adjust or deliver tools and services for improvements in healthcare organizations or to enable citizens to respond to the challenges of dealing with health systems. Papers are grouped under the headings: standards and interoperability, implementation and evaluation, knowledge management, decision support, modeling and analytics, health informatics education and learning systems, and patient-centered services. Attention is also given to development for sustainable use, educational strategies and workforce development, and the book will be of interest to both developers and practitioners of healthcare services.

Author: Nordic Council of Ministers
Publisher: Nordic Council of Ministers
ISBN: 9289325267
Category : Science
Languages : en
Pages : 122

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Book Description
The Nordic eHealth Research Network was established in 2012 as a forum for policy makers and researchers to jointly work towards measurable policy goals and data that can be exploited to steer decision making related to goals and their implementation. This report describes first results of the Network: eHealth policy analysis and first common Nordic eHealth indicators. The results show similarities and also some differences in the eHealth policies, priorities and implementation. Interesting similarities and differences in availability and use of eHealth services in the Nordic countries were found with the first comparable eHealth indicators. The results create a basis for Evidence-based policy making as well as benchmarking and learning best practices from each other.

Author: Ursula H. Hübner
Publisher: Springer Nature
ISBN: 303091237X
Category : Medical
Languages : en
Pages : 850

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Book Description
This new edition of the classic textbook on health informatics provides readers in healthcare practice and educational settings with an unparalleled depth of information on using informatics methods and tools. However, this new text speaks to nurses and — in a departure from earlier editions of this title — to all health professionals in direct patient care, regardless of their specialty, extending its usefulness as a textbook. This includes physicians, therapists, pharmacists, dieticians and many others. In recognition of the evolving digital environments in all healthcare settings and of interprofessional teams, the book is designed for a wide spectrum of healthcare professions including quality officers, health information managers, administrators and executives, as well as health information technology professionals such as engineers and computer scientists in health care. The book is of special interest to those who bridge the technical and caring domain, particularly nurse and medical informaticians and other informaticians working in the health sciences. Nursing Informatics: An Interprofessional and Global Perspective contains real-life case studies and other didactic features to illustrate the theories and principles discussed, making it an ideal resource for use within health and nursing informatics curricula at both undergraduate and graduate level, as well as for workforce development. It honors the format established by the previous editions by including a content array and questions to guide the reader. Readers are invited to look out of the box through a dedicated global perspective covering health informatics applications in different regions, countries and continents.

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: Centers of Disease Control
Publisher: World Health Organization
ISBN: 928905137X
Category : Law
Languages : en
Pages : 116

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Book Description
"The principal authors were Carrie Beth Peterson (Consultant in eHealth and Innovation, WHO Regional Office for Europe), Clayton Hamilton (Editor-in-chief and Unit Leader, eHealth and Innovation in the Division of Information, Evidence, Research and Innovation, WHO Regional Office for Europe) and Per Hasvold (WHO Collaborating Centre for eHealth and Telemedicine at the Norwegian Centre for Integrated Care and Telemedicine, Troms, Norway)."--Page viii.

Author: Hanna Falk Erhag
Publisher: Springer Nature
ISBN: 3030780635
Category : Social Science
Languages : en
Pages : 254

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Book Description
This open access book provides insight on how to interpret capability in ageing – one’s individual ability to perform actions in order to reach goals one has reason to value – from a multidisciplinary approach. With for the first time in history there being more people in the world aged 60 years and over than there are children below the age of 5, the book describes this demographic trends as well as the large global challenges and important societal implications this will have such as a worldwide increase in the number of persons affected with dementia, and in the ratio of retired persons to those still in the labor market. Through contributions from many different research areas, it discussed how capability depends on interactions between the individual (e.g. health, genetics, personality, intellectual capacity), environment (e.g. family, friends, home, work place), and society (e.g. political decisions, ageism, historical period). The final chapter summarizes the differences and similarities in these contributions. As such this book provides an interesting read for students, teachers and researchers at different levels and from different fields interested in capability and multidisciplinary research.