Atjaunināt sīkdatņu piekrišanu

Privacy and Healthcare Data: 'Choice of Control' to 'Choice' and 'Control' [Hardback]

  • Formāts: Hardback, 264 pages, height x width: 234x156 mm, weight: 635 g
  • Izdošanas datums: 15-Dec-2015
  • Izdevniecība: Routledge
  • ISBN-10: 147242686X
  • ISBN-13: 9781472426864
Citas grāmatas par šo tēmu:
  • Hardback
  • Cena: 210,77 €
  • Grāmatu piegādes laiks ir 3-4 nedēļas, ja grāmata ir uz vietas izdevniecības noliktavā. Ja izdevējam nepieciešams publicēt jaunu tirāžu, grāmatas piegāde var aizkavēties.
  • Daudzums:
  • Ielikt grozā
  • Piegādes laiks - 4-6 nedēļas
  • Pievienot vēlmju sarakstam
  • Formāts: Hardback, 264 pages, height x width: 234x156 mm, weight: 635 g
  • Izdošanas datums: 15-Dec-2015
  • Izdevniecība: Routledge
  • ISBN-10: 147242686X
  • ISBN-13: 9781472426864
Citas grāmatas par šo tēmu:
In order for the information society to realise its full potential, personal data has to be disclosed, used and often shared. This book explores the disclosure and sharing of data within the area of healthcare. Including an overview of how health information is currently managed, the authors argue that with changes in modern society, the idea of personal relationships with a local GP who solely holds and controls your health records is becoming rapidly outdated. The authors aim to encourage and empower patients to make informed choices about sharing their health data. They do this by developing a three-stage theoretical model for change to the roles of the NHS and the individual. The study generates debate to stimulate and inspire new models and policy, and to provoke new visions for the sharing of healthcare data. Such discussion is framed through an exploration of the changing concept of 'privacy' and 'patient control' in healthcare information management. The volume draws on best practices from Europe and the USA and combines these to form a suggested vision for the UK as an early adopter of change. The volume will be essential reading for academics in the field of privacy and data protection, as well as healthcare and informatics professionals across different jurisdictions.

Recenzijas

"The question of how to balance individual privacy interests and community interests in the exploitation of healthcare data is one of the most vexing issues facing privacy scholars. In this important contribution Munns and Basu, by putting patient choice and technology at the centre of the debate, make a key contribution that must be read by all interested parties." - Andrew Murray, London School of Economics, UK

"I found this study of health informatics to be an invaluable addition to the literature on technology regulation and the disruptive capacity of technological innovation, demonstrating our need to re-evaluate core concepts of privacy and data ownership under the forces of information technology." - Robert Lee, University of Birmingham, UK

"Writing in the shadow of 'care.data' the authors suggest that, by an imaginative use of online portals and platforms, the collective interest in sharing healthcare data can be reconciled with the individual interest in controlling access to one's personal health records. The proposal in this timely book merits serious consideration." - Roger Brownsword, King's College London, UK

"This book provides a very important contribution to the debate about consent and the use of health information that we should be having increasingly with the public. Transparency is not only ethically correct but also incredibly empowering, breaking down barriers to information sharing which so often jeopardise safe care. This novel proposal unites traditional privacy theory with innovation, offering mechanisms to make such empowerment a reality." - Dame Fiona Caldicott, FRCPsych, FRCP; National Data Guardian; Chair, Independent Information Governance Oversight Panel (IIGOP)

List of Figures and Tables
vii
Foreword ix
Philip Leith
Acknowledgements xi
PART I INTRODUCTION AND BACKGROUND
1(98)
1 Individual Privacy versus Collective Transparency
3(50)
Aims and Rationale
3(5)
Content and Structure of the Book
8(5)
Information Society and the Need for `Collective Transparency' to Ensure the NHS Survives
13(2)
Definitions as Part of the Issue
15(11)
Current Political Framework
26(7)
The Legal Framework
33(18)
Summary
51(2)
2 Sharing Healthcare Data in Europe and the USA
53(46)
Introduction
53(2)
E-Healthcare in Europe
55(9)
Healthcare Data in Europe
64(17)
E-Healthcare in the USA
81(3)
Healthcare Data in the USA
84(11)
Conclusion
95(4)
PART II THE PROBLEM
99(64)
3 The Theoretical Problem. The Three Issues Necessitating Change: Mindset, Information, Innovation
101(30)
Introduction
101(3)
The Theoretical Problem
104(2)
Informational Privacy in the NHS: Mindset
106(16)
Informational Privacy in the NHS: Information
122(6)
Informational Privacy in the NHS: Innovation
128(2)
Conclusions
130(1)
4 The Practical Problem. Historical Role Reversal: Law and Technology as Vehicles with the Wrong Drivers
131(32)
Introduction
131(1)
Inherent Irony of the Information Revolution
132(6)
Information Governance Controls
138(3)
Access Control
141(8)
Access Monitoring
149(8)
Classifications of Data: the Grey Area
157(2)
Conclusions: The Need for a Technical Consent Recording Mechanism
159(4)
PART III THE PROPOSED SOLUTION
163(66)
5 The Theoretical Solution
165(32)
Introduction
165(6)
Privacy as a Multidimensional Construct: Four Major Shifts
171(7)
The Individual's (MI) Information Revolution: Freedom of Choice
178(11)
The NHS as Information Users: Less Governance and More Transparency for Individuals
189(4)
Conclusion
193(4)
6 The Choice of Control: Putting the Solution into Practice
197(32)
Introduction
197(1)
Innovation -- WIi and MIi Fit Portals
198(18)
Sharing information with other Agencies
216(2)
Implementation: How Can This Be Delivered?
218(3)
Conclusion. Control as an Alter Ego of Privacy -- Empowering and `Control'
221(8)
Bibliography 229(18)
Index 247
Christina Munns is an informatics professional, specialising in the strategic application of information governance and security. She has worked within the national health and care informatics arena for the last decade, holding senior positions across strategy, policy and operations. Recent positions have included Theme Lead and Steering Group member on Dame Fiona Caldicotts 2013 Information Governance Review and Programme Head for Dame Fiona Caldicotts Independent Information Governance Oversight Panel. She was Lead Author of the Confidentiality Guide and managed the development of the 2014 statutory Code of Practice on Confidential Information for health and social care. National appointments include membership of the Care Quality Commissions National Information Governance Committee (CQCs NIGC), acting in an advisory capacity to the CQC Board. Subhajit Basu is Associate Professor in Cyber Law at the School of Law, University of Leeds and a Fellow of the Royal Society for the Encouragement of Arts, Manufactures and Commerce (FRSA) and Research Fellow of African Centre for Cyberlaw and Cybercrime Prevention (ACCP). His principal research and writing is on emerging technologies, especially in the context of the regulation of cyberspace. His scholarship focuses on the regulatory challenges and gaps brought about by the development, use and ubiquitousness of such technologies, in what for many is the unique legal environment of the Internet. As a realist he cares about the opportunities created by these technologies, in particular ensuring an effective adaptive regulatory framework. He is author of the critically acclaimed monograph titled `Global Perspectives on E-Commerce Taxation Law. In addition, he is author of a large number of articles and chapters in scholarly journals and books covering a variety of topics including data protection, privacy, freedom of expression, cybercrime, digital divide, patent e-commerce consumer protec