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This new text is a complete guide to patient engagement and participation in healthcare, which is a central theme of health policy in the UK and internationally. Based on 250 systematic reviews in the area, this is the most current and comprehensive text on the market.
Spanning 250 years and six generations of one family, these mini-biographies cover a period of dramatic change in British history from the Georgian period up to the twentieth century.
An evidence-based analysis of the opportunities and challenges of moving towards more person-centred health systems.
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This book reports the results of a major study carried out in eight different European countries to look at health policy dilemmas through the eyes of the patient. Drawing on literature reviews, focus groups and a survey of 1,000 people in each of the eight countries, the book addresses how patients no longer see themselves as passive recipients of care: increasingly they expect to be involved in all decisions that affect them.
Despite a policy focus on involving patients in health care and increasing patient autonomy, much covert coercion of patients takes place in everyday healthcare. This book, by a leading patient activist, examines for the first time how the patient movement, which works to improve the quality of healthcare, can actually be considered an emancipation movement when led by its radical elements. In this highly original book the author argues that radical patient groups and individual activists who repeatedly challenge or oppose some standards in healthcare, can be seen as working in the direction of freeing patients from coercion and from its associated injustice and inequality. Combining new academic theory with rich empirical evidence, the book explains how looking at healthcare from an emancipatory perspective could improve its quality as patients experience it. It will appeal to health professionals, managers, patient activists, policy makers and others concerned with the quality of healthcare.
An authoritative, topical, and comprehensive reference to the key concepts and most important traditional and contemporary issues in medical sociology. Contains 35 chapters by recognized experts in the field, both established and rising young scholars Covers standard topics in the field as well as new and engaging issues such as bioterrorism, bioethics, and infectious disease Chapters are thematically arranged to cover the major issues of the sub-discipline Global range of contributors and an international perspective
The detection, reporting, measurement, and minimization of medical errors and harms is now a core requirement in clinical organizations throughout developed societies. This book focuses on this major new area in health care. It explores the nature of medical error, its incidence in different health care settings, and strategies for minimizing errors and their harmful consequences to patients. Written by leading authorities, it discusses the practical issues involved in reducing errors in health care - for the clinician, the health policy adviser, and ethical and legal health professionals.
Improving patient experience is a global priority for health policy-makers and care providers. This book critically examines the various ways in which people's experience of health and healthcare can be recorded, analysed and therefore improved.
From the political and social turmoil of early nineteenth century Britain, a young Welsh doctor emerged in Birmingham to play a leading role in the transformation of the town as physician, political activist, medical reformer, and the borough’s first and most distinctive coroner. Fearless campaigner, socially aware, driven, and fiercely independent, John Birt Davies had unique access to the lives and deaths of ordinary citizens during this turbulent time. He looked after the health of all classes of people, from the families of Lunar Society celebrities to those of the poor and vulnerable living in slums and workhouses. And he played a major role in establishing Birmingham’s first medica...