Judith Healy - Böcker

Health care systems in developed countries must respond to increasingly diverse populations given greater population movements as a result of globalization. We all share a common humanity yet we each have different health care needs, depending on whether we are young or old, men or women, rich or poor, disabled or able-bodied, from different ethnic and indigenous groups, or citizens or asylum-seekers. Our membership of these societal groups shapes to some extent our health needs and our use of health services. But policy-makers and professionals often seem blind to this diversity. Some groups make special claims upon the state and have different expectations regarding health care. What are the barriers to people receiving equitable health care? Should mainstream services be made more responsive to the needs of different people, or is it necessary to set up alternative health care services? The chapters in this book discuss countries and population groups that illustrate different responses to claimant groups and different ways of delivering health services.For the first time this book brings draws together examples of how to deal with diversity from health systems across the industrialized world. It considers population groups within countries and takes a broad approach, studying inherent population diversity (age, sex), citizen issues (migrants, asylum seekers) and ethnic and indigenous groups (multiculturalism in the UK, Roma in Europe, New Zealand Maori, Australian Aborigines). It identifies barriers to accessing health care services by diverse populations and cultural groups within different countries and considers the advantages and disadvantages of different delivery models for different population groups.This book provides an unparalleled breadth of perspectives from which to draw conclusions about how to meet the needs of societies characterised by diversity.

Responding to the public concern caused by recent hospital scandals and accounts of unintended harm to patients, this author draws on her experience of analysing the health care systems of over a dozen countries and examines whether greater regulation has increased patient safety and health care quality. The book adopts a new approach to mapping developments in health care systems in Europe, North America and Australia and pieces together evidence of which regulatory strategies and mechanisms work well to ensure safer patient care. It identifies the regulatory bodies, the regulatory principles and the implementation strategies adopted to improve governance in health care systems and suggests a conceptual framework for responsive regulation. The book will be of interest to government actors, health care professionals and medico-legal scholars.