社会福祉・社会保障 — 全 下位分類

The COVID-19 pandemic in the United States is a classic tragedy of destruction following errors in judgment. Naomi Zack presents social and political aspects of this disaster as it unfolded in public health through federal and local government structures, society, culture, and the economy. Federalism combined with politics in facing and denying the SARS-CoV2 pandemic has revealed both weaknesses and strengths.
Preparation was woefully inadequate for the 2020 tidal wave of COVID-19 that broke over the medical system, the educational system, the lives of the poor, essential workers, racial and ethnic minorities, the elderly, and women, especially. Rhetoric and conspiracy theories flourished, as Red and Blue Americans politicized the pandemic. Police reform became urgent after billions witnessed George Floyd's death. The war of the statues evoked new conflicts over free speech.
The X-ray nature of COVID-19 has revealed the United States to itself, in character, incompetence, superstition, and injustice, but also in dedication to caring for others and abiding resilience. The core of democracy held after the 2020 election but vigilance is newly important and required. As a record of this US Plague Year and an argument for why we need to prepare for Climate Change, as well as the next pandemic, this book is an essential resource for every student, scholar, and citizen.

This multidisciplinary volume combines academic research with first-hand accounts of homelessness. It describes how people affected by homelessness are perceived as objects through the process of Othering. It also provides examples of how such Othering can be overcome through collaboration, and by providing a platform for people affected by homelessness.

The volume argues that stereotypical representations of homelessness, while useful for charity fundraising, do more harm than good. It concludes that organisations tasked with dealing with homelessness must include greater representation from people with direct 'lived experience' of homelessness.

This book analyzes how COVID-19 impacted politics and how politics shaped the response to the pandemic in Latin America, the region which has become the epicenter of the global health crisis started in China. The volume brings together studies carried out in eight countries of the region - Argentina, Brazil, Chile, Colombia, Ecuador, Mexico, Nicaragua and Uruguay - and show how the impacts and outcomes varied a lot across the region depending on the political processes under way in each country in the years preceding the pandemic and on the political responses adopted by each government to deal with the health crisis.

The volume is divided into four parts, each one dedicated to a specific dimension of the relation between politics and COVID-19 in Latin America. The first part is dedicated to denialism, and presents three case studies of governments that denied the importance of the health crisis: Brazil, Mexico and Nicaragua. The second part takes Uruguay and Colombia as two opposite examples of successful and failed state action against COVID-19. The third part analyzes how social movements faced the pandemic in Brazil and Chile. Finally, the fourth part analyzes how public opinion reacted to political responses to COVID-19 in four countries: Argentina, Brazil, Ecuador and Mexico.

COVID-19's Political Challenges in Latin America will be a valuable resource for political scientists, sociologists and other social scientists interested in understanding how the pandemic affected politics and how politics affected the fight against the biggest health crisis faced by humanity in the last hundred years.

How the authority of medicine is continuously shaped by relationships among physicians, industry, colleagues, and organizations

Exploring how the authority of medicine is controlled, negotiated, and organized, Managing Medical Authority asks: How is knowledge shared throughout the profession? Who makes decisions when your heart malfunctions-physicians, hospital administrators, or private companies who sell pacemakers? How do physicians gain and keep their influence? Arguing that medicine's authority is managed in collegial competition across venues, Daniel Menchik examines the full range of stakeholders driving the direction of the field: medical trainees, clinicians, researchers, administrators, and even the corporations that develop groundbreaking technologies enabling longer and better lives.

Menchik takes us into Superior Hospital to witness surgeries and executive negotiations. He moves outside the hospital to watch professional committees craft standards for treatments, case management, and professional ethics. At industry-sponsored meetings, he observes company representatives who train some experienced doctors on their technologies, while deterring others who they think might injure patients. Using an innovative ethnographic approach tying individual actions and their collective consequences, he considers how stakeholders ally across the various venues of medicine, even as they are sometimes pressed into competition within those venues. Menchik finds that these alliances and rivalries strengthen the authority of medicine as a whole. From place to place, and group to group, we see how a medical specialty renews and reinvigorates itself.

Beginning within the walls of the hospital, and moving to the professional and commercial venues that shape it, Managing Medical Authority offers an agenda-setting take on the social organization of medical authority.

This book is a collection of essays from across Africa which highlight the roles of beliefs and traditions in health behaviour. Chapters address mental health, risk perception, stigma, reproductive health, religion and health. The book also examines conceptual approaches in health communication and community development, both western and indigenous.

Specific topics include Alzheimer's, HIV and stigma; perception of risk from obesity, HIV prevention and preeclampsia; doctor-patient relationship and health beliefs of birth attendants; culture and mental health access and social media effects on mental health; the complementary use of contemporary and indigenous communication strategies and the accommodation of science by religious leaders during the COVID 19 pandemic.

The book, which starts by examining global inequalities in health, proposes an African approach informed by problematisation as theorised by Foucault and Freire, to unpack habits and social problems. It ends by asking the question: "Is science enough" and making a strong case for health enabling environments alongside science communication.

Healthcare history is more than leeches and drilling holes in skulls. It is stories of scientific failures and triumphs.
Exploring American Healthcare through 50 Historic Treasures presents a visual and narrative history of health and medicine in the United States, tracing paradigm shifts such as the introduction of anesthesia, the adoption of germ theory, and advances in public health. In this book, museum artifacts are windows into both famous and ordinary people's experiences with healthcare throughout American history, from patent medicines and faith healing to laboratory science.
With 50 vignette-like chapters and 50 color photographs, Exploring American Healthcare through 50 Historic Treasures showcases little-known objects that illustrate the complexities of our relationship with health, such as a bottle from the short period when the Schlitz beer company sold lager that was supposed to be high in vitamin D during the first vitamin craze. It also highlights famous moments in medicine, such as the discovery of penicillin, as illustrated by a mold-culturing pan. Each artifact tells some piece of the story of how its creators or users approached fundamental questions in health. Some of these questions are, "What causes sickness, and what causes health?" and "How much can everyone master the principles of health, and how much do laypeople need to rely on outside authorities?"
Exploring American Healthcare through 50 Historic Treasures describes the days when surgeons worked on patients without anesthesia and wiped their scalpels on their coats, and the day that EMTs raced to provide help when the Twin Towers were attacked in 2001. The book discusses social and cultural influences that have shaped healthcare, providing insight relevant to today's problems and colorful anecdotes along the way.

Drawing on Sir Ian Kennedy's extensive experience in healthcare law, ethics and public policy-making, this book explores vital issues in the law surrounding healthcare and regulation. The book contains a range of published and unpublished essays and speeches with the addition of notes and commentaries by the author that bring the pieces up to the present day.

Those who want to understand developments, from transplants to confidentiality, from COVID-19 to public inquiries to regulation will find a rich seam of rigorous, informed analysis. The author's unique range of experience allows him to share insights on a variety of issues; from the conduct of the disgraced breast surgeon, Ian Paterson, to research at Porton Down, to the economics of innovation in drug development at NICE. His abiding interest in the welfare of children informs his trenchant forensic examination of how children fare in the NHS.

Those involved in or with an interest in law, moral philosophy, and public policy will find much food for thought.

This eminently relevant and thoroughly entertaining book reminds us that understanding more about health care helps us understand the larger world around us.

With technological advances and information sharing so prevalent, health care should be more transparent and easier to access than ever before. So why does it seem like everything about it-from pricing, drug development, and the emergence of new diseases to the intricacies of biologic and precision medicine therapies-is becoming more complex, not less?

Rohit Khanna's Misunderstanding Health examines some of today's most revealing health care trends while imploring us to look at these issues with alacrity, humor, and vigilance. Over the course of eighteen short, engaging chapters, Khanna explains

* how unexamined beliefs can endanger patients, drive cost, and increase bureaucracy
* the "Dr. Google" effect on the ways that we seek (or eschew) care
* why our health care costs more than in any other country
* the unintended consequences of using rating sites like Yelp
* what we can learn about health care from hurricanes
* how social media influencers impact health care
* how artificial intelligence can improve health care
* why health screening programs are so complicated
* what the industry is doing to combat health care fraud
* what the big deal about legalizing medical cannabis is
* how to think about behavioral "nudges" designed to improve health
* why understanding how data are collected is critical to understanding what they can tell us
* and much more

Each provocative and easy-to-read chapter covers a familiar aspect of health care in a clear and succinct way. Offering inquisitive readers a warts-and-all view of American health care, Misunderstanding Health is the book that you'll want to read if you know enough to be frustrated by the system but want a deeper dive into its challenges and opportunities.

Through a tumultuous 20th-century period of revolution and foreign wars, Vietnam's public health system was praised by international observers as a "bright light in an epidemiologically dark world," standing out for its accomplishments in infectious disease control. Since the country's transition to a "market economy with socialist orientation" in the mid-1980s, however, some of these achievements have been reversed as the "renovation" of national systems for welfare and health leaves gaps in the social safety net. A series of cholera outbreaks that spread through Northern Vietnam in 2007-2010 revealed the paradoxes, contradictions, and challenges that Vietnam faces in its post-transition period.

This book presents an anthropological analysis of the political, economic, and infrastructural inputs to these epidemics and suggests how the most commonly repeated accounts of disease spread misdirected public attention and suppressed awareness of risk factors in Vietnam's capital. Drawing a parallel to the experience of novel coronavirus in Asia and beyond, this book reflects on how political priorities, economic forces, and cultural struggles influence the experience and the epidemiology of infectious disease.

This book, written decades into the HIV epidemic, reflects critically on the idea that the socially excluded populations often focused on in HIV research are in fact difficult to access and reach. The author broadly applies the concept 'hard to reach' to characterize populations that researchers find difficult to engage with. Social factors that produce marginalization and ultimately result in people choosing not to engage in research are not captured by the concept of 'hard to reach'. Limited attention has focused on how researchers can address the social factors that result in decisions to not engage in research. Disrupting the ways in which people are conceptualized as 'hard to reach' so as to refocus on transforming social systems and personal values, beliefs and approaches is understudied. This book uses case examples based on HIV research with Indigenous youth, internally displaced women, LGBTQ communities in the Global North and Global South, and persons at the intersection of these identities, to identify successful approaches to working with marginalized and often vulnerable communities and groups. The chapters signal the need for attention to five key social factors when developing successful approaches: context and storytelling; cultural humility; critical hope; imagination and possibility; and love, intimate inquiry, and the beloved community, if nations, individuals and communities are to address the epidemic in a sustainable and impactful way.

The COVID-19 pandemic has disrupted life as we knew it. Lockdowns, self-isolation and quarantine have become a normal part of everyday life. Pandemic surveillance allows governments and corporations to monitor and surveil the spread of the virus and to make sure citizens follow the measures they put in place. This is evident in the massive, unprecedented mobilization of public health data to contain and combat the virus, and the ballooning of surveillance technologies such as contact-tracing apps, facial recognition, and population tracking. This can also be seen as a pandemic of surveillance.

In this timely book, David Lyon tracks the development of these methods, examining different forms of pandemic surveillance, in health-related and other areas, from countries around the world. He explores their benefits and disadvantages, their legal status, and how they relate to privacy protection, an ethics of care, and data justice. Questioning whether this new culture of surveillance will become a permanent feature of post-pandemic societies and the long-term negative effects this might have on social inequalities and human freedoms, Pandemic Surveillance highlights the magnitude of COVID-19-related surveillance expansion. The book also underscores the urgent need for new policies relating to surveillance and data justice in the twenty-first century.

With a global commitment to achieve gender equality by 2030, the SDGs present a historic opportunity to place gender as central to human progress across the globe. Gender equality, which requires the empowerment of all women and girls, is an explicit goal, in addition to being a fundamental prerequisite to and facilitator of most other SDGs. This edited collection provides a range of geographical and geospatial insights, from a variety of disciplinary and country-specific perspectives, to better understand gender and sustainable development. In addition to several African countries, Mexico, Japan, Canada, USA, and Cambodia are featured. A range of topical case studies examine women's domestic and care work, including water collection, breastfeeding, food purchasing, and caring for elderly family members. Access to health care services is examined in the case of breast screening and antenatal care. Women's engagement in the labour force is also addressed, with a specific look at the renewable energy sector; structural barriers to employment are discussed across a number of chapters, with clear strategies to break through these barriers. Finally, theoretical insights are proposed in better understanding and engaging in gendered inequalities in health.

The New Sociology of Ageing explores the challenges and opportunities of ageing as a global force. Alongside globalisation, urbanisation, new technology, climate change, and global pandemics, ageing is transforming life in the twenty-first century.

Through the eyes of a young sociology student and her multigenerational family, this book sets out a new sociological framework to interpret ageing societies. It explores how the 'New Old' - the baby boomer generation - might be mobilised as an agency of social change in transforming later life. It proposes this generation as the co-architects of a new intergenerational social contract for the era ahead, rather than as the recipients of a post-war twentieth-century social contract that society can no longer support. Taking Britain as a case study and societies across the world as examples, Slattery explores emerging revolutions in work and retirement, potential crises in pensions, healthcare and housing, as well as transformations in family life and in our attitudes to sex and death in later life.

This book provides a clear overview of the sociology of ageing. It introduces students to demography as a sociological force of the future, and to the perils and the promises of longevity as societies across the world approach the Hundred-Year Life. This book will be of interest to undergraduate students and early scholars in the social sciences, particularly in sociology, gerontology, social policy, and public health.

This book assesses the implications of the COVID-19 pandemic for the European Union (EU), as well as its response in dealing with an overarching, multidimensional crisis with consequences extending beyond public health safety to political, economic, legal, and institutional arenas.

It argues the pandemic represents a symmetric crisis cutting across countries with different social, economic and political characteristics and which yet - despite favouring cooperative solutions at the supranational level - has largely been met with initial responses of a national, even local, nature. So, how well did the EU perform as a crisis manager in the pandemic crisis?

This book will be of key interest to scholars, students and readers of crisis, pandemic and health management, European Union politics and governance.

Exploring both the intrapersonal (moral) and interpersonal (ethical) nature of death and dying in the context of their development (philosophical), Dying in a Transhumanist and Posthuman Society shows how death and dying have been and will continue to be governed in any given society.

Drawing on transhumanism and discourses about posthumanity, life prolongation and digital life, the book analyses death, dying and grief via the governance of dying. It states that the bio-medical dimensions of our understanding of death and dying have predominated not only the discourses about death in society and the care of the dying, but their policy and practice as well. It seeks to provoke thinking beyond the benefits of technology and within the confinements of the world transhumanists describe.

This book is written for all who have an interest in thanatology (i.e. death studies) but will be useful specifically to those investigating the experiences of dying and grieving in contemporary societies, wherein technology, biology and medicine continuously advance. Thus, the manuscript will be of interest to researchers in a broad range of areas including health and social care, social policy, anthropology, sociology, philosophy, cultural studies, and, of course, thanatology.

A sweeping germ's-eye view of history from human origins to global pandemics

Plagues upon the Earth is a monumental history of humans and their germs. Weaving together a grand narrative of global history with insights from cutting-edge genetics, Kyle Harper explains why humanity's uniquely dangerous disease pool is rooted deep in our evolutionary past, and why its growth is accelerated by technological progress. He shows that the story of disease is entangled with the history of slavery, colonialism, and capitalism, and reveals the enduring effects of historical plagues in patterns of wealth, health, power, and inequality. He also tells the story of humanity's escape from infectious disease-a triumph that makes life as we know it possible, yet destabilizes the environment and fosters new diseases.

Panoramic in scope, Plagues upon the Earth traces the role of disease in the transition to farming, the spread of cities, the advance of transportation, and the stupendous increase in human population. Harper offers a new interpretation of humanity's path to control over infectious disease-one where rising evolutionary threats constantly push back against human progress, and where the devastating effects of modernization contribute to the great divergence between societies. The book reminds us that human health is globally interdependent-and inseparable from the well-being of the planet itself.

Putting the COVID-19 pandemic in perspective, Plagues upon the Earth tells the story of how we got here as a species, and it may help us decide where we want to go.

The 20th volume of Advances in Health Care Management showcases how health care management research helps to further understand grand challenges in health care: what they are, why they exist, the consequences that they have, and what can be done to address them. Grand challenges are large, unresolved problems. "Grand health care challenges" include current events such as the COVID-19 pandemic, and ongoing challenges related to the quadruple aim of health care: improving the health of populations, reducing the cost of healthcare, improving patient care experiences, and improving the experience of working in health care. The book demonstrates that these challenges are amenable to organizational and managerial solutions, and therefore health care management research has many important lessons to contribute.

For this volume, The Contributions of Health Care Management to Grand Health Care Challenges, we define health care management as the planning, direction, and coordination of health services and the management of health care professionals. Included chapters consider five grand challenges facing the health care sector: (1) caring for vulnerable populations; (2) maintaining the health care workforce; (3) translating innovation into practice; (4) sustaining organizations; and (5) navigating pandemics. Each challenge is discussed in its own section and addressed by two chapters that offer different perspectives and approaches to the challenge. Across chapters a variety of methodologies are used including ethnographic case studies, survey data analysis, interviews, literature review, and informed commentary. Together, the chapters in this volume synthesize current information in the field, direct future research efforts, and generate actionable insights for managers and policymakers.

This book discusses preventive actions that have led to reduction in the prevalence of child labor across the world over the 21^st century. It identifies exemplary programs in the area of community prevention that have had exceptional results; for example, the involvement of children in hazardous work globally being reduced by half. It documents a wide range of contexts where concerted action has counteracted social permissiveness towards child labor, including psycho-educational interventions in preventing early school leaving and conditional cash benefits which counteract family poverty. The book presents a set of evidence-based practices that are particularly useful for psychologists, educators, and social workers. More broadly, this book is also of interest to policymakers, professionals, and activists involved in child protection policy or in implementing programs to promote the psychological well-being of children.