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Cet ouvrage porte sur la communication pharmaceutique et son évolution; la médiatisation des découvertes pharmacologiques; la couverture des crises entourant certains médicaments vedettes; le rôle que joue Internet; la promotion d'une meilleure utilisation des médicaments; la régulation de la publicité; et, l'éducation des consommateurs.
With computerized health information receiving unprecedented government support, a group of health policy scholars analyze the intricate legal, social, and professional implications of the new technology. These essays explore how Health Information Technology (HIT) may alter relationships between physicians and patients, physicians and other providers, and physicians and their home institutions. Taken together, these investigations cast new light on the challenges and opportunities presented by HIT.
The Political Economy of Pharmaceutical Clinical Trials
Focusing on the professional roles of those involved, as well as key research practices, Fisher assesses the risks and advantages for physicians and patients alike when pharmaceutical drug studies are used as an alternative to standard medical care.
The Human and Ecological Cost of Colonial Silver Mining in the Andes
On the basis of an examination of the colonial mercury and silver production processes and related labor systems, Mercury, Mining, and Empire explores the effects of mercury pollution in colonial Huancavelica, Peru, and Potosí, in present-day Bolivia. The book presents a multifaceted and interwoven tale of what colonial exploitation of indigenous peoples and resources left in its wake. It is a socio-ecological history that explores the toxic interrelationships between mercury and silver production, urban environments, and the people who lived and worked in them. Nicholas A. Robins tells the story of how native peoples in the region were conscripted into the noxious ranks of foot soldiers of proto-globalism, and how their fate, and that of their communities, was -- and still is -- chained to it.
Égales devant la santé?
Le système de santé canadien, bien qu’universel, présente un portrait contrasté des états de santé et de l’espérance de vie. Si les résidents de Richmond en Colombie-Britannique peuvent espérer vivre 81 ans, ceux de la région du Nunavik ne peuvent guère imaginer dépasser 65 ans. Revenu, éducation et littératie sont quelques uns des déterminants qui entraînent une variation dans la distribution de la bonne et de la mauvaise santé.Qu’advient-il lorsqu’on compare les profils de santé des communautés de langue officielle minoritaire à la communauté linguistique majoritaire? Ces communautés ont-elles accès aux mêmes services de santé et dans les mêmes conditions? Ce sont là les questions sur lesquelles se penchent les auteurs en analysant les enquêtes nationales de santé produites par Statistique Canada, plus particulièrement l’Enquête nationale de santé dans les collectivités canadiennes (ESCC). Ils examinent en premier lieu le concept même de minorité nationale et de groupe en situation minoritaire dans le contexte canadien ainsi que la situation démographique et sociopolitique de ces groupes. Ils posent ensuite le cadre théorique qui leur a permis d’intégrer le fait minoritaire parmi les déterminants de la santé et présentent les résultats de recherche qui exposent les différences en matière de santé en défaveur des minorités linguistiques. Enfin, ils ouvrent la réflexion sur la perspective canadienne sur la santé, notamment en termes de politique et d’équité.
Truth and Lies in the Age of AIDS
In the era of the Internet and Oprah, in which formerly taboo information is readily available or freely confided, secrecy and privacy have in many ways given way to an onslaught of confession. Yet for those who are HIV positive, decisions about disclosure of their diagnosis force them to confront intimate, fundamental, and rarely discussed questions about truth, lies, sex, and trust. Drawing from interviews with over seventy gay men and women, intravenous drug users, sex workers, bisexual men, and heterosexual men and women, the authors provide a detailed portrait of moral, social, and psychological decision making. The interviews convey the complex emotions of love, lust, longing, hope, despair, and fear that shape individual dilemmas about whether to disclose to, deceive, or trust others concerning this disease. Some of those interviewed revealed their diagnosis widely; others told no one. Some struggled and ultimately told their partners; others spoke in codes or half-truths. One woman discovered her husband's diagnosis in a diary; when confronted, he denied it. Each year in the United States, 40,000 new cases of HIV arise, yet approximately one-third of the 900,000 Americans who are infected do not know it. As treatments have improved, unsafe sexual behavior has increased and efforts at prevention have stalled. Many of those infected continue to fear and experience rejection and discrimination. Addressing broad debates about the nature of secrecy, morality, and silence, this book explores public policy questions in the light of the nuanced, private decisions that are shaping the course of an epidemic and have broader indications for all.
Cultural and Biocultural Perspectives
Drunk Driving since 1900
Don’t drink and drive. It's a deceptively simple rule, but one that is all too often ignored. And while efforts to eliminate drunk driving have been around as long as automobiles, every movement to keep drunks from driving has hit some alarming bumps in the road. Barron H. Lerner narrates the two strong—and vocal—sides to this debate in the United States: those who argue vehemently against drunk driving, and those who believe the problem is exaggerated and overregulated. A public health professor and historian of medicine, Lerner asks why these opposing views exist, examining drunk driving in the context of American beliefs about alcoholism, driving, individualism, and civil liberties. Angry and bereaved activist leaders and advocacy groups like Mothers Against Drunk Driving campaign passionately for education and legislation, but even as people continue to be killed, many Americans remain unwilling to take stronger steps to address the problem. Lerner attributes this attitude to Americans’ love of drinking and love of driving, an inadequate public transportation system, the strength of the alcohol lobby, and the enduring backlash against Prohibition of the 1920s. The stories of people killed and maimed by drunk drivers are heartrending, and the country’s routine rejection of reasonable strategies for ending drunk driving is frustratingly inexplicible. This book is a fascinating study of the culture of drunk driving, grassroots and professional efforts to stop it, and a public that has consistently challenged and tested the limits of individual freedom. Why, despite decades and decades of warnings, do people still choose to drive while intoxicated? One for the Road provides crucial historical lessons for understanding the old epidemic of drunk driving and the new epidemic of distracted driving. Praise for Barron H. Lerner’s award-winning When Illness Goes Public: Celebrity Patients and How We Look at Medicine "Lerner has done a beautiful job of tracing the degree to which celebrity patients have reflected and shaped the modern American understanding of doctors, patients, and illness."—New England Journal of Medicine "Lerner has created a powerful prism through his thoughtful exploration of celebrity illness, highlighting societal and cultural forces that widely affect public and private health care decisions."—Journal of the American Medical Association "We can learn quite a bit about our society, culture, and values from the way celebrities' illnesses are publicly portrayed . . . Lerner is at his best when he uses his considerable narrative skills to place these stories into their broader historical, cultural, and ethical contexts."—American Journal of Bioethics "In Lerner's capable hands, these dozen stories in their retelling are both colorfully dramatic narratives, ripped from the headlines (as the saying now goes) and also probing samples of historically specific contingencies and shifting attitudes."—Bulletin of the History of Medicine
People and bubonic plague have a long and tragic history. When health officials in San Francisco thought they discovered plague in their city’s Chinatown in 1900, they responded with intrusive, controlling, and arbitrary measures that touched off a sociocultural clash still relevant today. Guenter B. Risse’s history of this epidemic features the tale of desperately ill Wong Chut King, believed to be the initial person infected, and is the first to incorporate the voices of those living in Chinatown at the time. Lasting until 1904, the plague in San Francisco's Chinatown reignited racial prejudices, re-sparked efforts to remove the Chinese from their district, and created new tensions among local, state, and federal public health officials quarreling over the presence of the deadly disease. Risse's rich, nuanced narrative of the event draws from a variety of sources, including Chinese-language news reports and other accounts. He addresses the ecology of Chinatown, the approaches taken by Chinese and Western medical practitioners, and the effects of quarantine plans on Chinatown and its residents. Risse explains how the presence of plague threatened California’s agricultural economy and San Francisco’s leading commercial role with Asia, discusses why it brought on a wave of fear mongering that drove perceptions and intervention efforts, and describes how Chinese residents organized and successfully opposed government quarantines and evacuation plans in federal court. In probing public health interventions in the context of one of the most visible ethnic communities in United States history, Plague, Fear, and Politics in San Francisco’s Chinatown offers insight into the clash of Eastern and Western cultures in a time of medical emergency.