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Author: Dora B. Weiner
Publisher:
ISBN:
Category : Medical
Languages : en
Pages : 472
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Book Description
In The Citizen-Patient in Revolutionary and Imperial Paris, Dora B. Weiner examines the experiences of the sick and handicapped indigent men, women, and children in Paris during the French Revolution and empire. Weiner argues that significant groups of Revolutionary physicians and reformers interpreted equality to include every citizen's right to health care. These reformers faced political, religious, and professional opposition, and daunting problems of funding. And they needed the participation of the poor as "citizen-patients", patients with both rights and duties, who acted as responsible partners in the pursuit and maintenance of public and personal health. Integrating the social history of medicine into the general history of the French Revolution, this book adds a new, medical facet to the meaning of equality while broadening the medical history of the Revolution by paying attention to the social history of the patient.
Author: Dora B. Weiner
Publisher:
ISBN:
Category : Medical
Languages : en
Pages : 472
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Book Description
In The Citizen-Patient in Revolutionary and Imperial Paris, Dora B. Weiner examines the experiences of the sick and handicapped indigent men, women, and children in Paris during the French Revolution and empire. Weiner argues that significant groups of Revolutionary physicians and reformers interpreted equality to include every citizen's right to health care. These reformers faced political, religious, and professional opposition, and daunting problems of funding. And they needed the participation of the poor as "citizen-patients", patients with both rights and duties, who acted as responsible partners in the pursuit and maintenance of public and personal health. Integrating the social history of medicine into the general history of the French Revolution, this book adds a new, medical facet to the meaning of equality while broadening the medical history of the Revolution by paying attention to the social history of the patient.
Author: Joan Costa-Font
Publisher: Cambridge University Press
ISBN: 1108474977
Category : Health & Fitness
Languages : en
Pages : 237
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Book Description
Provides an international, unifying perspective, based on the 'public choice' tradition, to explain how patient-citizens interact with their country's political institutions to determine health policies and outcomes. This volume will appeal to undergraduate and graduate students studying health economics, health policy and public policy.
Author: Alyshia Galvez
Publisher: Rutgers University Press
ISBN: 081355201X
Category : Social Science
Languages : en
Pages : 230
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Book Description
According to the Latina health paradox, Mexican immigrant women have less complicated pregnancies and more favorable birth outcomes than many other groups, in spite of socioeconomic disadvantage. Alyshia Gálvez provides an ethnographic examination of this paradox. What are the ways that Mexican immigrant women care for themselves during their pregnancies? How do they decide to leave behind some of the practices they bring with them on their pathways of migration in favor of biomedical approaches to pregnancy and childbirth? This book takes us from inside the halls of a busy metropolitan hospital’s public prenatal clinic to the Oaxaca and Puebla states in Mexico to look at the ways Mexican women manage their pregnancies. The mystery of the paradox lies perhaps not in the recipes Mexican-born women have for good perinatal health, but in the prenatal encounter in the United States. Patient Citizens, Immigrant Mothers is a migration story and a look at the ways that immigrants are received by our medical institutions and by our society
Author: Council of Europe. Committee of Ministers
Publisher: Council of Europe
ISBN: 9789287145659
Category : Health & Fitness
Languages : en
Pages : 68
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Book Description
Author: Robert Picard
Publisher: Elsevier
ISBN: 0081027591
Category : Science
Languages : en
Pages : 274
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Book Description
Value of Connected Things for Healthcare is based on feedback from members of the LLSA Forum, patients, healthcare professionals, Living Labs, industrialists, researchers and institutional actors confronted with the design, development, implementation and use of these types of tools that penetrate health and communicate data. The term connected object refers to devices that continuously collect data through these objects, providing the state of health of people wherever they are and whatever they do. These objects allow clinical researchers to study new phenomena that have hitherto escaped observations in institutions. However, the mobilization of these technologies in this context poses technical questions because the requirements of a remote, continuous operation are high. What is termed connected health emphasizes the human dimension of the subject, i.e., citizens, patients, health professionals, territorial communities, professional networks, institutions and associations. The questions of who benefits and ethical considerations are paramount to this discussion. - Brings awareness of the complexity of connected objects - Presents examples that highlight the use of connected codes - Describes new devices and related services - Identifies the challenges associated with solving these problems
Author: Nortin M. Hadler, M.D.
Publisher: Univ of North Carolina Press
ISBN: 0807869236
Category : Health & Fitness
Languages : en
Pages : 273
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Book Description
For those fortunate enough to reside in the developed world, death before reaching a ripe old age is a tragedy, not a fact of life. Although aging and dying are not diseases, older Americans are subject to the most egregious marketing in the name of "successful aging" and "long life," as if both are commodities. In Rethinking Aging, Nortin M. Hadler examines health-care choices offered to aging Americans and argues that too often the choices serve to profit the provider rather than benefit the recipient, leading to the medicalization of everyday ailments and blatant overtreatment. Rethinking Aging forewarns and arms readers with evidence-based insights that facilitate health-promoting decision making. Over the past decades, Hadler has established himself as a leading voice among those who approach the menu of health-care choices with informed skepticism. Only the rigorous demonstration of efficacy is adequate reassurance of a treatment's value, he argues; if it cannot be shown that a particular treatment will benefit the patient, one should proceed with caution. In Rethinking Aging, Hadler offers a doctor's perspective on the medical literature as well as his long clinical experience to help readers assess their health-care options and make informed medical choices in the last decades of life. The challenges of aging and dying, he eloquently assures us, can be faced with sophistication, confidence, and grace.
Author: Walter Lorenzo Sheldon
Publisher:
ISBN:
Category : Citizenship
Languages : en
Pages : 480
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Book Description
Author: Agency for Healthcare Research and Quality/AHRQ
Publisher: Government Printing Office
ISBN: 1587634333
Category : Medical
Languages : en
Pages : 385
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Book Description
This User’s Guide is intended to support the design, implementation, analysis, interpretation, and quality evaluation of registries created to increase understanding of patient outcomes. For the purposes of this guide, a patient registry is an organized system that uses observational study methods to collect uniform data (clinical and other) to evaluate specified outcomes for a population defined by a particular disease, condition, or exposure, and that serves one or more predetermined scientific, clinical, or policy purposes. A registry database is a file (or files) derived from the registry. Although registries can serve many purposes, this guide focuses on registries created for one or more of the following purposes: to describe the natural history of disease, to determine clinical effectiveness or cost-effectiveness of health care products and services, to measure or monitor safety and harm, and/or to measure quality of care. Registries are classified according to how their populations are defined. For example, product registries include patients who have been exposed to biopharmaceutical products or medical devices. Health services registries consist of patients who have had a common procedure, clinical encounter, or hospitalization. Disease or condition registries are defined by patients having the same diagnosis, such as cystic fibrosis or heart failure. The User’s Guide was created by researchers affiliated with AHRQ’s Effective Health Care Program, particularly those who participated in AHRQ’s DEcIDE (Developing Evidence to Inform Decisions About Effectiveness) program. Chapters were subject to multiple internal and external independent reviews.
Author: L. Sayce
Publisher: Palgrave
ISBN: 9780312227333
Category : Political Science
Languages : en
Pages : 292
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Book Description
This book proposes theoretical models and practical strategies for tackling the widespread social exclusion faced by people diagnosed mentally ill. Based primarily on research in the US and UK but with reference to other international examples, it analyses evidence of discrimination and the effectiveness of different remedies: disability discrimination law, work to re-frame media and cultural images, grassroots inclusion programmes, challenges to the 'nimby' factor. It places the growing user/survivor and disability movements as central to achieving any radical change.
Author: Annemarie Mol
Publisher: Routledge
ISBN: 1134053177
Category : Health & Fitness
Languages : en
Pages : 142
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Book Description
What is ‘good care’ and does more choice lead to better care? This innovative and compelling work investigates good care and argues that the often touted ideal of ‘patient choice’ will not improve healthcare in the ways hoped for by its advocates.
