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164 books match the query 'Medical care' and 11 start with b

cover of Battle: The Nature and Consequences of Civil War Combat

Battle

The Nature and Consequences of Civil War Combat

Edited by Kent Gramm

University of Alabama Press, 2008

A critical, multidisciplinary examination of Civil War combat that interrogates the technological, medical, psychological, and cultural forces shaping battlefield experience and its enduring national legacy.

“In our youth, our hearts were touched with fire,” wrote Oliver Wendell Holmes of his generation’s Civil War days. Through the ages, war stories have gleamed with romantic glory, and American memories of the cataclysmic Civil War inspire pageantry and poetry even today.

The essays in Battle form a corrective to such celebratory histories by examining the lethal realities of Civil War combat—Enlightenment science applied to the creation of weapons that maimed and killed, which far outpaced advances in diet, sanitation, and medical treatment. The book reveals that behind the drums and trumpets, sashes and swords, the armies of the Union and Confederacy alike were haunted by fear, pain, and death.

The collection includes an introduction and afterword by editor Kent Gramm, who also contributes an essay titled “Numbers” that reveals the war in statistics. Paul Fussell contributes a powerful essay titled “The Culture of War.” D. Scott Hartwig examines the face of battle at Gettysburg. Bruce A. Evans discusses medical technology in “Wounds, Death, and Medical Care in the Civil War.” Eric T. Dean challenges the meanings and consequences of combat in “The Awful Shock and Rage of Battle.” The collection is rounded out by Alan T. Nolan’s masterful review of the national consequences of battle and the resultant myth of the Confederacy’s Lost Cause.

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cover of Before the Storm: A Year in the Pribilof Islands, 1941-1942

Before the Storm

A Year in the Pribilof Islands, 1941-1942

Fredericka Martin

University of Alaska Press, 2010

From June of 1941 through the following summer, Fredericka Martin lived with her husband, Dr. Samuel Berenberg, on remote St. Paul Island in Alaska. During that time, Martin delved into the complex history of the Unangan people, and Before the Storm draws from her personal accounts of that year and her research to present a fascinating portrait of a time and a people facing radical change. A government-ordered evacuation of all Aleuts from the island in the face of World War II, which Martin recounts in her journal, proved but the first step in a long struggle by native peoples to gain independence, and, as editor Raymond L. Hudson explains, Martin came to play a significant role in the effort.

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cover of Beyond Method: Philosophical Conversations in Healthcare Research and Scholarship

Beyond Method

Philosophical Conversations in Healthcare Research and Scholarship

Edited by Pamela M. Ironside

University of Wisconsin Press, 2005

Beyond Method provides a forum for scholars across health and human sciences disciplines to explore issues surrounding philosophy, methodology, and epistemology in the context of interpretive scholarship. The essays comprising this volume move beyond the practical descriptions or the "how to" of interpretive methods commonly found in textbooks to explore the contributions, underlying assumptions, limitations, and possibilities embedded within and across particular philosophical, methodological, and epistemological perspectives. They reveal the complexity and richness of understanding that emerges when philosophical issues are explicated within contemporary contexts, illuminating new possibilities for healthcare and human science scholarship.
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cover of Beyond the Siege of Leningrad: One Woman’s Life during and after the Occupation: The Recollections of Evdokiia Vasil’evna Baskakova-Bogacheva

Beyond the Siege of Leningrad

One Woman’s Life during and after the Occupation: The Recollections of Evdokiia Vasil’evna Baskakova-Bogacheva

Pavel Gavrilov

Central European University Press, 2024

This memoir about the experiences of German occupation during the siege of Leningrad (now Saint Petersburg) was written by Moscow-born Evdokiia Vasil’evna Baskakova-Bogacheva (1888–1976), an émigré in Australia, at the age of eighty-one. The text had been forgotten in the Museum of Russian Culture in San Francisco since 1970 until the editors of this volume discovered it.

In the memoirs, after accounting on her youth spent against the background of the First World War and of the two Russian revolutions of 1917, Evdokiia describes the inferno of the Nazi occupation as experienced in a suburb of Leningrad in 1941-43. She survived for nearly two years almost on the front line, within a few kilometers of the blockade ring. As a medical practitioner, she became useful for the occupational authorities and the ever-shrinking town population, until her family was evacuated to the west in October 1943. Besides hunger, discord, disease, the hunt for food and firewood, along with violence and death, Evdokiia’s account deals with various forms of cooperation between Soviet citizens and the new authorities.

All the events she recalls can be confirmed through other sources. The introduction and the detailed notes to the text help the reader to locate Evdokiia’s recollections in time and place, and situate them in their historical context. 

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cover of Bioethics Mediation: A Guide to Shaping Shared Solutions, Revised and Expanded Edition

Bioethics Mediation

A Guide to Shaping Shared Solutions, Revised and Expanded Edition

Nancy Neveloff Dubler

Vanderbilt University Press, 2011

Bioethics Mediation offers stories about patients, families, and health care providers enmeshed in conflict as they wrestle with decisions about life and death. It provides guidance for those charged with supporting the patient's traditional and religious commitments and personal wishes. Today's medical system, without intervention, privileges those within shared cultures of communication and disadvantages those lacking power and position, such as immigrants, the poor, and nonprofessionals. This book gives clinical ethics consultants, palliative care providers, and physicians, nurses, and other medical staff the tools they need to understand and manage conflict while respecting the values of patients and family members.


Conflicts come in different guises, and the key to successful resolution is early identification and intervention. Every bioethics mediator needs to be prepared with skills to listen, "level the playing field," identify individual interests, explore options, and help craft a "principled resolution" -- a consensus that identifies a plan aligned with accepted ethical principles, legal stipulations, and moral rules and that charts a clear course of future intervention.


The organization of the book makes it ideal for teaching or as a handbook for the practitioner. It includes actual cases, modified to protect the privacy of patients, providers, and institutions; detailed case analyses; tools for step-by-step mediation; techniques for the mediator; sample chart notes; and a set of actual role plays with expert mediator and bioethics commentaries. The role plays include:


- discharge planning for a dying patient

- an at-risk pregnancy

- HIV and postsurgical complications in the ICU

- treatment for a dying adolescent

- dialysis and multiple systems failure
Expanded by two-thirds from the 2004 edition, the new edition features two new role plays, a new chapter on how to write chart notes, and a discussion of new understandings of the role of the clinical ethics consultant.

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cover of Biomedicine in an Unstable Place: Infrastructure and Personhood in a Papua New Guinean Hospital

Biomedicine in an Unstable Place

Infrastructure and Personhood in a Papua New Guinean Hospital

Alice Street

Duke University Press, 2014

Biomedicine in an Unstable Place is the story of people's struggle to make biomedicine work in a public hospital in Papua New Guinea. It is a story encompassing the history of hospital infrastructures as sites of colonial and postcolonial governance, the simultaneous production of Papua New Guinea as a site of global medical research and public health, and people's encounters with urban institutions and biomedical technologies. In Papua New Guinea, a century of state building has weakened already inadequate colonial infrastructures, and people experience the hospital as a space of institutional, medical, and ontological instability.

In the hospital's clinics, biomedical practitioners struggle amid severe resource shortages to make the diseased body visible and knowable to the clinical gaze. That struggle is entangled with attempts by doctors, nurses, and patients to make themselves visible to external others—to kin, clinical experts, global scientists, politicians, and international development workers—as socially recognizable and valuable persons. Here hospital infrastructures emerge as relational technologies that are fundamentally fragile but also offer crucial opportunities for making people visible and knowable in new, unpredictable, and powerful ways.
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cover of Birthing Black Mothers

Birthing Black Mothers

Jennifer C. Nash

Duke University Press, 2021

In Birthing Black Mothers Black feminist theorist Jennifer C. Nash examines how the figure of the “Black mother” has become a powerful political category. “Mothering while Black” has become synonymous with crisis as well as a site of cultural interest, empathy, fascination, and support. Cast as suffering and traumatized by their proximity to Black death—especially through medical racism and state-sanctioned police violence—Black mothers are often rendered as one-dimensional symbols of tragic heroism. In contrast, Nash examines Black mothers’ self-representations and public performances of motherhood—including Black doulas and breastfeeding advocates alongside celebrities such as Beyoncé, Serena Williams, and Michelle Obama—that are not rooted in loss. Through cultural critique and in-depth interviews, Nash acknowledges the complexities of Black motherhood outside its use as political currency. Throughout, Nash imagines a Black feminist project that refuses the lure of locating the precarity of Black life in women and instead invites readers to theorize, organize, and dream into being new modes of Black motherhood.
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cover of Body and Soul: The Black Panther Party and the Fight against Medical Discrimination

Body and Soul

The Black Panther Party and the Fight against Medical Discrimination

Alondra Nelson

University of Minnesota Press, 2013

Between its founding in 1966 and its formal end in 1980, the Black Panther Party blazed a distinctive trail in American political culture. The Black Panthers are most often remembered for their revolutionary rhetoric and militant action. Here Alondra Nelson deftly recovers an indispensable but lesser-known aspect of the organization’s broader struggle for social justice: health care. The Black Panther Party’s health activism—its network of free health clinics, its campaign to raise awareness about genetic disease, and its challenges to medical discrimination—was an expression of its founding political philosophy and also a recognition that poor blacks were both underserved by mainstream medicine and overexposed to its harms.

Drawing on extensive historical research as well as interviews with former members of the Black Panther Party, Nelson argues that the Party’s focus on health care was both practical and ideological. Building on a long tradition of medical self-sufficiency among African Americans, the Panthers’ People’s Free Medical Clinics administered basic preventive care, tested for lead poisoning and hypertension, and helped with housing, employment, and social services. In 1971, the party launched a campaign to address sickle-cell anemia. In addition to establishing screening programs and educational outreach efforts, it exposed the racial biases of the medical system that had largely ignored sickle-cell anemia, a disease that predominantly affected people of African descent.

The Black Panther Party’s understanding of health as a basic human right and its engagement with the social implications of genetics anticipated current debates about the politics of health and race. That legacy—and that struggle—continues today in the commitment of health activists and the fight for universal health care.

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cover of Borders of Care: Immigrants, Migrants, and the Fight for Health Care in the United States

Borders of Care

Immigrants, Migrants, and the Fight for Health Care in the United States

Beatrix Hoffman

University of Chicago Press, 2025

Probes the relationship between the immigration and health care systems in the United States.
 
For the roughly ten million undocumented immigrants living in the United States, federal health care coverage is out of reach. Barred from Medicare, Medicaid, and the Affordable Care Act, most rely on hospital emergency rooms when they get sick, or clinics that don’t inquire about immigration status. Further obstacles to health care, including discrimination and the fear of deportation, mean that immigrants, undocumented or not, seek and receive less medical attention than any other population in the country. Yet immigrants haven’t always been ostracized from health care in the United States—providers and activists have for over a century worked to make medical services available to newcomers and migrants, including, at times, the undocumented.
 
Drawing together stories from diverse communities from the mid-nineteenth century to the present, Borders of Care examines how health care in the United States has both included and excluded immigrants. Beatrix Hoffman analyzes both the health and immigration systems, adding to our understanding of why these structures, and the policies that support them, have resisted reform. Moreover, she shows that immigrants, often scapegoated as burdens on the health-care system, have strengthened it through their responses to systemic exclusion. By creating hospitals and clinics, serving as practitioners, fighting for safer workplaces, filing lawsuits, organizing and protesting, immigrants and migrants have improved medical access for everybody and advanced the idea of health care as a universal right. As accessible as it is authoritative, Hoffman’s survey could not be more timely.
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cover of Building Confianza: Empowering Latinos/as Through Transcultural Health Care Communication

Building Confianza

Empowering Latinos/as Through Transcultural Health Care Communication

Dalia Magaña

The Ohio State University Press, 2021

Dalia Magaña’s Building Confianza demonstrates that effective doctor-patient communication in Spanish requires that practitioners not only have knowledge of Spanish but also have transcultural knowledge of Latino/a values and language use. Using linguistic analysis to study real-time doctor-patient interactions, Magaña probes the role of interpersonal language and transcultural competency in improving patient-centered health care with Spanish-speaking Latino/as, highlighting successful examples of how Latino/a cultural constructs of confianza (trust), familismo (family-orientation), personalismo (friendliness), respeto (respect), and simpatía (kindness) can be deployed in medical interactions. She proposes that transcultural interactions entail knowing patients’ cultural values and being mindful about creating an interpersonal connection with patients through small talk, humor, self-disclosure, politeness, and informal language, including language switching and culturally appropriate use of colloquialisms. By explicitly articulating discourse strategies doctors can use in communicating with Spanish-speaking patients, Building Confianza will aid both students and providers in connecting to communities of Spanish speakers in health care contexts and advancing transcultural competence.
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cover of Bullets and Bacilli: The Spanish-American War and Military Medicine

Bullets and Bacilli

The Spanish-American War and Military Medicine

Cirillo, Vincent J.

Rutgers University Press, 2003

For each soldier killed in combat during the Spanish-American War, more than seven died from diseases such as typhoid fever and malaria - a rate higher than that of the Civil War. During a time of rapid medical innovation and discovery, why did these soldiers die so needlessly? This work focuses primarily on military medicine during this conflict. Historian Vincent J. Cirillo argues that there is a universal element of military culture that stifles medical progress. This war gave army medical officers an opportunity to introduce to the battlefield new medical technology, including the X-ray, aseptic surgery and sanitary systems derived from the germ theory. With few exceptions, however, their recommendations were ignored almost completely. Scientific knowledge was not sufficient; putting these ideas into military practice required the co-peration of line officers and volunteer soldiers as well as a restructuring of military education. The influence of military experiences on the history of American medicine is often overlooked. Cirillo shows how preventable deaths during the Spanish-American War led to reforms that continue to save the lives of both soldiers and civilians to the present day.
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