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Author: Publisher: ISBN: Category : Languages : en Pages : 10
Book Description
Socioeconomic position (SEP) refers to a range of dimensions that describe absolute and relative position in society including income, education, poverty, deprivation, and social status. The ultimate goal of the proposed work is to inform our understanding of racial and ethnic disparities in breast cancer care and the contribution of SEP and linguistic barriers, particularly for Hispanic women. This work has the potential to contribute to our understanding of disparities in breast cancer care, and to inform strategies to improve access to and quality of care for all women with breast cancer.
Author: Publisher: ISBN: Category : Languages : en Pages : 10
Book Description
Socioeconomic position (SEP) refers to a range of dimensions that describe absolute and relative position in society including income, education, poverty, deprivation, and social status. The ultimate goal of the proposed work is to inform our understanding of racial and ethnic disparities in breast cancer care and the contribution of SEP and linguistic barriers, particularly for Hispanic women. This work has the potential to contribute to our understanding of disparities in breast cancer care, and to inform strategies to improve access to and quality of care for all women with breast cancer.
Author: Brinda Venkatesh Publisher: ISBN: Category : Languages : en Pages : 81
Book Description
Despite significant advances that have been made in breast cancer diagnosis and treatment, a disproportionate burden of the disease continues to fall on women from minority groups. Studies suggest that differentials in the quality of breast cancer care in the treatment stage influence breast cancer disparities. Because treatment is defined by medical intervention, the health system plays a critical role in understanding breast cancer disparities and needs to be further examined. Moreover, studies examining such differentials have focused on aggregated racial data, which may be masking smaller ethnic groups that may be at higher risk. This dissertation attempts to clarify the health system contribution to breast cancer quality of care disparities and highlights the need to examine breast cancer quality of care disparities using disaggregated racial/ethnic data in order to help inform the design of more targeted quality improvement efforts. Paper #1 examines the relationship between designated specialty cancer centers and breast cancer quality of care. In cancer care delivery, there has been an emerging trend for cancer centers to obtain special designations from one or more of the following institutions: the National Cancer Institute (NCI), the National Comprehensive Cancer Network (NCCN), and the American College of Surgeon’ Commission on Cancer. These designations are markers for high quality cancer care, yet little is known about the actual effectiveness of the care they provide or the communities that they tend to serve. Paper #2 examines breast cancer quality of care differences between Asian women (aggregated and disaggregated) and non-Hispanic White women. Cancer disparities research often focus on examining communities in aggregate. Recently, more scholars are utilizing disaggregated ethnic data when assessing cancer disparities in order to acknowledge the diversity of these large communities. Little is known about breast cancer quality of care disparities among Asian American ethnic groups. Paper #3 examines the relative contribution of within hospital and between hospital effects on racial/ethnic disparities on the quality of breast cancer treatment. Existing literature posits that there are two mechanisms at the health systems level that contribute to disparities in the quality of care received by minority groups. Some studies suggest that disparities are due to minorities receiving differential treatment within the same institution as White patients, while others propose that minorities tend to receive care from lower quality health care settings. Studies to date have not examined the ways in which the health system may be contributing to breast cancer quality of care disparities. Data from the California Cancer Registry (CCR) was used for the analyses. The study population consisted of women ages 20 years or older and who have had a first invasive primary breast cancer diagnosis between 2011-2014. This dissertation contributes to the existing literature on breast cancer disparities by clarifying the mechanism of the health system contribution to breast cancer disparities and uncovering disparities in disaggregated ethnic groups. Findings from this dissertation will provide important information for the development of quality improvement efforts in cancer care delivery.
Author: Michael Feuerstein Publisher: ISBN: 9783319774312 Category : Cancer Languages : en Pages : 419
Book Description
"The timely revision of this authoritative handbook gives a wide range of health care providers practical insights and strategies for treating cancer survivors' long-term physical and mental health issues and promoting healthy lifestyle habits. Details of new and emerging trends in research and practice enhance readers' awareness of issues faced by survivors so they may better detect, monitor, intervene in, and if possible prevent distressing conditions and potentially harmful outcomes. Of particular emphasis are different models of care that may be applicable to diverse clinical settings around the world. New or updated chapters cover major challenges to survivors' quality of life and options for health care delivery across key life domains, including: Adaptation and coping post-treatment. Problems of aging in survivorship, including disparities and financial hardship. Well-being concerns including physical activity, weight loss, nutrition, and smoking cessation. Core functional areas such as work, sleep, relationships, and cognition. Large-scale symptoms including pain, distress, and fatigue. Models of care including primary care and comprehensive cancer center. International perspectives. PLUS, insights about lessons learned and challenges ahead"--Publisher's description
Author: Amelie G. Ramirez Publisher: Springer Nature ISBN: 303029286X Category : Medical Languages : en Pages : 320
Book Description
This open access book gives an overview of the sessions, panel discussions, and outcomes of the Advancing the Science of Cancer in Latinos conference, held in February 2018 in San Antonio, Texas, USA, and hosted by the Mays Cancer Center and the Institute for Health Promotion Research at UT Health San Antonio. Latinos – the largest, youngest, and fastest-growing minority group in the United States – are expected to face a 142% rise in cancer cases in coming years. Although there has been substantial advancement in cancer prevention, screening, diagnosis, and treatment over the past few decades, addressing Latino cancer health disparities has not nearly kept pace with progress. The diverse and dynamic group of speakers and panelists brought together at the Advancing the Science of Cancer in Latinos conference provided in-depth insights as well as progress and actionable goals for Latino-focused basic science research, clinical best practices, community interventions, and what can be done by way of prevention, screening, diagnosis, and treatment of cancer in Latinos. These insights have been translated into the chapters included in this compendium; the chapters summarize the presentations and include current knowledge in the specific topic areas, identified gaps, and top priority areas for future cancer research in Latinos. Topics included among the chapters: Colorectal cancer disparities in Latinos: Genes vs. Environment Breast cancer risk and mortality in women of Latin American origin Differential cancer risk in Latinos: The role of diet Overcoming barriers for Latinos on cancer clinical trials Es tiempo: Engaging Latinas in cervical cancer research Emerging policies in U.S. health care Advancing the Science of Cancer in Latinos proves to be an indispensable resource offering key insights into actionable targets for basic science research, suggestions for clinical best practices and community interventions, and novel strategies and advocacy opportunities to reduce health disparities in Latino communities. It will find an engaged audience among researchers, academics, physicians and other healthcare professionals, patient advocates, students, and others with an interest in the broad field of Latino cancer.
Author: National Research Council Publisher: National Academies Press ISBN: 0309164818 Category : Social Science Languages : en Pages : 502
Book Description
Hispanics and the Future of America presents details of the complex story of a population that varies in many dimensions, including national origin, immigration status, and generation. The papers in this volume draw on a wide variety of data sources to describe the contours of this population, from the perspectives of history, demography, geography, education, family, employment, economic well-being, health, and political engagement. They provide a rich source of information for researchers, policy makers, and others who want to better understand the fast-growing and diverse population that we call "Hispanic." The current period is a critical one for getting a better understanding of how Hispanics are being shaped by the U.S. experience. This will, in turn, affect the United States and the contours of the Hispanic future remain uncertain. The uncertainties include such issues as whether Hispanics, especially immigrants, improve their educational attainment and fluency in English and thereby improve their economic position; whether growing numbers of foreign-born Hispanics become citizens and achieve empowerment at the ballot box and through elected office; whether impending health problems are successfully averted; and whether Hispanics' geographic dispersal accelerates their spatial and social integration. The papers in this volume provide invaluable information to explore these issues.
Author: Institute of Medicine Publisher: National Academies Press ISBN: 030908265X Category : Medical Languages : en Pages : 781
Book Description
Racial and ethnic disparities in health care are known to reflect access to care and other issues that arise from differing socioeconomic conditions. There is, however, increasing evidence that even after such differences are accounted for, race and ethnicity remain significant predictors of the quality of health care received. In Unequal Treatment, a panel of experts documents this evidence and explores how persons of color experience the health care environment. The book examines how disparities in treatment may arise in health care systems and looks at aspects of the clinical encounter that may contribute to such disparities. Patients' and providers' attitudes, expectations, and behavior are analyzed. How to intervene? Unequal Treatment offers recommendations for improvements in medical care financing, allocation of care, availability of language translation, community-based care, and other arenas. The committee highlights the potential of cross-cultural education to improve provider-patient communication and offers a detailed look at how to integrate cross-cultural learning within the health professions. The book concludes with recommendations for data collection and research initiatives. Unequal Treatment will be vitally important to health care policymakers, administrators, providers, educators, and students as well as advocates for people of color.
Author: David Osoba Publisher: CRC Press ISBN: 1000142035 Category : Medical Languages : en Pages : 374
Book Description
This book is comprised of extensive reviews and instructional chapters that discuss the quality of life in several aspects of cancer. The first six chapters deal with conceptual issues relating to measuring quality of life in adult and pediatric populations with cancer. The next five chapters provide practical information on how to select quality-of-life measures, the statistical analysis of trials, economic evaluations to be considered, and some possible abuses of quality-of-life measures. Five chapters review the results of studies using selected quality-of-life measures and provide recent information on their performance. These are followed by three chapters dealing with specific issues relating to nausea and vomiting associated with cancer therapy. Three chapters are devoted to the problems of assessing and controlling pain in patients who have cancer. There are also two chapters that deal with the quality of life in palliative care. Effect of Cancer on Quality of Life is intended for all who have an interest in measuring the quality of life in patients with cancer. This includes investigators who are just entering the field and can benefit from instructions on how to conduct quality-of-life research, as well as those who are experienced in conducting this kind of research.
Author: National Research Council Publisher: National Academies Press ISBN: 0309166136 Category : Medical Languages : en Pages : 310
Book Description
Disparities in health and health care across racial, ethnic, and socioeconomic backgrounds in the United States are well documented. The reasons for these disparities are, however, not well understood. Current data available on race, ethnicity, SEP, and accumulation and language use are severely limited. The report examines data collection and reporting systems relating to the collection of data on race, ethnicity, and socioeconomic position and offers recommendations.
Author: Institute of Medicine Publisher: National Academies Press ISBN: 0309140129 Category : Medical Languages : en Pages : 286
Book Description
The goal of eliminating disparities in health care in the United States remains elusive. Even as quality improves on specific measures, disparities often persist. Addressing these disparities must begin with the fundamental step of bringing the nature of the disparities and the groups at risk for those disparities to light by collecting health care quality information stratified by race, ethnicity and language data. Then attention can be focused on where interventions might be best applied, and on planning and evaluating those efforts to inform the development of policy and the application of resources. A lack of standardization of categories for race, ethnicity, and language data has been suggested as one obstacle to achieving more widespread collection and utilization of these data. Race, Ethnicity, and Language Data identifies current models for collecting and coding race, ethnicity, and language data; reviews challenges involved in obtaining these data, and makes recommendations for a nationally standardized approach for use in health care quality improvement.
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Author: Brinda Venkatesh
Author: Michael Feuerstein
Author: David Joseph Delgado
Author: Amelie G. Ramirez
Author: National Research Council
Author: Institute of Medicine
Author: David Osoba
Author: National Research Council
Author: Institute of Medicine