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Author: Georg Bollig
Publisher: BoD – Books on Demand
ISBN: 085466050X
Category : Medical
Languages : en
Pages : 374
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Book Description
The need for Palliative Care is increasing around the world due to demographic change, the extension of the lifespan in general and the advances of medical and oncological treatment. In Palliative Care quality of life and family-centred care are paramount. The book, entitled Palliative Care - Current Practice and Future Perspectives, offers an insightful introduction to different concepts and approaches, presenting a multidisciplinary perspective and diverse ways of insights provided by a team of authors from various disciplines and regions across Europe, Asia, and Africa. The different chapters divided into five sections provide an insight into current practices from different fields and countries. It highlights current knowledge and experiences and discusses ideas for the future development of Palliative Care.
Author: Georg Bollig
Publisher: BoD – Books on Demand
ISBN: 085466050X
Category : Medical
Languages : en
Pages : 374
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Book Description
The need for Palliative Care is increasing around the world due to demographic change, the extension of the lifespan in general and the advances of medical and oncological treatment. In Palliative Care quality of life and family-centred care are paramount. The book, entitled Palliative Care - Current Practice and Future Perspectives, offers an insightful introduction to different concepts and approaches, presenting a multidisciplinary perspective and diverse ways of insights provided by a team of authors from various disciplines and regions across Europe, Asia, and Africa. The different chapters divided into five sections provide an insight into current practices from different fields and countries. It highlights current knowledge and experiences and discusses ideas for the future development of Palliative Care.
Author: Bernd Alt-Epping
Publisher: Springer
ISBN: 3662462028
Category : Medical
Languages : en
Pages : 302
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Book Description
Palliative care provides comprehensive support for severely affected patients with any life-limiting or life-threatening diagnosis. To do this effectively, it requires a disease-specific approach as the patients’ needs and clinical context will vary depending on the underlying diagnosis. Experts in the field of palliative care and oncology describe in detail the needs of patients with advanced cancer in comparison to those with non-cancer disease and also identify the requirements of patients with different cancer entities. Basic principles of symptom control are explained, with careful attention to therapy for pain associated with either the cancer or its treatment and to symptom-guided antineoplastic therapy. Complex therapeutic strategies for palliative cancer patients are highlighted that involve both cancer- and symptom-directed options and address a range of therapeutic aims. Issues relating to drug use in palliative cancer care are fully explored, and a separate section is devoted to care in the final phase. A range of organizational and policy issues are also discussed, and the book concludes by considering likely future developments in palliative care for cancer patients. Palliative Care in Oncology will be of particular interest to palliative care physicians who are interested in broadening the scope of their disease-specific knowledge, as well as to oncologists who wish to learn more about modern palliative care concepts relevant to their day-to-day work with cancer patients.
Author: Libby Sallnow
Publisher: Routledge
ISBN: 1136631992
Category : Medical
Languages : en
Pages : 258
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Book Description
Public health approaches to palliative care have been growing in policy importance and practice acceptance. This innovative volume explores the major concepts, practice examples, and practice guidelines for this new approach. The goal of ‘comprehensive care’ – seamless support for patients as they transition between home based care and inpatient services – relies on the principles of health promotion and community development both to ensure services are available and importantly appropriate for patients’ needs. In developing contexts, where hospitals and hospices may be inaccessible, a public health approach provides not only continuity of care but greater access to good end of life care. This book provides both a historical and conceptual overview whilst offering practical case examples from affluent and developing contexts, in a range of clinical settings. Finally, it draws together research-based guidelines for future practice. Essential reading for public health researchers and practitioners with an interest in end of life care and global health as well as those involved in developing palliative care provision, International Perspectives on Public Health and Palliative Care is the first volume to present an overview of theory and practice in this emerging field.
Author: Committee on Care at the End of Life
Publisher: National Academies Press
ISBN: 0309518253
Category : Medical
Languages : en
Pages : 457
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Book Description
When the end of life makes its inevitable appearance, people should be able to expect reliable, humane, and effective caregiving. Yet too many dying people suffer unnecessarily. While an "overtreated" dying is feared, untreated pain or emotional abandonment are equally frightening. Approaching Death reflects a wide-ranging effort to understand what we know about care at the end of life, what we have yet to learn, and what we know but do not adequately apply. It seeks to build understanding of what constitutes good care for the dying and offers recommendations to decisionmakers that address specific barriers to achieving good care. This volume offers a profile of when, where, and how Americans die. It examines the dimensions of caring at the end of life: Determining diagnosis and prognosis and communicating these to patient and family. Establishing clinical and personal goals. Matching physical, psychological, spiritual, and practical care strategies to the patient's values and circumstances. Approaching Death considers the dying experience in hospitals, nursing homes, and other settings and the role of interdisciplinary teams and managed care. It offers perspectives on quality measurement and improvement, the role of practice guidelines, cost concerns, and legal issues such as assisted suicide. The book proposes how health professionals can become better prepared to care well for those who are dying and to understand that these are not patients for whom "nothing can be done."
Author: Anne C. Mosenthal
Publisher:
ISBN: 0190858362
Category : Medical
Languages : en
Pages : 385
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Book Description
Part of the Integrating Palliative Care series, this volume on surgical palliative care guides readers through the core palliative skills and knowledge needed to deliver high value care for patients with life-limiting, critical, and terminal illness under surgical care. Surgical Palliative Care is an ideal resource for surgeons, surgical nurses, intensivists, and other practitioners who wish to learn more about integrating palliative care into the surgical field.
Author: Joachim Cohen
Publisher: Oxford University Press
ISBN: 0199599408
Category : Medical
Languages : en
Pages : 270
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Book Description
Focusing on population health and discussing studies using different methodologies, this title presents a synthesis and overview of relevant research and empirical data on the end of life that can bear a basis for a more systematic 'public health of the end of life'.
Author: Eleanor L. Stevenson, PhD, RN
Publisher: Springer Publishing Company
ISBN: 0826172547
Category : Medical
Languages : en
Pages : 394
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Book Description
Delivers current knowledge from global experts at the forefront of fertility and ART healthcare The first publication of its kind, this book on fertility and assisted reproductive technology (ART) is a globally focused, authoritative guide to state-of-the-art information about modern fertility and ART healthcare. Written for clinicians, public health officials, women’s health experts, scientists, students, scholars, and other interested individuals, the book encompasses theoretical, research, policy, and clinical practice aspects of fertility and ART healthcare. The book features the diverse contributions of multidisciplinary researchers, scholars, and clinicians from eight countries who explore contemporary health care perspectives regarding individuals and families dealing with infertility and fertility challenges including such advanced technologies as in-vitro fertilization, intrauterine insemination, and oocyte preservation. The book addresses theoretical underpinnings of fertility and ART healthcare including new ways of conceptualizing research and theoretical concepts. Practical aspects involved with administering and treating the many women and men whose lives are affected by fertility challenges are illuminated. Complex policy concerns resulting from the rapid advances in fertility and ART are considered. The health care needs of those seeking fertility evaluation and treatment including access to care locally and globally are examined in depth. The book also includes discussions about novel approaches and emerging populations in fertility and ART healthcare that expand the scope of care. Thought-provoking case examples from contemporary care practices will help the reader to synthesize information. Key Features: Delivers thought provoking ART research and practice issues for health care clinicians, scholars, and scientists Synthesizes evolving theory, research, clinical practice, and public policy concerns Addresses complex considerations within the practice and delivery of fertility and ART services Written by international thought leaders and emerging scholars on the forefront of ART technologies and other issues Includes case study exemplars to stimulate critical thinking and transform discussion about modern fertility and ART care
Author: Michael Silbermann
Publisher: Springer Nature
ISBN: 3030545261
Category : Medical
Languages : en
Pages : 566
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Book Description
The new global cancer data suggests that the global burden has risen to 18.1 million new cases per year and 9.6 million cancer deaths per year. A number of factors appear to be driving this increase, in particular, a growing and aging global population and an increase of exposure to cancer risk factors linked to social and economic development. For rapidly-growing economies, the data suggests a shift from poverty- or infection-related cancers to those associated with lifestyles more typical in industrialized countries. There is still large geographical diversity in cancer occurrence and variations in the magnitude and profile of the disease between and within world regions. There are specific types of cancer that dominate globally: lung, female breast and colorectal cancer, and the regional variations in common cancer types signal the extent to which societal, economic and lifestyle changes interplay to deferentially impact on the profile of this most complex group of diseases. Unfortunately, despite advances in cancer care, a significant proportion of patients at home, experience sub-optimal outcomes. Barriers to successful treatment outcomes include, but are not limited to: access to oncologists in the primary health centers, non-adherence, lack of experienced oncology and palliative care nurses in the community, inadequate monitoring and the lack of training of family and pediatric physicians. Telemedicine approaches, including telephone triage/education, telemonitoring, teleconsultation and status tracking through mobile applications, have shown promise in further improving outcomes, in particular for chronic cancer patients following their hospitalization. Lessons can be learned from existing hospices in North America, the United Kingdom, Australia, Centers of Excellence in African (Uganda) and modern community services in India (Kerala). An important goal of this book is to describe and encourage professionals to develop new community programs in palliative care, which include training and empowering physicians and nurses in the community on the principles of palliative care. The Middle East Cancer Consortium (MECC) together with the American Society of Clinical Oncology (ASCO) and the American Oncology Nursing Society (ONS) have conducted multiple courses ranging from basic palliative care to more specialized training in palliative care for multiple nationalities in Europe, Asia and Africa. Our experience clearly indicates that, to promote such activities, one needs strong leadership and confirmed political will to support the endeavor. The new book will emphasize the importance of having a core of multiple stakeholders including community leaders, government, NGOs and media to be actively involved in advocating for the cause and generating public awareness. This text will provide the reader with a comprehensive understanding of the outside-of-the-hospital treatment of cancer patients by medical, paramedical and volunteer personnel. In doing so, this text will encourage the creation of new palliative care services improving upon the existing ones and stimulate further research in this field. Part 1 of the text will begin with an overview of the current state of affairs of services provided to cancer patients while being cared for by primary health centers. It will also review the current literature regarding medical and psychological-based therapy options in the community for cancer patients at different stages of their disease. Part 2 will address the unique role of the community nurse, within the framework of the multidisciplinary team treating the patient, in the attempt to provide optimal evaluation and care in very challenging situations (such as with terminal patients). Part 3 will provide insightful models of this new discipline and serve as a valuable resource for physicians, nurses, social workers and others involved in the care of cancer patients. The book will take a multidisciplinary approach, integrating clinical and environmental data for practical management to enhance the efficacy of treatment while relieving suffering. Part 4 will also discuss the application of modern technological approaches to track symptoms, quality of life, diet, mobility, duration of sleep and medication use (including pain killers) in chronic cancer patients in the community. Part 5 of the book will also be devoted to modes of developing a collaborative program between governmental and non-governmental organization sectors. This includes volunteer workers in close collaboration with medical professionals for providing emotional and spiritual support, nursing care, nutritional support and empowering family caregivers. Such a model makes palliative care in the community a “people’s movement”, thus transferring part of the responsibility and ownership to the community.
Author: Ivette Motola
Publisher:
ISBN: 9781908438706
Category : Medical care
Languages : en
Pages : 36
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Book Description
Author: Julia M Addington-Hall
Publisher: Oxford University Press
ISBN: 0198530250
Category : Medical
Languages : en
Pages : 328
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Book Description
The research base for palliative care must improve as it continues to develop in increasingly evidence-based health care systems, and to provide the needs of patients and families. This is the first research methods textbook focusing on the unique needs of palliative care, aimed at improving current research and stimulating new research in the field.
