Author: Imogen Goold
Publisher: Bloomsbury Publishing
ISBN: 1509928588
Category : Law
Languages : en
Pages : 432
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Book Description
In the wake of the Charlie Gard and Alfie Evans cases, a wide-ranging international conversation was started regarding alternative thresholds for intervention and the different balances that can be made in weighing up the rights and interests of the child, the parent's rights and responsibilities and the role of medical professionals and the courts. This collection provides a comparative perspective on these issues by bringing together analysis from a range of jurisdictions across Europe, North and South America, Africa and Asia. Contextualising the differences and similarities, and drawing out the cultural and social values that inform the approach in different countries, this volume is highly valuable to scholars across jurisdictions, not only to inform their own local debate on how best to navigate such cases, but also to foster inter-jurisdictional debate on the issues. The book brings together commentators from the fields of law, medical ethics, and clinical medicine across the world, actively drawing on the view from the clinic as well as philosophical, legal and sociological perspectives on the crucial question of who should decide about the fate of a child suffering from a serious illness. In doing so, the collection offers comprehensive treatment of the key questions around whether the current best interests approach is still appropriate, and if not, what the alternatives are. It engages head-on with the concerns seen in both the academic and popular literature that there is a need to reconsider the orthodoxy in this area.
Author: Betty Ferrell
Publisher:
ISBN: 0190244186
Category : Family & Relationships
Languages : en
Pages : 161
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Book Description
Pediatric palliative care is a field of significant growth as health care systems recognize the benefits of palliative care in areas such as neonatal intensive care, pediatric ICU, and chronic pediatric illnesses. Pediatric Palliative Care, the fourth volume in the HPNA Palliative Nursing Manuals series, highlights key issues related to the field. Chapters address pediatric hospice, symptom management, pediatric pain, the neonatal intensive care unit, transitioning goals of care between the emergency department and intensive care unit, and grief and bereavement in pediatric palliative care. The content of the concise, clinically focused volumes in the HPNA Palliative Nursing Manuals series is one resource for nurses preparing for specialty certification exams and provides a quick-reference in daily practice. Plentiful tables and patient teaching points make these volumes useful resources for nurses.
Author: James Cameron
Publisher: Taylor & Francis
ISBN: 1003826776
Category : Law
Languages : en
Pages : 250
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Book Description
A series of recent high-profile court cases has demonstrated the inadequacy of current laws in addressing issues relating to medical treatment decisions involving seriously ill children. The challenges of determining that life-sustaining medical treatment is not in a young child’s best interests have resulted in criticism of the best interests principle. This book explores the theoretical foundations of the best interests principle, and alternatives offered in the academic literature, to allow readers to understand why the principle remains contentious despite its prevalence. It provides theoretical background, exploration of what occurs in practice, and proposes a novel approach to address these challenges. Frameworks for decision-making identified in the academic literature are used to examine the application of the best interests principle in practice in England and Wales, Australia, and New Zealand through a review of the case law and qualitative research with paediatric doctors. The exploration of current practice allows readers to understand the challenges of applying the best interests principle, but also the need to retain a focus on the child. Readers are introduced to a human-rights based approach, which ensures that the focus remains on upholding the child’s best interests but also provides a more comprehensive explanation of the situation. Progressing the debate around end-of-life decision-making and children, the book will be a valuable resource for academics, researchers and policy-makers. It will also provide practical guidance to both legal and medical practitioners in managing disputes about the provision of life-sustaining treatment.
Author: Christopher Danbury
Publisher:
ISBN: 0198817169
Category : Medical
Languages : en
Pages : 277
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Book Description
Every day, intensive care medicine raises multiple legal and ethical issues, making it increasingly difficult to know whom to admit and when, at what stage invasive management should be withdrawn, and who, crucially, should deride? These profound dilemmas, already complicated in a setting of scarce resources, demand an understanding of law and ethics for those working in intensive care medicine. When are 'Do Not Attempt Resuscitation' decisions appropriate? When doctors, patients, and relatives cannot agree, what options are available outside the courts? Who protects the rights of those who lack capacity? And, after Covid-19, what if rationing of intensive care treatment is necessary? Clinically focused, the book explains the relevance of leading cases to aid day-to-day decision making. A spectrum of ethical and legal controversies in critical care is addressed to demonstrate how law and ethics shape the practice of intensive care medicine. Featuring contributions from leading legal and medical experts, this important reference book should be read by critical care professionals, lawyers, and ethicists. Book jacket.
Author: Elisabeth (Boetzkes) Gedge
Publisher: Broadview Press
ISBN: 1554810388
Category : Philosophy
Languages : en
Pages : 675
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Book Description
Readings in Health Care Ethics provides a wide-ranging selection of important and engaging contributions to the field of health care ethics. The second edition adds a chapter on health care in Canada, and the introduction has been expanded to include discussion of a new direction in feminist naturalized ethics. The book presupposes no prior knowledge, only an interest in the bioethical issues that are shaping our world.
Author: Fiona McDonald
Publisher: Bloomsbury Publishing
ISBN: 1350310638
Category : Medical
Languages : en
Pages : 388
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Book Description
Understanding ethics and law in health care is an essential part of nurse and midwife professional standards, and a core component of qualifying programmes. Ethics, Law and Health Care teaches applied ethics and law in a way that illustrates the real world applications of these essential aspects of practice. It enables readers to not only recognise but also address legal and ethical issues that will arise in their professional practice. The book approaches these issues using the Australian Nursing and Midwifery Codes of Ethics, the Codes of Professional Conduct and the four principles of biomedical ethics: - Autonomy - Non-maleficence - Beneficence - Justice. Filled with case studies, review questions and useful further reading, this book gives readers a solid understanding of ethics and law in health care, and a clear decision-making framework so they can take action confidently. Please note, this book is written specifically for the Australian market. New to this Edition: - A new chapter on health, law, ethics and Aboriginal and Torres Strait Islanders - Illustrated with 'real world' applications, the bookensures students understand how core components of the nursing and midwifery curriculum are put in to practice - Copies of the Codes of Ethics and Professional Conduct for Nurses and Midwives are provided as appendixes for ease of reference
Author: Rebecca Weintraub Brendel
Publisher: Elsevier Health Sciences
ISBN: 0323835694
Category : Medical
Languages : en
Pages : 161
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Book Description
This issue of Psychiatric Clinics, guest edited by Drs. Rebecca Brendel and Michelle will discuss a number of important topics surrounding Psychiatric Ethics and impact on clinical practice. This issue is one of four each year selected by our series consulting editor, Dr. Harsh Trivedi of Sheppard Pratt Health System. Topics in this issue include: Ethics in Psychiatric Research, Ethical Aspects of Trauma Informed Care, Ethical Challenges in Addiction Psychiatry, Ethics in Child and Adolescent Psychiatry, Forensic Psychiatric Ethics, Geriatric Psychiatry Ethics, Ethics of emerging technologies, Ethical considerations in Psychiatric Genetics, Organizational Ethics, Suicide and the end of life, Psychiatry in public spaces, Autonomy and Multiculturalism, and Justice and Parity in Mental Health Treatment, among others.
Author: Betty R. Ferrell
Publisher: Oxford University Press, USA
ISBN: 0199332347
Category : Medical
Languages : en
Pages : 1249
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Book Description
The Oxford Textbook of Palliative Nursing is the definitive text on nursing care of the seriously ill and dying. It is a comprehensive work addressing all aspects of palliative care including physical, psychological, social and spiritual needs. The text is written by leaders in the field and includes an impressive section on international palliative care. Each chapter includes case examples and a strong evidence base to support the highest quality of care. The book is rich with tables and figures offering practical resources for clinical practice across all settings of care and encompassing all ages from pediatrics to geriatrics.
Author: Clayton Ó Néill
Publisher: Routledge
ISBN: 100038926X
Category : Health & Fitness
Languages : en
Pages : 315
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Book Description
This book examines the idea of a fundamental entitlement to health and healthcare from a human rights perspective. The volume is based on a particular conceptual reasoning that balances critical thinking and pragmatism in the context of a universal right to health. Thus, the primary focus of the book is the relationship or contrast between rights-based discourse/jurisprudential arguments and real-life healthcare contexts. The work sets out the constraints that are imposed on a universal right to health by practical realities such as economic hardship in countries, lack of appropriate governance, and lack of support for the implementation of this right through appropriate resource allocation. It queries the degree to which the existence of this legally enshrined right and its application in instruments such as the International Covenant on Economic, Social and Cultural Rights (ICESCR) and the Universal Declaration of Human Rights (UDHR) can be more than an ephemeral aspiration but can, actually, sustain, promote, and instil good practice. It further asks if social reality and the inequalities that present themselves therein impede the implementation of laudable human rights, particularly within marginalised communities and cadres of people. It deliberates on what states and global bodies do, or could do, in practical terms to ensure that such rights are moved beyond the aspirational and become attainable and implementable. Divided into three parts, the first analyses the notion of a universal inalienable right to health(care) from jurisprudential, anthropological, legal, and ethical perspectives. The second part considers the translation of international human rights norms into specific jurisdictional healthcare contexts. With a global perspective it includes countries with very different legal, economic, and social contexts. Finally, the third part summarises the lessons learnt and provides a pathway for future action. The book will be an invaluable resource for students, academics, and policymakers working in the areas of health law and policy, and international human rights law.
Author: Michelle O′Reilly
Publisher: SAGE
ISBN: 1446291685
Category : Education
Languages : en
Pages : 316
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Book Description
Thought-provoking, pertinent and engaging, this book provides an overview of every aspect of carrying out research with children. It is unique in its particular focus on vulnerable groups of children such as those with mental-health problems, physical health problems and learning disabilities, along with young offenders and looked after children. The book helpfully addresses each stage of the research process: -Part I introduces the main elements of doing research with children, including seeking ethical approval for sensitive research topics. -Part II guides the reader through the initial stages of the research project including recruitment issues and communicating with gatekeepers. -Part III outlines the data collection, data analysis, writing up and dissemination stages of research and covers both quantitative and qualitative methods. Filled with practical advice and useful activities for each chapter, this book is an essential resource for any student, academic or professional working with, or doing research with, children.
