Routledge handbook of global health rights
著者
書誌事項
Routledge handbook of global health rights
Routledge, c2021
- : pbk
大学図書館所蔵 全1件
  青森
  岩手
  宮城
  秋田
  山形
  福島
  茨城
  栃木
  群馬
  埼玉
  千葉
  東京
  神奈川
  新潟
  富山
  石川
  福井
  山梨
  長野
  岐阜
  静岡
  愛知
  三重
  滋賀
  京都
  大阪
  兵庫
  奈良
  和歌山
  鳥取
  島根
  岡山
  広島
  山口
  徳島
  香川
  愛媛
  高知
  福岡
  佐賀
  長崎
  熊本
  大分
  宮崎
  鹿児島
  沖縄
  韓国
  中国
  タイ
  イギリス
  ドイツ
  スイス
  フランス
  ベルギー
  オランダ
  スウェーデン
  ノルウェー
  アメリカ
内容説明・目次
内容説明
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.
目次
Part A
Chapter 1: An introduction to health rights as they apply in a global landscape
Chapter 2: Universal Declaration of Human Rights Part I: Articles 1, 2 3, 5 and 6
Chapter 3: Universal Declaration of Human Rights Part II: Articles 7, 12, 16, 18, 19 and 25
Chapter 4: A global right to health amid global health emergencies
Chapter 5: Global Health Rights in the Inter-American Court of Human Rights:On the Doctrine of the Minimum Core Obligations and a Co-Responsibility to Care
Part B
Beginning of life and children
Chapter 6: Assisted Reproductive Technologies in Uganda: Law and Practice
Chapter 7: Abortion and conscience: a crossroads for Northern Ireland
Chapter 8: The standard of care and implications for paediatric decision-making: the Swedish viewpoint
Middle of Life
Chapter 9: The right to health in Hong King: incorporation, implementation and balancing
Chapter 10: 'Dignity' in the adjudication of health rights in India
Chapter 11: Universal health coverage and the right to health in Nigeria
Chapter 12: Realising the right to health in Kenya: connecting health governance outcomes to patient safety perspectives
Chapter 13: Developing an intrinsic patient safety culture in health systems: the NHS experience
Chapter 14: Clinical Negligence Litigation Procedure, Policy and Practice in England: the product of a legal cycle rather than an application of a right to health?
Chapter 15: Patient Safety and Human Rights
Chapter 16: Fundamental rights to health care and charging overseas visitors for NHS treatment: Diversity across the the United Kingdom's devolved jurisdictions
Chapter 17: Public reporting, transparency and patient autonomy in the province of Quebec
End-of-life
Chapter 18: Human tissue, human rights and humanity
Chapter 19: Autonomy and the right to (end one's?) life: a German perspective
Chapter 20: End of Life Issues in Australia and New Zealand
Chapter 21: Comparative perspectives on medical aid in dying: the United States and Canada
Part C
Chapter 22: A right to health: a right granted, agreed, but limited or denied?
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