Search results for 'Terminal care Law and legislation' (try it on Scholar)

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  1. Joan McCarthy (ed.) (2011). End-of-Life Care: Ethics and Law. Cork University Press.
     
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  2.  5
    Stefania Negri (ed.) (2012). Self-Determination, Dignity and End-of-Life Care: Regulating Advance Directives in International and Comparative Perspective. M. Nijhoff Pub..
    By providing an interdisciplinary reading of advance directives regulation in international, European and domestic law, this book offers new insights into the most controversial legal issues surrounding the debate over dignity and autonomy ...
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  3. Hamide Tacir (2011). Hastanın Kendi Geleceğini Belirleme Hakkı. Xii Levha.
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  4.  4
    Sheila McLean (2007). Impairment and Disability: Law and Ethics at the Beginning and End of Life. Routledge-Cavendish.
    pt. 1. Background you need. -- What is brain-compatible teaching -- The old and new of it -- When brain research is applied to the classroom everything will change -- Change can be easy -- We're not in Kansas anymore -- Where's the proof -- Tools for exploring the brain -- Ten reasons to care about brain research -- The evolution of brain models -- Be a brain-smart consumer: recognizing good research -- Action or theory: who wants to read (...)
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  5. Merja Kuuppelomäki (2002). The Decision-Making Process When Starting Terminal Care as Assessed by Nursing Staff. Nursing Ethics 9 (1):20-35.
    This article deals with making decisions about starting terminal care. The results are part of a larger survey on nurses’ conceptions of terminal care in community health centres in Finland. The importance, frequency and timing of decision making as well as communication and the number of investigations and procedures carried out are examined. The relationship between decision making and the size of a health centre’s catchment population is also discussed. The results make it possible to compare (...)
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  6.  15
    Lois L. Shepherd (2009). If That Ever Happens to Me: Making Life and Death Decisions After Terri Schiavo. University of North Carolina Press.
    Disorders of consciousness and the permanent vegetative state -- Legal and political wrangling over Terri's life -- In context--law and ethics -- Terri's wishes -- The limits of evidence -- The implications of surrogacy -- Qualities of life -- Feeding -- The preservation of life -- Respect and care : an alternative framework.
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  7.  23
    Sally Sheldon & Michael Thomson (eds.) (1998). Feminist Perspectives on Health Care Law. Cavendish Pub..
    This book brings together new work by some of the foremost writers in the health care law arena. It presents exciting new insights,drawing on feminist theory and methodology to further our understanding of health care law. Whilst the book makes a real contribution to both feminist debates and the analysis of this area of law, it is also accessible to the undergraduate student who is approaching this area of legal scholarship and feminist jurisprudence for the first time. Its (...)
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  8.  4
    J. Savulescu (2013). Elective Ventilation and Interests. Journal of Medical Ethics 39 (3):129-129.
    This paper examines questions concerning elective ventilation, contextualised within English law and policy. It presents the general debate with reference both to the Exeter Protocol on elective ventilation, and the considerable developments in legal principle since the time that that protocol was declared to be unlawful. I distinguish different aspects of what might be labelled elective ventilation policies under the following four headings: ‘basic elective ventilation’; ‘epistemically complex elective ventilation’; ‘practically complex elective ventilation’; and ‘epistemically and practically complex elective ventilation’. (...)
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  9. Charles Foster (2009). Choosing Life, Choosing Death: The Tyranny of Autonomy in Medical Ethics and Law. Hart Pub..
  10.  2
    Søren Holm (2008). Best Interests: What Problems in Family Law Should Health Care Law Avoid? [REVIEW] Health Care Analysis 16 (3):252-254.
    This article comments briefly on three specific issues in Shazia Choudhry’s paper “‘Best Interests’ What can healthcare law learn from family law?” The three issues are: (1) the implications of ‘best interests’ and ‘welfare science’ for women within the family law and the health care law context, (2) the risk of capture by the ‘welfare science’ industry, and (3) the proposal that a committee of medical experts and medical ethicists should be set up to provide reports to the Court (...)
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  11.  2
    Yi-Chen Su (2014). When Ethical Reform Became Law: The Constitutional Concerns Raised by Recent Legislation in Taiwan. Journal of Medical Ethics 40 (7):484-487.
    In an effort at ethical reform, Taiwan recently revised the Hospice Palliative Care Law authorising family members or physicians to make surrogate decisions to discontinue life-sustaining treatment if an incompetent terminally ill patient did not express their wishes while still competent. In particular, Article 7 of the new law authorises the palliative care team, namely the physicians, to act as sole decision-makers on behalf of the incompetent terminally ill patient's best interests if no family member is available. However, (...)
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  12.  6
    Rien Janssens (1998). Terminal Care and Self-Determination. A Provocative Perspective. Medicine, Healthcare and Philosophy 1 (3):283-285.
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  13.  2
    Micheline Garel, Laurence Caeymaex, François Goffinet, Marina Cuttini & Monique Kaminski (2011). Ethically Complex Decisions in the Neonatal Intensive Care Unit: Impact of the New French Legislation on Attitudes and Practices of Physicians and Nurses. Journal of Medical Ethics 37 (4):240-243.
    Next SectionObjectives A statute enacted in 2005 modified the legislative framework of the rights of terminally ill persons in France. Ten years after the EURONIC study, which described the self-reported practices of neonatal caregivers towards ethical decision-making, a new study was conducted to assess the impact of the new law in neonatal intensive care units (NICU) and compare the results reported by EURONIC with current practices. Setting and design The study was carried out in the same two NICU as (...)
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  14.  12
    George P. Smith (1998). Terminal Sedation as Palliative Care: Revalidating a Right to a Good Death. Cambridge Quarterly of Healthcare Ethics 7 (4):382-387.
    Not everyone finds a in suffering. Indeed, even those who do subscribe to this interpretation recognize the responsibility of each individual to show not only sensitivity and compassion but render assistance to those in distress. Pharmacologic hypnosis, morphine intoxication, and terminal sedation provide their own type of medical to the terminally ill patient suffering unremitting pain. More and more states are enacting legislation that recognizes this need of the dying to receive relief through regulated administration of controlled substances. (...)
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  15. Mansoor Elahi (2011). Medical Ethics: A Practical Guide to Patient Care, Related Ethics, Conventions and Laws. Mtro Medical Publishing.
     
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  16. Michael D. A. Freeman (ed.) (2008). Law and Bioethics / Edited by Michael Freeman. Oxford University Press.
     
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  17. Mark Henaghan (2011). Health Professionals and Trust: The Cure for Healthcare Law and Policy. Routledge-Cavendish.
  18.  9
    Judith Hendrick (2004). Law and Ethics. Nelson Thornes.
    Provides an insight into the general principles of the professional-patient relationship.
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  19.  21
    Y. Michael Barilan (2003). Revisiting the Problem of Jewish Bioethics: The Case of Terminal Care. Kennedy Institute of Ethics Journal 13 (2):141-168.
    : This paper examines the main Jewish sources relevant to end-of-life ethics, two Talmudic stories, the early modern code of law (Shulhan Aruch), and contemporary Halakhaic (religious law) responsa. Some Orthodox rabbis object to the use of artificial life support that prolongs the life of a dying patient and permit its active discontinuation when the patient is suffering. Other rabbis believe that every medical measure must be taken in order to prolong life. The context of the discussion is the recent (...)
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  20.  13
    Robert F. Rizzo (2000). Physician-Assisted Suicide in the United States: The Underlying Factors in Technology, Health Care and Palliative Medicine – Part One. Theoretical Medicine and Bioethics 21 (3):277-289.
    In an age of rapid advances inlife-prolonging treatment, patients and caregivers areincreasingly facing tensions in making end-of-lifedecisions. An examination of the history of healthcare in the United States reveals technological,economic, and medical factors that have contributed tothe problems of terminal care and consequently to themovement of assisted suicide. The movement has itsroots in at least two fundamental perceptions andexpectations. In the age of technological medicineenergized by the profit motive, dying comes at a highprice in suffering and in personal (...)
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  21. Jeanne Fitzpatrick (2010). A Better Way of Dying: How to Make the Best Choices at the End of Life. Penguin Books.
    Foreword -- Prologue -- Attorney Eileen Fitzpatrick -- Dr. Jeanne Fitzpatrick -- section 1. Death and dying in America -- 1. The need for change : the cautionary tale of Phyllis Shattuck -- Dr. Fitzpatrick tells Phyllis Shattuck's story -- Reflections -- How this book will help -- Lessons to learn -- New name, old concept -- 2. Your right to die -- Your right to die is born : the case of Karen Ann Quinlan -- The Supreme Court weights (...)
     
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  22.  23
    Charles D. Douglas, Ian H. Kerridge & Rachel A. Ankeny (2013). Narratives of 'Terminal Sedation', and the Importance of the Intention-Foresight Distinction in Palliative Care Practice. Bioethics 27 (1):1-11.
    The moral importance of the ‘intention–foresight’ distinction has long been a matter of philosophical controversy, particularly in the context of end-of-life care. Previous empirical research in Australia has suggested that general physicians and surgeons may use analgesic or sedative infusions with ambiguous intentions, their actions sometimes approximating ‘slow euthanasia’. In this paper, we report findings from a qualitative study of 18 Australian palliative care medical specialists, using in-depth interviews to address the use of sedation at the end of (...)
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  23. George J. Annas (1993). Standard of Care the Law of American Bioethics. Monograph Collection (Matt - Pseudo).
     
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  24.  28
    Leonard M. Fleck (2011). Just Caring: Health Care Rationing, Terminal Illness, and the Medically Least Well Off. Journal of Law, Medicine & Ethics 39 (2):156-171.
    What does it mean to be a “just” and “caring” society in meeting the health care needs of the terminally ill when we have only limited resources to meet virtually unlimited health care needs? That question is the focus of this essay. Put another way: relative to all the other health care needs in our society, especially the need for lifesaving or life-prolonging health care, how high a priority ought the health care needs of persons (...)
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  25.  4
    S. Brannan, R. Campbell, M. Davies, V. English, R. Mussell & J. C. Sheather (2014). Ethics Briefing. Journal of Medical Ethics 40 (1):69-70.
    In February 2014, the Belgian Parliament passed legislation allowing euthanasia for terminally ill children of all ages by 86 votes to 44, with 12 abstentions. The Bill became law in early March after being signed by the King, making Belgium the first country in the world to abolish age restrictions for euthanasia. Previously, the youngest age at which euthanasia was permitted was 12 years old in The Netherlands.1Euthanasia was legalised in Belgium in 2002, and the new legislation introduces (...)
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  26.  34
    Virginia Held (2011). Morality, Care, and International Law. Ethics and Global Politics 4 (3):173-194.
    Whether we should respect international law is in dispute. In the United States, international law is dismissed by the left as merely promoting the interests of powerful states. It is attacked by the right as irrelevant and an interference with the interests and mission of the United States. And it follows from the arguments of many liberals that in the absence of world government the world is in a Hobbesian state of nature and international law inapplicable. This article reviews the (...)
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  27.  2
    Matty Van Niekerk, Ames Dhai & Yolande Guidozzi (2014). Is There a Foundation in South African Legislation to Require Students to Disclose Their Academic Status to Patients When Involved in Their Care? South African Journal of Bioethics and Law 7 (1):9.
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  28. Leonard M. Fleck (2011). Just Caring: Health Care Rationing, Terminal Illness, and the Medically Least Well Off. Journal of Law, Medicine and Ethics 39 (2):156-171.
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  29. Ian E. Thompson (1979). Dilemmas of Dying a Study in the Ethics of Terminal Care. Monograph Collection (Matt - Pseudo).
     
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  30. Alireza Bagheri (2013). Medical Futility: A Cross-National Study. Imperial College Press.
    So-called futile care : the experience of the Unied States -- The reality of medical futility in Brazil -- Medical futility and end-of-lfe issues in Belgium -- The concept of medical futility in Venezuela -- Medical futility in Russian Federation -- Medical futility in Australia -- Medical futility in Japan -- Ethical issues and policy in medical futility in China -- Medical futility in Korea -- Medical futility from Swiss perspective -- Medical futility in Turkey -- Medical futility in (...)
     
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  31.  4
    Camillia Kong (2015). The Space Between Second-Personal Respect and Rational Care in Theory and Mental Health Law. Law and Philosophy 34 (4):433-467.
    In recent human rights and legal instruments, individuals with impairments are increasingly recognised as agents who are worthy of respect for their inherent dignity and capacity to make autonomous decisions regarding treatment and care provisions. These legal developments could be understood using Stephen Darwall’s normative framework of the second person standpoint. However, this paper draws upon phenomena – both in legal developments and recent court cases – to illustrate theoretical difficulties with the contractualist underpinnings of Darwall’s account if applied (...)
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  32.  1
    Viktoras Justickis & Vidmantas Egidijus Kurapka (2009). Criminogenic Security of Law in the EU and Lithuanian Legislation. Jurisprudence 117 (3):217-238.
    The study focuses on the phenomenon of crime-causing (criminogenic) law. It includes a review of related studies on such laws and their criminal side-effects, the change in the legislator’s liability for effects of enacted laws, and the effects of the legislator’s afflatus on the potential criminogenic effects of law. Of special concern are cases where the legislator is aware of the potential criminogenic side-effects of a new law but carelessly neglects them. The study evaluates the tool for detection of probable (...)
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  33. Kenneth W. Goodman (ed.) (2010). The Case of Terri Schiavo: Ethics, Politics, and Death in the 21st Century. Oxford University Press.
    The case of Terri Schiavo, a young woman who spent 15 years in a persistent vegetative state, has emerged as a watershed in debates over end-of-life care. While many observers had thought the right to refuse medical treatment was well established, this case split a family, divided a nation, and counfounded physicians, legislators, and many of the people they treated or represented. In renewing debates over the importance of advance directives, the appropriate role of artificial hydration and nutrition, and (...)
     
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  34.  87
    Helga Varden (2012). A Kantian Critique of the Care Tradition: Family Law and Systemic Justice. Kantian Review 17 (2):327-356.
    Liberal theories of justice have been rightly criticized for two things by care theorists. First, they have failed to deal with private care relations’ inherent (inter)dependency, asymmetry and particularity. Second, they have been shown unable properly to address the asymmetry and dependency constitutive of care workers’ and care-receivers’ systemic conditions. I apply Kant’s theory of right to show that current care theories unfortunately reproduce similar problems because also they argue on the assumption that good (...) requires only virtuous private individuals. Giving up this assumption enables us to solve the problems regarding both private care relations and systemic injustice. (shrink)
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  35.  8
    Roberta M. Berry, Lisa Bliss, Sylvia Caley, Paul A. Lombardo & Leslie E. Wolf (2013). Recent Developments in Health Care Law: Culture and Controversy. [REVIEW] HEC Forum 25 (1):1-24.
    This article reviews recent developments in health care law, focusing on controversy at the intersection of health care law and culture. The article addresses: emerging issues in federal regulatory oversight of the rapidly developing market in direct-to-consumer genetic testing, including questions about the role of government oversight and professional mediation of consumer choice; continuing controversies surrounding stem cell research and therapies and the implications of these controversies for healthcare institutions; a controversy in India arising at the intersection of (...)
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  36. Robert F. Weir (1989). Abating Treatment with Critically Ill Patients: Ethical and Legal Limits to the Medical Prolongation of Life. Oxford University Press.
    This book offers an in-depth analysis of the wide range of issues surrounding "passive euthanasia" and "allow-to-die" decisions. The author develops a comprehensive conceptual model that is highly useful for assessing and dealing with real-life situations. He presents an informative historical overview, an evaluation of the clinical settings in which treatment abatement takes place, and an insightful discussion of relevant legal aspects. The result is a clearly articulated ethical analysis that is medically realistic, philosophically sound, and legally viable.
     
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  37.  44
    Arthur L. Caplan, James J. McCartney & Dominic A. Sisti (eds.) (2006). The Case of Terri Schiavo: Ethics at the End of Life. Prometheus Books.
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  38. David Larios Risco & Fernando Abellán-García Sánchez (eds.) (2009). Error Sanitario y Seguridad de Pacientes: Bases Jurídicas Para Un Registro de Sucesos Adversos En El Sistema Nacional de Salud. Comares.
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  39. Anne Rilliet Howald (2004). La Réforme des Régimes de Soins de Santé: Cadre International Et Communautaire, Thématiques Actuelles. Presses Universitaires d'Aix-Marseille.
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  40.  8
    H. Hinkka (2002). Factors Affecting Physicians' Decisions to Forgo Life-Sustaining Treatments in Terminal Care. Journal of Medical Ethics 28 (2):109-114.
    Objectives: Treatment decisions in ethically complex situations are known to depend on a physician's personal characteristics and medical experience. We sought to study variability in decisions to withdraw or withhold specific life-supporting treatments in terminal care and to evaluate the association between decisions and such background factors.Design: Readiness to withdraw or withhold treatment options was studied using a terminal cancer patient scenario with alternatives. Physicians were asked about their attitudes, life values, experience, and training; sociodemographic data were (...)
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  41.  13
    M. Berry Roberta, Sylvia Caley Lisa Bliss, A. Lombardo Paul, Jonathan Todres Jerri Nims Rooker & E. Wolf Leslie (forthcoming). Recent Developments in Health Care Law: Partners in Innovation. HEC Forum.
    This article reviews recent developments in health care law, focusing on the engagement of law as a partner in health care innovation. The article addresses: the history and contents of recent United States federal law restricting the use of genetic information by insurers and employers; the recent federal policy recommending routine HIV testing; the recent revision of federal policy regarding the funding of human embryonic stem cell research; the history, current status, and need for future attention to advance (...)
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  42.  8
    Roberta Berry, Lisa Bliss, Sylvia Caley, Paul Lombardo, Jerri Rooker, Jonathan Todres & Leslie Wolf (2010). Recent Developments in Health Care Law: Partners in Innovation. [REVIEW] HEC Forum 22 (2):85-116.
    This article reviews recent developments in health care law, focusing on the engagement of law as a partner in health care innovation. The article addresses: the history and contents of recent United States federal law restricting the use of genetic information by insurers and employers; the recent federal policy recommending routine HIV testing; the recent revision of federal policy regarding the funding of human embryonic stem cell research; the history, current status, and need for future attention to advance (...)
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  43.  5
    C. Cowley (2010). Justifying Terminal Care by 'Retrospective Quality-Adjusted Life-Years'. Journal of Medical Ethics 36 (5):290-292.
    A lot of medical procedures can be justified in terms of the number of quality-adjusted life-years (QALYs) they can be expected to generate; that is, the number of extra years that the procedure will provide, with the quality of life during those extra years factored in. QALYs are a crude tool, but good enough for many decisions. Notoriously, however, they cannot justify spending any money on terminal care (and indeed on older people in general). In this paper I (...)
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  44.  5
    M. Strätling, V. E. Scharf & P. Schmucker (2004). Mental Competence and Surrogate Decision-Making Towards the End of Life. Medicine, Health Care and Philosophy 7 (2):209-215.
    German legislation demands that decisions about the treatment of mentally incompetent patients require an ‘informed consent’. If this was not given by the patient him-/herself before he/she became incompetent, it has to be sought by the physician from a guardian, who has to be formally legitimized before. Additionally this surrogate has to seek the permission of a Court of Guardianship (Vormundschaftsgericht), if he/she intends to consent to interventions, which pose significant risks to the health or the life of the (...)
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  45. André den Exter (ed.) (2010). Human Rights and Biomedicine. Maklu.
     
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  46. Noritoshi Tanida (2000). Japanese Religious Organizations' View on Terminal Care. Eubios Journal of Asian and International Bioethics 10 (2):34-36.
    Religion may be an influential factor for care of terminally ill patients. Since there was no information of how Japanese religions thought of terminal care, a questionnaire survey was conducted among a total of 388 religious corporations, including 143 Shinto, 157 Buddhist, 58 Christian and 30 miscellaneous religious groups. Respondents were asked to answer questions based on their religious faith regarding a living will, and the introduction or withdrawal of life-sustaining treatments at the terminal stage. Results (...)
     
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  47. Akiva Tatz (2010). Dangerous Disease & Dangerous Therapy in Jewish Medical Ethics: Principles and Practice. Targum Press.
     
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  48. David N. Weisstub (ed.) (1998). Research on Human Subjects: Ethics, Law, and Social Policy. Pergamon.
    There have been serious controversies in the latter part of the 20th century about the roles and functions of scientific and medical research. In whose interests are medical and biomedical experiments conducted and what are the ethical implications of experimentation on subjects unable to give competent consent? From the decades following the Second World War and calls for the global banning of medical research to the cautious return to the notion that in controlled circumstances, medical research on human subjects is (...)
     
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  49.  10
    Kenneth S. Reinker & David Rosenberg (2011). Improve Medical Malpractice Law by Letting Health Care Insurers Take Charge. Journal of Law, Medicine & Ethics 39 (3):539-542.
    This essay discusses unlimited insurance subrogation (UIS) as a means of improving the deterrence and compensation results of medical malpractice law. Under UIS, health care insureds could assign their entire potential medical malpractice claims to their first-party commercial and government insurers. UIS should improve deterrence by establishing first-party insurers as plaintiffs to confront liability insurers on the defense side, leading to more effective prosecution of meritorious claims and reducing meritless and unnecessary litigation. UIS should improve compensation outcomes by converting (...)
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  50.  4
    Linda Delany (1993). Health Care Law. Health Care Analysis 1 (1):74-80.
    One probable success (the case of Mrs Tonge) is not a great deal to set against the courts' overwhelming reluctance to play a part in challenging resource allocation decisions. Nevertheless, where such decisions are inherently unreasonable—for example, as Margaret Brazier has suggested,11 a refusal to treat patients because they are divorced, or because they are Labour Party members—a remedy would be available through the courts. Presumably gender biased rationing decisions would similarly be susceptible to judicial review, although there might be (...)
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