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This book explores the challenges of informed consent in medical intervention and research ethics, considering the global reality of multiculturalism and religious diversity.
Informed consent (Medical law) --- Consent, Informed --- Consent to treatment --- Disclosure, Medical --- Medical disclosure --- Treatment, Consent to --- Consent (Law) --- Medical ethics --- Medical personnel --- Patient education --- Involuntary treatment --- Patient refusal of treatment --- Malpractice --- Religion and beliefs
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A timely, authoritative discussion of an important clinical topic, this useful book outlines the history, function, nature and requirements of informed consent, focusing on patient autonomy as central to the concept. Primarily a philosophical analysis, the book also covers legal aspects, with chapters on disclosure, comprehension, and competence.
Informed consent (Medical law) --- Consent (Law) --- Declaration of intention --- Justification (Law) --- Consent, Informed --- Consent to treatment --- Disclosure, Medical --- Medical disclosure --- Treatment, Consent to --- Medical ethics --- Medical personnel --- Patient education --- Involuntary treatment --- Patient refusal of treatment --- History. --- Malpractice --- Informed consent (Medical law) - United States - History
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Increasingly, notions of individual autonomy, personal ""choice"" and preference have become woven into our reproductive expectations. With respect to prenatal screening, the choices sought, offered or denied are shaped and interpreted through a range of so
Prenatal diagnosis --- Informed consent (Medical law) --- Genetic screening --- Consent, Informed --- Consent to treatment --- Disclosure, Medical --- Medical disclosure --- Treatment, Consent to --- Consent (Law) --- Medical ethics --- Medical personnel --- Patient education --- Involuntary treatment --- Patient refusal of treatment --- Antenatal diagnosis --- Intrauterine diagnosis --- Prenatal testing --- Diagnosis --- Obstetrics --- Moral and ethical aspects. --- Malpractice
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Alasdair Maclean analyses the ethical basis for consent to medical treatment, providing both an extensive reconsideration of the ethical issues and a detailed examination of English law. Importantly, the analysis is given a context by situating consent at the centre of the healthcare professional-patient relationship. This allows the development of a relational model that balances the agency of the two parties with their obligations that arise from that relationship. That relational model is then used to critique the current legal regulation of consent. To conclude, Alasdair Maclean considers the future development of the law and contrasts the model of relational consent with Neil Manson and Onora O'Neill's recent proposal for a model of genuine consent.
Informed consent (Medical law) --- Consent, Informed --- Consent to treatment --- Disclosure, Medical --- Medical disclosure --- Treatment, Consent to --- Consent (Law) --- Medical ethics --- Medical personnel --- Patient education --- Involuntary treatment --- Patient refusal of treatment --- Malpractice --- Medical law and ethics --- Social ethics --- Professional ethics. Deontology --- Medical law --- Law --- General and Others --- Informed consent (Medical law) - England --- Droit médical --- Royaume-Uni
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This second edition has been revised and updated to reflect current changes in legislation on consent in the medical and healthcare setting. This book explores the law relating to consent, covering both the general principles where the patient is a mentally competent adult, and also the specialist areas of mental incapacity, children and parents. The text is written for all health professionals who care for the patient, and for patient service managers, patient groups, relatives, lecturers a...
Informed consent (Medical law) --- Medical laws and legislation --- Patients --- Persons --- Sick --- Consent, Informed --- Consent to treatment --- Disclosure, Medical --- Medical disclosure --- Treatment, Consent to --- Consent (Law) --- Medical ethics --- Medical personnel --- Patient education --- Involuntary treatment --- Patient refusal of treatment --- Civil rights --- Legal status, laws, etc. --- Malpractice
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Respect for autonomy has become a fundamental principle in human research ethics. Nonetheless, this principle and the associated process of obtaining informed consent do have limitations. This can lead to some groups, many of them vulnerable, being left understudied. This book considers these limitations and contributes through legal and philosophical analyses to the search for viable approaches to human research ethics. It explores the limitations of respect for autonomy and informed consent both in law and through the examination of cases where autonomy is lacking (infants), diminished (addicts), and compromised (low socio-economic status). It examines alternative and complementary concepts to overcome the limits of respect for autonomy, including beneficence, dignity, virtue, solidarity, non-exploitation, vulnerability and self-ownership. It takes seriously the importance of human relationality and community in qualifying, tempering and complementing autonomy to achieve the ultimate end of human research - the good of humankind.
Informed consent (Medical law) --- Medicine --- Biology --- Bioethics. --- Health Workforce --- Consent, Informed --- Consent to treatment --- Disclosure, Medical --- Medical disclosure --- Treatment, Consent to --- Consent (Law) --- Medical ethics --- Medical personnel --- Patient education --- Involuntary treatment --- Patient refusal of treatment --- Life sciences --- Biomass --- Life (Biology) --- Natural history --- Biomedical ethics --- Life sciences ethics --- Science --- Research --- Moral and ethical aspects. --- Malpractice --- Moral and ethical aspects --- Medicina --- Biología --- Bioética --- Aspectos morales
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Access to medical treatment for trans youth occupies a haphazard and dynamic legal landscape. In this comprehensive scholarly analysis of the historical and current legal principles, Steph Jowett examines the medico-legal nexus of regulation of this healthcare in Australia and in England and Wales. This is informed by an in-depth discussion of the medical literature on treatment for trans youth, including clinical guidelines, the outcomes of treatment and outcomes for trans youth who are unable to be treated. With illustrative examples and clear language, Jowett argues that legal barriers to clinical practice should be congruent with and reflect the current state of medical knowledge. Not only does Jowett assess the extent to which key legal decisions have been consistent with medical knowledge in the past, but she offers a nuanced, comparative perspective that will inform reform efforts in the future.
Gender-nonconforming youth --- Gender identity --- Informed consent (Medical law) --- Medical care --- Law and legislation --- Sex identity (Gender identity) --- Sexual identity (Gender identity) --- Identity (Psychology) --- Sex (Psychology) --- Queer theory --- Youth --- Consent, Informed --- Consent to treatment --- Disclosure, Medical --- Medical disclosure --- Treatment, Consent to --- Consent (Law) --- Medical ethics --- Medical personnel --- Patient education --- Involuntary treatment --- Patient refusal of treatment --- Malpractice --- Gender dysphoria --- Transsexual youth
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This book focuses on informed consent in African Traditional Medicine (ATM). ATM forms a large portion of the healthcare systems in Africa. WHO statistics show that as much as 80% of the population in Africa uses traditional medicine for primary health care. With such a large constituency, it follows that ATM and its practices should receive more attention in bioethics. By comparing the ethics of care approach with the ATM approach to Relational Autonomy In Consent (RAIC), the authors argue that the ATM focus on consent based on consensus constitutes a legitimate informed consent. This book is distinctive insofar as it employs the ethics of care as a hermeneutic to interpret ATM. The analysis examines the ethics of care movement in Western bioethics to explore its relational approach to informed consent. Additionally, this is the first known study that discusses healthcare ethics committees in ATM.
Medical ethics --- Traditional medicine --- Informed consent (Medical law) --- Biomedical ethics --- Clinical ethics --- Ethics, Medical --- Health care ethics --- Medical care --- Medicine --- Bioethics --- Professional ethics --- Nursing ethics --- Social medicine --- Consent, Informed --- Consent to treatment --- Disclosure, Medical --- Medical disclosure --- Treatment, Consent to --- Consent (Law) --- Medical personnel --- Patient education --- Involuntary treatment --- Patient refusal of treatment --- Moral and ethical aspects --- Malpractice --- Ethics. --- Medical ethics. --- Theory of Medicine/Bioethics. --- Deontology --- Ethics, Primitive --- Ethology --- Moral philosophy --- Morality --- Morals --- Philosophy, Moral --- Science, Moral --- Philosophy --- Values
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Disclosure of information --- -Informed consent (Medical law) --- -Patients --- -#GBIB:CBMER --- 351.84*1 --- 17.023.33 --- 614.253.8 --- Persons --- Sick --- Consent, Informed --- Consent to treatment --- Disclosure, Medical --- Medical disclosure --- Treatment, Consent to --- Consent (Law) --- Medical ethics --- Medical personnel --- Patient education --- Involuntary treatment --- Patient refusal of treatment --- Information, Disclosure of --- Truthfulness and falsehood --- Law and legislation --- -Moral and ethical aspects --- Legal status, laws, etc --- -Malpractice --- -Disclosure of information --- Medical care --- Netherlands --- Informed consent (Medical law) --- Patients --- #GBIB:CBMER --- Moral and ethical aspects --- Malpractice
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Informed consent (Medical law) --- Human experimentation in medicine --- Genomics --- Moral and ethical aspects --- Law and legislation --- Consent, Informed --- Consent to treatment --- Disclosure, Medical --- Medical disclosure --- Treatment, Consent to --- Consent (Law) --- Medical ethics --- Medical personnel --- Patient education --- Involuntary treatment --- Patient refusal of treatment --- Genome research --- Genomes --- Molecular genetics --- Malpractice --- Research --- Human experimentation in medicine - Moral and ethical aspects --- Genomics - Law and legislation --- Droit médical --- Bioéthique --- Sciences de la santé --- Médecine expérimentale --- Droit international
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