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A practical guide for health and social care professionals on the Mental Capacity Act 2005, enabling more informed and effective practice.
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This volume addresses the proper character of patient informed consent to medical treatment and clinical research. The goal is critically to explore the current individually oriented approach to informed consent which grew out of the dominant bioethics movement that arose in the United States in the 1970s. In contrast to that individually oriented approach, this volume explores the importance of family-oriented approaches to informed consent for medical treatment and clinical research. It draws on both East Asian moral resources as well as a critical response to the ways in which the practice of informed consent has developed in the United States.
Philosophy. --- Ethics. --- Theory of Medicine/Bioethics. --- Philosophy of Medicine. --- Philosophy (General). --- medicine --- Medical ethics. --- Morale --- Ethique médicale --- Informed consent (Medical law). --- Patient participation. --- Therapeutics -- Decision making. --- Philosophy --- Philosophy & Religion --- Ethics --- Informed consent (Medical law) --- Bioethics. --- Biology --- Biomedical ethics --- Life sciences --- Life sciences ethics --- Clinical ethics --- Ethics, Medical --- Health care ethics --- Medical care --- Medicine --- Consent, Informed --- Consent to treatment --- Disclosure, Medical --- Medical disclosure --- Treatment, Consent to --- Moral and ethical aspects --- Bioethics --- Professional ethics --- Nursing ethics --- Social medicine --- Consent (Law) --- Medical ethics --- Medical personnel --- Patient education --- Involuntary treatment --- Patient refusal of treatment --- Science --- Malpractice --- Medicine-Philosophy. --- Deontology --- Ethics, Primitive --- Ethology --- Moral philosophy --- Morality --- Morals --- Philosophy, Moral --- Science, Moral --- Values --- Medicine—Philosophy.
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This important book proposes revising the current informed consent protocol for predictive genetic testing to reflect the trend toward patient-centered medicine. Emphasizing the predictive aspect of testing, the author analyzes the state of informed consent procedure in terms of three components: comprehension of risk assessment, disclosure to select appropriate treatment, and voluntariness. The book's revised model revisits these cornerstones, restructuring the consent process to allow for expanded comprehension time, enhanced patient safety, greater patient involvement and autonomy, and reduced chance of coercion by family or others. A comparison of the current and revised versions and case studies showing the new model in real-world applications add extra usefulness to this resource. Included in the coverage: The science behind PGT. Understanding genetic risks and probability. The history of informed consent. Revised model of informed consent: comprehension, disclosure, voluntariness, patient safety. Applications of the model in DTC and pleiotropic genetic testing. Implementation of the revised model, and assessing its effectiveness. A milestone in the bioethics literature, Informed Consent in Predictive Genetic Testing will be of considerable interest to genetic counselors, medical and bioethicists, and public health professionals.
Medicine & Public Health. --- Maternal and Child Health. --- Psychotherapy and Counseling. --- Human Genetics. --- Health Psychology. --- Medicine. --- Human genetics. --- Maternal and infant welfare. --- Applied psychology. --- Psychology, clinical. --- Médecine --- Génétique humaine --- Medicine --- Health & Biological Sciences --- Gynecology & Obstetrics --- Pediatrics --- Human chromosome abnormalities --- Informed consent (Medical law) --- Genetic screening. --- Diagnosis. --- Consent, Informed --- Consent to treatment --- Disclosure, Medical --- Medical disclosure --- Treatment, Consent to --- Genetic diagnosis --- Genetic testing --- Maternal and child health services. --- Psychotherapy. --- Counseling. --- Health psychology. --- Consent (Law) --- Medical ethics --- Medical personnel --- Patient education --- Involuntary treatment --- Patient refusal of treatment --- Medical screening --- Malpractice --- Diagnosis --- Genetics --- Heredity, Human --- Human biology --- Physical anthropology --- Applied psychology --- Psychagogy --- Psychology, Practical --- Social psychotechnics --- Psychology --- Infant welfare --- Infants --- Maternity welfare --- Child welfare --- Mothers --- Women --- Maternal health services --- Charities, protection, etc. --- Charities --- Health psychology --- Health psychology, Clinical --- Psychology, Clinical health --- Psychology, Health --- Salutogenesis --- Clinical psychology --- Medicine and psychology --- Counselling --- Helping behavior --- Psychology, Applied --- Clinical sociology --- Interviewing --- Personal coaching --- Social case work --- Therapy (Psychotherapy) --- Mental illness --- Mental health counseling --- Treatment
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This volume presents a number of controversial cases of enforced medical treatment from around the globe, providing for the first time a common, biopolitcal framework for all of them. Bringing together all these real cases guarantees that a new, more complete understanding of the topic will be within grasp for readers unacquainted with the aspects involved in these cases. On the one hand, readers interested mainly in the legal and medical dimensions of cases like those considered will benefit from the explanation of the biopolitical framework within which each case develops. On the other hand, those focusing on only one of the situations presented here will find the parallels between the cases an interesting expansion of the complexity of the problem. Despite the book's ambitious goal, for those willing to use it as supplemental material or interested in only one of the cases, the chapters can function as self-standing pieces to be read separately. This volume will be a valuable tool for both academics and professionals. Bioethicists in both the analytic and continental traditions, will find the book interesting for not only the specific concepts and issues considered, but also for its constructive bridging of the two schools of thought. In addition to philosophers, the structure of this work will also appeal to lawyers, doctors, human rights activists, and anyone concerned in the most disparate way with real-life cases of enforced medical treatment.
Philosophy. --- Ethics. --- Theory of Medicine/Bioethics. --- Medical Law. --- Neurosciences. --- Political Science, general. --- Philosophy (General). --- Medical ethics. --- Public health laws. --- Neurosciences --- Morale --- Ethique médicale --- Santé publique --- Droit --- Ethics --- Philosophy --- Philosophy & Religion --- Involuntary treatment. --- Involuntary treatment --- Moral and ethical aspects. --- Coerced treatment --- Coercive care --- Coercive treatment --- Compulsory treatment --- Enforced treatment --- Forced treatment --- Treatment, Involuntary --- Political science. --- Medical laws and legislation. --- Political Science. --- Patients --- Therapeutics --- Informed consent (Medical law) --- Legal status, laws, etc. --- Administration --- Civil government --- Commonwealth, The --- Government --- Political theory --- Political thought --- Politics --- Science, Political --- Social sciences --- State, The --- Neural sciences --- Neurological sciences --- Neuroscience --- Medical sciences --- Nervous system --- Communicable diseases --- Public health --- Medical laws and legislation --- Biomedical ethics --- Clinical ethics --- Ethics, Medical --- Health care ethics --- Medical care --- Medicine --- Bioethics --- Professional ethics --- Nursing ethics --- Social medicine --- Deontology --- Ethics, Primitive --- Ethology --- Moral philosophy --- Morality --- Morals --- Philosophy, Moral --- Science, Moral --- Values --- Law and legislation --- Moral and ethical aspects --- Law, Medical --- Medical personnel --- Medical registration and examination --- Physicians --- Surgeons --- Medical policy --- Medical jurisprudence
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Zorgverleners en patiënten beslissen samen over de behandeling De juiste kennis en tools om samen met patiënten keuzes te maken. Het overlegmodel zit in de lift. Veel zorggebruikers willen mee beslissen over de zorg en zijn daar, mede dankzij het internet, steeds beter op voorbereid. Zorgverstrekkers erkennen het belang van patiëntgerichte zorg. Immers, in veel keuzesituaties is de beste optie mede afhankelijk van de waarden en voorkeuren van de patiënt. Dit vereist nieuwe kennis, attitudes en competenties van iedereen die in de zorg actief is. Gelukkig bestaan er tools die zorgverstrekkers en gebruikers ondersteunen. Maar hoe ga je ermee aan slag? In dit boek wordt ieder aspect van deze kwestie behandeld zodat de zorgverstrekker met kennis van zaken aan de slag kan. patiënt, houdt rekening met hun verschillende perspectieven en biedt praktische tips om kiezen in overleg in de praktijk te brengen. Zo vormt het de perfecte kennismaking met een arts-patiëntcommunicatie die is aangepast aan de noden van onze tijd.
Care and treatment --- Consent [Informed ] --- Consent to treatment --- Consentement au traitement --- Consentement du malade --- Consentement éclairé (Droit médical) --- Disclosure [Medical ] --- Geneeskundige zorgen--Planning --- Gestion des soins--Planification (Soins médicaux) --- Geïnformeerde toestemming (Medisch recht) --- Informed consent (Medical law) --- Malades--Consentement au traitement --- Managed care plans (Medical care) --- Managed care programs (Medical care) --- Managed care systems (Medical care) --- Medical disclosure --- Medische zorgen--Planning --- Plans [Managed care (Medical care) ] --- Program [Managed care (Medical care) ] --- Soins et traitement --- Systems [Managed care (Medical care) ] --- Toestemming met kennis van zaken (Medisch recht) --- Treatment [Consent to ] --- Verzorgingen en behandeling --- Zorgen [Geneeskundige ]--Planning --- Zorgen [Medische ]--Planning --- Zorgplanning (Gezondheidszorg) --- Patiëntenrecht --- Arts-patiënt relatie --- Besliskunde (medische besliskunde) --- Informed consent --- 601.3 --- verpleegkunde --- geneeskunde --- zorgrelatie --- communicatie --- patiënt-verpleegkundige relatie --- overleg --- 614.253.83 --- Rechten en plichten van patiënten. Verantwoordelijkheid van de arts voor de behandeling. Veronachtzaming van de patiënt. Nalaten van behandeling. Afwijzing van behandeling --- Patiëntenbegeleiding --- Persoonsgerichte zorg --- patiëntenparticipatie --- Human medicine --- arts-patiënt relatie --- gespreksmodellen --- eerstelijnsgezondheidszorg --- Hygiene. Public health. Protection --- informed consent --- Mass communications --- Patiëntenbegeleiding. --- Arts en patiënt --- Physicians --- Professional ethics --- Patients --- Legal status, laws, etc. --- Belgium --- Handbooks, manuals, etc. --- PXL-Healthcare 2016 --- patiëntenbegeleiding --- Academic collection --- #gsdb5 --- Relatie arts - patiënt --- Arts en patiënt
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