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ویرایش: 4
نویسندگان: Udo Schüklenk. Peter Singer
سری: Blackwell philosophy anthologies
ISBN (شابک) : 9781119635116, 9781119635154
ناشر: John Wiley & Sons, Inc.
سال نشر: 2022
تعداد صفحات: 941
زبان: English
فرمت فایل : PDF (درصورت درخواست کاربر به PDF، EPUB یا AZW3 تبدیل می شود)
حجم فایل: 9 مگابایت
در صورت تبدیل فایل کتاب Bioethics: An Anthology به فرمت های PDF، EPUB، AZW3، MOBI و یا DJVU می توانید به پشتیبان اطلاع دهید تا فایل مورد نظر را تبدیل نمایند.
توجه داشته باشید کتاب اخلاق زیستی: گلچین نسخه زبان اصلی می باشد و کتاب ترجمه شده به فارسی نمی باشد. وبسایت اینترنشنال لایبرری ارائه دهنده کتاب های زبان اصلی می باشد و هیچ گونه کتاب ترجمه شده یا نوشته شده به فارسی را ارائه نمی دهد.
Cover Title Page Copyright Page Contents Acknowledgments Introduction Notes Part I Abortion Introduction Chapter 1 Abortion and Infanticide I Abortion and Infanticide II Terminology: “Person” versus “Human Being” III The Basic Issue: When is a Member of the Species Homo sapiens a Person? IV Some Critical Comments on Alternative Proposals V Refutation of the Conservative Position VI Summary and Conclusions Notes Chapter 2 A Defense of Abortion Notes Chapter 3 The Wrong of Abortion Embryos and Fetuses are Complete (though Immature) Human Beings No-Person Arguments: The Dualist Version No-Person Arguments: The Evaluative Version The Argument that Abortion is Justified as Non-intentional Killing Notes Chapter 4 Why Abortion is Immoral I II III IV V VI Notes Part II Issues in Reproduction Introduction Assisted Reproduction Prenatal Screening, Sex Selection, and Cloning Assisted Reproduction Chapter 5 The McCaughey Septuplets: God’s Will or Human Choice?1 Notes Chapter 6 The Meaning of Synthetic Gametes for Gay and Lesbian People and Bioethics Too Controversial Parenthood Protecting Children from Some Possible Parents Conclusions References Chapter 7 Rights, Interests, and Possible People Notes Prenatal Screening, Sex Selection, and Cloning Chapter 8 Genetics and Reproductive Risk: Can Having Children Be Immoral? Huntington’s Disease Possible Children and Potential Parents Notes Chapter 9 Sex Selection and Preimplantation Genetic Diagnosis Background The General Ethical Debate Preimplantation Genetic Diagnosis and Sex Selection: Joining the Particular Issues Recommendations Chapter 10 Sex Selection and Preimplantation Diagnosis: A Response to the Ethics Committee of the American Society of Reproductive Medicine Introduction References Chapter 11 Why We Should Not Permit Embryos to Be Selected as Tissue Donors Children as Things What Kind of Ethics Do We Need? Chapter 12 The Moral Status of Human CloningNeo-Lockean Persons versus Human Embryos Introduction 1 A Crucial Concept: neo-Lockean Persons 1.1 John Locke’s concept of a person 1.2 The concept of a neo-Lockean person 1.3 Distortions of the concept of a neo-Lockean person 1.4 Neo-Lockean persons and the right to life 2 Cloning to Produce Human Organisms that Will Never Become Persons 2.1 Cloning for medical purposes or scientific research 2.2 Cloning to produce a human organ bank 2.3 Arguments Against Such Cloning 2.3.1 Appeals to immaterial minds or souls 3 Cloning to Produce Persons 3.1 Is cloning that aims at producing future persons intrinsically wrong? 3.2 Consequentialist objections to cloning to produce persons 3.3 Arguments in favor of cloning to produce persons Conclusion Note References Part III Genetic Manipulation Introduction Chapter 13 Questions about Some Uses of Genetic Engineering Avoiding the Debate about Genes and the Environment Methods of Changing the Genetic Composition of Future Generations The Positive–Negative Distinction The View that Overall Improvement is Unlikely or Impossible The Family and Our Descendants Risks and Mistakes Not Playing God The Genetic Supermarket A Mixed System Values Notes Chapter 14 The Moral Significance of the Therapy–Enhancement Distinction in Human Genetics Introduction Somatic versus Germline Interventions The Concepts of Health and Disease The Goals of Medicine Our Humanness The Rights of the Unborn Eugenics Conclusion: The Significance of the Distinction Notes Chapter 15 In Defense of Posthuman Dignity Transhumanists vs. Bioconservatives Two Fears about the Posthuman Is Human Dignity Incompatible with Posthuman Dignity? Why We Need Posthuman Dignity Notes Chapter 16 Statement on NIH Funding of Research Using Gene-Editing Technologies in Human Embryos Chapter 17 Genome Editing and Assisted Reproduction: Curing Embryos, Society or Prospective Parents? Introduction: Genetic Diseases, Genome Editing and Existing Alternatives PGD and Assisted Reproduction CRISPR and Assisted Reproduction Assisted Reproduction and PGD, or Assisted Reproduction and CRISPR? The Case for Genome Editing: Two Sets of Arguments Selection versus Therapy Curing Embryos, Society or Prospective Parents? Reproductive autonomy, child welfare and the interests of society Societal interests and the costs of introducing genome editing in the context of assisted reproduction Conclusions: Context Matters References Notes Chapter 18 Who’s Afraid of the Big Bad (Germline Editing) Wolf? References Chapter 19 An Ethical Pathway for Gene Editing Notes Part IV Life and Death Issues Introduction Killing and Letting Die Newborns Brain Death Advance Directives Voluntary Euthanasia and Medically Assisted Suicide Notes Chapter 20 The Sanctity of Life 1 Direct Objections and Side-Effects 2 Stating the Principle of the Sanctity of Life 3 The Boundary between Life and Death 4 ‘Being Alive Is Intrinsically Valuable’ 5 ‘Being Conscious Is Intrinsically Valuable’ 6 ‘Being Human Is Intrinsically Valuable’ 7 The Concept of a ‘Life Worth Living’ 8 Is the Desire to Live the Criterion of a Worthwhile Life? 9 Length of Life 10 The ‘No Trade-Off’ View 11 The Social Effects of Abandoning the Sanctity of Life References Chapter 21 Declaration on Euthanasia: Sacred Congregation for the Doctrine of the Faith I The Value of Human Life II Euthanasia III The Meaning of Suffering for Christians and the Use of Painkillers IV Due Proportion in the Use of Remedies Conclusion Notes Chapter 22 Active and Passive Euthanasia Reference Killing and Letting Die Chapter 23 The Morality of Killing: A Traditional View The Morality of Killing Chapter 24 Is Killing No Worse Than Letting Die? 2 3 4 Notes Chapter 25 Why Killing is Not Always Worse – and Sometimes Better – Than Letting Die I II III Notes Chapter 26 Moral Fictions and Medical Ethics The Concept of Moral Fictions Exposing the Moral Fictions Suicide Causation Intention Moral responsibility Differential moral assessment The Moral Work of Moral Fictions Abandoning the Moral Fictions Notes Newborns Chapter 27 Can a Physician Ever Justifiably Euthanize a Severely Disabled Newborn? The Case of the Ill-fated Newborn References Chapter 28 No to Infant Euthanasia References Chapter 29 Physicians Can Justifiably Euthanize Certain Severely Impaired Neonates Discussion Infants lack decision-making capacity Sanctity of life versus quality of life Quality-of-life ethic and infanticide Quality-of-life ethic and terminal sedation Parental and health care professionals’ interests matter Resource allocation justice Slippery slope concerns Unfair discrimination against the disabled? Human dignity Conclusions References Chapter 30 You Should Not Have Let Your Baby Die Chapter 31 After-Birth AbortionWhy Should the Baby Live? Introduction Abortion and After-Birth Abortion The Newborn and the Fetus are Morally Equivalent The Fetus and the Newborn are Potential Persons Adoption as an Alternative to After-Birth Abortion? Conclusions References Chapter 32 Does a Human Being Gain the Right to Live after He or She is Born? References Chapter 33 Hard LessonsLearning from the Charlie Gard Case Parents’ Role In Decision-Making for Children: We Need to Clarify Harm Decisions for Adults Versus Decisions for Children: Allow Adults to Choose Treatment for Themselves even if Suboptimal Experimental Treatment: We Should Have A Lower Threshold For Allowing Access Where Patients Have No Other Options, And Allow Earlier Innovative Treatment The Role of Resources: We Need to Talk about Limited Resources The Role of the Courts: We Need a Fair, Expedient Way of Resolving Disputes Ethical Decisions versus Clinical Decisions: Allow and Support Reasonable Disagreement Medical Tourism: Allow Families to Travel Unless Illegal or Risks Significant Harm Challenging Normative and Conceptual Issues: Need for Further Ethical Analysis Reflective Equilibrium, Reasons and Evidence: Need for Humility and Transparency References Brain Death Chapter 34 A Definition of Irreversible Coma Characteristics of Irreversible Coma Other Procedures Legal commentary Comment Summary Reference Chapter 35 The Challenge of Brain Death for the Sanctity of Life Ethic I Introduction II The Origins of the New Definition of Death III Death as the Irreversible Loss of Integrated Organic Functioning IV What do the Standard Tests for Brain Death Show? V President George W. Bush’s Council on Bioethics Enters the Debate VI The significance of irreversible unconsciousness VII The Centrality of Ethics VIII Conclusion Notes References Chapter 36 The Philosophical Debate I Position One: There Is No Sound Biological Justification for Today’s Neurological Standard II Position Two: There Is a Sound Biological Justification for Today’s Neurological Standard A The Work of the Organism as a Whole B Comparison with the UK Standard Notes References Chapter 37 An Alternative to Brain Death Some Common but Mistaken Assumptions about Death An Alternative Understanding of Death Reference Advance Directives Chapter 38 Life Past Reason Autonomy Notes Chapter 39 Dworkin on Dementia: Elegant Theory, Questionable Policy Advance Directives and Precedent Autonomy Critical and Experiential Interests: Problems with the Model The State’s Interest in Margo’s Life Notes Chapter 40 The Note Statement Voluntary Euthanasia and Medically Assisted Suicide Chapter 41 When Self-Determination Runs Amok Self-Determination Killing and Allowing to Die Calculating the Consequences Euthanasia and Medical Practice Chapter 42 When Abstract Moralizing Runs Amok Notes Chapter 43 Physician-Assisted Death and Severe, Treatment-Resistant Depression Terminology Terminal Illness Defining and Identifying Treatment-Resistant Depression Can Patients with Severe Major Depressive Disorder Be Competent to Request Assisted Dying? Role Responsibility Slippery-Slope Concerns Public Policy Considerations Notes Chapter 44 Are Concerns about Irremediableness, Vulnerability, or Competence Sufficient to Justify Excluding All Psychiatric Patients from Medical Aid in Dying? Introduction Irremediableness What are treatment outcomes like for patients with treatment resistant depression? Discerning between irremediable and remediable cases Irremediableness cannot be understood as certainty that no treatment will succeed Defending irremediableness that admits of false positives Does the availability of MAID for non-terminal patients negatively impact care? Vulnerability Why are psychiatric patients especially vulnerable? Is vulnerability a useful concept? Does vulnerability shift the burden of proof? Assessing Competence Can physicians effectively perform capacity assessments? Arbitrarily high capacity test score cut-offs as an alternative to a ban The Netherlands Opposition to the Dutch system Physician disagreement Specific concerns about capacity assessment in the Netherlands Trust in physicians Conclusion Notes References Part V Resource Allocation Introduction Chapter 45 In a Pandemic, Should We Save Younger Lives?: YES – Peter Singer NO – Lucy Winkett YES NO YES NO Chapter 46 The Value of Life I The Moral Significance of Age The anti-ageist argument The fair innings argument Numbers of lives and numbers of years Extra life-time versus extra lives The fallacy of life-time views Worthwhile life-time Fair innings or no ageism? Notes Chapter 47 Bubbles under the Wallpaper: Healthcare Rationing and Discrimination Bubbles under the Wallpaper Example A Rights-Based Approach? Randomness to the Rescue? Conclusion Notes References Chapter 48 Rescuing Lives: Can’t We Count? Notes Chapter 49 Should Alcoholics Compete Equally for Liver Transplantation? Should Patients with ARESLD Receive Transplants? Nonrenewable resource Comparison with cardiac transplantation Expensive technology General guideline proposed Objections to Proposal Alcoholism: How is it similar to and different from other diseases? Are we discriminating against alcoholics? Reasons Patients with ARESLD Should Have a Lower Priority on Transplant Waiting Lists Fairness Policy considerations regarding public support for liver transplantation Should Any Alcoholics Be Considered for Transplantation? Need for Further Research Comment References Part VI Obtaining Organs Introduction Chapter 50 Organ Donation and Retrieval: Whose Body is it Anyway? Note Chapter 51 The Case for Allowing Kidney Sales References Chapter 52 Ethical Issues in the Supply and Demand of Kidneys Brief Background: The Status Quo Systems of Kidney Procurement Anti-Market Considerations Does a Market Ban Necessarily Decrease the Supply of Available Organs? Vulnerability Weak Agency Equal Status Considerations The Integrity of the Body Policy Notes Chapter 53 The Survival Lottery Note Part VII Ethical Issues in Research Experimentation with Humans Chapter 54 Belmont Report: Ethical Principles and Guidelines for the Protection of Human Subjects of Research A Boundaries between Practice and Research B Basic Ethical Principles 1 Respect for persons 2 Beneficence 3 Justice C Applications 1 Informed consent 2 Assessment of risks and benefits 3 Selection of subjects Notes Chapter 55 Scientific Research is a Moral Duty Do No Harm Fairness The Moral Imperative for Research Do Universal Moral Principles Deny This Claim? Is There an Enforceable Obligation to Participate in Research? Mandatory Contribution to Public Goods Benefit Sharing A New Principle of Research Ethics On Whom Does the Obligation to Participate in Research Fall? Me and My Kind Children and the Incompetent Inducements to Participate in Research Conclusion Notes References Chapter 56 Participation in Biomedical Research is an Imperfect Moral Duty: A Response to John Harris The Principle of Beneficence The Principle of Fairness Conclusions Notes References Chapter 57 Unethical Trials of Interventions to Reduce Perinatal Transmission of the Human Immunodeficiency Virus in Developing Countries Asking the Wrong Research Question Inadequate Analysis of Data from ACTG 076 and Other Sources Defining Placebo as the Standard of Care in Developing Countries Justifying Placebo-Controlled Trials by Claiming They Are More Rapid Toward a Single International Standard of Ethical Research References Chapter 58 We’re Trying to Help Our Sickest People, Not Exploit Them Chapter 59 Pandemic Ethics: The Case for Risky Research1 The Principle of Risk Parity Applying the Principle of Risk Parity to COVID-19 Research – Three Examples Notes References Experimentation with Animals Chapter 60 Duties towards Animals Chapter 61 A Utilitarian View Note Chapter 62 The Harmful, Nontherapeutic Use of Animals in Research is Morally Wrong Methods Some Distracting Issues not Discussed in Detail Activists’ behavior “Rights” “Equality,” “importance,” “status” and “standing” Some Objections: “Animal Experimentation is Morally Permissible Because . . .” “Scientific” arguments “Necessary condition” arguments “Group-based” arguments “Benefits” arguments “Necessity” arguments “No alternatives” arguments “Necessary condition” arguments Group-based arguments A Positive, Cumulative Case in Defense of Animals References Chapter 63 The Use of Nonhuman Animals in Biomedical Research Arguments Against the Use of Animals in Scientific Research Claim: Humans do not benefit from animal research Claim: Animal research has a very low success rate Claim: Researchers must prove animals are necessary for their work Claim: Animal models are not predictive of human responses Claim: Basic research is knowledge for knowledge’s sake Claim: Alternatives to animal research already exist Ethics of Animal Research The Moral Status of Animals Rejecting the Extremes of the Spectrum Equal Consideration of Equal Interests Human Ability to Challenge Nature and Suffering is Unique Utilitarian Considerations What About Marginal Cases? Human Relationships Are Unique: The Human Family Assuming Responsibility and Stewardship Conclusion References Chapter 64 Ethical Issues When Modelling Brain Disorders in Non-Human Primates Introduction Trends in Disease Modelling Post-CRISPR Methodological Starting Point Animal welfare Available alternatives Expectation of benefit Conclusion Notes References Academic Freedom and Research Chapter 65 On Liberty Chapter II: Of The Liberty of Thought and Discussion Chapter 66 Should Some Knowledge Be Forbidden?: The Case of Cognitive Differences Research 1 Introduction 2 A Case Study: The Right to Equality versus the Right to Freedom of Research 3 Past Precedents 4 The Third Precedent 5 Conclusion References Chapter 67 Academic Freedom and Race: You Ought Not to Believe What You Think May Be True 1 An Intelligible Hypothesis 2 Not Believing What You Think May Be True 3 Not Discussing What Some Think To Be True 4 Not Using Science to Investigate the Truth 5 From Advice to Sanctions 6 The Dead Hand of Ignorance 7 The Appeal to Paradigms of Irrationality 8 Compromises 9 The Bright Light of Knowledge 10 Armageddon 11 Some History and Rhetoric Part VIII Public Health Issues Introduction Reference Chapter 68 Ethics and Infectious Disease I Distribution of Research Resources II The Ethical Importance of Infectious Disease 1 Consequences 2 Difficult ethical questions 3 Justice III Why the Neglect? 1 High tech medicine 2 Optimism in medicine 3 ‘The other’ 4 Complexity 5 Apparent ease 6 Religious hijacking Conclusion Notes Chapter 69 XDR-TB in South Africa: No Time for Denial or Complacency The Threat to Regional and Global Health The True Extent of the Problem Factors Fuelling the Outbreak Factors That Could Undermine Efforts to Tackle the Outbreak Is There a Role for Involuntary Detention? Conclusion References Chapter 70 Clinical Ethics During the Covid-19 Pandemic: Missing the Trees for the Forest Introduction Clinical Ethics Challenges Arising in the Care of Covid-19 Patients Treatment of Covid-19 patients as a means to an end Working with uncertain evidence and unproven therapies Duty to care versus right to protection Rationing of scarce resources in pandemic situations Dignity in death Clinical Ethics Considerations in the Care of “Non-Covid-19” Patients Moral Distress of Healthcare Providers References Chapter 71 The Moral Obligation to be Vaccinated: Utilitarianism, Contractualism, and Collective Easy Rescue Introduction From Collective to Individual Responsibility The Utilitarian Approach: Group Beneficence and Imperceptible Contributions The Deontological Approach Vaccination and the generalization test Vaccination and contractualism Duty of Easy Rescue and Fairness: A Further Argument for an Individual Moral Obligation to be Vaccinated Easy rescue, collective obligations, and the individual duty to be vaccinated High cost vaccinations Conclusion Notes References Chapter 72 Taking Responsibility for Responsibility Responsibility for Health The Social Determinants of Health Taking Responsibility for Responsibility Notes References Part IX Ethical Issues in the Practice of Healthcare Introduction When do Doctors have a Duty to Treat? Confidentiality Truth-Telling Informed Consent and Patient Autonomy Notes When do Doctors have a Duty to Treat? Chapter 73 What Healthcare Professionals Owe Us: Why Their Duty to Treat During a Pandemic is Contingent on Personal Protective Equipment (PPE) Introduction What Healthcare Professionals Owe Us Neoliberalism and the Fetishisation of ‘Efficiency’ Implications for Healthcare Professionals’ Obligations Conclusion References Chapter 74 Conscientious Objection in Health Care Introduction What is Conscientious Objection? Assessing Approaches to Conscientious Objection in Health Care Conscience absolutism Incompatibilism Reasonable accommodation Conscientious Objection vs. Obstruction Conclusion Notes Chapter 75 Conscientious Objection in Medicine: Accommodation versus Professionalism and the Public Good Introduction Conscience – What Is It, and Does It Matter? Conscience Claims – Should They be Reasonable and Genuine? Conscience and Professionalism Voluntariness and Monopoly Equality of Opportunity Diversity Equal Citizenship Peaceful Co-existence Conclusion References Confidentiality Chapter 76 Confidentiality in Medicine: A Decrepit Concept Two Aspects of Medical Confidentiality Confidentiality and third-party interests Confidentiality and the patient’s interest The Role of Confidentiality in Medicine Possible Solutions to the Confidentiality Problem Afterthought: Confidentiality and Indiscretion Conclusion Chapter 77 A Defense of Unqualified Medical Confidentiality The Case of the Infected Spouse Clearing the Ground: What Professional Obligations Are Not Law Personal morality Personal values The Concept of a Professional Obligation The Duty to Diminish Risks to Third Parties A Defense of Unqualified Confidentiality Concluding Remarks References Truth-Telling Chapter 78 On a Supposed Right to Lie from Altruistic Motives Chapter 79 Should Doctors Tell the Truth? Chapter 80 On Telling Patients the Truth Notes Informed Consent and Patient Autonomy Chapter 81 On Liberty Chapter 82 From Schloendorff v. NewYork Hospital Chapter 83 Informed Consent: Its History, Meaning, and Present Challenges The Historical Foundations of Informed Consent The Concept of Informed Consent Current Challenges to Informed Consent The limits of the law in biomedical ethics The quality of consent Problems of broad consent The regulation of consent and the research–treatment distinction Conclusion Notes Chapter 84 The Doctor–Patient Relationship in Different Cultures “Physicians Treat Patients Badly” Similarities and Differences Conceptions of Autonomy: East and West Truth-Telling Notes Chapter 85 Transgender Children and the Right to Transition: Medical Ethics When Parents Mean Well But Cause Harm 1 Introduction 2 Gender Dysphoria and Treatment for Transgender Youth 2.1 Gender dysphoria and its consequences 2.2 Do children own their bodies? 2.3 Persisting and desisting 2.4 PBT is the best route, regardless 3 Psychological Harm and Epistemic Barriers 4 The Physical Risks 5 Justifying Intervention 5.1 A child’s right to their body 5.2 Putting rights into practice 6 Spreading the Word and the Role of Schools 7 Objections and How to Answer Them 7.1 Parental rights to raise their children 7.2 Funding issues 7.3 Why not take it further? 8 Review and Concluding Remarks Notes References Chapter 86 Amputees by Choice Editors’ Note Notes Chapter 87 Rational Desires and the Limitation of Life-Sustaining Treatment The President’s Commission Report Part I. What is Autonomy? An argument for rational desiring Two objections to vivid imagination Two senses of rational desiring Autonomy as a dispositional concept Ulysses and the Sirens: an example of obstructive desire One objection Part II. “No Man Ever Threw Away Life, While It Was Worth Keeping” Adaptation to disability Hurdles to evaluation: loss aversion and contrast Part III. Limitations of Treatment of Incompetent Patients When is limitation of treatment in a patient’s best interests? Limitation of Treatment of Competent Patients Two Objections 1. Respect only articulated desires? 2. Autonomy and false beliefs Conclusion Notes Part X Disability Introduction Chapter 88 Valuing Disability, Causing Disability I The Bad-Difference/Mere-Difference Distinction II A Problem for the Mere-Difference View? III Causing a Nondisabled Person to Become Disabled IV Causing a Nondisabled Person to Become Disabled Without Transition Costs V Causing a Disabled Person to Exist Instead of a Nondisabled Person VI Causing and “Curing” VII Conclusion Notes Chapter 89 Is Disability Mere Difference? Introduction Disability and Quality of Life Disability and Society The Indirect Strategy Conclusion References Chapter 90 Prenatal Diagnosis and Selective Abortion: A Challenge to Practice and Policy Contrasting Medical and Social Paradigms of Disability Prenatal diagnosis for disability prevention Rationales for prenatal testing Implications for People with Disabilities Implications for Family Life Implications for Professional Practice References Chapter 91 Down Syndrome Screening Isn’t about Public HealthIt’s about Eliminating a Group of People Chapter 92 I Would’ve Aborted a Fetus with Down Syndrome: Women Need that Right Part XI Neuroethics Introduction Chapter 93 Neuroethics: Ethics and the Sciences of the Mind The Ethics of Neuroscience Memory Modification and Enhancement Note References Chapter 94 Engineering Love Chapter 95 Unrequited Love Hurts: Should Doctors Treat Broken Hearts? Unrequited Love Hurts Two Arguments Against the Medicalization of Unrequited Love The peculiarity-of-heartbreak objection The arts objection Conclusions Acknowledgment Notes Chapter 96 Stimulating Brains, Altering Minds Empirical Evidence: Benefits and Risks A Case Study Autonomy and Identity Conclusion References Chapter 97 Authenticity or Autonomy? When Deep Brain Stimulation Causes a Dilemma Introduction: Feelings of Authenticity and Alienation under Deep Brain Stimulation A Patient’s Dilemma: Choosing between Mental Competence and Well-Being Authenticity or Autonomy? A Philosophical Reinterpretation Is ‘Authenticity’ the New ‘Autonomy’ in Neuroethics? Conclusions References Chapter 98 On the Necessity of Ethical Guidelines for Novel Neurotechnologies Novel Neurotechnologies and Their Future Use Ethical and Societal Issues Raised by Novel Neurotechnologies Developing Ethical Principles for Neurotechnologies The Importance of Novel Neurotechnology for the Progress of Humankind References Index EULA