INFORMED CONSENT Some Philosophical Puzzles Professor David Archard

Slides:



Advertisements
Similar presentations
Legal Capacity, Personhood and Supported Decision Making
Advertisements

Confidentiality, Consent and Data Protection Elizabeth M Robertson Deputy Medical Director Grampian University Hospitals Trust.
Informed Consent Hemantha Senanayake Chairman, Research Ethics Committee, Faculty of Medicine, University of Colombo.
Informed consent in research ethics
Ethics Relating to Children in Research in FP7
DAVID ARCHARD PROFESSOR OF PHILOSOPHY What does it mean to have a right of participation?
Chapter 10 Ethical Issues in Nursing Research. Perspectives for Assessing Ethical Acceptability Utilitarian Perspective - the good of a project is defined.
Ethical regulations for health research involving human subjects in Cambodia By Chap Seak Chhay, MD, MPH, MHPEd Public Health and Health Professions Educator.
Informed Consent: Requirements Ben Faneye, OP, DHCE West African Bioethics Training Program.
© HRP Associates, Inc. Informed Consent, Parental Permission & Assent Jeffrey M. Cohen, Ph.D., CIP President, HRP Associates, Inc.
Ethical and Moral Issues in Counseling
Vicki Hammen, Vice Chair, IRB IRB Brown Bag February 9, 2009.
ETHICS In Field Of Dental Hygiene BY Dr. Shahzadi Tayyaba Hashmi.
REFUSAL OF TREATMENT – ADOLESCENT WITH CANCER Rabbi Prof. Avraham Steinberg.
Obtaining Informed Consent: 1. Elements Of Informed Consent 2. Essential Information For Prospective Participants 3. Obligation for investigators.
Justification of Research in Humans Impossible to reach the important conclusions without studying humans Impossible to reach the important conclusions.
Detectives in the Classroom - Investigation 2-3: What's Wrong with This Picture? What's Wrong with This Picture?
Chapter 4 Legal and Ethical Considerations for Counselors
1 Consent for treatment A summary guide for health practitioners about obtaining consent for treatment Bridie Woolnough Resolution Officer Health Care.
Ethics in research involving human subjects
Research Ethics John Porter London School of Hygiene and Tropical Medicine.
IRB Discussion Consent and Assent Issues in Vulnerable Populations December
Practical Ethics Introduction to practical ethical issues and philosophical concepts. What is Practical Ethics? An area of moral philosophy looking at.
Idara C.E.. Three ethical principles guides research with human participants. principle of Autonomy 1. The principle of Autonomy requires investigators.
Proxy Consent. Civil code of the Philippines Competency of minors  Art. 38. Minority, insanity or imbecility, the state of being a deaf-mute, prodigality.
SOCIAL WORK ETHICS Issue in Child Welfare. GOALS & OBJECTIVES 1. To discuss how we define ethics. 2. To examine personal values related to ethics. 3.
Prepared by : Dr. Reem A.Jarra d. Introduction In their daily work nurses deal with events of : birth, death, & suffering. So they will be faced by many.
Ethics and End-of-Life Care Part 2: Autonomy and Futility Michael Wassenaar, PhD February 9, 2012.
Patient Understanding in Informed Consent Robert F. Dunton, MD Chief, Division of Cardiothoracic Surgery Upstate Medical University.
HUMAN RESEARCH HISTORICAL PERSPECTIVE. Objectives Identify the history events that lead to the development of principles, regulations, and guidance.
The Eighth Asian Bioethics Conference Biotechnology, Culture, and Human Values in Asia and Beyond Confidentiality and Genetic data: Ethical and Legal Rights.
Case Study: Medical Research Jillian Cudmore Mallory Anne Andrea Currie Amy DeBaie.
Sex, Drugs, Rock and Role, and Other Ethical Dilemmas in Community Based Research Robert T. Trotter, II General Motors Sigma Xi Lecture Dec. 4, 2003.
1 Protection of Vulnerable Subjects in Research Melody Lin, Ph.D. December 2012.
ETHICS IN FIELD OF DENTAL HYGIENE Dr. Shahzadi Tayyaba Hashmi
Professor David Stanley Northumbria University.  “Human participants or subjects are defined as including living human beings, human beings who have.
Introduction to Ethics Lecture 20 Cohen & The Case for the Use of Animals in Biomedical Research By David Kelsey.
Are There Limits to Patient Autonomy? Elizabeth Heitman, PhD Vanderbilt University Medical Center Center for Biomedical Ethics and Society Challenges in.
 the study of the rightness or wrongness of human conduct.  In any situation involving two or more individuals, values may come into conflict and ethical.
MEDICAL ETHICS and The End of Life. PRIMA FACIE DUTIES AUTONOMY BENEFICENCE NON - MALEFICENCE JUSTICE UTILITY.
THOMPSON & HENDERSON (2011): CHAPTER 4 Legal and Ethical Considerations for Counselors.
The Ethics of Research on Human Subjects. Research Activity on Human Subjects: Any systematic attempt to gain generalizable knowledge about humans A systematic.
Consent Procedures. What is Informed Consent? Consent by a patient to a surgical or medical procedure or participation in a clinical study after achieving.
1 [INSERT SPEAKER NAME DATE & LOCATION HERE] Ethics of Tuberculosis Prevention, Care and Control MODULE 10: RESEARCH IN TB CARE AND CONTROL Insert country/ministry.
Applicability of principles Reidar K. Lie, MD, PhD Department of Clinical Bioethics, NIH and University of Bergen, Norway.
Consent & Vulnerable Adults Aim: To provide an opportunity for Primary Care Staff to explore issues related to consent & vulnerable adults.
Medical law and its place in the system of law and legislation in Ukraine. Legislative provision in healthcare in Ukraine.  The concept, object, method.
MEDICAL ETHICS and The End of Life. ETHICAL THEORIES DEONTOLOGY CONSEQUENTIALISM VIRTUE ETHICS.
Idara C.E.. Three ethical principles guides research with human participants. principle of Autonomy 1. The principle of Autonomy requires investigators.
Chapter 24 Ethical Obligations and Accountability Fundamentals of Nursing: Standards & Practices, 2E.
HUMAN TESTING: Ethical or unethical?. What is human testing? ■Human subjects research: any research or clinical investigation that involves human subjects.
By MUREREREHE Julienne BDT(Hons) KHI..  Informed consent is a legal document, prepared as an agreement for treatment, non-treatment, or for an invasive.
Chapter 5 Ethical Concerns in Research. Historical Perspective on Ethics Nazi Experimentation in WWII –“medical experiments” –Nuremberg War Crime Trials.
Pediatric Research Ethics and the Research Subject Advocate Tomas Jose Silber, MD, MASS RSA and Director, Office of Ethics, CNMC Professor of Pediatrics,
0 Ethics Lecture Essentials of Informed Consent. ACADEMY OF OPHTHALMOLOGY The speaker has no financial interest in the subject matter.
Dr Hidayathulla Shaikh Lecturer, College Of Dentistry, Majmaah University.
Research ethics.
Dr.Amira Yahia, Ph.D (N), M.Sc (N), B.Sc (N).  By the end of this session the student will be able to:  Define some terms related to ethic  Explain.
Ethical Dilemma Research that is most likely to reveal something important about human nature is also the most likely to violate human rights. A number.
Reconsidering requirements for research ethics in Lithuania
Chapter 2 Ethical and Legal Issues
J. Andrew Bertolatus MD Internal Medicine IRB/HSO 13 Sept 2017
J. Andrew Bertolatus MD Internal Medicine IRB/HSO 12 Apr 2017
J. Andrew Bertolatus MD Internal Medicine IRB/HSO 13 September 2017
universalizability & reversibility
بنام خداوند جان و خرد كزين برتر انديشه بر نگذرد
Ethics in Research.
Greg Nezat CRNA, PhD CDR/NC/USN Chairman, IRB II
Research, Experimentation, & Clinical Trials
Ethical Theories and Principles in Clinical and Research
Presentation transcript:

INFORMED CONSENT Some Philosophical Puzzles Professor David Archard

GENERAL BACKGROUND Sane competent adults should be free to make their own decisions Sane competent adults should be free to make their own decisions ‘…this doctrine is meant to apply only to human beings in the maturity of their faculties’ ‘…this doctrine is meant to apply only to human beings in the maturity of their faculties’

Informed Consent: Background A requirement of informed consent as a key principle of medical research and practice A requirement of informed consent as a key principle of medical research and practice Nothing shall be done to an individual without that individual’s consent Nothing shall be done to an individual without that individual’s consent Negatively: revulsion at abuse of medical practices during World War II Negatively: revulsion at abuse of medical practices during World War II Positively: reflecting an underlying view of the sovereign individual as final and authoritative source of an decision of what shall be done to her. Positively: reflecting an underlying view of the sovereign individual as final and authoritative source of an decision of what shall be done to her.

Principles of consent Nothing shall be done to a person without that person’s consent Nothing shall be done to a person without that person’s consent Something done to a person with her consent is morally permissible Something done to a person with her consent is morally permissible ‘Moral magic’: consent is a basic normative power to transform the moral relationships in which individuals stand to one another ‘Moral magic’: consent is a basic normative power to transform the moral relationships in which individuals stand to one another

From assault to sport…..

International Codes of Bioethics 1. The voluntary consent of the human subject is absolutely essential. This means that the person involved should have legal capacity to give consent; should be situated as to be able to exercise free power of choice, …..and should have sufficient knowledge and comprehension of the elements of the subject matter involved as to enable him to make an understanding and enlightened decision. (Nuremberg Code, a ten point statement delimiting permissible medical experimentation on human subjects). 1. The voluntary consent of the human subject is absolutely essential. This means that the person involved should have legal capacity to give consent; should be situated as to be able to exercise free power of choice, …..and should have sufficient knowledge and comprehension of the elements of the subject matter involved as to enable him to make an understanding and enlightened decision. (Nuremberg Code, a ten point statement delimiting permissible medical experimentation on human subjects). The subjects must be volunteers and informed participants in the research project. ([World Medical Association] Helsinki Declaration, 1964) The subjects must be volunteers and informed participants in the research project. ([World Medical Association] Helsinki Declaration, 1964) For all biomedical research involving humans the investigator must obtain the voluntary informed consent of the prospective subject or, in the case of an individual who is not capable of giving informed consent, the permission of a legally authorized representative in accordance with applicable law. Waiver of informed consent is to be regarded as uncommon and exceptional, and must in all cases be approved by an ethical review committee. (CIOMS International Ethical Guidelines for Biomedical Research Involving Human Subjects, Guidline 4) For all biomedical research involving humans the investigator must obtain the voluntary informed consent of the prospective subject or, in the case of an individual who is not capable of giving informed consent, the permission of a legally authorized representative in accordance with applicable law. Waiver of informed consent is to be regarded as uncommon and exceptional, and must in all cases be approved by an ethical review committee. (CIOMS International Ethical Guidelines for Biomedical Research Involving Human Subjects, Guidline 4)

The ‘triumph of autonomy’ Autonomy as one principle amongst others (beneficence, non-maleficence, justice) Autonomy as one principle amongst others (beneficence, non-maleficence, justice) ‘For better or for worse …autonomy has emerged as the most powerful principle in American bioethics, the basis of much theory and much regulation, and has become the “default” principle.’ ‘For better or for worse …autonomy has emerged as the most powerful principle in American bioethics, the basis of much theory and much regulation, and has become the “default” principle.’

The Roots of Consent The ideal of self- ownership (John Locke) The ideal of self- ownership (John Locke) The ideal of (rational) autonomy (Immanuel Kant) The ideal of (rational) autonomy (Immanuel Kant)

Two Very Different Kinds of Claim It’s my body and you can’t do that to me It’s my body and you can’t do that to me It’s my life and I’ll lead it as I choose It’s my life and I’ll lead it as I choose

Conditions of Consent Voluntary: given freely and not, e.g., as a result of coercive pressure. Voluntary: given freely and not, e.g., as a result of coercive pressure. Informed: given in possession and understanding of the principal, relevant information. Informed: given in possession and understanding of the principal, relevant information. Competent: given by somebody able, in virtue of their age and maturity, of making a free, considered choice. Competent: given by somebody able, in virtue of their age and maturity, of making a free, considered choice.

Challenges to the Principles within Medical Research and Practice Is it necessary to obtain consent to what will only minimally affect the individual but will be productive of great good? Is it necessary to obtain consent to what will only minimally affect the individual but will be productive of great good? The good could be for the individual. Or The good could be for the individual. Or For society For society Consider the painless, relatively costless obtaining (and use) of some kinds of very important information without consent Consider the painless, relatively costless obtaining (and use) of some kinds of very important information without consent

The autonomy of the patient/subject? Decisions made under conditions of considerable personal stress and short time scale Decisions made under conditions of considerable personal stress and short time scale The influence of doctors (as authority figures or as sources of inducement) The influence of doctors (as authority figures or as sources of inducement) The influence of family and loved ones The influence of family and loved ones

Informed? Much medical information is surely too complex for ordinary individuals to understand Much medical information is surely too complex for ordinary individuals to understand Is this a problem of the information as such or the manner in which doctors choose to communicate it? Is this a problem of the information as such or the manner in which doctors choose to communicate it? Some features of information – e.g. risk – may be impossible successfully to communicate Some features of information – e.g. risk – may be impossible successfully to communicate

Understanding Risk ‘This experimental drug will reduce your chances of contracting a certain fatal disease by a 100. But there is a 1 in 5 chance of some unpleasant side effects’ Take it? ‘This experimental drug will reduce your chances of contracting a certain fatal disease by a 100. But there is a 1 in 5 chance of some unpleasant side effects’ Take it? Your initial chances of contracting the disease are 1 in 1,000,000 Your initial chances of contracting the disease are 1 in 1,000,000

The scope of consent Opacity: consent to something under one description need not be consent to that same thing under another description (a life-saving operation v. an excruciatingly painful procedure) Opacity: consent to something under one description need not be consent to that same thing under another description (a life-saving operation v. an excruciatingly painful procedure) Consequential uncertainty: consent to something may not be consent to what might follow from it (an operation and its possible side-effects) Consequential uncertainty: consent to something may not be consent to what might follow from it (an operation and its possible side-effects)

The subjects of consent A (Western?) presumption that the subjects of consent are individuals A (Western?) presumption that the subjects of consent are individuals But we are relational subjects defined by our membership of, e.g., families But we are relational subjects defined by our membership of, e.g., families Who then should be the author of consent: the individual or her family? Who then should be the author of consent: the individual or her family?

Trust and Autonomy Trust (between professional and client) involves the confident reliance upon the professional to act in the client’s best interests Trust (between professional and client) involves the confident reliance upon the professional to act in the client’s best interests Such trust may be in tension with the demand for information that is a condition of consent Such trust may be in tension with the demand for information that is a condition of consent

Slippery Slopes The more information we demand the less we trust our informant (and vice versa) The more information we demand the less we trust our informant (and vice versa) Abandoning informed consent could lead to greater abuses Abandoning informed consent could lead to greater abuses

The future of consent Should a principle of informed consent remain a fundamental, basic principle of medical practice and research? Should a principle of informed consent remain a fundamental, basic principle of medical practice and research? Or should we use a principle of restricted scope and limited weight? Or should we use a principle of restricted scope and limited weight? Or should medical practice and research be regulated by other principles? Or should medical practice and research be regulated by other principles?