ࡱ> '` bjbj$$ BFF+\\\\\\\p+++8+,|p  -^~----///$h\ 5."/ 5 5\\--gÑC9C9C9 5X\-\-C9 5C9C9\\-- 1j+e5 Ltّ0 q6z\8</0:C92 3///8X/// 5 5 5 5ppp$$+ppp+ppp\\\\\\  National Ethics Teleconference The Basics of Informed Consent: History, Ethics, and Law September 21, 2010 INTRODUCTION Dr. Berkowitz: Good day everyone. This is Ken Berkowitz. I am the Chief of the Ethics Consultation Service at the National Center for Ethics in Health Care and a physician at the VA NY Harbor Healthcare System. I am very pleased to welcome you all to today's National Ethics Teleconference. By sponsoring this series of calls, the Center provides an opportunity for regular education and open discussion of ethical concerns relevant to VHA. Each call features an educational presentation on an interesting ethics topic followed by an open, moderated discussion of that topic. After the discussion, we reserve the last few minutes of each call for our From the Field section. This will be your opportunity to speak up and let us know what is on your mind regarding ethics related topics other than the focus of today's call. ANNOUNCEMENTS AND GROUND RULES CME credits are available for listeners of this call. To receive CME credit for this course, you must attend 100% of the call, and complete the registration and evaluation process on the LMS website: https://www.lms.va.gov/plateau/user/login.jsp. To get a CME credit hour for participating in the conference call you must complete the registration and evaluation process within 30 days of the conference date. If you have any questions about this process or about the LMS website, please contact the Project Manager, Charles Johnston, at (205) 731-1812 X315 or by e-mail at  HYPERLINK "mailto:charles.johnston3@va.gov" charles.johnston3@va.gov. Many of our regular listeners will notice that the frequency of our National Ethics Teleconferences has decreased. This is due to staffing shortages at the National Center for Ethics in Health Care. We hope that this will be temporary, but in the mean time the frequency of these calls will decrease to about one per quarter, or more as we are able, for the foreseeable future. Ground Rules: We ask hat when you talk, you please begin by telling us your name, location and title so that we continue to get to know each other better. During the call, please try to minimize background noise and PLEASE do not put the call on hold. Due to the interactive nature of these calls, and the fact that at times we deal with sensitive issues, we think it is important to make two final points: First, it is not the specific role of the National Center for Ethics in Health Care to report policy violations. However, please remember that there are many participants on the line. You are speaking in an open forum and ultimately you are responsible for your own words, and Lastly, please remember that these Ethics Teleconference calls are not an appropriate place to discuss specific cases or confidential information. If, during the discussions we hear people providing such information we may interrupt and ask them to make their comments more general PRESENTATION The topic of todays call is The Basics of Informed Consent: History, Ethics, and Law. Questions about decision making in the health care setting are often vexing, and are often the reasons that ethics consultations are requested. In fact, of the 1964 documented FY2010 ethics consults in the VAs ECWeb system so far this year, 70% were categorized by the consultants as falling primarily into the domain of shared decision making! In many ways shared decision making is fundamental to health care ethics, and informed consent is fundamental to shared decision making. So, we thought it would be helpful to step back and provide some perspective on the origins of the doctrine of informed consent in ethics and law and to highlight some of the ways in which the ethical and legal bases of informed consent is reflected in VHA Handbook 1004.01: Informed Consent for Treatments and Procedures. Also, because of the breadth of this topic, we can only address informed consent for treatment or procedures today, not for research. My colleagues, Drs. Virginia Ashby Sharpe, Karen Rasmussen and David Alfandre from the National Center for Ethics Policy and Consultation Services are here today to talk to us. Ashby, Karen, David, welcome Dr. Berkowitz: Let me just get us started with what should be a familiar axiom here in VHA: Patients have a fundamental right to direct what happens to their bodies. In turn, health care professionals have an ethical obligation to involve patients in a process of shared decision making and to seek patients informed consent for treatments and procedures. Id like to ask our faculty to unpack that by helping us to understand where the patients right comes from, and how it shapes the health care providers obligation. Ashby can you get us started? Dr. Sharpe: Sure Ken. I think its helpful to understand that informed consent has three overlapping dimensions (Berg et al, 2001): First, its an ethical doctrine. Second, its a set of legal rules and policies that prescribe the behaviors of health care providers. Third, its an interpersonal process thats one part of shared decision making in medicine. I think for many health care practitioners, informed consent is understood pretty straightforwardly as a legal requirement that needs to be met and documented in order to authorize a health care intervention. Often what goes with this perception is that the requirement is met by getting a patients signature on a consent form. But informed consent is much more than a legal requirement or a matter of compliance, and its much more than a signature on a form. In terms of its history, informed consent is rooted in the Enlightenment principles of individual liberty and the right to self determination that are enshrined in the U.S. Constitution and Bill of Rights. These principles of individual liberty and the right to self determination are the basis for all three dimensions of informed consent that I mentioned before: Theyre the basis for: First, the ethical doctrine that patients have the right to make an autonomous decision about the medical interventions that are performed on them. This is an alternative to what is known in the clinical ethics literature as the tradition of paternalism which is the idea that the doctors know and will decide whats best for you as a patient. Second, the legal doctrine is grounded in both the Constitutional principle of liberty and in the common law right of bodily integrity reflected in civil and criminal laws of assault and battery. Third, the right to self determination is an important ingredient in the interpersonal process of shared decision making -- of which informed consent is a part -- because it means that the patient should be respected as a partner in the decision making. Dr. Berkowitz: OK, thanks. So to restate it, the patients right to direct what happens to their bodies is part of the American tradition of individual liberty; it is grounded in both Constitutional and common law, federal regulations, VA policy, and it is part of a non-paternalistic approach to shared decision making which is about making decisions WITH and not FOR patients. Dr. Sharpe: Right! Dr. Berkowitz: As I already mentioned, this is more than just interesting theory. Dr. Rasmussen, can you jump in here to give some examples of a few common clinical challenges that frequently come up when we talk about patient autonomy and informed consent? Dr. Rasmussen: Sure Ken, First, consider what happens if a patients autonomous choice is contrary to medically recommended treatment? For example, a situation where a patient declines a treatment that could easily save her life, say the amputation of a gangrenous foot? How can practitioners respect the patients autonomous decision when they feel it compromises the medical care they are responsible for providing? Second, if patients have individual liberty and autonomy, so do clinicians. What is the limit of patient autonomy? Are practitioners required to do whatever the patient wants? For example, a situation where a patient is demanding antibiotics from a practitioner for a condition where antibiotics wont work? Third, how can practitioners respect the patients autonomy when the patient lacks decision-making capacity? For example, how should decision making about artificial nutrition or hydration proceed for a patient with advanced dementia? Dr. Berkowitz: Yes, youre absolutely right; those are common concerns that are raised about informed consent and patient autonomy. Lets see if we can address them as we go forward. Let me first have you and David talk about the elements of a valid informed consent. David, can you start us off? Dr. Alfandre: Sure Ken. A valid informed consent is based on the following 5 elements (Faden and Beauchamp, 1986; Berg et al, 2001): Capacity Disclosure Comprehension Voluntariness, and Communication of the decision. Let me say a bit about capacity and then trade off with Dr. Rasmussen to cover the rest. Capacity In the context of informed consent, capacity means that the patient has capacity to make the specific treatment decision at the specific time. That is, the patient can understand whats being recommended and why, can appreciate the recommended options based on his or her values, can reason about the consequences of various options, and can communicate his or her choice. In keeping with what Ashby said about informed consent having its roots in individual liberty and the right to self-determination, unless there is reason to doubt it, the presumption is always that the patient has decision making capacity. Also, by the same reasoning, if a patients capacity is anticipated to be restored within a reasonable amount of time (e.g., temporary effects of general anesthesia) then the practitioner should defer the informed consent process until the patient is capable of participating. In some cases, though, it will be obvious that the patient lacks capacity and wont regain it within the timeframe needed to make a decision, for example, the patient is unconscious or has advanced dementia. Also, there are a variety of reasons why a patients decision making capacity might legitimately be questioned: for example, if the patient, who is otherwise well known to the clinician, isnt making sense, or if the patient is confused, groggy, or delirious. Importantly, the fact that a patient might disagree with a practitioners recommendation is never sufficient evidence alone to suspect or claim that the patient lacks decision making capacity. Dr. Berkowitz: So what happens if the practitioner thinks the patient lacks capacity? Dr. Alfandre: The key to capacity assessment for the purposes of informed consent is that capacity is decision-specific and time-specific. In other words, were not assessing the patients global capacity to live independently, do their taxes, drive a car, and do long division. Were just assessing whether the patient can understand and make a decision about a particular medically recommended treatment or procedure. A person is determined to have capacity to make a particular decision if they: understand and appreciate the information relevant to the decision can use or weigh relevant information in making their decision, including information on benefits and risks of the recommended treatment options, and benefits and risks of no treatment can communicate their decision to others. Dr. Berkowitz: So who should actually do the capacity assessment? Dr. Alfandre: In general, the capacity assessment can be done by the practitioner obtaining informed consent. But as our Informed Consent Policy (Handbook 1004.01) says: if the determination of lack of decision-making capacity is based on a diagnosis of mental illness, a psychiatrist or licensed psychologist must be consulted in order to ensure that the underlying cause of the lack of decision-making capacity is adequately addressed. I also want to make one last point about decision-making capacity, which is that decision-making capacity is a clinical determination made by health care professionals; as distinguished from incompetence which is a legal determination made by a judge or a court of law. If a patient is determined clinically to lack decision making capacity, then the informed consent process is carried out on behalf of the patient with the patients surrogate. In the case of a patient who has been declared incompetent by a court of law, a legal guardian or special guardian is appointed by a court of appropriate jurisdiction as the surrogate decision maker. Otherwise, the surrogate may be the patients Health Care Agent (the person named by the patient in a Durable Power of Attorney for Health Care), the Next-of-kin, or a Close friend. So, to get back to Dr. Rasmussens examples of common concerns, if a patient lacks decision making capacity, they lack autonomy. But that doesnt mean that the patients perspective is somehow lost. In means that in those cases, the surrogate makes decisions on the patients behalf. Also, again, even if a patient lacks autonomy now, they may have identified their wishes in a living will or other advance directive. In that case, they have exercised their autonomy prospectively so that if they lose capacity, there will be a valid statement of their wishes that can guide the surrogate and health care team. Dr. Berkowitz: So, in other words, value so much liberty, autonomy, and self-determination that we have mechanisms, such as informed consent and advance directives to enable patients to play a role in decision making, including making statements about their preferences regarding future medical care in the event that they lose autonomy. Dr. Sharpe: Right, and its no coincidence then that an important mechanism of advance care planning was codified in law by something called the Patient Self Determination Act. Dr. Berkowitz: Karen, can you give us an overview of the disclosure element of informed consent? Dr. Rasmussen: Sure Ken. But I also wanted to follow on what David was saying about decision-making capacity to underscore that patients are vulnerable in lots of ways that might diminish their autonomy. When patients are very sick, their whole world can change. Theyre suddenly dependent on others for information and assistance. In the health care setting they have to expose their bodies and share personal information with strangers and can become afraid and uncertain. All these factors can affect the way they usually process information and make it more difficult for them to make decisions. Dr. Sharpe: Thats so true. Autonomy literally means self law (auto nomos) and when were sick, we often lose control over our lives. In those cases, autonomy is really more of an ideal rather than a reality. That having been said, though, when someone becomes a patient, they dont cease being a person or having all the rights that they would otherwise have. So even when or especially when someone is a patient, health care providers should treat them in ways that minimize their vulnerability and empower them in ways that are respectful of them as persons. The role of a professional isn't to take over someone's life and make decisions for them but to help them to regain and/or maintain control as a way of advancing their health care goals. Actively participating in shared decision making through a real informed consent process is one way that health care practitioners show respect for the patient as a person. Assessing a patients decisional capacity lets you include them or, when appropriate, their surrogate in care planning. Dr. Rasmussen: Yes and the disclosure element of informed consent is another way of respecting a patients right to self determination, and empowering them to make decisions about their care. Disclosure The goal of the informed consent process is to ensure that patients have an opportunity to be empowered participants in decisions about their health care. The informed part of informed consent begins with the obligation of health care practitioners to disclose information to the patient (or surrogate) that is relevant to the decision that needs to be made. Although the law of informed consent began to develop in the early 1900s, it wasnt until the 1950s, 60s, and 70s that the law spelled out the range of information that needs to be provided. The Salgo case in 1955 and the Natanson and Canterbury cases in 1960 and 1970 clarified that practitioners need to explain the patients condition and diagnosis; they must inform the patient (or authorized surrogate) about treatment options and alternatives, including the risks and benefits of each, providing the information that a reasonable person in similar circumstances would want to know in making the treatment decision. A key element of the process is that the practitioner explains why he or she believes recommended treatments or procedures will be more beneficial than alternatives in the context of the patients diagnosis. Youll all be familiar with these requirements from Handbook 1004.01. The Salgo case involved a 55 year old man with arteriosclerosis whose doctor advised him to undergo diagnostic aortography. He was anesthetized, his aorta was injected with radiographic contrast, and X-rays were taken of the abdominal aorta. The next morning Mr. Salgo discovered that his lower extremities were paralyzed. What was precedent setting about the Salgo case the first legal decision to use the term informed consent -- was that the court found that the doctor had failed to explain the risks of the procedure, including possible paralysis. What was precedent-setting about the Natanson and Canterbury cases was that they established that the standard of disclosure should be what a person in similar circumstances would likely want to know, not, as was the practice, what the health care professional thought was relevant. In Canterbury, a 19 year old man became paralyzed after surgical removal of a vertebra and a fall from his hospital bed. The court found that the doctor had not sufficiently informed the patient of the risks, stating [r]isk is thus material when a reasonable person, in what the physician knows or should know to be the patients position, would be likely to attach significance to the risk or cluster of risks in deciding whether or not to forego the proposed therapy. This is also known as the reasonable person standard. Dr. Berkowitz: Thanks Karen, so whats important about the informational part of informed consent is that the practitioner should provide information that a reasonable person in a similar circumstance would want to know and it should be inclusive of the benefits, risks, and alternatives, including the alternative of no treatment. Dr. Rasmussen: Right. And again, these are the legal cases that provide the common law basis for informed consent as it is practiced today. Comprehension Less well-defined in law is the requirement that the patient must comprehend the information that the practitioner discloses in the informed consent process. From a common sense perspective, if a patient doesnt understand the information that theyre given they really arent in a position to consent to or decline a recommended treatment. Likewise, from an ethical perspective, a person cant exercise autonomy if they dont understand what they are being asked to choose between. Whats important is that the practitioner recognizes each patients ability to understand the relevant information and employ the necessary range of skills to respectfully help the patient understand their clinical situation, the choices they have, and the potential consequences of the decision they make. To assess and augment understanding, practitioners can use a variety of strategies, including having the patient state in their own words what they understand; encouraging the patient to bring someone they trust to take be part in the conversation, take notes, write down and ask questions if time permits; encouraging the patient to go home and think about the decision and come back for a follow-up visit; supporting a patients request to obtain a second opinion; and certainly ensuring a translator is present for patients who speak a language that the practitioner does not speak fluently. This takes time and is one of the reasons why informed consent is better understood as a multistep process rather than a singular event. Dr. Berkowitz: OK, now the voluntariness part of a valid informed consent. David, can you say a bit about that? Voluntariness Dr. Alfandre: Yes, the key here is that patients not be coerced into making a decision since force takes away the patients true choice which is obviously incompatible with respect for autonomy. Of course there is a lot of philosophical literature about free will and whether and how much anyone has including how free a patients choice really is if they are faced with a dire illness and few options but thats not so much what were talking about. What were really concerned about here is how the practitioner uses their power to influence the patients decision. All of us know that doctors can phrase their recommendation for a treatment in ways that are more or less persuasive and that there is a continuum from straight-forward recommendation to persuasion, to manipulation, to coercion. The goal of shared decision making in general, and of voluntariness as an element of informed consent, is to ensure that the patient is enabled to make a decision that is best for them (or the surrogate is enabled to make a decision that is best for the patient) even if its a decision that the practitioner wouldnt make or recommend. Dr. Rasmussen: Right, and that gets us back to one of the common concerns that I mentioned earlier: What if a patients autonomous choice is contrary to medically recommended treatment? Think back to the example I gave before, the situation where a patient declines a treatment that could easily save her life, say the amputation of a gangrenous foot? How can clinicians respect the patients autonomous decision when it compromises the medical care clinicians are responsible for providing? Dr. Sharpe: Yes, thanks for bringing us back to those issues. Youre right, practitioners are trained to provide medical care and so it sometimes may seem frustrating to them if a patient doesnt want them to do their job or let me help them. Medical ethics in general and the law and ethics of informed consent, in particular, requires a change of perspective from the patient as an object of medical care, to the patient as a partner in medical care. Heres an analogy from one of the other traditional professions education that might help: a friend of mine who is a professor in a philosophy department was asked what she taught. She didnt say she taught philosophy, she said that she taught students! Likewise, doctors and other health care practitioners arent treating diseases, theyre treating patients. To be patient-centered means among other things that the patients values need to be incorporated into the decision making process. So, doctors who might be frustrated by a patients refusal of recommended treatment need to remember that to be patient-centered means to recognize that patients are individuals who have individual needs. To practice patient-centered care means, among other things, to take seriously the patients values and preferences. Also, from a legal perspective, as Justice Benjamin Cardozo said in his opinion for the landmark 1914 Schloendorff case: Every human being of adult years and sound mind has a right to determine what shall be done with his own body; and a surgeon who performs an operation without his patients consent commits an assault, for which he is liable in damages. That opinion became a basis for the patients legal right to self-determination; a right that is also manifested in the bioethical principle of autonomy. Justice Cardozos famous statement codified in law the ethical principle of respect for persons when they happen to be patients. Dr. Berkowitz: Thanks Ashby, now, back to another example that Karen mentioned earlier: If patients have individual liberty and autonomy, so do practitioners. What is the limit of patient autonomy and are practitioners required to do whatever the patient wants? Dr. Sharpe: No, they arent and the VHA policy on Informed Consent for Clinical Treatments and Procedures is clear on this: In VHA, patients have the right to accept or refuse any medical treatment or procedure that is recommended to them. However, practitioners are not obligated to recommend treatments that in their clinical judgment will have no effect or be disproportionately harmful. The aim of shared decision making is for the practitioner to contribute knowledge of the patients medical condition and prognosis, and the patient (or surrogate) to bring knowledge of the patients values, preferences, and life plans so that together they can mutually establish the goals of care and a treatment plan. Of course in cases of conflict further discussions or strategies, or sometimes an ethics consultation, may be needed to try to work through differences between practitioners or the practitioners and the patient/surrogate/family. Dr. Berkowitz: OK, let me just remind folks of where we are. Weve talked about four of the five elements of informed consent: capacity, disclosure, comprehension, and voluntariness. Now, back to David for a look at the fifth element, that is the consent itself the patients ability to communicate a choice. Dr. Alfandre: So, for the actual consent, what is meant is that the patient can acknowledge orally or in writing that they understand and agree to the treatment or procedure. Of course, patients or surrogates can decline rather than consent to a treatment. And, with a few specific exceptions, including emergencies, it is the patients (or surrogates) consent that authorizes a practitioner to proceed with a medically recommended treatment or procedure. As folks know from the Informed Consent Handbook, sometimes the consent must be documented with the patients signature, sometimes oral consent is sufficient. The key here is that patients who may have a difficult time communicating their decision, for example, they can no longer use their hands to write, or cannot use their voice, should be appropriately assisted to ensure that their decision is understood by their caregivers. One of the unintended consequences of the consent requirement is that busy health care providers are tempted to reduce the informed consent process to the single simplified act of obtaining a patients signature on a consent form. But, as weve said, the final statement of the patients decision (i.e., the consent or refusal), is only one element in a much more comprehensive informed consent process. Dr. Sharpe: Yes, thats right. I think another problematic practice is the attempt by health care practitioners to use blanket consent forms; these are catch-all documents intended to cover any and all eventuality that might arise during a given episode of care. These forms are ethically problematic because they ask the patient to agree to care that may never be needed without providing relevant information in real-time for the patient to use in making an informed decision. Frequently these forms might contain vague language like, quote, any treatment your doctors think is necessary, or quote routine procedures as needed, or quote the use of blood products if needed for any reason during your hospitalization. We have also seen blanket consent used on admission to ICUs, where patients (or surrogates) are asked to provide a blanket consent for common critical care interventions, quote, if needed. Such practices fail to meet the requirement that consent be specific to the recommended treatment or treatment plan. To be decision-specific, informed consent should be sought for individual procedures that are part of a plan of care, and are clinically indicated, or are recommended for that individual patient at the time consent is being obtained. Catch all or blanket consent isnt decision-specific and so its not patient-centered, and not an ethically sound practice. Dr. Berkowitz: So, to recap, informed consent is always specific to the individual patient, the clinical situation, and the recommended plan of care or recommended treatment(s) or procedure(s). Decision-making capacity is decision-specific rather than global. Informed consent should be understood as a process that is patient-centered, rather than simply as a singular event that meets the practitioners legal requirement to obtain permission to proceed with a treatment. Lets look at one more example of a common concern.. If patient autonomy is so important that its the basis of the ethics and law of informed consent and a fundamental element of health care ethics, what do we do about patients who dont want to shoulder the burden of autonomous decision making? Do we force them to be the decision maker? Karen, do you want to help us think through that? Dr. Rasmussen: Sure Ken. The issue here is whether a patient who is autonomous can decide that they dont want to participate in the decision making process, or essentially choose to opt out of shared decision making. If decision making is supposed to be shared and a patient with capacity is supposed to play an active role in the process of informed consent for which practitioners are legally liable, can they waive their autonomy? Dr. Sharpe: There are people who have argued that autonomy should be mandatory because they think that patients shouldnt shirk their difficult responsibilities -- but this is a pretty uncommon view. For many cultures decision making is more communal rather than individual. Similarly, some cultures view receiving bad news as inherently harmful. Ethically-speaking, forcing a patient to participate in decision making, for example, compelling a patient to receive information that they dont want may be inconsistent with respect for their self-determination or inconsistent with respect for their other cultural beliefs. (Carrese and Rhodes, 1995; Gostin, 1995) Its also not practical to try to force a patient to participate in decision making. Trying to coerce participation could easily be counterproductive, undermining the trust relationship between practitioner and patient. Fortunately, this doesnt come up too often, and if it does it might be another good time to consider requesting an ethics consultation! MODERATED DISCUSSION Dr. Berkowitz: We saved time for you our listeners to continue the discussion. So now is your chance to ask questions about informed consent. Please begin by stating your name and where you are from What is on your mind? Ware Kushner, Palo Alto: Informed Consent with respect to research, one of the criticisms is that it can be a very lengthy process in terms of the documents. With the boiler plate language that the VA requires, the document can be incredibly lengthy in research. Do you have any thoughts about this lengthening increase? Dr. Berkowitz: We hear from people that things have gotten too burdensome and I ask Dr. Sharpe and Dr. Rasmussen to weigh in on how do we balance the need for good disclosure and assurance of comprehension without making things too burdensome and impractical for the patient? Dr. Rasmussen: I think you bring up a valid point, when were talking about the disclosure of information that the patient needs to know in order to make a sound decision about their healthcare; there really is a lot of information that needs to be conveyed to them. One of the points in the Informed Consent policy is the idea that it needs to be a process. We encourage that people talk to patients over a period of time; convey and reinforcing the information the patient needs to know and answering the questions the patient might have so they can make informed decisions. The content of the form is very rigidly mandated and frequently the patient is given the consent form in one sitting that may take several hours. I think its important to think about what the real process needs to be for patients making informed decisions and that being patient-centered means both giving patients the kind of information they need plus the time they need to think about the decision theyre making. Dr. Sharpe: I think its so ironic we have to talk about patient informed consent because as weve laid out in the call basically is that informed consent is based on the idea of respect for patients as persons and their individual autonomy and right to be self-determining. I think its one of the paradoxes of informed consent as a legal requirement that prescribes the behavior of healthcare professionals and researchers that informed consent is a tool for compliance and in order for people to protect themselves as they conduct important research and clinical work; they need to make sure they have met these obligations. There needs to be a balance obviously between the very legalistic language that intended to protect the providers and the language that needs to be more explanatory and sensible to patients and research subjects. FROM THE FIELD Now is the portion of the call that you can either continue todays discussion, or ask questions about ethics-related topics other than the main focus of todays call. CONCLUSION Id like to take the last minute of the call to thank everyone who worked hard on the development, planning, and implementation of the call. It is not a trivial task and I appreciate everyones efforts, including the members of the Ethics Center, EES and VANTS staff that support these calls; and in particular for this call, Drs. Sharpe, Rasmussen and Alfandre. Note that our web site vaww.ethics.va.gov contains all of the summaries of prior National Ethics Teleconferences. If you are on our email mailing list you will receive details about the posting of the summary of this call, any references we described, and announcements for upcoming National Ethics Teleconferences. Let us know if you or someone you know doesnt receive our e-mails and you want to be put on our list. Please also let us know if you have suggestions about topics for future calls or any questions and again, our e-mail address is HYPERLINK "mailto:vhaethics@va.gov"vhaethics@va.gov. The date for the next NET call has not yet been determined Stay tuned to your Outlook e-mail and our Web site for further details of the call when the time gets closer. Thank you everyone, and have a great day! REFERENCES Berg, Jessica W., Paul Appelbaum, Charles W. Lidz, Lisa J. Parker. Informed Consent: Legal Theory and Clinical Practice. Oxford; New York: Oxford University Press, 2001. Carrese, Joseph A., Rhodes, Lorna A. Western Bioethics on the Navajo Reservation. JAMA 1995; 274(10). Faden, Ruth R., Tom L. Beauchamp. A History and Theory of Informed Consent. New York: Oxford University Press, 1986. Salgo v. Leland Stanford Jr. University Board of Trustees: 125-127 Natanson v. Kline: 129-133 Canterbury v. Spence: 133-137 Schloendorff v. Society of New York Hospitals: 123-127. Gostin, Lawrence O. Informed Consent, Cultural Sensitivity, and Respect for Persons. JAMA 1995; 27410:844-5. Patient Self-Determination Act [1990], Pub L 101-508 [Sections] 4206, 4751 (OBRA), 42 USC 1395 cc (a) et seq (1990). VHA Handbook 1004.01, Informed Consent for Clinical Treatments & Procedures. HYPERLINK "http://vaww.ethics.va.gov/activities/policy.asp"http://vaww.ethics.va.gov/activities/policy.asp Additional research articles on informed consent: Doyal, L. Informed consent: moral necessity or illusion? Quality and Safety in Health Care 2001; 10; 29-33.  HYPERLINK "http://qshc.bmj.com/content/10/suppl_1/i29.full" http://qshc.bmj.com/content/10/suppl_1/i29.full Wirshing, Donna A., Wirshing, William C., Marder, Stephen R., Liberman, Robert P., Mintz, Jim. Informed Consent: Assessment of Comprehension. American Journal of Psychiatry 1998; 155; 1508-1511.  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Questions about decision making in the health care setting are often vexing, and are often the reasons that ethics consultations are requested. In fact, of the 1964 docAethics, bioethics, NET, teleconference, informed consent, consentnDepartment of Veterans Affairs, Veterans Health Administration, National Center for Ethics in Health Care 10E Michael Ford#                           ! " Oh+'0$$$p|      |National Ethics Teleconference The Basics of Informed Consent: History, Ethics, and Law - US Department of Veterans AffairsThe topic of todays call is The Basics of Informed Consent: History, Ethics, and Law. Questions about decision making in the health care setting are often vexing, and are often the reasons that ethics consultations are requested. In fact, of the 1964 documented FY2010 ethics consults in the VAs ECWeb system so far this year, 70% were categorized by the consultants as falling primarily into the domain of shared decision making! In many ways shared decision making is fundamental to health care ethics, and informed consent is fundamental to shared decision making. So, we thought it would be helpful to step back and provide some perspective on the origins of the doctrine of informed consent in ethics and law and to highlight some of the ways in which the ethical and legal bases of informed consent is reflected in VHA Handbook 1004.01: Informed Consent for Treatments and Procedures.pDepartment of Veterans Affairs, Veterans Health Administration, National Center for Ethics in Health Care 10E Dethics, bioethics, NET, teleconference, informed consent, consent Normal.dotMichael Ford2Microsoft Office Word@G@ )SY@1j@1jUy՜.+,D՜.+, px  hteaching materialI' |National Ethics Teleconference The Basics of Informed Consent: History, Ethics, and Law - US Department of Veterans Affairs Title8Nbn _PID_HLINKS datecreated Language datereviewedAJJ =http://ajp.psychiatryonline.org/cgi/content/full/155/11/1508d q 0http://qshc.bmj.com/content/10/suppl_1/i29.fulld l)0http://vaww.ethics.va.gov/activities/policy.aspd  ,mailto:vhaethics@va.govd Fe mailto:charles.johnston3@va.govd  20100921en 20101012  !"#$%&'()*+,-./0123456789:;<=>?@ABCDEFGHIJKLMNOPQRSTUVWXYZ[\]^_`abcdefghijklmnopqrstuvwxyz{|}~      !#$%&'()+,-./0123456789:;<=>?@ABCDEFGHIJKLMNOPQRSTUVWXYZ[\]^_`abcdefghijklmnopqrstuvwyz{|}~Root Entry FЫ1jData "1Table*=WordDocumentBSummaryInformation(xDocumentSummaryInformation8CompObjq  FMicrosoft Office Word Document MSWordDocWord.Document.89q