Published in JAMA on April 15, 1992
Do-not-resuscitate order. What happens after hospital discharge? West J Med (1993) 2.06
Substituted judgment: the limitations of autonomy in surrogate decision making. J Gen Intern Med (2008) 1.88
A comparison of methods to communicate treatment preferences in nursing facilities: traditional practices versus the physician orders for life-sustaining treatment program. J Am Geriatr Soc (2010) 1.51
Minor cognitive impairments in cancer patients magnify the effect of caregiver preferences on end-of-life care. J Pain Symptom Manage (2012) 1.47
Advance Care Planning in Dementia: Do Family Carers Know the Treatment Preferences of People with Early Dementia? PLoS One (2016) 1.39
Preferences of physicians and their patients for end-of-life care. J Gen Intern Med (1997) 1.32
Ethics review: 'Living wills' and intensive care--an overview of the American experience. Crit Care (2007) 1.23
Empathy and life support decisions in intensive care units. J Gen Intern Med (2008) 1.18
Bioethics for clinicians: 5. Substitute decision-making. CMAJ (1996) 1.07
Family members' experiences of "wait and see" as a communication strategy in end-of-life decisions. Intensive Care Med (2011) 1.02
Limiting risks by curtailing rights: a response to Dr Ryan. J Med Ethics (1996) 0.96
Physicians' views on the importance of patient preferences in surrogate decision-making. J Am Geriatr Soc (2010) 0.92
Comparing utilization of life-sustaining treatments with patient and public preferences. J Gen Intern Med (1998) 0.89
A conceptual model of the role of communication in surrogate decision making for hospitalized adults. Patient Educ Couns (2011) 0.87
Competency and the Capacity to Make Treatment Decisions: A Primer for Primary Care Physicians. Prim Care Companion J Clin Psychiatry (1999) 0.86
Procedures for making medical decisions for incompetent adults. JAMA (1992) 0.85
Making decisions for hospitalized older adults: ethical factors considered by family surrogates. J Clin Ethics (2013) 0.84
Ethical questions in the treatment of subjects with dementia. Part I. Respecting autonomy: awareness, competence and behavioural disorders. Neurol Sci (2007) 0.80
Caregiver perspectives on cancer screening for persons with dementia: "why put them through it?". J Am Geriatr Soc (2013) 0.77
Current status of percutaneous endoscopic gastrostomy (PEG) in a general hospital in Japan: a cross-sectional study. J Rural Med (2016) 0.75
Is there such a thing as a life not worth living? BMJ (2001) 0.75
Issues surrounding end-of-life decision-making. Patient Prefer Adherence (2013) 0.75
Advance directives: a computer assisted approach to assuring patients' rights and compliance with PSDA (Patient Self-Determination Act) and JCAHO standards. HEC Forum (1997) 0.75
Ethical considerations in neuroclinical trials. Neurosurg Rev (1997) 0.75
A Legal and Ethical Analysis of the Effects of Triggering Conditions on Surrogate Decision-Making in End-of-Life Care in the US. HEC Forum (2016) 0.75
Better palliative care for people with a dementia: summary of interdisciplinary workshop highlighting current gaps and recommendations for future research. BMC Palliat Care (2017) 0.75
Four models of the physician-patient relationship. JAMA (1992) 12.91
The economics of dying. The illusion of cost savings at the end of life. N Engl J Med (1994) 4.92
Medical professionalism in society. N Engl J Med (1999) 4.09
The patient-physician relationship. Ensuring competency in end-of-life care: communication and relational skills. JAMA (2000) 2.82
The promise of a good death. Lancet (1998) 2.67
Understanding the experience of pain in terminally ill patients. Lancet (2001) 2.66
Attitudes and desires related to euthanasia and physician-assisted suicide among terminally ill patients and their caregivers. JAMA (2000) 2.62
Understanding economic and other burdens of terminal illness: the experience of patients and their caregivers. Ann Intern Med (2000) 2.52
What is accountability in health care? Ann Intern Med (1996) 2.22
Shared expectations for protection of identifiable health care information: report of a national consensus process. J Gen Intern Med (2001) 1.81
Planning for the end of life. Lancet (2000) 1.68
Hospital informed consent for procedure forms: facilitating quality patient-physician interaction. Arch Surg (2000) 1.61
Assistance from family members, friends, paid care givers, and volunteers in the care of terminally ill patients. N Engl J Med (1999) 1.44
Crisis, ethics, and the American Medical Association 1847 and 1997. JAMA (1997) 1.44
Advance directives. JAMA (1991) 1.39
Preserving community in health care. J Health Polit Policy Law (1997) 1.28
Physician participation in executions: time to eliminate anonymity provisions and protest the practice. Ann Intern Med (2001) 1.24
How well is the Patient Self-Determination Act working?: an early assessment. Am J Med (1993) 1.21
Can goals of care be used to predict intervention preferences in an advance directive? Arch Intern Med (1997) 1.18
Ethics and the structures of healthcare. Camb Q Healthc Ethics (2000) 1.01
Knowledge: insufficient for change. J Palliat Med (2001) 0.94
The search for low-cost, high-quality care: what are the assumptions and what are the questions now? J Gen Intern Med (1995) 0.82
Coding and reimbursement mechanisms for physician services in hospice and palliative care. J Palliat Med (2000) 0.81
Living wills: past, present, and future. J Clin Ethics (1990) 0.78
A manual on manners and courtesies for the shared care of patients. J Clin Ethics (1997) 0.76
Is our AIDS policy ethical? Am J Med (1987) 0.75
Advance directives. Ann Intern Med (1992) 0.75
Relationships, relationships, relationships.... J Clin Ethics (1997) 0.75
Physician aid in dying and the relief of patients' suffering: physicians' attitudes regarding patients' suffering and end-of-life decisions. J Clin Ethics (1995) 0.75
Going beyond a 'philosophy of care'. Health Aff (Millwood) (1998) 0.75