 |
 |

Hospital Policy on Advance DirectivesDo Institutions Ask Patients About Living Wills?
S. Van McCrary, JD, MPH;
Jeffrey R. Botkin, MD, MPH
JAMA. 1989;262(17):2411-2414.
Abstract
 |  |
Surveys have shown that a substantial proportion of the population has prepared an advance directive. The purpose of this exploratory study was to assess the existence and nature of hospital policy regarding these documents. A survey questionnaire was sent to 394 randomly selected hospitals in the United States. Of the 219 responding hospitals, 146 (67%) reported having a formal policy regarding advance directives. The large majority of those with a policy require the patient to notify the hospital of an advance directive, while only 4% of the respondents actively inquire about these documents. Hospitals in states with legislation that sanctions advance directives were significantly more likely to have a formal policy regarding these documents than hospitals in states without such legislation. Forty-six percent of the respondents reported having an ethics committee; however, the presence of an ethics committee was not significantly associated with the presence of a formal policy. Of the 69 hospitals that had both a formal policy and an ethics committee, only 30 (43%) reported that the policy had been reviewed by the ethics committee. Ethical and legal issues regarding hospital policy on advance directives are discussed. Hospitals should adopt formal policies to ask all adult patients at the time of admission whether they have prepared a living will, durable power of attorney, or similar document; and ethics committees should play a more active role in policy development.
(JAMA. 1989;262:2411-2414)
Author Affiliations
From The Program on Law, Ethics and Health, Department of Health Policy and Management, The Johns Hopkins University School of Hygiene and Public Health, Baltimore, Md. Mr McCrary is now with the Institute for the Medical Humanities, University of Texas Medical Branch at Galveston. Dr Botkin is now with the Department of Pediatrics and the Center for Biomedical Ethics, Case Western Reserve University School of Medicine, Cleveland, Ohio.
Footnotes
Reprint requests to the Institute for the Medical Humanities, University of Texas Medical Branch, Galveston, TX 77550 (Mr McCrary).
CiteULike Connotea Del.icio.us Digg Reddit Technorati Twitter
What's this?
THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES
The High Costs of Dying: A Way Out
Gillick
Arch Intern Med 1994;154:2134-2137.
ABSTRACT
Living Will Completion in Older Adults
Stelter et al.
Arch Intern Med 1992;152:954-959.
ABSTRACT
Consumer Competence and the Reform of American Health Care
Reiser
JAMA 1992;267:1511-1515.
ABSTRACT
The Patient Self-Determination Act and the Future of Advance Directives
Greco et al.
ANN INTERN MED 1991;115:639-643.
ABSTRACT
Life and Death Choices After Cruzan
Gostin
J Law Med Ethics 1991;19:9-12.
Decisions to Abate Life-Sustaining Treatment for Nonautonomous Patients: Ethical Standards and Legal Liability for Physicians After Cruzan
Weir and Gostin
JAMA 1990;264:1846-1853.
ABSTRACT
The Values History: An Innovation in Surrogate Medical Decision-Making
Lambert et al.
J Law Med Ethics 1990;18:202-212.
Advance Medical Directives
Orentlicher
JAMA 1990;263:2365-2367.
|