You are seeing this message because your Web browser does not support basic Web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.


ABOUT ARCHIVES
Advanced Search

Welcome   | My Account | E-mail Alerts | Access Rights | Sign In


  Vol. 155 No. 10, 22 MAY 1995 TABLE OF CONTENTS
  Archives
  •  Online Features
  Original Investigations
 This Article
 •References
 •Full text PDF
 •Send to a friend
 • Save in My Folder
 •Save to citation manager
 •Permissions
 Citing Articles
 •Citation map
 •Citing articles on HighWire
 •Contact me when this article is cited
 Related Content
 •Similar articles in this journal
 Social Bookmarking
  Add to CiteULike Add to Connotea Add to Del.icio.us Add to Digg Add to Reddit Add to Technorati Add to Twitter What's this?

The Discussion About Advance Directives

Patient and Physician Opinions Regarding When and How It Should Be Conducted

Sarah Coate Johnston, MD; Mark P. Pfeifer, MD; Robert McNutt, MD; End of Life Study Group; Harold M. Adelman, MD; Paul M. Wallach, MD; Joseph F. Boero, MD; Dennis Crnkovich, MD; Kevin A. Halbritter, MD; Sarah C. Johnston, MD; Rita Layson, MD; Robert McNutt, MD; Mark P. Pfeifer, MD; Jaan E. Sidorov, MD; Arthur Evans, MD, MPH; Miriam B. Settle, PhD

Arch Intern Med. 1995;155(10):1025-1030.


Abstract

Background
Widely publicized court cases have focused national attention on the importance of advance directives. In spite of initiatives such as the Patient Self-Determination Act of 1991, fewer than 10% of Americans have prepared advance directives. One way to increase the preparation of advance directives may be to increase the frequency and quality of discussions about them between individual patients and their physicians. We performed a multicenter observational study to assess the opinions of primary care patients and physicians regarding these discussions.

Methods
This was a cross-sectional descriptive survey of randomly selected primary care patients and physicians in eight primary care internal medicine clinics in the eastern and midwestern United States. Quantitative questionnaires were used to elicit subjects' demographic characteristics, and their opinions regarding the timing, content, and location of discussions about advance directives.

Results
The 883 subjects included 329 adult outpatients, 282 resident physicians, and 272 practicing physicians. Physician and patient response rates were 75% and 76%, respectively. Patients felt that the discussion should occur earlier than did the physicians: at an earlier age, earlier in the natural history of disease, and earlier in the patient-physician relationship. Most subjects agreed it was the physician's responsibility to initiate the discussion.

Conclusion
We defined a discrepancy between the preferences of primary care patients and physicians regarding the timing of the discussion about advance directives. We propose physician education regarding patient preferences as the most effective way to accomplish the goal of improving the frequency and quality of discussions about advance directives.

(Arch Intern Med. 1995;155:1025-1030)



Author Affiliations

University of South Florida, Tampa; University of Illinois, Rockford; University of Illinois, Peoria; West Virginia University, Morgantown; University of Kansas—Wichita; University of North Carolina—Greensboro; University of Wisconsin at Milwaukee; University of Louisville (Ky); Geisinger Medical Center, Danville, Pa; University of North Carolina—Chapel Hill.

From the Departments of Internal Medicine, University of Kansas School of Medicine—Wichita (Dr Johnston); University of Louisville (Ky) (Dr Pfeifer); and University of Wisconsin at Milwaukee (Dr McNutt). Members of the End of Life Study Group are listed at the end of the article.



Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter     What's this?

THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Do Older Adults Know Their Spouses' End-of-Life Treatment Preferences?
Moorman et al.
Research on Aging 2009;31:463-491.
ABSTRACT  

Clinician perceived good practice in end-of-life care for patients with COPD
Roberts et al.
Palliat Med 2008;22:855-858.
ABSTRACT  

Role of advance directives in palliative care units: a prospective study
Pautex et al.
Palliat Med 2008;22:835-841.
ABSTRACT  

Residency Training in Advance Care Planning: Can It Be Done in the Outpatient Clinic?
Alderman et al.
AM J HOSP PALLIAT CARE 2008;25:190-194.
ABSTRACT  

Outcomes After Hematopoietic Stem-Cell Transplantation for Hematologic Malignancies in Patients With or Without Advance Care Planning
Ganti et al.
JCO 2007;25:5643-5648.
ABSTRACT | FULL TEXT  

End-of-Life Health Care Planning Among Young-Old Adults: An Assessment of Psychosocial Influences
Carr and Khodyakov
Journals of Gerontology Series B: Psychological Sciences and Social Science 2007;62:S135-S141.
ABSTRACT | FULL TEXT  

Hope and advance care planning in patients with end stage renal disease: qualitative interview study
Davison and Simpson
BMJ 2006;333:886.
ABSTRACT | FULL TEXT  

Facilitating Advance Care Planning for Patients with End-Stage Renal Disease: The Patient Perspective
Davison
CJASN 2006;1:1023-1028.
ABSTRACT | FULL TEXT  

End-of-Life Treatment Preferences of Persons With Serious Mental Illness
Foti et al.
Psychiatr. Serv. 2005;56:585-591.
ABSTRACT | FULL TEXT  

Advance care planning redux: It's time to talk
Reisfield and Wilson
AM J HOSP PALLIAT CARE 2004;21:7-9.
 

Meaning and Agency in Discussing End-of-Life Care: A Study of Elderly Veterans' Values and Interpretations
Young et al.
Qual Health Res 2003;13:1039-1062.
ABSTRACT  

The Value of Disease Severity in Predicting Patient Readiness to Address End-of-Life Issues
Pfeifer et al.
Arch Intern Med 2003;163:609-612.
ABSTRACT | FULL TEXT  

Psychosocial-- spiritual correlates of death distress in patients with life-threatening medical conditions
Chibnall et al.
Palliat Med 2002;16:331-338.
ABSTRACT  

Patients' Knowledge of Options at the End of Life: Ignorance in the Face of Death
Silveira et al.
JAMA 2000;284:2483-2488.
ABSTRACT | FULL TEXT  

Practice Parameter: The Care of the Patient with Amyotrophic Lateral Sclerosis (An Evidence-Based Review): Report of the Quality Standards Subcommittee of the American Academy of Neurology
Miller et al.
Neurorehabil Neural Repair 1999;13:93-107.
 

Dialysis Patients' Preferences for Family-Based Advance Care Planning
Hines et al.
ANN INTERN MED 1999;130:825-828.
ABSTRACT | FULL TEXT  

Practice parameter: The care of the patient with amyotrophic lateral sclerosis (an evidence-based review): Report of the Quality Standards Subcommittee of the American Academy of Neurology
Miller et al.
Neurology 1999;52:1311-1311.
FULL TEXT  

Assessment of competence to complete advance directives: validation of a patient centred approach
Fazel et al.
BMJ 1999;318:493-497.
ABSTRACT | FULL TEXT  

A Systemic Perspective of Life-Prolonging Treatment Decision Making
Shidler
Qual Health Res 1998;8:254-269.
ABSTRACT  

Can Goals of Care Be Used to Predict Intervention Preferences in an Advance Directive?
Fischer et al.
Arch Intern Med 1997;157:801-807.
ABSTRACT  

Publications in Subspecialty Journals on End-of-Life Ethics
Heffner et al.
Arch Intern Med 1997;157:685-690.
ABSTRACT  

Procedure-Specific Do-Not-Resuscitate Orders: Effect on Communication of Treatment Limitations
Heffner et al.
Arch Intern Med 1996;156:793-797.
ABSTRACT  





HOME | CURRENT ISSUE | PAST ISSUES | TOPIC COLLECTIONS | CME | SUBMIT | SUBSCRIBE | HELP
CONDITIONS OF USE | PRIVACY POLICY | CONTACT US | SITE MAP
 
© 1995 American Medical Association. All Rights Reserved.