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.


Advertisement

ABOUT ARCHIVES
Advanced Search

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


  Vol. 169 No. 10, May 25, 2009 TABLE OF CONTENTS
  Online Only
 •  Online First Table of
Contents
  Original Investigation
 •Online Features
 This Article
 •Full text
 •PDF
 • Reply to article
 •Send to a friend
 • Save in My Folder
 •Save to citation manager
 •Permissions
 Citing Articles
 •Citation map
 •Citing articles on HighWire
 •Citing articles on Web of Science (12)
 •Contact me when this article is cited
 Related Content
 •Related article
 •Similar articles in this journal
 Topic Collections
 •Medical Practice
 •Medical Practice, Other
 •Oncology
 •Lung Cancer
 •Oncology, Other
 •Pain
 •Patient-Physician Communication
 •End-of-life Care/ Palliative Medicine
 •Pulmonary Diseases, Other
 •Alert me on articles by topic
 Social Bookmarking
  Add to CiteULike Add to Connotea Add to Delicious Add to Digg Add to Facebook Add to Reddit Add to Technorati Add to Twitter What's this?

Discussions With Physicians About Hospice Among Patients With Metastatic Lung Cancer

Haiden A. Huskamp, PhD; Nancy L. Keating, MD, MPH; Jennifer L. Malin, MD, PhD; Alan M. Zaslavsky, PhD; Jane C. Weeks, MD, MSc; Craig C. Earle, MD; Joan M. Teno, MD, MS; Beth A. Virnig, PhD, MPH; Katherine L. Kahn, MD; Yulei He, PhD; John Z. Ayanian, MD, MPP

Arch Intern Med. 2009;169(10):954-962.

Background  Many terminally ill patients enroll in hospice only in the final days before death or not at all. Discussing hospice with a health care provider could increase awareness of hospice and possibly result in earlier use.

Methods  We used data on 1517 patients diagnosed as having stage IV lung cancer from a multiregional study. We estimated logistic regression models for the probability that a patient discussed hospice with a physician or other health care provider before an interview 4 to 7 months after diagnosis as reported by either the patient or surrogate or documented in the medical record.

Results  Half (53%) of the patients had discussed hospice with a provider. Patients who were black, Hispanic, non-English speaking, married or living with a partner, Medicaid beneficiaries, or had received chemotherapy were less likely to have discussed hospice. Only 53% of individuals who died within 2 months after the interview had discussed hospice, and rates were lower among those who lived longer. Patients who reported that they expected to live less than 2 years had much higher rates of discussion than those expecting to live longer. Patients reporting the most severe pain or dyspnea were no more likely to have discussed hospice than those reporting less severe or no symptoms. A third of patients who reported discussing do-not-resuscitate preferences with a physician had also discussed hospice.

Conclusions  Many patients diagnosed as having metastatic lung cancer had not discussed hospice with a provider within 4 to 7 months after diagnosis. Increased communication with physicians could address patients' lack of awareness about hospice and misunderstandings about prognosis.


Author Affiliations: Department of Health Care Policy, Harvard Medical School (Drs Huskamp, Keating, Zaslavsky, He, and Ayanian), Division of General Internal Medicine, Brigham and Women's Hospital (Drs Keating and Ayanian), and Division of Population Sciences, Dana-Farber Cancer Institute (Dr Weeks), Boston, Massachusetts; Department of Medicine (Dr Malin) and Division of General Internal Medicine (Dr Kahn), David Geffen School of Medicine, University of California, Los Angeles, and Veterans Affairs Health Care System, Greater Los Angeles (Dr Malin), Los Angeles; RAND Corporation, Santa Monica, California (Drs Malin and Kahn); Institute for Clinical Evaluative Sciences, Sunnybrook Health Sciences Center, Toronto, Ontario, Canada (Dr Earle); Center for Gerontology and Health Care Research, Department of Community Health, Warren Alpert Medical School, Brown University, Providence, Rhode Island (Dr Teno); and Department of Health Policy and Management, University of Minnesota, Minneapolis (Dr Virnig).



Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Delicious Delicious   Add to Digg Digg   Add to Facebook Facebook   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter     What's this?

RELATED ARTICLE

Bereavement Practices of Physicians in Oncology and Palliative Care
Nicole G. Chau, Camilla Zimmermann, Clement Ma, Nathan Taback, and Monika K. Krzyzanowska
Arch Intern Med. 2009;169(10):963-971.
ABSTRACT | FULL TEXT  


THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

It Takes a Village
Earle
JCO 2012;30:353-354.
FULL TEXT  

A Population-based Study of the Pattern of Terminal Care and Hospital Death in Patients with Non-small Cell Lung Cancer
NIEDER et al.
Anticancer Res 2012;32:189-194.
ABSTRACT | FULL TEXT  

Documentation of Information and Care Planning for Patients with Advanced Cancer: Associations with Patient Characteristics and Utilization of Hospital Care
Sharma and Dy
AM J HOSP PALLIAT CARE 2011;28:543-549.
ABSTRACT  

Palliative Care and the Quality of Life
Meier and Brawley
JCO 2011;29:2750-2752.
FULL TEXT  

The Quality of Care Provided to Hospitalized Patients at the End of Life
Walling et al.
Arch Intern Med 2010;170:1057-1063.
ABSTRACT | FULL TEXT  

Missing Data Analysis Using Multiple Imputation: Getting to the Heart of the Matter
He
Circ Cardiovasc Qual Outcomes 2010;3:98-105.
ABSTRACT | FULL TEXT  





HOME | CURRENT ISSUE | PAST ISSUES | TOPIC COLLECTIONS | CME | PHYSICIAN JOBS | SUBMIT | SUBSCRIBE | HELP
CONDITIONS OF USE | PRIVACY POLICY | CONTACT US | SITE MAP
 
© 2009 American Medical Association. All Rights Reserved.