Cited by 2,788Palliative Care and End-of-Life IssuesPalliative and Oncologic CarePatient-Provider Communication in Healthcare

The DOI matches its Crossref record; 49 of the 50 references it cites were found in a registry or an index; none of the 18 sources its claims cite is checked for support yet.

Associations Between End-of-Life Discussions, Patient Mental Health, Medical Care Near Death, and Caregiver Bereavement Adjustment

Open access
Wright, Alexi A.·2008·JAMA

Abstract

CONTEXT: Talking about death can be difficult. Without evidence that end-of-life discussions improve patient outcomes, physicians must balance their desire to honor patient autonomy against a concern of inflicting psychological harm. OBJECTIVE: To determine whether end-of-life discussions with physicians are associated with fewer aggressive interventions. DESIGN, SETTING, AND PARTICIPANTS: A US multisite, prospective, longitudinal cohort study of patients with advanced cancer and their informal caregivers (n = 332 dyads), September 2002-February 2008. Patients were followed up from enrollment to death, a median of 4.4 months later. Bereaved caregivers' psychiatric illness and quality of life was assessed a median of 6.5 months later. MAIN OUTCOME MEASURES: Aggressive medical care (eg, ventilation, resuscitation) and hospice in the final week of life. Secondary outcomes included patients' mental health and caregivers' bereavement adjustment. RESULTS: One hundred twenty-three of 332 (37.0%) patients reported having end-of-life discussions before baseline. Such discussions were not associated with higher rates of major depressive disorder (8.3% vs 5.8%; adjusted odds ratio [OR], 1.33; 95% confidence interval [CI], 0.54-3.32), or more worry (mean McGill score, 6.5 vs 7.0; P = .19). After propensity-score weighted adjustment, end-of-life discussions were associated with lower rates of ventilation (1.6% vs 11.0%; adjusted OR, 0.26; 95% CI, 0.08-0.83), resuscitation (0.8% vs 6.7%; adjusted OR, 0.16; 95% CI, 0.03-0.80), ICU admission (4.1% vs 12.4%; adjusted OR, 0.35; 95% CI, 0.14-0.90), and earlier hospice enrollment (65.6% vs 44.5%; adjusted OR, 1.65;95% CI, 1.04-2.63). In adjusted analyses, more aggressive medical care was associated with worse patient quality of life (6.4 vs 4.6; F = 3.61, P = .01) and higher risk of major depressive disorder in bereaved caregivers (adjusted OR, 3.37; 95% CI, 1.12-10.13), whereas longer hospice stays were associated with better patient quality of life (mean score, 5.6 vs 6.9; F = 3.70, P = .01). Better patient quality of life was associated with better caregiver quality of life at follow-up (beta = .20; P = .001). CONCLUSIONS: End-of-life discussions are associated with less aggressive medical care near death and earlier hospice referrals. Aggressive care is associated with worse patient quality of life and worse bereavement adjustment.

Overview

Integrity signals

Registry

Crossref · 10.1001/jama.300.14.1665

Cites

49 of 49 references verified0 citation errors · 0 not checkable

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Claims the paper makes

36 Own result · 7 Not checked yet · 7 Own method · 4 Own interpretation · 1 No basis given

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Show all 48 claims

  • It may state two separate claims as one. 6
  • Probably not a substantial claim. 1
7 of 7
  • The paper relies on this without support.

    Patient self-report accurately identifies whether an end-of-life discussion occurred.

    “Absent such independent validation, the accuracy of patients’ reported rates of discussions remains unknown”
    “we do not know who initiated the conversation, when it happened, or what was said.”
  • The paper relies on this without support.

    Caregiver report accurately reflects the patient's quality of life near death.

    “In a post-mortem interview, research staff interviewed the formal/informal caregiver involved in the patients’ care during the final week of life to assess the patient’s QoL near death.”
    “source of report for patient QoL”
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Metadata

Authors
Wright, A. A.
Affiliations
Dana-Farber Cancer Institute (US)
Corresponding author
Wright, Alexi A.
Venue
JAMA
Published
2008-10-08
Volume
300
Issue
14
Pages
1665
ISSN
  • 0002-9955 (ISSN-L)
  • 0098-7484
OpenAlex
W2137401089
Cited by
2,788
References
50
Citations by year
2026: 115 · 2025: 132 · 2024: 152 · 2023: 167 · 2022: 186 · 2021: 221 · 2020: 215 · 2019: 225 · 2018: 178 · 2017: 207 · 2016: 179 · 2015: 159 · 2014: 143 · 2013: 136 · 2012: 110
FWCI
84.45
Type
journal article
Language
en
Open access
Locations
  • JAMA (publishedVersion)
  • PubMed (publishedVersion)
  • Europe PMC (PubMed Central) (acceptedVersion)
  • PubMed Central (acceptedVersion)
  • Digital Access to Scholarship at Harvard (DASH) (Harvard University) (acceptedVersion)
Funders
  • McGill University
  • National Institute on Aging (K24AG033640)
  • National Institute of Mental Health (MH-63892, R01MH063892)
  • National Cancer Institute (R01CA106370, CA106370, CA 92044343, T32CA009172)
Topics
  • Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Palliative Care and End-of-Life Issues
  • Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Palliative and Oncologic Care
  • Health Sciences › Health Professions › General Health Professions › Patient-Provider Communication in Healthcare
Keywords
end-of-life discussions, advance care planning, mechanical ventilation, cardiopulmonary resuscitation, hospice enrollment, advanced cancer, patient mental health, major depressive disorder, informal caregivers, quality of life, intensive care unit admission, physician-patient communication, patient autonomy
MeSH terms
Adaptation, Psychological, Aged, Attitude to Death, Bereavement, Female, Humans, Longitudinal Studies, Male, Mental Health, Middle Aged, Neoplasms, Physician-Patient Relations, Physician's Role, Quality of Life, Resuscitation, Terminal Care, Caregivers, Hospice Care, Terminally Ill, Advance Care Planning

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