Literature DB >> 19110677

Mental health, treatment preferences, advance care planning, location, and quality of death in advanced cancer patients with dependent children.

Matthew E Nilsson1, Paul K Maciejewski, Baohui Zhang, Alexi A Wright, Elizabeth D Trice, Anna C Muriel, Robert J Friedlander, Karen M Fasciano, Susan D Block, Holly G Prigerson.   

Abstract

BACKGROUND: Clinicians observe that advanced cancer patients with dependent children agonize over the impact their death will have on their children. The objective of this study was to determine empirically whether advanced cancer patients with and without dependent children differ in treatment preferences, mental health, and end-of-life (EOL) outcomes.
METHODS: Coping with Cancer is a National Cancer Institute/National Institute of Mental Health-funded, multi-institutional, prospective cohort study of 668 patients with advanced cancer. Patients with and without dependent children were compared on rates of psychiatric disorders, advance care planning (ACP), EOL care, quality of their last week of life, and location of death.
RESULTS: In adjusted analyses, patients with advanced cancer who had dependent children were more likely to meet panic disorder criteria (adjusted odds ratio [AOR], 5.41; 95% confidence interval [95% CI], 2.13-13.69), more likely to be worried (mean difference in standard deviations [delta], 0.09; P=.006), and more likely to prefer aggressive treatment over palliative care (AOR, 1.77; 95% CI, 1.07-2.93). Patients with dependent children were less likely to engage in ACP (eg, do not resuscitate orders: AOR, 0.44; 95% CI, 0.26-0.75) and had a worse quality of life in the last week of life (delta, 0.15; P=.007). Among spousal caregivers, those with dependent children were more likely to meet criteria for major depressive disorder (AOR, 4.53; 95% CI, 1.47-14) and generalized anxiety disorder (AOR, 3.95; 95% CI, 1.29-12.16).
CONCLUSIONS: Patients with dependent children were more anxious, were less likely to engage in ACP, and were more likely to have a worse quality of life in their last week of life. Advanced cancer patients and spousal caregivers with dependent children represent a particularly distressed group that warrants further clinical attention, research, and support. Copyright (c) 2009 American Cancer Society.

Entities:  

Mesh:

Year:  2009        PMID: 19110677      PMCID: PMC2630701          DOI: 10.1002/cncr.24002

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  16 in total

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2.  Validity of the McGill Quality of Life Questionnaire in the palliative care setting: a multi-centre Canadian study demonstrating the importance of the existential domain.

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4.  The McGill Quality of Life Questionnaire: a measure of quality of life appropriate for people with advanced disease. A preliminary study of validity and acceptability.

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Journal:  Palliat Med       Date:  1995-07       Impact factor: 4.762

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7.  Peace, Equanimity, and Acceptance in the Cancer Experience (PEACE): validation of a scale to assess acceptance and struggle with terminal illness.

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Journal:  J Health Soc Behav       Date:  1992-12

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Authors:  S B Yellen; D F Cella
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10.  The effect of psychological interventions on anxiety and depression in cancer patients: results of two meta-analyses.

Authors:  T Sheard; P Maguire
Journal:  Br J Cancer       Date:  1999-08       Impact factor: 7.640

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  42 in total

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5.  Understanding health-related quality of life in adult women with metastatic cancer who have dependent children.

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6.  Enhancing Connections-Palliative Care: A Quasi-Experimental Pilot Feasibility Study of a Cancer Parenting Program.

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Review 9.  Communication in end-stage cancer: review of the literature and future research.

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