Literature DB >> 20171827

Provider communication and patient understanding of life-limiting illness and their relationship to patient communication of treatment preferences.

Glenn J Wagner1, Deborah Riopelle, Jillisa Steckart, Karl A Lorenz, Kenneth E Rosenfeld.   

Abstract

Medical decision making in the context of serious illness ideally involves a patient who understands his or her condition and prognosis and can effectively formulate and communicate his or her care preferences. To understand the relationships among these care processes, we analyzed baseline interview data from veterans enrolled in a randomized controlled trial of a palliative care intervention. Participants were 400 inpatient veterans admitted with a physician-estimated risk of one-year mortality more than 25%; 260 (65%) had cancer as the primary diagnosis. Patients who believed that they had a life-limiting illness (89% of sample) reported that their provider had communicated this to them more frequently than those who did not share that belief (78% vs. 22%, P<0.001). Over half (53%) of the participants reported discussing their care preferences with their providers and 66% reported such discussions with their family; 35% had a living will. In multivariate analysis, greater functional impairment was associated with patients having discussed their care preferences with providers (P<0.05), whereas patient understanding of prognosis (P<0.05), better quality of life (P<0.01), and not being African American (P<0.05) were associated with patients having discussed their care preferences with family; higher education (P<0.001), and not being African American (P<0.01) were associated with having a living will. Patients with poor understanding of prognosis are less likely to discuss care preferences with family members, suggesting the importance of provider communication with patients regarding prognosis. Because functional decline may prompt physicians to discuss prognosis with patients, patients with relatively preserved function may particularly need such communication. (c) 2010 U.S. Cancer Pain Relief Committee. All rights reserved.

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Year:  2010        PMID: 20171827     DOI: 10.1016/j.jpainsymman.2009.07.012

Source DB:  PubMed          Journal:  J Pain Symptom Manage        ISSN: 0885-3924            Impact factor:   3.612


  10 in total

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4.  Advance directives in patients with advanced cancer receiving active treatment: attitudes, prevalence, and barriers.

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Authors:  Wendy G Anderson; Susan Kools; Audrey Lyndon
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6.  Effect of Default Options in Advance Directives on Hospital-Free Days and Care Choices Among Seriously Ill Patients: A Randomized Clinical Trial.

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7.  The Effect of Prognostic Communication on Patient Outcomes in Palliative Cancer Care: a Systematic Review.

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8.  Socioeconomic position and use of hospital-based care towards the end of life: a mediation analysis using the English Longitudinal Study of Ageing.

Authors:  Joanna M Davies; Matthew Maddocks; Kia-Chong Chua; Panayotes Demakakos; Katherine E Sleeman; Fliss E M Murtagh
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Review 9.  Perceptions and Misperceptions of Early Palliative Care Interventions for Patients With Hematologic Malignancies Undergoing Bone Marrow Transplantation.

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  10 in total

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