Literature DB >> 28827369

Discordance between patients' stated values and treatment preferences for end-of-life care: results of a multicentre survey.

Daren K Heyland1,2,3, Rebecca Heyland3, Peter Dodek4, John J You5, Tasnim Sinuff6,7, Tim Hiebert8, Xuran Jiang3, Andrew G Day3.   

Abstract

BACKGROUND: Medical orders for the use of life-supports should be informed by patients' values and treatment preferences. The purpose of this study was to explore the internal consistency of patients' (or their family members') stated values, and the relationship between these values and expressed preferences.
METHODS: We conducted a prospective study in 12 acute care hospitals in Canada. We administered a questionnaire to elderly patients and their family members about their values related to end-of-life (EOL) care, treatment preferences and decisional conflict.
RESULTS: Of 513 patients and 366 family members approached, 278 patients (54%) and 225 family members (61%) consented to participate. Participants' most important stated values were to be comfortable and suffer as little as possible, to have more time with family, to avoid being attached to machines and tubes and that death not be prolonged. The least important stated value was that life be preserved. Based on prespecified expected associations between the various values measured, there were inconsistencies in participants' expressed value statements. With few exceptions, participants' expressed values were not associated with expected corresponding treatment preferences. Of the 109 (40%) patients and 95 (42%) family members who had made decisions about use of life-supports, 68 (56%) patients and 60 (59%) family members had decisional conflict.
CONCLUSIONS: Decision-making regarding medical treatments at the EOL is inadequate. To reduce decisional conflict, patients and their families need more support to clarify their values and ensure that their preferences are grounded in adequate understanding of their illness and treatment options. TRIAL REGISTRATION NUMBER: NCT01362855. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/.

Entities:  

Keywords:  Clinical decisions; Communication; Ethics; Hospital care

Mesh:

Year:  2016        PMID: 28827369     DOI: 10.1136/bmjspcare-2015-001056

Source DB:  PubMed          Journal:  BMJ Support Palliat Care        ISSN: 2045-435X            Impact factor:   3.568


  24 in total

1.  Giving Voice to Patient Values Throughout Cancer: A Novel Nurse-Led Intervention.

Authors:  Andrew S Epstein; Anjali V Desai; Camila Bernal; Danielle Romano; Peter J Wan; Molly Okpako; Kelly Anderson; Kimberly Chow; Dana Kramer; Claudia Calderon; Virginia V Klimek; Robin Rawlins-Duell; Diane L Reidy; Jessica I Goldberg; Elizabeth Cruz; Judith E Nelson
Journal:  J Pain Symptom Manage       Date:  2019-04-26       Impact factor: 3.612

2.  A novel decision aid to help plan for serious illness: a multisite randomized trial.

Authors:  Daren K Heyland; Rebecca Heyland; Alice Bailey; Michelle Howard
Journal:  CMAJ Open       Date:  2020-04-28

3.  Influence of clinical context on interpretation and use of an advance care planning policy: a qualitative study.

Authors:  Marta Shaw; Shelley Raffin Bouchal; Lauren Hutchison; Reanne Booker; Jayna Holroyd-Leduc; Deborah White; Andrew Grant; Jessica Simon
Journal:  CMAJ Open       Date:  2020-01-07

Review 4.  Achieving Goal-Concordant Care: A Conceptual Model and Approach to Measuring Serious Illness Communication and Its Impact.

Authors:  Justin J Sanders; J Randall Curtis; James A Tulsky
Journal:  J Palliat Med       Date:  2017-11-01       Impact factor: 2.947

5.  Patient Activation: A Key Component of Successful Advance Care Planning.

Authors:  Daniel David; Deborah E Barnes; Ryan D McMahan; Ying Shi; Mary T Katen; Rebecca L Sudore
Journal:  J Palliat Med       Date:  2018-08-21       Impact factor: 2.947

6.  Outcomes That Define Successful Advance Care Planning: A Delphi Panel Consensus.

Authors:  Rebecca L Sudore; Daren K Heyland; Hillary D Lum; Judith A C Rietjens; Ida J Korfage; Christine S Ritchie; Laura C Hanson; Diane E Meier; Steven Z Pantilat; Karl Lorenz; Michelle Howard; Michael J Green; Jessica E Simon; Mariko A Feuz; John J You
Journal:  J Pain Symptom Manage       Date:  2017-09-01       Impact factor: 3.612

7.  Quality versus quantity in end-of-life choices of cancer patients and support persons: a discrete choice experiment.

Authors:  Amy Waller; Rob Sanson-Fisher; Scott D Brown; Laura Wall; Justin Walsh
Journal:  Support Care Cancer       Date:  2018-05-03       Impact factor: 3.603

8.  Physician Orders for Life-Sustaining Treatment and ICU Admission Near the End of Life-Reply.

Authors:  Robert Y Lee; J Randall Curtis; Erin K Kross
Journal:  JAMA       Date:  2020-08-11       Impact factor: 56.272

9.  Instability in End-of-Life Care Preference Among Heart Failure Patients: Secondary Analysis of a Randomized Controlled Trial in Singapore.

Authors:  Chetna Malhotra; Meibo Hu; Rahul Malhotra; David Sim; Fazlur Rehman Jaufeerally; Filipinas G Bundoc; Eric A Finkelstein
Journal:  J Gen Intern Med       Date:  2020-02-26       Impact factor: 5.128

10.  Patient Risk Factor Profiles Associated With the Timing of Goals-of-Care Consultation Before Death: A Classification and Regression Tree Analysis.

Authors:  Lauren T Starr; Connie M Ulrich; Paul Junker; Liming Huang; Nina R O'Connor; Salimah H Meghani
Journal:  Am J Hosp Palliat Care       Date:  2020-06-30       Impact factor: 2.500

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