Literature DB >> 24793077

Family involvement at the end-of-life and receipt of quality care.

Rebecca L Sudore1, David Casarett2, Dawn Smith3, Diane M Richardson3, Mary Ersek4.   

Abstract

CONTEXT: Most patients will lose decision-making capacity at the end of life. Little is known about the quality of care received by patients who have family involved in their care.
OBJECTIVES: To evaluate differences in the receipt of quality end-of-life care for patients who died with and without family involvement.
METHODS: We retrospectively reviewed the charts of 34,290 decedents from 146 acute and long-term care Veterans Affairs facilities between 2010 and 2011. Outcomes included: (1) palliative care consult, (2) chaplain visit, and 3) death in an inpatient hospice or palliative care unit. We also assessed "do not resuscitate" (DNR) orders. Family involvement was defined as documented discussions with the health care team in the last month of life. We used logistic regression adjusted for demographics, comorbidity, and clustered by facility. For chaplain visit, hospice or palliative care unit death, and DNR, we additionally adjusted for palliative care consults.
RESULTS: Mean (SD) age was 74 (±12) years, 98% were men, and 19% were nonwhite. Most decedents (94.2%) had involved family. Veterans with involved family were more likely to have had a palliative care consult, adjusted odds ratio (AOR) 4.31 (95% CI 3.90-4.76); a chaplain visit, AOR 1.18 (95% CI 1.07-1.31); and a DNR order, AOR 4.59 (95% CI 4.08-5.16) but not more likely to die in a hospice or palliative care unit.
CONCLUSION: Family involvement at the end of life is associated with receipt of palliative care consultation and a chaplain visit and a higher likelihood of a DNR order. Clinicians should support early advance care planning for vulnerable patients who may lack family or friends. Published by Elsevier Inc.

Entities:  

Keywords:  End-of-life care; communication; quality assessment; veterans

Mesh:

Year:  2014        PMID: 24793077     DOI: 10.1016/j.jpainsymman.2014.04.001

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


  12 in total

1.  Evaluation of Family Characteristics and Multiple Hospitalizations at the End of Life: Evidence from the Utah Population Database.

Authors:  Djin L Tay; Katherine A Ornstein; Huong Meeks; Rebecca L Utz; Ken R Smith; Caroline Stephens; Mia Hashibe; Lee Ellington
Journal:  J Palliat Med       Date:  2021-08-27       Impact factor: 2.947

2.  Development and Validation of Filial Piety Representations at Parents' End of Life Scale.

Authors:  Sok-Leng Che; Wai-I Ng; Xiang Li; Mingxia Zhu
Journal:  Healthcare (Basel)       Date:  2022-06-06

3.  Quality of End-of-Life Care Provided to Patients With Different Serious Illnesses.

Authors:  Melissa W Wachterman; Corey Pilver; Dawn Smith; Mary Ersek; Stuart R Lipsitz; Nancy L Keating
Journal:  JAMA Intern Med       Date:  2016-08-01       Impact factor: 21.873

4.  Adapting an Early Palliative Care Intervention to Family Caregivers of Persons With Advanced Cancer in the Rural Deep South: A Qualitative Formative Evaluation.

Authors:  J Nicholas Dionne-Odom; Richard Taylor; Gabrielle Rocque; Carol Chambless; Thomas Ramsey; Andres Azuero; Nataliya Ivankova; Michelle Y Martin; Marie A Bakitas
Journal:  J Pain Symptom Manage       Date:  2018-02-21       Impact factor: 3.612

5.  Predictors of spiritual care provision for patients with dementia at the end of life as perceived by physicians: a prospective study.

Authors:  Jenny T van der Steen; Marie-José He Gijsberts; Cees Mpm Hertogh; Luc Deliens
Journal:  BMC Palliat Care       Date:  2014-12-19       Impact factor: 3.234

6.  Evaluation of a strategy for enrolling the families of critically ill patients in research using limited human resources.

Authors:  Alison E Turnbull; Mohamed D Hashem; Anahita Rabiee; An To; Caroline M Chessare; Dale M Needham
Journal:  PLoS One       Date:  2017-05-25       Impact factor: 3.240

7.  Nurses' decision-making about cancer patients' end-of-life skin care in Wales: an exploratory mixed-method vignette study protocol.

Authors:  Ray Samuriwo; Candida Lovell-Smith; Sally Anstey; Claire Job; Jane Hopkinson
Journal:  BMJ Open       Date:  2020-07-05       Impact factor: 2.692

Review 8.  Conceptualizing and Counting Discretionary Utilization in the Final 100 Days of Life: A Scoping Review.

Authors:  Paul R Duberstein; Michael Chen; Michael Hoerger; Ronald M Epstein; Laura M Perry; Sule Yilmaz; Fahad Saeed; Supriya G Mohile; Sally A Norton
Journal:  J Pain Symptom Manage       Date:  2019-10-19       Impact factor: 3.612

Review 9.  Deconstructing the Complexities of Advance Care Planning Outcomes: What Do We Know and Where Do We Go? A Scoping Review.

Authors:  Ryan D McMahan; Ismael Tellez; Rebecca L Sudore
Journal:  J Am Geriatr Soc       Date:  2020-09-07       Impact factor: 5.562

10.  'Take more laxatives was their answer to everything': A qualitative exploration of the patient, carer and healthcare professional experience of constipation in specialist palliative care.

Authors:  Felicity Hasson; Deborah Muldrew; Emma Carduff; Anne Finucane; Lisa Graham-Wisener; Phil Larkin; Noleen Mccorry; Paul Slater; Sonja McIlfatrick
Journal:  Palliat Med       Date:  2019-12-23       Impact factor: 4.762

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