Literature DB >> 25194877

Correlates of a good death and the impact of hospice involvement: findings from the national survey of households affected by cancer.

John G Cagle1, Jolynn Pek, Maggie Clifford, Jack Guralnik, Sheryl Zimmerman.   

Abstract

PURPOSE: Knowing how to improve the dying experience for patients with end-stage cancer is essential for cancer professionals. However, there is little evidence on the relationship between clinically relevant factors and quality of death. Also, while hospice has been linked with improved outcomes, our understanding of factors that contribute to a "good death" when hospice is involved remains limited. This study (1) identified correlates of a good death and (2) provided evidence on the impact of hospice on quality of death.
METHODS: Using data from a survey of US households affected by cancer (N = 930, response rate 51 %), we fit regression models with a subsample of 158 respondents who had experienced the death of a family member with cancer. Measures included quality of death (good/bad) and clinically relevant factors including: hospice involvement, symptoms during treatment, whether wishes were followed, provider knowledge/expertise, and compassion.
RESULTS: Respondents were 60 % female, 89 % White, and averaged 57 years old. Decedents were most often a respondent's spouse (46 %). While 73 % of respondents reported a good death, Hispanics were less likely to experience good death (p = 0.007). Clinically relevant factors, including hospice, were associated with good death (p < 0.05)--an exception being whether the physician said the cancer was curable/fatal. With adjustments, perceptions of provider knowledge/expertise was the only clinical factor that remained associated with good death.
CONCLUSIONS: Enhanced provider training/communication, referrals to hospice and greater attention to symptom management may facilitate improved quality of dying. Additionally, the cultural relevance of the concept of a "good death" warrants further research.

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Mesh:

Year:  2014        PMID: 25194877      PMCID: PMC5484523          DOI: 10.1007/s00520-014-2404-z

Source DB:  PubMed          Journal:  Support Care Cancer        ISSN: 0941-4355            Impact factor:   3.603


  27 in total

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Review 2.  Part 1: Home-based family caregiving at the end of life: a comprehensive review of published quantitative research (1998-2008).

Authors:  Ki Stajduhar; L Funk; C Toye; Ge Grande; S Aoun; Cj Todd
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3.  Decision-making in serious illness: a matter of life, death and words.

Authors:  James A Tulsky
Journal:  Patient Educ Couns       Date:  2010-07

Review 4.  Review: the quality of dying and death: a systematic review of measures.

Authors:  Sarah Hales; Camilla Zimmermann; Gary Rodin
Journal:  Palliat Med       Date:  2010-01-19       Impact factor: 4.762

5.  Knowledge About Hospice Care and Beliefs About Pain Management: Exploring Differences Between Hispanics and Non-Hispanics.

Authors:  Iraida V Carrion; John G Cagle; Daniel J Van Dussen; Krystal L Culler; Seokho Hong
Journal:  Am J Hosp Palliat Care       Date:  2014-06-05       Impact factor: 2.500

6.  Navigating the advanced cancer experience of underserved Latinas.

Authors:  Frances R Nedjat-Haiem; Iraida V Carrion; Kathleen Ell; Lawrence Palinkas
Journal:  Support Care Cancer       Date:  2012-03-15       Impact factor: 3.603

7.  Improving end-of-life experience and care in the community: a conceptual framework.

Authors:  I Byock; K Norris; J R Curtis; D L Patrick
Journal:  J Pain Symptom Manage       Date:  2001-09       Impact factor: 3.612

8.  A "good death" for whom? Quality of spouse's death and psychological distress among older widowed persons.

Authors:  Deborah Carr
Journal:  J Health Soc Behav       Date:  2003-06

9.  The health impact of health care on families: a matched cohort study of hospice use by decedents and mortality outcomes in surviving, widowed spouses.

Authors:  Nicholas A Christakis; Theodore J Iwashyna
Journal:  Soc Sci Med       Date:  2003-08       Impact factor: 4.634

10.  Satisfaction of families using end-of-life care: current successes and challenges in the hospice industry.

Authors:  Penny J Miceli; Deirdre E Mylod
Journal:  Am J Hosp Palliat Care       Date:  2003 Sep-Oct       Impact factor: 2.500

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  9 in total

1.  Culture and Sanity at the End of Life.

Authors:  Daniel D Matlock; Stacy M Fischer
Journal:  J Am Geriatr Soc       Date:  2019-07-09       Impact factor: 5.562

2.  Priorities of a "good death" according to cancer patients, their family caregivers, physicians, and the general population: a nationwide survey.

Authors:  Young Ho Yun; Kyoung-Nam Kim; Jin-Ah Sim; EunKyo Kang; Jihye Lee; Jiyeon Choo; Shin Hye Yoo; Miso Kim; Young Ae Kim; Beo Deul Kang; Hyun-Jeong Shim; Eun-Kee Song; Jung Hun Kang; Jung Hye Kwon; Jung Lim Lee; Soon Nam Lee; Chi Hoon Maeng; Eun Joo Kang; Young Rok Do; Yoon Seok Choi; Kyung Hae Jung
Journal:  Support Care Cancer       Date:  2018-04-22       Impact factor: 3.603

3.  Using a Non-Fit Message Helps to De-Intensify Negative Reactions to Tough Advice.

Authors:  Ilona Fridman; Karen A Scherr; Paul A Glare; E Tory Higgins
Journal:  Pers Soc Psychol Bull       Date:  2016-08

4.  Communication among cancer patients, caregivers, and hospice nurses: Content, process and change over time.

Authors:  Lee Ellington; Margaret F Clayton; Maija Reblin; Gary Donaldson; Seth Latimer
Journal:  Patient Educ Couns       Date:  2017-09-22

5.  Elements of healthy death: a thematic analysis.

Authors:  Fatemeh Estebsari; Mohammad Hossein Taghdisi; Davood Mostafaei; Zahra Rahimi
Journal:  Med J Islam Repub Iran       Date:  2017-03-23

6.  Family perceptions of quality of end of life in LGBTQ+ individuals: a comparative study.

Authors:  S Alexander Kemery
Journal:  Palliat Care Soc Pract       Date:  2021-03-31

7.  "It's Like a Death Sentence but It Really Isn't" What Patients and Families Want to Know About Hospice Care When Making End-of-Life Decisions.

Authors:  Channing E Tate; Grace Venechuk; Elinor J Brereton; Pilar Ingle; Larry A Allen; Megan A Morris; Daniel D Matlock
Journal:  Am J Hosp Palliat Care       Date:  2019-12-31       Impact factor: 2.500

8.  The Impact of Varying Levels of Advance Care Planning Engagement on Perceptions of the End-of-Life Experience Among Caregivers of Deceased Patients With Cancer.

Authors:  Kristin Levoy; Harleah Buck; Victoria Behar-Zusman
Journal:  Am J Hosp Palliat Care       Date:  2020-04-13       Impact factor: 2.500

Review 9.  Patient Portals to Support Palliative and End-of-Life Care: Scoping Review.

Authors:  M Pilar Ingle; Cristina Valdovinos; Kelsey L Ford; Shou Zhou; Sheana Bull; Starlynne Gornail; Xuhong Zhang; Jennifer Portz; Susan Moore
Journal:  J Med Internet Res       Date:  2021-09-16       Impact factor: 5.428

  9 in total

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