Literature DB >> 25050607

Association between quality of end-of-life care and possible complicated grief among bereaved family members.

Kaya Miyajima1, Daisuke Fujisawa, Kimio Yoshimura, Masaya Ito, Satomi Nakajima, Joichiro Shirahase, Masaru Mimura, Mitsunori Miyashita.   

Abstract

BACKGROUND: Little is known about the association between quality of end-of-life care of a patient and complicated grief among bereaved family members.
OBJECTIVE: This study aims to examine the impact of quality of end-of-life care on complicated grief among bereaved family members in a Japanese general population sample.
METHODS: A mail-based cross-sectional questionnaire survey was used. A total of 641 individuals aged 40 to 79 years in the general population who lost their loved one within the period between 6 months and 10 years were enrolled. Complicated grief was assessed using the Brief Grief Questionnaire, and the bereaved family members' perceptions on quality of end-of-life care were assessed using the Care Evaluation Scale and the Good Death Inventory. Logistic regression analysis was used to identify the variables that associated with possible complicated grief.
RESULTS: Possible complicated grief was observed in 24.5% of the participants. Three components of quality of end-of-life care, namely, dissatisfaction with the explanation to the family about the patient's expected outcome, unreasonable cost of care, and family's perception that the deceased person had not achieved a sense of completion about his or her life, were significantly associated with possible complicated grief. Spousal relationship, primary caregiver, and high psychological distress also had significant association.
CONCLUSIONS: Perceptions on quality of end-of-life care were significantly associated with complicated grief. Providing sufficient information to patients' family about expected outcome and enhancing patients' sense of completion about their life may prevent bereaved family members from developing complicated grief.

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Year:  2014        PMID: 25050607     DOI: 10.1089/jpm.2013.0552

Source DB:  PubMed          Journal:  J Palliat Med        ISSN: 1557-7740            Impact factor:   2.947


  12 in total

1.  End-of-life experiences of mothers with advanced cancer: perspectives of widowed fathers.

Authors:  Eliza M Park; Allison M Deal; Justin M Yopp; Teresa P Edwards; Douglas J Wilson; Laura C Hanson; Donald L Rosenstein
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Review 2.  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

3.  Comparison of the quality of death between primary malignant brain tumor patients and other cancer patients: results from a nationwide bereavement survey in Japan.

Authors:  Maho Aoyama; Kento Masukawa; Ikuko Sugiyama; Tatsuya Morita; Yoshiyuki Kizawa; Satoru Tsuneto; Yasuo Shima; Mitsunori Miyashita
Journal:  J Neurooncol       Date:  2022-04-18       Impact factor: 4.130

4.  Development of an Assessment to Examine Training of the Hospice Primary Caregiver.

Authors:  Eleanor L DiBiasio; Joan M Teno; Melissa A Clark; Carol Spence; David Casarett
Journal:  J Palliat Med       Date:  2016-05-25       Impact factor: 2.947

5.  Posttraumatic growth in bereaved family members of patients with cancer: a qualitative analysis.

Authors:  Kayo Hirooka; Hiroki Fukahori; Kanako Taku; Sakiko Izawa; Asao Ogawa
Journal:  Support Care Cancer       Date:  2018-08-30       Impact factor: 3.603

6.  Development the Care Evaluation Scale Version 2.0: a modified version of a measure for bereaved family members to evaluate the structure and process of palliative care for cancer patient.

Authors:  Mitsunori Miyashita; Maho Aoyama; Misato Nakahata; Yuji Yamada; Mutsumi Abe; Kazuhiro Yanagihara; Akemi Shirado; Mariko Shutoh; Yoshiaki Okamoto; Jun Hamano; Aoi Miyamoto; Saki Yoshida; Kazuki Sato; Kei Hirai; Tatsuya Morita
Journal:  BMC Palliat Care       Date:  2017-01-23       Impact factor: 3.234

Review 7.  Still Searching: A Meta-Synthesis of a Good Death from the Bereaved Family Member Perspective.

Authors:  Kelly E Tenzek; Rachel Depner
Journal:  Behav Sci (Basel)       Date:  2017-04-25

8.  Associations between informal care costs, care quality, carer rewards, burden and subsequent grief: the international, access, rights and empowerment mortality follow-back study of the last 3 months of life (IARE I study).

Authors:  Irene J Higginson; Deokhee Yi; Bridget M Johnston; Karen Ryan; Regina McQuillan; Lucy Selman; Stephen Z Pantilat; Barbara A Daveson; R Sean Morrison; Charles Normand
Journal:  BMC Med       Date:  2020-11-03       Impact factor: 8.775

9.  Good Quality Care for Cancer Patients Dying in Hospitals, but Information Needs Unmet: Bereaved Relatives' Survey within Seven Countries.

Authors:  Dagny Faksvåg Haugen; Karl Ove Hufthammer; Christina Gerlach; Katrin Sigurdardottir; Marit Irene Tuen Hansen; Grace Ting; Vilma Adriana Tripodoro; Gabriel Goldraij; Eduardo Garcia Yanneo; Wojciech Leppert; Katarzyna Wolszczak; Lair Zambon; Juliana Nalin Passarini; Ivete Alonso Bredda Saad; Martin Weber; John Ellershaw; Catriona Rachel Mayland
Journal:  Oncologist       Date:  2021-06-17

Review 10.  Supporting Adults Bereaved Through COVID-19: A Rapid Review of the Impact of Previous Pandemics on Grief and Bereavement.

Authors:  Catriona R Mayland; Andrew J E Harding; Nancy Preston; Sheila Payne
Journal:  J Pain Symptom Manage       Date:  2020-05-15       Impact factor: 3.612

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