Literature DB >> 29567822

Families' Sense of Abandonment When Patients Are Referred to Hospice.

Takuya Odagiri1, Tatsuya Morita2, Maho Aoyama3, Yoshiyuki Kizawa4, Satoru Tsuneto5, Yasuo Shima6, Mitsunori Miyashita3.   

Abstract

BACKGROUND: Terminally ill patients with cancer and their families may have a sense of abandonment when they are referred to hospice. This study aimed to clarify the prevalence of families' sense of abandonment, explore the association between the sense of abandonment and the oncologists' behaviors, and investigate the association between the sense of abandonment and the families' depression and complicated grief. PATIENTS AND METHODS: This was part of a nationwide self-reported questionnaire survey of bereaved families of patients with cancer who died in inpatient hospices. We sent questionnaires to 947 bereaved families of patients with cancer who died in 133 certified hospices between May 2012 and January 2014.
RESULTS: Among 707 responses obtained, a total of 189 (26.7%) families felt abandoned. The factors significantly associated with a greater sense of abandonment were that the oncologists said there was nothing more to do for the patient, the patient's age of less than 60 years, and being the patient's spouse. The factors significantly associated with a lower sense of abandonment were that the oncologists reassured the patients that they had received the best anticancer treatment, that the oncologists recommended hospices as one potential choice rather than mandatory, and that a palliative care team provided care. Families with a sense of abandonment had higher scores on the Patient Health Questionnaire-9 (p = .096) and Brief Grief Questionnaire (p < .001).
CONCLUSION: Approximately a quarter of bereaved families had a sense of abandonment, which was associated with a higher rate of complicated grief. Oncologists may reduce the sense of abandonment by reassuring that the patients received the best anticancer treatment, recommending hospices as a potential choice rather than as mandatory, and by not saying there is nothing that can be done for the patients. IMPLICATIONS FOR PRACTICE: This self-reported questionnaire study investigated the prevalence of families' feelings of abandonment when they were referred to hospice care, focusing on the association of sense of abandonment and the behavior of their physicians. Nearly a quarter of families felt abandoned by the referral to hospice, and the behavior of some oncologists was associated with the sense of abandonment. © AlphaMed Press 2018.

Entities:  

Keywords:  Hospice; Palliative care; Sense of abandonment; Transition

Mesh:

Year:  2018        PMID: 29567822      PMCID: PMC6192602          DOI: 10.1634/theoncologist.2017-0547

Source DB:  PubMed          Journal:  Oncologist        ISSN: 1083-7159


  21 in total

1.  The PHQ-9: validity of a brief depression severity measure.

Authors:  K Kroenke; R L Spitzer; J B Williams
Journal:  J Gen Intern Med       Date:  2001-09       Impact factor: 5.128

2.  On saying goodbye: acknowledging the end of the patient-physician relationship with patients who are near death.

Authors:  Anthony L Back; Robert M Arnold; James A Tulsky; Walter F Baile; Kelly A Fryer-Edwards
Journal:  Ann Intern Med       Date:  2005-04-19       Impact factor: 25.391

3.  Palliative care services, patient abandonment, and the scope of physicians' responsibilities in end-of-life care.

Authors:  Paul K J Han; Robert M Arnold
Journal:  J Palliat Med       Date:  2005-12       Impact factor: 2.947

4.  "When patients and families feel abandoned".

Authors:  Daniel E Epner; Vinod Ravi; Walter F Baile
Journal:  Support Care Cancer       Date:  2010-09-19       Impact factor: 3.603

5.  Abandonment at the end of life from patient, caregiver, nurse, and physician perspectives: loss of continuity and lack of closure.

Authors:  Anthony L Back; Jessica P Young; Ellen McCown; Ruth A Engelberg; Elizabeth K Vig; Lynn F Reinke; Marjorie D Wenrich; Barbara B McGrath; J Randall Curtis
Journal:  Arch Intern Med       Date:  2009-03-09

6.  Administration of chemotherapy with palliative intent in the last 30 days of life: the balance between palliation and chemotherapy.

Authors:  N Zdenkowski; J Cavenagh; Y C Ku; A Bisquera; A Bonaventura
Journal:  Intern Med J       Date:  2013-11       Impact factor: 2.048

7.  The patient health questionnaire, Japanese version: validity according to the mini-international neuropsychiatric interview-plus.

Authors:  Kumiko Muramatsu; Hitoshi Miyaoka; Kunitoshi Kamijima; Yoshiyuki Muramatsu; Masahito Yoshida; Tempei Otsubo; Fumitake Gejyo
Journal:  Psychol Rep       Date:  2007-12

8.  The Japan HOspice and Palliative Care Evaluation Study 3: Study Design, Characteristics of Participants and Participating Institutions, and Response Rates.

Authors:  Maho Aoyama; Tatsuya Morita; Yoshiyuki Kizawa; Satoru Tsuneto; Yasuo Shima; Mitsunori Miyashita
Journal:  Am J Hosp Palliat Care       Date:  2016-05-02       Impact factor: 2.500

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Authors:  T E Quill; C K Cassel
Journal:  Ann Intern Med       Date:  1995-03-01       Impact factor: 25.391

10.  Brief measure for screening complicated grief: reliability and discriminant validity.

Authors:  Masaya Ito; Satomi Nakajima; Daisuke Fujisawa; Mitsunori Miyashita; Yoshiharu Kim; M Katherine Shear; Angela Ghesquiere; Melanie M Wall
Journal:  PLoS One       Date:  2012-02-14       Impact factor: 3.240

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  2 in total

Review 1.  Easing the Journey-an Updated Review of Palliative Care for the Patient with High-Grade Glioma.

Authors:  Rita C Crooms; Margaret O Johnson; Heather Leeper; Ambereen Mehta; Michelle McWhirter; Akanksha Sharma
Journal:  Curr Oncol Rep       Date:  2022-02-22       Impact factor: 5.075

2.  What will happen to my mom? A grounded theory on nurses' support of relatives' end-of-life decision-making process for residents living with dementia in long-term care homes.

Authors:  Stéphanie Daneau; Anne Bourbonnais; Alain Legault
Journal:  Dementia (London)       Date:  2022-03-25
  2 in total

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