Literature DB >> 19939305

The meaning of being in transition to end-of-life care for female partners of spouses with cancer.

Nisha Sutherland1.   

Abstract

OBJECTIVE: Female partners of cancer patients are at high risk for psychological distress. However, the majority of studies have focused on measurement of female partners' psychological distress during diagnosis and early treatment. There is a gap in the literature with regard to qualitative studies that examine the experiences of female partners of spouses with cancer during the transition to end-of-life care. The purpose of this qualitative study was to explore the meaning of being in transition to end-of-life care among female partners of spouses with cancer.
METHODS: An interpretive phenomenological approach based on Gadamer's (1960/1975) philosophy was used to gain a deeper understanding of the phenomenon of end-of-life transition. Eight female partners from two in-patient hospices and a community-based palliative care service were interviewed using a semistructured approach.
RESULTS: Three major themes and associated subthemes were identified that outlined female partners' experiences. One major theme, Meaning of Our Lives, included the subthemes Our Relationship, Significance of His Life, and Searching for Understanding. In another theme, Dying with Cancer, partners undertook the Burden of Caring, experienced an Uncertain Path and were Looking for Hope. In the last theme, Glimpses of the Future, participants Faced Tomorrow and confirmed their Capacity to Survive. SIGNIFICANCE OF
RESULTS: The results centered on three major concepts: meaning making, anticipatory mourning, and hope. Although meaning making has been identified as a fundamental way in which bereaved individuals cope with loss, results of this study suggested that female partners made meaning of their situations before their spouses' deaths. Participants also spontaneously described aspects of anticipatory mourning, thus, validating a concept that has been widely accepted despite limited research. Another finding was that participants shouldered the responsibility of adjusting spouses' hopes in order to help them to cope. Implications for practice and research are drawn from these findings.

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Year:  2009        PMID: 19939305     DOI: 10.1017/S1478951509990435

Source DB:  PubMed          Journal:  Palliat Support Care        ISSN: 1478-9515


  5 in total

1.  The family's experience of the child and/or teenager in palliative care: fluctuating between hope and hopelessness in a world changed by losses.

Authors:  Maira Deguer Misko; Maiara Rodrigues dos Santos; Carolliny Rossi de Faria Ichikawa; Regina Aparecida Garcia de Lima; Regina Szylit Bousso
Journal:  Rev Lat Am Enfermagem       Date:  2015 May-Jun

2.  Association between advanced cancer patient-caregiver agreement regarding prognosis and hospice enrollment.

Authors:  Kelly M Trevino; Holly G Prigerson; Megan Johnson Shen; Daniel J Tancredi; Guibo Xing; Michael Hoerger; Ronald M Epstein; Paul R Duberstein
Journal:  Cancer       Date:  2019-05-30       Impact factor: 6.860

Review 3.  Transitions as experienced by persons in palliative care circumstances and their families - a qualitative meta-synthesis.

Authors:  André Fringer; Mareike Hechinger; Wilfried Schnepp
Journal:  BMC Palliat Care       Date:  2018-02-05       Impact factor: 3.234

4.  The experience of family caregivers of patients with cancer in an Asian country: A grounded theory approach.

Authors:  Martina Sinta Kristanti; Christantie Effendy; Adi Utarini; Myrra Vernooij-Dassen; Yvonne Engels
Journal:  Palliat Med       Date:  2019-03-27       Impact factor: 4.762

5.  "You begin to give more value in life, in minutes, in seconds": spiritual and existential experiences of family caregivers of patients with advanced cancer receiving end-of-life care in Brazil.

Authors:  Andrea Carolina Benites; Gary Rodin; Érika Arantes de Oliveira-Cardoso; Manoel Antônio Dos Santos
Journal:  Support Care Cancer       Date:  2021-11-24       Impact factor: 3.603

  5 in total

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