Literature DB >> 20576673

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

L Funk1, Ki Stajduhar, C Toye, S Aoun, Ge Grande, Cj Todd.   

Abstract

Family caregivers are crucial for supporting home death. We reviewed published qualitative research on home-based family caregiving at end of life (1998-2008), synthesizing key findings and identifying gaps where additional research is needed. Multiple databases were searched and abstracts reviewed for a focus on family caregiving and palliative care; full articles were reviewed to extract data for this review. In total, 105 articles were included. Findings are presented in the following areas: the caregiving experience and contextual features; supporting family caregivers at end of life; caregiving roles and decision-making; and rewards, meaning and coping. We noted a lack of definitional clarity; a reliance on interview methods and descriptive, thematic analyses, and a relative lack of diversity of patient conditions. Research needs are identified in several areas, including the bereavement experience, caregiver ambivalence, access to services, caregiver meaning-making, and relational and contextual influences on family caregiving at end of life.

Entities:  

Mesh:

Year:  2010        PMID: 20576673     DOI: 10.1177/0269216310371411

Source DB:  PubMed          Journal:  Palliat Med        ISSN: 0269-2163            Impact factor:   4.762


  55 in total

1.  Experience of meaning in life in bereaved informal caregivers of palliative care patients.

Authors:  Monika Brandstätter; Monika Kögler; Urs Baumann; Veronika Fensterer; Helmut Küchenhoff; Gian Domenico Borasio; Martin Johannes Fegg
Journal:  Support Care Cancer       Date:  2014-01-03       Impact factor: 3.603

2.  Research priorities in geriatric palliative care: informal caregiving.

Authors:  Richard Schulz
Journal:  J Palliat Med       Date:  2013-07-24       Impact factor: 2.947

3.  Caregivers needing care: the unmet needs of the family caregivers of end-of-life cancer patients.

Authors:  Maryam Hashemi; Alireza Irajpour; Fariba Taleghani
Journal:  Support Care Cancer       Date:  2017-09-27       Impact factor: 3.603

4.  Caring at home until death: enabled determination.

Authors:  Carole A Robinson; Joan L Bottorff; Erin McFee; Laura J Bissell; Gillian Fyles
Journal:  Support Care Cancer       Date:  2016-12-06       Impact factor: 3.603

5.  Role recognition and changes to self-identity in family caregivers of people with advanced cancer: a qualitative study.

Authors:  Anna Ugalde; Meinir Krishnasamy; Penelope Schofield
Journal:  Support Care Cancer       Date:  2011-05-25       Impact factor: 3.603

6.  Family as the primary caregiver: palliative care in the Golan Heights.

Authors:  Elon Richman; Amit Ringel; Jonah Susser Kreniske; Wajdi Safadi
Journal:  BMJ Case Rep       Date:  2015-04-09

7.  Anxiety among informal hospice caregivers: an exploratory study.

Authors:  Karla T Washington; George Demiris; Kenneth C Pike; Robin L Kruse; Debra Parker Oliver
Journal:  Palliat Support Care       Date:  2014-02-13

8.  Does Caregiving Strain Increase as Patients With and Without Dementia Approach the End of Life?

Authors:  Judith B Vick; Katherine A Ornstein; Sarah L Szanton; Sydney M Dy; Jennifer L Wolff
Journal:  J Pain Symptom Manage       Date:  2018-11-17       Impact factor: 3.612

9.  An overview and evaluation of the oncology family caregiver project: improving quality of life and quality of care for oncology family caregivers.

Authors:  Betty Ferrell; Jo Hanson; Marcia Grant
Journal:  Psychooncology       Date:  2012-10-14       Impact factor: 3.894

10.  Activities of daily living in Mexican American caregivers: the key to continuing informal care.

Authors:  Bronwynne C Evans; Michael J Belyea; David W Coon; Ebere Ume
Journal:  J Fam Nurs       Date:  2012-06-26       Impact factor: 3.818

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