Literature DB >> 27657662

The experience of family caregivers caring for a terminal patient at home: A research review.

J Martín Martín1, M Olano-Lizarraga2, M Saracíbar-Razquin3.   

Abstract

INTRODUCTION: One of the key aspects of the care of terminal patients is care delivered in their own home. Increasingly, the process of dying is moving from hospitals to homes. Although this process is directly related to the support of the social health environment, the involvement of family caregivers is essential. Given the impact that caring for a terminally ill family member has on people's lives, it is necessary to comprehend their personal experience in a holistic way.
OBJECTIVE: To reveal the experience of family caregivers who are caring for a terminal patient in their home.
DESIGN: A qualitative systematic review of articles published from 2000 to 2015 was conducted between March and September of 2015. The following databases were consulted: CINAHL, PubMed, PsycINFO, Cochrane Library, SciELO and Dialnet. After applying the selection criteria, 12 relevant studies were identified. Subsequently, two of the reviewers jointly performed a qualitative content analysis of them.
RESULTS: The analysis permitted the caregivers' experiences to be grouped into five themes: 1) Learning the diagnosis: uncertainty about the future and the prospects of death; 2) Feeling the physical and emotional burden of care; 3) Experiencing a limited life; 4) Redefining the relationship with the person being cared for; and 5) Valuing the importance of the support of the environment.
CONCLUSIONS: This review shows that caring for a family member with advanced illness in the home has a great impact on the personal realm of the caregiver and in the relationship he or she maintains with the ill family member. Being involved in the process of dying translates into a prodigious physical and psychological effort, together with a substantial limitation on the normal development of their own life. Additionally, the caregiver must face and establish a new relationship with the family member, in accordance with the new ethos, without the help of a formal structure providing the necessary support. These results may help to focus attention on family caregiver needs and to develop the knowledge necessary to meet the current demands of end-of-life health care in the home. Copyright Â
© 2016 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  End of life care; Experience; Family caregiver; Home care; Nursing; Terminally ill

Mesh:

Year:  2016        PMID: 27657662     DOI: 10.1016/j.ijnurstu.2016.09.010

Source DB:  PubMed          Journal:  Int J Nurs Stud        ISSN: 0020-7489            Impact factor:   5.837


  11 in total

1.  Facilitators and barriers in using comics to support family caregivers of patients receiving palliative care at home: A qualitative study.

Authors:  Maaike M Haan; Jelle Lp van Gurp; Marjan Knippenberg; Gert Olthuis
Journal:  Palliat Med       Date:  2022-05-03       Impact factor: 5.713

2.  A drive for structure: A longitudinal qualitative study of the implementation of the Carer Support Needs Assessment Tool (CSNAT) intervention during hospital discharge at end of life.

Authors:  Alex Hall; Gail Ewing; Christine Rowland; Gunn Grande
Journal:  Palliat Med       Date:  2020-06-03       Impact factor: 4.762

3.  Haematology nurses' perspectives of their patients' places of care and death: A UK qualitative interview study.

Authors:  Dorothy McCaughan; Eve Roman; Alexandra G Smith; Anne C Garry; Miriam J Johnson; Russell D Patmore; Martin R Howard; Debra A Howell
Journal:  Eur J Oncol Nurs       Date:  2019-02-07       Impact factor: 2.398

4.  Perspectives of bereaved relatives of patients with haematological malignancies concerning preferred place of care and death: A qualitative study.

Authors:  Dorothy McCaughan; Eve Roman; Alexandra G Smith; Anne C Garry; Miriam J Johnson; Russell D Patmore; Martin R Howard; Debra A Howell
Journal:  Palliat Med       Date:  2019-01-30       Impact factor: 4.762

5.  [The first moments of the carer: The process of becoming a caregiver of a dependent elderly relative].

Authors:  Lourdes Moral-Fernández; Antonio Frías-Osuna; Sara Moreno-Cámara; Pedro A Palomino-Moral; Rafael Del-Pino-Casado
Journal:  Aten Primaria       Date:  2017-07-21       Impact factor: 1.137

6.  Understanding the Experience of Cancer Pain From the Perspective of Patients and Family Caregivers to Inform Design of an In-Home Smart Health System: Multimethod Approach.

Authors:  Virginia LeBaron; Rachel Bennett; Ridwan Alam; Leslie Blackhall; Kate Gordon; James Hayes; Nutta Homdee; Randy Jones; Yudel Martinez; Emmanuel Ogunjirin; Tanya Thomas; John Lach
Journal:  JMIR Form Res       Date:  2020-08-26

7.  Caregivers' Experience of End-of-Life Stage Elderly Patients: Longitudinal Qualitative Interview.

Authors:  Eliza Lai-Yi Wong; Janice Ying-Chui Lau; Patsy Yuen-Kwan Chau; Roger Yat-Nork Chung; Samuel Yeung-Shan Wong; Jean Woo; Eng-Kiong Yeoh
Journal:  Int J Environ Res Public Health       Date:  2022-02-13       Impact factor: 3.390

Review 8.  Psychological Aspects of Care in Cancer Patients in the Last Weeks/Days of Life.

Authors:  Sujin Ann-Yi; Eduardo Bruera
Journal:  Cancer Res Treat       Date:  2022-06-28       Impact factor: 5.036

9.  Caregivers of Patients with Hematological Malignancies within Home Care: A Phenomenological Study.

Authors:  Isabella Capodanno; Mirta Rocchi; Rossella Prandi; Cristina Pedroni; Enrica Tamagnini; Pierluigi Alfieri; Francesco Merli; Luca Ghirotto
Journal:  Int J Environ Res Public Health       Date:  2020-06-05       Impact factor: 3.390

10.  The start of caring for an elderly dependent family member: a qualitative metasynthesis.

Authors:  Lourdes Moral-Fernández; Antonio Frías-Osuna; Sara Moreno-Cámara; Pedro A Palomino-Moral; Rafael Del-Pino-Casado
Journal:  BMC Geriatr       Date:  2018-09-25       Impact factor: 3.921

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