Literature DB >> 27635764

Caregivers burden in palliative care patients: a problem to tackle.

Verónica Inés Veloso1, Vilma Adriana Tripodoro.   

Abstract

PURPOSE OF REVIEW: To revise the family caregiver's burden concept and to understand the implications for the patient, family and healthcare system. We analyzed recent literature in three main areas: the role of family caregiver at the end of life, the family caregiver's burden and the involvement of social care networks. RECENT
FINDINGS: The family caregiver often accepts the caring as a natural action, presumably imposed by the society. A recent review described seven main roles of care which, according to family system and society, consist of different tasks and activities. To assume this role is not stress free. It is likely to develop a 'burden' by the assumed task.
SUMMARY: Family members who are close to the patient may play the role of caregiver, well-being enhancer, diversity of tasks fulfiller, minimizer and managing suffering, palliative care facilitator and responsible for the continuity of care, apprentice and participant of health teams. The family caregiver often gives priority to the problems of his dependent family member, becoming almost 'invisible' to the health system. It should also be consider the relevance of this issue into future bereavement process. Considering all these aspects, the family caregiver is often considered by the healthcare teams as 'overall tasks' performers'.

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Mesh:

Year:  2016        PMID: 27635764     DOI: 10.1097/SPC.0000000000000239

Source DB:  PubMed          Journal:  Curr Opin Support Palliat Care        ISSN: 1751-4258            Impact factor:   2.302


  6 in total

1.  "Never at ease" - family carers within integrated palliative care: a multinational, mixed method study.

Authors:  Gülay Ateş; Anne Frederieke Ebenau; Csilla Busa; Ágnes Csikos; Jeroen Hasselaar; Birgit Jaspers; Johan Menten; Sheila Payne; Karen Van Beek; Sandra Varey; Marieke Groot; Lukas Radbruch
Journal:  BMC Palliat Care       Date:  2018-03-01       Impact factor: 3.234

2.  Caregiver burden among informal caregivers in the largest specialized palliative care unit in Malaysia: a cross sectional study.

Authors:  Zati Sabrina Ahmad Zubaidi; Farnaza Ariffin; Cindy Teoh Cy Oun; Diana Katiman
Journal:  BMC Palliat Care       Date:  2020-12-08       Impact factor: 3.234

3.  Burden of Care and Perceived Psycho-Social Outcomes among Family Caregivers of Patients Living with Cancer.

Authors:  Chiemerigo Anne Onyeneho; Rose Ekama Ilesanmi
Journal:  Asia Pac J Oncol Nurs       Date:  2021-02-04

4.  What does it mean to be the main caregiver to a terminally ill family member in Lithuania?: A qualitative study.

Authors:  Jolanta Kuznecovienė; Rūta Butkevičienė; W David Harrison; Eimantas Peičius; Gvidas Urbonas; Kristina Astromskė
Journal:  PLoS One       Date:  2022-05-12       Impact factor: 3.752

5.  Palliative care and its own identity, through an autoethnography: do you recognize these patterns?

Authors:  Isabel Galriça Neto
Journal:  Palliat Care Soc Pract       Date:  2022-09-14

6.  Perceptions, knowledge and attitudes towards the concept and approach of palliative care amongst caregivers: a cross-sectional survey in Karachi, Pakistan.

Authors:  Sameena Shah; Faizan Qaisar; Iqbal Azam; Khairunnisa Mansoor
Journal:  BMC Palliat Care       Date:  2020-11-26       Impact factor: 3.234

  6 in total

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