Literature DB >> 24999578

The education of family caregivers as an ethical issue.

M Pennacchini1, D Tartaglini2.   

Abstract

Family caregiving represents the first and predominant source of care for 75% to 80% of people with chronic illness in industrialized countries. They have a fundamental role in assisting, providing care, and support to their relatives throughout all the history of the illness. Despite the significant value of informal caregiving, studies consistently report unmet needs among informal caregivers, particularly with regard to obtaining the information and education necessary to care for an older adult experiencing a chronic health condition. Health care professionals talk to patients and their relatives about their disease and about how to manage them daily, forgetting to consider the healthy component that still accompanies their disease though to differing degrees. In the twentieth century some philosophers highlighted that health is still very frequently a hidden asset, an asset that human beings forget not only to possess, but mostly to guard. This paper argues that the family can be an entity responsible not only for the treatment and care of a sick person, but also to building the health of this and the other members Family caregivers can build families capable of "building health" even when caring for a chronically ill. Therefore the education of family caregivers is an important ethical issue. Health care providers should be supportive of family caregivers and help them acquire knowledge and skills in order to maximize quality care. In addition, it is very important that family caregivers: 1. acquire the ability to direct the family's attitude to the enhancement of the health of a sick person, 2. lead the family and not just the sick person to have an adequate and proper life style in order to manage both his/her pathology and his/her health; 3. contribute to improve the quality of life both of the patient and of the family considered as a "unit of care"

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Year:  2014        PMID: 24999578     DOI: 10.7417/CT.2014.1723

Source DB:  PubMed          Journal:  Clin Ter        ISSN: 0009-9074


  3 in total

1.  Differences in COPD patient care by primary family caregivers: an age-based study.

Authors:  Peng-Ching Hsiao; Chi-Ming Chu; Pei-Yi Sung; Wann-Cherng Perng; Kwua-Yun Wang
Journal:  PLoS One       Date:  2014-09-24       Impact factor: 3.240

2.  Developing education materials for caregivers of culturally and linguistically diverse patients: Insights from a qualitative analysis of caregivers' needs, access and understanding of information.

Authors:  Jamie L Schaffler; Sarah Tremblay; Andréa M Laizner; Sylvie Lambert
Journal:  Health Expect       Date:  2019-02-14       Impact factor: 3.377

3.  Migrant Caregivers of Older People in Spain: Qualitative Insights into Relatives' Experiences.

Authors:  María José Morales-Gázquez; Epifanía Natalia Medina-Artiles; Remedios López-Liria; José Manuel Aguilar-Parra; Rubén Trigueros-Ramos; Jerónimo J González-Bernal; Patricia Rocamora-Pérez
Journal:  Int J Environ Res Public Health       Date:  2020-04-24       Impact factor: 3.390

  3 in total

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