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1.
BMC Res Notes ; 8: 280, 2015 Jun 30.
Artigo em Inglês | MEDLINE | ID: mdl-26122085

RESUMO

BACKGROUND: Much of what is known about family caregiving at end-of-life in Canada has been studied within the context of various disease categories or across different care settings, rather than in relation to specific ethnic/cultural identities. Such homogeneity belies the impact of cultural and social factors on the experiences and outcomes of palliative and end-of-life (P/EOL) care. We know little about the end-of-life experiences of Vietnamese-Canadian families. Consequently, there is a lack of understanding around how to best meet the needs of Vietnamese care recipients, caregivers, and their families via the health service system, whose services of which we know they have limited access. RESULTS: To determine a set of service recommendations for health care settings (including the home) specific to caring for Vietnamese (P/EOL) care recipients, caregivers and their families, a qualitative instrumental case-study design was employed. The perspectives of 18 adult Vietnamese family caregivers (FCGs) were obtained. In addition, seven semi-structured key informant interviews were implemented with a range of personnel from community service providers to front-line health care professionals. The ways in which caregiving was perceived and expressed were reflected in three thematic findings: (1) Natural: identity and care work; (2) Intentional: whole person care; and (3) Intensive: standards, struggle, and the context of care. Ten main recommendations have been vetted with service provider leaders and confirmed as being appropriate for uptake. CONCLUSIONS: The ten service recommendations for health care settings (including the home), if implemented, would contribute to improved P/EOL services for the Vietnamese population. Further research involves the evaluation of these policy and programs.


Assuntos
Cuidadores/psicologia , Assistência à Saúde Culturalmente Competente/etnologia , Serviços de Saúde/normas , Cuidados Paliativos/psicologia , Guias de Prática Clínica como Assunto/normas , Assistência Terminal/psicologia , Adulto , Canadá/etnologia , Humanos , Pesquisa Qualitativa , Vietnã/etnologia
2.
Health Soc Care Community ; 23(1): 79-87, 2015 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-25328018

RESUMO

The objective of this study was to examine how Vietnamese family caregivers (FCGs) perceive, manage and experience end-of-life care-giving for seriously ill family members. Using an instrumental case study design, this longitudinal qualitative research employed the use of cultural brokers/language interpreters to help ensure that the research was conducted in a culturally-appropriate manner. Participants (n = 18) discussed their experiences of care-giving within the context of a traditional cultural framework, which was found to influence their motivations and approaches to care-giving, as well as their propensities towards the use of various supports and services. The study was carried out in southern Ontario, Canada, and participants were providing home-based care-giving in the community. Data were collected throughout 2010 and 2011. The ways in which care-giving was perceived and expressed are reflected in three themes: (i) Natural: identity and care work; (ii) Intentional: whole-person care; and (iii) Intensive: standards, struggle and the context of care. This research confirms the need for culturally-appropriate services and supports while illustrating that Vietnamese FCGs not only value, but are also likely to use healthcare and social services if they are language-accessible, built on trust and demonstrate respect for their values as individuals, regardless of culture.


Assuntos
Cuidadores/psicologia , Família/etnologia , Assistência Terminal , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Canadá , Cultura , Feminino , Humanos , Estudos Longitudinais , Masculino , Pessoa de Meia-Idade , Ontário/epidemiologia , Pesquisa Qualitativa , Apoio Social , Fatores Socioeconômicos , Vietnã/etnologia , Adulto Jovem
3.
Soc Sci Med ; 72(3): 338-46, 2011 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-21095052

RESUMO

Families are facing increased pressure to provide care to their terminally-ill or dying kin in the home. It is known that balancing care with other personal and social roles can adversely affect family caregivers' (FCGs) health, yet access to supportive services which can mitigate burden is often inadequate. Cultural factors are known to shape the experience of caregiving; however, most research to date tends to neglect the experiences of FCGs from different cultural groups. This understanding is necessary to ensure that supportive services are both meaningful and culturally-appropriate. Using qualitative methods, we undertook longitudinal research with a sample of Dutch Reformed FCGs (n = 5) to understand their experiences of caregiving and bereavement. The results of the study are suggestive of a cultural specificity with respect to caregiving that impacts both responsibilities and reactions to care. Three themes were salient to this group as a cultural entity: cultural attitudes towards care, religious beliefs and coping, and culturally-informed care-seeking behaviours. These three themes were seen to be a function of their religious and ethnic identities and were reinforced by ties to the communities in which they resided. Cultural identity provided a framework through which to understand and make sense of the experience, while group membership provided access to networks of informal support. This research contributes to the geographical literature on care/caregiving by providing insight into the social, cultural and religious context of informal family caregiving with a population who live in close geographic proximity. On a practical level, this case study indicates the importance of considering how these factors may operate in other settings in order to implement timely and appropriate interventions to better support FCGs who are caring for their terminally-ill loved-ones at home.


Assuntos
Cuidadores/psicologia , Características Culturais , Assistência Domiciliar/organização & administração , Cuidados Paliativos , Adaptação Psicológica , Atitude Frente a Saúde , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Ontário , Estudos de Casos Organizacionais , Aceitação pelo Paciente de Cuidados de Saúde , Pesquisa Qualitativa , Religião
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