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1.
Am J Hosp Palliat Care ; 36(4): 282-289, 2019 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-30556405

RESUMO

This study was conducted to examine cultural appropriateness and readiness for the Blackfeet people in the United States talking about end of life. In the past, a taboo perception of Blackfeet traditional belief in end-of-life discussion was identified as a core barrier for hospice use. However, a recent anecdotal increase in hospice interest triggered the research team to investigate community-wide interest as well as traditional appropriateness of hospice introduction. The community-based participatory research approach was used to conduct the study. Using convenience sampling, we interviewed 10 tribally recognized Elders and surveyed 102 tribal members who were over 18 years old using a modified Duke End-of-Life Care Survey. Here, our report focused on the perception changes on end-of-life discussion. The elders' statements were divided into two, saying that an end-of-life discussion was not against tradition and that sickness and death would break the living spirit, thus no such discussion. Despite, the importance of a family gathering and the need for knowledge about end-of-life care were confirmed. The survey (response rate 100%; n = 92) showed that 90% of the respondents thought dying was a normal part of life and 76% felt comfortable talking about death. In conclusion, there was a shift in the Blackfeet Indians' attitude toward end-of-life discussion from reluctance to at ease. Recommendations specific to the Blackfeet-related entities are presented.


Assuntos
Atitude Frente a Morte/etnologia , Indígenas Norte-Americanos/psicologia , Assistência Terminal/psicologia , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Pesquisa Participativa Baseada na Comunidade , Competência Cultural , Feminino , Conhecimentos, Atitudes e Prática em Saúde/etnologia , Cuidados Paliativos na Terminalidade da Vida/psicologia , Humanos , Entrevistas como Assunto , Masculino , Pessoa de Meia-Idade , Percepção , Fatores Socioeconômicos , Tabu , Estados Unidos , Adulto Jovem
2.
Am J Hosp Palliat Care ; 34(6): 584-591, 2017 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-26984856

RESUMO

This study was conducted to highlight Native American (NA) perspectives on death taboo in order to examine the cultural appropriateness of hospice services for NA patients, if any. Searching literature that addressed taboo and death from historical, psychological, sociological, and anthropological aspects, a comparison of death perspectives was made between NAs and European Americans. A culturally sensitive transition from palliative care to hospice care was suggested for NA patients and their family.


Assuntos
Atitude Frente a Morte/etnologia , Cuidados Paliativos na Terminalidade da Vida/psicologia , Indígenas Norte-Americanos/psicologia , Cuidados Paliativos/psicologia , Tabu/psicologia , População Branca/psicologia , Adulto , Idoso , Idoso de 80 Anos ou mais , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , América do Norte
4.
Am J Hosp Palliat Care ; 31(5): 503-12, 2014 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-23779233

RESUMO

This study explored American Indians' end-of-life experiences in treatment decision making. Scarce knowledge about this population's perspective regarding end-of-life treatments has resulted in health care providers (HCPs) functioning at less than optimum levels. Using a community-based participatory research approach, open-ended interview data were collected and analyzed using a grounded theory method. Patient and family participants generally stated that the physicians made the treatment decisions for them, while HCPs believed that patients participated in informed autonomous treatment decision making. Both parties (HCPs and patients and families) were not aware of American Indian's psychological aspect that interfered with the exercise of the right of informed consent. This additional understanding would benefit them in order to result in ethically and legally sound practice of patient's autonomous treatment decision making.


Assuntos
Tomada de Decisões , Família/etnologia , Indígenas Norte-Americanos , Participação do Paciente/psicologia , Assistência Terminal/organização & administração , Adulto , Idoso , Idoso de 80 Anos ou mais , Pesquisa Participativa Baseada na Comunidade , Feminino , Humanos , Entrevistas como Assunto , Masculino , Pessoa de Meia-Idade , Relações Médico-Paciente , Religião
5.
J Fam Nurs ; 13(2): 201-25, 2007 May.
Artigo em Inglês | MEDLINE | ID: mdl-17452603

RESUMO

This exploratory study describes decision making at end of life among Japanese American families. Using qualitative methods including a one-time, semistructured interview, 16 Japanese American family participants described their experiences with the death of 22 family members. A grounded theory analysis led to the development of a model of a process that reflected the influence of age-cohort generational differences and health care providers' involvement. The model also included four dimensions of family understanding. The four dimensions were awareness of the seriousness of the family members' condition, decision making about life-sustaining treatment, readiness for impending death, and experience of the dying process. Each dimension reflected a continuum from low to high understanding. The results suggest that nurses and other health care providers can impact the level of understanding within each of the dimensions in culturally sensitive ways and contribute to improving the experience with end-of-life decision making for Japanese Americans.


Assuntos
Asiático/psicologia , Tomada de Decisões , Assistência Terminal/psicologia , Adulto , Diretivas Antecipadas , Idoso , Idoso de 80 Anos ou mais , Características Culturais , Enfermagem Familiar , Feminino , Humanos , Entrevistas como Assunto , Japão/etnologia , Masculino , Pessoa de Meia-Idade , Avaliação em Enfermagem , Estados Unidos
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