Qualities of Culturally and Religiously Sensitive Practice: A Cross-Sectional Study

2021 ◽  
pp. 082585972110507
Author(s):  
Panagiotis Pentaris ◽  
Panayiota Christodoulou

Background: Culture and religion influence lived experience and particularly dying and grieving. Research has largely focused on exploring culturally and religiously sensitive practices, but not necessarily in palliative and hospice care or across nations. Acquired knowledge from the more advanced end-of-life care systems (eg the UK) tends to be generalized to other contexts where its cultural appropriation is not tested. Aim: This study explored the different qualities, among hospice and palliative professionals in Cyprus, describing cultural competence, cultural humility, and religious literacy. Design: A cross-sectional study of 41 palliative and hospice professionals in Cyprus, with the use of a 5-point Likert style questionnaire ( a = 0.898). Setting: The study took place in Cyprus and participants were recruited from across palliative and hospice care organizations, including the only hospice in Cyprus, Cyprus Association of Cancer Patients and Friends (PASYKAF), and the Cyprus Anti-Cancer Society (CACS). Results: This study found that there are four main qualities that lead to effective culturally and religiously sensitive practice—informed decision-making, respect, adaptability, and nonjudgmental practice. Conclusions: Future education and training of professionals can consider these findings to appropriate approaches in practice that fit the Cypriot end-of-life care context more effectively.

2020 ◽  
pp. 003022282093692
Author(s):  
Radka Bužgová ◽  
Radka Kozáková ◽  
Michal Bar ◽  
Monika Škutová ◽  
Pavel Ressner ◽  
...  

The objective was to identify the attitudes of progressive neurological disease (PND) patients and their family members regarding end-of-life care, and their worries about dying. The sample included 327 participants. The Attitudes of Patients with PND to End-of-Life Care questionnaire was used to collect the data. Statistically significant differences in the assessment of attitudes towards end-of-life care between patients and family members were identified (p < 0.001). Family members more frequently favored patients being kept alive at any cost; patients more commonly wished to have their end of life under control. Respondents most frequently deferred to doctors when it came to decisions on treatment to keep patients alive. However, both patients and family members wanted patients to be able to decide on their treatment by leaving a written record of their previously stated wishes. The demands of patients and their families regarding end-of-life care should be documented in individual care plans.


2016 ◽  
Vol 30 (9) ◽  
pp. 843-853 ◽  
Author(s):  
Charis Wei Ling Ng ◽  
SK Cheong ◽  
A Govinda Raj ◽  
WSK Teo ◽  
IYO Leong

2020 ◽  
Vol 76 (11) ◽  
pp. 3014-3025
Author(s):  
Amy Waller ◽  
Sally Chan ◽  
Carmen W. H. Chan ◽  
Meyrick C. M. Chow ◽  
Miyoung Kim ◽  
...  

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