Abstract
BackgroundA sizeable cohort of Chinese migrants in high-income non-Asian countries is reaching old age and many will develop life-limiting illnesses. They may benefit from palliative care, which is integrated into universal health coverage in many of these countries, but the uptake of this care among migrant communities remains low. Cultural differences between the Chinese and the host community, and poor language skills may be barriers to access, yet understanding the reasons hindering uptake are obscure.AimsTo understand the cultural perspective of how first generation Chinese migrants and their families perceive the provision of palliative care, to identify what exists which may limit their access in high-income non-Asian countries.DesignA systematic review and three-stage thematic synthesis of qualitative studies. Citations and full texts were reviewed against predefined inclusion criteria. All included studies were appraised for quality.Data sourceMEDLINE, EMBASE, PsycINFO, CINAHL and PubMed were searched to July 2019.ResultsSeven qualitative studies were identified (from USA, UK, Canada and Australia). Across the studies analytical themes that impacted on the use of palliative care services were identified: (1) migrants’ intrinsic perceptions of cultural practices, (2) their expectations of and preparation for care at the end of life, (3) perspectives and influences of family and (4) knowledge and communication with palliative care providers in the host country. Key elements found that challenge access to palliative care services in the host countries were: Chinese culture is rooted in the core values of the family as opposed to the individual; migrants’ limited experience in their place of origin in accessing healthcare; and practical issues including a lack of language skills of their host country.ConclusionsPalliative care services do not always match the needs of Chinese migrants in non-Asian high-income countries. Engagement and education on multiethnic cultural awareness in both the host non-migrant and the migrant communities is needed.
Funder
Marie Curie: Care and support through terminal illness
Subject
Public Health, Environmental and Occupational Health,Health Policy
Reference44 articles.
1. Who definition of palliative care, 2019. Available: https://www.who.int/cancer/palliative/definition/en/
2. The difference between palliative care and end of life care: more than semantics;Krau;Nurs Clin North Am,2016
3. Putting palliative care on the global health agenda;Powell;Lancet Oncol,2015
4. Connor S , Sepulveda C . The global atlas of palliative care at the end of life, 2014.
5. Mapping pediatric palliative care development in the WHO-European region: children living in Low-to-Middle-Income countries are less likely to access it;Arias-Casais;J Pain Symptom Manage,2020
Cited by
20 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献