Kreling, B., Selsky, C., Perret-Gentil, M., Huerta, E.E. and Mandelblatt, J.S. (2010) The Worst Thing about Hospice Is That They Talk about Death: Contrasting Hospice Decisions and Experience among Immigrant Central and South American Latinos with US-Born White, Non-Latino Cancer Caregivers. Palliative Medicine, 24, 427-434.
http://dx.doi.org/10.1177/0269216310366605

has been cited by the following article:

• TITLE: A Systematic Review of Cultural Preferences for Receiving Medical “Bad News” in the United States

  AUTHORS: Christine Larkin, H. Russell Searight

  KEYWORDS: Medical Ethics, Health Care Communication, Cross Cultural Health

  JOURNAL NAME: Health, Vol.6 No.16, September 12, 2014

  ABSTRACT: According to the dominant models of medical ethics in the United States and many Western countries, physician disclosure of information such as diagnosis, treatment options, and prognosis is considered an essential precondition for patient informed consent. While being consistent with the principle of patient autonomy stressed in many Western healthcare systems, full disclosure—particularly of life-threatening diagnoses and poor prognoses—is inconsistent with the cultural values of many ethnic communities within the United States. A systematic review of research examining cultural preferences for disclosure of medical “bad news” was conducted. Results suggested that cultural preferences are more heterogeneous than has often been portrayed. Particularly when communicating with patients and families from culturally and ethnically diverse backgrounds, health care professionals should ask about preferences for receiving medical information and making treatment decisions.