IN THIS ARTICLE

Citations

1. Heyland DK, et al. (2006). What matters most in end-of-life care: Perceptions of seriously ill patients and their family members. Canadian Medical Association Journal, 174(5): 1–9.

2. Teno JM, et al. (2004). Family perspectives on end-of-life care at the last place of care. JAMA, 291(1): 88–93.

Other Works Consulted

• Arnold R (2012). Care of dying patients and their families. In L Goldman, A Shafer, eds., Goldman’s Cecil Medicine, 24th ed., pp. 9–15. Philadelphia: Saunders.

• Byock I (1997). Dying Well. New York: Riverhead Books.

• Byock I (2004). Four Things That Matter Most: A Book About Living. New York: Free Press.

• Collins JJ (2006). End-of-life care for pediatric patients. In FD Burg et al., eds., Current Pediatric Therapy, 18th ed., pp. 242–245. Philadelphia: Saunders Elsevier.

• Federal Trade Commission (accessed April 2010). Funerals: Consumer Rights Under the Funeral Rule. Available online: http://www.ftc.gov/bcp/edu/microsites/funerals.

• Kliegman RM (2007). Grief and bereavement. In RM Kliegman et al., eds., Nelson Textbook of Pediatrics, 18th ed., pp. 206–208. Philadelphia: Saunders Elsevier.

• Lampert R, et al. (2010). HRS Expert consensus statement on the management of cardiovascular implantable electronic devices (CIEDs) in patients nearing end of life or requesting withdrawal of therapy. Heart Rhythm, 7(7): 1088–1026. Available online: http://www.hrsonline.org/Policy/ClinicalGuidelines/upload/ceids_mgmt_eol.pdf.

• Liben S (2007). The care of children with life-limiting illness. In RM Kliegman et al., eds., Nelson Textbook of Pediatrics, 18th ed., pp. 200–206. Philadelphia: Saunders Elsevier.