BACKGROUND: Increasing numbers of Americans die in nursing homes. Little is known about the roles and experiences of family members of persons who die in nursing homes. METHODS: The authors conducted 54 qualitative telephone interviews of close family or friends of individuals who had spent at least 48 hours in the last month of life in a nursing home. Respondents had earlier participated in a national survey that found 587 of 1578 decedents (37.2%) received end-of-life nursing home care. In qualitative interviews respondents described the last year of life, focusing on the nursing home experience. Interviews were analyzed by a multidisciplinary team to identify key themes of areas of concern. RESULTS: An important interview theme revealed families often felt the need to advocate for their dying relative because of low expectations or experiences with poor quality nursing home care. They noted staff members who did not fully inform them about what to expect in the dying process. Respondents reported burden and gratification in care they themselves provided, which sometimes entailed collaboration with staff. Interviews also identified ways hospice care impacted families, including helping to relieve family burden. CONCLUSIONS: End-of-life advocacy takes on increased urgency when those close to the dying resident have concerns about basic care and do not understand the dying course. Enhancing communication, preparing families at the end of life, and better understanding of hospice are likely to increase family trust in nursing home care, improve the care of dying residents, and help reduce family burden.
BACKGROUND: Increasing numbers of Americans die in nursing homes. Little is known about the roles and experiences of family members of persons who die in nursing homes. METHODS: The authors conducted 54 qualitative telephone interviews of close family or friends of individuals who had spent at least 48 hours in the last month of life in a nursing home. Respondents had earlier participated in a national survey that found 587 of 1578 decedents (37.2%) received end-of-life nursing home care. In qualitative interviews respondents described the last year of life, focusing on the nursing home experience. Interviews were analyzed by a multidisciplinary team to identify key themes of areas of concern. RESULTS: An important interview theme revealed families often felt the need to advocate for their dying relative because of low expectations or experiences with poor quality nursing home care. They noted staff members who did not fully inform them about what to expect in the dying process. Respondents reported burden and gratification in care they themselves provided, which sometimes entailed collaboration with staff. Interviews also identified ways hospice care impacted families, including helping to relieve family burden. CONCLUSIONS: End-of-life advocacy takes on increased urgency when those close to the dying resident have concerns about basic care and do not understand the dying course. Enhancing communication, preparing families at the end of life, and better understanding of hospice are likely to increase family trust in nursing home care, improve the care of dying residents, and help reduce family burden.
Authors: Jane L Givens; Ruth Palan Lopez; Kathleen M Mazor; Susan L Mitchell Journal: Alzheimer Dis Assoc Disord Date: 2012 Jul-Sep Impact factor: 2.703
Authors: Lena K Makaroun; Joan M Teno; Vicki A Freedman; Judith D Kasper; Pedro Gozalo; Vincent Mor Journal: J Am Geriatr Soc Date: 2018-07-04 Impact factor: 5.562
Authors: L Ashley Gage; Karla Washington; Debra Parker Oliver; Robin Kruse; Alexandra Lewis; George Demiris Journal: Am J Hosp Palliat Care Date: 2014-11-23 Impact factor: 2.500
Authors: Ruth Palan Lopez; Kathleen M Mazor; Susan L Mitchell; Jane L Givens Journal: Am J Alzheimers Dis Other Demen Date: 2013-10-01 Impact factor: 2.035
Authors: Nan Tracy Zheng; Dana B Mukamel; Bruce Friedman; Thomas V Caprio; Helena Temkin-Greener Journal: J Am Med Dir Assoc Date: 2014-10-07 Impact factor: 4.669