Location of end-of-life care of children with cancer: A systematic review of parent experiences

被引:14
作者
Noyes, Michelle [1 ,2 ]
Herbert, Anthony [2 ,3 ,4 ]
Moloney, Susan [1 ]
Irving, Helen [4 ]
Bradford, Natalie [2 ,3 ,4 ,5 ]
机构
[1] Gold Coast Univ Hosp, Oncol Serv, Gold Coast, Qld, Australia
[2] Queensland Univ Technol, Sch Nursing, Fac Hlth, Brisbane, Qld, Australia
[3] Childrens Hlth Queensland Hosp & Hlth Serv, Oncol Serv Grp, Queensland Paediat Palliat Care Haematol & Onco, Brisbane, Qld, Australia
[4] Queensland Univ Technol, Canc & Palliat CareOutcome Ctr, Brisbane, Qld, Australia
[5] Childrens Hlth Queensland Hosp & Hlth Serv, Ctr Childrens Hlth Res, Brisbane, Qld, Australia
关键词
adolescent; child; decision making; neoplasms; parents; place of death; qualitative research; terminal care; PALLIATIVE CARE; BEREAVED PARENTS; DEATH; PERCEPTIONS; PLACE; HOME; DIE;
D O I
10.1002/pbc.29621
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective To synthesize existing qualitative research exploring the experiences of parents caring for children with cancer during the end-of-life phase, and the factors that influence parental decision-making when choosing the location of end-of-life care and death for their child. Results This review included 15 studies of 460 parents of 333 children and adolescents who died from progressive cancer. Where reported, the majority (58%) of children died at home or in a hospital (39%), with only a small fraction dying in a hospice. Factors impacting decision-making for the location of care included the quality of communication and the quality of care available. Themes related to choosing home for end-of-life care and death included honoring the child's wishes, the familiarity of home, and parents' desire to be their child's primary carer. Preference for the location of death in the hospital included trust in hospital staff, practical logistics, and the safety of the hospital environment.
引用
收藏
页数:12
相关论文
共 50 条
  • [1] [Anonymous], 2018, CRIT APPR SKILLS PRO
  • [2] Parents' responses to prognostic disclosure at diagnosis of a child with a high-risk brain tumor: Analysis of clinician-parent interactions and implications for clinical practice
    Bluebond-Langner, Myra
    Hall, Nicolas
    Vincent, Katherine
    Henderson, Ellen M.
    Russell, Jessica
    Beecham, Emma
    Bryan, Gemma
    Gains, Jennifer E.
    Gaze, Mark N.
    Slater, Olga
    Langner, Richard W.
    Hargrave, Darren
    [J]. PEDIATRIC BLOOD & CANCER, 2021, 68 (03)
  • [3] Preferred place of death for children and young people with life-limiting and life-threatening conditions: A systematic review of the literature and recommendations for future inquiry and policy
    Bluebond-Langner, Myra
    Beecham, Emma
    Candy, Bridget
    Langner, Richard
    Jones, Louise
    [J]. PALLIATIVE MEDICINE, 2013, 27 (08) : 705 - 713
  • [4] Family meetings in paediatric palliative care: an integrative review
    Bradford, Natalie
    Rolfe, Melanie
    Ekberg, Stuart
    Mitchell, Geoffrey
    Beane, Theresa
    Ferranti, Kahli
    Herbert, Anthony
    [J]. BMJ SUPPORTIVE & PALLIATIVE CARE, 2021, 11 (03) : 288 - 295
  • [5] Palliative Care Afterhours: A Review of a Phone Support Service
    Bradford, Natalie
    Irving, Helen
    Smith, Anthony C.
    Pedersen, Lee-Anne
    Herbert, Anthony
    [J]. JOURNAL OF PEDIATRIC ONCOLOGY NURSING, 2012, 29 (03) : 141 - 150
  • [6] Principles of a paediatric palliative care consultation can be achieved with home telemedicine
    Bradford, Natalie K.
    Armfield, Nigel R.
    Young, Jeanine
    Herbert, Anthony
    Mott, Christine
    Smith, Anthony C.
    [J]. JOURNAL OF TELEMEDICINE AND TELECARE, 2014, 20 (07) : 360 - 364
  • [7] Paediatric palliative care by video consultation at home: a cost minimisation analysis
    Bradford, Natalie K.
    Armfield, Nigel R.
    Young, Jeanine
    Smith, Anthony C.
    [J]. BMC HEALTH SERVICES RESEARCH, 2014, 14
  • [8] Barriers in care for children with life-threatening conditions: a qualitative interview study in the Netherlands
    Brouwer, Marije
    Maeckelberghe, Els L. M.
    van der Heide, Agnes
    Hein, Irma
    Verhagen, Eduard
    [J]. BMJ OPEN, 2020, 10 (06): : e035863
  • [9] Pediatric Brain Tumors: Narrating Suffering and End-of-Life Decisionmaking
    Brouwer, Marije
    Maeckelberghe, Els
    Ten Brincke, Henk-Jan
    Meulenbeek-Ten Brincke, Marloes
    Verhagen, Eduard
    [J]. CAMBRIDGE QUARTERLY OF HEALTHCARE ETHICS, 2020, 29 (03) : 338 - 345
  • [10] Childhood Cancer Statistics, 2021, CANC NET