The Parents' Ability to Attend to the "Voice of Their Child" With Incurable Cancer During the Palliative Phase

被引:30
|
作者
Kars, Marijke C. [1 ]
Grypdonck, Mieke H. F. [2 ]
de Bock, Leonie C. [1 ]
van Delden, Johannes J. M. [1 ]
机构
[1] Univ Med Ctr Utrecht, Dept Med Eth, NL-3508 GA Utrecht, Netherlands
[2] Univ Ghent, Dept Nursing Sci, B-9000 Ghent, Belgium
关键词
child participation; decision-making; parenting; pediatric oncology; pediatric palliative care; LIFE DECISION-MAKING; OF-LIFE; PEDIATRIC ONCOLOGY; CARE; COMMUNICATION;
D O I
10.1037/hea0000166
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Objective: In pediatric oncology, parents want, and are expected, to act and decide in the best interest of their child. A recent qualitative study (PRESENCE study) indicated that parents had difficulty in doing so. The aim of this subanalysis was to describe and offer an explanation for the parents' actions in expressing and handling of "the voice of the child." Method: A multicenter, qualitative research study comprising 37 interviews conducted with 34 parents of 17 children with incurable cancer, cared for at home, during the palliative phase. A thematic analysis was conducted. Results: The "voice of the child" becomes manifest in the parents' expressions of the child's needs and perceptions. Parents who actively searched to understand their child's inner perspective used direct and indirect strategies. Parents preferred indirect strategies when their child avoided talking or when they considered the conversation as threatening for the child, or for themselves. Even if the parents show an intense involvement in the care and support of their child; they can still have difficulty acknowledging the child's perspective. An inability to take into account the child's perspective was largely due to the parents' own struggle to cope with loss. Conclusions: Whether or not the voice of children approaching the end-of-life is heard, often depends on their parents' ability to give them a voice. Professional caregivers have a difficult task in supporting parents in giving their child his or her voice, while at the same time preserving their, and their parents', ability to cope.
引用
收藏
页码:446 / 452
页数:7
相关论文
共 50 条
  • [31] Fatigue in informal caregivers of cancer patients during active treatment in the palliative phase
    Peters, M. E. W. J.
    Goedendorp, M. M.
    Verhagen, C. A. H.
    Bleijenberg, G.
    Van der Graaf, W. T. A.
    EUROPEAN JOURNAL OF CANCER, 2013, 49 : S372 - S372
  • [32] Nature of Discussions About Systemic Therapy Discontinuation or Hospice among Patients, Families, and Palliative Care Clinicians during Care for Incurable Cancer: A Qualitative Study
    Traeger, Lara
    Rapoport, Chelsea
    Wright, Emily
    El-Jawahri, Areej
    Greer, Joseph A.
    Park, Elyse R.
    Jackson, Vicki A.
    Temel, Jennifer S.
    JOURNAL OF PALLIATIVE MEDICINE, 2020, 23 (04) : 542 - 547
  • [33] Decision Making by Parents of Children With Incurable Cancer Who Opt for Enrollment on a Phase I Trial Compared With Choosing a Do Not Resuscitate/Terminal Care Option
    Maurer, Scott H.
    Hinds, Pamela S.
    Spunt, Sheri L.
    Furman, Wayne L.
    Kane, Javier R.
    Baker, Justin N.
    JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (20) : 3292 - 3298
  • [34] Complementary and alternative medicine use in pediatric cancer reported during palliative phase of disease
    Deborah Tomlinson
    Tanya Hesser
    Marie-Chantal Ethier
    Lillian Sung
    Supportive Care in Cancer, 2011, 19 : 1857 - 1863
  • [35] Including the Oncologist in Palliative Oncology: A Response to Nature of Discussions about Systemic Therapy Discontinuation or Hospice among Patients, Families, and Palliative Care Clinicians during Care for Incurable Cancer: A Qualitative Study
    Newport, Kristina
    Sivendran, Shanthi
    JOURNAL OF PALLIATIVE MEDICINE, 2020, 23 (04) : 451 - 452
  • [36] Complementary and alternative medicine use in pediatric cancer reported during palliative phase of disease
    Tomlinson, Deborah
    Hesser, Tanya
    Ethier, Marie-Chantal
    Sung, Lillian
    SUPPORTIVE CARE IN CANCER, 2011, 19 (11) : 1857 - 1863
  • [37] Caring for a child with cancer during COVID-19 pandemic: an assessment of the parents' perception and stress level
    Nawi, Muhamad Aizat
    Lau, Sie Chong Doris
    Chin, Shi Tying
    Teh, Kok Hoi
    Ho, Lee Sue Betty
    Alias, Hamidah
    FRONTIERS IN PUBLIC HEALTH, 2024, 12
  • [38] Who is supporting the parents during their child's cancer treatment? A qualitative study through the lens of compassion
    Nielsen, Camilla Littau
    Clemensen, Jane
    Callesen, Michael Thude
    Jensen, Claus Sixtus
    Smith, Anthony C.
    Holm, Kristina Garne
    EUROPEAN JOURNAL OF ONCOLOGY NURSING, 2024, 70
  • [39] A prospective analysis on fatigue and experienced burden in informal caregivers of cancer patients during cancer treatment in the palliative phase
    Peters, Marlies E. W. J.
    Goedendorp, Martine M.
    Verhagen, Stans A. H. H. V. M.
    Smilde, Tineke J.
    Bleijenberg, Gijs
    van der Graaf, Winette T. A.
    ACTA ONCOLOGICA, 2015, 54 (04) : 500 - 506
  • [40] Quality of life of palliative care cancer patients during COVID-19 lockdown phase
    Das Adhikari, Shreya
    Pandit, Anuja
    Pangaria, Bhawesh
    Bhatnagar, Sushma
    PALLIATIVE MEDICINE IN PRACTICE, 2022, 16 (04): : 212 - 219