Parents and end-of-life decision-making for their child: roles and responsibilities

被引:22
作者
Sullivan, Jane [1 ,2 ]
Gillam, Lynn [1 ,2 ]
Monagle, Paul [3 ,4 ,5 ]
机构
[1] Royal Childrens Hosp, Childrens Bioeth Ctr, Parkville, Vic 3052, Australia
[2] Univ Melbourne, Ctr Hlth & Soc, Melbourne, Vic 3010, Australia
[3] Royal Childrens Hosp, Melbourne, Vic, Australia
[4] Univ Melbourne, Dept Paediat, Melbourne, Vic, Australia
[5] Murdoch Childrens Res Inst, Crit Care & Neurosci Theme, Melbourne, Vic, Australia
关键词
BEREAVEMENT RESEARCH; SUPPORT DECISIONS; ISSUES; AUTONOMY;
D O I
10.1136/bmjspcare-2013-000558
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Background Whether parents want to be and should be the decision-maker for their child in end-of-life matters are contested clinical and ethical questions. Previous research outcomes are equivocal. Method A qualitative interview method was used to examine the views and experiences of 25 bereaved parents in end-of-life decision-making for their child. Data were analysed thematically. Results Three types of decision-making roles were identified: self-determined, guided (both involving active decision-making) and acquiescent (passive). The majority of parents had been active in the decision-making process for their child. They perceived themselves as the ultimate end-of-life decision-maker. This was perceived as part of their parental responsibility. A minority of parents did not consider that they had been an active, ultimate decision-maker. Generally, parents in the self-determined and guided groups reported no negative consequences from their decision-making involvement. Importantly, parents in the acquiescent group described their experience as difficult at the time and subsequently, although not all difficulties related directly to decision-making. Parents considered that in principle parents should be the end-of-life decision-maker for their child, but understood personal characteristics and preference could prevent some parents from taking this role. Conclusions This study unequivocally supports parents' desire to fulfil the end-of-life decision-making role. It provides a nuanced understanding of parents' roles and contributes evidence for the ethical position that parents should be the end-of-life decision-makers for their child, unless not in the child's best interests. On the whole, parents want this role and can manage its consequences. Indeed, not being the end-of-life decision-maker could be detrimental to parents' well-being.
引用
收藏
页码:240 / 248
页数:9
相关论文
共 34 条
  • [1] Armentrout D, 2009, CRIT CARE NURS CLIN, V21, P53
  • [2] Bandura A, 2008, ANN REV PSYC, V52, P1
  • [3] Tragic Choices: Autonomy and Emotional Responses to Medical Decisions
    Botti, Simona
    Orfali, Kristina
    Iyengar, Sheena S.
    [J]. JOURNAL OF CONSUMER RESEARCH, 2009, 36 (03) : 337 - 352
  • [4] One size fits all? What counts as quality practice in (reflexive) thematic analysis?
    Braun, Virginia
    Clarke, Victoria
    [J]. QUALITATIVE RESEARCH IN PSYCHOLOGY, 2021, 18 (03) : 328 - 352
  • [5] Brinchmann BS, 2005, NEWBORN INFANT NURS, V5, P77, DOI 10.1053/j.nainr.2005.03.005
  • [6] Qualitative bereavement research: incongruity between the perspectives of participants and research ethics boards
    Buckle, Jennifer L.
    Dwyer, Sonya Corbin
    Jackson, Marlene
    [J]. INTERNATIONAL JOURNAL OF SOCIAL RESEARCH METHODOLOGY, 2010, 13 (02) : 111 - 125
  • [7] Perceived role in end-of-life decision making in the NICU affects long-term parental grief response
    Caeymaex, Laurence
    Jousselme, Catherine
    Vasilescu, Caroline
    Danan, Claude
    Falissard, Bruno
    Bourrat, Marie-Michele
    Gare, Micheline
    Speranza, Mario
    [J]. ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION, 2013, 98 (01): : F26 - F31
  • [8] Living with a Crucial Decision: A Qualitative Study of Parental Narratives Three Years after the Loss of Their Newborn in the NICU
    Caeymaex, Laurence
    Speranza, Mario
    Vasilescu, Caroline
    Danan, Claude
    Bourrat, Marie-Michele
    Garel, Micheline
    Jousselme, Catherine
    [J]. PLOS ONE, 2011, 6 (12):
  • [9] Parental involvement in treatment decisions regarding their critically ill child: A comparative study of France and Quebec
    Carnevale, Franco A.
    Canoui, Pierre
    Cremer, Robin
    Farrell, Catherine
    Doussau, Amelie
    Seguin, Marie-Josee
    Hubert, Philippe
    Leclerc, Francis
    Lacroix, Jacques
    [J]. PEDIATRIC CRITICAL CARE MEDICINE, 2007, 8 (04) : 337 - 342
  • [10] Carnevale Franco A, 2006, J Child Health Care, V10, P69