Literature DB >> 24917616

Parents who wish no further treatment for their child.

Mirjam A de Vos1, Antje A Seeber2, Sjef K M Gevers3, Albert P Bos4, Ferry Gevers5, Dick L Willems1.   

Abstract

BACKGROUND: In the ethical and clinical literature, cases of parents who want treatment for their child to be withdrawn against the views of the medical team have not received much attention. Yet resolution of such conflicts demands much effort of both the medical team and parents.
OBJECTIVE: To discuss who can best protect a child's interests, which often becomes a central issue, putting considerable pressure on mutual trust and partnership.
METHODS: We describe the case of a 3-year-old boy with acquired brain damage due to autoimmune-mediated encephalitis whose parents wanted to stop treatment. By comparing this case with relevant literature, we systematically explored the pros and cons of sharing end-of-life decisions with parents in cases where treatment is considered futile by parents and not (yet) by physicians.
CONCLUSIONS: Sharing end-of-life decisions with parents is a more important duty for physicians than protecting parents from guilt or doubt. Moreover, a request from parents on behalf of their child to discontinue treatment is, and should be, hard to over-rule in cases with significant prognostic uncertainty and/or in cases with divergent opinions within the medical team. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.

Entities:  

Keywords:  Allowing Minors to Die; End of Life Care; Family; Minors/Parental Consent; Right to Refuse Treatment

Mesh:

Year:  2014        PMID: 24917616     DOI: 10.1136/medethics-2013-101395

Source DB:  PubMed          Journal:  J Med Ethics        ISSN: 0306-6800            Impact factor:   2.903


  7 in total

1.  When and Why Do Neonatal and Pediatric Critical Care Physicians Consult Palliative Care?

Authors:  Claire A Richards; Helene Starks; M Rebecca O'Connor; Erica Bourget; Taryn Lindhorst; Ross Hays; Ardith Z Doorenbos
Journal:  Am J Hosp Palliat Care       Date:  2017-11-27       Impact factor: 2.500

2.  End-of-life care in the Pediatric Intensive Care Units: Challenges and ethical principles.

Authors:  Brenda M Morrow
Journal:  Indian J Crit Care Med       Date:  2015-03

3.  "It scares me to know that we might not have been there!": a qualitative study into the experiences of parents of seriously ill children participating in ethical case discussions.

Authors:  Reidun Førde; Trude Linja
Journal:  BMC Med Ethics       Date:  2015-06-06       Impact factor: 2.652

4.  Conceptualization of Idle (Laghw) and its relation to medical futility.

Authors:  Mohsen Rezaei Aderyani; Mohsen Javadi; Saeid Nazari Tavakkoli; Mehrzad Kiani; Mahmood Abbasi
Journal:  J Med Ethics Hist Med       Date:  2016-04-01

5.  Harm is all you need? Best interests and disputes about parental decision-making.

Authors:  Giles Birchley
Journal:  J Med Ethics       Date:  2015-09-23       Impact factor: 2.903

6.  Physicians Perceptions of Shared Decision-Making in Neonatal and Pediatric Critical Care.

Authors:  Claire A Richards; Helene Starks; M Rebecca O'Connor; Erica Bourget; Ross M Hays; Ardith Z Doorenbos
Journal:  Am J Hosp Palliat Care       Date:  2017-10-08       Impact factor: 2.090

7.  How doctors actually (do not) involve families in decisions to continue or discontinue life-sustaining treatment in neonatal, pediatric, and adult intensive care: A qualitative study.

Authors:  A Aranka Akkermans; J M W J Joyce Lamerichs; M J Marcus Schultz; T G V Thomas Cherpanath; J B M Job van Woensel; M Marc van Heerde; A H L C Anton van Kaam; M D Moniek van de Loo; A M Anne Stiggelbout; E M A Ellen Smets; M A Mirjam de Vos
Journal:  Palliat Med       Date:  2021-06-28       Impact factor: 4.762

  7 in total

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