什么是儿童的最大利益?儿童肿瘤学环境中父母、儿童和医生的观点

M. D. de Vries, D. Bresters, G. Kaspers, Mirjam Houtlosser, J. Wit, D. P. Engberts, E. van Leeuwen
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引用次数: 12

摘要

背景:在儿科学中,“最佳利益”标准已成为决策的主流标准,尽管在实践中难以应用。价值观的不同会导致家庭和医生对什么是儿童利益的不同看法。我们的目标是深入了解儿童肿瘤环境中家长、儿童和医生的观点。方法:我们进行了一项定性多中心研究,采用深度半结构化访谈,包括21名8-18岁接受癌症治疗的儿童、26名家长和15名儿科肿瘤学家。结果:在治疗开始时,父母、儿童和医生对什么是符合儿童利益的观点是一致的:通过遵循治疗方案来生存。然而,在治疗过程中会发生转变。对家庭而言,构成最大利益的因素超出了医疗方面的考虑,还包括过正常生活的愿望、控制治疗的某些方面以及保持自己的身份(例如,通过宗教)。这些方面有时会与医学方面发生冲突,导致专业和家庭对什么是合适的行动方案有不同的看法。结论:医生在治疗过程中应明确讨论家长和家属的关切和意见,以认识个人观点,避免冲突。我们提出了一个“交际伦理”的模型,使这些问题成为讨论的主题。家庭在确定什么符合儿童的最大利益方面的作用,只有在它意味着对儿童造成(不可逆转的)伤害的重大医疗风险时,才应加以限制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
What Constitutes the Best Interest of a Child? Views of Parents, Children, and Physicians in a Pediatric Oncology Setting
Background: In pediatrics, the “best interest” standard has become the prevailing standard in decision making even though it proves difficult to apply in practice. Differences in values can lead to different views by families and physicians of what is in the interest of a child. Our aim was to gain insight into the views of parents, children, and physicians in a pediatric oncology setting. Methods: We conducted a qualitative multicenter study, using in-depth semistructured interviews, with 21 children aged 8–18 years undergoing cancer treatment, 26 parents, and 15 pediatric oncologists. Results: At the onset of treatment, parents, children, and physicians had the same views on what is in the interest of the child: survival by following the treatment protocol. In the course of treatment, however, a transition takes place. For families, what constitutes the best interests expands beyond medical considerations, to include the wish to lead a normal life, having control over certain aspects of treatment, and maintaining one's identity (e.g., through religion). These aspects sometimes collide with medical aspects, leading to different professional and familial views about what course of action is appropriate. Conclusions: In order to recognize personal views and avoid conflicts, physicians should explicitly discuss parent and family concerns and opinions in the course of treatment. We present a model of “communicative ethics” to make these issues a subject of discussion. The role of the family in determining what is in the best interest of the child should only be limited when it implies a substantial medical risk of (irreversible) harm to the child.
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