Richards Claire A, Starks Helene, O'Connor M Rebecca, Bourget Erica, Hays Ross M, Doorenbos Ardith Z
1 Health Services Research and Development, Veterans Affairs Puget Sound Health Care System, Seattle, WA, USA.
2 Department of Health Services, School of Public Health, University of Washington, Seattle, WA, USA.
Am J Hosp Palliat Care. 2018 Apr;35(4):669-676. doi: 10.1177/1049909117734843. Epub 2017 Oct 8.
Most children die in neonatal and pediatric intensive care units after decisions are made to withhold or withdraw life-sustaining treatments. These decisions can be challenging when there are different views about the child's best interest and when there is a lack of clarity about how best to also consider the interests of the family.
To understand how neonatal and pediatric critical care physicians balance and integrate the interests of the child and family in decisions about life-sustaining treatments.
Semistructured interviews were conducted with 22 physicians from neonatal, pediatric, and cardiothoracic intensive care units in a single quaternary care pediatric hospital. Transcribed interviews were analyzed using content and thematic analysis.
We identified 3 main themes: (1) beliefs about child and family interests; (2) disagreement about the child's best interest; and (3) decision-making strategies, including limiting options, being directive, staying neutral, and allowing parents to come to their own conclusions. Physicians described challenges to implementing shared decision-making including unequal power and authority, clinical uncertainty, and complexity of balancing child and family interests. They acknowledged determining the level of engagement in shared decision-making with parents (vs routine engagement) based on their perceptions of the best interests of the child and parent.
Due to power imbalances, families' values and preferences may not be integrated in decisions or families may be excluded from discussions about goals of care. We suggest that a systematic approach to identify parental preferences and needs for decisional roles and information may reduce variability in parental involvement.
大多数儿童在做出停止或撤销维持生命治疗的决定后,死于新生儿和儿科重症监护病房。当对于儿童的最大利益存在不同观点,以及对于如何最好地兼顾家庭利益缺乏明确认识时,这些决定可能具有挑战性。
了解新生儿和儿科重症监护医生在关于维持生命治疗的决策中如何平衡和整合儿童及家庭的利益。
在一家单一的四级儿科医院,对来自新生儿、儿科和心胸重症监护病房的22名医生进行了半结构化访谈。对转录的访谈内容进行了内容和主题分析。
我们确定了3个主要主题:(1)关于儿童和家庭利益的信念;(2)对儿童最大利益的分歧;(3)决策策略,包括限制选择、给予指导、保持中立以及让父母自行得出结论。医生们描述了实施共同决策面临的挑战,包括权力和权威不平等、临床不确定性以及平衡儿童和家庭利益的复杂性。他们承认根据对儿童和父母最大利益的认知来确定与父母进行共同决策(相对于常规参与)的参与程度。
由于权力失衡,家庭的价值观和偏好可能无法纳入决策,或者家庭可能被排除在关于护理目标的讨论之外。我们建议,一种识别父母对决策角色和信息的偏好及需求的系统方法,可能会减少父母参与程度的差异。