Institute for Philosophy and Public Policy, George Mason University, Fairfax, USA.
Arthur Labatt Family School of Nursing, Western University, London, Canada.
BMC Med Ethics. 2021 Jul 28;22(1):105. doi: 10.1186/s12910-021-00674-8.
Severe brain injury is a leading cause of death and disability. Diagnosis and prognostication are difficult, and errors occur often. Novel neuroimaging methods can improve diagnostic and prognostic accuracy, especially in patients with prolonged disorders of consciousness (PDoC). Yet it is currently unknown how family caregivers understand this information, raising ethical concerns that disclosure of neuroimaging results could result in therapeutic misconception or false hope.
To examine these ethical concerns, we conducted semi-structured interviews with caregivers of patients with PDoC who were enrolled in a concurrent neuroimaging research program designed to detect covert consciousness following severe brain injury. Caregivers held surrogate decision-making status for a patient. Interviews were conducted at two time points for each caregiver. The first interview occurred before the disclosure of neuroimaging results. The second occurred after disclosure. Descriptive analysis was applied to the data of four interview topics: (1) expectations for neuroimaging; (2) reactions to evidence of preserved cognition; (3) reactions to null results; and (4) understanding of the results and study.
Twelve caregivers participated in the study; two caregivers shared surrogate decision-making status for one patient with PDoC. Twenty-one interviews were completed; one caregiver declined to participate in the post-disclosure interview. Three patients with PDoC associated with the study displayed evidence of covert consciousness. Overall, caregivers understood the neuroimaging research and results. Caregivers who received results of covert consciousness were generally pleased. However, there was some variation in expectations and reactions to these data and null results.
This study, for the first time, reveals caregiver expectations for and reactions to neuroimaging evidence of covert consciousness in patients with PDoC. Caregivers understood the neuroimaging research and results, casting doubt on speculative ethical concerns regarding therapeutic misconception and false hope. However, disclosure of neuroimaging result could be improved. Pre-disclosure consultations might assist professionals in shaping caregiver expectations. Standardization of disclosure might also improve comprehension of the results.
严重脑损伤是导致死亡和残疾的主要原因。诊断和预后都很困难,而且经常出错。新的神经影像学方法可以提高诊断和预后的准确性,特别是在长时间意识障碍(PDoC)的患者中。然而,目前尚不清楚家庭照顾者如何理解这些信息,这引发了一个伦理问题,即披露神经影像学结果可能导致治疗误解或虚假希望。
为了研究这些伦理问题,我们对参加一项旨在检测严重脑损伤后隐匿性意识的神经影像学研究项目的 PDoC 患者的照顾者进行了半结构化访谈。照顾者为患者担任代理决策人。每位照顾者在两个时间点接受访谈。第一次访谈在披露神经影像学结果之前进行,第二次访谈在披露之后进行。对四个访谈主题的数据进行描述性分析:(1)对神经影像学的期望;(2)对保留认知证据的反应;(3)对零结果的反应;以及(4)对结果和研究的理解。
共有 12 名照顾者参与了研究,其中 2 名照顾者共同为一名 PDoC 患者担任代理决策人。完成了 21 次访谈,有 1 名照顾者拒绝参加披露后访谈。研究中共有 3 名 PDoC 患者显示出隐匿性意识的证据。总体而言,照顾者理解神经影像学研究和结果。接受隐匿性意识神经影像学结果的照顾者通常感到高兴。然而,对这些数据和零结果的期望和反应存在一些差异。
这项研究首次揭示了照顾者对 PDoC 患者隐匿性意识神经影像学证据的期望和反应。照顾者理解神经影像学研究和结果,对治疗误解和虚假希望的推测性伦理问题提出了质疑。然而,神经影像学结果的披露可以得到改善。披露前的咨询可能有助于专业人员塑造照顾者的期望。结果的标准化也可能提高对结果的理解。