Nunez Eduardo R, Schenker Yael, Joel Ian D, Reynolds Charles F, Dew Mary Amanda, Arnold Robert M, Barnato Amber E
1University of Pittsburgh School of Medicine, Pittsburgh, PA. 2Section of Palliative Care and Medical Ethics, Division of General Internal Medicine, Department of Medicine, University of Pittsburgh and Palliative and Supportive Institute, University of Pittsburgh Medical Center, Pittsburgh, PA. 3Department of Medicine, University of California Los Angeles, Los Angeles, CA. 4Department of Psychiatry, University of Pittsburgh, Pittsburgh, PA. 5Section of Decision Sciences, Division of General Internal Medicine, Department of Medicine, University of Pittsburgh School of Medicine, Pittsburgh, PA.
Crit Care Med. 2015 Nov;43(11):2387-93. doi: 10.1097/CCM.0000000000001270.
Participating in a decision to limit life support for a loved one in the ICU is associated with adverse mental health consequences for surrogate decision makers. We sought to describe acutely bereaved surrogates' experiences surrounding this decision.
Qualitative analysis of interviews with surrogates approximately 4 weeks after a patient's death in one of six ICUs at four hospitals in Pittsburgh, PA.
Adults who participated in decisions about life support in the ICU.
Not applicable.
We collected participant demographics, previous advance care planning, and decision control preferences. We used qualitative content analysis of transcribed interviews to identify themes in surrogates' experiences. The 23 participants included the spouse (n = 7), child/stepchild (7), sibling (5), parent (3), or other relation (1) of the deceased patient. Their mean age was 55, 61% were women, all were whites, 74% had previous treatment preference discussions with the patient, and 43% of patients had written advance directives. Fifteen of 23 surrogates (65%) preferred an active decision-making role, 8 of 23 (35%) preferred to share responsibility with the physician, and no surrogates preferred a passive role. Surrogates report that key stressors in the ICU are the uncertainty and witnessed or empathic suffering. These factors contributed to surrogates' sense of helplessness in the ICU. Involvement in the decision to limit life support allowed surrogates to regain a sense of agency by making a decision consistent with the patient's wishes and values, counteracting surrogates' helplessness and ending the uncertainty and suffering.
In this all-white sample of surrogates with nonpassive decision control preferences from a single US region, participating in decision making allowed surrogates to regain control, counteract feelings of helplessness, and end their empathic suffering. Although previous research highlighted the distress caused by participation in a decision to limit life support, the act of decision making may, counterintuitively, help some surrogates cope with the experience.
在重症监护病房(ICU)参与决定限制所爱的人的生命支持,会给替代决策者带来不良的心理健康后果。我们试图描述刚经历丧亲之痛的替代决策者围绕这一决定的经历。
对宾夕法尼亚州匹兹堡市四家医院六个ICU之一的患者死亡约四周后对替代决策者进行的访谈进行定性分析。
参与ICU生命支持决策的成年人。
不适用。
我们收集了参与者的人口统计学信息、先前的预先护理计划以及决策控制偏好。我们对访谈转录本进行定性内容分析,以确定替代决策者经历中的主题。23名参与者包括已故患者的配偶(n = 7)、子女/继子女(7)、兄弟姐妹(5)、父母(3)或其他亲属(1)。他们的平均年龄为55岁,61%为女性,均为白人,74%曾与患者讨论过治疗偏好,43%的患者有书面预先指示。23名替代决策者中有15名(65%)倾向于积极的决策角色,23名中有8名(35%)倾向于与医生分担责任,没有替代决策者倾向于被动角色。替代决策者报告说,ICU中的关键压力源是不确定性以及目睹的痛苦或感同身受的痛苦。这些因素导致替代决策者在ICU中产生无助感。参与限制生命支持的决策使替代决策者能够通过做出符合患者意愿和价值观的决定来重新获得掌控感,抵消替代决策者的无助感,并结束不确定性和痛苦。
在这个来自美国单一地区、具有非被动决策控制偏好的全白人替代决策者样本中,参与决策使替代决策者能够重新获得控制权,抵消无助感,并结束他们的感同身受的痛苦。尽管先前的研究强调了参与限制生命支持决策所带来的痛苦,但决策行为可能与直觉相反,有助于一些替代决策者应对这一经历。