Center of Innovation for Veteran-Centered and Value-Driven Care.
Nephrology Section, Hospital and Specialty Medicine Service, and.
Clin J Am Soc Nephrol. 2018 Jul 6;13(7):1022-1029. doi: 10.2215/CJN.14261217.
The highly specialized and technologically focused approach to care inherent to many health systems can adversely affect patients' emotional experiences of illness, while also obscuring these effects from the clinician's view. We describe what we learned from patients with advanced kidney disease about the emotional impact of illness and care.
DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: As part of an ongoing study on advance care planning, we conducted semistructured interviews at the VA Puget Sound Healthcare System in Seattle, Washington, with 27 patients with advanced kidney disease between April of 2014 and May of 2016. Of these, ten (37%) were receiving center hemodialysis, five (19%) were receiving peritoneal dialysis, and 12 (44%) had an eGFR≤20 ml/min per 1.73 m and had not started dialysis. Interviews were audiotaped, transcribed, and analyzed inductively using grounded theory methods.
We here describe three emergent themes related to patients' emotional experiences of care and illness: () emotional impact of interactions with individual providers: when providers seemed to lack insight into the patient's experience of illness and treatment, this could engender a sense of mistrust, abandonment, isolation, and/or alienation; () emotional impact of encounters with the health care system: just as they could be affected emotionally by interactions with individual providers, patients could also be affected by how care was organized, which could similarly lead to feelings of mistrust, abandonment, isolation, and/or alienation; and () emotional impact of meaning-making: patients struggled to make sense of their illness experience, worked to apportion blame, and were often quick to blame themselves and to assume that their illness could have been prevented.
Interactions with individual providers and with the wider health system coupled with patients' own struggles to make meaning of their illness can take a large emotional toll. A deeper appreciation of patients' emotional experiences may offer important opportunities to improve care.
许多医疗系统固有的高度专业化和技术导向的护理方法可能会对患者的疾病情感体验产生不利影响,同时也使临床医生无法看到这些影响。我们描述了从患有晚期肾病的患者那里了解到的关于疾病和护理的情感影响。
设计、地点、参与者和测量:作为一项关于预先护理计划的正在进行的研究的一部分,我们在华盛顿州西雅图的 VA Puget Sound Healthcare System 进行了半结构化访谈,采访了 2014 年 4 月至 2016 年 5 月期间的 27 名患有晚期肾病的患者。其中,有 10 名(37%)正在接受中心血液透析,5 名(19%)正在接受腹膜透析,12 名(44%)的 eGFR≤20 ml/min per 1.73 m 且尚未开始透析。访谈进行了录音、转录,并使用扎根理论方法进行了归纳分析。
我们在这里描述了与患者护理和疾病的情感体验相关的三个主题:(1)与个体提供者互动的情感影响:当提供者似乎缺乏对患者疾病和治疗体验的洞察力时,这可能会引起不信任、被遗弃、孤立和/或疏远感;(2)与医疗保健系统遭遇的情感影响:就像他们可能会受到与个体提供者互动的情感影响一样,患者也可能会受到护理组织方式的影响,这同样可能导致不信任、被遗弃、孤立和/或疏远感;(3)意义构建的情感影响:患者努力理解自己的疾病体验,试图归咎于他人,并且常常很快就自责并认为自己的疾病本来是可以预防的。
与个体提供者和更广泛的医疗系统的互动,加上患者自己对疾病体验的意义的理解,可能会对情感造成巨大的损失。更深入地了解患者的情感体验可能会提供改善护理的重要机会。