Department of Medicine, University of Washington, Seattle, Washington
Hospital and Specialty Medicine, Geriatrics and Extended Care and Seattle-Denver Health Services Research and Development Center for Innovation, Veterans Affairs Puget Sound Health Care System, Seattle, Washington.
J Am Soc Nephrol. 2020 Nov;31(11):2667-2677. doi: 10.1681/ASN.2020040473. Epub 2020 Aug 6.
Patients with advanced kidney disease are less likely than many patients with other types of serious illness to enroll in hospice. Little is known about real-world clinical decision-making related to hospice for members of this population.
We used a text search tool to conduct a thematic analysis of documentation pertaining to hospice in the electronic medical record system of the Department of Veterans Affairs, for a national sample of 1000 patients with advanced kidney disease between 2004 and 2014 who were followed until October 8, 2019.
Three dominant themes emerged from our qualitative analysis of the electronic medical records of 340 cohort members with notes containing hospice mentions: () hospice and usual care as antithetical care models: clinicians appeared to perceive a sharp demarcation between services that could be provided under hospice versus usual care and were often uncertain about hospice eligibility criteria. This could shape decision-making about hospice and dialysis and made it hard to individualize care; () hospice as a last resort: patients often were referred to hospice late in the course of illness and did not so much choose hospice as accept these services after all treatment options had been exhausted; and () care complexity: patients' complex care needs at the time of hospice referral could complicate transitions to hospice, stretch the limits of home hospice, and promote continued reliance on the acute care system.
Our findings underscore the need to improve transitions to hospice for patients with advanced kidney disease as they approach the end of life.
与其他许多患有严重疾病的患者相比,晚期肾病患者不太可能参加临终关怀。对于这一人群的临终关怀相关的实际临床决策知之甚少。
我们使用文本搜索工具,对 2004 年至 2014 年间随访至 2019 年 10 月 8 日的 1000 名晚期肾病患者的退伍军人事务部电子病历系统中的临终关怀文档进行主题分析,该研究纳入了一个全国性样本。
对 340 名队列成员的电子病历进行定性分析后出现了三个主要主题,这些成员的病历中包含临终关怀的记录:(1)临终关怀和常规护理是对立的护理模式:临床医生似乎认为可以在临终关怀下提供的服务和常规护理之间有明显的界限,并且经常对临终关怀的资格标准不确定。这可能会影响对临终关怀和透析的决策,并使个性化护理变得困难;(2)临终关怀是最后的手段:患者通常在疾病过程的晚期被转介到临终关怀,他们并不是选择临终关怀,而是在所有治疗方案都用尽后接受这些服务;(3)护理的复杂性:患者在临终关怀转介时的复杂护理需求可能会使向临终关怀的过渡复杂化,使家庭临终关怀的极限受到挑战,并促进对急性护理系统的持续依赖。
我们的研究结果强调了需要改善晚期肾病患者临终关怀的过渡,因为他们即将走到生命的尽头。