Department of Medicine, UCSF, San Francisco, California.
UCSF School of Medicine, San Francisco, California.
J Pain Symptom Manage. 2018 Feb;55(2):256-264. doi: 10.1016/j.jpainsymman.2017.09.018. Epub 2017 Sep 22.
Documenting patients' advance care planning (ACP) wishes is essential to providing value-aligned care, as is having this documentation readily accessible. Little is known about ACP documentation practices in the electronic health record.
The objective of this study was to describe ACP documentation practices and the accessibility of documented discussions in the electronic health record.
Participants were primary care patients at the San Francisco Veterans Affairs Medical Center, were ≥60 years old, and had ≥2 chronic/serious health conditions. In this cross-sectional study, we assessed the prevalence of ACP documentation, including any legal forms/orders and discussions in the prior five years. We also determined accessibility of discussions (i.e., accessible centralized posting vs. inaccessible free text in progress notes).
The mean age of 414 participants was 71 years (SD ± 8), 9% were women, 43% were nonwhite, and 51% had documented ACP including 149 (36%) with forms/orders and 138 (33%) with discussions. Seventy-four participants (50%) with forms/orders lacked accompanying explanatory documentation. Most (55%) discussions were not easily accessible, including 70% of those documenting changes in treatment preferences from prior forms/orders.
Half of chronically ill, older participants had documented ACP, including one-third with documented discussions. However, half of the patients with completed legal forms/orders had no accompanying documented explanatory discussions, and the majority of documented discussions were not easily accessible, even when wishes had changed. Ensuring that patients' preferences are documented and easily accessible is an important patient safety and quality improvement target to ensure patients' wishes are honored.
记录患者的预先医疗护理计划(ACP)意愿对于提供符合价值观的护理至关重要,并且要有便于获取这些记录的途径。电子健康记录中的 ACP 记录实践知之甚少。
本研究的目的是描述 ACP 记录实践以及在电子健康记录中记录讨论的可及性。
参与者是旧金山退伍军人事务医疗中心的初级保健患者,年龄≥60 岁,患有≥2 种慢性/严重健康状况。在这项横断面研究中,我们评估了 ACP 记录的流行率,包括在过去五年中任何合法形式/命令和讨论。我们还确定了讨论的可及性(即,可访问的集中发布与不可访问的进展记录中的自由文本)。
414 名参与者的平均年龄为 71 岁(标准差±8),9%为女性,43%为非白人,51%有记录的 ACP 包括 149 名(36%)有表格/订单和 138 名(33%)有讨论。74 名(50%)有表格/订单的参与者缺乏伴随的解释性记录。大多数(55%)讨论不易获取,包括 70%记录了治疗偏好变化的讨论,而这些变化来自之前的表格/订单。
一半的慢性病、老年患者有记录的 ACP,包括三分之一有记录的讨论。然而,一半完成了合法表格/订单的患者没有伴随的记录解释性讨论,并且大多数记录的讨论不易获取,即使愿望已经改变。确保患者的偏好得到记录和易于获取是一个重要的患者安全和质量改进目标,以确保患者的意愿得到尊重。