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患者和照护者对姑息治疗和临终癌症护理质量措施的优先排序。

Patient and Caregiver Prioritization of Palliative and End-of-Life Cancer Care Quality Measures.

机构信息

Center for the Study of Healthcare Innovation, Implementation and Policy (CSHIIP), VA Greater Los Angeles Health Care System, Los Angeles, CA, USA. Claire.O'

Center for Innovation to Implementation (Ci2i), VA Palo Alto Health Care System, Palo Alto, CA, USA.

出版信息

J Gen Intern Med. 2022 May;37(6):1429-1435. doi: 10.1007/s11606-021-07041-8. Epub 2021 Aug 17.

Abstract

BACKGROUND

Development and prioritization of quality measures typically relies on experts in clinical medicine, but patients and their caregivers may have different perspectives on quality measurement priorities.

OBJECTIVE

To inform priorities for health system implementation of palliative cancer and end-of-life care quality measures by eliciting perspectives of patients and caregivers.

DESIGN

Using modified RAND-UCLA Appropriateness Panel methods and materials tailored for knowledgeable lay participants, we convened a panel to rate cancer palliative care process quality measure concepts before and after a 1-day, in-person meeting.

PARTICIPANTS

Nine patients and caregivers with experience living with or caring for patients with cancer.

MAIN MEASURES

Panelists rated each concept on importance for providing patient- and family-centered care on a nine-point scale and each panelist nominated five highest priority measure concepts ("top 5").

KEY RESULTS

Cancer patient and caregiver panelists rated all measure concepts presented as highly important to patient- and family- centered care (median rating ≥ 7) in pre-panel (mean rating range, 6.9-8.8) and post-panel ratings (mean rating range, 7.2-8.9). Forced choice nominations of the "top 5" helped distinguish similarly rated measure concepts. Measure concepts nominated into the "top 5" by three or more panelists included two measure concepts of communication (goals of care discussions and discussion of prognosis), one measure concept on providing comprehensive assessments of patients, and three on symptoms including pain management plans, improvement in pain, and depression management plans. Patients and caregivers nominated one additional measure concept (pain screening) back into consideration, bringing the total number of measure concepts under consideration to 21.

CONCLUSIONS

Input from cancer patients and caregivers helped identify quality measurement priorities for health system implementation. Forced choice nominations were useful to discriminate concepts with the highest perceived importance. Our approach serves as a model for incorporating patient and caregiver priorities in quality measure development and implementation.

摘要

背景

质量措施的制定和优先排序通常依赖于临床医学专家,但患者及其护理人员可能对质量衡量重点有不同的看法。

目的

通过征求患者和护理人员的意见,为姑息治疗癌症和临终关怀质量措施在卫生系统中的实施确定优先事项。

设计

使用改良的 RAND-UCLA 适宜性小组方法和针对有知识的非专业参与者定制的材料,我们召集了一个小组,在为期一天的面对面会议前后对癌症姑息治疗过程质量测量概念进行评分。

参与者

9 名有癌症患者生活或护理经验的患者和护理人员。

主要措施

小组成员根据对提供以患者和家庭为中心的护理的重要性,对每个概念进行了 9 分制的评分,每位小组成员提名了五个最重要的措施概念(“前 5 名”)。

主要结果

癌症患者和护理人员小组成员对所有提出的措施概念都给予了高度评价,认为这些概念对以患者和家庭为中心的护理非常重要(预小组评分中位数为≥7;后小组评分中位数为 7.2-8.9)。强制性选择提名“前 5 名”有助于区分评分相似的措施概念。由 3 名或更多小组成员提名的“前 5 名”措施概念包括两个沟通措施概念(治疗目标讨论和预后讨论)、一个对患者进行全面评估的措施概念、以及三个关于症状的措施概念,包括疼痛管理计划、疼痛改善和抑郁管理计划。患者和护理人员提名了一个额外的措施概念(疼痛筛查),使其重新进入考虑范围,考虑的措施概念总数达到 21 个。

结论

来自癌症患者和护理人员的意见有助于确定卫生系统实施的质量衡量优先事项。强制性选择提名有助于区分具有最高感知重要性的概念。我们的方法为将患者和护理人员的优先事项纳入质量测量的制定和实施提供了一个模式。

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