Department of Behavioral Science, College of Medicine, University of Kentucky, Lexington, Kentucky, USA; Center for Health Equity Transformation, University of Kentucky, Lexington, Kentucky, USA; Markey Cancer Center, University of Kentucky, Lexington, Kentucky, USA.
Markey Cancer Center, University of Kentucky, Lexington, Kentucky, USA; Department of Health, Behavior, and Society, College of Public Health, University of Kentucky, Lexington, Kentucky, USA.
J Pain Symptom Manage. 2024 Apr;67(4):337-345.e2. doi: 10.1016/j.jpainsymman.2024.01.013. Epub 2024 Jan 14.
Patient misperceptions are a strong barrier to early palliative care discussions and referrals during advanced lung cancer treatment.
We developed and tested the acceptability of a web-based patient-facing palliative care education and screening tool intended for use in a planned multilevel intervention (i.e., patient, clinician, system-level targets).
We elicited feedback from advanced lung cancer patients (n = 6), oncology and palliative care clinicians (n = 4), and a clinic administrator (n = 1) on the perceived relevance of the intervention. We then tested the prototype of a patient-facing tool for patient acceptability and preliminary effects on patient palliative care knowledge and motivation.
Partners agreed that the intervention-clinician palliative care education and an electronic health record-integrated patient tool-is relevant and their feedback informed development of the patient prototype. Advanced stage lung cancer patients (n = 20; age 60 ± 9.8; 40% male; 70% with a technical degree or less) reviewed and rated the prototype on a five-point scale for acceptability (4.48 ± 0.55), appropriateness (4.37 ± 0.62), and feasibility (4.43 ± 0.59). After using the prototype, 75% were interested in using palliative care and 80% were more motivated to talk to their oncologist about it. Of patients who had or were at risk of having misperceptions about palliative care (e.g., conflating it with hospice), 100% no longer held the misperceptions after using the prototype.
The palliative care education and screening tool is acceptable to patients and may address misperceptions and motivate palliative care discussions during treatment.
患者的误解是在晚期肺癌治疗中进行早期姑息治疗讨论和转诊的一个强大障碍。
我们开发并测试了一种基于网络的面向患者的姑息治疗教育和筛选工具的可接受性,该工具旨在用于计划中的多层次干预(即患者、临床医生、系统层面的目标)。
我们向 6 名晚期肺癌患者、4 名肿瘤学和姑息治疗临床医生和 1 名诊所管理人员征求了对干预措施的感知相关性的反馈意见。然后,我们测试了面向患者的工具原型,以了解患者的可接受性以及对患者姑息治疗知识和动机的初步影响。
合作伙伴一致认为干预-临床医生姑息治疗教育和电子病历集成的患者工具是相关的,他们的反馈为患者原型的开发提供了信息。20 名晚期肺癌患者(年龄 60 ± 9.8;40%为男性;70%具有技术学位或以下)使用五分量表对原型进行了可接受性(4.48 ± 0.55)、适当性(4.37 ± 0.62)和可行性(4.43 ± 0.59)的评估。使用原型后,75%的患者对使用姑息治疗感兴趣,80%的患者更有动力与他们的肿瘤医生谈论姑息治疗。在使用原型后,100%的患者消除了对姑息治疗的误解(例如,将姑息治疗与临终关怀混为一谈)。
姑息治疗教育和筛选工具可被患者接受,并且可能会解决误解,并在治疗期间促进姑息治疗讨论。