Department of Medical Social Sciences, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, United States.
Robert H Lurie Comprehensive Cancer Center, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, United States.
J Am Med Inform Assoc. 2024 Oct 1;31(10):2190-2201. doi: 10.1093/jamia/ocae180.
To assess the use of a co-designed patient-reported outcome (PRO) clinical dashboard and estimate its impact on shared decision-making (SDM) and symptomatology in adults with advanced cancer or chronic kidney disease (CKD).
We developed a clinical PRO dashboard within the Northwestern Medicine Patient-Reported Outcomes system, enhanced through co-design involving 20 diverse constituents. Using a single-group, pretest-posttest design, we evaluated the dashboard's use among patients with advanced cancer or CKD between June 2020 and January 2022. Eligible patients had a visit with a participating clinician, completed at least two dashboard-eligible visits, and consented to follow-up surveys. PROs were collected 72 h prior to visits, including measures for chronic condition management self-efficacy, health-related quality of life (PROMIS measures), and SDM (collaboRATE). Responses were integrated into the EHR dashboard and accessible to clinicians and patients.
We recruited 157 participants: 66 with advanced cancer and 91 with CKD. There were significant improvements in SDM from baseline, as assessed by collaboRATE scores. The proportion of participants reporting the highest level of SDM on every collaboRATE item increased by 15 percentage points from baseline to 3 months, and 17 points between baseline and 6-month follow-up. Additionally, there was a clinically meaningful decrease in anxiety levels over study period (T-score baseline: 53; 3-month: 52; 6-month: 50; P < .001), with a standardized response mean (SRM) of -0.38 at 6 months.
PRO clinical dashboards, developed and shared with patients, may enhance SDM and reduce anxiety among patients with advanced cancer and CKD.
评估经共同设计的患者报告结局(PRO)临床仪表盘的使用情况,并评估其对晚期癌症或慢性肾脏病(CKD)成人患者的共享决策(SDM)和症状的影响。
我们在西北医学患者报告结局系统中开发了一个临床 PRO 仪表盘,通过涉及 20 名不同参与者的共同设计对其进行了增强。我们采用单组、预测试-后测试设计,评估了 2020 年 6 月至 2022 年 1 月期间患有晚期癌症或 CKD 的患者对该仪表盘的使用情况。符合条件的患者与参与的临床医生进行了一次就诊,至少完成了两次符合仪表盘要求的就诊,并同意接受随访调查。PRO 在就诊前 72 小时收集,包括慢性病管理自我效能、健康相关生活质量(PROMIS 量表)和 SDM(collaboRATE)的测量。这些反应被整合到电子健康记录(EHR)仪表盘,并提供给临床医生和患者。
我们招募了 157 名参与者:66 名患有晚期癌症,91 名患有 CKD。collaboRATE 评分显示,SDM 从基线开始显著改善。从基线到 3 个月,报告每项 collaboRATE 项目最高 SDM 水平的参与者比例增加了 15 个百分点,从基线到 6 个月随访时增加了 17 个百分点。此外,在研究期间焦虑水平有临床意义的下降(T 评分基线:53;3 个月:52;6 个月:50;P<0.001),6 个月时的标准化反应均值(SRM)为-0.38。
与患者共同设计和共享的 PRO 临床仪表盘,可能会增强晚期癌症和 CKD 患者的 SDM,并降低其焦虑水平。