新颖的数字健康平台与健康指导,优化手术患者:大型学术医疗系统的可行性研究。

Stephen Andrew Esper, Jennifer Holder-Murray, Katie Ann Meister, Hsing-Hua Sylvia Lin, David Kojo Hamilton, Yram Jan Groff, Brian Scott Zuckerbraun, Aman Mahajan
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引用次数: 0

摘要

背景介绍Pip 是一种新型数字健康平台 (DHP),它将人类健康顾问 (HC) 和面向患者的内容技术相结合。目前尚未在围手术期手术优化中对这一组合进行过研究:本研究旨在测试 Pip 平台的可行性,以便在围手术期的预定时间间隔内,在健康顾问的协助下为择期手术患者提供面向患者的数字化围手术期优化指南:我们在 2022 年 11 月 22 日至 2023 年 3 月 27 日期间,在一家学术医疗中心对计划接受择期手术并受邀在术前 2.5 至 4 周至术后 4 周加入 Pip 的患者进行了一项机构审查委员会批准的描述性前瞻性可行性研究。描述性主要终点是患者报告的结果,包括患者满意度和参与度以及 Pip HC 评估。次要终点包括平均或中位住院时间(LOS)、7 天和 30 天内的再入院情况以及 30 天内急诊科的使用情况。次要终点在接受 Pip 治疗的患者与未接受 Pip 治疗的患者之间进行比较,采用的是稳定的反向治疗概率加权法:共邀请了 283 名患者,其中 172 人(60.8%)接受了 Pip 治疗。其中,80.2%(138/172)的患者接受了≥1次HC治疗并进行了手术,70.3%(97/138)的注册患者在术后参与了Pip治疗。平均参与时间为手术前 27 天。Pip 显示了 82% 的每周 HC 参与率。患者平均参加了 6.7 次 HC 会话。在完成调查的患者中(95/138,68.8%),满意度很高(平均 4.8/5;n=95)。患者非常认同医护人员在整个围手术期过程中对他们的帮助(平均 4.97/5;n=33)。净促进者平均得分为 9.7 分(满分 10 分)。在分析样本中,非 Pip 组共有 268 名患者,Pip 组共有 128 名患者,其治疗加权的稳定反概率分布有适当的重叠。与非 Pip 组相比,Pip 组患者的 LOS 缩短(平均 2.4 天 vs 3.1 天;中位数 1.9,IQR 1.0-3.1 vs 中位数 3.0,IQR 1.1-3.9 天;平均比值比 0.76;95% CI 0.62-0.93;P=.009)。Pip队列的7天再入院风险降低了49%(相对风险[RR] 0.51,95% CI 0.11-2.31;P=.38),30天再入院风险降低了17%(RR 0.83,95% CI 0.30-2.31;P=.73),但未达到统计学意义。两组患者在急诊科的30天复诊率相似(RR 1.06,95% CI 0.56-2.01,P=.85):Pip是一种新型移动DHP,结合了人类HCs和围手术期优化内容,可让患者参与围手术期治疗,并缩短住院时间。需要进一步研究评估在围手术期使用 Pip 或类似的 DHP 人机交互组合对临床和患者报告结果的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Novel Digital Health Platform With Health Coaches to Optimize Surgical Patients: Feasibility Study at a Large Academic Health System.

Background: Pip is a novel digital health platform (DHP) that combines human health coaches (HCs) and technology with patient-facing content. This combination has not been studied in perioperative surgical optimization.

Objective: This study's aim was to test the feasibility of the Pip platform for deploying perioperative, digital, patient-facing optimization guidelines to elective surgical patients, assisted by an HC, at predefined intervals in the perioperative journey.

Methods: We conducted an institutional review board-approved, descriptive, prospective feasibility study of patients scheduled for elective surgery and invited to enroll in Pip from 2.5 to 4 weeks preoperatively through 4 weeks postoperatively at an academic medical center between November 22, 2022, and March 27, 2023. Descriptive primary end points were patient-reported outcomes, including patient satisfaction and engagement, and Pip HC evaluations. Secondary end points included mean or median length of stay (LOS), readmission at 7 and 30 days, and emergency department use within 30 days. Secondary end points were compared between patients who received Pip versus patients who did not receive Pip using stabilized inverse probability of treatment weighting.

Results: A total of 283 patients were invited, of whom 172 (60.8%) enrolled in Pip. Of these, 80.2% (138/172) patients had ≥1 HC session and proceeded to surgery, and 70.3% (97/138) of the enrolled patients engaged with Pip postoperatively. The mean engagement began 27 days before surgery. Pip demonstrated an 82% weekly engagement rate with HCs. Patients attended an average of 6.7 HC sessions. Of those patients that completed surveys (95/138, 68.8%), high satisfaction scores were recorded (mean 4.8/5; n=95). Patients strongly agreed that HCs helped them throughout the perioperative process (mean 4.97/5; n=33). The average net promoter score was 9.7 out of 10. A total of 268 patients in the non-Pip group and 128 patients in the Pip group had appropriate overlapping distributions of stabilized inverse probability of treatment weighting for the analytic sample. The Pip cohort was associated with LOS reduction when compared to the non-Pip cohort (mean 2.4 vs 3.1 days; median 1.9, IQR 1.0-3.1 vs median 3.0, IQR 1.1-3.9 days; mean ratio 0.76; 95% CI 0.62-0.93; P=.009). The Pip cohort experienced a 49% lower risk of 7-day readmission (relative risk [RR] 0.51, 95% CI 0.11-2.31; P=.38) and a 17% lower risk of 30-day readmission (RR 0.83, 95% CI 0.30-2.31; P=.73), though these did not reach statistical significance. Both cohorts had similar 30-day emergency department returns (RR 1.06, 95% CI 0.56-2.01, P=.85).

Conclusions: Pip is a novel mobile DHP combining human HCs and perioperative optimization content that is feasible to engage patients in their perioperative journey and is associated with reduced hospital LOS. Further studies assessing the impact on clinical and patient-reported outcomes from the use of Pip or similar DHPs HC combinations during the perioperative journey are required.

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