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基于网络的患者报告结局测量用于个性化治疗和护理(PROMPT-Care):多中心实用非随机试验。

Web-Based Patient-Reported Outcome Measures for Personalized Treatment and Care (PROMPT-Care): Multicenter Pragmatic Nonrandomized Trial.

机构信息

Centre for Oncology Education and Research Translation, Ingham Institute for Applied Medical Research, Sydney, Australia.

Faculty of Medicine, The University of New South Wales, Sydney, Australia.

出版信息

J Med Internet Res. 2020 Oct 29;22(10):e19685. doi: 10.2196/19685.

Abstract

BACKGROUND

Despite the acceptability and efficacy of e-patient-reported outcome (ePRO) systems, implementation in routine clinical care remains challenging.

OBJECTIVE

This pragmatic trial implemented the PROMPT-Care (Patient Reported Outcome Measures for Personalized Treatment and Care) web-based system into existing clinical workflows and evaluated its effectiveness among a diverse population of patients with cancer.

METHODS

Adult patients with solid tumors receiving active treatment or follow-up care in four cancer centers were enrolled. The PROMPT-Care intervention supported patient management through (1) monthly off-site electronic PRO physical symptom and psychosocial well-being assessments, (2) automated electronic clinical alerts notifying the care team of unresolved clinical issues following two consecutive assessments, and (3) tailored online patient self-management resources. Propensity score matching was used to match controls with intervention patients in a 4:1 ratio for patient age, sex, and treatment status. The primary outcome was a reduction in emergency department presentations. Secondary outcomes were time spent on chemotherapy and the number of allied health service referrals.

RESULTS

From April 2016 to October 2018, 328 patients from four public hospitals received the intervention. Matched controls (n=1312) comprised the general population of patients with cancer, seen at the participating hospitals during the study period. Emergency department visits were significantly reduced by 33% (P=.02) among patients receiving the intervention compared with patients in the matched controls. No significant associations were found in allied health referrals or time to end of chemotherapy. At baseline, the most common patient reported outcomes (above-threshold) were fatigue (39%), tiredness (38.4%), worry (32.9%), general wellbeing (32.9%), and sleep (24.1%), aligning with the most frequently accessed self-management domain pages of physical well-being (36%) and emotional well-being (23%). The majority of clinical feedback reports were reviewed by nursing staff (729/893, 82%), largely in response to the automated clinical alerts (n=877).

CONCLUSIONS

Algorithm-supported web-based systems utilizing patient reported outcomes in clinical practice reduced emergency department presentations among a diverse population of patients with cancer. This study also highlighted the importance of (1) automated triggers for reviewing above-threshold results in patient reports, rather than passive manual review of patient records; (2) the instrumental role nurses play in managing alerts; and (3) providing patients with resources to support guided self-management, where appropriate. Together, these factors will inform the integration of web-based PRO systems into future models of routine cancer care.

TRIAL REGISTRATION

Australian New Zealand Clinical Trials Registry ACTRN12616000615482; https://www.anzctr.org.au/Trial/Registration/TrialReview.aspx?id=370633.

INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): RR2-10.1186/s12885-018-4729-3.

摘要

背景

尽管电子患者报告结局(ePRO)系统具有可接受性和有效性,但在常规临床护理中的实施仍然具有挑战性。

目的

本实用临床试验将基于网络的 PROMPT-Care(用于个性化治疗和护理的患者报告结局测量)系统实施到现有的临床工作流程中,并评估其在癌症患者的多样化人群中的有效性。

方法

在四个癌症中心接受积极治疗或随访护理的成年实体瘤患者入组。PROMPT-Care 干预措施通过以下方式支持患者管理:(1)每月进行场外电子 PRO 身体症状和心理社会健康评估;(2)在连续两次评估后,自动电子临床警报通知护理团队未解决的临床问题;(3)提供个性化的在线患者自我管理资源。采用倾向评分匹配,将对照组与干预组患者按照年龄、性别和治疗状态以 4:1 的比例进行匹配。主要结局是减少急诊就诊。次要结局是化疗时间和转介的辅助医疗服务数量。

结果

从 2016 年 4 月至 2018 年 10 月,四家公立医院的 328 名患者接受了干预。对照组(n=1312)包括在研究期间参加医院就诊的癌症患者的一般人群。与对照组患者相比,接受干预的患者急诊就诊率显著降低 33%(P=.02)。在辅助医疗转介或化疗结束时间方面,未发现显著关联。在基线时,最常见的患者报告结局(超过阈值)是疲劳(39%)、疲倦(38.4%)、担忧(32.9%)、总体幸福感(32.9%)和睡眠(24.1%),与身体幸福感(36%)和情绪幸福感(23%)最常访问的自我管理领域页面一致。大多数临床反馈报告由护理人员(729/893,82%)审查,主要是对自动临床警报(n=877)的响应。

结论

基于算法的网络系统在临床实践中利用患者报告结局,减少了癌症患者多样化人群的急诊就诊率。本研究还强调了(1)在患者报告中,自动触发以审查超过阈值的结果,而不是被动地手动审查患者记录的重要性;(2)护士在管理警报方面的重要作用;(3)在适当情况下为患者提供支持引导性自我管理的资源。这些因素共同为基于网络的 PRO 系统纳入未来常规癌症护理模式提供了信息。

试验注册

澳大利亚和新西兰临床试验注册中心 ACTRN12616000615482;https://www.anzctr.org.au/Trial/Registration/TrialReview.aspx?id=370633。

国际标准化报告标识符(IRRID):RR2-10.1186/s12885-018-4729-3。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16ba/7661255/d295eb12ef17/jmir_v22i10e19685_fig1.jpg

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