Kapoor Alok, Hayes Anna, Patel Jay, Patel Harshal, Andrade Andreza, Mazor Kathleen, Possidente Carl, Nolen Kimberly, Hegeman-Dingle Rozelle, McManus David
Department of Medicine, University of Massachusetts Chan Medical School, Worcester, MA, United States.
Division of Medical Affairs, Pfizer Inc, New York, NY, United States.
JMIR Cardio. 2021 Nov 19;5(2):e27016. doi: 10.2196/27016.
Although the American Heart Association and other professional societies have recommended shared decision-making as a way for patients with atrial fibrillation (AF) or atrial flutter to make informed decisions about using anticoagulation (AC), the best method for facilitating shared decision-making remains uncertain.
The aim of this study is to assess the AFib 2gether mobile app for usability, perceived usefulness, and the extent and nature of shared decision-making that occurred for clinical encounters between patients with AF and their cardiology providers in which the app was used.
We identified patients visiting a cardiology provider between October 2019 and May 2020. We measured usability from patients and providers using the Mobile App Rating Scale. From the 8 items of the Mobile App Rating Scale, we reported the average score (out of 5) for domains of functionality, esthetics, and overall quality. We administered a 3-item questionnaire to patients relating to their perceived usefulness of the app and a separate 3-item questionnaire to providers to measure their perceived usefulness of the app. We performed a chart review to track the occurrence of AC within 6 months of the index visit. We also audio recorded a subset of the encounters to identify evidence of shared decision-making.
We facilitated shared decision-making visits for 37 patients visiting 13 providers. In terms of usability, patients' average ratings of functionality, esthetics, and overall quality were 4.51 (SD 0.61), 4.26 (SD 0.51), and 4.24 (SD 0.89), respectively. In terms of usefulness, 41% (15/37) of patients agreed that the app improved their knowledge regarding AC, and 62% (23/37) agreed that the app helped clarify to their provider their preferences regarding AC. Among providers, 79% (27/34) agreed that the app helped clarify their patients' preferences, 82% (28/34) agreed that the app saved them time, and 59% (20/34) agreed that the app helped their patients make decisions about AC. In addition, 32% (12/37) of patients started AC after their shared decision-making visits. We audio recorded 25 encounters. Of these, 84% (21/25) included the mention of AC for AF, 44% (11/25) included the discussion of multiple options for AC, 72% (18/25) included a provider recommendation for AC, and 48% (12/25) included the evidence of patient involvement in the discussion.
Patients and providers rated the app with high usability and perceived usefulness. Moreover, one-third of the patients began AC, and approximately 50% (12/25) of the encounters showed evidence of patient involvement in decision-making. In the future, we plan to study the effect of the app on a larger sample and with a controlled study design.
ClinicalTrials.gov NCT04118270; https://clinicaltrials.gov/ct2/show/NCT04118270.
INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): RR2-21986.
尽管美国心脏协会和其他专业学会推荐共同决策,作为心房颤动(AF)或心房扑动患者就使用抗凝治疗(AC)做出明智决策的一种方式,但促进共同决策的最佳方法仍不确定。
本研究的目的是评估AFib 2gether移动应用程序的可用性、感知有用性,以及在使用该应用程序的AF患者与其心脏病学提供者的临床会诊中发生的共同决策的程度和性质。
我们确定了2019年10月至2020年5月期间就诊于心脏病学提供者的患者。我们使用移动应用程序评分量表测量患者和提供者的可用性。从移动应用程序评分量表的8个项目中,我们报告了功能、美学和整体质量领域的平均得分(满分5分)。我们向患者发放了一份3项问卷,询问他们对应用程序的感知有用性,并向提供者发放了一份单独的3项问卷,以测量他们对应用程序的感知有用性。我们进行了病历审查,以跟踪索引就诊后6个月内AC的使用情况。我们还对一部分会诊进行了录音,以确定共同决策的证据。
我们为37名就诊于13名提供者的患者提供了共同决策会诊。在可用性方面,患者对功能、美学和整体质量的平均评分分别为4.51(标准差0.61)、4.26(标准差0.51)和4.24(标准差0.89)。在有用性方面,41%(15/37)的患者同意该应用程序提高了他们关于AC的知识,62%(23/37)的患者同意该应用程序有助于向他们的提供者阐明他们对AC的偏好。在提供者中,79%(27/34)的人同意该应用程序有助于阐明他们患者的偏好,82%(28/34)的人同意该应用程序节省了他们的时间,59%(20/34)的人同意该应用程序帮助他们的患者就AC做出决策。此外,32%(12/37)的患者在共同决策会诊后开始使用AC。我们对25次会诊进行了录音。其中,84%(21/25)提到了AF的AC,44%(11/25)包括了对AC多种选择的讨论,72%(18/25)包括了提供者对AC的推荐,48%(12/25)包括了患者参与讨论的证据。
患者和提供者对该应用程序的可用性和感知有用性评价很高。此外,三分之一的患者开始使用AC,并且大约50%(12/25)的会诊显示有患者参与决策的证据。未来,我们计划在更大样本和对照研究设计中研究该应用程序的效果。
ClinicalTrials.gov NCT04118270;https://clinicaltrials.gov/ct2/show/NCT04118270。
国际注册报告识别码(IRRID):RR2-21986。