Paul Tenes J, Tran Khanh-Van, Mehawej Jordy, Lessard Darleen, Ding Eric, Filippaios Andreas, Howard-Wilson Sakeina, Otabil Edith Mensah, Noorishirazi Kamran, Naeem Syed, Hamel Alex, Han Dong, Chon Ki H, Barton Bruce, Saczynski Jane, McManus David
Division of Cardiovascular Medicine, Department of Medicine, University of Massachusetts Medical School, Worcester, Massachusetts.
Department of Population and Quantitative Health Sciences, University of Massachusetts Medical School, Worcester, Massachusetts.
Cardiovasc Digit Health J. 2023 May 4;4(4):118-125. doi: 10.1016/j.cvdhj.2023.04.002. eCollection 2023 Aug.
The detection of atrial fibrillation (AF) in stroke survivors is critical to decreasing the risk of recurrent stroke. Smartwatches have emerged as a convenient and accurate means of AF diagnosis; however, the impact on critical patient-reported outcomes, including anxiety, engagement, and quality of life, remains ill defined.
To examine the association between smartwatch prescription for AF detection and the patient-reported outcomes of anxiety, patient activation, and self-reported health.
We used data from the Pulsewatch trial, a 2-phase randomized controlled trial that included participants aged 50 years or older with a history of ischemic stroke. Participants were randomized to use either a proprietary smartphone-smartwatch app for 30 days of AF monitoring or no cardiac rhythm monitoring. Validated surveys were deployed before and after the 30-day study period to assess anxiety, patient activation, and self-rated physical and mental health. Logistic regression and generalized estimation equations were used to examine the association between smartwatch prescription for AF monitoring and changes in the patient-reported outcomes.
A total of 110 participants (mean age 64 years, 41% female, 91% non-Hispanic White) were studied. Seventy percent of intervention participants were novice smartwatch users, as opposed to 84% of controls, and there was no significant difference in baseline rates of anxiety, activation, or self-rated health between the 2 groups. The incidence of new AF among smartwatch users was 6%. Participants who were prescribed smartwatches did not have a statistically significant change in anxiety, activation, or self-reported health as compared to those who were not prescribed smartwatches. The results held even after removing participants who received an AF alert on the watch.
The prescription of smartwatches to stroke survivors for AF monitoring does not adversely affect key patient-reported outcomes. Further research is needed to better inform the successful deployment of smartwatches in clinical practice.
检测卒中幸存者的房颤对于降低复发性卒中风险至关重要。智能手表已成为一种方便且准确的房颤诊断手段;然而,其对包括焦虑、参与度和生活质量在内的关键患者报告结局的影响仍不明确。
探讨用于房颤检测的智能手表处方与患者报告的焦虑、患者激活度及自我报告健康状况之间的关联。
我们使用了来自Pulsewatch试验的数据,这是一项两阶段随机对照试验,纳入了年龄在50岁及以上且有缺血性卒中病史的参与者。参与者被随机分为使用一款专有的智能手机-智能手表应用程序进行30天的房颤监测或不进行心律监测。在30天研究期前后部署经过验证的调查问卷,以评估焦虑、患者激活度以及自我评定的身心健康状况。使用逻辑回归和广义估计方程来检验用于房颤监测的智能手表处方与患者报告结局变化之间的关联。
共研究了110名参与者(平均年龄64岁,41%为女性,91%为非西班牙裔白人)。70%的干预组参与者是智能手表新手用户,而对照组这一比例为84%,两组之间焦虑、激活度或自我评定健康的基线率无显著差异。智能手表用户中新发房颤的发生率为6%。与未配备智能手表的参与者相比,配备智能手表的参与者在焦虑、激活度或自我报告健康方面没有统计学上的显著变化。即使排除了手表收到房颤警报的参与者,结果依然成立。
为卒中幸存者开具智能手表用于房颤监测的处方不会对关键的患者报告结局产生不利影响。需要进一步研究以更好地指导智能手表在临床实践中的成功应用。