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使用基于网络的移动医疗应用程序测量心力衰竭患者的健康状况和症状负担。

Measuring health status and symptom burden using a web-based mHealth application in patients with heart failure.

机构信息

1 School of Nursing, Columbia University, USA.

2 Department of Healthcare Policy and Research, Weill Cornell Medicine, USA.

出版信息

Eur J Cardiovasc Nurs. 2019 Apr;18(4):325-331. doi: 10.1177/1474515119825704. Epub 2019 Jan 25.

Abstract

BACKGROUND

Symptoms of heart failure markedly impair a patient's health status. The aim of this study was to identify predictors of health status in a sample of racially and ethnically diverse patients with heart failure using a web-based mobile health application, mi.Symptoms.

METHODS

We conducted a cross-sectional study at an urban academic medical center. Patients with heart failure self-reported symptoms using validated symptom instruments (e.g. patient-reported outcome measurement information system) by way of the mobile health application, mi.Symptoms. The primary study outcome was health status, measured with the Kansas City cardiomyopathy questionnaire clinical summary score. Data were analyzed using descriptive statistics and multiple linear regression.

RESULTS

The mean age of the sample ( n=168) was 58.7 (±12.5) years, 37% were women, 36% were Black, 36% identified as Hispanic/Latino, 48% were classified as New York Heart Association class III, and 44% reported not having enough income to make ends meet. Predictors of better health status in heart failure included higher physical function ( β=0.89, p=0.001) and ability to participate in social roles and activities ( β=0.58, p=0.002), and predictors of poorer health status were New York Heart Association class IV ( β=-11.68, p=0.006) and dyspnea ( β=-0.77, p<0.001). The predictors accounted for 73% of the variance in health status.

CONCLUSION

Patient-centered interventions should focus on modifiable risk factors that reduce dyspnea, improve functional status, and enhance engagement in social roles to improve the health status of patients with heart failure.

摘要

背景

心力衰竭的症状显著影响患者的健康状况。本研究旨在通过基于网络的移动健康应用程序 mi.Symptoms 识别种族和民族多样化的心力衰竭患者样本中健康状况的预测因素。

方法

我们在城市学术医疗中心进行了一项横断面研究。心力衰竭患者通过移动健康应用程序 mi.Symptoms 使用经过验证的症状量表(例如患者报告的结果测量信息系统)自我报告症状。主要研究结果是健康状况,用堪萨斯城心肌病问卷临床总结评分来衡量。使用描述性统计和多元线性回归分析数据。

结果

样本(n=168)的平均年龄为 58.7(±12.5)岁,37%为女性,36%为黑人,36%为西班牙裔/拉丁裔,48%为纽约心脏协会(NYHA)III 级,44%报告收入不足以维持生计。心力衰竭患者健康状况较好的预测因素包括较高的身体功能(β=0.89,p=0.001)和参与社会角色和活动的能力(β=0.58,p=0.002),而健康状况较差的预测因素包括 NYHA 分级 IV(β=-11.68,p=0.006)和呼吸困难(β=-0.77,p<0.001)。这些预测因素占健康状况变异的 73%。

结论

以患者为中心的干预措施应侧重于减轻呼吸困难、改善功能状态和增强参与社会角色的可改变风险因素,以改善心力衰竭患者的健康状况。

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