在急性缺血性中风患者中使用智能手表验证血压测量
Yu-Hsuan Liu1, Li-Ching Chen2, Yi-Shian Guo3
1Department of Neurology, E-DA Hospital, Kaohsiung, Taiwan.
这项研究验证了智能手表在急性缺血性中风患者的血压 (BP) 测量精度. 阿苏斯VivoWatch SP表现出可靠的血压读数,符合无袖设备的国际标准.
科学领域:
- 生物医学工程 生物医学工程
- 心血管研究研究心血管研究
- 医疗器械 医疗器械
背景情况:
- 精确的血压 (BP) 监测对于管理急性缺血性中风至关重要.
- 传统的血压测量方法可能很麻烦,特别是在中风患者中.
- 可穿戴技术为连续和方便的BP监测提供了潜力.
研究的目的:
- 在被诊断为急性缺血性中风的患者中,通过智能手表 (ASUS VivoWatch SP) 获得的血压测量的准确性.
- 在这个特定的患者群体中评估无袖血压监测的可靠性.
主要方法:
- 将来自ASUS VivoWatch SP的140对血压测量与血压计 (参考设备) 进行比较.
- 遵循ANSI/AAMI/ISO 81060-2:2018标准,适用于急性缺血性中风患者的无袖设备.
- 在智能手表和参考设备之间分析了心压和腹压血压的差异.
主要成果:
- 平均差异为静脉血压的1.8 ± 5.7 mm Hg,而静脉血压的0.7 ± 3.6 mm Hg (标准1).
- 平均差异为静脉血压的1.8 ± 5.6 mm Hg,而静脉血压的0.7 ± 3.6 mm Hg (第二标准).
- 结果符合两个验证标准,麻和非麻组之间没有显著差异.
结论:
- 在ASUS VivoWatch SP,利用光聚缩学传感器,在急性缺血性中风患者提供准确和可靠的血压测量.
- 智能手表血压监测是这个患者群体的可行选择,遵循既定的验证标准.
- 这项技术有望改善中风护理中的血压管理.
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