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A New Cuffless Device for Measuring Blood Pressure: A Real-Life Validation Study

机译:一种新型的无袖血压测量装置:一项真实的验证研究

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摘要

BACKGROUND: Cuffless blood pressure (BP) monitoring devices, based on pulse transit time, are being developed as an easy-to-use, more convenient, fast, and relatively cheap alternative to conventional BP measuring devices based on cuff occlusion. Thereby they may provide a great alternative to BP self-measurement. OBJECTIVE: The objective of our study was to evaluate the performance of the first release of the Checkme Health Monitor (Viatom Technology), a cuffless BP monitor, in a real-life setting. Furthermore, we wanted to investigate whether the posture of the volunteer and the position of the device relative to the heart level would influence its outcomes. METHODS: Study volunteers fell into 3 BP ranges: high (>160 mmHg), normal (130-160 mmHg), and low (<130 mmHg). All requirements for test environment, observer qualification, volunteer recruitment, and BP measurements were met according to the European Society of Hypertension International Protocol (ESH-IP) for the validation of BP measurement devices. After calibrating the Checkme device, we measured systolic BP with Checkme and a validated, oscillometric reference BP monitor (RM). Measurements were performed in randomized order both in supine and in sitting position, and with Checkme at and above heart level. RESULTS: We recruited 52 volunteers, of whom we excluded 15 (12 due to calibration failure with Checkme, 3 due to a variety of reasons). The remaining 37 volunteers were divided into low (n=14), medium (n=13), and high (n=10) BP ranges. There were 18 men and 19 women, with a mean age of 54.1 (SD 14.5) years, and mean recruitment systolic BP of 141.7 (SD 24.7) mmHg. BP results obtained by RM and Checkme correlated well. In the supine position, the difference between the RM and Checkme was >5 mmHg in 17 of 37 volunteers (46%), of whom 9 of 37 (24%) had a difference >10 mmHg and 5 of 37 (14%) had a difference >15 mmHg. CONCLUSIONS: BP obtained with Checkme correlated well with RM BP, particularly in the position (supine) in which the device was calibrated. These preliminary results are promising for conducting further research on cuffless BP measurement in the clinical and outpatient settings.
机译:背景技术:基于脉搏传播时间的无袖血压(BP)监测设备正被开发为基于袖套阻塞的常规BP测量设备的一种易于使用,更方便,快速且相对便宜的替代产品。因此,它们可以为BP自测提供很好的选择。目的:我们的研究目的是在现实环境中评估Checkme Health Monitor(Viatom Technology)(一种无袖带BP监护仪)首次发布的性能。此外,我们想调查志愿者的姿势和设备相对于心脏水平的位置是否会影响其结果。方法:研究志愿者分为3个BP范围:高(> 160 mmHg),正常(130-160 mmHg)和低(<130 mmHg)。测试环境,观察员资格,志愿者招募和BP测量的所有要求均已根据欧洲高血压学会国际协议(ESH-IP)的要求满足,以验证BP测量设备。校准Checkme设备后,我们使用Checkme和经过验证的示波参考BP监视器(RM)测量了收缩压。在仰卧位和坐位以及Checkme处于或高于心脏水平时,均以随机顺序进行测量。结果:我们招募了52名志愿者,其中我们排除了15名(12名因Checkme的校准失败,3名出于各种原因)。其余37名志愿者分为低(n = 14),中(n = 13)和高(n = 10)血压范围。男18例,女19例,平均年龄54.1(SD 14.5)岁,平均收缩压为141.7(SD 24.7)mmHg。 RM和Checkme获得的BP结果具有很好的相关性。在仰卧位,在37名志愿者中,有17名(46%)的RM和Checkme之间的差异> 5 mmHg,其中37名志愿者中有9名(24%)的差异> 10 mmHg,37名参与者中有5名(14%)的差异> 10 mmHg相差> 15毫米汞柱。结论:用Checkme获得的BP与RM BP相关性很好,特别是在校准设备的位置(仰卧)。这些初步结果有望在临床和门诊患者中进行无袖血压测量的进一步研究。

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