Boubouchairopoulou N, Kollias A, Chiu B, Chen B, Lagou S, Anestis P, Stergiou G S
Hypertension Center STRIDE-7, Third Department of Medicine, National and Kapodistrian University of Athens, School of Medicine, Sotiria Hospital, Athens, Greece.
Maisense Inc., Zhubei, Taiwan.
J Hum Hypertens. 2017 Jul;31(7):479-482. doi: 10.1038/jhh.2016.101. Epub 2017 Jan 26.
A pocket-size cuffless electronic device for self-measurement of blood pressure (BP) has been developed (Freescan, Maisense Inc., Zhubei, Taiwan). The device estimates BP within 10 s using three embedded electrodes and one force sensor that is applied over the radial pulse to evaluate the pulse wave. Before use, basic anthropometric characteristics are recorded on the device, and individualized initial calibration is required based on a standard BP measurement performed using an upper-arm BP monitor. The device performance in providing valid BP readings was evaluated in 313 normotensive and hypertensive adults in three study phases during which the device sensor was upgraded. A formal validation study of a prototype device against mercury sphygmomanometer was performed according to the American National Standards Institute/Association for the Advancement of Medical Instrumentation/International Organization for Standardization (ANSI/AAMI/ISO) 2013 protocol. The test device succeeded in obtaining a valid BP measurement (three successful readings within up to five attempts) in 55-72% of the participants, which reached 87% with device sensor upgrade. For the validation study, 125 adults were recruited and 85 met the protocol requirements for inclusion. The mean device-observers BP difference was 3.2±6.7 (s.d.) mm Hg for systolic and 2.6±4.6 mm Hg for diastolic BP (criterion 1). The estimated s.d. (inter-subject variability) were 5.83 and 4.17 mm Hg respectively (criterion 2). These data suggest that this prototype cuffless BP monitor provides valid self-measurements in the vast majority of adults, and satisfies the BP measurement accuracy criteria of the ANSI/AAMI/ISO 2013 validation protocol.
已研发出一种用于自我测量血压(BP)的袖珍无袖电子设备(Freescan,台湾新竹迈新科技公司)。该设备使用三个嵌入式电极和一个力传感器在桡动脉脉搏上进行评估,以在10秒内估算血压。使用前,需在设备上记录基本人体测量特征,并根据使用上臂血压监测仪进行的标准血压测量进行个性化初始校准。在三个研究阶段对313名血压正常和高血压成年人进行了评估,在此期间设备传感器进行了升级,以评估该设备提供有效血压读数的性能。根据美国国家标准学会/医疗仪器促进协会/国际标准化组织(ANSI/AAMI/ISO)2013协议,对该原型设备与汞柱式血压计进行了正式验证研究。测试设备在55%-72%的参与者中成功获得了有效的血压测量值(最多五次尝试中有三次成功读数),随着设备传感器升级,这一比例达到了87%。在验证研究中,招募了125名成年人,其中85名符合纳入方案要求。收缩压的平均设备-观察者血压差异为3.2±6.7(标准差)mmHg,舒张压为2.6±4.6 mmHg(标准1)。估计的标准差(受试者间变异性)分别为5.83和4.17 mmHg(标准2)。这些数据表明,这种原型无袖血压监测仪在绝大多数成年人中提供了有效的自我测量,并满足了ANSI/AAMI/ISO 2013验证方案的血压测量准确性标准。