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An Automated Blood Pressure Display for Self-Measurement in Patients With Chronic Kidney Disease (iHealth Track): Device Validation Study

机译:慢性肾病患者自测自动血压显示器(IHealth Track):设备验证研究

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Background Hypertension is a global public health issue and is closely related to chronic kidney disorder (CKD). In people with CKD, strict monitoring of blood pressure is an important part of therapy. Objective The aim of this research was to validate the iHealth Track blood pressure monitoring device for patients with CKD according to the European Society of Hypertension International Protocol 2010 (ESH-IP2). Methods In total, 33 patients who received hemodialysis in Plasencia participated in the study. There were 9 successive measurements made, which conformed to the ESH-IP2. We calculated the differences between the standard reference device (Omron M3 Intellisense) and the test device (iHealth Track) for blood pressure and heart rate values. For 99 total comparisons of paired measurements, we classified differences into various categories (≤5 mmHg, ≤10 mmHg, and ≤15 mmHg for blood pressure; ≤3, ≤5, and ≤8 beats per minute for heart rate). Results In 90 of 99 systolic blood pressure and 89 of 99 diastolic blood pressure comparisons between the devices, measurement differences were within 5 mmHg. In 81 of 99 heart rate comparisons between the devices, measurement differences were within 3 beats per minute. The mean differences between the test and reference standard measurements were 3.27 (SD 2.99) mmHg for systolic blood pressure, 3.59 (SD 4.55) mmHg for diastolic blood pressure, and 2.18 (SD 2.75) beats per minute for heart rate. We also observed that for both systolic and diastolic blood pressure, 31 of 33 participants had at least two of three comparisons between the devices with measurement differences less than 5 mmHg. For heart rate, 28 of 33 patients had at least two of three comparisons between the devices with measurement differences less than 3 beats per minute. Conclusions To our knowledge, this is the first study to show that iHealth Track meets the requirements of the ESH-IP2 in patients with CKD. Therefore, the iHealth Track is suitable for use in renal patients.
机译:背景技术高血压是全球公共卫生问题,与慢性肾脏疾病(CKD)密切相关。在CKD的人们中,严格监测血压是治疗的重要组成部分。客观本研究的目的是根据欧洲高血压国际协议2010(ESH-IP2)验证CKD患者的iHealth轨道血压监测装置。方法总共33例接受Plasencia中血液透析的患者参加了该研究。制作了9个连续测量,符合ESH-IP2。我们计算了标准参考装置(OMRON M3 IntelliSense)与血压和心率值的测试装置(iHealth曲目)之间的差异。对于99个配对测量的总比较,我们将差异分为各种类别(≤5mmHg,≤10mmHg,血压≤15mmHg;≤3,≤5,心率为≤8次)。结果999个收缩压和99个舒张压血压比较的89个装置,测量差异在5mmHg范围内。在99个心率比较的81个设备中,测量差异在每分钟3次左右内。测试和参考标准测量之间的平均差异为3.27(SD 2.99)mmHg,用于收缩压,3.59(SD 4.55)mmHg用于舒张压,2.18(SD 2.75)每分钟为心率为每分钟。我们还观察到,对于收缩系统和舒张压,33名参与者中的31种具有至少两个在具有小于5mmHg的测量差异之间的三种比较中的三种比较中的至少两个。对于心率,33名患者中的28例在装置之间至少有两种比较,测量差异小于每分钟3次。结论我们的知识,这是第一次表明iHealth曲目符合CKD患者ESH-IP2的要求。因此,iHealth轨道适用于肾患者。

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