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Are Automated Blood Pressure Apparatus Reliable? Automated versus Manual Measurement of Blood Pressure

机译:自动血压仪是否可靠?自动与手动测量血压

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With hypertension becoming a global burden, it is necessary to validate the Blood Pressure (BP) recordings, used to screen and follow-up patients for hypertension. Since three different devices (mercury manometer, aneroid meter, and digital) are commonly used throughout the world, a study was proposed to compare the recordings of the three devices.Aim: To evaluate the validity of aneroid and digital BP monitors as compared to mercury manometer.Materials and Methods: BP was measured in 240 healthy subjects of both sex (Male=127, Female=113) using mercury manometer, aneroid and digital BP monitor from the same arm consecutively with five minutes interval between each recording. The data were analysed using SPSS 21, Systolic Blood Pressure (SBP) and Diastolic Blood Pressure (DBP) readings of aneroid and digital monitors were compared with mercury manometer. British Hypertension Society (BHS) protocol, Association for the Advancement of Medical Instrumentation (AAMI) standards and Bland Altman scatter plots were used to validate the aneroid and digital BP monitors.Results: The difference in SBP measured using mercury manometer and aneroid meter was 0.675±7.12 mmHg and mercury manometer and digital monitor was 1.65±11.08 mmHg. The difference in DBP using mercury manometer and aneroid meter was 1.75±6.3 mmHg and mercury manometer and digital was 2.76±8.8 mmHg. While aneroid meter satisfied the AAMI criteria, digital monitor did not. The BHS grade for aneroid meter was C (poor) and digital D (very poor). According to Bland-Altman plot, the bias in SBP for aneroid was minimal with 0.675 (-13.28-14.63), for digital -1.41 (-21.66-18.84) and in DBP for aneroid was 1.75 (-10.6-14.1), for digital was the highest with 2.76 (-14.47-20.01).Conclusion: BP measured using aneroid and digital monitors varied significantly from the mercury manometer and showed higher levels of inaccuracy and hence should be used with caution in clinical setting.
机译:随着高血压成为全球负担,有必要验证血压(BP)记录,以筛查和随访患者的高血压。由于全世界普遍使用三种不同的设备(水银压力计,无液仪表和数字设备),因此提出了一项研究以比较这三种设备的记录。目的:评估无液和数字BP监护仪的有效性, 材料与方法:使用汞压力计,无液尿素和数字BP监护仪从同一手臂连续五分钟间隔两次,对240名男女健康受试者(男性= 127,女性= 113)进行血压测量。每次录音。使用SPSS 21对数据进行分析,将无液尿素的收缩压(SBP)和舒张压(DBP)读数与数字监测仪与水银压力计进行比较。使用英国高血压学会(BHS)协议,美国医疗器械先进协会(AAMI)标准和Bland Altman散点图来验证无液和数字BP监护仪。水银压力计为0.675±7.12 mmHg,水银压力计和数字监控器为1.65±11.08 mmHg。使用水银压力计和无水线仪的DBP差异为1.75±6.3 mmHg,水银压力计与数字仪的差异为2.76±8.8 mmHg。虽然无液水准仪满足AAMI标准,但数字监视器却没有。无液水准仪的BHS等级为C(差)和D(非常差)。根据Bland-Altman曲线,无液的SBP偏差最小,为0.675(-13.28-14.63),数字的为-1.41(-21.66-18.84),无液的DBP为1.75(-10.6-14.1),数字的结论是最高的,为2.76(-14.47-20.01)。结论:使用无液和数字监测仪测量的BP与水银压力计差异很大,并且显示出较高的不准确度,因此在临床环境中应谨慎使用。

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