Amoore J N
Department of Medical Physics and Medical Engineering, Royal Infirmary of Edinburgh, Edinburgh, UK.
Blood Press Monit. 2000 Apr;5(2):69-79.
Oscillometric pressure is measured by analysing, in relation to the cuff pressure, low-amplitude cuff-pressure pulsations generated by each arterial pulse. The cuff pressure is sampled at the pulse rate, introducing measurement variations, which are compounded by artefactual pulses.
To study the consistency of measurements with and without artefacts using simulated waveforms.
The Propaq Smartcuf (with and without electrocardiographic synchronization), the Welch Allyn 52 000 (before and after its software had been upgraded), the Critikon DINAMAP 8100 and Compact TS and the Criticare 507 NJC were evaluated. Each monitor recorded 15 determinations at 120/80 (93) mmHg without and with either low-frequency or high-frequency artefacts generated by the Bio-Tek BP-Pump simulator. Consistency of measurements was defined as SD of less than 2 mmHg for at least two of the systolic, diastolic and mean arterial pressures with all less than 3 mmHg.
All monitors except the Critikon 8100 satisfied the consistency criteria without artefacts with most SD less than 1 mmHg. Several satisfied the criteria with a severe low-frequency artefact (all recorded SD were less than 6 mmHg). None satisfied the criteria with a severe high-frequency artefact. High systolic blood pressures were typically recorded with a severe tremor artefact, though the Criticare device, which measures during cuff inflation, recorded lower systolic blood pressures. The Propaq device with electrocardiographic synchronization had the lowest variability, with synchronization increasing determination time.
Oscillometric monitors are more sensitive to a high-frequency artefact than they are to a low-frequency artefact. Signal-processing techniques can improve consistency of measurements. Simulators can evaluate a monitor's consistency with and without artefacts.
示波法测量血压是通过分析与袖带压力相关的、由每次动脉搏动产生的低振幅袖带压力脉动来实现的。袖带压力以脉搏频率进行采样,这会引入测量变化,而伪脉冲会使这种变化更加复杂。
使用模拟波形研究有无伪影时测量的一致性。
对Propaq Smartcuf(有无心电图同步功能)、Welch Allyn 52 000(软件升级前后)、Critikon DINAMAP 8100和Compact TS以及Criticare 507 NJC进行评估。每个监测仪在120/80(93)mmHg下记录15次测量值,分别在无伪影以及有Bio-Tek BP-Pump模拟器产生的低频或高频伪影的情况下进行。测量的一致性定义为收缩压、舒张压和平均动脉压中至少两项的标准差小于2 mmHg,且所有标准差均小于3 mmHg。
除Critikon 8100外,所有监测仪在无伪影时均满足一致性标准,大多数标准差小于1 mmHg。有几种监测仪在存在严重低频伪影时满足标准(所有记录的标准差均小于6 mmHg)。在存在严重高频伪影时,没有一种监测仪满足标准。在存在严重震颤伪影时,通常会记录到较高的收缩压,不过在袖带充气时进行测量的Criticare设备记录的收缩压较低。具有心电图同步功能的Propaq设备变异性最低,同步功能会增加测量时间。
示波监测仪对高频伪影比对低频伪影更敏感。信号处理技术可以提高测量的一致性。模拟器可以评估监测仪在有无伪影情况下的一致性。