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[示波法血压监测仪的评估:Dinamap 1846和惠普M-1008B]

[Evaluation of the oscillometric blood pressure monitors: Dinamap 1846 and HP M-1008B].

作者信息

Papadopoulos G, Mieke S, Kuhn H J, Apenburg C

机构信息

Klinik für Anaesthesiologie und operative Intensivmedizin, Universitätsklinikum Benjamin Franklin, FU Berlin.

出版信息

Anaesthesist. 1996 May;45(5):453-9. doi: 10.1007/s001010050280.

Abstract

Using the PTB simulator, which emits real signals from patients, we examined the precision of the oscillometric blood pressure measurement with the Dinamap 1846 (Critikon) and the HP M-1008B (Hewlett Packard). For this purpose we simultaneously registered invasive arterial pulsewave, cuff pressure and cuff pressure oscillations of 20 patients from our intensive care unit and stored them in the database of the simulator. The invasive reference blood pressure values were determined following the recommendations given by the Association for the Advancement of Medical Instrumentation. The invasive system showed a cut-off frequency of 35 Hz; the damping constant was 0.21. With 49 record signals from patients we carried out 15 simulated measurements each. From a total of 49 bio-signals from patients the Dinamap 1846 was able to process 41 signals and the HP M-1008B 47 signals. The mean error of the oscillometric blood pressure measurement of the systolic, diastolic and mean arterial pressure amounted to -2.50 mmHg, 3.35 mmHg (P < 0.05) and 1.51 mmHg with the Dinamap 1846 and to -8.5 mmHg (P < 0.001), -5.15 mmHg (P < 0.001) and -5.58 mmHg (P < 0.001) for the HP M-1008B. The 95% confidence limit for the systolic, diastolic and the mean arterial pressure amounts to 56 mmHg, 30 mmHg and 35 mmHg for the Dinamap 1846 and 50 mmHg, 38 mmHg and 35 mmHg for the HP M-1008B. The differences between that two instruments could be caused by the different algorithms for the calculation of blood pressure values and different artefact detection and elimination techniques. The results of the performance tests we achieved with the PTB simulator correspond to the results of other clinical examinations. The American Association for the Advancement of Medical Instrumentation recommends a maximum mean error of 5 +/- 8 mmHg. None of the examined instruments lay within these limits. Due to the systematic and stochastic errors, we think that the Dinamap 1846 (Critikon) and the HP M-1008B (Hewlett Packard) do not achieve performance levels that are adequate for measuring critically ill patients.

摘要

我们使用能够发出真实患者信号的PTB模拟器,检测了Dinamap 1846(Critikon公司)和惠普M - 1008B(惠普公司)示波法测量血压的精度。为此,我们同步记录了重症监护病房20名患者的有创动脉脉搏波、袖带压力及袖带压力振荡,并将其存储于模拟器数据库中。有创参考血压值依据医疗仪器促进协会给出的建议来确定。有创系统的截止频率为35Hz,阻尼常数为0.21。我们利用49个患者记录信号,对每台仪器各进行了15次模拟测量。在总共49个患者生物信号中,Dinamap 1846能够处理41个信号,惠普M - 1008B能够处理47个信号。使用Dinamap 1846测量收缩压、舒张压及平均动脉压的示波法平均误差分别为-2.50mmHg、3.35mmHg(P < 0.05)和1.51mmHg;使用惠普M - 1008B测量时,上述指标的平均误差分别为-8.5mmHg(P < 0.001)、-5.15mmHg(P < 0.001)和-5.58mmHg(P < 0.001)。Dinamap 1846测量收缩压、舒张压及平均动脉压的95%置信区间分别为56mmHg、30mmHg和35mmHg;惠普M - 1008B的相应值分别为50mmHg、38mmHg和35mmHg。这两种仪器之间的差异可能是由于计算血压值的算法不同以及伪差检测和消除技术不同所致。我们用PTB模拟器进行性能测试的结果与其他临床检查结果相符。医疗仪器促进协会建议最大平均误差为5±8mmHg。所检测的仪器均未达到此标准。鉴于存在系统误差和随机误差,我们认为Dinamap 1846(Critikon公司)和惠普M - 1008B(惠普公司)的性能水平不足以用于测量重症患者的血压。

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