Abstract

We know that a 10cm departure from the reference level of pressure transducer position is equal to a 7.5mmHg change of invasive hemodynamic pressure monitoring in a fluid-filled system. However, the relationship between the site level of a variable arterial pressure transducer and the pulse contour-derived parameters has yet to be established in critically ill patients. Moreover, the related quantitative analysis has never been investigated. Forty-two critically ill patients requiring PiCCO-Plus cardiac output monitoring were prospectively studied. The phlebostatic axis was defined as the zero reference level; the arterial pressure transducer was then vertically adjusted to different positions (+5, +10, +15, +20, -20, -15, -10, -5cm) of departure from the zero reference site. The pulse contour waveform-derived parameters were recorded at each position. Elevation of the pressure transducer caused significantly positive changes in the continuous cardiac index (+CCI), stroke volume index (+SVI), and stroke volume variation (+SVV), and negative changes in the rate of left ventricular pressure rise during systole (-dP/dtmax), the systemic vascular resistance index (-SVRI), and vice versa. At the 5cm position, the SVRI changes reached statistical significance with error. At the 10cm position, the changes in CCI and dP/dtmax reached statistical significance with error, while the change in SVV reached statistical significance at 15cm. The change rate of CCI was more than 5% at the 15cm position and approximately 10% at the 20cm position. On average, for every centimeter change of the transducer, there was a corresponding 0.014L/min/m(2) CCI change and 0.36% change rate, a 1.41mmHg/s dP/dtmax change and 0.13% change rate, and a 25dyne/s/cm(5) SVRI change and 1.2% change rate. The variation of arterial transducer position can result in inaccurate measurement of pulse contour waveform-derived parameters, especially when the transducer's vertical distance is more than 10cm from the phlebostatic axis. These findings have clinical implications for continuous hemodynamic monitoring.

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