Original Contribution
Comparison of noninvasive cardiac output measurements using the Nexfin monitoring device and the esophageal Doppler

https://doi.org/10.1016/j.jclinane.2011.08.014Get rights and content

Abstract

Study Objective

To evaluate the validity of cardiac output (CO) measurements obtained using the Nexfin device in comparison to those obtained with the esophageal Doppler in steady-state conditions and after phenylephrine administration.

Design

Prospective observational study.

Setting

Operating room of a North American academic medical center.

Patients

25 ASA physical status 1, 2, and 3 patients referred for abdominal or orthopedic surgeries.

Interventions

After endotracheal intubation, patients who presented with a 20% or greater decrease in mean arterial pressure (MAP) received an intravenous (IV) bolus of 100 μg of phenylephrine. If MAP was still 20% lower than the patient's baseline level at least 10 minutes after the first vasopressor treatment, a second bolus of 100 μg of phenylephrine was given.

Measurements

CO was measured simultaneously by esophageal Doppler (COED) and Nexfin (CONXF) at baseline and when blood pressure peaked after an IV 100 μg phenylephrine bolus. Comparisons were then made between the two devices to evaluate the ability of the Nexfin device to track changes in CO.

Main Results

66 pairs of data were obtained. Mean COED and CONXF were 4.7 ± 1.8 L/min and 5.6 ± 2.0 L/min, respectively. There was a significant relationship between COED and CONXF (r2 = 0.82; P < 0.001). The agreement between COED and CONXF was 0.88 ± 0.86 L/min (Bland Altman). The mean percent error (Critchley and Critchley) of CONXF versus COED was 37%. Trending analysis found a 94% concordance between changes in COED and CONXF after phenylephrine administration.

Conclusions

Intraoperative CO measurement using the Nexfin device has a strong correlation with CO measured by esophageal Doppler.

Introduction

In recent years there has been increasing interest in perioperative hemodynamic management through the incorporation of cardiac output (CO) measurements [1], [2], [3], [4]. Several technologies are now available for minimally invasive or noninvasive CO monitoring in the perioperative setting [5], [6]. However, most of these are either operator-dependent (esophageal Doppler) or require the use of intra-arterial catheters (pulse contour analysis). A new CO monitoring system based on the volume-clamp method (Nexfin; BMEYE B.V, Amsterdam, The Netherlands) was recently proposed for noninvasive and continuous CO monitoring. This method uses the area under the systolic part of the blood pressure waveform as input into an algorithm incorporating patient-specific aortic vascular characteristics to calculate beat-to-beat stroke volume (SV) and CO [7], [8]. This device is noninvasive, relatively simple, and nonoperator-dependent [7], and it has been tested in healthy volunteers during orthostasis and for optimization of cardiac resynchronization therapy [9], [10]. It has also been compared with thermodilution CO measurements in 25 awake patients after coronary artery bypass surgery [11]. All of these previous studies suggest that Nexfin CO readings have the potential to be used for intraoperative hemodynamic optimization. Currently we lack data focusing on the accuracy and trending abilities of this device during general anesthesia. Moreover, pulse contour analysis methods may be impacted by the administration of vasopressors [12], [13], [14] such as phenylephrine [15].

The esophageal Doppler is a minimally invasive hemodynamic monitoring device that measures beat-to-beat blood flow in the descending aorta. Cardiac output is then determined by multiplying the cross-sectional area of the aorta by blood flow velocity integrated over time [16], [17]. Hemodynamic optimization using Doppler-derived CO measurements leads to a decrease in perioperative morbidity and in postoperative intensive care unit (ICU) length of stay [18], [19]. This device was an acceptable surrogate for an invasive CO trending monitor in studies that evaluated the accuracy of new CO monitors [20], [21] and in studies focusing on fluid responsiveness [22], [23].

The goals of our study were to compare the CO measuring capabilities of the Nexfin device with those of the esophageal Doppler during general anesthesia and after phenylephrine administration.

Section snippets

Patients

After Institutional Review Board approval from the University of California, Irvine Medical Center and written, informed consent, 25 patients undergoing abdominal or orthopedic surgery in the supine position were enrolled. Six patients were classified as ASA physical status 1, 16 were ASA physical status 2, and three patients were ASA physical status 3. Eleven patients underwent lower leg surgery, 5 had urologic surgery, 6 patients had rectal surgery, and three had a hip replacement. Exclusion

Results

Twenty-five patients (15 men and 10 women, age 41 ± 12 yrs, weight 92 ± 17 kg, and height 172 ± 18 cm) were enrolled in our study. Seventeen patients received one bolus of 100 μg of phenylephrine, while 8 patients received two phenylephrine boluses. Consequently, 66 pairs of CO data were obtained, including 33 pairs before the IV phenylephrine bolus and 33 pairs after the phenylephrine bolus. The quality of the arterial waveform from the Nexfin device was classified as good or excellent in all

Discussion

This study is the first to evaluate the accuracy and tracking abilities of CONXF during surgery and to show clinically acceptable agreement and strong tracking abilities for CO measurements between the Nexfin and esophageal Doppler after phenylephrine administration. These data suggest that the Nexfin device was not impacted by changes in vasomotor tone (direct result of phenylephrine administration).

Cardiac output monitoring is of major importance during surgery; recent studies suggest that CO

Acknowledgment

We would like to thank Shen-yi Yang for his assistance in data collection and analysis.

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    Supported by departmental funding only.

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