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* From the Medical Intensive Care Unit, Bicêtre Hospital, University Paris XI, France.
Correspondence to: Frédéric Michard, MD, PhD, Service de Réanimation Médicale, CHU de Bicêtre, 78 rue du Général Leclerc, 94275, le Kremlin-Bicêtre cedex, France; e-mail: michard.frederic{at}free.fr
| Abstract |
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Design: Prospective clinical study.
Setting: Medical ICU of a university hospital (20 beds).
Patients: Thirty-six patients with septic shock.
Interventions: Volume loading and dobutamine infusion.
Measurements and results: Hemodynamic parameters were evaluated in triplicate by the transpulmonary thermodilution technique: (1) before and after 66 fluid challenges in 27 patients, and (2) before and after 28 increases in dobutamine infusion rate in 9 patients. Volume loading induced a significant (p < 0.001) increase in central venous pressure (CVP) from 10 ± 4 to 13 ± 4 mm Hg, in GEDV index from 711 ± 164 to 769 ± 144 mL/m2, in stroke volume index (SVI) from 36 ± 12 to 42 ± 12 mL/m2, and in cardiac index (CI) from 3.4 ± 1.1 to 3.9 ± 1.2 L/min/m2 (mean ± SD). Changes in GEDV index were correlated (r = 0.72, p < 0.001) with changes in SVI, while changes in CVP were not. The increase in SVI was > 15% in 32 of 66 instances (positive response). The preinfusion GEDV index was lower (637 ± 134 mL/m2 vs 781 ± 161 mL/m2, p < 0.001) in the cases of positive response, and was negatively correlated with the percentage increase in GEDV index (r = - 0.65, p < 0.001) and in SVI (r = - 0.5, p < 0.001). Dobutamine infusion induced an increase in SVI (32 ± 11 mL/m2 vs 35 ± 12 mL/m2, p < 0.05) and in CI (2.8 ± 0.6 L/min/m2 vs 3.2 ± 0.6 L/min/m2, p < 0.001) but no significant change in CVP (13 ± 3 mm Hg vs 13 ± 3 mm Hg) and in GEDV index (823 ± 221 mL/m2 vs 817 ± 202 mL/m2).
Conclusion: In patients with septic shock, our findings demonstrate that, in contrast to CVP, the transpulmonary thermodilution GEDV index behaves as an indicator of cardiac preload.
Key Words: cardiac preload central venous pressure dobutamine fluid responsiveness global end-diastolic volume septic shock transpulmonary thermodilution volume expansion
| Introduction |
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Various methods for preload determination are commonly used today, principally the measurement of the central venous pressure (CVP) and pulmonary artery wedge pressure6 ; however, cardiac filling pressures are not always accurate indicators of ventricular preload because of erroneous readings of pressure tracings,7 discrepancy between measured and transmural pressures,8 and changes in ventricular compliance.9 Therefore, other parameters have been proposed to assess cardiac preload at the bedside, such as right ventricular end-diastolic volume evaluated by fast response pulmonary artery catheters,10 11 12 left ventricular end-diastolic area measured by echocardiography,13 14 15 and the intrathoracic blood volume evaluated by the double-indicator (thermo-dye) dilution technique.16 17 18
The benefit/risk ratio of pulmonary artery catheter is a subject of ongoing controversy,19 20 21 and echocardiography is an operator-dependent technique, which is not available in all ICUs and is not appropriate for monitoring of hemodynamically unstable patients. Moreover, the estimation of left ventricular end-diastolic area by echocardiography does not always accurately reflect left ventricular end-diastolic volume22 and hence left ventricular preload. Although effective at the bedside, the double-indicator dilution technique is relatively time consuming (due to preparation of the indocyanine green solution), cumbersome, and expensive. More recently, the single-indicator (cold bolus) dilution, also called the transpulmonary thermodilution, has been proposed as an alternative technique for assessing cardiac preload.23 24 Indeed, the mathematical analysis of the transpulmonary thermodilution curve25 26 allows the assessment of the largest volume of blood contained in the four heart chambers, called the global end-diastolic volume (GEDV).23 24 Most septic patients with acute circulatory failure are instrumented with a central venous line (at least for vasoactive agents administration) and estimation of BP using a cuff is commonly inaccurate in shock states, such that the use of an arterial cannula is recommended.27 In this context, transpulmonary thermodilution simply requires the use of a specific thermodilution-tipped arterial catheter, and GEDV measurements the central venous injection of a cold saline solution bolus. The GEDV is a parameter closely related to the intrathoracic blood volume, since the intrathoracic blood volume is composed of the GEDV and the pulmonary blood volume23 24 ; however, the clinical value of the transpulmonary thermodilution GEDV as an indicator of cardiac preload remains to be proved.
The aim of the present study was to test the hypothesis that the GEDV behaves as an indicator of cardiac preload in patients with septic shock. In this hypothesis, the GEDV should increase with volume loading but not with dobutamine, and the lower the preinfusion GEDV, the more marked should be the hemodynamic effects of volume loading.
| Materials and Methods |
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Patients
We studied 36 patients with a diagnosis of septic shock. This group comprised 28 men and 8 women (age range, 32 to 89 years; mean ± SD age, 61 ± 16 years). All patients were receiving mechanical ventilation and vasopressors (dopamine, > 5 µg/kg/min, or norepinephrine). Twelve patients also received dobutamine. Inclusion criteria were as follows: (1) septic shock as defined by the criteria of the American College of Chest Physicians/Society of Critical Care Medicine Consensus Conference,28
(2) instrumentation with a central venous (jugular or subclavian) catheter and a thermodilution femoral arterial catheter (PulsioCath PV 2015L20; Pulsion Medical Systems; Munich, Germany) for hemodynamic monitoring, and (3) the clinical requirement for a volume challenge of 500 mL of 6% hydroxyethylstarch or for an increase in dobutamine infusion rate according to the attending physician, at any time during the course of septic shock.
Hemodynamic Measurements
Patients were studied in a supine position, and zero pressure was measured at the midaxillary line. The CVP was recorded throughout the respiratory cycle and measured at end-expiration. Cardiac output and GEDV were evaluated in triplicate by transpulmonary thermodilution using a commercially available device (PiCCO; Pulsion Medical Systems). After injection of a cold saline solution bolus in the superior vena cava, a thermistor in the tip of the femoral arterial catheter is used to measure the downstream temperature changes. The cardiac output is then calculated by the analysis of the thermodilution curve using the Stewart-Hamilton algorithm. The measurement of cardiac output by transpulmonary thermodilution has been previously validated against the pulmonary thermodilution and the Fick method.29
30
31
32
33
The monitor (PiCCO; Pulsion Medical Systems) also calculates the mean transit time and the exponential downslope time of the transpulmonary thermodilution curve. The product of cardiac output and mean transit time is the volume of distribution of the thermal indicator.25
This volume of distribution, the so-called "intrathoracic thermal volume," is made up of the intrathoracic blood volume and the extravascular lung water. The product of cardiac output and exponential downslope time is the "pulmonary thermal volume," which is composed of the pulmonary blood volume and the extravascular lung water26
; therefore, the GEDV is calculated by the monitor as the difference between the intrathoracic thermal volume and the pulmonary thermal volume.23
24
Cardiac index (CI), stroke volume index (SVI), GEDV index, and systemic vascular resistance index (SVRI) were calculated using standard formula. The reproducibility (SD/mean of three successive measurements) of cardiac output and GEDV measurement was 4 ± 2% and 5 ± 3%, respectively (mean ± SD).
Study Protocol
Measurements were performed before and immediately after volume loading using 500 mL of 6% hydroxyethylstarch (Hestéril; Frésénius Kabi; Sévres, France) over a short period (< 30 min) or, in patients who were already receiving dobutamine, before and 20 to 30 min after an increase in dobutamine infusion rate. In all instances, the decision regarding volume loading and an increase in dobutamine infusion rate was made by the treating physician. Ventilatory settings and dosages of vasopressors were held constant.
Statistical Analysis
Results were expressed as mean ± SD. The hemodynamic effects of volume loading and of dobutamine infusion were assessed using a Wilcoxon nonparametric rank-sum test. Volume challenges were divided into three equal GEDV groups (low, intermediate, and high) according to the preinfusion GEDV index value. The fluid challenges associated with the lowest preinfusion values of GEDV constituted the low GEDV group. Similarly, the fluid challenges associated with the highest preinfusion values of GEDV constituted the high GEDV group. The remaining fluid challenges were considered to belong to the intermediate GEDV group. Assuming that a 15% change in SVI was needed for clinical significance, a positive response to volume loading was defined by an increase in SVI > 15%. A 2 x 3 contingency table was used to compare the rates of positive response between the three (low, intermediate, and high) GEDV groups. A nonparametric Mann-Whitney U test was used to compare hemodynamic parameters before volume loading in the cases of positive and negative responses to volume loading. Linear correlations were tested using the Spearman rank method. A p value < 0.05 was considered statistically significant.
| Results |
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Fluid Challenges
Sixty-six fluid challenges were studied in 27 patients. Fifteen patients received two fluid challenges, and 12 patients received three fluid challenges. The hemodynamic effects of volume loading are presented in Table 1
and Figure 1
. Volume loading induced a significant (p < 0.05) decrease in heart rate and a significant (p < 0.001) increase in CVP, GEDV index, SVI, CI, and mean arterial pressure. The preinfusion GEDV index was significantly correlated (r = - 0.65, p < 0.001) with the percentage increase in GEDV index such that the lower GEDV index before volume loading, the greater was the increase in GEDV index (Fig 2
). Volume loading-induced changes in GEDV index were significantly correlated with changes in SVI (r = 0.72, p < 0.001) [Fig 3
], changes in CI (r = 0.67, p < 0.001), and changes in mean arterial pressure (r = 0.55, p < 0.001). In contrast, volume loading-induced changes in CVP were not correlated in anyway with changes in SVI, CI, and mean arterial pressure.
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The preinfusion GEDV index ranged from 413 to 611 mL/m2 (mean, 546 ± 52 mL/m2) in the low GEDV group (n = 22), from 615 to 781 mL/m2 (mean, 681 ± 60 mL/m2) in the intermediate GEDV group (n = 22), and from 816 to 1,174 mL/m2 (mean, 907 ± 86 mL/m2) in the high GEDV group (n = 22). The rate of positive response to volume loading was significantly different between the three groups (p = 0.0013): 77% in the low GEDV group, 45% in the intermediate GEDV group, and 23% in the high GEDV group (Fig 4 ). The rate of positive response was 20% (2 of 10 instances) and 0% (0 of 5 instances) when the preinfusion GEDV index was > 900 mL/m2 and 950 mL/m2, respectively; conversely, the rate of positive response was 89% (8 of 9 instances) and 100% (4 of 4 instances) when the GEDV index was < 550 mL/m2 and < 500 mL/m2, respectively.
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| Discussion |
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According to the Frank-Starling mechanism, the greater the increase in preload, the greater should be the increase in stroke volume.35 We also observed a significant relationship between volume loading-induced changes in GEDV index and changes in SVI such that the greater the increase in GEDV index, the greater was the increase in SVI (Fig 3) .
Interestingly, the preinfusion GEDV index was also significantly correlated with the percentage increase in SVI that resulted from the volume loading. In this regard, the preinfusion GEDV index was significantly lower in the cases of patients who had a positive response compared with those who had a negative response to volume loading. These findings are consistent with echocardiographic studies14 15 reporting lower preinfusion left ventricular end-diastolic area in responders compared with nonresponders to volume loading, and a significant relationship between the preinfusion left ventricular end-diastolic area and the percentage increase in SVI in response to volume loading.
Because the slope of the relationship between preload and stroke volume depends on ventricular contractility,35 the preinfusion cardiac preload is not the only factor influencing the response to volume loading.34 However, when preload is low, an increase in preload usually induces a significant increase in stroke volume whatever the ventricular function; similarly, when preload is high, a significant increase in stroke volume is rarely observed (Fig 5 ). In contrast, for the intermediate values of preload, the increase in stroke volume depends more on ventricular function (ie, on the slope of the curve) than on the preinfusion cardiac preload (Fig 5) . In this regard, the rate of response to volume loading was high (77%) in patients with a low preinfusion GEDV index, low (23%) in patients with a high preinfusion GEDV index, and approximately 50% in the intermediate group (Fig 4) . These findings are consistent with other studies demonstrating that a positive response to volume loading is frequently observed in patients with a low (< 90 mL/m2) preinfusion right ventricular end-diastolic volume index, rarely observed when the right ventricular end-diastolic volume index is > 140 mL/m2, and unpredictable for the intermediate values.10 11 12 Therefore, our findings are quite consistent with cardiac physiology, in agreement with previous clinical studies,10 11 12 and suggest that the easily obtainable GEDV may help in the decision-making process concerning volume loading. However, it must be noted that our results have been observed in a population of patients with septic shock, and hence that they cannot necessarily be extrapolated to other clinical situations.
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As expected, volume loading induced a significant increase in CVP; however, the volume loading-induced changes in CVP were not proportional to the changes in stroke volume and the preinfusion CVP was not significantly lower in cases of positive response than in cases of negative response to volume loading. These findings are in agreement with previous reports,10 11 12 17 18 34 and confirm the limited value of CVP both as an indicator of cardiac preload and as a predictor of fluid responsiveness. Like CVP, the pulmonary artery wedge pressure is widely used to guide fluid therapy in critically ill patients.6 Although the pulmonary artery wedge pressure is probably useful to identify patients at risk of acquiring pulmonary edema, several clinical studies have already emphasized its little value in accurately reflecting cardiac preload9 40 or predicting fluid responsiveness.34 Because our patients were not instrumented with a pulmonary artery catheter, we were not able to confirm these previous studies.
An important consideration concerns the possible mathematical coupling between GEDV and cardiac output since both of these parameters are derived from the same thermodilution curve.41 Such mathematical coupling may be advocated to explain, at least in part, some of the significant relationships reported in the present study. Nevertheless, McLuckie and Bihari42 have shown that the mean transit time of an indicator may change independently of changes in cardiac output. Perhaps more importantly, in patients receiving a volume load, we observed a positive relationship between changes in GEDV index and changes in mean arterial pressure. Because GEDV and mean arterial pressure cannot be mathematically coupled (these parameters are evaluated by independent techniques), and because volume loading does not increase systemic vascular tone (systemic vascular resistance remained unchanged), such a relationship confirms that the greater was the increase in GEDV index, the more marked was the increase in SVI. Furthermore, by increasing CI with dobutamine and observing GEDV index to be unchanged, we have also demonstrated in the present study that the GEDV index and the CI can change independently. Our findings are consistent with those of another study43 that reported large changes in cardiac output without any contemporary change in GEDV during esmolol administration in cardiac surgery patients. In summary, these findings strongly support the notion that the relationships reported in the present study are not due to a mathematical coupling but are related to the physiologic relationship between an indicator of preload (ie, GEDV) and the stroke volume.
Since most patients with septic shock are instrumented with central venous and arterial lines, the transpulmonary thermodilution technique can be regarded as a less invasive method than pulmonary artery catheterization to assess cardiac preload. Moreover, in contrast to echocardiography, transpulmonary thermodilution provides an operator-independent determination of cardiac output and cardiac preload with a reproducibility close to 5%, as often as is necessary.
To summarize, our study demonstrates that the GEDV increases with volume loading but not with dobutamine, and the lower the preinfusion GEDV, the more marked the hemodynamic effects of volume loading. Therefore, in patients with septic shock, we conclude that the GEDV behaves as an indicator of cardiac preload. Further studies are required to confirm the usefulness of transpulmonary thermodilution for assessing cardiac preload in other clinical situations.
| Acknowledgements |
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| Footnotes |
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Received for publication October 24, 2002. Accepted for publication April 3, 2003.
| References |
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