Comparison Between Mixed Venous Oxygen Saturation and Thermodilution Cardiac Output in Monitoring Patients with Severe Heart Failure Treated with Milrinone and Dobutamine

Authors: Stefanie Nuñez, MD, Alan Maisel, MD, Division of Cardiology, Veterans Affairs Medical Center and University of California, San Diego, Calif.

BackIntroduction

Since the introduction of the Swan-Ganz pulmonary artery catheter, thermodilution cardiac output (COtd) has become the accepted method for monitoring patients with heart failure in the intensive care unit.[1] Although COtd is in theory the most direct bedside measure of hemodynamic status, most authors agree that this technique-dependent method estimates cardiac output at best to within 15% to 20% of true output.[2,3] It is widely known that thermodilution cardiac output measurements are particularly inaccurate in low-flow states and in the presence of tricuspid regurgitation or left-to-right shunt. In addition, COtd does not reflect the interaction between oxygen delivery and tissue oxygen extraction.[4,5] Recent studies have focused on the use of oxygen transport variables as therapeutic targets in critically ill patients and as predictors of survival.[4-9] Mixed venous oxygen saturation (SvO2), both as an intermittent and continuous measure, has been proposed as an alternative to conventional hemodynamic monitoring.

Several studies have attempted with varying success to show the usefulness of monitoring mixed venous oxygen saturation in critically ill patients. Some groups suggest that the ability of SvO2 to serve as a therapeutic indicator is highly dependent on patient characteristics; others dismiss SvO2 in favor of variables more representative of metabolic rate.[4-11] Although many of these studies have evaluated the direct relation between thermodilution cardiac output and mixed venous oxygen saturation in various patient populations, no one has reported a comparison of COtd with SvO2 as a measure of hemodynamic response during trials of inotropic therapy.

The purpose of this study was to determine whether SvO2 has added benefit over COtd for monitoring hemodynamic response to inotropic therapy in patients with heart failure in whom thermodilution technique is known to be less accurate. To this end we compared the relation between COtd and increasing drug dose with the relation between SvO2 and increasing drug dose during therapeutic trials of milrinone and dobutamine in patients with severe heart failure.

BackDiscussion

Accurate and reliable measures of hemodynamics are an essential part of the evaluation and treatment of patients with heart failure in the intensive care unit. Although thermodilution cardiac output has become the accepted measure of hemodynamic status, it is least accurate in precisely those patients in whom invasive monitoring is critical. Patients with heart failure not only have low cardiac output but also frequently have secondary tricuspid regurgitation,[12] two variables that have been associated with inaccurate COtd. Mixed venous oxygen saturation has emerged as an attractive alternative for hemodynamic monitoring. Although many studies have examined the relation between COtd and SvO2, little consensus has developed as to which measurement should be used during evaluation and therapy. Our study set out to show the usefulness of SvO2 monitoring compared with routine thermodilution techniques during trials of two inotropic drugs, milrinone and dobutamine, known to be of benefit in patients with congestive heart failure.

The relation between thermodilution cardiac output and mixed venous oxygen saturation has been debated by several groups. Jain et al.[4] found a good linear correlation coefficient in the subset of patients with cardiac index <2 L/min/m2 and SvO2 <55% in a group with symptomatic heart failure and no evidence of tricuspid regurgitation; however, in the same group of patients we found a nonlinear relation between SvO2 and cardiac output over a wide range of confidence intervals. Our study shows that mixed venous oxygen saturation was more highly correlated with increasing drug dose compared with thermodilution cardiac output in a group of patients with severely depressed systolic function and some degree of tricuspid regurgitation during trials of milrinone therapy; furthermore SvO2 was a more reproducible measure of hemodynamic status compared with COtd in the same group of patients. In addition, SvO2 was comparable to thermodilution cardiac output as a measure of hemodynamic status in a similar group of patients during trials of dobutamine.

Our results support the hypothesis that monitoring SvO2 has added benefit over COtd, particularly in patients with severe heart failure (left ventricular ejection fraction <30%). One study found SvO2 to be a better predictor of survival than cardiac index in a group of patients with acute myocardial infarction because of its ability to reflect peripheral tissue oxygen demand and use.[9] In addition, several studies have suggested that SvO2 monitoring may be the preferred method for early recognition of hemodynamic change in the critically ill patient.[6,13,14]

We also found that SvO2 was a more reproducible measure of hemodynamic status than COtd in the milrinone trials; in the dobutamine trials the differences observed in reproducibility of measurements was not significant. These data support previous studies that showed thermodilution cardiac output measurements are less reproducible than other methods for determining cardiac output because of the many sources of error in thermodilution technique.[3]

Limitations

This was a retrospective study in which there was interobserver and intraobserver variability; however, the data acquired were part of a prospective study on the efficacy of milrinone treatment in heart failure. The assumption that changes in SvO2 represent actual changes in cardiac function is not entirely correct, because the data did not include arterial oxygen saturation, hemoglobin level, and total body oxygen consumption; however, patients did receive supplemental oxygen, had no gross bleeding, and were at bedrest generally afebrile and without seizures over the short period of time encompassing the therapeutic trials. Finally, although SvO2 correlates well with increasing dose of inotrope, the authors do not mean to suggest that it is possible to predict SvO2 or the magnitude of improvement in hemodynamic status at any particular dose of inotropic therapy.

Clinical Significance

We believe that insufficient attention is paid to SvO2 and that it is rarely used for the purpose of intensive care monitoring compared with the widespread use of COtd. The knowledge that a significant relation exists between SvO2 and increasing dose of inotropic drug in patients with severe heart failure and tricuspid regurgitation has practical value for physicians monitoring these patients in the intensive care unit. We believe this study demonstrates the worth of SvO2 in detecting hemodynamic change during trials of inotropic therapy and that this parameter may in fact be more reproducible than traditional thermodilution methods. This appears to be especially true in patients with very low levels of cardiac output and in patients with significant tricuspid regurgitation, two cases in which thermodilution measurements are notoriously unreliable.