Chest
Volume 84, Issue 4, October 1983, Pages 418-422
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Cardiac Output By Thermodilution Technique: Effect of Injectate’s Volume and Temperature on Accuracy and Reproducibility in the Critically III Patient

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We compared determinations of cardiac output using various combinations of injectate volumes and temperatures to results obtained with 10 ml of iced (0°C) injectate (standard technique) in 33 critically ill patients. The use of a 10-ml injectate at room temperature resulted in comparable reproducibility (12.7 vs 10.8 percent; not significant) and a small and nonsignificant error (–0.013 ± 0.543 L/min). Five milliliters at room temperature resulted in markedly decreased reproducibility (17.9 vs 8.9 percent; p<0.05); however, the error associated with the technique was still not significant (0.136 ± 0.829 L/min). When a 5-ml injectate at 0°C was used, a reproducibility comparable to that of 10 ml at 0°C was obtained (12.3 vs 7.5 percent; not significant). The results underestimated values obtained with 10 ml at 0°C (–0.360 ± 0.857 L/minute); however, the difference did not reach statistical significance. The use of 3 ml at 0°C was associated with a substantial increase in variability, with a coefficient of variation of 32.0 percent (10.4 percent for 10 ml of iced injectate; p<0.01); however, the differences between the average value of cardiac output obtained with this technique and the standard technique were only minimal (error, –0.063 ± 0.455; not significant). We reached the following conclusions: (1) the use of 10 ml at room temperature and 5 ml at 0°C as the indicator for thermodilution determinations of cardiac output results in small and insignificant differences in reproducibility and accuracy from the standard technique; (2) five milliliters at room temperature and 3 ml at 0°C are associated with markedly decreased reproducibility; however, the error in values for cardiac output obtained with these techniques is not statistically significant; and (3) the ability to use injectate at room temperature and in small volume should substantially simplify the technique, lowering its cost, and should prevent volume overloading.

Section snippets

Population of Patients

A validation of our thermodilution technique against dye dilution was performed in 15 men and 12 women between the ages of 26 and 66 years. All patients had undergone diagnostic cardiac catheterization for cardiac symptoms at the University of California Irvine Medical Center. Twenty-two patients had coronary arterial disease, and two patients had rheumatic mitral valvular disease. One patient had a combination of coronary arterial disease and mitral valvular prolapse, one patient had an aortic

RESULTS

Table 1 presents the reproducibility of the dye dilution and thermodilution techniques for measuring cardiac output. Shown in the table are the mean values for cardiac output, intrapatient SD, and coefficient of variation for each technique and the number of determinations. Using the first two, first three, and all five determinations of cardiac output by the thermodilution technique produced results which were not less reproducible than that using two measurements by the dye dilution method

DISCUSSION

Although the thermodilution technique for the measurement of cardiac output has been widely used, there are few data available dealing with its accuracy and reproducibility in the clinical setting. In the setting of the cardiac catheterization laboratory, where the study was performed in hemodynamically stable, mildly sedated patients, our results confirm previous reports2,3 demonstrating close agreement between thermodilution and dye dilution for measurement of cardiac output. The

ACKNOWLEDGMENT

We are greatly indebted to the nurses of the Cardiac Care Unit and the Catheterization Laboratory of the University of California Irvine Medical Center for their invaluable help in this study. We also thank Michael Mumford, M.D., and Johnathan Tobis, M. D., for their support and Mrs. Dione Fosdick for her excellent secretarial assistance.

REFERENCES (12)

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Manuscript received March 7; revision accepted May 31.

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