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Critical Care Nurse. 2004;24: 74-78
Copyright © 2004 by the American Association of Critical-Care Nurses.
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Protocols for Practice

Measuring Cardiac Output: Intermittent Bolus Thermodilution Method

Anna Gawlinski, RN, DNSc, CS-ACNP


Anna Gawlinski is a clinical nurse specialist in the cardiac care unit and cardiac observation unit at UCLA Medical Center and is an assistant professor of nursing at the UCLA School of Nursing, Los Angeles, Calif.

To purchase reprints, contact The InnoVision Group, 101 Columbia, Aliso Viejo, CA 92656. Phone, (800) 809-2273 or (949) 362-2050 (ext 532); fax, (949) 362-2049; e-mail, reprints{at}aacn.org.


Q What are the physiological principles underlying the intermittent bolus thermodilution (TDCO) method of determining cardiac output?

The TDCO method is the one clinicians use most often to measure cardiac output. It is based on the principles of dilution. A known quantity of an indicator (ie, a contrast agent) is injected into the bloodstream. Blood flow and blood volume are calculated by measuring the concentration of the indicator downstream at a distal arterial site at selected times. The TDCO method uses a cold solution to create a thermal deficit as a variant of the indicator-dilution method. A bolus of sterile solution (ie, the injectate) that is colder than the patient s blood is injected into the proximal port of a pulmonary artery catheter located in the right atrium. In the atrium, the injectate mixes with the blood and passes through the tricuspid valve into the right ventricle. A thermistor within the catheter senses the change in blood temperature as the blood passes the catheter tip located in the pulmonary artery.1 A curve that shows the change in temperature over time is calculated by a computer and converted into a measurement of cardiac output. Cardiac output is inversely proportional to the area under the curve.

The normal cardiac output curve has a rapid smooth upstroke and a gradual downstroke (Figure 1Go). A small area under the curve indicates a high cardiac output. The faster blood flows through the heart, the earlier the peak and sharper the drop, because the catheter senses temperature change over a short period. A low cardiac output results in a larger area under the curve. When blood flows slowly (low cardiac output), the area under the curve (temperature change over time) is greater because the catheter senses changes in temperature over a longer period. The curves vary according to the patient’s clinical condition and according to deviations in technique (Figure 2Go).



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Figure 1 An ideal thermodilution curve. Administration of the injectate is characterized by a rapid upslope to a peak, a gradual downslope, and an exponential decay of the thermal signals. The cardiac output computer begins integration of the area under the thermodilution curve at the instant of injection and terminates integration when the exponential decay reaches a value of about 30%. The computer then extrapolates the exponential decay to baseline. In this way, any artifact introduced by recirculation of indicator is minimized.

 


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Figure 2 A, Variations in the normal cardiac output curve seen in certain clinical conditions. B, Abnormal cardiac output curves that will produce an erroneous cardiac output value.

Reprinted with permission from Love M, Lough ME, Bloomquist J. Cardiovascular laboratory assessment and diagnostic procedures. In: Thelan LA, Davie JK, Urden LD. Textbook of Critical Care Nursing: Diagnosis and Management. St Louis, Mo: CV Mosby;1990:246.

 
Concerns about contamination of prefilled syringes of injectate and warming of injectate due to handling led to the design of closed delivery systems (Figure 3Go). The closed system is designated for use with a pulmonary artery catheter and a cardiac output computer or with iced and room-temperature injectate. The closed system also incorporates a flow-through temperature probe that measures the temperature of the injectate near the site of injection. The obvious advantages are that closed systems do not require preparation of individual syringes, eliminate inefficiencies, and reduce multiple entries into a sterile system.2



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Figure 3 Schematic illustration of the closed injectate delivery system for use with iced injectate for determination of cardiac output.

Reprinted with permission from Abbott Critical Care, Mountain View, Calif.

 
Q: How accurate is the TDCO method?

The accuracy of the method is related to how closely the observed signal (ie, measurement of cardiac output) matches an accepted standard value. Forrester et al3 found a correlation coefficient of 0.993 between a mechanical pump with a known flow and TDCO measurements. In other studies4–6 with flowmeters, correlation coefficients were 0.97 to 1.0. Other researchers have used the direct Fick method as the gold standard for measurement of cardiac output. The Fick principle states that the amount of a substance taken up by the body per unit of time is equal to the arterial level of the substance minus the venous level of the substance multiplied by the flow.6,7 Cardiac output can be calculated by the Fick method by dividing the amount of oxygen consumed by the body by the arterial-venous oxygen difference.8 Numerous studies4,9–14 have addressed the correlation between the direct Fick method and the TDCO method. In all but 2 studies,15,16 the correlations between values obtained with the 2 methods were 0.91 to 0.98.6 The TDCO method is an acceptable substitute for the Fick method or the indicator-dilution method.

Many of the derived hemodynamic indexes and the clinical therapies for critically ill patients depend on accurate measurement of cardiac output. Critical care nurses routinely use the TDCO method to measure cardiac output in critically ill patients and are responsible for the accuracy and analysis of the obtained values. Several technical considerations must be understood in order to minimize the potential for error. These include the position of the pulmonary artery catheter, volume and temperature of the injectate, the phase in the respiratory cycle for administration of the injectate, the patient’s body position, effects of concomitant intravenous infusions, and the effect of positive end-expiratory pressure. Even under ideal circumstances, TDCO measurements have a 10% error.17,18

Q: Is the continuous cardiac output (CCO) method as accurate is the TDCO method?

Clinical studies have also compared the accuracy of the CCO and the TDCO methods. These studies are synthesized and critiqued in the "Annotated Bibliography" section of the research-based protocol on measurement of cardiac output.19 Although the studies report good correlations (0.84 to 0.94) between measurements obtained with the 2 methods, comparisons between CCO and TDCO values have intrinsic methodological issues. The TDCO method itself is not a gold standard for measurement of cardiac output. Under ideal circumstances, TDCO measurements have a 10% error rate related to operator error, temperature transduction, and instrument inaccuracies. Studies that compare values obtained with the CCO method with values obtained with an inaccurate gold standard such as the TDCO method may lead to erroneous estimation of the accuracy of the CCO device. Further studies are necessary to compare CCO values with more precise measurement of cardiac output (such as those obtained by using the Fick or the indicator-dilution method) in a variety of critically ill patients. Such confirmatory studies are necessary to verify the accuracy of CCO technology.

Other methodological problems limit the generalizability of these studies to other critically ill populations. The majority of the studies were done during periods of hemodynamic stability in patients who had had coronary artery bypass graft surgery. Many of these studies used small sample sizes (N = 12 to 35) and multiple observations. Therefore, measurements within each study were not completely independent of one another. For example, if a subject in a study had some characteristic that led to errors in measurement, multiple measurements in that subject would lead to overrepresentation and possibly negative bias in the results. Using larger sample sizes and limiting the number of data points per patient would control for this possible variation. Power analysis was not used to determine appropriate sample size (see the "Annotated Bibliography" in the protocol19 for more details). Rigorous studies that control for the issues just described are needed in critically ill patients to establish the accuracy of newer technologies of noninvasive measurements of cardiac output.

Q: What is the procedure for obtaining a TDCO measurement?

For accurate TDCO curves, the signal-to-noise ratio must be adequate for the cardiac output monitor to sense a change in temperature over time. The signal is the temperature difference between the injectate and the patient’s blood; the noise is the cycling variation in blood temperature. The difference between the temperature of the injectate and the temperature of the patient’s blood should be 10°C.2 Theoretically, 10 mL of iced injectate produces a greater signal-to-noise ratio than does 10 mL of room-temperature injectate or smaller volumes (eg, 5 mL) of either iced or room-temperature injectate. Use of room-temperature injectate or smaller volumes of injectate may decrease the temperature difference (signal) and may yield erroneous values for cardiac output. In most normothermic patients, 5 mL of iced injectate can be used if fluid restriction is warranted. Before using a smaller volume, clinicians must verify that the values obtained with the smaller volume are comparable to values obtained with a larger volume.

• To ensure the validity and reliability of the measurement, check the following:

– position of the pulmonary artery catheter,
computation constant,
– catheter size,
– temperature of the injectate,
– volume of injectate, 10 mL (or 5 mL if iced), and
– patient’s body position.

• Use appropriate TDCO technique:

– Inject 10 mL within 4 seconds; 5 mL, within 2 seconds.
– Administer the injectate when the patient is at end-expiration.
– Obtain 3 measurements.
– Assess the cardiac output curve.
– Average values that are within 10% of the median value.
– Starting at baseline, a normal cardiac output curve has a smooth rapid upstroke and a gradual downstroke.

Q: What further research on measurement of cardiac output is needed?

Although many research studies have been done on measurement of cardiac output and on newer methods, additional investigation and replication are needed. Further research is needed to do the following:

Note

This article was first published in Critical Care Nurse April 2000.

This article is based on the protocol Cardiac Output Monitoring by Anna Gawlinski. It was taken from the Hemodynamic Monitoring series (Product #170709) of AACN’s Protocols for Practice. Protocols can be obtained from AACN, 101 Columbia, Aliso Viejo, CA 92656-1491, (800) 899-AACN, (949) 362-2000. Product #170704: $11, AACN members; $14, nonmembers.

References

  1. Kallasian KG, Raffin, TA. The technique of thermodilution cardiac output measurement. J Crit Illness. 1996;11:249–256.
  2. Gardner PE, Bridges ET. Hemodynamic monitoring. In: Woods SL, Sivarajan-Froelicher ES, Halpenny CJ, Motzer SU, eds. Cardiac Nursing. 3rd ed. Philadelphia, Pa: JB Lippincott; 1995:424–458.
  3. Forrester JS, Ganz W, Diamond G, McHugh T, Chonette DW, Swan HJC. Thermodilution cardiac output determination with a single flow-directed catheter. Am Heart J. 1972;83:306–311.[Medline]
  4. Hoel BL. Some aspects of the clinical use of thermodilution in measuring cardiac output. Scand J Clin Lab Invest. 1978;38:383–388.[Medline]
  5. Sanmarco ME, Philips CM, Marquez LC, Hall D, Davila JA. Measurement of cardiac output by thermodilution. Am J Cardiol. 1971;29:54–58.
  6. Sommers MS, Woods SL, Courtade MA. Issues in methods and measurement of thermodilution cardiac output. Nurs Res. 1993;42:228–233.[Medline]
  7. Ganong WF. Review of Medical Physiology. 16th ed. East Norwalk, Conn: Appleton & Lange; 1993.
  8. Berne RM, Levy MN. Cardiovascular Physiology. 6th ed. St Louis, Mo: Mosby-Year Book; 1992.
  9. Kadota LT. Theory and application of thermodilution cardiac output measurement: a review. Heart Lung. 1985;14;605–616.[Medline]
  10. Wyse SD, Pfitzner J, Rees A, Lincoln JCR, Branthwaite MA. Measurement of cardiac output by thermal dilution in infants and children. Thorax. 1975;30:262–265.[Abstract/Free Full Text]
  11. Freed MD, Keane JF. Cardiac output measured by thermodilution in infants and children. J Pediatr. 1978;92:39–42.[Medline]
  12. Branthwaite MA, Bradley RD. Measurement of cardiac output by thermodilution in man. J Appl Physiol. 1968;24:434–438.[Free Full Text]
  13. Vandermoten P, Bernard R, de Hamptinne J, Gillet JM, Lenaers A. Cardiac output monitoring during the acute phase of myocardial infarction: accuracy and precision of the thermodilution method. Cardiology. 1977;62:291–295.[Medline]
  14. Zisserman D, Mantle JA, Smith LR, Rogers WJ, Russell RO Jr, Rackley CE. Clinical comparison of thermal dilution cardiac output to the Fick and angiographic methods [abstract]. Clin Res. 1979;27:736A.
  15. Hodges M, Downs JB, Mitchell LA. Thermodilution and Fick cardiac index determinations following cardiac surgery. Crit Care Med. 1975;3:182–184.[Medline]
  16. Stawicki JJ, Holford FD, Michelson EL, Josephson ME. Multiple cardiac output measurements in man. Chest. 1979;76:193–197.[Abstract/Free Full Text]
  17. Moore FA, Haenel JB, Moore EE. Alternatives to Swan-Ganz cardiac output monitoring. Surg Clin North Am. 1991;71:699–721.[Medline]
  18. Burchell SA, Yu M, Takiguchi SA, Ohta RM, Myers SA. Evaluation of a continuous cardiac output and mixed venous oxygen saturation catheter in critically ill surgical patients. Crit Care Med. 1997;25:388–391.[Medline]
  19. Gawlinski A. Cardiac Output Monitoring. Aliso Viejo, Calif: American Association of Critical Care Nurses: 1997.



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