eISSN: 1897-4252
ISSN: 1731-5530
Kardiochirurgia i Torakochirurgia Polska/Polish Journal of Thoracic and Cardiovascular Surgery
Current issue Archive Manuscripts accepted About the journal Supplements Editorial board Reviewers Abstracting and indexing Contact Instructions for authors Ethical standards and procedures
Editorial System
Submit your Manuscript
SCImago Journal & Country Rank
1/2013
vol. 10
 
Share:
Share:

YOUNG CLINICIANS’ FORUM
Correlation between mixed venous blood saturation and cardiac output in patients undergoing cardiac surgery procedures

Bartosz Szurlej
,
Magda Piekarska
,
Dariusz Szurlej
,
Andrzej Węglarzy
,
Tomasz Latusek
,
Ryszard Bachowski

Kardiochirurgia i Torakochirurgia Polska 2013; 10 (1): 79–83
Online publish date: 2013/04/05
Article file
- 15 Szurlej.pdf  [0.70 MB]
Get citation
 
PlumX metrics:
 

Introduction

Cardiac surgery with cardiopulmonary bypass (CPB) is a source of stress reaction and burdens the organism. Also the surgical wounds lead to permanent adrenergic stimulation and pain which requires the use of strong analgesics. The blood supply of the organs begins to be dependent on the CPB and short episodes of blood pressure drops affect the incidence of periods of temporary ischemia in organs. Removing the blood from the operation field by suction leads to erythrocyte damage. Cardiopulmonary bypass is also associated with the risk of organ micro- and macroembolization.

The activation of coagulation (the intrinsic and the extrinsic coagulation pathway), and the fibrinolysis process are the causes of consumptive coagulopathy. Coagulation failure is intensified by heparin. The manifestation of all of the physiological aberrations in the function of the organism is the occurrence of systemic inflammatory response syndrome (SIRS) in every patient after cardiac surgery with the use of CPB [1].

Evaluation of blood oxygen status in patients during cardiac surgery procedures is routinely carried out by oxygen partial pressure (PaO2), carbon dioxide partial pressure (PaCO2) and arterial blood saturation (SaO2). These parameters allow an intermediate assessment of the oxygen delivery. If there were indications for Swan-Ganz catheter (SGC) insertion, it was used during the cardiac surgery operation to monitor the hemodynamic and the gas exchange parameters [2-4]. Initially, we get ten parameters which describe the cardiovascular system efficiency and four parameters of the systemic oxygen transport: mixed venous oxygen saturation (SvO2), dissolved oxygen (DO2), oxygen uptake (VO2) and oxygen extraction ratio (O2ER).

Some of the hemodynamic parameters should be shown as an index value, that means calculated per 1 m2 of the body surface area (BSA). In the case of cardiac output (CO) it is the cardiac index (CI) [5]. By the use of the SGC it is also possible to take samples of the venous blood from the right atrium and samples of the mixed venous blood from the pulmonary artery. Some types of SGC give the ability of continuous monitoring of SvO2. The value of SvO2 shows both the oxygen delivery and the oxygen consumption. This value is dependent on the hemoglobin concentration (CHb), arterial blood saturation and CO [5]. A proper compensation reaction of the decrease of CO is the increase of oxygen extraction (O2ER) from the capillary vessels, which is necessary to keep a constant value of the oxygen uptake (VO2). Oxygen extraction adjustment, depending on the requirement, is especially intensified in life-threatening states; thus decrease of SvO2 may indicate a decrease of CO. Not every patient reacts with an increase of O2ER to a decrease of blood flow. Often severely ill patients are not capable of such an adaptive reaction [6, 7]. In these patients oxygen concentration will not change due to the changes in CO; thus the value of SvO2 will not be a reliable indicator of the blood flow [6].

Aim of the study

The aim of the study was to determine the reliability of the correlation between hemodynamic parameters and indices of tissue oxygenation in patients undergoing cardiac surgery procedures and to assess the correlation between SvO2 and CI in the study group.

Material and methods

A retrospective analysis was performed for 19 patients undergoing cardiac surgery procedures at the 2nd Department of Cardiac Surgery, Medical University of Silesia in Katowice between February 2010 and April 2010. The study inclusion criterion was the requirement for hemodynamic and systemic oxygen transport monitoring by the use of the SGC. The study group is shown in Table I.

In all patients surgical anesthesia was performed by the same method of analgesic anesthesia by using etomidate, fentanyl and pancuronium. Anesthesia was maintained by using isoflurane and during CPB by continuous infusion of propofol and fentanyl.

Dopamine, adrenaline and noradrenaline were used for inotropic support as a monotherapy or in different combinations depending on the circulatory system condition. Values of CI, SvO2, SaO2 and BEecf (base excess in extracellular fluid) were analyzed.

Measurements by the SGC were taken in every patient at three time points: T0 – after the intubation and after the insertion of the SGC; T1 – 15 minutes after discontinuing CPB; and T2 – 30 minutes after admitting the patient to the postoperative unit.

Obtained values were compared with the parameters used for the assessment of intermediate oxygen delivery: PaO2, PaCO2, SaO2 and CHb. DO2, VO2 and O2ER were also analyzed.

Results

Statistical analysis was performed using Statistica PL v.5.0. Data from time points T0 and T2 were analyzed. The analysis did not contain data from time point T1 because of the large range of obtained values.

Increase of the average value of CI after the operation (Fig. 1) in comparison with the value before the operation (p < 0.05) was observed.

In the study group there was a decrease of SvO2 after the operation (Fig. 2) in comparison with the preoperative period (p < 0.05).

In two patients at time point T0 high values of SvO2 were noted: 95% and 96%.

There was a positive correlation between the trends of SvO2 and CI in patients before and after the surgery. The correlation coefficient (r) before the operation (Fig. 3) was 0.38 (p > 0.05) and after the operation (Fig. 4) it was 0.52 (p < 0.05).

The CI increased in 63% of patients, it decreased in 16%, while in 21% of patients it did not change. Correct values of CI in the study group before the operation were noted in 31% of patients and in 69% of patients this value was below the lower reference limit (reference limits: 2.4-4.0 l/min/m2). After the operation CI within the correct reference limits was noted in 42% of patients.

The VO2 after the operation increased in 84% of patients, a decrease was noted in 11%, and in 5% of patients this value did not change (p < 0.05). In 15% of patients before the operation values of VO2 were noted within the reference limits (reference limits: 110-160 ml/min × m2). In 85% of patients the value of VO2 was below the lower reference limit while after the cardiac surgery procedure values within the reference limits were noted in 31% of patients. Values below the lower reference limit were noted in 69% of patients.

An increase of DO2 took place in 58% of patients, a decrease in 37%, and in 5% of patients this value did not change. Before the operation in 90% of patients values below the lower reference limit (reference limits: 520-570 ml/min × m²) were noted. None of the patients had a DO2 within the reference limits after the operation.

The O2ER was within the reference limits (reference limits: 20-30%) in 53% of patients. An increase of O2ER was noted in 84% of patients. After the cardiac surgery procedure an increase of O2ER above the upper reference limit was noted in 58% of patients. In 5% of patients the value of O2ER was below the lower reference limit. Values within the reference limits were noted in 27% of patients.

The BEecf before the operation was below the lower reference limit in 10% of patients and above the upper reference limit in 5% of patients. After the operation BEecf was below the lower reference limit in 53% of patients and above the upper reference limit in 5% of patients.

In 50% of patients the postoperative course was complicated with atrial fibrillation (n = 4), increased postoperative drainage (n = 2), thrombocytopenia (n = 2), infection of the upper respiratory tract (n = 2) and urinary infection (n = 1). There was one death in the study group.

Discussion

The mean value of cardiac index (CI) after cardiac surgery using cardiopulmonary bypass was increased compared with the value before the operation, which leads to a positive result of the surgery. A gradual reduction of the dose of anesthetic drugs, restoration of homeostasis, reverse of the anticoagulant effect of heparin, the transfusion of fluids and effective analgesic therapy ultimately allow stabilization of the cardiovascular system. In some patients postoperatively the cardiac index has decreased or its value did not change. Perhaps that group of patients needed a longer period of time to achieve homeostasis, when the positive outcome of the operation showed its effect.

Many of the patients had a BMI indicating obesity (Table I). We did not analyze in the study group the liver and kidney function, adipose tissue content, serum protein concentration after cardiac operation, fluid balance type or the volume of transfusion fluids. We did not observe in every patient a return to normal values of the cardiac index after the operation. However, it was not surprising. Achieving the correct value of CI in cardiac surgery patients, who have a long-term coronary heart disease or organic changes of the heart, because of, for example, coexisting valvular defects, is a process that occurs gradually and takes time [8]. The correct physiological reaction that we expected in patients after cardiac surgery was an increase of oxygen consumption by tissues. Because hemodilution used during cardiac surgery procedures impacts on the oxygen supply to the tissues, it is highly important to carry out an evaluation of the oxygen transport in patient who undergo these procedures. In patients after the operation there is an increase of the VO2 value. It can be explained by the phenomenon of the body’s reflex hyperemia after ischemia, a phenomenon that is referred to in the literature as the “overshoot effect”. The periodic increase of VO2 is required to compensate the oxygen debt acquired during the operation [6]. Increase of VO2 is related to the growth of the value of O2ER that we observed in our study.

When the metabolism is increased, even normal values of oxygen consumption are not sufficient to maintain the body’s needs and the metabolism enters an anaerobic phase [9]. In most patients after the operation there was a decrease of mixed venous oxygen saturation, which was probably related to inadequate tissue perfusion and anaerobic metabolism of cells. This situation occurs after using cardiopulmonary bypass. After the operation the correct body compensatory response should be based on the increase of CI and VO2 [9, 10].

An increase of VO2 is related to a decrease of SvO2, because the oxygen uptake from blood by the tissues is associated with a decrease of SvO2 [9]. The ability to adapt to the oxygen extraction of the body’s needs is one of the identifying features of a life-threatening condition; thus a reduction of SvO2 may signal a decrease of cardiac output [11]. Not every organism reacts with an increase of O2ER to a decrease in blood flow. In some patients the oxygen concentration will stay in the range of initial values despite the changes in cardiac output, so the final value of SvO2 is not a reliable indicator of blood flow. Some of the patients in the study group responded to a decrease of SvO2 with an increase of cardiac output after the operation [12]. Perhaps the compensatory physiological response after cardiac surgery is the reason for this phenomenon. In these patients an increase of CI and a decrease of SvO2 indicate an accelerated metabolism and higher oxygen demand

[2, 7, 13-15]. Positive correlations between SvO2 and cardiac index before and after the operations were, respectively: r = 0.38 (average correlation) and r = 0.52 (high correlation). We found similar studies in the available literature where the statistical results differ from the material. Krauss et al. presented a very high correlation (r = 0.78) between the values of mixed venous oxygen saturation and cardiac index in patients undergoing heart or lung surgery [16]. Waller et al. when examining patients undergoing coronary artery bypass surgery, with continuous monitoring of SvO2 by SGC, found a strong correlation between changes in SvO2 and CI values: r = 0.69 [17]. The high values of SvO2 at T0 may indicate a leak caused by the change of direction of arterial blood flow (shunting) in peripheral tissues. This phenomenon occurs in states such as sepsis, and cirrhosis of the liver [18]. After excluding the possibility of existence of such diseases in patients, a probable cause of such high values of SvO2 was the admixture of oxygenated blood coming from the alveolar capillaries. To further characterize the patients after determining BMI (28.02 ±2.8 kg/m2) we calculated the rate of BSA. We analyzed the BSA value, which, although it is not very specific, is however a better indicator of metabolic body weight, because it is less influenced by the excess amount of body adipose tissue. In three patients the BSA was greater than 2.0 m2, and these patients had a decrease of SvO2 and a decrease of CI values after surgery.

The values of BEecf were below the lower reference limit, and there was a decrease of DO2. Perhaps the adipose tissue has the main impact on the value of these parameters. That phenomenon is connected with greater cardiovascular burden and the need to use higher doses of medication during the procedure and a longer return to normal body temperature [19-22].

Parameters such as SaO2, PaO2 and PaCO2 do not give the ability of assessing the transport of oxygen through the circulatory system.

Furthermore, the correct values of these parameters do not mean that at the subcellular level the processes involved in the extraction of oxygen proceed physiologically. Only the values of SvO2 and CI obtained with the SGC allow the assessment of the supply of oxygen and its consumption by the tissue.

Results enriched with information such as DO2, VO2 and O2ER can be very useful in treatment of patients with severe conditions, in whom the body is unable to restore homeostasis after surgery [13, 23-25].

Conclusions

1. An increase of CI after the operation in comparison with CI before the operation was observed.

2. In the study group there was a decrease of SvO2 after the operation in comparison with the values of SvO2 before the operation.

3. There was a positive correlation between the trends of SvO2 and CI before and after the cardiac surgery.

4. In the study group there was an increase of VO2 after the operation in comparison with the VO2 before the operation.

5. In the study group there was an increase of O2ER after the operation in comparison with O2ER before the operation.

References

1. Rogowski J, Jarmoszewicz K, Siondalski P, Pawlaczyk R. Opieka pooperacyjna po zabiegach kardiochirurgicznych. Choroby Serca i Naczyń 2006; 3: 115-122.

2. Duarte JJ, Pontes JC, Gomes OM, Silva GV, Gardenal N, Silva AF, Viola MD. Correlation between right atrial venous blood gasometry and cardiac index in cardiac surgery postoperative period. Rev Bras Cir Cardiovasc 2010; 25: 160-165.

3. Harvey S, Young D, Brampton W, Cooper AB, Doig G, Sibbald W, Rowan K. Pulmonary artery catheters for adult patients in intensive care. Cochrane Database Syst Rev 2006; 3: CD003408.

4. Neya K. Swan-Ganz catheter (pulmonary artery catheter). Kyobu Geka 2009; 62 (8 Suppl): 677-681.

5. Aitkenhead AR, Smith G, Rowbotham DJ. Anestezjologia Polish 2nd edition. Kübler A (ed.). Urban & Partner, Wrocław 2008.

6. Marino PL. Intensywna terapia. Polish 1st edition. Kübler A (ed.). Urban &Partner, Wrocław 1991.

7. Jain A, Shroff SG, Janicki JS, Reddy HK, Weber KT. Relation between mixed venous oxygen saturation and cardiac index. Nonlinearity and normalization for oxygen uptake and hemoglobin. Chest 1991; 99: 1403-1409.

8. Wesslén O, van der Linden J, Ekroth R, Joachimsson PO, Nordgren L, Nyström SO. Myocardial recovery after cardiac surgery: a study of hemodynamic performance and electrophysiology during the first 18 postoperative hours. J Cardiothorac Anesth 1990; 4: 672-80.

9. Routsi C, Vincent JL, Bakker J, De Backer D, Lejeune P, d’Hollander A, Le Clerc JL, Kahn RJ. Relation between oxygen consumption and oxygen delivery in patients after cardiac surgery. Anesth Analg 1993; 77: 1104-1110.

10. Gerbode F, Norlander O, Herzog P, Johansson L, Osborn JJ. Oxygen uptake during anesthesia in patients before and after total body perfusion. Ann Surg 1964; 159: 481-488.

11. Andersen MN, Senning Å. Studies in oxygen consumption during extracorporeal circulation with a pump-oxygenator. Ann Surg 1958; 148: 59-65.

12. Pölönen P, Hippeläinen M, Takala R, Ruokonen E, Takala J. Relationship between intra-and postoperative oxygen transport and prolonged intensive care after cardiac surgery: a prospective study. Acta Anaesthesiol Scand 1997; 41: 810-817.

13. Videcoq M, Desmonts JM. What is the role of monitoring of mixed venous blood saturation in cardiac surgery? Ann Fr Anesth Reanim 1989; 8: 696-702.

14. Richard C, Thuillez C, Pezzano M, Bottineau G, Giudicelli JF, Auzepy P. Relationship between mixed venous oxygen saturation and cardiac index in patients with chronic congestive heart failure. Chest 1989; 95: 1289-1294.

15. Tulla H, Takala J, Alhava E, Huttunen H, Kari A. Hypermetabolism after coronary artery bypass. J Thorac Cardiovasc Surg 1991; 101: 598-600.

16. Krauss XH, Verdouw PD, Hughenholtz PG, Nauta J. On-line monitoring of mixed venous oxygen saturation after cardiothoracic surgery. Thorax 1975; 30: 636-643.

17. Waller JL, Kaplan JA, Bauman DI, Craver JM. Clinical evaluation of a new fiberoptic catheter oximeter during cardiac surgery. Anesth Analg 1982; 61: 676-679.

18. Maclntyre NR, Branson RD, Wentylacja mechaniczna. Polish 1st edition. Gaszyński W (ed.). Wydawnictwo ADI, Łódź 2008.

19. Francischetti EA, Genelhu VA. Obesity-hypertension – an ongoing pandemic. Int J Clin Pract 2007; 61: 269-280.

20. Molfino A, Rossi Fanelli F, Laviano A. Sympathetic nervous system activity may link hyperphagia and fat deposition in human obesity. Am J Physiol Endocrinol Metab 2007; 293: E1129.

21. Collis T, Devereux RB, Roman MJ, de Simone G, Yeh J, Howard BV, Fabsitz RR, Welty TK. Relations of stroke volume and cardiac output to body composition: the strong heart study. Circulation 2001; 103: 820-825.

22. Troisi RJ, Weiss ST, Parker DR, Sparrow D, Young JB, Landsberg L. Relation of obesity and diet to sympathetic nervous system activity. Hypertension 1991; 17: 669-677.

23. Shah MR, Hasselblad V, Stevenson LW, Binanay C, O’Connor CM, Sopko G, Califf RM. Impact of the pulmonary artery catheter in critically ill patients: meta-analysis of randomized clinical trials. JAMA 2005; 294: 1664-1670.

24. Sommers MS, Stevenson JS, Hamlin RL, Ivey TD, Russell AC. Mixed venous oxygen saturation and oxygen partial pressure as predictors of cardiac index after coronary artery bypass grafting. Heart Lung 1993; 22: 112-120.

25. Bartlett R. Fizjologia stanów krytycznych. Wydawnictwo Lekarskie PZWL, Warszawa 1999.
Copyright: © 2013 Polish Society of Cardiothoracic Surgeons (Polskie Towarzystwo KardioTorakochirurgów) and the editors of the Polish Journal of Cardio-Thoracic Surgery (Kardiochirurgia i Torakochirurgia Polska). This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License (http://creativecommons.org/licenses/by-nc-sa/4.0/), allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
Quick links
© 2024 Termedia Sp. z o.o.
Developed by Bentus.