The Use of the Ratio between the Veno-arterial Carbon Dioxide Difference and the Arterial-venous Oxygen Difference to Guide Resuscitation in Cardiac Surgery Patients with Hyperlactatemia and Normal Central Venous Oxygen Saturation

Wei Du, Yun Long, Xiao-Ting Wang, Da-Wei Liu, Wei Du, Yun Long, Xiao-Ting Wang, Da-Wei Liu

Abstract

Background: After cardiac surgery, central venous oxygen saturation (ScvO 2 ) and serum lactate concentration are often used to guide resuscitation; however, neither are completely reliable indicators of global tissue hypoxia. This observational study aimed to establish whether the ratio between the veno-arterial carbon dioxide and the arterial-venous oxygen differences (P(v-a)CO 2 /C(a-v)O 2 ) could predict whether patients would respond to resuscitation by increasing oxygen delivery (DO 2 ).

Methods: We selected 72 patients from a cohort of 290 who had undergone cardiac surgery in our institution between January 2012 and August 2014. The selected patients were managed postoperatively on the Intensive Care Unit, had a normal ScvO 2 , elevated serum lactate concentration, and responded to resuscitation by increasing DO 2 by >10%. As a consequence, 48 patients responded with an increase in oxygen consumption (VO 2 ) while VO 2 was static or fell in 24.

Results: At baseline and before resuscitative intervention in postoperative cardiac surgery patients, a P(v-a)CO 2 /C(a-v)O 2 ratio ≥1.6 mmHg/ml predicted a positive VO 2 response to an increase in DO 2 of >10% with a sensitivity of 68.8% and a specificity of 87.5%.

Conclusions: P(v-a)CO 2 /C(a-v)O 2 ratio appears to be a reliable marker of global anaerobic metabolism and predicts response to DO 2 challenge. Thus, patients likely to benefit from resuscitation can be identified promptly, the P(v-a)CO 2 /C(a-v)O 2 ratio may, therefore, be a useful resuscitation target.

Conflict of interest statement

Conflict of Interest: None declared.

Figures

Figure 1
Figure 1
Study flow chart. PiCCO: Pulse contour continuous cardiac output; ScvO2: Central venous oxygen saturation; DO2: Oxygen delivery.
Figure 2
Figure 2
Receiver operating characteristic (ROC) curve. ROC curve comparing the P(v−a)CO2/C(a−v)O2 ratio to an increase in oxygen consumption (VO2) brought about by increasing oxygen delivery (DO2) by >10% in cardiac surgical patients. Area under the curve: 0.77 ± 0.10, P = 0.032, The cutoff of the P(v−a)CO2/C(a−v)O2 ratio value was 1.6 for predicting cardiac surgery patients in whom VO2 would increase when DO2 increased by >10%, resulting in a sensitivity of 68.8% and a specificity of 87.5%.

References

    1. Leavy JA, Weil MH, Rackow EC. ‘Lactate washout’ following circulatory arrest. JAMA. 1988;260:662–4.
    1. Gasparovic H, Plestina S, Sutlic Z, Husedzinovic I, Coric V, Ivancan V, et al. Pulmonary lactate release following cardiopulmonary bypass. Eur J Cardiothorac Surg. 2007;32:882–7.
    1. James JH, Luchette FA, McCarter FD, Fischer JE. Lactate is an unreliable indicator of tissue hypoxia in injury or sepsis. Lancet. 1999;354:505–8.
    1. Levy B, Gibot S, Franck P, Cravoisy A, Bollaert PE. Relation between muscle Na+K+ATPase activity and raised lactate concentrations in septic shock: A prospective study. Lancet. 2005;365:871–5.
    1. Fink MP. Cytopathic hypoxia. Mitochondrial dysfunction as mechanism contributing to organ dysfunction in sepsis. Crit Care Clin. 2001;17:219–37.
    1. Pope JV, Jones AE, Gaieski DF, Arnold RC, Trzeciak S, Shapiro NI, et al. Multicenter study of central venous oxygen saturation (ScvO (2)) as a predictor of mortality in patients with sepsis. Ann Emerg Med. 2010;55:40–6e1.
    1. Monnet X, Julien F, Ait-Hamou N, Lequoy M, Gosset C, Jozwiak M, et al. Lactate and venoarterial carbon dioxide difference/arterial-venous oxygen difference ratio, but not central venous oxygen saturation, predict increase in oxygen consumption in fluid responders. Crit Care Med. 2013;41:1412–20.
    1. Friedman G, De Backer D, Shahla M, Vincent JL. Oxygen supply dependency can characterize septic shock. Intensive Care Med. 1998;24:118–23.
    1. Perz S, Uhlig T, Kohl M, Bredle DL, Reinhart K, Bauer M, et al. Low and “supranormal” central venous oxygen saturation and markers of tissue hypoxia in cardiac surgery patients: A prospective observational study. Intensive Care Med. 2011;37:52–9.
    1. Figge J, Jabor A, Kazda A, Fencl V. Anion gap and hypoalbuminemia. Crit Care Med. 1998;26:1807–10.
    1. Mekontso-Dessap A, Castelain V, Anguel N, Bahloul M, Schauvliege F, Richard C, et al. Combination of venoarterial PCO2 difference with arteriovenous O2 content difference to detect anaerobic metabolism in patients. Intensive Care Med. 2002;28:272–7.
    1. Randall HM, Jr, Cohen JJ. Anaerobic CO2 production by dog kidney in vitro. Am J Physiol. 1966;211:493–505.
    1. Rhodes A, Lamb FJ, Malagon I, Newman PJ, Grounds RM, Bennett ED. A prospective study of the use of a dobutamine stress test to identify outcome in patients with sepsis, severe sepsis, or septic shock. Crit Care Med. 1999;27:2361–6.
    1. Sladen RN. Temperature and ventilation after hypothermic cardiopulmonary bypass. Anesth Analg. 1985;64:816–20.
    1. Tulla H, Takala J, Alhava E, Huttunen H, Kari A. Hypermetabolism after coronary artery bypass. J Thorac Cardiovasc Surg. 1991;101:598–600.
    1. Zwischenberger JB, Kirsh MM, Dechert RE, Arnold DK, Bartlett RH. Suppression of shivering decreases oxygen consumption and improves hemodynamic stability during postoperative rewarming. Ann Thorac Surg. 1987;43:428–31.
    1. Bihari D, Smithies M, Gimson A, Tinker J. The effects of vasodilation with prostacyclin on oxygen delivery and uptake in critically ill patients. N Engl J Med. 1987;317:397–403.
    1. Jeppsson A, Ekroth R, Friberg P, Kirnö K, Milocco I, Nilsson F, et al. Renal effects of amino acid infusion in cardiac surgery. J Cardiothorac Vasc Anesth. 2000;14:51–5.
    1. Jacobson ED. Effects of histamine, acetylcholine, and norepinephrine on gastric vascular resistance. Am J Physiol. 1963;204:1013–7.
    1. Durán WN, Renkin EM. Oxygen consumption and blood flow in resting mammalian skeletal muscle. Am J Physiol. 1974;226:173–7.
    1. McCord JM. Oxygen-derived free radicals in postischemic tissue injury. N Engl J Med. 1985;312:159–63.
    1. Duke T, Butt W, South M, Karl TR. Early markers of major adverse events in children after cardiac operations. J Thorac Cardiovasc Surg. 1997;114:1042–52.
    1. Cheifetz IM, Kern FH, Schulman SR, Greeley WJ, Ungerleider RM, Meliones JN. Serum lactates correlate with mortality after operations for complex congenital heart disease. Ann Thorac Surg. 1997;64:735–8.
    1. Murray D, Grant D, Murali N, Butt W. Unmeasured anions in children after cardiac surgery. J Thorac Cardiovasc Surg. 2007;133:235–40.
    1. Cheung PY, Chui N, Joffe AR, Rebeyka IM, Robertson CM. Western Canadian Complex Pediatric Therapies Project, Follow-up Group. Postoperative lactate concentrations predict the outcome of infants aged 6 weeks or less after intracardiac surgery: A cohort follow-up to 18 months. J Thorac Cardiovasc Surg. 2005;130:837–43.
    1. Amark K, Berggren H, Björk K, Ekroth A, Ekroth R, Nilsson K, et al. Blood cardioplegia provides superior protection in infant cardiac surgery. Ann Thorac Surg. 2005;80:989–94.
    1. Bendjelid K, Treggiari MM, Romand JA. Transpulmonary lactate gradient after hypothermic cardiopulmonary bypass. Intensive Care Med. 2004;30:817–21.
    1. Pearse RM, Hinds CJ. Should we use central venous saturation to guide management in high-risk surgical patients? Crit Care. 2006;10:181.
    1. Rivers E, Nguyen B, Havstad S, Ressler J, Muzzin A, Knoblich B, et al. Early goal-directed therapy in the treatment of severe sepsis and septic shock. N Engl J Med. 2001;345:1368–77.
    1. Du W, Liu DW, Wang XT, Long Y, Chai WZ, Zhou X, et al. Combining central venous-to-arterial partial pressure of carbon dioxide difference and central venous oxygen saturation to guide resuscitation in septic shock. J Crit Care. 2013;28:1110e1–5.
    1. Van der Linden P, Rausin I, Deltell A, Bekrar Y, Gilbart E, Bakker J, et al. Detection of tissue hypoxia by arteriovenous gradient for PCO2 and pH in anesthetized dogs during progressive hemorrhage. Anesth Analg. 1995;80:269–75.
    1. Zhang H, Vincent JL. Arteriovenous differences in PCO2 and pH are good indicators of critical hypoperfusion. Am Rev Respir Dis. 1993;148:867–71.
    1. Lamia B, Monnet X, Teboul JL. Meaning of arterio-venous PCO2 difference in circulatory shock. Minerva Anestesiol. 2006;72:597–604.
    1. Vallet B, Teboul JL, Cain S, Curtis S. Venoarterial CO(2) difference during regional ischemic or hypoxic hypoxia. J Appl Physiol (1985) 2000;89:1317–21.
    1. Durward A, Tibby SM, Skellett S, Austin C, Anderson D, Murdoch IA. The strong ion gap predicts mortality in children following cardiopulmonary bypass surgery. Pediatr Crit Care Med. 2005;6:281–5.
    1. Bellomo R, Lipcsey M, Calzavacca P, Haase M, Haase-Fielitz A, Licari E, et al. Early acid-base and blood pressure effects of continuous renal replacement therapy intensity in patients with metabolic acidosis. Intensive Care Med. 2013;39:429–36.
    1. Van der Linden P, Gilbart E, Engelman E, Schmartz D, Vincent JL. Effects of anesthetic agents on systemic critical O2 delivery. J Appl Physiol (1985) 1991;71:83–93.
    1. Miwa K, Mitsuoka M, Takamori S, Hayashi A, Shirouzu K. Continuous monitoring of oxygen consumption in patients undergoing weaning from mechanical ventilation. Respiration. 2003;70:623–30.

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