Arterial, Mixed Venous or Central Venous Hemogasometry and End Tidal CO2 in Dogs under Different Hemodynamic States
DOI:
https://doi.org/10.22456/1679-9216.80007Keywords:
acid-base balance, hypotension, venous oxygen saturation, blood analysis.Abstract
Background: Hemogasometric analysis is used in the interpretation of acid-base balance (ABB) and to access pulmonary ventilation. Already mixed venous oxygen saturation obtained at pulmonary artery correlates with tissue oxygenation. However, both samples can be difficult to access because of the difficulties in arterial and pulmonary catheterization. The aim of this study was to evaluate the feasibility of replacing the arterial and mixed venous bloods, the end tidal pressure of carbon dioxide (EtCO2) and central venous blood in the analysis of pulmonary ventilation, tissue oxygenation and ABB in dogs under different hemodynamic states.
Material, Methods & Results: Nine dogs were used with an average weight of 19.6 ± 1.3 kg, anesthetized with isoflurane at 1.4 V% diluted on oxygen 60% (Baseline), and subsequently undergoing mechanical ventilation (MV) and the hypodinamic state (Hypo) with isoflurane at 3.5V% and mean arterial pressure (MAP) lower than 50 mmHg and hyperdynamic state (Hyper) by dobutamine infusion at 5 μg/kg/min and with MAP 30% higher than baseline. For each time allowed a 15 min of stabilization by each hemodynamic status. Simultaneously were collected samples of 0.6 mL of arterial blood by metatarsal artery, mixed and central venous blood by pulmonary artery and right atrium for hemogasometric analysis. To access lung function we correlated and compared the EtCO2 values obtained by gas analyzer with expired carbon dioxide pressure in the arterial blood (PaCO2), mixed venous blood (PmvCO2) and central venous blood (PcvCO2). For the interpretation of tissue oxygenation we correlated and compared the values of mixed (SmvO2) and central (ScvO2) venous oxygen saturation. For the acid-base balance we used the correlation of potencial hydrogen (pH); carbon dioxide pressure (PCO2); bicarbonate ion (HCO3-); base excess (BE); anion GAP (AG); sodium ions (Na+), chlorine ions (Cl-), potassium ions (K+) and ionized calcium (iCa) of arterial (a) mixed venous (mv) and central venous (CV) bloods. Statistical analysis was performed using ANOVA-RM followed by Dunnet test for differences between times and Tukey’s test for differences among the samples (P ≤ 0.05). Pearson correlation analysis was performed using linear regression and for comparison methods we used the Bland-Altman analysis The EtCO2 values correlated (r = 0.87) and were according to Bland-Altman analysis with PaCO2 values (mean difference of -1.6 ± 2,9 mmHg for PaCO2. There were no differences (P ≤ 0.05) from SmvO2 and ScvO2. ScvO2 correlated (r = 0.91) with SmvO2 at different hemodynamic states and with a mean difference of -0.4 ± 2.5%. Both venous bloods were correlated with the analysis of arterial blood acid-base balance and electrolytes in different hemodynamic states. However, the ionized calcium levels were 40% lower in arterial blood.
Discussion: EtCO2 measurement depends of monitor technology and proper pulmonar ventilation and perfusion. In this study the limiting factor in replacing the PaCO2 hair EtCO2 was spontaneous ventilation because in this state pulmonary ventilation is compromissed. With the use of MV was possible get up similar results in the pulmonar function analysis using the EtCO2 and PaCO2. The use of central venous blood instead mixed venous blood at oxygen saturation analysis provided adequate estimate this parameter. This being easier and less invasive technique. ABB was possible with all samples with own reference values for venous and arterial samples. This is an interesting result for critical patients where the arterial sample is difficult. In electrolytes the sample was indifferent except for calcium because pH interfere in this values. It was conclude that the values of EtCO2 and central venous blood are correlated and can replace arterial and mixed venous bloods in the analysis of lung function, tissue oxygenation and acid base balance.
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Alenka S., Alenka N. & Butinar J. 2006. The relationship between end-tidal CO2, mean arterial blood pressure and neuroendocrine response in canine haemorrhagic shock. Acta Veterinaria. 56(4): 295-304.
Andriolo A., Ballarati C.A.F., Galoro C.A.O., Mendes M.E., Melo M.R. & Sumita N.M. 2014. Recomendações da sociedade brasileira de patologia clínica/ medicina laboratorial (SBPC/ML):Coleta e Preparo da Amostra Biológica. Barueri: Manole : Minha Editora, 261p.
Blasco V., Leone M., Textoris J., Visintini P., Albanèse J. & Martin C. 2008. Venous oximetry: physiology and therapeutic implications. Annales Françaises D’Anesthésie et de Réanimation. 27(1): 74-82.
Brainard B.M., Boller M. & Fletcher D.J. 2012. RECOVER evidence and knowledge gap analysis on veterinary CPR. Part 5: Monitoring. Journal of Veterinary Emergency and Critical Care. 22(1): 65-84.
Conti-Patara A., Araújo Caldeira J., Mattos-Junior E., Carvalho H.S., Reinoldes A., Pedron B.G., Patara M., Francisco Talib M.S., Faustino M., Oliveira C.M. & Cortopassi S.R. 2012. Changes in tissue perfusion parameters in dogs with severe sepsis/septic shock in response to goal-directed hemodynamic optimization at admission to ICU and the relation to outcome. Journal of Veterinary Emergency and Critical Care. 22(4): 409-418.
Crapo R. O. 1994. Pulmonary-Function Testing. Current Concepts. 331(1): 25-30.
De Morais H. A. 2008. Metabolic acid-base disorders in the critical care unit. The Veterinary Clinics of North America. Small Animal Practice. 38(3): 559–574.
Dibartola S.P. 2007. Fluid, electrolyte and acid base disorders in small animal practice. 3rd edn. St. Louis: Saunders Elsevier, 661 p.
Duarte J.J., Pontes J.C.D.V., Gomes O.M., Silva G.V.R., Gardenal N., Silva A.F. & Viola M.D.Z. 2010. Correlação entre gasometria atrial direita e índice cardíaco no pós-operatório de cirurgia cardíaca. Revista Brasileira de Cirugia Cardiovasular. 25(2): 160-165.
Hayes G.M., Mathews K., Boston S. & Dewey C. 2011. Low central venous oxygen saturation is associated with increased mortality in critically ill dogs. Journal of Small Animal Practice. 52(8): 433-440.
Hopper K. & Epstein S. E. 2012. Incidence, nature, and etiology of metabolic acidosis in dogs and cats. Journal of Veterinary Internal Medicine / American College of Veterinary Internal Medicine. 26(5): 1107-1114.
Hopper K., Epstein S.E., Kass P.H. & Mellema M.S. 2014. Evaluation of acid-base disorders in dogs and cats presenting to an emergency room. Part 1: Comparison of three methods of acid-base analysis. Journal of Veterinary Emergency and Critical Care. 24(5): 493-501.
Ilkiw J.E., Rose R.J. & Martin I.C. 1991. A Comparison of Simultaneously Collected Arterial, Mixed Venous, Jugular Venous and Cephalic Venous Blood Samples in the Assessment of Blood-Gas and Acid-Base Status in the Dog. Journal of Veterinary Internal Medicine. 5(5): 294-298.
Kruljc P., Alenka N., Neli V. & Butinar J. 2003. Relation between end-tidal and arterial carbon dioxide partial pressure during general anaesthesia with spontaneous breathing and controlled ventilation in dogs – an experimental study. Acta Veterinaria (Beograd). 53(5): 283-296.
Machado F.R., Carvalho R.B., Freitas F.G., Sanches L.C., Jackiu M., Mazza B.F., Assunção M., Guimarães H.P. & Amaral J.L. 2008. Saturação venosa central e mista de oxigênio no choque séptico: existe diferença clinicamente relevante? Revista Brasileira de Terapia Intensiva. 20(3): 398-404.
Marx G. & Reinhart K. 2006. Venous oximetry. Current Opinion in Critical Care.12(3): 263–268.
Proulx J. 1999. Respiratory monitoring: arterial blood gas analysis, pulse oximetry, and end-tidal carbon dioxide analysis. Clinical Techniques in Small Animal Practice. 14(4): 227-230.
Ralston S.H. 1985. Venous and arterial blood gases during and after cardiopulmonary resuscitation in dogs. The American Journal of Emergency Medicine. 3(2): 132-136.
Reinhart K., Rudolph T., Bredle D.L., Hannemann L. & Cain S.M. 1989. Comparison of central-venous to mixedvenous oxigen saturation during changes in oxigen supply/demand. Chest. 95(6): 1216-1221.
Rieser T.M. 2013. Arterial and Venous Blood Gas Analyses. Topics in Company Animal Medicine. 28(3): 86-90.
Stillion R. S & Fletcher D.J. 2012. Admission base excess as a predictor of transfusion requirement and mortality in dogs with blunt trauma: 52 cases (2007-2009). Journal of Veterinary Emergency and Critical Care. 22(5): 588-594.
Teixeira-Neto F.J., Carregaro A.B., Mannarino R., Cruz M.L. & Luna S.P. 2002. Comparison of a sidestream capnograph and a mainstream capnograph in mechanically ventilated dogs. Journal of the American Veterinary Medical Association. 22(11): 1582-1585.
Valezi A.C., Mali Junior J., Oliveira R.G. & Storti L.H. 2003. Correlação entre as pressões parciais de CO2 no ar expirado e no sangue arterial, em porcas submetidas a pneumoperitônio. Revista do Colégio Brasileiro de Cirurgiões. 30(3): 177-182.
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