Newsletter

Sign up for our quarterly newsletter and get the newest articles from acutecaretesting.org

Printed from acutecaretesting.org

Article

June 2002

Transcutaneous carbon dioxide monitoring: Applications in the operating room

The intraoperative monitoring of the partial pressure of carbon dioxide in arterial blood (pCO2) is used to assess the adequacy of ventilation and guide clinical interventions. 

Although end-tidal CO2 monitoring remains the most frequently used non-invasive technology in the intraoperative setting to provide a continuous estimate of pCO2, given its potential for inaccuracy with alterations in pulmonary function, there is a continued need for other non-invasive means of monitoring pCO2

Although transcutaneous (TC) CO2 monitoring has been used in the ICU setting, there are little data regarding its use in the intraoperative setting. This manuscript reviews the reports regarding the intraoperative applications of TC-CO2 monitoring and discusses the potential intraoperative applications of this non-invasive monitoring modality.

INTRODUCTION

The monitoring of the partial pressure of carbon dioxide (pCO2) in the arterial blood is used to assess the adequacy of ventilation during both spontaneous and controlled ventilation.

Although the gold standard for monitoring pCO2 remains intermittent arterial blood gas (ABG) analysis, ABGs provide only an intermittent sample of what is often a dynamic and rapidly changing value. To overcome such problems, non-invasive monitors are used both in the ICU and intraoperatively to provide a continuous estimate of pCO2.

Routine monitoring in the operating room includes end-tidal CO2 (ET-CO2) measurement; however, several patient-related issues such as ventilation-perfusion mismatch may influence the correlation of the ET-CO2 with pCO2 [1,2]. Grenier et al have demonstrated that there is a significant influence of patient positioning on the correlation between ET-CO2 and pCO2 as well as a significant variation or instability of the gradient over time, thereby questioning the utility of ET-CO2 monitoring during neurosurgical procedures [3].

Transcutaneous (TC) CO2 devices provide another option for the continuous, non-invasive estimation of pCO2. Although these devices have been shown to be accurate in infants, children, and adolescents in the Neonatal or Pediatric ICU setting [4,5], there remains limited information regarding the intraoperative applications of TC-CO2 monitoring.

INTRAOPERATIVE APPLICATIONS -  Adults

Because of its effects on cerebral blood flow and intracranial pressure, the intraoperative control of pCO2 can be of great significance during neurosurgical procedures. Given the inherent inaccuracies noted in the study of Grenier et al [3] and the importance of monitoring pCO2 during neurosurgical procedures, we carried out a prospective study to determine the accuracy of ET- and TC-CO2 monitoring during neurosurgical procedures in adults [6].

The patient population included patients 18 years of age or older presenting for neurosurgical procedures in which intra-arterial access was deemed necessary by the attending anesthesiologist. ET-CO2 was measured using standard intraoperative, infrared spectroscopy with a sidestream aspirator connected at the elbow between the endotracheal tube (ETT) and the anesthesia circuit.

Prior to placement, the electrode was cleaned, a new membrane applied, and calibration performed according to the manufacturer’s recommendations. The working temperature of the electrode was set at 45 °C.

ABGs were obtained as clinically indicated during the surgical procedure and compared to the values from the two non-invasive monitors. The cohort for the study included 30 adults ranging in age from 18 to 76 years and in weight from 49 to 130 kilograms undergoing a craniotomy for various indications.

No patient was receiving an inotropic agent or adrenergic agonist. None of the patients had significant tissue edema or manifested signs of a low cardiac output state. Fifty-seven sample sets (pCO2, ET-CO2, and TC-CO2) were obtained from the 30 patients, Fig. 1. 

The actual pCO2 ranged from 26 to 62 mmHg. The ET-CO2-to-pCO2 difference was 6.1 ± 5.6 mmHg, while the TC-CO2-to-pCO2 difference was 3.7 ± 2.9 mmHg (p=0.005).

The difference between the pCO2 and ET-CO2 was 3 mmHg or less in 17 of 57 values, while the difference between the pCO2 and TC-CO2 was 3 mmHg or less in 35 of 57 values (p = 0.002, odds ratio of 3.942). The difference between the pCO2 and ET-CO2 was 5 mmHg or less in 31 of 57 values, while the difference between the pCO2 and TC-CO2 was 5 mmHg or less in 47 of 57 values (p = 0.00139, odds ratio of 3.743).

Linear regression analysis of ET-CO2 versus pCO2 revealed a slope of 0.381, r value = 0.5531, and r2 = 0.3025. Linear regression analysis of TC-CO2 versus pCO2 revealed a slope of 1.17, r value = 0.8824, and r2 = 0.7786.

Trans car dio mon fig 1

FIG. 1. Difference in pCO2 (ABG) in relation to TC and ET grouped by  ≤3 mmHg; ≤5 mmHg and > 5 mmHg (n = 57).

INTRAOPERATIVE APPLICATIONS – Infants and Children

ET-CO2 monitoring may also be notoriously inaccurate in infants and smaller children given their smaller tidal volumes and additional problems imposed by the type of mechanical ventilator used (continuous versus intermittent gas flow) and the site of ET-CO2 monitoring (distal or proximal end of the ETT) [7,8]. The latter is true regardless of the clinical scenario (Pediatric/Neonatal ICU or intraoperative care).

We carried out a prospective study to determine the accuracy of ET- and TC-CO2 monitoring during intraoperative care in infants and children [9]. The patient population included patients 18 years of age or younger for whom intra-arterial access was deemed necessary by the attending anesthesiologist. ET- and TC-CO2 were measured as in our previously described intraoperative study (see above).

The cohort for the study included 30 patients ranging in age from 6 months to 15 years and in weight from 4.7 to 73 kilograms. Sixty-four sample sets (pCO2, ET-CO2, and TC-CO2) were obtained from the 30 patients. The ET-CO2-to-pCO2 difference was 4.4 ± 7.1 mmHg, while the TC-CO2-to-pCO2 difference was 2.8 ± 2.9 mmHg.

The difference between the pCO2 and ET-CO2 was 3 mmHg or less in 37 of 64 values, while the difference between the pCO2 and TC-CO2 was 3 mmHg or less in 49 of 64 values (p<0.05). The difference between the pCO2 and ET-CO2 was 5 mmHg or less in 55 of 64 values, while the difference between the pCO2 and TC-CO2 was 5 mmHg or less in 62 of 64 values. (Fig. 2.).

Trans car dio mon fig 2

Fig. 2. Difference in pCO2 (ABG) in relation to TC and ET grouped by  ≤3 mmHg;  ≤5 mmHg and > 5 mmHg (n = 64).

Linear regression analysis of ET-CO2 versus pCO2 revealed a slope of 0.434 ± 0.007, r value = 0.8761, and r2 = 0.7676, while linear regression analysis of TC-CO2 versus pCO2 revealed a slope of 0.914, r value = 0.9140, and r2 = 0.8972.

The true utility of TC-CO2 monitoring is demonstrated by one of the patients in the current study who developed intraoperative bronchospasm. Despite an ET-CO2 of only 70 mmHg, the TC-CO2 was reading 110 mmHg with a pCO2 that was 122 mmHg.

DISCUSSION

Since its inception, TC-CO2 monitoring has received the greatest use in the neonatal population. Previous studies have also validated the accuracy of TC-CO2 monitoring in the Pediatric ICU population with respiratory failure of various etiologies and following cardiothoracic surgical procedures [4,5].

In these studies, TC-CO2 monitoring proved especially efficacious in settings where ventilation-perfusion disturbances or other patient factors can be expected to interfere with the gradient between the ET and pCO2 [24,5].

Intraoperative monitoring

We have also found that intraoperative TC-CO2 monitoring can be a clinically useful adjunct to standard intraoperative monitoring techniques. As outlined above in our two intraoperative studies, we noted, in both clinical intraoperative scenarios (adult and pediatric patients), that TC-CO2 monitoring was more accurate and provided a closer estimation of pCO2 than ET-CO2 monitoring.

To date, there remains limited other information concerning intraoperative TC-CO2 monitoring. Bhavani-Shankar et al reported the use of TC-CO2 during intraoperative anesthetic care for a laparoscopic cholecystectomy in a parturient [10].

Their use of TC-CO2 monitoring was prompted by reports of the potential problems with ET-CO2 monitoring during laparoscopy. Since there was no indication for placement of an indwelling arterial catheter and since there was a limited increase in the TC-CO2, ABG analysis was not performed.

The authors noted an increase in the TC-CO2 from a baseline of 39.1 ± 0.1 mmHg to a maximum of 45.7 ± 0.1 mmHg as well as an increase in the TC-to-ET gradient from 6.6 ± 0.3 mmHg to 13.7 ± 0.2 mmHg during peritoneal insufflation with CO2.

Reid et al compared ET- with TC-CO2 monitoring during general anesthesia in 22 adults during 3 different levels of mechanical ventilation [11].

A total of 66 data sets with the pCO2 ranging from 28 to 62 mmHg demonstrated an ET-to-arterial gradient of 7.0 ± 3.1 mmHg with a correlation coefficient of r = 0.89 and a TC-to-arterial gradient of 2.3 ± 2.4 mmHg (p < 0.05 when compared to TC-to-arterial gradient) with r = 0.92. The differences were greatest at the higher pCO2 values.

Phan et al also compared ET- and TC-CO2 monitoring during general anesthesia in 24 adults [12]. The correlation coefficient, bias, and precision for the ET-to-arterial comparison were 0.67, –7.8 mmHg, and ± 6.1 mmHg, while the correlation coefficient, bias, and precision for the TC-to-arterial comparison were 0.87, –1.6 mmHg, and ± 4.3 mmHg.

By following some important caveats and technical suggestions, we have found that TC-CO2 monitoring will provide an excellent and clinically acceptable estimate of pCO2, which we have found is better than that obtained with conventional, intraoperative ET-CO2 monitoring.

When reviewing the literature concerning TC-CO2 monitoring, the type and manufacturer of the monitor and whether a “calibration factor” is used by the monitor can affect the accuracy of the monitoring and thereby the results of the study. Regardless of the monitor used, the tissue CO2 and therefore the TC-CO2 is invariably higher than the pCO2 unlike the ET-CO2, which is invariably lower than the pCO2.

Technical aspects of TC monitoring – temperature corrections

The TC-CO2 monitor used in our intraoperative studies, corrects for the alterations in CO2 caused by heating the skin to 43-45 °C. Heating of the skin is necessary to ensure capillary vasodilatation and an equilibration between the tissue and capillary pCO2.

With heating of the skin, the uncorrected TC-CO2 is significantly above the pCO2 (measured at 37 °C) because of increased CO2 production from the elevated local tissue metabolism and the altered solubility of CO2 at higher temperatures.

The importance of these factors is illustrated by the study of Tremper et al [13]. The authors, without correcting the TC-CO2 value for temperature differences, compared the transcutaneous and arterial values of CO2 in 435 data sets in 44 patients in a mixed OR/ICU setting [8].

Although they noted a wide difference between the TC and the CO2 value (23 ± 11 mmHg), linear regression analysis yielded a correlation coefficient of 0.80. They also noted that, with a low cardiac output state (cardiac index less than 1.5 L/min/m2), there was a further increase in the TC-to-arterial CO2 gradient and the TC-CO2 trended inversely with the cardiac index and not the pCO2.

A similar effect of cardiovascular performance and the gradient between arterial and TC carbon dioxide has been reported by other investigators [14-17]. No patient in either of our intraoperative studies manifested clinical signs or symptoms of cardiovascular dysfunction or a low cardiac output state.

Technical aspects of TC monitoring – preparation time

When compared with ET-CO2 monitoring, TC-CO2 monitoring requires a much longer preparation time including a 5-minute calibration period prior to placement and then an additional 10- to 15-minute equilibration period after placement on the patient to allow for an equilibration between the TC and arterial CO2 values.

Once the electrode is placed, recalibration and replacement at another site every 4 hours is recommended by the manufacturer, making this monitor more labor intensive than ET-CO2 monitoring. This may be problematic if access is limited to the patient intraoperatively when replacement at another site is needed due to the duration of the surgical procedure.

Technical aspects of TC monitoring – others

Although we found that TC-CO2 monitoring provided a more accurate reflection of pCO2 in most patients, several factors related to the monitor itself may affect this accuracy including technical variables such as trapped air bubbles, improper placement technique, damaged membranes, and inappropriate calibration techniques. In addition to technical problems, patient problems may affect the accuracy of TC-CO2 monitoring.

These may include variations in skin thickness, the presence of edema, tissue hypoperfusion, or the administration of vasoconstricting drugs [4,14-17]. Following our clinical experience, we would recommend keeping the working temperature of the probe at 44-45 °C. As this can leave a superficial blister, we always warn the patient of this preoperatively and change the site every 2.5 to 3 hours.

Our clinical experience also suggests that more accurate readings are provided when the probe is placed over specific areas of the body such as the ventral (volar) aspect of the forearm.

Conclusion

Because no technique can be expected to be 100 % reliable, periodic calibration with pCO2 values is recommended.

In our clinical experience, although TC-CO2 monitoring is a more accurate means of estimating pCO2, ET-CO2 is still required during intraoperative care as it documents the intratracheal position of the endotracheal tube and serves as an additional safety monitor to alert one to a ventilator disconnection, functions not provided by ET-CO2 monitoring.

Author 

Joseph D. Tobias
The University of Missouri
Department of Child Health
M658 Health Sciences Center
One Hospital Drive
Columbia, Missouri 65212
USA

References
  1. Bhavani-Shankar K, Moseley H, Kumar AY, Delph Y. Capnometry and anesthesia. Can J Anaesth 1992; 39: 617-32.
  2. Pansard JL, Cholley B, Devilliers C, et al. Variation in arterial to end-tidal CO2 tension differences during anesthesia in the “kidney rest” lateral decubitus position. Anesth Analg 1992; 75: 506-10.
  3. Grenier B, Verchere E, Meslie A, et al. Capnography monitoring during neurosurgery: reliability in relation to various intraoperative positions. Anesthesiology 1999; 88: 43-48.
  4. Tobias JD, Wilson WR Jr, Meyer DJ. Transcutaneous monitoring of carbon dioxide tension after cardiothoracic surgery in infants and children. Anesth Analg 1999; 88: 531-34.
  5. Tobias JD, Meyer DJ. Noninvasive monitoring of carbon dioxide during respiratory failure in toddlers and infants: end-tidal versus transcutaneous carbon dioxide. Anesth Analg 1997; 85: 55-58.
  6. McBride DS, Johnson JO, Tobias JD. Noninvasive carbon dioxide monitoring during neurosurgical procedures in adults: end-tidal versus transcutaneous techniques. South Med J (in press).
  7. Badgwell JM, Heavener JE, May WS, et al. End-tidal pCO2 monitoring in infants and children ventilated with either a partial rebreathing or non-rebreathing circuit. Anesthesiology 1987; 66: 405-10.
  8. Badgwell JM, McLeod ME, Lerman J, et al. End-tidal pCO2 measurements sampled at the distal and proximal ends of the endotracheal tube in infants and children. Anesth Analg 1987; 66: 959-64.
  9. Nosovitch MA, Johnson JO, Tobias JD. Noninvasive intraoperative monitoring of carbon dioxide in children: end-tidal versus transcutaneous techniques. Paediatr Anaesth 2002; 12: 480-52.
  10. Bhavani-Shankar K, Steinbrook RA, Mushlin PS, et al. Transcutaneous CO2 monitoring during laparoscopic cholecystectomy during pregnancy. Can J Anaesth 1998; 45: 164-69.
  11. Reid CW, Martineau RJ, Miller DR, et al. A comparison of transcutaneous, end-tidal and arterial measurements of carbon dioxide during general anesthesia.  Can J Anaesth 1992; 39: 31-36.
  12. Phan CQ, Tremper KK, Lee SE, Barker SJ. Noninvasive monitoring of carbon dioxide: a comparison of the partial pressure of transcutaneous and end-tidal carbon dioxide with the partial pressure of arterial carbon dioxide. J Clin Monitor 1987; 3: 149-54.
  13. Tremper KK, Shoemaker WC, Shippy CR, Nolan LS. Transcutaneous pCO2 monitoring on adult patients in the ICU and the operating room. Crit Care Med 1981; 9: 752-55.
  14. Rithalia SVS, Ng YN, Tinker J. Measurement of transcutaneous pCO2 in critically ill patients. Resuscitation 1982; 10: 13-18.
  15. Rithalia SVS, Clutton-Brock TH, Tinker J. Characteristics of transcutaneous carbon dioxide tension monitors in normal adults and critically ill patients. Intens Care Med 1984; 10: 149-53.
  16. Shoemaker WC. Physiologic and clinical significance of ptcCO2 and ptcCO2. Crit Care Med 1981; 9: 689-90.
  17. Hasibeder W, Haisjackl M, Sparr H, et al. Factors influencing transcutaneous oxygen and carbon dioxide measurements in adult intensive care patients. Intens Care Med 1991; 17: 272-75.
+ View more
References
  1. Bhavani-Shankar K, Moseley H, Kumar AY, Delph Y. Capnometry and anesthesia. Can J Anaesth 1992; 39: 617-32.
  2. Pansard JL, Cholley B, Devilliers C, et al. Variation in arterial to end-tidal CO2 tension differences during anesthesia in the “kidney rest” lateral decubitus position. Anesth Analg 1992; 75: 506-10.
  3. Grenier B, Verchere E, Meslie A, et al. Capnography monitoring during neurosurgery: reliability in relation to various intraoperative positions. Anesthesiology 1999; 88: 43-48.
  4. Tobias JD, Wilson WR Jr, Meyer DJ. Transcutaneous monitoring of carbon dioxide tension after cardiothoracic surgery in infants and children. Anesth Analg 1999; 88: 531-34.
  5. Tobias JD, Meyer DJ. Noninvasive monitoring of carbon dioxide during respiratory failure in toddlers and infants: end-tidal versus transcutaneous carbon dioxide. Anesth Analg 1997; 85: 55-58.
  6. McBride DS, Johnson JO, Tobias JD. Noninvasive carbon dioxide monitoring during neurosurgical procedures in adults: end-tidal versus transcutaneous techniques. South Med J (in press).
  7. Badgwell JM, Heavener JE, May WS, et al. End-tidal pCO2 monitoring in infants and children ventilated with either a partial rebreathing or non-rebreathing circuit. Anesthesiology 1987; 66: 405-10.
  8. Badgwell JM, McLeod ME, Lerman J, et al. End-tidal pCO2 measurements sampled at the distal and proximal ends of the endotracheal tube in infants and children. Anesth Analg 1987; 66: 959-64.
  9. Nosovitch MA, Johnson JO, Tobias JD. Noninvasive intraoperative monitoring of carbon dioxide in children: end-tidal versus transcutaneous techniques. Paediatr Anaesth 2002; 12: 480-52.
  10. Bhavani-Shankar K, Steinbrook RA, Mushlin PS, et al. Transcutaneous CO2 monitoring during laparoscopic cholecystectomy during pregnancy. Can J Anaesth 1998; 45: 164-69.
  11. Reid CW, Martineau RJ, Miller DR, et al. A comparison of transcutaneous, end-tidal and arterial measurements of carbon dioxide during general anesthesia.  Can J Anaesth 1992; 39: 31-36.
  12. Phan CQ, Tremper KK, Lee SE, Barker SJ. Noninvasive monitoring of carbon dioxide: a comparison of the partial pressure of transcutaneous and end-tidal carbon dioxide with the partial pressure of arterial carbon dioxide. J Clin Monitor 1987; 3: 149-54.
  13. Tremper KK, Shoemaker WC, Shippy CR, Nolan LS. Transcutaneous pCO2 monitoring on adult patients in the ICU and the operating room. Crit Care Med 1981; 9: 752-55.
  14. Rithalia SVS, Ng YN, Tinker J. Measurement of transcutaneous pCO2 in critically ill patients. Resuscitation 1982; 10: 13-18.
  15. Rithalia SVS, Clutton-Brock TH, Tinker J. Characteristics of transcutaneous carbon dioxide tension monitors in normal adults and critically ill patients. Intens Care Med 1984; 10: 149-53.
  16. Shoemaker WC. Physiologic and clinical significance of ptcCO2 and ptcCO2. Crit Care Med 1981; 9: 689-90.
  17. Hasibeder W, Haisjackl M, Sparr H, et al. Factors influencing transcutaneous oxygen and carbon dioxide measurements in adult intensive care patients. Intens Care Med 1991; 17: 272-75.
Disclaimer

May contain information that is not supported by performance and intended use claims of Radiometer's products. See also Legal info.

Joseph D. Tobia

 

Department of Anesthesiology
Pediatric Critical Care/Pediatric Anesthesiology
University of Missouri
Department of Anesthesiology, 3W40H
One Hospital Drive
Columbia, Missouri 65212
USA

Articles by this author
Acutecaretesting handbook

Acute care testing handbook

Get the acute care testing handbook

Your practical guide to critical parameters in acute care testing. 

Download now
Webinar on demand: Evolution of blood gas testing - Part 1

Related webinar

Evolution of blood gas testing Part 1

Presented by Ellis Jacobs, PhD, Assoc. Professor of Pathology, NYU School of Medicine.

Watch the webinar
Webinar: Evolution of blood gas testing - Part 2

Related webinar

Evolution of blood gas testing Part 2

Presented by Ellis Jacobs, PhD, Assoc. Professor of Pathology, NYU School of Medicine.

Watch the webinar
Preanalytical errors handbook

Blood gas Preanalytics app

Get the Blood gas Preanalytics app for your smartphone

This smartphone app focuses on the preanalytical phase of blood gas testing and what operators can do to avoid errors.

Download app

Sign up for the Acute Care Testing newsletter

Sign up
About this site About Radiometer Contact us Legal notice Privacy Policy
This site uses cookies Read more