Abstract
Deterioration of gas exchange during one-lung ventilation (OLV) is caused by both total collapse of the nondependent lung and partial collapse of the dependent lung. Alveolar recruitment maneuver improves lung function during general anesthesia. The objective of this study was to investigate whether there is an indirect relationship between the changes of CO2 expirogram and the selective lung recruitment. To further improve the oxygenation and gas exchange, we compare adjust setting of ventilated parameters based on CO2 expirogram and a preset setting of ventilated parameters during OLV in patients undergoing right-side thoracic surgery.
Thirty patients met the requirements criteria that were studied at 3 time points: during two-lung ventilation (TLV), during OLV with preset ventilation parameters (OLV-PP), and during OLV with adjustable ventilation parameters (OLV-AP) that are in accordance with CO2 expirogram. Adjustable ventilation parameters such as tidal volume (VT), respiratory rate (RR), positive end-expiratory pressure (PEEP), and the ratio of inspiratory to expiratory were adjusted by utilizing the phase III slopes of CO2 expirogram, which together with the relationship between the changes of CO2 expirogram and the selective lung recruitment.
During OLV, the phase III slopes of CO2 expirogram in patients with pulse oxymetry (SpO2) decreased less than 93% after the OLV-PP, and were absolutely different from that during TLV. After OLV-AP, the phase III slopes of CO2 expirogram and SpO2 were similar to those during TLV. During OLV, however, parameters of ventilation setting in both OLV-PP and OLV-AP are obviously different.
This study indicates that alveolar recruitment by utilizing CO2 expirogram probably improves SpO2 level during one-lung ventilation.
Keywords: alveolar recruitment maneuver, CO2 expirogram, hypoxemic, one-lung ventilation
1. Introduction
During lung operations or in instances when the collapse of the lung increases access to the operation field, one-lung ventilation (OLV) is almost always now in thoracic operations. Although nonventilated lung leads inevitably to transpulmonary shunting, and, occasionally, to hypoxemia, not all cases of hypoxemia are altered by shunt and uneven ventilation perfusion ratios during OLV. In patients undergoing general anesthesia, 1 study showed that lung recruitment maneuvers were both easy to perform and effective in reverting alveolar collapse, hypoxemia, and decreased compliance.[1] Hypoxemia during OLV is associated with operation side.[2] Schwarzkopf et al[3] showed the mean arterial oxygen tension during OLV was respectively around 280 and 170 mm Hg during left-sided thoracic surgery and right-sided operation under ventilation with a fraction of inspired oxygen (FiO2) of 1. Therefore, oxygenation during OLV is better during left thoracotomy, since the right lung is larger than the left one.[4] Moreover, OLV anesthesia in the lateral position leads to total collapse of the nondependent lung and increase of dead space in the dependent lung, which results in pulmonary shunt ranging from 15% to 40% and atelectasis due to impaired arterial oxygenation, respectively.[5] Therefore, gas exchange and ventilation efficiency during general anesthesia can be evaluated by the analysis of lung recruitment maneuvers and lung CO2 removal, as shunt is closely associated with dead space.
Selective recruitment of a collapsed lung lobe on gas exchange and lung efficiency during OLV by using the single-breath test of CO2.[6] Schulz et al[7] confirmed that although clear asymmetries in lung structure exist, filling and emptying of the lungs occurs in a remarkably symmetrical fashion. Further, the lungs are robust to changes in ventilatory patterns. The dynamics on the intrapulmonary gas transport is not yet clear because comprehensive studies are lacking. Thus, it is important to provide for further recruitment maneuver to keep the alveoli opened and avoiding uniform alveolar distension. Our study is focused on allowing a more comprehensive characterization of the single-breath expirogram than does the consideration of dead space volumes alone during OLV undergoing thoracic surgeries. The aim of this study was to evaluate the efficacy of alveolar recruitment maneuver followed by utilizing the shape of a carbon dioxide expirogram that is altered with different setting parameters of mechanical ventilation and as a label for gas changes during OLV.
2. Methods
This study was approved by the Ethics Board of Affiliated Third Hospital of Anhui Medical University. Between January 2014 and October 2014, consecutive patients scheduled for undergoing elective thoracic surgical procedures (right lobectomy or esophageal neoplasia resection) requiring left one lung ventilation (OLV) and have developed an episode from intermittent droping in pulse oxymetry (SpO2) less than 90% appeared 2 times after initial OLV were considered for this study if they met the requirements of the experimental protocol. Written informed consent was obtained from all patients. All patients were enrolled in the prospective longitudinal study and were selected on the following criteria: preoperative evaluation major included a physical examination, patients underwent pulmonary function tests and blood gases, cardiac evaluation (and echocardiography if ordered by the cardiologist), and cardiorespiratory polygraphy if acute respiratory distress syndrome or severe threatened by the presence of a right-to-left transpulmonary shunt were suspected. Exclusion criteria were documented any cardiovascular disease, hypertension or arrhythmia, or major obstructive or restrictive pulmonary disease (defined as <70% of predicted values for pulmonary function test variables of volume and flow), and anemic (hemoglobin <9 g/dL), or liver and renal dysfunction, or inability to maintain an appropriate SpO2 or end-tidal carbon dioxide partial pressure (PETCO2). In addition, patients who required absolutely right-sided double-lumen tube and presented a distorted anatomy of the tracheobronchial tree on chest radiograph were not included in this study.
No premedication was given. Before the induction of anesthesia, an IV infusion of normal Ringer lactate was started. After 3 minutes of preoxygenation, anesthesia was induced with midazolam 0.1 mg/kg, propofol 1.5 mg/kg, fentanyl 2 μg/kg, and vecuronium 0.08 mg/kg IV and isoflurane concentrations up to 1 MAC. The trachea and the left bronchus were intubated with a left-sided double-lumen tube (DLT) of the appropriate size, and then it was connected to the anesthesia circuit. After clinical confirmation of correct DLT (by inspection and auscultation) with the patient in both the supin and lateral decubitus positions. Effective lung isolation was confirmed by the absence of a leak from the nonventilated lumen of the endobronchial tube. Upon opening of the pleura, direct observation of the collapsed nonventilated lung and the absence of a leak from this lung provided further confirmation. Anesthesia was maintained with low concentration isoflurane (≦1%), and propofol (75 mg/kg/min) and remifentanil (0.1 mg/kg/min). Vecuronium (0.03 mg/kg) was administrated if required muscular relaxing.
All patients were ventilated with Datex-Ohmeda Aestive/5 Smart Ventilator (Madison, WI). Patients were randomized to receive one of the following ventilatory regimens. Before starting OLV, two lung ventilation (TLV) started with 100% FiO2, VT of 8 mL/kg predicted body weight, positive end-expiratory pressure (PEEP) of 0 cmH2O, inspiratory to expiratory (I:E) ratio of 1: 2, and initial respiratory rate (RR) of 12 breaths/min. After starting OLV, ventilation parameters were fixed at 6 mL/kg VT under 100% FiO2, a 14 to 16 breaths/min RR to keep PETCO2 between 30 and 35 mm Hg, I: E was 1: 2, and a 6 to 10 cm H2O PEEP.
Standard monitoring including electrocardiogram, heart rate (HR), invasive arterial blood pressure, and SpO2 was collected by the Datex Ohmeda S/5 monitor during the entire study period. Prior to use, the PETCO2 was measured using an infrared analyzer with a side stream sampler attached at the elbow between the endotracheal tube and the anesthesia circuit and the device was calibrated according to the manufacturer's recommendations. The CO2 waveform was obtained by monitoring PETCO2 on a monitor following tracheal cannulation during the two lung ventilation and as a basic CO2 waveform. However, CO2 waveforms are characterized by a triphasic shape that has been described in normal (see Fig. 1),[8] therefore it is referenced as a basic CO2 waveform during TLV.
The primary target variable of this study was CO2 waveform by monitoring PETCO2. The null hypothesis was that CO2 waveform of TLV and OLV modes was propinquity and the alternative hypothesis that they were different. The primary outcome variable was determined by whether arterial oxygenation. (≤93%) once again after restarting OLV (9.6 ± 2.7 min) with PP setting. The patients were carried out by randomization and step-wise approach in both the preset parameters (OLV-PP) setting and adjustable parameters (OLV-AP) setting to the management of arterial oxygenation during OLV. In the OLV-PP setting, ventilation parameters were fixed as described above for an initial control period during OLV. In the OLV-AP setting, the same 100% FiO2 was used, the ventilation parameters were randomly adjusted any at a time to following CO2 waveform aiming to make its sample with basic CO2 waveform as similar as possible. Primary outcome variable was SpO2 during TLV, OLV, and period after OLV-AP setting. VT, RR, PEEP, I:E, peak inspiratory pressure (PIP), and PETCO2 during mechanical ventilation were recorded. Seven time points were observed and recorded according to the SpO2 change. SpO2 were a typical normal by TLV and a time point of OLV beginning (T0). And the processing of hypoxemia included the first time when SpO2 decreased to less than 90% (T1), surgery was temporarily interrupted to resume TLV (performed with continuous positive airway pressure (CPAP)) using the hand bag until SpO2 recovered to at least 97% (T2), once again SpO2 decreased to less than 93% after restarting OLV (T3); SpO2 recovered to more than 97% with second attempts of CPAP and AP setting was adopted (T4), a period after OLV-AP setting was adopted (T5), and the end of OLV (T6). That is, OLV-PP setting for T1, T2, T3, and OLV-AP setting for T4, T5 and T6. VT, RR, I:E, PEEP, PIP, and PETCO2 were recorded continuously. At frequent intervals, a mean value of all SpO2 was obtained during OLV.
3. Statistical analysis
Data are presented as mean standard deviation and range. Student t test was applied for statistical comparisons of changes occurring within each study condition. A P value of <0.05 was considered to achieve statistical significance.
4. Results
Thirty patients who met the requirements criteria were included in the study, their physical status I or II, aged 43 to 75 years, and patients characteristics are listed in Table 1.
Table 1.
Thirty patients were presented a SpO2 decrease less than 90% (as cases of an episode of hypoxemia) during OLV and randomized or step-wise to receive ventilation parameters with both OLV-PP setting and OLV-AP setting. No patient was excluded from 30 patients due to any preoperative or intraoperative criteria, and in all patients left-double lumen tubes were used.
Fig. 2a (a real sample) was obtained from a patient undergoing OLV and TLV during thoracic surgery. (a)-(A) During TLV, rising segment (phase II) rapidly reaches a height, usually attained only CO2 exhaled from rapidly emptying alveoli, whereas alveolar plateau (phase III) would be nearly horizontal. However, this ideal situation does not occur, even in normal lungs. The waveform analysis was performed on theirs difference as the intersection angle between lines B to C (phase II) and lines C to D (phase III) along with principle axis. The beginning of OLV with PP setting depicted a CO2 waveform. Fig. 2a-(B) shows that application of PP setting increased the intersection angle between phase II and phase III slopes [beta angle (β = 130°) vs. alpha angle (α = 105°)]. Application of AP setting significantly decreased the angle between phase II and phase III slopes [gamma angle (γ = 110°) vs. beta angle (β = 130°)]. In other words, phase II rapidly reaches a height, whereas phase III would be nearly horizontal, and there is a rapid S-shaped upstroke on the tracing due to the CO2 rich exhalation from the alveoli.
In Fig. 2b, the plot shows the entire sequence from intraoperative in SpO2 less than 90% in 30 patients during TLV and OLV in accordance with a sample CO2 waveform at below 7 time points.
The period before T0 indicates that SpO2 were a typical normal (≥99%) by TLV.
T0 to T1 indicates that SpO2 were declined (≤90%) of short period (18.5±3.7 min) by OLV according to the PP setting. T1 to T2 indicates that SpO2 were rose rapidly (2.1 ± 1.5 min) by TLV with CPAP. T2 to T3 indicates that SpO2 decreased (≤93%) once again after were restarted OLV (9.6 ± 2.7 min) with PP setting. T3 to T4 indicates that SpO2 were rose again by TLV (2.2 ± 1.8 min) with CPAP. T4 to T5 indicates that SpO2 were declined briefly by OLV (8.3 ± 3.2 min) with AP setting. T5 to T6 indicates that SpO2 can be retained normal level by AP setting during OLV (117.6 ± 23.7 min).
Table 2 shows the key characteristics of each setting. They were significantly different with respect to VT, RR, I:E, PEEP, PIP, and PETCO2. Arterial oxygenation (SpO2) with a mode of the OLV-AP setting was significantly improved compared to the OLV-PP setting. The beginning of OLV with OLV-PP setting produced a significant high in RR and end-tidal carbon dioxide partial pressure (PETCO2), whereas comparison of the OLV-PP and OLV-AP showed a significant difference in VT, I:E, PEEP, and PIP.
Table 2.
5. Discussion
The ventilatory pattern should be directed toward minimizing dynamic hyperinflation and auto-PEEP by using small VT and preserving expiratory time.[9] Although hyperinflation is unlikely with low VT, especially during high FiO2, it may lead to more atelectasis and poor oxygenation.[10] Therefore, low VT must be applied with PEEP to avoid atelectasis. We ventilated patients undergoing left-side OLV for right-side thoracic surgery with a low VT as a fixing parameters setting and found that it was difficulty maintaining arterial oxygenation or decrease the occurrence of SpO2 less than 90%. In contrast, ventilating patients with selectable lung recruitment maneuver by some transform parameters that mainly based on the change with “CO2 expirogram” approach, results in improving the efficiency on oxygenation and gas exchange.
Lung recruitment maneuver has been considered the conventional approach to mechanical ventilation of patients undergoing thoracic surgery and OLV. However, the collapsed lungs could be reexpanded via various strategies during general anesthesia. Atelectatic lung can be completely reexpanded just with 15 seconds of an airway pressure of 40 cm H2O. This pressure is corresponding to inflation to vital capacity, and therefore this maneuver is termed vital capacity maneuver.[11] Talab et al[8] demonstrated this maneuver requires to be maintained by PEEP 10 cm H2O with the purpose of reexpanding all previously collapsed lung tissues. But during OLV, the recruitment effect of a single vital capacity maneuver may be lost after reduced tidal volumes (5–6 mL/kg) or may be decreased by the intrinsic PEEP because of the accompanying need for increased respiratory rates.[12] For this reason, we believe that as a net result, recruitment maneuvers should protect collapse-prone lungs despite an increase in VT at a slight high PIP. Selective recruitment of the collapsed lung region by adjusting the parameters of ventilation constant only in CO2 expirogram for reference never reported to be effective as a last resort for oxygenation of the collapsed lungs.
The SpO2 did not decrease less than 97% in any of the 30 patients during TLV with a FiO2 of 1.0 in this study. Since mean difference between SpO2 and O2Hb during OLV was 2.9% ± 0.1%, and the SpO2 to O2Hb difference decreased with increasing FiO2.[3] The SpO2 decreased less than 90% is defined as hypoxemia in this study. However, the oxygenation of patients is affected also by the duration of OLV, being the lowest at about 27 minutes with a peak at about 1 hour and 25 minutes.[13] To minimize the impact of this intraoperative variation in oxygenation,[14] we used the 3 stepwise sequence for SpO2 decreased less than 93% at 2 times in random order. Although we tried to maintain the parameters of ventilation constant as a preset approach during initial OLV, we had to use an interference of continuous positive pressure (using hand bag) to recover SpO2 with oxygenation. This may explain why the improvement in oxygenation with adjustable parameters setting being based on the shape of CO2 expirogram was effective in our study.
The time period between the beginning of OLV and applying adjustable parameters setting ranged approximately from 20 to 38 minutes. Our study shows that initial stage during OLV with a predetermined parameter values including VT, RR, I:E, and PEEP, then the graphic of CO2 expirogram was correspondingly changed after switching from TLV to OLV. This means quite unlike with other previous results[6,15–18] and can be explained by a recruitment effect on both the function state of small airway or alveolar and dead space, taking into account that hemodynamic, delivered tidal volume, and ventilatory conditions during OLV were different during TLV. This means that graphic changes of CO2 expirogram may be an effective means of decreasing oxygenation or affect gas exchange or lead to hypoxemia during OLV. The CO2 expirogram (capnogram) has been characterized for adult patients with normal and abnormal pulmonary function,[19] and factors directly related to the airway pressure, the alveolar opening, and ventilation compliance and lung function influence the shape change of a CO2 expirogram.[7,20,21] Whether the parameters setting of ventilation according to the shape change of CO2 expirogram during the relatively long period of OLV may be “optimize” oxygenation approach is indeed unclear. However, a similar relationship between the shape change of CO2 expirogram and the selectable lung recruitment maneuver, and CO2 expirogram are significantly more sensitive to the function of the alveolar state than the artificial setting for ventilation parameters in the clinical study. Furthermore, such as application of selectable lung recruitment maneuver by CO2 expirogram to the nonventilated lungs, may at least obviate the need for CPAP during OLV.
The results of this study indicate an improved efficiency in gas exchange after a lung recruitment maneuver with ventilation parameters setting by CO2 expirogram during OLV. CO2 expitogram is a technical monitor of the estimated alveolar PCO2 (PACO2) and consequently of the estimated arterial PCO2 (PaCO2) as well as the overall adequacy of alveolar ventilation. In contrast, PETCO2 measures the average PACO2 accurately only if the volume-weighted alveolar plateau is nearly horizontal on the capnogram. What are the mechanisms that cause or increase the positive slope of the alveolar plateau? Since the chronic obstructive pulmonary disease is accompanied with ineffective ventilated lung units with high PCO2, the sequential emptying of parallel alveolar units with different PCO2 can generate a sharp slope of alveolar plateau.[22] Our real-time simulation and clinical studies show close relationships between the magnitude of ventilation parameters and the alveolar plateau or the phase III slope. In our study, the VT, PEEP, and PIP after the adjustable parameters setting were higher as compared with preset parameters setting during OLV. This means that a full tidal volume can create a common alveolar opening to the collapsed lungs and constant inspired flow toward the peak inspiratory pressure, and for maximum improvement in oxygenation, continuous PEEP was applied with prior inflation of the lung. We had to use a slow respiratory rate and a setting for I:E ratio of 1 to 2.5 applied by adjustable setting in order to be unanimous in CO2 expirogram with one during TLV, which acquiring appropriate expiratory flow process and maintaining the set expiratory pressure (the alveolar plateau of the CO2 expirogram will be flatter than applied without prior inflation). Thus, when expiration is prolong and progresses to a lung volume below closing capacity, expired CO2 concentration may rise sharply at the end of the alveolar plateau. This may explain why the positive slope of the alveolar plateau is the continued accumulation of CO2 from the pulmonary blood into a shrinking alveolar volume during exhalation.[23] The resultant expiratory alteration with flow and pressure had only primary influence on CO2 expirogram position and shape of phase II. The general condition of the patient actually represents one of the major factors determining the arterial oxygenation during OLV. Theoretically, however, “optimum” ventilation parameters such as the PEEP, I:E, and PIP may result in more homogeneous distribution of VT, improvement in static and dynamic lung compliance, better oxygenation, and dead space ventilation.
In conclusion, the appropriate lung recruitment improves gas exchange and ventilation efficiency during OLV anesthesia. CO2 expirogram by PETCO2 monitoring provides an indirect guide of the lung recruitment maneuver gained by ventilation parameters setting. Based on our finding, we believe that CO2 expirogram monitoring should be incorporated into “optimize” recruitment approach during OLV and the outcome in connection with ventilation setting to provide insight into the condition of patients suffering hypoxemia.
Acknowledgments
We thank Dr Jun Zhang and Dr Peng Sun for providing additional patient data.
Footnotes
Abbreviations: CPAP = continuous positive airway pressure, DLT = double-lumen tube, FiO2 = fraction of inspired oxygen, I:E = inspiratory to expiratory ratio, OLV = one-lung ventilation, OLV-AP = OLV with adjustable ventilation parameters, OLV-PP = OLV with preset ventilation parameters, PEEP = positive end-expiratory pressure, PETCO2 = end-tidal carbon dioxide partial pressure, RR = respiratory rate, SpO2 = pulse oxymetry, TLV = two-lung ventilation, VT = tidal volume.
CD, JY, and YL contributed to the conception and design. QL, JY, and CW did the data collection. CD, JY, and YL did the analysis and interpretation. CD and YL did the writing, critical revision of the article. All authors reviewed and approved the final manuscript.
This study was supported by department funding.
The authors have no conflicts of interest to disclose.
References
- [1].Tusman G, Böhm SH, Vazquez de Anda GF, et al. ‘Alveolar recruitment strategy’ improves arterial oxygenation during general anaesthesia. Br J Anaesth 1999;82:8–13. [DOI] [PubMed] [Google Scholar]
- [2].Slinger P, Suissa S, Triolet W. Predicting arterial oxygenation during one-lung anaesthesia. Can J Anaesth 1992;39:1030–5. [DOI] [PubMed] [Google Scholar]
- [3].Schwarzkopf K, Klein U, Schreiber T, et al. Oxygenation during one-lung ventilation: the effects of inhaled nitric oxide and increasing levels of inspired fraction of oxygen. Anesth Analg 2001;92:842–7. [DOI] [PubMed] [Google Scholar]
- [4].Katz Y, Zisman E, Isserles SA, et al. Left, but not right, one-lung ventilation causes hypoxemia during endoscopic transthoracic sympathectomy. J Cardiothorac Vasc Anesth 1996;10:207–9. [DOI] [PubMed] [Google Scholar]
- [5].Torda TA, McCulloch CH, O’Brien HD, et al. Pulmonary venous admixture during one-lung anaesthesia. The effect of inhaled oxygen tension and respiratory rate. Anaesthesia 1974;29:272–9. [DOI] [PubMed] [Google Scholar]
- [6].Tusman G, Bohm SH, Sipmann FS, et al. Lung recruitment improves the efficiency of ventilation and gas exchange during one-lung ventilation anesthesia. Anesth Analg 2004;98:1604–9. [DOI] [PubMed] [Google Scholar]
- [7].Schulz H, Schulz A, Eder G, et al. Labeled carbon dioxide (C18O2): an indicator gas for phase II in expirograms. J Appl Physiol 2004;97:1755–62. [DOI] [PubMed] [Google Scholar]
- [8].Talab HF, Zabani IA, Abdelrahman HS, et al. Intraoperative ventilatory strategies for prevention of pulmonary atelectasis in obese patients undergoing laparoscopic bariatric surgery. Anesth Analg 2009;109:1511–6. [DOI] [PubMed] [Google Scholar]
- [9].Blanch L, Bernabe F, Lucangelo U. Measurement of air trapping intrinsic positive end-expiratory pressure, and dynamic hyperinflation in mechanically ventilated patients. Respir Care J 2005;50:110–23. [PubMed] [Google Scholar]
- [10].Duggan M, Kavanagh BP. Pulmonary atelectasis: a pathogenic perioperative entity. Anesthesiology 2005;102:838–54. [DOI] [PubMed] [Google Scholar]
- [11].Rothen HU, Sporre B, Englberg G, et al. Re-expansion of atelectasis during general anaesthesia: a computed tomography study. Br J Anaesth 1993;71:788–95. [DOI] [PubMed] [Google Scholar]
- [12].de Durante G, del Turco M, Rustichini L, et al. ARDSNet lower tidal volume ventilatory strategy may generate intrinsic positive end-expiratory pressure in patients with acute respiratory distress syndrome. Am J Respir Crit Care Med 2002;165:1271–4. [DOI] [PubMed] [Google Scholar]
- [13].Ishikawa S. Oxygenation may improve with time during one lung ventilation. Anesth Analg 1999;89:258–9. [DOI] [PubMed] [Google Scholar]
- [14].Watanabe S, Noguchi E, Yamada S, et al. Sequential changes of arterial oxygentension in the supine position during one-lung ventilation. Anesth Analg 2000;90:28–34. [DOI] [PubMed] [Google Scholar]
- [15].Hickling KG. The pressure-volume curve is greatly modified by recruitment: a mathematical model of ARDS lungs. Am J Respir Crit Care Med 1998;158:194–202. [DOI] [PubMed] [Google Scholar]
- [16].Tusman G, Böhm SH, Melkun F, et al. Alveolar recruitment strategy increases arterial oxygenation during one-lung ventilation. Ann Thorac Surg 2002;73:1204–9. [DOI] [PubMed] [Google Scholar]
- [17].Gal TJ. Con: low tidal volumes are indicated during one-lung ventilation. Anesth Analg 2006;103:271–3. [DOI] [PubMed] [Google Scholar]
- [18].Montes FR, Pardo DF, Charris H, et al. Comparison of two protective lung ventilatory regimes on oxygenation during one-lung ventilation: a randomized controlled trial. J Cardiothorac Surg 2010;5:99. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [19].Yaron M, Padyk P, Hutsinpiller M, et al. Utility of the expiratory capnogram in the assessment of bronchospasm. Ann Emerg Med 1996;28:403–7. [DOI] [PubMed] [Google Scholar]
- [20].Breen PH, Mazumdar B, Skinner SC. Comparison of end-tidal PCO2 and average alveolar expired PCO2 during positive end-expiratory pressure. Anesth Analg 1996;82:368–73. [DOI] [PubMed] [Google Scholar]
- [21].Tang Y, Turner MJ, Baker AB. Systematic errors and susceptibility to noise of four methods for calculating anatomical dead space from the CO2 expirogram. Br J Anaesth 2007;98:828–34. [DOI] [PubMed] [Google Scholar]
- [22].Fletcher R. The arterial-end-tidal CO2 difference during cardiothoracic surgery. J Cardiothoracic Anesth 1990;4:105–17. [DOI] [PubMed] [Google Scholar]
- [23].Dubois AB, Britt AG, Fenn WO. Alveolar CO2 during the respiratory cycle. J Appl Physiol 1952;4:535–48. [DOI] [PubMed] [Google Scholar]