The main findings of this study are provided below:
The main conclusion is that ORi is sensitive and specific in predicting hypoxemia defined as SpO2 values of less than 95% while the FiO2 is 50% or higher on a pulse oximetry device at 5 min after intubation in the supine position (sensitivity of 92.3%, specificity of 81.1% and, an accuracy of 84.0%) [7,8,9, 13, 15, 17,18,19,20,21].
There are other time points where there is statistically good report of sensitivity, specificity and accuracy for time points at ORiDL5, and during OLV until OLV30 where sensitivity of 43.8%, specificity of 64%, and an accuracy of 56.1% are recorded. These findings correlated to the previous reports that HPV increases and intrapulmonary shunting decreases after the start of OLV within 30 to 60 min [4, 8, 13, 14].
In our study group of patients, a total of 19 patients (38%) developed hypoxemia at various recorded time points during the surgical procedure. ORi provides information for impending hypoxemia that a change in ORi value can be detected 5 to 6 min earlier than pulse oximetry value. Therefore, ORi can provide a valuable time to the anesthesiologist to provide an increase in FiO2 values, to perform necessary mechanical ventilation adjustments, to perform aspiration or other anesthetic management techniques to prevent hypoxemia [7,8,9, 13, 15, 17,18,19,20,21].
During OLV, hypoxemia can develop not only by the intrapulmonary shunt in the non-ventilated lung but also by the ventilation-perfusion mismatch in the ventilated lung or hemodynamic instability [4, 5]. In our study, patients with coronary artery disease and an ejection fraction below 40% were not included into the study. Patients with heart failure were also excluded. During OLV, atelectasis occurs during general anesthesia induction, which causes ventilation/perfusion mismatch even before switching to OLV [5, 6, 10]. During OLV, oxygen delivery to the patient under general anesthesia occurs during various interactions between hemoglobin, oxygen saturation, cardiac output, and normal physiological mechanisms such as HPV and intrapulmonary shunts [3, 4]. Although the causes of OLV-induced hypoxemia are multifactorial, early detection of hypoxemia before the onset of OLV allows the application of different ventilation strategies to improve oxygenation [3,4,5,6]. The role of HPV and intrapulmonary shunting are also discussed earlier [4, 10, 14, 22].
A significant correlation between ORi and SpO2 was found at time points of DS5, DL5 and, at OLV10. The relationship between SpO2 values and ORi equals to zero values for predicting hypoxemia during anesthesia induction and maintenance is supported by these statistical findings. There are previous studies that support these correlations [7,8,9, 13, 15, 17,18,19,20,21]. In our study group, hypoxemia episodes were observed at various time points throughout the surgery however, the reports were not able to demonstrate a fall of pulse oximeter values below 95% as FiO2 values were set at 50% and may have been rised up to 70% after anesthesia management throughout the surgical procedures. In addition to temporary rises in FiO2 throughout surgery, mechanical ventilation and anesthetic maneuvers were performed by the anesthesiologists. Because of these interventions, in our opinion, we were not able to show a continuous a correlation between ORi and SpO2 values at all measured time points. When ORi which is an oximeter-related parameter is used along with the pulse oximeter monitoring, ORi values may present and record early signs of the downward trend of PaO2 in comparison to a pulse oximetry value. In a previous study, at 1 min after start of OLV the measurements show that; hypoxemia was 27.5% where SpO2 value was less than 90% whereas; a negative predictive value was reported as 12.9% in those patients who did not achieve an ORi value of 0 at 1 min after the lung collapsed. It has been reported that median time until desaturation was approximately 5.5 to 6 min. Therefore, FiO2 values should be kept between 50 to 60% to avoid hyperoxemia and its related adverse effects such as atelectasis [7,8,9, 13, 17, 18, 20, 21].
Our findings show similarity with a recent study by Alday and his colleagues [8] however, they also suggested that these values may be used to prevent unnecessary hyperoxemia. In our study, it is clear that during anesthetic management FiO2 values are kept at a value of 50 to 70% in our patients whereas other studies investigated the use of ORi for hyperoxemia as well [7,8,9, 13, 17, 18, 20, 21]. In a study by Applegate and his colleagues, a positive correlation between ORi values and PaO2 values of 240 mmHg or lower (r = 0.536, p < 0.01) in comparison to ORi values and PaO2 values of higher than 240 mmHg (r = 0.0016, p > 0.05) [9]. In our study, we were not able to measure PaO2 values on each time point because of hospital policies to decrease medical costs. In our study, at the measurement time of arterial blood gas analysis at DL5, we found that 4 patients had a PaO2 value above 240 mmHg and ORi values showed statistically significant negative correlation (r = − 1.0, p < 0.001). In another study, 15 patients undergoing elective thoracic surgery using OLV were evaluated for correlation between PaO2 and ORi parameters throughout the surgical procedure and showed that ORi has a significant correlation with PaO2 (r = 0.671, p < 0.001) [18]. There are a few studies that provide evidence that PaO2 values show positive correlation with ORi values [7, 9, 11, 18, 20, 21].
During pulse oximetry monitoring, there is a sigmoidal relationship between arterial oxygenation in blood gas value and peripheral oxygenation reported as SpO2 value on the pulse oximetry device. This relationship causes no change in pulse oximeter values until PaO2 falls below 80 mmHg. Afterward, there is a sudden drop in pulse oximetry value; however, the PaO2 is unacceptable for more than 3 to 5 min. Therefore, there is a need to investigate a larger scale of several wavelengths to detect quantitative measurement of methemoglobin, carboxyhemoglobin, and total hemoglobin, and a newly presented device achieved this. Masimo Rainbow Signal Extraction Technology introduced the device [14,15,16, 19]. ORi is a parameter-driven from this device that is between 0 and 1 values, and it is sensitive to the changes in arterial oxygenation in the blood, with the range of 100 to 200 mmHg [2, 7,8,9, 13, 15, 18, 20, 21]. When oxygenation is in the moderate hyperoxic content showing an arterial blood oxygenation value of 100–240 mmHg in arterial blood gas analysis, the pulse oximeter SpO2 value remains 100%, whereas, there is a decrease in the value of ORi [2, 7,8,9, 13, 18, 20, 21]. In our study, Fig. 1 and Table 4 provides data on time-dependent correlations between ORi with SpO2.
Increased intrathoracic pressure with respiration leads to more immediate reductions in peripheral perfusion in patients with a fluid deficit. In this case, a decrease in the PI value of the patient is observed. As a result of these changes with respiration, the highest and lowest PI ratio corresponds to the PVI. High PVI values are observed in patients with a high fluid deficit or those who do not respond to fluid application changes with changes in the PI [11, 12, 15,16,17, 23, 24]. In our study, we investigated the ORi and PVI values at different time points during anesthesia induction and maintenance of thoracic surgery and our findings are in correspondence with the previous findings that; fluid deficit or fluid overload causes changes in PI and PVI values. This can be observed in our representative trend graphs in Figs. 2 and 3 [16,17,18, 23, 24].
Our study provides valuable data for the investigation of correlations between ORi and PI, and PVI. OLV with DLT has significant cardiopulmonary physiological changes, as has been discussed elsewhere [14, 16, 17, 19]. Our study provides data that at a time point of DS5, there is a significant negative correlation with PI (r = − 0.332, p = 0.019), whereas; no correlations with PVI were noted. This finding is thought to result from anesthesia drugs that are use during anesthesia induction and especially the use of opioid medications [3,4,5,6, 10, 12].
The use of FiO2 values higher than 50% during anesthesia is related to hyperoxemia, and this high oxygenation decreases cardiac output by reducing heart rate and causing systemic vasoconstriction. Furthermore, hyperoxemia is a potent vasoconstrictor stimulus to the coronary circulation, functioning at the level of the microvascular resistance vessels [7, 21]. Tsuchiya et al. demonstrated that the PVI could be used to evaluate hypotension that is caused secondary to anestethic drugs in patients undergoing general anesthesia without age group classification [23]. This technique has been used in patients undergoing mechanical ventilation in the intensive care unit to detect fluid responsiveness through respiratory patterns and peripheral perfusion changes [11]. There are insufficient data to distinguish the cause of hypotension due to peripheral vasodilatation and fluid redistribution or cardiac output decrease after general anesthesia [23, 24]. High PVI values are observed in patients with a high fluid deficit or those who do not respond to fluid application changes with changes in the PI [24].
In our study, we demonstrated a time-dependent correlation between PVI and MAP at the time point of OLV90, indicating that PVI showed a relation to MAP at a late stage of the surgical procedure. Recently, it is pointed out in a meta-analysis that PVI is a reliable marker in evaluating a response to fluid management [16].