A randomised controlled trial on roles of prostaglandin E1 nebulization among patients undergoing one lung ventilation

Abstract

Background

Prostaglandin E1 (PGE1) has been reported to maintain adequate oxygenation among patients under 60% FiO₂ one-lung ventilation (OLV). This research aimed to explore whether PGE1 is safe in pulmonary shunt and oxygenation under 40% FiO₂ OLV and provide a reference concentration of PGE1.

Methods

Totally 90 esophageal cancer patients treated with thoracotomy were enrolled in this study, randomly divided into three groups (n = 30/group): Group A (60% FiO₂ and 0.1 µg/kg PGE1), Group B (40% FiO₂ and 0.1 µg/kg PGE1), and Group C (40% FiO₂, 0.2 µg/kg PGE1). Primary outcomes were oxygenation and pulmonary shunt during OLV. Secondary outcomes included oxidative stress after OLV.

Results

During OLV, patients in Group C and B had lower levels of PaO₂, SaO₂, SpO₂, MAP, and Qs/Qt than those in Group A (P < 0.05). At T2 (OLV 10 min), patients in Group C and B exhibited a lower level of PaO₂/FiO₂ than those in Group A, without any statistical difference at other time points. The IL-6 levels of patients in different groups were different at T8 (F = 3.431, P = 0.038), with IL-6 in Group C being lower than that in Group B and A. MDA levels among the three groups differed at T5 (F = 4.692, P = 0.012) and T7 (F = 5.906, P = 0.004), with the MDA level of Group C being lower than that of Group B and A at T5, and the MDA level of Group C and B being lower than that of Group A at T7. In terms of TNF-α level, patients in Group C had a lower level than those in Group B and A at T8 (F = 3.598, P = 0.033). Compared with patients who did not use PGE1, patients in Group C had comparable complications and lung infection scores.

Conclusion

The concentration of FiO₂ could be reduced from 60 to 40% to maintain oxygenation. 40% FiO₂ + 0.2 µg/kg PGE1 is recommended as a better combination on account of its effects on the inflammatory factors.

Trial registration: Chictr.org.cn identifier: ChiCTR1800018288, 09/09/2018.

Background

Open radical esophagectomy with extended lymph node dissection is vital for treating esophageal cancer (EC), whether EC is early and locally advanced [1, 2]. One-lung ventilation (OLV) has been extensively used throughout thoracic surgery, being conducive to surgical exposure [3]. However, OLV can decrease the partial pressure of arterial oxygen (PaO₂) and lead to hypoxemia by increasing intrapulmonary shunts and alveolar death space [4, 5]. Furthermore, it has been reported that hypoxemia is associated with an increased risk of complications, such as cognitive impairment, atrial fibrillation, renal failure, and pulmonary hypertension [6, 7]. Therefore, the prevention and treatment of hypoxemia during OLV is an essential part in intraoperative anesthesia management.

A high fraction of inspiration O₂ (FiO₂) has been usually adopted to prevent hypoxemia in clinical practice [8]. However, a recent large multicenter cohort study found that high FiO₂ (FiO₂ > 60%) could promote expiratory pulmonary collapse and atelectasis, with long-term high FiO₂ exposure being associated with worsening oxygenation index [9]. According to current protective ventilation strategies, the FiO₂ should be controlled to the lowest level in the case of sufficient oxygenation, without specific reference of FiO₂ concentrations [10]. Prostaglandin E1 (PEG1), a kind of selective pulmonary arterial vasodilator, has been reported to decrease pulmonary shunts and increase PaO₂ during OLV [11], with a debated optimal dosage [12,13,14] Our previous study has demonstrated that PGE1 can maintain adequate oxygenation in patients under 60% FiO₂ OLV [15]. To the best of our knowledge, the effects of PGE1 on pulmonary shunt and oxygen supply of patients under 40% FiO₂ OLV are still unclear.

Herein, a randomized controlled trial was designed to explore the effect of PGE1 nebulization of ventilated lungs under 40% FiO₂ OLV on maintaining adequate oxygenation based on 90 patients from the Affiliated Cancer Hospital of Nanjing Medical University between 2015 and 2017.

Methods

Study population

Patients with EC scheduled to undergo selective open radical resection were recruited from Affiliated Cancer Hospital of Nanjing Medical University between 2015 and 2017. Diagnosis of EC patients was based on clinical, laboratory, histopathological, and gastroscopy assessment. Exclusion Criteria: (1) percutaneous oxygen saturation (SpO₂) was below 90% during the trial and SpO₂ did not rise to more than 90% or further reduced to less than 88% within 3 min; (2) severe arrhythmia and hemodynamic instability occurred during the whole surgery; (3) surgical duration was more than 6 h or less than 1 h; (4) liver dysfunction and kidney dysfunction were determined based on laboratory test parameters, history of coronary heart disease, cerebral infarction and glaucoma. Random number table was used for group assignment (Fig. 1): Group A (FiO₂ = 60%, PGE1 dose = 0.1 µg/kg, n = 30), Group B (FiO₂ = 40%, PGE1 dose = 0.1 µg/kg, n = 30), Group C (FiO₂ = 40%, PGE1 dose = 0.2 µg/kg, n = 30). This randomized controlled clinical trial was registered at chictr.org.cn (identifier: ChiCTR1800018288, 09/09/2018), approved by the Ethics Committee of the Nanjing Medical University [2017–550].

Fig. 1

Flow diagram of study participants

Anesthesia and intervention

After completing pre-operation preparation, all participants underwent general anesthesia and intubation with a left-side double-lumen tube (DLT). Thirty minutes before admission to the operating room, patients received phenobarbital 0.1 g and atropine 0.5 mg. A central venous catheter was inserted via the right internal jugular vein. Midazolam (0.05 mg/kg), fentanyl (3–4 µg/kg), propofol (1 mg/kg), and cis-atracurium (0.2 mg/kg) were adopted for anesthesia induction. A left-side DLT was then inserted, with fiber bronchoscopy being used to confirm its position. Parameters of the ventilator were set as follows: tidal volume (VT), 6–8 ml/predicted body weight; respiratory rate (RR), 12–14/min; the ratio of inspiratory to expiratory time (I:E rate), 1:2; end-tidal carbon dioxide (ETCO₂), 35–45 mmHg; FiO₂, 60%; positive end-expiratory pressure (PEEP), 5 cmH₂O. The settings of VT and PEEP were kept initially unchanged throughout OLV. When the oxygen partial pressure dropped rapidly below 90%, I:E rate was adjusted to 1:1.5 by increasing RR. If SpO₂ did not rise above 90% or further dropped below 88% within 3 min, 100% O₂ ventilation, continuous positive airway pressure (CPAP) on non-ventilated side lungs, and resumed ventilation of double lungs were performed in sequence if necessary. The unventilated lungs were directly connected to the room air. Group B and Group C were treated with 40% FiO₂ throughout the surgery. Depth of anesthesia was monitored by the bispectral index (BIS), keeping it between 40 and 60.

After confirming the placement of a DLT with a fiberoptic bronchoscope, the patient was repositioned to a right lateral decubitus position, and double lungs were ventilated to nebulization. All the three groups were treated with PGE1 (Beijing Tide Pharmaceutical Co., Ltd., 10 µg/2 ml, diluted to 10 ml with normal saline) nebulization to the right lung through a reconstructed breathing circuit, all nebulization being maintained for 10 min. The Yuyue 402A ultrasonic nebulizer was modified in 2 steps: firstly, seal the bottom of the sprayer tank to remove the air inlet; secondly, isolate the two original atomizer outlets to ensure that one of the exits was a new intake, and the other was the only outlet towards the patients. The device was then connected to the designated breathing circuit [16].

Observed indicators

PaO₂, arterial oxygen saturation (SaO₂), SpO₂, and arterial partial pressure of carbon dioxide (PaCO₂) were determined from the artery and venous blood samples, which were taken at post-anesthesia/pre-nebulization (T1), OLV 10 min (T2), OLV 15 min (T3), OLV 30 min (T4), OLV 60 min (T5), OLV 120 min (T6). Mean arterial pressure (MAP) and airway pressure (PAW) were also recorded. Shunt fraction was calculated using the following formula:

$$\begin{aligned} {\text{Qs}}/{\text{Qt}} & = \left( {{\text{CcO}}_{{2}} - {\text{CaO}}_{{2}} } \right)/\left( {{\text{CcO}}_{{2}} - {\text{CvO}}_{{2}} } \right) [17, 18] \\ {\text{CaO}}_{{2}} & = {\text{PaO}}_{{2}} * 0.00{31} + \left( {{\text{Hb }}*{ 1}.{36 }*{\text{SaO}}_{{2}} } \right) \\ {\text{CvO}}_{{2}} & = \left( {{\text{PvO}}_{{2}} * 0.00{31}} \right) + \left( {{\text{Hb }}*{ 1}.{36 }*{\text{ SvO}}_{{2}} } \right) \\ {\text{CcO}}_{{2}} & = \left[ {{\text{FiO}}_{{2}} *\left( {{\text{P}}_{{\text{B}}} - {\text{P}}_{{{\text{H}}_{{2}} {\text{O}}}} } \right) - {\text{PaCO}}_{{2}} /{\text{R}}} \right]\\ &\quad*0.0031 + \left( {{\text{Hb }}*{ 1}.{36}} \right) \\ \end{aligned}$$

CcO₂, pulmonary capillary blood oxygen content; CaO₂, arterial blood oxygen content; CvO₂, mixed venous blood oxygen content; PvO₂, mixed venous oxygen partial pressure; SvO₂, mixed venous oxygen saturation, we replaced SvO₂ with central venous oxygen saturation (ScvO₂); P_B, atmospheric pressure (760 mmHg); P_H2O, 37 °C water vapor pressure (47 mmHg); R, respiratory quotient (0.8).

Measurement of serum malondialdehyde (MDA) and superoxide dismutase (SOD), Tumor necrosis factor-α (TNF-α), and interleukin 6 (IL-6)

Venous blood sampling through the central line was collected at T1, T5, 30 min after restarting two-lung ventilation (TLV) (T7) and 24 h after surgery (T8). After centrifugation (3000 rpm, 4 °C, 20 min), the serum was stored at − 80 °C until being assayed. According to the manufacturer’s instructions, the concentrations of MDA, SOD, TNF-α, and IL-6 were measured by human MDA, SOD, TNF-α, and IL-6 ELISA Kits.

Postoperative characteristics

Clinical pulmonary infection score (CPIS) [19], complications (pleural effusion, pneumothorax, anastomotic leakage and incision infection), length of stay in the hospital or ICU, and the grade of wound healing were used as our prognostic indicators.

Outcomes

The primary outcomes were oxygenation and pulmonary shunt during OLV, including the observed and measurement indicators of PaO₂, PaO₂/FiO₂ and Qs/Qt, which were determined at T2-T6. Secondary outcomes were oxidative stress after OLV, including MDA, SOD, TNF-α, and IL-6 at T1, T5, T7 and T8.

Statistical analysis

All data analyses were performed by R4.0.3. At least 24 patients were required in each group to achieve a power of 0.8 and a two-sided Alpha level of 0.05. Thirty patients were included in each group considering the drop-out rate of 20%. The measurement data were expressed as mean ± standard deviation (M ± SD) or median [interquartile range, M (Q₁, Q₃)], and intergroup analysis was made by one-way ANOVA, Kruskal–Wallis rank test, or repeated-measures ANOVA of three factors, as appropriate. In addition, Student–Newman–Keuls (SNK) was used for comparisons between groups at each time point. Counting data was tested by the chi-square test. P < 0.05 was considered statistically significant.

Results

Baseline characteristics

A total of 90 patients [71 (78.89%) male, 19 (21.11%) females] were enrolled and randomly divided into three groups, with an average age of (63.32 ± 6.46) years old (Table 1). No patient developed hypoxemia among the two groups. No significant differences in gender, age, BMI, duration of surgery, and duration of OLV were observed among those patients (P > 0.05). Table 2 shows the clinical characteristics of all the patients.

Table 1 Basic situation of studied patients [n (%)/Mean ± SD]

Table 2 Characteristic of patients with esophageal cancer [n (%)/Mean ± SD]

Effects of PGE1 nebulization of ventilated lungs under different FiO₂ OLV on oxygenation and pulmonary shunt

Data acquired at each time point were statistically analyzed using analysis of variance. The results showed that, during OLV, patients in Group C and B had lower levels of PaO₂, SaO₂, SpO₂, MAP, and Qs/Qt than those in Group A (Table 3). At T2 (OLV 10 min), patients in Group C and B exhibited a lower PaO₂/FiO₂ than those in Group A, without any statistical difference at other time points (Table 3).

Table 3 The levels of PaO₂, PaO₂/FiO₂, SaO₂, SPO₂, ETCO₂, PaCO₂, MAP, PAW and QS/QT among three groups

Effects of PGE1 nebulization of ventilated lungs under different FiO₂ OLV on inflammatory factors and postoperative characteristics

Data of inflammatory factors collected at each time point were compared by analysis of variance. The results presented that the IL-6 levels of patients in different groups were different at T8 (F = 3.431, P = 0.038), with the level of IL-6 in Group C being lower than that of Group B and A (Table 4 and Fig. 2A). MDA levels among the three groups were different at T5 (F = 4.692, P = 0.012) and T7 (F = 5.906, P = 0.004), with the MDA level of Group C being lower than that of Group B and A at T5, and the MDA level of Group C and B being lower than that of Group A at T7 (Table 4 and Fig. 2B). In terms of TNF-α level, patients in Group C had a lower level than Group B and A at T8 (F = 3.598, P = 0.033) (Table 4 and Fig. 2C). Differences in the level of SOD were not statistically significant (Table 4 and Fig. 2D). Regarding postoperative characteristics, the lung infection scores of patients in Group C and B were lower than those of Group A, and the difference was statistically significant (P < 0.05) (Table 5). In addition, there was no significant difference in lung infection scores, complications, length of stay in hospital and ICU, and grade of wound healing between patients in Group C and those who did not use PGE1 (Table 6).

Table 4 Levels of inflammatory biomarkers

Fig. 2

IL-6 (A), MDA (B), TNF-α (C), and SOD (D) levels of patients in different time points and different groups. A 60% FiO₂ + 0.1 µg/kg PGE₁; B 40% FiO₂ + 0.1 µg/kg PGE₁; C 40% FiO₂ + 0.2 µg/kg PGE₁.T1, pre-nebulization; T5, one-lung ventilation (OLV) 60 min, T7, two-lung ventilation (TLV) 30 min; T8, 24 h after surgery. ^aP < 0.05 compared with Group A; ^bP < 0.05 compared with Group B

Table 5 Postoperative characteristics of patients in Group A, C and B [M (Q₁, Q₃)/n (%)]

Table 6 Postoperative characteristics of patients in Group C and those who did not use PGE1 under 40% FiO₂ [M (Q₁, Q₃)/n (%)]

Discussion

PGE1 has been reported to maintain adequate oxygenation among patients under 60% FiO₂ one-lung ventilation (OLV) [15]. However, the effects of PGE1 on patients under 40% FiO₂ OLV remain uncertain. We intended to study the effects of PGE1 on pulmonary shunt and oxygenation of patients under 40% FiO₂ OLV and provide a reference concentration of PGE1. Although the levels of PaO₂, SaO₂, MAP, and SaO₂ decreased when the concentration of FiO₂ decreased from 60 to 40%, PaO₂ and SaO₂ remained at a safe level. Furthermore, no statistical difference among patients treated with 60% FiO₂ and 40% FiO₂ was observed regarding PaCO₂, ETCO₂, and PAW levels. In addition, the level of PaO₂/FiO₂ decreased at T2, but the difference at other moments was not statistically significant, with Qs/Qt of patients treated with 40% FiO₂ being lower than 60%. Those results indicated that the concentration of FiO₂ could be reduced from 60 to 40%. In addition, among patients treated with 40% FiO₂, increasing the concentration of PGE1 could reduce the levels of IL-6, MDA, and TNF-α. 40%FiO₂ + 0.2 µg/kg PGE1 is recommended as a better combination on account of its effects on the inflammatory factors.

Previous research illustrated that 58% of patients under 50% FiO₂ OLV had hypoxemia and needed higher FiO₂ to maintain 95% SpO₂ [20]. However, our result showed that no patient (FiO₂ = 40% + 0.2 µg/kg PGE1) developed hypoxemia, indicating that PGE1 could be conducive to maintaining adequate oxygenation under 40% FiO₂ OLV.

During OLV, blood flow is distributed in the collapsed lung without ventilation, and the ventilation/perfusion ratio (V/Q) is almost zero, which results in pulmonary blood flow, without oxygenation, flowing directly into the left atrium and then into the systemic circulation, causing pulmonary shunt [14]. This study showed that once OLV was initiated, the patients’ level of Qs/Qt declined compared to before, which is consistent with the previous research. Inhaling PEG1, a kind of selective pulmonary artery dilator, by ultrasonic atomization during OLV could dilate the pulmonary artery, which causes stealing blood from the shunt area to the non-shunt area, reducing intrapulmonary shunt [21, 22]. In addition, a previous study demonstrated that PGE1 could decrease pulmonary shunt and increase PaO₂ in a dose-dependent manner during OLV [11]. The results showed that the Qs/Qt of patients using 0.2 µg/kg PGE1 and 0.1 µg/kg PGE1 under the condition of 40% FiO₂ was significantly lower than that of patients using 0.1 µg/kg PGE1 under 60% FiO₂. This may be because pre-nebulization of PGE1 to the ventilated lung of OLV during two-lung ventilation could reduce shunt and improve oxygenation. However, our results showed that there was no statistical difference in the levels of Qs/Qt and PaO₂/FiO₂ between patients treated by 0.2 µg/kg PGE1 and 0.1 µg/kg PGE1 under 40% FiO₂, suggesting that 0.1 µg/kg and 0.2 µg/kg PGE1 would maintain sufficient oxygenation, and further studies are needed to explore whether the mechanism of PGE1 is different under different concentrations of FiO₂. In a word, our research results showed that even under 40% FiO₂ OLV, PGE1 could keep lower pulmonary shunt. The mechanisms may be multifaceted. It has been proved experimentally that hypoxic pulmonary vasoconstriction (HPV) could improve oxygenation function in vivo by reducing intrapulmonary shunt [23, 24]. We speculate that PGE1 might affect Qs/Qt by regulating HPV.

Patients treated with 40% FiO₂ had lower levels of IL-6 and MDA than those who used 60% FiO₂. In addition, we found that patients receiving 0.2 µg/kg PGE1 had lower levels of IL-6, MDA, and TNF-α than those receiving 0.1 µg/kg PGE1 under 40% FiO₂. Previous research exhibited that MDA levels were indirect indicators of oxidative stress, and MDA was associated with lung injury [25]. Animal experiments and clinical studies showed that intravenous infusion of PGE1 could lower serum IL-6 and TNF-α levels, reducing organ inflammatory damage [26, 27]. Considering the effects of the inflammatory factors mentioned, 40% FiO₂ + 0.2 µg/kg PGE1 is recommended as a better combination, which may decrease the risk of infection at the time point we have observed.

Prior research indicated that 60% FiO₂ + 0.1 µg/kg PGE1 could maintain adequate oxygenation during OLV, improving oxidative stress and complications after OLV. This study further found that 0.1 µg/kg and 0.2 µg/kg PGE1 could be adopted to maintain the patients’ oxygenation under 40% FiO₂. Additionally, patients under 40% FiO₂ could benefit more from 0.2 µg/kg PGE1 than from 0.1 µg/kg PGE1 in terms of inflammatory factors.

Limitation

Nevertheless, several limitations in this study could not be ignored. Firstly, further subgroup analysis based on complications, age, or gender was unable to be performed due to the small sample size. Secondly, participants with pulmonary dysfunction were not be enrolled in this study. Whether the recommended combination (40% FiO₂ + 0.2 µg/kg PGE1) is suitable for different populations remains to be further verified. Thirdly, we used ScvO₂ instead of SvO₂ in the calculation of shunt fraction. ScvO₂ measures the oxygen saturation of the superior vena cava, while SvO₂ measures the oxygen saturation of the whole body, including the abdomen and lower extremities, so the absolute value is different. Using ScvO₂ to estimate SvO₂ in calculating the shunt fraction was imperfect, and ScvO₂ depended on catheter placement, patient anatomy and physiological state [17]. Fourthly, we speculated that pre-nebulization of PGE1 to the ventilated lung of OLV during two-lung ventilation could reduce shunt and improve oxygenation, but FiO₂ changes may also have an impact on the shunt. Based on the existing results in this article, we are not sure whether the reduction in the shunt fraction is affected by PGE1. More rigorously designed prospective researches with larger sample sizes are required to confirm our results.

Conclusion

PGE1 nebulized on the ventilated lung and FiO₂ reduced to 40% for OLV could reduce the shunt fraction and maintain oxygenation. We recommend a PGE1 concentration of 0.2 µg/kg, which could reduce the levels of inflammatory factors IL-6, MDA and TNF-α during surgery to a certain extent.