- 1Laboratório de Fisiologia da Respiração, Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil
- 2Instituto de Educação, Ciência e Tecnologia do Rio de Janeiro, Rio de Janeiro, Brazil
- 3Hospital Federal dos Servidores do Estado, Rio de Janeiro, Brazil
- 4Laboratório de Investigação Pulmonar, Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil
- 5Programa Doutor Empreendedor, Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro, Rio de Janeiro, Brazil
- 6Instituto D’or de Pesquisa e Ensino, Rio de Janeiro, Brazil
- 7Hospital Barra D’Or, Rio de Janeiro, Brazil
Introduction: During pneumoperitoneum (PNP), airway driving pressure (ΔPRS) increases due to the stiffness of the chest wall and cephalic shift of the diaphragm, which favors atelectasis. In addition, depending on the mechanical power (MP) formulas, they may lead to different interpretations.
Methods: Patients >18 years of age with body mass index >35 kg/m2 were included in a single-center randomized controlled trial during their admission for bariatric surgery by abdominal laparoscopy. Intra-abdominal pressure was set at 15 mmHg at the pneumoperitoneum time point (PNP). After the recruitment maneuver, the lowest respiratory system elastance (ERS) was detected during the positive end-expiratory pressure (PEEP) step-wise decrement. Patients were randomized to the 1) CTRL group: ventilated with PEEP of 5 cmH2O and 2) PEEPIND group: ventilated with PEEP value associated with ERS that is 5% higher than its lowest level. Respiratory system mechanics and mean arterial pressure (MAP) were assessed at the PNP, 5 min after randomization (T1), and at the end of the ventilation protocol (T2); arterial blood gas was assessed at PNP and T2. ΔPRS was the primary outcome. Three MP formulas were used: MPA, which computes static PEEP × volume, elastic, and resistive components; MPB, which computes only the elastic component; and MPC, which computes static PEEP × volume, elastic, and resistive components without inspiratory holds.
Results: Twenty-eight patients were assessed for eligibility: eight were not included and 20 patients were randomized and allocated to CTRL and PEEPIND groups (n = 10/group). The PEEPIND ventilator strategy reduced ΔPRS when compared with the CTRL group (PEEPIND, 13 ± 2 cmH2O; CTRL, 22 ± 4 cmH2O; p < 0.001). Oxygenation improved in the PEEPIND group when compared with the CTRL group (p = 0.029), whereas MAP was comparable between the PEEPIND and CTRL groups. At the end of surgery, MPA and MPB were correlated in both the CTRL (rho = 0.71, p = 0.019) and PEEPIND (rho = 0.84, p = 0.020) groups but showed different bias (CTRL, −1.9 J/min; PEEPIND, +10.0 J/min). At the end of the surgery, MPA and MPC were correlated in both the CTRL (rho = 0.71, p = 0.019) and PEEPIND (rho = 0.84, p = 0.020) groups but showed different bias (CTRL, −1.9 J/min; PEEPIND, +10.0 J/min).
Conclusion: Individualized PEEP was associated with a reduction in ΔPRS and an improvement in oxygenation with comparable MAP. The MP, which solely computes the elastic component, better reflected the improvement in ΔPRS observed in the individualized PEEP group.
Clinical Trial Registration: The protocol was registered at the Brazilian Registry of Clinical Trials (U1111-1220-7296).
Introduction
Millions of laparoscopic procedures are performed globally every year (Boberg et al., 2022), which involve the insufflation of carbon dioxide into the peritoneal cavity to produce a pneumoperitoneum (PNP). PNP can cause dramatic changes in respiratory mechanics due to the stiffness of the chest wall and cephalic shift of the diaphragm, which favors atelectasis (Andersson et al., 2005; Cinnella et al., 2013). Furthermore, the combination of laparoscopic surgery, PNP, and obesity may further increase the negative consequences for the respiratory system (Regli et al., 2019), as observed by an increase in airway driving pressure (ΔPRS). In addition, the cardiac output may decrease with a subsequent decrease in the mean arterial pressure (MAP) after an increase in intra-abdominal pressure (IAP) during the PNP procedure (Regli et al., 2019). Different ventilatory strategies have been adopted during the intraoperative period. The recruitment maneuver (RM) followed by the fixed positive end-expiratory pressure (PEEP) level has been associated with an improvement in intraoperative oxygenation in morbidly obese patients and also with hemodynamic instability (Whalen et al., 2006) or functional improvement occurred only after repetitive RM followed by fixed PEEP level titration (Almarakbi et al., 2009; Talab et al., 2009; Edmark et al., 2016). Individualization of the PEEP level after the application of RM has also been done in laparoscopic surgeries in obese patients using pulse oximetry (Ferrando et al., 2018), electrical impedance tomography (EIT) (Nestler et al., 2017), best respiratory system compliance (D Antini et al., 2018; Boesing et al., 2023), or by transpulmonary pressure (Eichler et al., 2018; Mazzinari et al., 2020). However, the use of these variables requires equipment that is not widely available in operating rooms or the introduction of an esophageal balloon, which is not feasible during bariatric surgery under PNP. In addition, the PEEP level has been individualized in laparoscopic surgery in obese patients using several techniques but with minimal changes in real-life ventilator settings in the perioperative period in obese patients. For instance, during the secondary analysis of the international multicenter LAS VEGAS study (Ball et al., 2018), 2,012 obese patients were ventilated with PEEP of 4 cmH2O. Recently, RM followed by PEEP titration according to the lowest respiratory system elastance (ERS) reduced ΔPRS and cardiovascular performance of the right ventricle in an experimental obesity model and in obese patients (Magder et al., 2021). Nevertheless, the PEEP value associated with minimal ERS may not be feasible during laparoscopic surgery due to hemodynamic instability. Whether ventilating at the PEEP level that corresponds to a 5% increase in ERS according to its minimal value obtained during PEEP titration can maintain the beneficial effects on respiratory system mechanics throughout the surgery without causing hemodynamic instability is not known. Therefore, we hypothesized that a ventilatory strategy based on individualized PEEP (PEEPIND; that is, the PEEP level associated with ERS that is 5% higher than the minimal ERS) can reduce airway driving pressure compared with PEEP of 5 cmH2O and would be hemodynamically feasible.
Material and methods
Study design
This is a single-center, randomized controlled trial that evaluated obese patients admitted for bariatric surgery by abdominal laparoscopy at the Hospital Federal dos Servidores do Estado do Rio de Janeiro between September 2018 and December 2019. This study was approved by the Co-substantiated Ethics and Research Committee of the Hospital Federal dos Servidores do Estado do Rio de Janeiro on 14 December 2015 (CAAE: 51623015.9.0000.5252), and written informed consent was obtained from all subjects participating in the trial. The trial was registered prior to patient enrollment at the Brazilian Registry of Clinical Trials (number U1111-1220-7296; http://www.ensaiosclinicos.gov.br/rg/RBR-68y7cz/; principal investigator: Tiago Batista Xavier; date of registration: 28 September 2018). This report follows the CONSORT 2010 Statement: updated guidelines for reporting parallel group randomized trials (Schulz et al., 2010).
Patient eligibility
The inclusion criteria were patients >18 years of age, with body mass index >35 kg/m2, and signed consent provided. The exclusion criteria were chronic obstructive pulmonary disease with forced expiratory volume at first second (FEV1) <80% or FEV1 divided by forced vital capacity 70% lower after a bronchodilator challenge; heart disease with an ejection fraction <65%; structural chest wall alterations due to obesity such as kyphosis, scoliosis, or hyperlordosis; the absence of consent; and pregnancy.
Experimental protocol
On the day of surgery, the procedure for anesthesia and pre-surgery care, such as fasting period, was followed according to the hospital protocols (Figure 1). Briefly, patients were intubated by endo-tracheal intubation (inner diameter, 7.0 mm), according to a rapid sequence intubation protocol with intravenous administration of fentanyl 1–2 μg/kg, lidocaine 1 mg/kg, propofol 1–2 mg/kg, and succinylcholine 1 mg/kg. General anesthesia was maintained with inhaled sevoflurane in expired concentrations ≥1.4% and intravenous fentanyl 1–2 μg/kg, according to the adequacy of the depth of anesthesia. Neuromuscular blockade after tracheal intubation was maintained with intravenous administration of rocuronium 0.1–0.3 mg/kg or cisatracurium 0.02–0.05 mg/kg every 20–30 min during PNP inflation. The lungs were mechanically ventilated (Aisys, Datex-Ohmeda, Madison, WI, United States) in the 35° dorsal recumbent position using the following parameters at baseline: volume-controlled ventilation (VCV), tidal volume (VT) = 8 mL/kg of the predicted body weight (PBW), the respiratory rate (RR) adjusted to between 10 and 20 bpm to achieve end-tidal carbon dioxide (PETCO2) of 35–45 mmHg, the inspiratory/expiratory (I:E) ratio of 1:2, PEEP 5 cmH2O, and FiO2 0.5–0.6. The heart rate (HR), PETCO2, MAP, and peripheral oxygen saturation (SpO2) were monitored using a multiparameter monitor (S/5; Datex-Ohmeda). After baseline, abdomen insufflation was done using a clinical CO2 insufflator (Baxter), which maintained the IAP at 15 mmHg (∼20 cmH2O) during the surgery. After clinical stabilization, the arterial blood was sampled (1 mL) at the PNP time point, and all patients underwent the initial RM, as is described later. After the initial RM, an additional RM was followed by PEEP titration to detect the PEEP level associated with the lowest ERS (so-called PEEPminERS). At this point, randomization and open allocation into the CTRL and PEEPIND groups were performed according to a computer-generated random number list: 1) the CTRL group was ventilated with the baseline ventilator parameters; 2) the PEEPIND group was ventilated with the same baseline ventilator parameters and the PEEP value associated with ERS that is 5% higher than its lowest level (Figure 2). The surgery was started after both PEEP adjustments were made. No further changes to the ventilation settings were made during the surgery. At the end of surgery, the arterial blood was sampled (1 mL) again, which was still under PNP pressure (15 mmHg).
Figure 1. Timeline of the experimental procedures. ABG, arterial blood gases; CTRL, control group ventilated with PEEP of 5 cmH2O; ERS, respiratory system elastance; MV, mechanical ventilation; PEEP, positive end-expiratory pressure; PEEPIND, PEEP adjusted at ERS that is 5% higher than the PEEPminERS; PNP, pneumoperitoneum; RM, recruitment maneuver; T1, at the beginning of surgery; T2, at the end of surgery.
Figure 2. Representative PEEP–ERS curve. In this patient, the PEEP associated with the lowest ERS was 23 cmH2O (PEEPminERS), and the PEEP associated with the 5% higher ERS than the lowest ERS was 18 cmH2O (PEEPIND). ERS, respiratory system elastance; PEEP, positive end-expiratory pressure.
Initial recruitment maneuver
For the initial RM, pressure-controlled ventilation was adjusted according to the following parameters: delta inspiratory pressure, 15 cmH2O; RR, 10 bpm; I:E ratio, 1:1; PEEP, 5 cmH2O; and FiO2, 1. PEEP was increased to 10 cmH2O for 10 s, followed by an increase to 20 cm H2O for 10 s and to 30 cmH2O for 30 s. After the initial maneuver, the ventilator parameters were adjusted according to the baseline condition.
PEEP titration maneuver
After a similar initial RM, the ventilation mode was rapidly adjusted to VCV under a square flow curve, VT of 8 mL/kg of PBW, RR of 20 bpm, I:E ratio of 1:1, and FiO2 = 1 and PEEP was reduced in steps of 2 cmH2O every 30 s, when feasible according to the MAP safe levels (>65 mmHg), starting at PEEP of 26 cmH2O down to PEEP of 6 cmH2O and ending at PEEP of 5 cmH2O.
The parameter chosen to individualize PEEP was ERS. The ERS at different PEEP levels during the PEEP titration maneuver was estimated in real time by the Bdalog software written in LabVIEW version 8.2 (National Instruments, Austin, TX, United States) using the least square fitting method according to the homogeneous one-compartmental linear model as follows:
where Paw is the airway pressure, Raw is the airway resistance, ERS is respiratory system elastance, and P0 is the airway pressure when the flow and volume are equal to zero. A PEEP–ERS curve was obtained for all patients. The PEEPminERS was recognized as the PEEP level associated with the lowest ERS. PEEPIND represented the lowest PEEP level associated with ERS that is 5% higher than the minimum ERS (Figure 2).
Data acquisition
Airflow, Paw, HR, PETCO2, MAP, and SpO2 data were collected using a multiparameter monitor. Airflow and Paw were also recorded using the serial port of the mechanical ventilator and the Bdalog software. Airflow and CO2 sensors were calibrated by the anesthesiologists. The time points were baseline, PNP, T1, and T2. Baseline and PNP were the time points after endotracheal intubation and during PNP, respectively. T1 and T2 were the time points at the beginning and end of surgery, respectively.
Mechanical power (MP, J/min) was calculated using the following formulas:
The formulas were obtained from previous clinical studies (Gattinoni et al., 2016; Guerin et al., 2016; Giosa et al., 2019). MPA computes the static PEEP × volume, elastic, and resistive components (Gattinoni et al., 2016), whereas MPB computes only the elastic component (Guerin et al., 2016). MPC computes the static PEEP × volume, elastic, and resistive components with the additional benefit that inspiratory holds are not necessary (Giosa et al., 2019).
Statistical analysis
According to previous pilot data from the respiratory physiology laboratory at the Institute of Biophysics Carlos Chagas, a sample of 10 patients per arm would provide the information (1 − β = 0.9) to identify significant (α = 0.05) differences in ΔPRS as the primary outcome between CTRL and PEEPIND (pilot data: CTRL, 12.0 ± 4.2 cmH2O vs. PEEPIND, 20.3 ± 4.5 cmH2O), taking into account an effect size d = 1.84, a two-sided test, and a sample size ratio of 1 (G*Power 3.1.9.2; University of Düsseldorf, Germany).
The primary outcome was airway driving pressure, while secondary outcomes were arterial blood gas and hemodynamic. The normality of the data was tested using the Shapiro–Wilk test. The number and relative frequency were compared by Fisher’s exact test (p < 0.05). The Student’s t-test and Mann–Whitney rank-sum test were used to compare parametric and non-parametric data, respectively. The mechanical data obtained at baseline and PNP time points were compared by paired Student’s t-test. Arterial blood gases, respiratory variables, and MAP obtained from the CTRL and PEEPIND groups at PNP and subsequent time points were compared by two-way ANOVA followed by the Holm–Sidak multiple comparisons test (p < 0.05).
Pearson correlation and Bland–Altman analyses were done between the MPA and MPB formulas and between the MPA and MPC formulas to determine the levels of agreement and bias obtained. The data are expressed as means and standard deviation (SD), medians and interquartile range (IQR), or number and relative frequency (%), as appropriate. The SPSS 25 (SPSS, IBM Inc., Armonk, NY, United States) and GraphPad Prism 9.0 for MacIOS (GraphPad Software, La Jolla, CA, United States) were used. A p < 0.05 was considered significant.
Results
From September 2018 to December 2019, 28 patients were assessed for eligibility at the study site. Eight patients did not meet the inclusion criteria due to chronic obstructive pulmonary disease (n = 4), heart disease with an ejection fraction <65% (n = 3), and pregnancy (n = 1); 20 patients underwent randomization (Figure 3). Overall, 90% of the patients were females, and the median age was 45 years (IQR, 45–52 years), the mean body mass index was 47.6 kg/m2 (SD, ±7.2 kg/m2), and most patients were American Society of Anesthesiologists physical status classification level III. Few patients were diagnosed with restrictive lung disease (15%), with 65% and 55% of them having arterial hypertension and diabetes mellitus, respectively. The surgery time was 71.5 min (IQR, 55.5–77.0 min) (Supplementary Table S1).
Figure 3. Enrolment, randomization, follow-up, and treatment. Twenty-eight patients were assessed for eligibility at the study site. Of these, 20 underwent randomization (10 to CTRL group and 10 to PEEPIND group), and eight patients were excluded for not meeting the inclusion criteria.
ΔPRS, MPA, and MPB increased after the PNP procedure when compared with the baseline (p < 0.001, p = 0.004, and p < 0.001, respectively) (Supplementary Figure S1). Supplementary Figure S2 depicts the PEEP–ERS curve for all the patients. The primary outcome ΔPRS was lower in the PEEPIND group at T1 and T2 than in the CTRL group (p < 0.001) (Table 1). PaO2/FiO2 was higher in the PEEPIND group than in the CTRL group at T2 (p = 0.029). pHa had decreased in both groups over time (p = 0.002 for both). HCO3− was lower in the PEEPIND group than in the CTRL group at T2 (p = 0.016). No differences were observed in PaCO2 and lactate levels (Table 1). MAP decreased in the CTRL group at T1 and T2 in relation to the respective PNP time points (p = 0.011 and p = 0.002, respectively). In addition, MAP decreased in the PEEPIND group at T2 in relation to the respective PNP time point (p = 0.032). No difference was observed between the PEEPIND and CTRL groups at T2 (p = 0.445) (Table 1).
No difference was observed in VT among the groups and over time (Table 1). RR increased in the PEEPIND group at T2 in relation to the PNP time point (p = 0.019). PEEP was higher in the PEEPIND group at T1 and T2 than in the CTRL group (p < 0.001 for both). PpeakRS was higher in the PEEPIND group at T1 than in the CTRL group (p = 0.048). ERS was lower in the PEEPIND group at T1 and T2 than in the CTRL group (p < 0.001). Raw decreased in the PEEPIND group at T1 and T2 in relation to the respective PNP time points (p < 0.001 for both). MPA and MPC were higher, whereas MPB was lower in the PEEPIND group than in CTRL groups at T1 and T2 (Table 1).
In the CTRL group at T2, MPA and MPB showed a positive correlation (rho = 0.71, p = 0.019), whereas the Bland–Altman plot showed a bias of −1.9 J/min between both the formulas for mechanical power (Figures 4A and B). In the PEEPIND group at T2, MPA and MPB showed a positive correlation (rho = 0.84, p = 0.020), while the Bland–Altman plot showed a bias of +10.0 J/min between both the formulas for MP (Figures 4C and D).
Figure 4. Correlations and Bland–Altman plot between MPA and MPB in CTRL and PEEPIND groups at T2. In the CTRL group at T2, MPA and MPB showed a positive correlation (rho = 0.71, p = 0.019), and the Bland–Altman plot showed a bias of −1.9 J/min between both formulas for mechanical power (A,B). In the PEEPIND group at T2, MPA and MPB showed a positive correlation (rho = 0.84, p = 0.020), and the Bland–Altman plot showed a bias of +10.0 J/min between both formulas for mechanical power (C,D). CTRL, control group ventilated with PEEP of 5 cmH2O; MPA, mechanical power formula: 0.098 × RR × VT × (PpeakRS − 0.5 ΔPRS); MPB, mechanical power formula: 0.098 × RR × VT × ΔPRS); PEEP, positive end-expiratory pressure; PEEPIND, PEEP adjusted at ERS that is 5% higher than the PEEPminERS; RR, respiratory rate; T2, at the end of surgery; VT, tidal volume.
In the CTRL group at T2, MPA and MPC showed a positive correlation (rho = 0.98, p < 0.001), whereas the Bland–Altman plot showed a bias of +1.18 J/min between both formulas for MP (Figures 5A and B). In the PEEPIND group at T2, MPA and MPC showed a positive correlation (rho = 0.98, p < 0.001), whereas the Bland–Altman plot showed a bias of +1.41 J/min between both the formulas for MP (Figures 5C and D). Figure 6 shows a summary of the respiratory variables in the PEEPIND group in relation to the CTRL group at T2 in percentage. The increase in MPA (+50%) was highly influenced by the increase in PEEP (+346%) and did not follow the decrease in ΔPRS and ERS (−41% and −42%, respectively). The decrease in MPB (−31%) followed the decrease in ΔPRS and ERS. MPA and MPC showed comparative increments.
Figure 5. Correlations and Bland–Altman plot between MPA and MPC in the CTRL and PEEPIND groups at T2. In the CTRL group at T2, MPA and MPC showed a positive correlation (rho = 0.98, p < 0.001), and the Bland–Altman plot showed a bias of 1.19 J/min between both formulas for MP (A,B). In the PEEPIND group at T2, MPA and MPC showed a positive correlation (rho = 0.98, p < 0.001), and the Bland–Altman plot showed a bias of 1.41 J/min between both formulas for MP (C,D). CTRL, control group ventilated with PEEP of 5 cmH2O; MPA, mechanical power formula: 0.098 × RR × VT × (PpeakRS − 0.5 ΔPRS); MPC, mechanical power formula: 0.098 × VT × RR × (PpeakRS + PEEP + F/6)/20; PEEP, positive end-expiratory pressure; PEEPIND, PEEP adjusted at ERS that is 5% higher than the PEEPminERS; RR, respiratory rate; T2, at the end of surgery; VT, tidal volume.
Figure 6. Summary of respiratory variables in the PEEPIND group in relation to the CTRL group at T2. The solid bars show the increase, and the hatched bars show the decrease in percentage. The MPA increase (+50%) was highly influenced by the increase in PEEP (+346%) and did not follow the decrease in ΔPRS and ERS (−41% and −42%, respectively). MPB (−31%) decrease followed the decrease in ΔPRS and ERS. CTRL, control group ventilated with PEEP of 5 cmH2O; ERS, respiratory system elastance; MPA, mechanical power formula: 0.098 × RR × VT × (PpeakRS − 0.5 ΔPRS); MPB, mechanical power formula: 0.098 × RR × VT × ΔPRS); MPC, mechanical power formula: 0.098 × VT × RR × (PpeakRS + PEEP + F/6)/20. PEEP, positive end-expiratory pressure; PEEPIND, PEEP adjusted at ERS that is 5% higher than the PEEPminERS; PpeakRS, peak airway pressure; Raw, airway resistance; RR, respiratory rate; T2, at the end of surgery; VT, tidal volume; ΔPRS, driving pressure.
Discussion
This single-center, randomized clinical trial on obese patients under PNP for bariatric surgery by abdominal laparoscopy showed that 1) a ventilatory strategy based on the PEEP level associated with ERS that is 5% higher than the lowest ERS was feasible and reduced ΔPRS when compared with a CTRL group ventilated at PEEP of 5 cmH2O; 2) oxygenation improved in the PEEPIND group compared with the CTRL group, with similar MAP; 3) the MPA and MPC formulas used to compute the static PEEP × volume, elastic, and resistive components did not follow the improvement observed in ΔPRS, whereas the MPB formula, which computes only the elastic component, did.
Laparoscopic surgery involves CO2 insufflation into the peritoneal cavity, producing a PNP. IAP of 15 mmHg during PNP increased ΔPRS, likely due to the cranial shift of the diaphragm, reduction of the lung tissue could sustain the strain, and formation of atelectasis (D Antini et al., 2018). After an increase in IAP, the cardiac output may decrease with a subsequent fall in MAP (Regli et al., 2019). Although the PEEPIND group showed increased levels of PEEP compared with the CTRL group, with the MAP being comparable in the two groups. Thus, we can infer that IAP was the main factor responsible for the reduction in MAP, likely due to the compression of the inferior vena cava.
RM followed by a fixed PEEP level of 12 cmH2O has been associated with improved oxygenation in morbidly obese patients, but it is associated with hemodynamic instability (Whalen et al., 2006). In a study on obese patients undergoing laparoscopic gastric banding (Almarakbi et al., 2009), the respiratory mechanics and oxygenation benefits were only achieved by repetitive RM followed by 10 cmH2O PEEP (Talab et al., 2009; Edmark et al., 2016). Nestler et al. (2017) showed that RM followed by individualized PEEP using EIT restored end-expiratory lung volume (EELV), regional ventilation distribution, and oxygenation during anesthesia. Hemodynamic instability was reported during surgery. It has been shown that PEEP levels up to 10 cmH2O (7.3 mmHg) cannot prevent a decline in functional residual capacity caused by grade I intra-abdominal hypertension (12–15 mmHg); they are associated with reduced oxygen delivery as a consequence of reduced cardiac output (Regli et al., 2019). To maintain EELV according to EIT or to keep ERS stable, as observed in our study, PEEP levels were adjusted to 18.5 cmH2O and 16.3 cmH2O, respectively. It has been shown that targeted PEEP levels of 10, 14, and 17 cmH2O at IAP of 8, 12, and 15 mmHg, respectively, resulted in lower transpulmonary driving pressure (Mazzinari et al., 2020). However, PEEP was not titrated and, thus, not individualized. PEEP can counteract the negative effects of intra-abdominal hypertension on lung volume, and the present study favors setting PEEP to allow ERS that is 5% higher than the minimal ERS.
The intraoperative ΔPRS, the ratio of VT to respiratory system compliance, reflects the strain applied on lung tissue available for ventilation during general anesthesia (Silva and Rocco, 2018). After RM and PEEPIND, ΔPRS decreased, likely due to an increase in lung tissue availability to accommodate VT. Because VT did not change, we may infer that overall respiratory system compliance improved. There are currently no data from large trials regarding safe ΔPRS levels for obese patients undergoing mechanical ventilation. Nevertheless, ΔPRS should ideally be limited to a maximum value of 15 cmH2O in non-acute respiratory distress syndrome (ARDS) obese patients (Ball and Pelosi, 2019). The ΔPRS observed in our PEEPIND group was 13 cmH2O, which is within the protective range, while ΔPRS was. In addition, hemodynamic instability is more frequent than respiratory impairment in obese patients without ARDS (Cinnella et al., 2013). In swine with obesity, the RM followed by PEEP titration according to the lowest ERS reduced the inspiratory load on the right ventricle. A similar behavior was observed in obese patients under protective ventilation (Magder et al., 2021), and likely the protection may not only be restricted to the lungs but may also protect the heart.
MP refers to the energy transferred to the respiratory system and, similarly, to ΔPRS, but there are no data regarding safe MP levels for obese patients. The suggested overall protective threshold is 17–20 J/min. ΔPRS and MP are dependent on chest wall elastance, which is increased in obese patients, especially during PNP (Loring et al., 2014; Ball et al., 2018). There are different formulas for MP (Gattinoni et al., 2016; Guerin et al., 2016; Giosa et al., 2019). The fundamental role of calculating MP is to inform lung protection and likely follow the behavior of key variables, such as ΔPRS. Here, PEEPIND led to not only a reduction in ΔPRS toward the protective range but also an increase in MP (>20 J/min) when the MPA and MPC formulas were used. The explanation relies on the contribution of the MP formula components during PEEPIND ventilation. PEEPIND led to a reduction in ΔPRS (elastic component) by 41% when compared with the CTRL. However, to achieve that reduction, PEEP (static PEEP × volume) had to increase by 346% when compared with the CTRL and bypass the improvement observed in the elastic component (Figure 6). No major changes were observed in Raw (resistive component). On applying the MPB formula, agreement with the behavior of ΔPRS was observed. Thus, the choice of the MP formula may have an impact on interpreting the results, as noted by the bias in the PEEPIND (+10.0 J/min) group. The MPC formula has the additional benefit that inspiratory holds are not necessary, which may facilitate the inclusion of an algorithm in mechanical ventilators (Giosa et al., 2019). Because MPC also computes the PEEP × volume and resistive components, it showed a similar behavior to the MPA formula and did not follow the improvement observed in ΔPRS. The rationale for using only the dynamic elastic component or including static elastic and resistive components has been debated extensively (Huhle et al., 2018; Vasques et al., 2018). In addition, a study of 4,549 patients with ARDS showed the concept of using 4 × ΔPRS + 1 × RR (4DPRR) to quantify the impact of changes in the ventilatory strategy on ventilator-induced lung injury (Costa et al., 2021). The 4DPRR formula only computes the dynamic elastic component, similar to the MPB used here. Thus, we believe that our data may provide additional discussion about ventilator settings in obese patients under laparoscopy.
Limitations
We did not compute the postoperative complications, which are highly prevalent in obese patients after laparoscopic surgeries under mechanical ventilation (Bluth et al., 2019). EIT measurements were not done and could add important information about the distribution of VT and EELV in obese patients. However, we conducted the PEEP titration according to the PEEP–ERS curve. We did not measure the transpulmonary pressure because there was no wide-caliber probe to keep the pylorus open, and thus, we could not pass the esophageal balloon. In addition, we did not measure invasive cardiac output and the related variables due to the absence of hemodynamic devices in the operating room.
Conclusion
The present single-center, randomized clinical trial on obese patients under abdominal laparoscopy showed that individualized PEEP was associated with a reduction in ΔPRS and improvement in oxygenation with comparable MAP. The MP, which solely computes the elastic component, better reflected the improvement in ΔPRS observed in individualized PEEP group.
Data availability statement
The original contributions presented in the study are included in the article/Supplementary Material; further inquiries can be directed to the corresponding author.
Ethics statement
The studies involving humans were approved by the Co-substantiated Ethics and Research Committee of the Hospital Federal dos Servidores do Estado do Rio de Janeiro, on 14 December 2015 (CAAE: 51623015.9.0000.5252), and written informed consent was obtained from all subjects participating in the trial. The studies were conducted in accordance with the local legislation and institutional requirements. The participants provided their written informed consent to participate in this study.
Author contributions
TX: Conceptualization, data curation, formal analysis, investigation, methodology, project administration, software, supervision, validation, manuscript writing—original draft, review, and editing. LeC: Data curation, formal analysis, investigation, methodology, manuscript writing—original draft, review, and editing. DF: Data curation, formal analysis, investigation, methodology, manuscript writing—original draft, review, and editing. JC: Data curation, formal analysis, investigation, methodology, manuscript writing—original draft, review, and editing. MD: Conceptualization, data curation, formal analysis, investigation, methodology, manuscript writing—original draft, review, and editing. LS: Formal analysis, methodology, validation, visualization, manuscript writing—original draft, review, and editing. GM-R: Data curation, formal analysis, methodology, software, validation, manuscript writing—original draft, review, and editing. LuC: Conceptualization, data curation, formal analysis, investigation, methodology, manuscript writing—original draft, review, and editing. AC: Conceptualization, data curation, formal analysis, investigation, software, validation, visualization, manuscript writing—original draft, review, and editing. PS: Data curation, formal analysis, funding acquisition, resources, supervision, validation, visualization, manuscript writing—original draft, review, and editing.
Funding
The authors declare that no financial support was received for the research, authorship, and/or publication of this article.
Acknowledgments
The authors would like to express their gratitude to Lorna O’Brien (authorserv.com) for editing assistance.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
The authors declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision.
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Supplementary material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fphys.2024.1383167/full#supplementary-material
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Glossary
Keywords: laparoscopy, obesity, pressure, positive end-expiratory, respiratory mechanics
Citation: Xavier TB, Coelho LV, Ferreira DAL, Cota y Raposeiras JM, Duran MS, Silva LA, Motta-Ribeiro GCd, Camilo LM, Carvalho ARS and Silva PL (2024) Individualized positive end-expiratory pressure reduces driving pressure in obese patients during laparoscopic surgery under pneumoperitoneum: a randomized clinical trial. Front. Physiol. 15:1383167. doi: 10.3389/fphys.2024.1383167
Received: 07 February 2024; Accepted: 19 March 2024;
Published: 05 April 2024.
Edited by:
Alberto Noto, University of Messina, ItalyReviewed by:
Lucia Mirabella, University of Foggia, ItalyAndrea Cortegiani, University of Palermo, Italy
Copyright © 2024 Xavier, Coelho, Ferreira, Cota y Raposeiras, Duran, Silva, Motta-Ribeiro, Camilo, Carvalho and Silva. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Pedro Leme Silva, cGVkcm9sZW1lQGJpb2YudWZyai5icg==