Slow Positive End-Expiratory Pressure Titration During General Anesthesia with Muscle Paralysis Improves Lung Function Without Compromising Hemodynamic Stability in Preschool Children: A Randomized Control Clinical Trial

authors:

avatar Ana Dragoljub Mandras ORCID 1 , * , avatar Ivan Soldatovic 2 , avatar Maja Sujica ORCID 1 , avatar Vesna Stevanovic ORCID 1 , avatar Dejan Markovic 3 , avatar Zoran Paunovic ORCID 4 , avatar Predrag Minic 5

Department of Anesthesiology and Intensive Care Therapy, Institute for Mother and Child Health Care, Belgrade, Serbia
Institute for Medical Statistics and Informatics, Medical Faculty University of Belgrade, Belgrade, Serbia
Department of Anesthesiology, Clinic for Cardiovascular Surgery, Clinical Center of Serbia, Belgrade, Serbia
Department of Orthopedics, Institute for Mother and Child Health Care, Belgrade, Serbia
Depratment of Pulmonolgy, Institute for Mother and Child Health Care, Belgrade, Serbia

how to cite: Mandras A D, Soldatovic I, Sujica M, Stevanovic V, Markovic D, et al. Slow Positive End-Expiratory Pressure Titration During General Anesthesia with Muscle Paralysis Improves Lung Function Without Compromising Hemodynamic Stability in Preschool Children: A Randomized Control Clinical Trial. Iran J Pediatr. 2019;29(6):e92269. https://doi.org/10.5812/ijp.92269.

Abstract

Background:

Mechanical ventilation impairs oxygenation and increases intrapulmonary shunt. Positive end-expiratory pressure (PEEP) slows derecruitment, improves lung function but can compromise hemodynamics.

Objectives:

To asses slow PEEP titration effect on intrapulmonary shunt, oxygenation and hemodynamics in preschool children on mechanical ventilation under general anesthesia.

Methods:

This was a single tertiary care center an open-label, randomized parallel group controlled clinical trial. Study included 70 children, 3 - 7 years, ASA I and II, under general anesthesia for non-cardiothoracic surgery. Children were randomly allocated either to receive PEEP titration 5 - 11 cmH2O 20 minutes before the end of anesthesia (intervention group) or to be ventilated until the end of anesthesia with constant positive end-expiratory pressure of 3 cmH2O (control group). Main outcome measures were changes in oxygenation index (PaO2/FiO2) and alveolar-arterial gradient (P(A-a)O2) between and within groups and changes in systolic blood pressure (SBP), mean arterial pressure (MAP) and heart rate (HR) in interventional group during PEEP trial.

Results:

Seventy children were recruited and analyzed. P(A-a)O2 and PaO2/FiO2 improved in interventional group comparing to control as consequence of PEEP titration (ΔPaO2/FiO2 -30.3 vs. 0.52; P < 0.001; ΔP(A-a)O2 6.7 vs. -1.0; P < 0.001) and within interventional group before and after PEEP titration (PaO2/FiO2 522.0 vs. 552.3; P < 0.01; P(A-a)O2 20.1 vs. 13.3; P < 0.001). Hypotension and bradycardia were not documented.

Conclusions:

Slow PEEP titration up to 11 cmH2O improves oxygenation, reduces intrapulmonary shunt without causing hemodynamic instability in preschool children during general anesthesia.

1. Background

Mechanical ventilation promotes alveolar derecruitment, atelectasis and increases physiological intrapulmonary shunt (1, 2). This can lead to impaired oxygen exchange. Positive end-expiratory pressure (PEEP) is used to counteract alveolar derecruitment and improve oxygen exchange. Literature data from human and animal studies show overall positive effect of PEEP on lung function (3-7). On the other hand, PEEP exerts negative hemodynamic effects. As distending pressure PEEP increases intrathoracic pressure, decreases venous return and cardiac output in normovolemic and hypovolemic patients (8). Depending on speed of titration and PEEP level these effects can be more or less clinically apparent (4, 7, 9). Slow PEEP titration up to 20 cmH2O during 15 minutes achieved recruitment, improved gas exchange and decreased intrapulmonary shunt without circulatory depression (4, 7).

2. Objectives

Based on data obtained from experimental model, we hypothesized that intraoperative preventive PEEP titration up to 11 cmH2O during 5 minutes can improve lung function without causing hypotension and bradycardia in preschool children with healthy lungs during general anesthesia for non-cardiothoracic surgery.

3. Methods

This was a prospective, randomized, two arms, unblinded, clinical trial in children undergoing general anesthesia for non-cardiothoracic surgery. Study was conducted at Institute for Mother and Child Health Care, Belgrade, Serbia between January 2017 and June 2017. Study was approved by Ethic Committee of Institute for Mother and Child Health Care (No 8/30, 2017.) and performed in accordance to criteria set by Declaration of Helsinki. All parents/legal guardians were informed about study protocol and children were enrolled only if parents/legal guardians gave informed consent. Study included 70 preschool children scheduled for general anesthesia for non-cardiothoracic surgery. They were randomly assigned into two groups; interventional (I group; n = 35) and control group (C group; n = 35). Inclusion criteria were: age 3 - 7 years, ASA I and II. Exclusion criteria were: current or recent (up to 4 weeks) upper airway infection, present cardiovascular and present respiratory comorbidity. All children were assessed preoperatively one day before surgery. Premedication and general anesthesia were the same in both groups. Children were premedicated with midazolam 0.1 mg/kg iv. Anesthesia induction was performed by thiopental 5 mg/kg iv, fentanyl 3 mcg/kg iv, sevoflurane 1 vol%, O2:air mixture 35%:65% and muscle paralysis with rocuronium 1 mg/kg. Trachea was intubated with proper sized tube. Anesthesia was maintained using sevoflurane 1.5 vol%/2 vol%, fentanyl 2 mcg/kg and rocuronium. Intravascular volume was maintained with Ringer lactate solution using 4:2:1 rule plus intraoperative losses (10). Both groups had the same initial ventilator settings (DatexOhmeda, Avance CS2, GE anesthesia machine) except for 20 minutes before the end of surgery. Initial ventilator settings were: PCV, Pinsp adjusted to achieve tidal volume (Vt) 6 - 8 mL/kg, respiratory rate adjusted to achieve end expiratory carbon dioxide (EtCO2) 35 mmHg - 45 mmHg, PEEP 3 cmH2O, air:oxygen 65%:35%. After intubation arterial line was placed and invasive monitoring of blood pressure set up. Monitoring during anesthesia was: hemoglobin oxygen saturation (SpO2), capnography and capnometry (EtCO2), invasive blood pressure (IBP), heart rate (HR), inspiratory pressure (Pins), peak airway pressure (Ppeak), mean airway pressure (Pmean) and dynamic lung compliance (Cdyn). We used monitoring incorporated in anesthesia machine (DatexOhmeda, Avance CS2, GE anesthesia machine). Arterial blood samples were analyzed immediately after obtaining the sample (ABL 90 Radiometer, Copenhagen, Denmark).

3.1. Allocation

Patients were randomly assigned in a 1:1 ratio into either interventional or control group. We used sealed envelope technique to allocate participants in groups. The box containing 70 envelopes with allocation instruction (I: interventional group; C: control group) was used to allocate patients randomly. Before first sampling of arterial blood anesthetist in charge pulled the envelope from the box and allocated patient to experimental or control group.

3.2. Intervention

Twenty minutes before the end of anesthesia and surgery PEEP was increased in interventional group by 2 cmH2 on every 5 breaths up to 11 cmH2. Ventilation was maintained on PEEP 11 cmH2 for 2 minutes. Then, PEEP was decreased by 2 cmH2 for every 5 breaths to 5 cmH2O. Ventilation with PEEP of 5 cmH2O was unchanged until extubation in order to keep re-aerated alveoli open. Total time to perform the PEEP maneuver was 5 minutes. Control group was ventilated the whole time with baseline PEEP setting (3 cmH2O). PEEP 3 cmH2O is lowest PEEP level used in clinical practice and is associated with derecrutiment. As a part of study design, we kept it constant in control group to be able to differences in PaO2/FiO2 index and P(A-a)O2 gradient between two groups. Arterial blood was collected in the same two time points in both groups (Figure 1): TIME I- before PEEP titration, which was 20 minutes before the end of surgery and TIME II before extubation. Criteria for aborting the procedure were hypotension, bradycardia, desaturation below SpO2 94% and sudden rise in Ppeak. Based on previous published data hypotension was defined as SBP < 70 mmHg and MAP < 55 mmHg (11, 12). Bradycardia was defined as heart rate ≤ 60/min.

Timing of blood sampling and PEEP maneuver. TI: 20 minutes before the end of operation; TII: before extubation.
Timing of blood sampling and PEEP maneuver. TI: 20 minutes before the end of operation; TII: before extubation.

3.3. Study Outcomes

To evaluate oxygen exchange we used PaO2/FiO2 index and to evaluate changes in intrapulmonary shunt we used P(A-a)O2 gradient. Hemodynamic changes during PEEP titration were evaluated using MAP, SBP, and HR.

3.4. Statistical Analysis

Sample size was calculated using available literature data on PEEP effect on oxygen exchange (PaO2/FiO2) (13) with α = 0.05 and study power of 80%. The number needed was 35 participants per group. All data were analyzed using IBM-SPSS 20.0 (IBM Corp, New York, USA) statistical software. Results are presented as mean and standard deviation with CI 95% or proportions. To evaluate size effect PEEP titration produced, we calculated delta (Δ) and compared it between groups. To test the difference between groups Student’s t-test for independent samples and Mann-Whitney U test were used depending on data distribution. To test the difference within intervention group before and after PEEP titration paired sample t-test was used. To test the difference in SBP, MAP and HR in interventional group on different PEEP levels repeated measurements ANOVA was used. All tests were 2-tailed and P < 0.05 was considered statistically significant.

4. Results

Between January and June 2017, 486 children were scheduled for surgery, 271 were younger than 3 and older than 7 years, 113 refused to participate, 10 had upper respiratory tract infection, 7 had present chronic heart and lung conditions and 15 didn’t show up at all on the day of surgery. All enrolled participants between January 2017 and June 2017 completed the study and were analyzed for outcomes (Figure 2). Baseline data of participants are presented in Table 1.

CONSORT 2010 flow diagram
CONSORT 2010 flow diagram
Table 1.

Characteristics of Patientsa

GroupP Value
InterventionalControl
Age, y4.9 ± 1.55.1 ± 1.60.728b
Body weight, kg18.8 ± 5.219.4 ± 5.30.682b
Gender (male)19 (54)25 (71)0.138c
Comorbidity present14 (40)6 (17)0.034c
Type of surgery0.328c
Abdominal12 (34)10 (29)
Urology7 (20)14 (40)
Orthopedics7 (20)5 (14)
Reconstructive surgery9 (26)6 (17)
Procedure duration > 60 min20 (57)22 (63)0.238c

4.1. Main Outcomes

Differences in P(A-a)O2 and PaO2/FiO2 between and within groups in TIME I and II are presented in Table 2. There was significant difference between groups in TI (before PEEP maneuver) in both parameters. Independent t-test for delta between groups (Δ TI - TII) revealed that there was a statistically significant difference in magnitude of change in P(A-a)O2 and PaO2/FiO2 between groups which means that intervention had effect. Comparison within I group showed that there was significant difference in both parameters before and after PEEP titration (TI vs. TII). Both parameters improved after PEEP maneuver. Table 3 displays changes in SBP, DBP, MAP and HR during PEEP titration in interventional group. There were no episodes of hypotension or bradycardia during PEEP titration, all subjects remained hemodynamically stabile. Figure 3 displays changes in MAP on different PEEP levels. Figure 4 displays HR on different PEEP levels.

Table 2.

Difference in Respiratory Parameters Between and Within Groups in TI and TIIa

GroupP Value
InterventionalControl
PaO2/FiO2
TI (Before)522.0 (508.2 - 535.9)554.7 (547.3 - 562.2)< 0.001b
TII (After)552.3 (545.2 - 559.4)554.2 (541.6 - 566.8)0.784b
P value (TI - TII)< 0.001c0.870c
Δ PaO2/FiO2-30.3 (-38.7 - -21.8)0.52 (-5.87 - 6.91)< 0.001b
P(A-a)O2
TI (Before)20.1 (15.5 - 24.7)8.7 (6.5 - 10.9)< 0.001d
TII (After)13.3 (10.8 - 15.9)9.7 (6.1 - 13.4)0.230d
P value (TI - TII)< 0.001c0.350c
Δ P(A-a)O26.7 (4.1 - 9.4)-1.0 (-3.2 - 1.1)< 0.001b
Table 3.

Differences in Hemodynamic Parameters During PEEP Titrationa

MeasurementMAPSystolic BPHeart Rate
PEEP 3 vs. 5 70.6 (67.5 - 73.6)100 (96.3 - 103.7)105.6 (97.7 - 113.4)
PEEP 5 vs. 7 75 (72 - 77.9)b102.3 (99.3 - 105.3)97 (90.8 - 103.2)b
PEEP 7 vs. 9 72.9 (69.8 - 76)b100.5 (96.9 - 104.2)b94.6 (88.3 - 101)b
PEEP 9 vs. 11 72.9 (69.5 - 76.3)99.1 (94.7 - 103.6)b94.4 (87.8 - 101)
PEEP 11 vs. 11 in 1st minute72.5 (68.6 - 76.4)98.6 (93.8 - 103.5)92.5 (86.2 - 98.7)b
PEEP 11 in 1st minute vs. 11 in 2nd minute72.3 (69 - 75.7)97.5 (93.9 - 101.2)93.8 (87.5 - 100.1)
PEEP 11 vs. 971.8 (68.8 - 74.9)96.9 (93.5 - 100.2)95.3 (88 - 102.5)
PEEP 9 vs. 774 (70.5 - 77.6)b100.2 (96.3 - 104.1)b97.7 (90.9 - 104.4)b
PEEP 7 vs. 575.1 (72 - 78.1)b99.4 (96 - 102.8)98.2 (91.7 - 104.7)
PEEP 5 vs. 5 in 2nd minute75.7 (72.5 - 79)99.6 (95.9 - 103.3)97.4 (91.3 - 103.5)
PEEP 5 in 2nd minute vs. PEEP 5 in 10th minute74.2 (70.9 - 77.5)96.3 (89.9 - 102.6)97.5 (91.5 - 103.6)
PEEP 5 in 10th minute vs. PEEP 5 before extubation73.3 (71.3 - 75.3)97.7 (95.1 - 100.4)95.2 (89.6 - 100.8)b
MAP changes during PEEP titration
MAP changes during PEEP titration
HR changes during PEEP titration
HR changes during PEEP titration

5. Discussion

For more than two decades PEEP was used to improve lung function on mechanically ventilated patients. Proposed values that should prevent perioperative deterioration of lung function are 7 - 15 cmH2O (14). Most of data regarding intraoperative preventive use of PEEP was pooled from adult studies and extrapolated to pediatric population. The aim of this study was to evaluate slow stepwise up and down PEEP titration effect from 5 - 11 cmH2O on intrapulmonary shunt, oxygenation and hemodynamics in preschool children in general anesthesia with muscle paralysis for non-cardiothoracic surgery. As markers of lung function we used alveolar-arterial gradient (P(A-a)O2) and oxygen exchange index (PaO2/FiO2). P(A-a)O2 is simple and reliable indicator of physiological shunt alterations in cardiorespiratory stable patients on constant FiO2. PaO2/FiO2 has been widely used to evaluate oxygen exchange and it is modified with PEEP and respiratory condition of the patient (15). Due to simplicity of bedside calculation of both parameters, absence of cardiorespiratory comorbidity in study population and ventilation with constant FiO2, we used those parameters to evaluate PEEP titration effect. In our study effect produced by PEEP maneuver was beneficial for patients in interventional group. P(A-a)O2 decreased within interventional group and compared to control. Improvement in P(A-a)O2 was a consequence of decrease in intrapulmonary shunt caused by applied PEEP maneuver. Similar results were presented in studies on adult patients and laboratory animals (4, 16). Ambrosio et al. observed decrease in P(A-a)O2 with increasing PEEP from 5 - 20 cmH2O (4). In pediatric patients, titration of PEEP decreased P(A-a)O2 1 hour after laparscopic surgery compered to children ventilated without PEEP (17). Positive pressure ventilation with PEEP 10 cmH2O also caused significant decrease of P(A-a)O2 in patients after coronary artery bypass grafting (16). The difference of mentioned studies on humans regarding our study was the study sample. We investigated effect on cardiorespiratory healthy preschool children. Nevertheless, in both studies authors mitigated conditions that could limit the use of P(A-a)O2 gradient. All samples in their study were obtained when patients were cardiorespiratory stable and on constant FiO2, similar to conditions in our study. Therefore we believe this is comparable to our study. As marker of oxygen exchange we investigated changes in PaO2/FiO2 index since it is influenced by PEEP. PEEP titration improved oxygen exchange within interventional group and compared to control group. Improvement in PaO2/FiO2 index was also demonstrated on isolated experimental lung when PEEP 5 and 10 was applied (5). In pediatric patients with ARDS, stepwise down PEEP titration from 25 cmH2O to “open lung PEEP” led to improvement in PaO2/FiO2 index (13). These results are similar to ours. On the other hand, we cannot ignore that sometimes PEEP application fails to improve PaO2/FiO2 index. In experimental model application of PEEP 5 - 7 failed to improve PaO2/FiO2 index but it did slow down raise of elastance that was used as marker of derecruitment (18). In pediatric patients after cardiopulmonary bypass (CBP) adding PEEP 8 cmH2O didn’t cause improvement in PaO2/FiO2 index compared to PEEP 0 (19). Our study group consisted of children with healthy lungs and atelectasis developed was consequence of mechanical ventilation only. In contrast, study population in the mentioned study was patients with injured lungs. Adding PEEP up to 11 cmH2O in our study was enough to improve oxygen exchange in healthy lungs but adding PEEP 8 wasn’t enough to improve oxygenation in injured lungs. Indeed, PEEP modifies PaO2/FiO2 index and the same index value can be obtained under different respiratory conditions and PEEP levels (20). Oxygenation changes when PEEP is applied better correlate with aerated lung parts than with poorly aerated or collapsed areas (21). So, the effect that PEEP produces regarding oxygenation depends not only on PEEP level but also on initial lung condition. Therefore, when evaluating lung function, especially in terms of lung recruitment, oxygenation exchange should not be used as the only marker.

Application of PEEP can have negative hemodynamic effect, regardless of its beneficial effect on lung function. To estimate its impact on hemodynamics we used MAP, SBP and HR. Besides the fact that they are easy to obtain, those parameters are advised as obligatory monitoring in every day practice. PEEP increases intrathoracic pressure. As a consequence, venous return decreases, right ventricular (RV) afterload increases, ventricular compliance and contractility decrease (8, 22). Increase in RV afterload leads to left shifting of septum, decrease in left ventricular end-diastolic diameter and left ventricular end-diastolic area (23). In hypovolemic and normovolemic patients, PEEP reduces cardiac output due to decreased venous return (22). Above mentioned changes in cardiac performance may or may not be clinically significant (23). During our PEEP trial there was not a single case of hypotension or/and bradycardia, as invasive blood pressure and ECG monitoring showed. All patients remained hemodynamically stable on each PEEP level. This is in accordance with previously published data. In systematic review Algera et al. analyzed hemodynamic effect of low PEEP (med 0, IQR 0 - 5) vs. high PEEP (med 10, IQR 3 - 20) in experimental animals with uninjured lungs. In 2 trials, application of high PEEP didn’t cause hypotension and bradycardia, 1 trial documented lower blood pressure (24). In study by Ambrosio et al. during 15 minutes PEEP titration up to 20 cmH2O cardiac output, cardiac index, systemic and pulmonary vascular resistance were significantly lower at PEEP of 20 cmH2O but this wasn’t clinically significant. Animals in both groups remained hemodynamically stable with no differences in HR and MAP within and between groups (4). Although this is experimental study, it is similar to ours in some points: uninjured lung, level of applied PEEP and the slow PEEP titration. Slow titration of PEEP up to 15, when compared to fast PEEP titration up to 10 and 20, causes less circulatory depression (7). In clinical setting, in hemodynamically stable children after repair of congenital cardiac defect, PEEP 4 - 12 cmH2O caused fall of cardiac index, but this reduction wasn’t clinically significant (25, 26). Several studies used MAP and HR to evaluate hemodynamic effect of PEEP in hemodynamically stable patients. Although MAP and HR can be reduced up to 5% with PEEP 10, this was not recognized as bradycardia or hypotension (27, 28). In their review article, Berger and Takala discussed impact of PEEP on hemodynamics, more precisely, on mean systemic filling pressure (MSFP) and venous return as major factors whose changes, induced by PEEP, influence CO. They pointed out controversy in experimental research, where some studies document unchanged venous return and CO or decreased CO with PEEP 10 - 20 cmH2O (22). Few years previously authors investigated impact of lower PEEP levels 5 - 10 cmH2O with stable airway pressure and found no effect on MSFP, venous return or resistance to venous return (29). None of CO determinants (and hemodynamics) was changed. As authors speculated, reason for these different results is probably a consequence of ventilator strategy with small pressures and tidal volumes. This is similar to our study since we used protective ventilation strategy, as mentioned earlier.

Limitation to our study is its open label design. We are aware that if the anesthesiologist who performed PEEP titration was not involved in data collection, and the observer who collected the data was unaware of the study groups, the results would be more convincing.

5.1. Conclusions

Our investigation confirmed hypothesis of study that preventive slow stepwise up and down PEEP titration form of 5 - 11 cmH2O improves oxygen exchange and decreases intrapulmonary shunt without compromising hemodynamics in preschool children in general anesthesia. Applied PEEP levels are sufficient to improve lung function and safe to use in everyday practice in children without cardiorespiratory comorbidity.

Acknowledgements

References

  • 1.

    Tusman G, Acosta CM, Bohm SH, Waldmann AD, Ferrando C, Marquez MP, et al. Postural lung recruitment assessed by lung ultrasound in mechanically ventilated children. Crit Ultrasound J. 2017;9(1):22. [PubMed ID: 29030754]. [PubMed Central ID: PMC5640559]. https://doi.org/10.1186/s13089-017-0073-0.

  • 2.

    Acosta CM, Tusman G, Costantini M, Echevarria C, Pollioto S, Abrego D, et al. Doppler images of intra-pulmonary shunt within atelectasis in anesthetized children. Crit Ultrasound J. 2016;8(1):19. [PubMed ID: 27910005]. [PubMed Central ID: PMC5133206]. https://doi.org/10.1186/s13089-016-0055-7.

  • 3.

    Suarez-Sipmann F, Bohm SH, Tusman G, Pesch T, Thamm O, Reissmann H, et al. Use of dynamic compliance for open lung positive end-expiratory pressure titration in an experimental study. Crit Care Med. 2007;35(1):214-21. [PubMed ID: 17110872]. https://doi.org/10.1097/01.CCM.0000251131.40301.E2.

  • 4.

    Ambrosio AM, Ida KK, Souto MT, Oshiro AH, Fantoni DT. Effects of positive end-expiratory pressure titration on gas exchange, respiratory mechanics and hemodynamics in anesthetized horses. Vet Anaesth Analg. 2013;40(6):564-72. [PubMed ID: 23848843]. https://doi.org/10.1111/vaa.12068.

  • 5.

    Michelet P, Roch A, Brousse D, D'Journo XB, Bregeon F, Lambert D, et al. Effects of PEEP on oxygenation and respiratory mechanics during one-lung ventilation. Br J Anaesth. 2005;95(2):267-73. [PubMed ID: 15980044]. https://doi.org/10.1093/bja/aei178.

  • 6.

    Spadaro S, Karbing DS, Mauri T, Marangoni E, Mojoli F, Valpiani G, et al. Effect of positive end-expiratory pressure on pulmonary shunt and dynamic compliance during abdominal surgery. Br J Anaesth. 2016;116(6):855-61. [PubMed ID: 27199317]. https://doi.org/10.1093/bja/aew123.

  • 7.

    Odenstedt H, Lindgren S, Olegard C, Erlandsson K, Lethvall S, Aneman A, et al. Slow moderate pressure recruitment maneuver minimizes negative circulatory and lung mechanic side effects: Evaluation of recruitment maneuvers using electric impedance tomography. Intensive Care Med. 2005;31(12):1706-14. [PubMed ID: 16177920]. https://doi.org/10.1007/s00134-005-2799-6.

  • 8.

    Luecke T, Pelosi P. Clinical review: Positive end-expiratory pressure and cardiac output. Crit Care. 2005;9(6):R607-22. [PubMed ID: 16356246]. [PubMed Central ID: PMC1414045]. https://doi.org/10.1186/cc3877.

  • 9.

    Ross PA, Khemani RG, Rubin SS, Bhalla AK, Newth CJ. Elevated positive end-expiratory pressure decreases cardiac index in a rhesus monkey model. Front Pediatr. 2014;2:134. [PubMed ID: 25520944]. [PubMed Central ID: PMC4253666]. https://doi.org/10.3389/fped.2014.00134.

  • 10.

    Mc Clain CD, Mc Manus ML. Fluid management. In: Cote CJ, Lerman J, Anderson BJ, editors. A practice of anesthesia for infants and children. 6th ed. Philadelphia: Elsevier; 2019. p. 982-1001.

  • 11.

    Haque IU, Zaritsky AL. Analysis of the evidence for the lower limit of systolic and mean arterial pressure in children. Pediatr Crit Care Med. 2007;8(2):138-44. [PubMed ID: 17273118]. https://doi.org/10.1097/01.PCC.0000257039.32593.DC.

  • 12.

    Shung J. Intra-operative hypotension in children: does it matter? South Afr J Anaesth Analgesia. 2014;16(2):42-4. https://doi.org/10.1080/22201173.2010.10872664.

  • 13.

    Cruces P, Donoso A, Valenzuela J, Diaz F. Respiratory and hemodynamic effects of a stepwise lung recruitment maneuver in pediatric ARDS: A feasibility study. Pediatr Pulmonol. 2013;48(11):1135-43. [PubMed ID: 23255291]. https://doi.org/10.1002/ppul.22729.

  • 14.

    Neves VC, Koliski A, Giraldi DJ. Alveolar recruitment maneuver in mechanic ventilation pediatric intensive care unit children. Rev Bras Ter Intensiva. 2009;21(4):453-60. [PubMed ID: 25307339].

  • 15.

    Sanchez Casado M, Quintana Diaz M, Palacios D, Hortiguela V, Marco Schulke C, Garcia J, et al. [Relationship between the alveolar-arterial oxygen gradient and PaO(2)/FiO(2)-introducing PEEP into the model]. Med Intensiva. 2012;36(5):329-34. Spanish. [PubMed ID: 22154281]. https://doi.org/10.1016/j.medin.2011.10.007.

  • 16.

    Marvel SL, Elliott CG, Tocino I, Greenway LW, Metcalf SM, Chapman RH. Positive end-expiratory pressure following coronary artery bypass grafting. Chest. 1986;90(4):537-41. [PubMed ID: 3530647]. https://doi.org/10.1378/chest.90.4.537.

  • 17.

    Abdel-Ghaffar HS, Youseff HA, Abdelal FA, Osman MA, Sayed JA, Riad MAF, et al. Post-extubation continuous positive airway pressure improves oxygenation after pediatric laparoscopic surgery: A randomized controlled trial. Acta Anaesthesiol Scand. 2019;63(5):620-9. [PubMed ID: 30761530]. https://doi.org/10.1111/aas.13324.

  • 18.

    Camilo LM, Avila MB, Cruz LF, Ribeiro GC, Spieth PM, Reske AA, et al. Positive end-expiratory pressure and variable ventilation in lung-healthy rats under general anesthesia. PLoS One. 2014;9(11). e110817. [PubMed ID: 25383882]. [PubMed Central ID: PMC4226529]. https://doi.org/10.1371/journal.pone.0110817.

  • 19.

    Scohy TV, Bikker IG, Hofland J, de Jong PL, Bogers AJ, Gommers D. Alveolar recruitment strategy and PEEP improve oxygenation, dynamic compliance of respiratory system and end-expiratory lung volume in pediatric patients undergoing cardiac surgery for congenital heart disease. Paediatr Anaesth. 2009;19(12):1207-12. [PubMed ID: 19863733]. https://doi.org/10.1111/j.1460-9592.2009.03177.x.

  • 20.

    Marini JJ, Wheeler AP. Respiratory monitoring. In: Marini JJ, Wheeler AP, editors. Critical care medicine. The essentials. 4th ed. Philadelphia: Lippincot Williams & Wilkins; 2010. p. 8-13.

  • 21.

    Henzler D, Pelosi P, Dembinski R, Ullmann A, Mahnken AH, Rossaint R, et al. Respiratory compliance but not gas exchange correlates with changes in lung aeration after a recruitment maneuver: An experimental study in pigs with saline lavage lung injury. Crit Care. 2005;9(5):R471-82. [PubMed ID: 16277708]. [PubMed Central ID: PMC1297611]. https://doi.org/10.1186/cc3772.

  • 22.

    Berger D, Takala J. Determinants of systemic venous return and the impact of positive pressure ventilation. Ann Transl Med. 2018;6(18):350. [PubMed ID: 30370277]. [PubMed Central ID: PMC6186556]. https://doi.org/10.21037/atm.2018.05.27.

  • 23.

    Gernoth C, Wagner G, Pelosi P, Luecke T. Respiratory and haemodynamic changes during decremental open lung positive end-expiratory pressure titration in patients with acute respiratory distress syndrome. Crit Care. 2009;13(2):R59. [PubMed ID: 19374751]. [PubMed Central ID: PMC2689506]. https://doi.org/10.1186/cc7786.

  • 24.

    Algera AG, Pisani L, Chaves RCF, Amorim TC, Cherpanath T, Determann R, et al. Effects of peep on lung injury, pulmonary function, systemic circulation and mortality in animals with uninjured lungs-a systematic review. Ann Transl Med. 2018;6(2):25. [PubMed ID: 29430442]. [PubMed Central ID: PMC5799137]. https://doi.org/10.21037/atm.2017.12.05.

  • 25.

    Ingaramo OA, Ngo T, Khemani RG, Newth CJ. Impact of positive end-expiratory pressure on cardiac index measured by ultrasound cardiac output monitor. Pediatr Crit Care Med. 2014;15(1):15-20. [PubMed ID: 24389709]. https://doi.org/10.1097/PCC.0b013e3182976251.

  • 26.

    Levett JM, Culpepper WS, Lin CY, Arcilla RA, Replogle RL. Cardiovascular responses to PEEP and CPAP following repair of complicated congenital heart defects. Ann Thorac Surg. 1983;36(4):411-6. [PubMed ID: 6354116]. https://doi.org/10.1016/s0003-4975(10)60479-1.

  • 27.

    Bernard D, Brandely A, Scatton O, Schoeffler P, Futier E, Lescot T, et al. Positive end-expiratory pressure does not decrease cardiac output during laparoscopic liver surgery: A prospective observational evaluation. HPB (Oxford). 2017;19(1):36-41. [PubMed ID: 27889250]. https://doi.org/10.1016/j.hpb.2016.10.009.

  • 28.

    Saner FH, Pavlakovic G, Gu Y, Gensicke J, Paul A, Radtke A, et al. Effects of positive end-expiratory pressure on systemic haemodynamics, with special interest to central venous and common iliac venous pressure in liver transplanted patients. Eur J Anaesthesiol. 2006;23(9):766-71. [PubMed ID: 16723056]. https://doi.org/10.1017/S026502150600072X.

  • 29.

    Berger D, Moller PW, Weber A, Bloch A, Bloechlinger S, Haenggi M, et al. Effect of PEEP, blood volume, and inspiratory hold maneuvers on venous return. Am J Physiol Heart Circ Physiol. 2016;311(3):H794-806. [PubMed ID: 27422991]. https://doi.org/10.1152/ajpheart.00931.2015.