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Positive end-expiratory pressure management in patients with severe ARDS: implications of prone positioning and extracorporeal membrane oxygenation
Critical Care volume 28, Article number: 277 (2024)
Abstract
The optimal strategy for positive end-expiratory pressure (PEEP) titration in the management of severe acute respiratory distress syndrome (ARDS) patients remains unclear. Current guidelines emphasize the importance of a careful risk–benefit assessment for PEEP titration in terms of cardiopulmonary function in these patients. Over the last few decades, the primary goal of PEEP usage has shifted from merely improving oxygenation to emphasizing lung protection, with a growing focus on the individual pattern of lung injury, lung and chest wall mechanics, and the hemodynamic consequences of PEEP. In moderate-to-severe ARDS patients, prone positioning (PP) is recommended as part of a lung protective ventilation strategy to reduce mortality. However, the physiologic changes in respiratory mechanics and hemodynamics during PP may require careful re-assessment of the ventilation strategy, including PEEP. For the most severe ARDS patients with refractory gas exchange impairment, where lung protective ventilation is not possible, veno-venous extracorporeal membrane oxygenation (V-V ECMO) facilitates gas exchange and allows for a “lung rest” strategy using “ultraprotective” ventilation. Consequently, the importance of lung recruitment to improve oxygenation and homogenize ventilation with adequate PEEP may differ in severe ARDS patients treated with V-V ECMO compared to those managed conservatively. This review discusses PEEP management in severe ARDS patients and the implications of management with PP or V-V ECMO with respect to respiratory mechanics and hemodynamic function.
Background
Positive end-expiratory pressure (PEEP) has been a cornerstone in the management of mechanically ventilated patients with acute respiratory distress syndrome (ARDS) since its description by Ashbaugh et al. in 1967 [1]. As part of a lung protective ventilation strategy, PEEP improves ventilation distribution and potentially limits ventilator-induced lung injury (VILI) [2]. Although different methods to titrate PEEP based on oxygenation and respiratory mechanics have been evaluated in randomized clinical trials, the optimal strategy to improve clinical outcomes remains undefined [3].
The current European Society of Intensive Care Medicine (ESICM) guideline on ARDS does not make a recommendation on higher versus lower oxygenation-based PEEP or PEEP titration guided by respiratory mechanics compared to oxygenation [4]. In contrast, the American Thoracic Society (ATS) guideline on ARDS management suggests using higher rather than lower PEEP in patients with moderate to severe ARDS [5] based on two meta-analyses showing an association between higher PEEP and improved survival in this ARDS subpopulation [6, 7].
Management of severe ARDS patients with prone positioning (PP) and veno-venous extracorporeal membrane oxygenation (V-V ECMO), along with the associated changes in respiratory mechanics and ventilatory strategies, may also affect the physiological effects of PEEP [8,9,10]. In these situations, “optimal” PEEP may differ and warrant careful re-titration to balance potential benefits and harms.
This article reviews PEEP management in patients with severe ARDS, focusing on the physiological effects of personalized PEEP with respect to respiratory mechanics and cardiopulmonary function, and the implications of management with PP and V-V ECMO.
PEEP in severe ARDS
Physiological effects and rationale
Almost 50 years ago, Suter et al. described that “optimal” PEEP titrated to respiratory mechanics and oxygen delivery (DO2) could potentially improve cardiopulmonary function in patients with respiratory failure [11]. Since then, the primary goal for the use of PEEP has shifted from merely improving oxygenation to emphasizing lung protection, with a growing focus on the individual pattern of lung injury, lung and chest wall mechanics, and the hemodynamic consequences of PEEP [3, 4, 12].
PEEP as part of a lung protective ventilation strategy can promote alveolar recruitment and limit atelectrauma, thereby reducing ventilation inhomogeneity and potentially preventing VILI [13] (Fig. 1). However, excessive PEEP may result in VILI due to alveolar overdistension and increased mechanical power (MP) transmission to the lung [14].
PEEP can adversely affect hemodynamics by decreasing the gradient for venous return, increasing pulmonary vascular resistance, and decreasing cardiac output [15] (Fig. 1). These hemodynamic consequences of excessive PEEP may increase the need for fluid administration and cardioactive drugs, which could impact patient outcomes [16, 17].
The balance between the benefits and harms of PEEP critically depends on its effect on lung recruitment, defined as reaeration of non- and poorly aerated lung parenchyma in response to increased airway pressures [18]. The application of PEEP increases transpulmonary pressure (PTP), i.e. the difference between airway and pleural pressure, in both non-dependent and dependent lung regions [19]. The resultant change in lung volume relative to the resting lung volume, termed functional residual capacity (FRC), represents lung strain. Lung strain is composed of static and dynamic components due to PEEP [end-expiratory lung volume (EELV) determined by PEEP relative to FRC] and tidal volume (VT) (VT relative to EELV), respectively.
In cases of significant recruitability, PEEP-induced increases in PTP lead to reaeration of lung parenchyma with minimal overdistension. While PEEP increases static strain, the corresponding increase in EELV significantly decreases dynamic strain with tidal ventilation, potentially improving gas exchange, lung protection, and limiting VILI [20, 21]. Conversely, excessive PEEP in cases of low recruitability fails to reaerate lung parenchyma significantly, increasing static strain without decreasing dynamic strain. This results in overdistension of aerated lung parenchyma, leading to increased lung stress and strain, and raising the risk for VILI as well as hemodynamic compromise (Fig. 1). It is important to note that due to the lung inhomogeneity in patients with ARDS, increasing PTP with PEEP always involves a trade-off between reaeration and overdistension of aerated lung parenchyma [22], with "recruitability" indicating this balance. Although increasing PEEP may decrease lung inhomogeneity in patients with mild and moderate ARDS, significant recruitment or reduced lung inhomogeneity may not be achievable in severe ARDS patients [23] when airway plateau pressures are limited to the recommended 30 cmH2O [4].
In these cases, PP may be employed to enhance ventilation distribution, thereby reducing overdistension and cyclical alveolar opening and closing [24]. In severe ARDS patients with refractory gas exchange impairment or inability to provide lung protective ventilation, V-V ECMO facilitates gas exchange and allows for an “ultraprotective” ventilation strategy [25].
Assessment and personalized PEEP strategy
Severe ARDS is characterized by a significant heterogeneity in the pattern of lung injury (focal vs. diffuse), lung and chest wall mechanics, hemodynamics, and potential multiorgan dysfunction [26, 27]. This variability, combined with the interaction of different ventilator strategies [28], complicates PEEP management and the definition of an optimal and personalized PEEP strategy [3, 4]. Although the optimal approach for managing PEEP in severe ARDS remains unclear, both the ESICM and ATS guidelines emphasize the importance of assessing the cardiopulmonary risk–benefit ratio when setting PEEP [4, 5].
Assessing lung recruitability to estimate the theoretical response to higher PEEP can be done using physiological parameters (e.g. oxygenation, ΔP, PTP) [29,30,31], bedside maneuvers (e.g. recruitment-to-inflation ratio) [32], and imaging techniques (e.g. computed tomography, electrical impedance tomography, ultrasound) [33,34,35]. However, PEEP management based solely on recruitability may not provide a truly personalized approach to ventilator management in severe ARDS patients [36]. A more comprehensive approach involves evaluating the interaction between PEEP, treatment strategies (PP, “ultraprotective” ventilation with very-low VT), resulting gas exchange and PTP, as well as considering the “biological” costs related to hemodynamic variables and fluid requirements (Fig. 2).
Possible algorithm for the risk–benefit assessment in PEEP titration and personalized therapy during prone positioning and V-V ECMO in patients with severe ARDS. PaO2/FiO2, arterial partial pressure of oxygen divided by the fraction of inspired oxygen; VT, tidal volume; PBW, predicted body weight; PEEP, positive end-expiratory pressure; V-V ECMO, veno-venous extracorporeal membrane oxygenation; PTP, transpulmonary pressure
The competing effects of PEEP in balancing lung protection and hemodynamic stability were highlighted in a reanalysis of the EPVent-2- trial. This study showed that the effect of PEEP strategy on mortality depended on the severity of multiorgan dysfunction [37]. PEEP titrated to end-expiratory PTP near 0 cmH2O was associated with improved survival compared to more positive or negative values [37], indicating the need to balance atelectrauma and overdistension [22]. At the bedside, this approach may be combined with non-invasive methods, such as electrical impedance tomography (EIT), to visualize ventilation distribution and estimate the response to PEEP semi-quantitatively [38, 39].
Given the high prevalence of hemodynamic impairment, including acute cor pulmonale, in severe ARDS patients [40], the effect of PEEP on hemodynamic variables and the need for cardioactive drugs and fluids should be considered. Monitoring the interaction between mechanical ventilation and cardiopulmonary function using echocardiography and advanced hemodynamic monitoring, such as pulmonary artery catheter and transpulmonary thermodilution, is recommended in this ARDS subgroup [15]. In the presence of right ventricular failure, which is associated with increased mortality [40], the response to PEEP concerning PTP, alveolar recruitment and overdistension, as well as the effects on cardiopulmonary function, should be periodically reassessed [41].
Management with PP and V-V ECMO may improve right ventricular function and optimize hemodynamics in severe ARDS patients [15, 42, 43]. These strategies can enhance oxygenation, homogenize regional PTP, and potentially reduce the intensity of ventilation.
Clinical implications
-
In the absence of an “optimal” PEEP, which simultaneously enhances alveolar recruitment and gas exchange while avoiding overdistension and hemodynamic impairment, a moderate level of PEEP that provides lung protection while minimizing hemodynamic compromise may be acceptable.
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Once PEEP is set, it is crucial to periodically reassess its effects on cardiopulmonary function.
Prone positioning
Physiological effects of prone positioning and interaction with PEEP
Current guidelines [4, 5] recommend PP for patients with moderate-to-severe ARDS (PaO2/FiO2 < 150 mmHg) to reduce mortality based on findings from the PROSEVA trial [44]. In the most severe ARDS patients with PaO2/FiO2 < 80 mmHg, both PP and V-V ECMO are associated with improved outcomes relative to low or moderate VT alone, according to a recent meta-analysis by Sud et al. [45]. Given that PP is a critical treatment for severe ARDS [46], understanding the physiological changes that occur during PP is essential for optimizing PEEP management. PP and PEEP can interact synergistically to influence respiratory mechanics, lung volumes, and gas exchange (Table 1).
In the supine position, gravity causes a vertical pleural pressure gradient that reduces PTP from ventral to dorsal lung regions [8]. This pleural pressure gradient is exacerbated in severe ARDS patients by the pressure of the edematous lung, sedation, and neuromuscular blockade [47, 48], leading to collapse of dorsobasal alveoli and ventilation inhomogeneity [49]. Experimental data suggest an increased pleural pressure gradient with lower PEEP levels, resulting in predominant ventilation of non-dependent lung regions in the supine position [8]. While increasing PEEP can promote dorsobasal alveolar recruitment, it may also cause overdistension of non-dependent lung regions [50]. PP alleviates the pleural pressure gradient by reducing the compressive force of the mediastinum, resulting in a more uniform distribution of regional end-expiratory and end-inspiratory PTP and thus ventilation [8]. Furthermore, PP increases EELV through lung recruitment associated with an uniform distribution of PTP [51]. This homogenization of ventilation distribution and lung recruitment reduces ventilation/perfusion mismatch and shunt, thereby improving gas exchange in ARDS patients during PP [24].
As mentioned earlier, PEEP alone may not induce significant lung recruitment in severe ARDS patients and could lead to overdistension of aerated lung parenchyma [23]. Experimental data suggest that the synergistic effects of PEEP and PP optimize regional compliance and minimize transpulmonary driving pressure (ΔPTP) in both dependent and non-dependent lung regions [8]. Therefore, by reducing the pleural pressure gradient, the combination of PEEP and PP facilitates recruitment of dependent lung regions without overdistending non-dependent lung regions, potentially mitigating VILI.
PP enhances lung recruitment and decreases alveolar instability and overdistension observed at high PEEP levels in ARDS patients [50]. Another important mechanism during PP is the increase in chest wall elastance [52, 53], which modifies regional PTP and induces recruitment by shifting lung aeration dorsally, thus improving ventilation homogeneity [54]. This improvement in ventilation/perfusion matching and reduced shunt improves gas exchange [55,56,57], while homogenized regional PTP may mitigate the cardiopulmonary effects of mechanical ventilation [15]. In severe ARDS patients with right ventricular failure, PP may help unload the right ventricle and optimize hemodynamics, potentially contributing to the improvement in patient outcomes [42, 43].
The dorsal ventilation shift and alveolar recruitment during PP may decrease ΔPTP, a surrogate for true lung stress independent of chest wall mechanics [8, 53]. Notably, experimental and clinical data recommend that minimal ΔPTP can be achieved with lower PEEP during PP compared to supine positioning [8, 58], suggesting recruitment of previously non-aerated lung units and/or improved mechanical properties of already ventilated lung units [59]. The optimal PEEP level during PP and whether it should be adjusted after changes in patient positioning remain debated in the absence of studies with patient-centered outcomes [60]. This challenge is compounded by the fact that ventilator-based measurements do not always correlate with changes in the lung-to-respiratory system elastance ratio, which significantly alters lung energy transfer during PP [61,62,63].
Clinical data
In the PROSEVA trial, which demonstrated a reduction in mortality with PP, patients were initially ventilated with a PEEP of approximately 10 cmH2O according to the lower PEEP/FiO2 table [44]. PEEP was gradually decreased to 8–9 cmH2O over the following seven days, without adjustment based on patient positioning [44]. Improved lung protection due to more uniform distribution of lung stress and strain during the respiratory cycle has been cited as a major factor contributing to improved outcomes in the PROSEVA trial [24, 50, 64]. Although a physiological study using the PROSEVA protocol did not reduce driving pressure (ΔP) or MP with PP, it did show increased EELV and decreased ΔPTP, suggesting more even distribution of lung stress and strain during PP [53]. Furthermore, PP may allow for reduced elastic power transfer per aerated lung volume, as comparable PTP and EELV can be achieved at lower airway pressures compared to supine positioning [58].
A recent physiological study by Morais et al. demonstrated the necessity of individualizing PEEP based on patient positioning due to significant changes in respiratory mechanics during PP [65]. Using EIT and esophageal manometry, the authors found a heterogeneous response in regional and global respiratory mechanics during PP, requiring PEEP adjustment of PEEP of at least 4 cmH2O in approximately 50% of patients [65]. Conversely, Mezidi et al. found no significant changes in PEEP adjusted to physiologic endpoints between supine positioning and PP [66]. In another recent study, PEEP was titrated based on the lowest static respiratory system compliance or positive end-expiratory PTP with respect to FiO2 [67] in both supine positioning and PP [53]. With both strategies, PEEP titration according to physiologic targets was lower during PP, resulting in reduced airway pressures and MP, while preserving EELV and improving oxygenation and hemodynamics. Esophageal pressure-guided ventilation targeting an end-expiratory PTP of 0 to 2 cmH2O [37] led to a median PEEP reduction of 5 cmH2O during PP compared to supine positioning, demonstrating lower elastic power transfer, improved gas exchange, and DO2 [58].
Implications of prone positioning for PEEP management
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The potential synergy between PP and PEEP may help to homogenize ventilation, recruit previously non-aerated lung units, and/or enhance the mechanical properties of already ventilated lung units without causing regional overdistension.
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PP may enable a reduction in PEEP, thereby reducing the energy required per aerated lung volume while preserving EELV, optimizing gas exchange, and maintaining hemodynamic stability.
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The significant variability in individual responses to PP, including changes in respiratory mechanics, PTP, and gas exchange, underscores the need for periodic reevaluation of PEEP settings during PP.
Veno-venous extracorporeal membrane oxygenation
Rationale and potential indications for V-V ECMO
In patients with the most severe ARDS and refractory gas exchange impairment, defined by eligibility criteria from the EOLIA trial (PaO2/FiO2 < 50 mmHg for > 3 h, or a PaO2/FiO2 of < 80 mmHg for > 6 h, or a pH of < 7.25 with a PaCO2 of ≥ 60 mmHg for > 6 h, with the respiratory rate increased to 35 breaths/min and mechanical ventilation settings adjusted to keep a plateau pressure of ≤ 32 cmH2O [68]), V-V ECMO is recommended according to current guidelines [4, 5]. The extracorporeal circuit facilitates gas exchange while employing an "ultraprotective” ventilation strategy aimed at achieving "lung rest" [10, 69]. This strategy is adopted by most medium-to-high volume ECMO centers and aims to reduce lung stress and strain by decreasing VT, respiratory rate, and airway pressures, thereby minimizing energy transfer to the inflamed lung parenchyma [70]. Although correcting refractory hypoxemia is critical, the primary benefit of managing severe ARDS patients with V-V ECMO is thought to be the reduced risk of VILI associated with less intensive mechanical ventilation [25].
Given that the extracorporeal circuit ensures adequate gas exchange, two primary objectives for ventilator management in severe ARDS patients undergoing V-V ECMO emerge: (1) Lung protection to minimize VILI; and (2) Reduction of the hemodynamic impact of mechanical ventilation to optimize DO2 (Table 2). The latter is particularly crucial for severe ARDS patients with right ventricular failure unresponsive to conservative treatments. In such cases, V-V ECMO can facilitate gas exchange while allowing for an "ultraprotective" ventilation strategy [15] that minimizes ventilatory settings and associated hemodynamic effects. This approach has been demonstrated to improve right ventricular function by reducing hypoxic pulmonary vasoconstriction and intrathoracic pressures, which lowers right ventricular afterload and enhances right ventricular coupling [71, 72].
PEEP as part of an ultraprotective ventilation strategy
The “ultraprotective” ventilation strategy facilitated by the extracorporeal circuit has important implications for PEEP management. Firstly, there is no reliance on PEEP to ensure oxygenation through alveolar recruitment, as gas exchange is primarily managed by the extracorporeal circuit [70, 73]. Secondly, the reduction in VT and respiratory rate during "ultraprotective" ventilation alters the role of adequate PEEP in increasing EELV and limiting dynamic strain during tidal ventilation. Moreover, the importance of sufficient PEEP to stabilize edematous alveoli and prevent cyclic alveolar collapse and reopening needs reevaluation in these patients [73].
While the reduction in VT during "ultraprotective" ventilation lowers the risk of overdistension, a VT of 2 to 4 ml/kg predicted body weight, combined with moderate PEEP levels and limited airway plateau pressures, may still lead to regional overdistension and VILI in patients with severe ARDS, particularly those with very low EELV [74, 75]. According to the current ARDS guidelines and using a PEEP/FiO2 table, patients eligible for V-V ECMO should initially be managed with an empirical PEEP of 16 to 24 cmH2O [4, 5]. The Extracorporeal Life Support Organization (ELSO) recommends PEEP levels between 10 and 24 cmH2O while maintaining an inspiratory plateau pressure lower than 25 cmH2O [70]. Consequently, PEEP management during V-V ECMO treatment shows considerable variation between centers [76], with participating centers in the LIFEGARDS study using a mean PEEP of 11 ± 3 cmH2O [10]. Similarly, the CESAR and EOLIA trials utilized a comparable PEEP range of 10 to 12 cmH2O to facilitate "lung rest" [68, 77]. Despite numerous studies evaluating the impact of ventilator settings, including PEEP, on patient outcomes during V-V ECMO [10, 76, 78, 79], findings regarding optimal PEEP have been inconsistent. Recent analyses identified more integrative ventilatory parameters such as ΔP and MP as independent predictors of mortality in this ARDS subgroup [80, 81]. To date, the optimal PEEP strategy to improve outcomes in severe ARDS patients managed with V-V ECMO remains unknown. Following the initiation of extracorporeal support and "ultraprotective" ventilation, using a moderate level of PEEP (10 to 15 cmH2O) may be reasonable to balance lung protection and hemodynamic stability in this ARDS subgroup. Further personalization of PEEP settings should then be guided by clinical assessment of the benefits and risks of PEEP in terms of cardiopulmonary function to minimize VILI, maintain hemodynamic stability, and optimize DO2 (Fig. 1).
Clinical and experimental data
In patients with the most severe ARDS requiring V-V ECMO treatment, recruitability varies widely [82], influencing the benefits and risks associated with PEEP. In a physiological study using EIT, Franchineau et al. identified an optimal PEEP of 15 cmH2O in 47% and 10 cmH2O in 40% of the included patients, defined as a compromise between preventing alveolar collapse and avoiding overdistension, which can lead to atelectrauma and volutrauma, respectively [83]. Graf et al., quantifying lung volumes via computed tomography in V-V ECMO patients, found that titrated PEEP increased static lung strain approximately 1.5-fold without recruiting dependent lung regions, resulting in significantly higher non-dependent lung strain [84]. Despite the moderate-to-high mean PEEP of 15.4 cmH2O, tidal recruitment was observed with a VT of 3 ml/kg predicted body weight. During V-V ECMO and "ultraprotective" ventilation, setting PEEP to minimize ΔP and prevent cyclic alveolar collapse while limiting airway plateau pressures to avoid overdistension in non-dependent lungs may prove challenging [23]. Accepting cyclic alveolar opening and closing (atelectrauma) while avoiding high airway pressures linked to volutrauma, mainly in non-dependent lungs, may be preferable for reducing pulmonary inflammation during the initial phases of V-V ECMO [85]. This approach minimizes energy transfer to lung parenchyma, which is reflected in MP [86]. Despite the ongoing discussions regarding the significance of each MP component, high overall MP increases the risk of VILI in patients with ARDS [14] and has been associated with mortality during V-V ECMO treatment [81].
Adopting a less invasive ventilatory strategy with moderate levels of PEEP to promote “lung rest” may provide a favorable balance between lung protection and cardiopulmonary function. In an experimental ARDS model managed with V-V ECMO, a moderate PEEP level of 10 cmH2O minimized lung injury while maintaining hemodynamic stability. Conversely, inadequate PEEP, whether too low or high, exacerbated lung injury or precipitated hemodynamic collapse, respectively [87]. Experimental studies comparing equivalent total MP with differing static and dynamic components revealed similar lung injury outcomes, with high PEEP exerting the greatest impact on hemodynamics and necessitating fluid administration [88]. However, inadequate PEEP during V-V ECMO treatment can lead to progressive alveolar collapse, which may subsequently increase pulmonary vascular resistance [89, 90]. Another aspect to consider when using moderate PEEP levels during “ultraprotective” ventilation in the most severe ARDS patients is the presence of complete airway closure, which may confound assessments of respiratory mechanics and contribute to atelectasis due to denitrogenation [91, 92].
Changes in regional PTP in response to PEEP determine the cardiopulmonary effects of mechanical ventilation, particularly in severe ARDS patients with marked ventilation heterogeneity [15]. Atelectasis due to insufficient PEEP can lead to right ventricular failure [89, 90], while lung overdistension due to excessive PEEP impairs pulmonary circulation, and reduces cardiac output [15]. Individual recruitability and the balance between lung reaeration and overdistension are therefore critical considerations in PEEP management to maintain hemodynamic stability and optimize DO2. A recent study in severe ARDS patients managed with V-V ECMO compared a moderate empirical PEEP level of 10 cmH2O, the lowest PEEP recommended by the ELSO, with individualized PEEP titration based on highest respiratory system compliance (mean 16.2 ± 4.7 cmH2O) and end-expiratory PTP of 0 cmH2O (mean 17.3 ± 4.7 cmH2O) during "ultraprotective" ventilation [93]. Although respiratory mechanics-guided PEEP titration decreased ΔPTP compared to empirical PEEP of 10 cmH2O, both approaches increased MP and lung stress, leading to reduced cardiac output and DO2, potentially compromising the extracorporeal circuit's goal of maintaining tissue normoxia. Notably, lung recruitability was not formally assessed using imaging or physiological maneuvers [32, 34], and higher PEEP did not significantly recruit lungs in the study cohort [93], consistent with previous findings in this ARDS subgroup [23]. The high disease severity and multiorgan dysfunction in the study cohort may have also contributed to the hemodynamic impairment associated with higher PEEP [37].
Implications of V-V ECMO for PEEP management
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Setting PEEP during “ultraprotective” ventilation in severe ARDS patients managed with V-V ECMO, especially during the initial phases of treatment involving multiorgan dysfunction and shock, should strive to balance lung protection with hemodynamic stability.
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A moderate level of PEEP (10 to 15 cmH2O), as part of a “lung rest” strategy, may be appropriate for this ARDS subgroup to minimize VILI, maintain hemodynamic stability, and optimize DO2.
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Further personalization of PEEP during V-V ECMO requires periodic assessment of the benefits and risks associated with PEEP in terms of cardiopulmonary function.
Conclusions
In patients with severe ARDS characterized by a significant heterogeneity in lung injury patterns, respiratory mechanics, hemodynamics, and potential multiorgan dysfunction, careful assessment of the benefits and risks associated with PEEP in terms of cardiopulmonary function is warranted. In these patients, the use of PP and its synergism with PEEP to homogenize ventilation distribution has important implication for PEEP management, necessitating reevaluation of PEEP settings during PP. Management of the most severe ARDS patients with V-V ECMO facilitates gas exchange and allows for a “lung rest” strategy. A moderate level of PEEP during “ultraprotective” ventilation may balance lung protection and hemodynamic stability in this ARDS subgroup. Individualized assessment and careful PEEP titration are crucial for optimizing ventilator management and improving patient outcomes.
Availability of data and materials
Not applicable.
Abbreviations
- ΔP:
-
Driving pressure
- ΔPTP :
-
Transpulmonary driving pressure
- ARDS:
-
Acute respiratory distress syndrome
- ATS:
-
American Thoracic Society
- DO2 :
-
Oxygen delivery
- EELV:
-
End-expiratory lung volume
- EIT:
-
Electrical impedance tomography
- ELSO:
-
Extracorporeal Life Support Organization
- ESICM:
-
European Society of Intensive Care Medicine
- FRC:
-
Functional residual capacity
- MP:
-
Mechanical power
- PaCO2 :
-
Arterial partial pressure of carbon dioxide
- PaO2/FiO2 :
-
Arterial partial pressure of oxygen divided by the fraction of inspired oxygen
- PEEP:
-
Positive end-expiratory pressure
- PP:
-
Prone positioning
- PTP :
-
Transpulmonary pressure
- VILI:
-
Ventilator-induced lung injury
- VT :
-
Tidal volume
- V-V ECMO:
-
Veno-venous extracorporeal membrane oxygenation
References
Ashbaugh DG, Bigelow DB, Petty TL, Levine BE. Acute respiratory distress in adults. Lancet (London, England). 1967;2(7511):319–23.
Slutsky AS, Ranieri VM. Ventilator-induced lung injury. N Engl J Med. 2013;369(22):2126–36.
Gattinoni L, Marini JJ. In search of the Holy Grail: identifying the best PEEP in ventilated patients. Intensive Care Med. 2022;48(6):728–31.
Grasselli G, Calfee CS, Camporota L, Poole D, Amato MBP, Antonelli M, Arabi YM, Baroncelli F, Beitler JR, Bellani G, et al. ESICM guidelines on acute respiratory distress syndrome: definition, phenotyping and respiratory support strategies. Intensive Care Med. 2023;49(7):727–59.
Qadir N, Sahetya S, Munshi L, Summers C, Abrams D, Beitler J, Bellani G, Brower RG, Burry L, Chen JT, et al. An update on management of adult patients with acute respiratory distress syndrome: an official American Thoracic Society Clinical practice guideline. Am J Respir Crit Care Med. 2024;209(1):24–36.
Briel M, Meade M, Mercat A, Brower RG, Talmor D, Walter SD, Slutsky AS, Pullenayegum E, Zhou Q, Cook D, et al. Higher vs lower positive end-expiratory pressure in patients with acute lung injury and acute respiratory distress syndrome: systematic review and meta-analysis. JAMA. 2010;303(9):865–73.
Dianti J, Tisminetzky M, Ferreyro BL, Englesakis M, Del Sorbo L, Sud S, Talmor D, Ball L, Meade M, Hodgson C, et al. Association of positive end-expiratory pressure and lung recruitment selection strategies with mortality in acute respiratory distress syndrome: a systematic review and network meta-analysis. Am J Respir Crit Care Med. 2022;205(11):1300–10.
Katira BH, Osada K, Engelberts D, Bastia L, Damiani LF, Li X, Chan H, Yoshida T, Amato MBP, Ferguson ND, et al. Positive end-expiratory pressure, pleural pressure, and regional compliance during pronation: an experimental study. Am J Respir Crit Care Med. 2021;203(10):1266–74.
Fan E. “There is nothing new except what has been forgotten”: the story of mechanical ventilation during extracorporeal support. Am J Respir Crit Care Med. 2019;199(5):550–3.
Schmidt M, Pham T, Arcadipane A, Agerstrand C, Ohshimo S, Pellegrino V, Vuylsteke A, Guervilly C, McGuinness S, Pierard S et al. Mechanical ventilation management during extracorporeal membrane oxygenation for acute respiratory distress syndrome. An international multicenter prospective cohort. Am J Respir Crit Care Med 2019;200(8):1002–1012.
Suter PM, Fairley B, Isenberg MD. Optimum end-expiratory airway pressure in patients with acute pulmonary failure. N Engl J Med. 1975;292(6):284–9.
Gattinoni L, Collino F, Maiolo G, Rapetti F, Romitti F, Tonetti T, Vasques F, Quintel M. Positive end-expiratory pressure: how to set it at the individual level. Ann Transl Med. 2017;5(14):288.
Cressoni M, Cadringher P, Chiurazzi C, Amini M, Gallazzi E, Marino A, Brioni M, Carlesso E, Chiumello D, Quintel M, et al. Lung inhomogeneity in patients with acute respiratory distress syndrome. Am J Respir Crit Care Med. 2014;189(2):149–58.
Gattinoni L, Collino F, Camporota L. Mechanical power: meaning, uses and limitations. Intensive Care Med. 2023;49(4):465–7.
Vieillard-Baron A, Matthay M, Teboul JL, Bein T, Schultz M, Magder S, Marini JJ. Experts’ opinion on management of hemodynamics in ARDS patients: focus on the effects of mechanical ventilation. Intensive Care Med. 2016;42(5):739–49.
Gattarello S, Pasticci I, Busana M, Lazzari S, Palermo P, Palumbo MM, Romitti F, Steinberg I, Collino F, Vassalli F, et al. Role of fluid and sodium retention in experimental ventilator-induced lung injury. Front Physiol. 2021;12: 743153.
Vignon P, Evrard B, Asfar P, Busana M, Calfee CS, Coppola S, Demiselle J, Geri G, Jozwiak M, Martin GS, et al. Fluid administration and monitoring in ARDS: Which management? Intensive Care Med. 2020;46(12):2252–64.
Gattinoni L, Caironi P, Cressoni M, Chiumello D, Ranieri VM, Quintel M, Russo S, Patroniti N, Cornejo R, Bugedo G. Lung recruitment in patients with the acute respiratory distress syndrome. N Engl J Med. 2006;354(17):1775–86.
Gattinoni L, Carlesso E, Caironi P. Stress and strain within the lung. Curr Opin Crit Care. 2012;18(1):42–7.
Gattinoni L, Pesenti A. The concept of “baby lung.” Intensive Care Med. 2005;31(6):776–84.
Protti A, Andreis DT, Monti M, Santini A, Sparacino CC, Langer T, Votta E, Gatti S, Lombardi L, Leopardi O, et al. Lung stress and strain during mechanical ventilation: Any difference between statics and dynamics? Crit Care Med. 2013;41(4):1046–55.
Madahar P, Talmor D, Beitler JR. Transpulmonary pressure-guided ventilation to attenuate atelectrauma and hyperinflation in acute lung injury. Am J Respir Crit Care Med. 2021;203(8):934–7.
Cressoni M, Chiumello D, Algieri I, Brioni M, Chiurazzi C, Colombo A, Colombo A, Crimella F, Guanziroli M, Tomic I, et al. Opening pressures and atelectrauma in acute respiratory distress syndrome. Intensive Care Med. 2017;43(5):603–11.
Guerin C, Albert RK, Beitler J, Gattinoni L, Jaber S, Marini JJ, Munshi L, Papazian L, Pesenti A, Vieillard-Baron A, Mancebo J. Prone position in ARDS patients: why, when, how and for whom. Intensive Care Med. 2020;46(12):2385–96.
Combes A, Peek GJ, Hajage D, Hardy P, Abrams D, Schmidt M, Dechartres A, Elbourne D. ECMO for severe ARDS: systematic review and individual patient data meta-analysis. Intensive Care Med. 2020;46(11):2048–57.
Calfee CS, Delucchi K, Parsons PE, Thompson BT, Ware LB, Matthay MA, Network NA. Subphenotypes in acute respiratory distress syndrome: latent class analysis of data from two randomised controlled trials. Lancet Respir Med. 2014;2(8):611–20.
Wilson JG, Calfee CS. ARDS subphenotypes: understanding a heterogeneous syndrome. Crit Care (London, England). 2020;24(1):102.
Constantin JM, Jabaudon M, Lefrant JY, Jaber S, Quenot JP, Langeron O, Ferrandiere M, Grelon F, Seguin P, Ichai C, et al. Personalised mechanical ventilation tailored to lung morphology versus low positive end-expiratory pressure for patients with acute respiratory distress syndrome in France (the LIVE study): a multicentre, single-blind, randomised controlled trial. Lancet Respir Med. 2019;7(10):870–80.
Goligher EC, Kavanagh BP, Rubenfeld GD, Adhikari NK, Pinto R, Fan E, Brochard LJ, Granton JT, Mercat A, Marie Richard JC et al. Oxygenation response to positive end-expiratory pressure predicts mortality in acute respiratory distress syndrome. A secondary analysis of the LOVS and ExPress trials. Am J Respir Crit Care Med 2014;190(1):70–76.
Chen L, Jonkman A, Pereira SM, Lu C, Brochard L. Driving pressure monitoring during acute respiratory failure in 2020. Curr Opin Crit Care. 2021;27(3):303–10.
Talmor D, Sarge T, Malhotra A, O’Donnell CR, Ritz R, Lisbon A, Novack V, Loring SH. Mechanical ventilation guided by esophageal pressure in acute lung injury. N Engl J Med. 2008;359(20):2095–104.
Chen L, Del Sorbo L, Grieco DL, Junhasavasdikul D, Rittayamai N, Soliman I, Sklar MC, Rauseo M, Ferguson ND, Fan E et al. Potential for lung recruitment estimated by the recruitment-to-inflation ratio in acute respiratory distress syndrome. A clinical trial. Am J Respir Crit Care Med 2020;201(2):178–187.
Malbouisson LM, Muller JC, Constantin JM, Lu Q, Puybasset L, Rouby JJ. Group CTSAS: computed tomography assessment of positive end-expiratory pressure-induced alveolar recruitment in patients with acute respiratory distress syndrome. Am J Respir Crit Care Med. 2001;163(6):1444–50.
Franchineau G, Jonkman AH, Piquilloud L, Yoshida T, Costa E, Roze H, Camporota L, Piraino T, Spinelli E, Combes A, et al. Electrical impedance tomography to monitor hypoxemic respiratory failure. Am J Respir Crit Care Med. 2024;209(6):670–82.
Chiumello D, Mongodi S, Algieri I, Vergani GL, Orlando A, Via G, Crimella F, Cressoni M, Mojoli F. Assessment of lung aeration and recruitment by CT scan and ultrasound in acute respiratory distress syndrome patients. Crit Care Med. 2018;46(11):1761–8.
Gattinoni L, Collino F, Camporota L. Assessing lung recruitability: Does it help with PEEP settings? Intensive Care Med. 2024;50(5):749–51.
Sarge T, Baedorf-Kassis E, Banner-Goodspeed V, Novack V, Loring SH, Gong MN, Cook D, Talmor D, Beitler JR. EPVent-2 study group: effect of esophageal pressure-guided positive end-expiratory pressure on survival from acute respiratory distress syndrome: a risk-based and mechanistic reanalysis of the EPVent-2 trial. Am J Respir Crit Care Med. 2021;204(10):1153–63.
Jonkman AH, Alcala GC, Pavlovsky B, Roca O, Spadaro S, Scaramuzzo G, Chen L, Dianti J, Sousa MLA, Sklar MC, et al. Lung recruitment assessed by electrical impedance tomography (RECRUIT): a multicenter study of COVID-19 acute respiratory distress syndrome. Am J Respir Crit Care Med. 2023;208(1):25–38.
Songsangvorn N, Xu Y, Lu C, Rotstein O, Brochard L, Slutsky AS, Burns KEA, Zhang H. Electrical impedance tomography-guided positive end-expiratory pressure titration in ARDS: a systematic review and meta-analysis. Intensive Care Med. 2024;50(5):617–31.
Mekontso Dessap A, Boissier F, Charron C, Begot E, Repesse X, Legras A, Brun-Buisson C, Vignon P, Vieillard-Baron A. Acute cor pulmonale during protective ventilation for acute respiratory distress syndrome: prevalence, predictors, and clinical impact. Intensive Care Med. 2016;42(5):862–70.
Cappio Borlino S, Hagry J, Lai C, Rocca E, Fouque G, Rosalba D, Fasan M, Shi R, Recanatini A, Cisterna I et al. The effect of PEEP on pulmonary vascular resistance depends on lung recruitability in ARDS patients. Am J Respir Crit Care Med 2024;Epub ahead of print.
Vieillard-Baron A, Boissier F, Pesenti A. Hemodynamic impact of prone position. Let’s protect the lung and its circulation to improve prognosis. Intensive Care Med. 2023;49(6):692–4.
Lai C, Monnet X, Teboul JL. Hemodynamic implications of prone positioning in patients with ARDS. Crit Care (London, England). 2023;27(1):98.
Guerin C, Reignier J, Richard JC, Beuret P, Gacouin A, Boulain T, Mercier E, Badet M, Mercat A, Baudin O, et al. Prone positioning in severe acute respiratory distress syndrome. N Engl J Med. 2013;368(23):2159–68.
Sud S, Fan E, Adhikari NKJ, Friedrich JO, Ferguson ND, Combes A, Guerin C, Guyatt G. Comparison of venovenous extracorporeal membrane oxygenation, prone position and supine mechanical ventilation for severely hypoxemic acute respiratory distress syndrome: a network meta-analysis. Intensive Care Med. 2024;50(7):1021–34.
Sud S, Friedrich JO, Adhikari NKJ, Fan E, Ferguson ND, Guyatt G, Meade MO. Comparative effectiveness of protective ventilation strategies for moderate and severe acute respiratory distress syndrome. A network meta-analysis. Am J Respir Crit Care Med 2021;203(11):1366–1377.
Pelosi P, Goldner M, McKibben A, Adams A, Eccher G, Caironi P, Losappio S, Gattinoni L, Marini JJ. Recruitment and derecruitment during acute respiratory failure: an experimental study. Am J Respir Crit Care Med. 2001;164(1):122–30.
Pelosi P, D’Andrea L, Vitale G, Pesenti A, Gattinoni L. Vertical gradient of regional lung inflation in adult respiratory distress syndrome. Am J Respir Crit Care Med. 1994;149(1):8–13.
Yoshida T, Amato MBP, Grieco DL, Chen L, Lima CAS, Roldan R, Morais CCA, Gomes S, Costa ELV, Cardoso PFG, et al. Esophageal manometry and regional transpulmonary pressure in lung injury. Am J Respir Crit Care Med. 2018;197(8):1018–26.
Cornejo RA, Diaz JC, Tobar EA, Bruhn AR, Ramos CA, Gonzalez RA, Repetto CA, Romero CM, Galvez LR, Llanos O, et al. Effects of prone positioning on lung protection in patients with acute respiratory distress syndrome. Am J Respir Crit Care Med. 2013;188(4):440–8.
Guerin C, Baboi L, Richard JC. Mechanisms of the effects of prone positioning in acute respiratory distress syndrome. Intensive Care Med. 2014;40(11):1634–42.
Riad Z, Mezidi M, Subtil F, Louis B, Guerin C. Short-term effects of the prone positioning maneuver on lung and chest wall mechanics in patients with acute respiratory distress syndrome. Am J Respir Crit Care Med. 2018;197(10):1355–8.
Boesing C, Graf PT, Schmitt F, Thiel M, Pelosi P, Rocco PRM, Luecke T, Krebs J. Effects of different positive end-expiratory pressure titration strategies during prone positioning in patients with acute respiratory distress syndrome: a prospective interventional study. Crit Care (London, England). 2022;26(1):82.
Gattinoni L, Marini JJ, Pesenti A, Quintel M, Mancebo J, Brochard L. The “baby lung” became an adult. Intensive Care Med. 2016;42(5):663–73.
Pelosi P, Tubiolo D, Mascheroni D, Vicardi P, Crotti S, Valenza F, Gattinoni L. Effects of the prone position on respiratory mechanics and gas exchange during acute lung injury. Am J Respir Crit Care Med. 1998;157(2):387–93.
Lamm WJ, Graham MM, Albert RK. Mechanism by which the prone position improves oxygenation in acute lung injury. Am J Respir Crit Care Med. 1994;150(1):184–93.
Richter T, Bellani G, Scott Harris R, Vidal Melo MF, Winkler T, Venegas JG, Musch G. Effect of prone position on regional shunt, aeration, and perfusion in experimental acute lung injury. Am J Respir Crit Care Med. 2005;172(4):480–7.
Boesing C, Krebs J, Conrad AM, Otto M, Beck G, Thiel M, Rocco PRM, Luecke T, Schaefer L. Effects of prone positioning on lung mechanical power components in patients with acute respiratory distress syndrome: a physiologic study. Crit Care (London, England). 2024;28(1):82.
Chiumello D, Marino A, Brioni M, Cigada I, Menga F, Colombo A, Crimella F, Algieri I, Cressoni M, Carlesso E, Gattinoni L. Lung recruitment assessed by respiratory mechanics and computed tomography in patients with acute respiratory distress syndrome. What is the relationship? Am J Respir Crit Care Med 2016;193(11):1254–1263.
Beitler JR, Guerin C, Ayzac L, Mancebo J, Bates DM, Malhotra A, Talmor D. PEEP titration during prone positioning for acute respiratory distress syndrome. Crit Care (London, England). 2015;19:436.
Keenan JC, Cortes-Puentes GA, Zhang L, Adams AB, Dries DJ, Marini JJ. PEEP titration: the effect of prone position and abdominal pressure in an ARDS model. Intensive Care Med Exp. 2018;6(1):3.
Chiumello D, Carlesso E, Cadringher P, Caironi P, Valenza F, Polli F, Tallarini F, Cozzi P, Cressoni M, Colombo A, et al. Lung stress and strain during mechanical ventilation for acute respiratory distress syndrome. Am J Respir Crit Care Med. 2008;178(4):346–55.
Gattinoni L, Chiumello D, Carlesso E, Valenza F. Bench-to-bedside review: chest wall elastance in acute lung injury/acute respiratory distress syndrome patients. Crit Care (London, England). 2004;8(5):350–5.
Broccard A, Shapiro RS, Schmitz LL, Adams AB, Nahum A, Marini JJ. Prone positioning attenuates and redistributes ventilator-induced lung injury in dogs. Crit Care Med. 2000;28(2):295–303.
Morais CCA, Alcala G, De Santis Santiago RR, Valsecchi C, Diaz E, Wanderley H, Fakhr BS, Di Fenza R, Gianni S, Foote S, et al. Pronation reveals a heterogeneous response of global and regional respiratory mechanics in patients with acute hypoxemic respiratory failure. Crit Care Explor. 2023;5(10): e0983.
Mezidi M, Parrilla FJ, Yonis H, Riad Z, Bohm SH, Waldmann AD, Richard JC, Lissonde F, Tapponnier R, Baboi L, et al. Effects of positive end-expiratory pressure strategy in supine and prone position on lung and chest wall mechanics in acute respiratory distress syndrome. Ann Intensive Care. 2018;8(1):86.
Beitler JR, Sarge T, Banner-Goodspeed VM, Gong MN, Cook D, Novack V, Loring SH, Talmor D. EPVent-2 study group: effect of titrating positive end-expiratory pressure (PEEP) with an esophageal pressure-guided strategy vs an empirical high PEEP-Fio2 strategy on death and days free from mechanical ventilation among patients with acute respiratory distress syndrome: a randomized clinical trial. JAMA. 2019;321(9):846–57.
Combes A, Hajage D, Capellier G, Demoule A, Lavoue S, Guervilly C, Da Silva D, Zafrani L, Tirot P, Veber B, et al. Extracorporeal membrane oxygenation for severe acute respiratory distress syndrome. N Engl J Med. 2018;378(21):1965–75.
Brodie D, Slutsky AS, Combes A. Extracorporeal life support for adults with respiratory failure and related indications: a review. JAMA. 2019;322(6):557–68.
Tonna JE, Abrams D, Brodie D, Greenwood JC, Rubio Mateo-Sidron JA, Usman A, Fan E. Management of adult patients supported with venovenous extracorporeal membrane oxygenation (VV ECMO): guideline from the extracorporeal life support organization (ELSO). ASAIO J. 2021;67(6):601–10.
Reis Miranda D, van Thiel R, Brodie D, Bakker J. Right ventricular unloading after initiation of venovenous extracorporeal membrane oxygenation. Am J Respir Crit Care Med. 2015;191(3):346–8.
Levy D, Desnos C, Lebreton G, Thery G, Pineton de Chambrun M, Leprince P, Hammoudi N, Schmidt M, Combes A, Hekimian G. Early reversal of right ventricular dysfunction after venovenous extracorporeal membrane oxygenation in patients with COVID-19 pneumonia. Am J Respir Crit Care Med 2023;207(6):784–787.
Del Sorbo L, Ranieri VM. We do not need mechanical ventilation any more. Crit Care Med. 2010;38(10 Suppl):S555-558.
Terragni PP, Rosboch G, Tealdi A, Corno E, Menaldo E, Davini O, Gandini G, Herrmann P, Mascia L, Quintel M, et al. Tidal hyperinflation during low tidal volume ventilation in acute respiratory distress syndrome. Am J Respir Crit Care Med. 2007;175(2):160–6.
Nieszkowska A, Lu Q, Vieira S, Elman M, Fetita C, Rouby JJ. Incidence and regional distribution of lung overinflation during mechanical ventilation with positive end-expiratory pressure. Crit Care Med. 2004;32(7):1496–503.
Schmidt M, Stewart C, Bailey M, Nieszkowska A, Kelly J, Murphy L, Pilcher D, Cooper DJ, Scheinkestel C, Pellegrino V, et al. Mechanical ventilation management during extracorporeal membrane oxygenation for acute respiratory distress syndrome: a retrospective international multicenter study. Crit Care Med. 2015;43(3):654–64.
Peek GJ, Mugford M, Tiruvoipati R, Wilson A, Allen E, Thalanany MM, Hibbert CL, Truesdale A, Clemens F, Cooper N, et al. Efficacy and economic assessment of conventional ventilatory support versus extracorporeal membrane oxygenation for severe adult respiratory failure (CESAR): a multicentre randomised controlled trial. Lancet (London, England). 2009;374(9698):1351–63.
Modrykamien AM, Hernandez OO, Im Y, Walters RW, Schrader CL, Smith LE, Lima B. Mechanical ventilation in patients with the acute respiratory distress syndrome and treated with extracorporeal membrane oxygenation: impact on hospital and 30 day postdischarge survival. ASAIO J. 2016;62(5):607–12.
Wang R, Sun B, Li X, Tang X, He H, Li Y, Yuan X, Li H, Chu H, Tong Z. Mechanical ventilation strategy guided by transpulmonary pressure in severe acute respiratory distress syndrome treated with venovenous extracorporeal membrane oxygenation. Crit Care Med. 2020;48(9):1280–8.
Serpa Neto A, Schmidt M, Azevedo LC, Bein T, Brochard L, Beutel G, Combes A, Costa EL, Hodgson C, Lindskov C, et al. Associations between ventilator settings during extracorporeal membrane oxygenation for refractory hypoxemia and outcome in patients with acute respiratory distress syndrome: a pooled individual patient data analysis: mechanical ventilation during ECMO. Intensive Care Med. 2016;42(11):1672–84.
Chiu LC, Lin SW, Chuang LP, Li HH, Liu PH, Tsai FC, Chang CH, Hung CY, Lee CS, Leu SW, et al. Mechanical power during extracorporeal membrane oxygenation and hospital mortality in patients with acute respiratory distress syndrome. Crit Care (London, England). 2021;25(1):13.
Camporota L, Caricola EV, Bartolomeo N, Di Mussi R, Wyncoll DLA, Meadows CIS, Amado-Rodriguez L, Vasques F, Sanderson B, Glover GW, et al. Lung recruitability in severe acute respiratory distress syndrome requiring extracorporeal membrane oxygenation. Crit Care Med. 2019;47(9):1177–83.
Franchineau G, Brechot N, Lebreton G, Hekimian G, Nieszkowska A, Trouillet JL, Leprince P, Chastre J, Luyt CE, Combes A, Schmidt M. Bedside contribution of electrical impedance tomography to setting positive end-expiratory pressure for extracorporeal membrane oxygenation-treated patients with severe acute respiratory distress syndrome. Am J Respir Crit Care Med. 2017;196(4):447–57.
Graf PT, Boesing C, Brumm I, Biehler J, Muller KW, Thiel M, Pelosi P, Rocco PRM, Luecke T, Krebs J. Ultraprotective versus apneic ventilation in acute respiratory distress syndrome patients with extracorporeal membrane oxygenation: a physiological study. J Intensive Care. 2022;10(1):12.
Guldner A, Braune A, Ball L, Silva PL, Samary C, Insorsi A, Huhle R, Rentzsch I, Becker C, Oehme L, et al. Comparative effects of volutrauma and atelectrauma on lung inflammation in experimental acute respiratory distress syndrome. Crit Care Med. 2016;44(9):e854-865.
Gattinoni L, Tonetti T, Cressoni M, Cadringher P, Herrmann P, Moerer O, Protti A, Gotti M, Chiurazzi C, Carlesso E, et al. Ventilator-related causes of lung injury: the mechanical power. Intensive Care Med. 2016;42(10):1567–75.
Araos J, Alegria L, Garcia A, Cruces P, Soto D, Erranz B, Salomon T, Medina T, Garcia P, Dubo S, et al. Effect of positive end-expiratory pressure on lung injury and haemodynamics during experimental acute respiratory distress syndrome treated with extracorporeal membrane oxygenation and near-apnoeic ventilation. Br J Anaesth. 2021;127(5):807–14.
Vassalli F, Pasticci I, Romitti F, Duscio E, Assmann DJ, Grunhagen H, Vasques F, Bonifazi M, Busana M, Macri MM, et al. Does iso-mechanical power lead to iso-lung damage? An experimental study in a porcine model. Anesthesiology. 2020;132(5):1126–37.
Duggan M, McCaul CL, McNamara PJ, Engelberts D, Ackerley C, Kavanagh BP. Atelectasis causes vascular leak and lethal right ventricular failure in uninjured rat lungs. Am J Respir Crit Care Med. 2003;167(12):1633–40.
Mekontso Dessap A, Charron C, Devaquet J, Aboab J, Jardin F, Brochard L, Vieillard-Baron A. Impact of acute hypercapnia and augmented positive end-expiratory pressure on right ventricle function in severe acute respiratory distress syndrome. Intensive Care Med. 2009;35(11):1850–8.
Chen L, Del Sorbo L, Grieco DL, Shklar O, Junhasavasdikul D, Telias I, Fan E, Brochard L. Airway closure in acute respiratory distress syndrome: an underestimated and misinterpreted phenomenon. Am J Respir Crit Care Med. 2018;197(1):132–6.
Coudroy R, Vimpere D, Aissaoui N, Younan R, Bailleul C, Couteau-Chardon A, Lancelot A, Guerot E, Chen L, Brochard L, Diehl JL. Prevalence of complete airway closure according to body mass index in acute respiratory distress syndrome. Anesthesiology. 2020;133(4):867–78.
Boesing C, Schaefer L, Graf PT, Pelosi P, Rocco PRM, Luecke T, Krebs J. Effects of different positive end-expiratory pressure titration strategies on mechanical power during ultraprotective ventilation in ARDS patients treated with veno-venous extracorporeal membrane oxygenation: a prospective interventional study. J Crit Care. 2024;79: 154406.
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Open Access funding enabled and organized by Projekt DEAL. PRMR was supported by Brazilian Council for Scientific and Technological Development (CNPq) and Carlos Chagas Filho, Rio de Janeiro State Foundation (FAPERJ). JK is supported by the Bundesministerium für Bildung und Forschung (BMBF).
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CB, PRMR, TL, and JK designed this review. All authors contributed equally to literature revision and manuscript writing. All authors revised and approved the final version of the manuscript.
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Boesing, C., Rocco, P.R.M., Luecke, T. et al. Positive end-expiratory pressure management in patients with severe ARDS: implications of prone positioning and extracorporeal membrane oxygenation. Crit Care 28, 277 (2024). https://doi.org/10.1186/s13054-024-05059-y
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DOI: https://doi.org/10.1186/s13054-024-05059-y