PEEP titration in moderate to severe ARDS: plateau versus transpulmonary pressure

Abstract

Background

Although lung protection with low tidal volume and limited plateau pressure (P_plat) improves survival in acute respiratory distress syndrome patients (ARDS), the best way to set positive end-expiratory pressure (PEEP) is still debated.

Methods

This study aimed to compare two strategies using individual PEEP based on a maximum P_plat (28–30 cmH₂O, the Express group) or on keeping end-expiratory transpulmonary pressure positive (0–5 cmH₂O, P_Lexpi group). We estimated alveolar recruitment (Vrec), end-expiratory lung volume and alveolar distension based on elastance-related end-inspiratory transpulmonary pressure (P_L,EL).

Results

Nineteen patients with moderate to severe ARDS (PaO₂/FiO₂ < 150 mmHg) were included with a baseline PEEP of 7.0 ± 1.8 cmH₂O and a PaO₂/FiO₂ of 91.2 ± 31.2 mmHg. PEEP and oxygenation increased significantly from baseline with both protocols; PEEP Express group was 14.2 ± 3.6 cmH₂O versus 16.7 ± 5.9 cmH₂O in P_Lexpi group. No patient had the same PEEP with the two protocols. Vrec was higher with the latter protocol (299 [0 to 875] vs. 222 [47 to 483] ml, p = 0.049) and correlated with improved oxygenation (R² = 0.45, p = 0.002). Two and seven patients in the Express and P_L,expi groups, respectively, had P_L,EL > 25 cmH₂O.

Conclusions

There is a great heterogeneity of P_Lexpi when P_plat is used to titrate PEEP but with limited risk of over-distension. A PEEP titration for a moderate positive level of P_Lexpi might slightly improve alveolar recruitment and oxygenation but increases the risk of over-distension in one-third of patients.

Background

Mechanical ventilation for acute respiratory distress syndrome (ARDS) may lead to ventilation-induced lung injury [1]. A lung protective ventilation strategy, with low tidal volume (V_T), limited plateau pressure and positive end-expiratory pressure (PEEP), aims to improve survival [2, 3]. Different protocols have been proposed to set PEEP in order to avoid alveolar collapse with limited end-inspiratory distension of the lungs [4]. Some of these strategies use a table of PEEP values which depend on inspired fraction of oxygen (FiO₂), while others are based on individual respiratory mechanics. The Express protocol, developed by Mercat et al., consists of attaining airway plateau pressure (P_plat) up to 28–30 cmH₂O with a fixed V_T of 6 ml kg⁻¹ predicted body weight [5]. These authors reported a significant reduction in morbidity but not mortality. Because airway pressure is an oversimplified surrogate for lung stress in patients with abnormal chest wall elastance, it could be relevant to assess lung distending pressure estimated from transpulmonary pressure (P_L). This later, in static airway conditions, can be estimated by measuring pleural via esophageal pressure [6]. This estimation can be affected by elastic recoil of the balloon, of the esophagus, esophageal muscular tone and pressures transmitted from the heart beat and mediastinum [7]. The relationship between esophageal and pleural pressure, and its measurement in ARDS patients with an important anteroposterior gradient in the supine position, requires the acceptance of several assumptions [8]. However, a recent study directly measured pleural pressure in pigs and human cadavers and found that esophageal pressure accurately reflects pleural pressure close to the balloon, corresponding to dependent lung regions to mid-chest [7]. Thus, collapse and trauma from recurrent alveolar collapse and re-opening can be related to end-expiratory P_L. [9, 10] Elastance-derived calculation of relative end-inspiratory P_L (P_L,EL) is close to direct measurement of pleural transpulmonary end-inspiratory pressure in the non-dependent lung region and might therefore give some information about alveolar distension in the non-dependent lung, more at risk for over-distension [11]. Different protocols have been proposed for setting PEEP according to P_L. The EPVent 1 and 2 trials titrated PEEP by measuring pleural pressure to achieve a positive end-expiratory transpulmonary pressure (P_Lexpi) between 0 to 10 cmH₂O according to a sliding scale based on FiO₂ [12, 13] Grasso et al. used P_L,EL to increase PEEP in severe ARDS until P_L,EL = 25 cmH₂O [14]. Some patients improved their oxygenation significantly and avoided extracorporeal membrane oxygenation.

The aim of this study was to compare estimated alveolar recruitment (Vrec) with end-expiratory lung volume (EELV) measurement, and alveolar distension with measurement of P_L,EL, during individual PEEP titration using two different targets: P_plat (28–30 cmH₂O) or positive P_Lexpi (0–5 cmH₂O).

Methods

Study design and participants

This multicenter, prospective crossover physiological study was conducted in severe ARDS patients admitted to three French intensive care units in Bordeaux (Robert Picqué Military Teaching Hospital; North Bordeaux Aquitaine Clinic; Thoracic Intensive Care Unit, Bordeaux University Hospital) between 2016 and 2017. All patients had recent (within a week) bilateral opacities not fully explained by cardiac failure or fluid overload with moderate to severe hypoxemia defined by their PaO₂/FiO₂ below 150 with 5–8 cmH₂O of PEEP and required volume-controlled mechanical ventilation [15]. The ventilator used was a carescape R860 (General Electrics, Madison WI, USA).

Exclusion criteria included esophageal disease, pulmonary leakage (major bronchopleural fistula, pneumothorax), severe coagulopathy, solid organ transplantation (hepatic, pulmonary) and refusal to participate.

Experimental protocol

Sedation was achieved with a midazolam-sufentanil infusion to obtain a bispectral index between 40 and 60. Subjects recieved cisatracurium to obtain myorelaxation, monitoring was Train Of Four of ulnar, 1 or 2 twitches out of 4 was considered appropriate. All subjects were placed in a 30° head up position. A validated nasogastric tube with an esophageal balloon-catheter (Nutrivent™; Sidam, Modena, Italy) was inserted to estimate pleural pressure [16]. The balloon was filled with 4 ml of air. The correct position of the Nutrivent tube was confirmed by an end-expiratory occlusion maneuver with four chest compressions and four ΔPes/ΔPaw ratio measurements as described previously and with thoracic radiography (radio-opaque markers) [6, 17]. At baseline, patients were ventilated with a V_T of 6 ml kg⁻¹ predicted body weight and a PEEP between 5–8 cmH₂O (PEEP_baseline). Twenty minutes later, PEEP was titrated according to the Express or P_Lexpi protocols in a randomized order. For the Express protocol, PEEP was titrated in order to obtain a P_plat between 28–30 cmH₂O. For the P_Lexpi protocol, PEEP was titrated in order to obtain a P_Lexpi between 0–5 cmH₂O. PEEP level according to each protocol was maintained for 20 min before recording all respiratory parameters and blood withdrawal for blood gas analysis. PEEP was returned to 0 cmH₂O between each protocol during less than 30 s. For hemodynamic assessment, respiratory variation of the arterial pulse pressure and the response to a passive leg raising test were used before PEEP titration, with an echocardiography. If positive, a fluid challenge was performed to avoid hypovolemia. After PEEP titration, echocardiography was done to assess right heart function and the occurrence of septal dyskinesia.

Measurement of variables

End-inspiratory and -expiratory airway and esophageal pressures were measured during a 5 s pause of the ventilator; V_T were monitored continuously. EELV was measured using the nitrogen washin/washout technique; FiO₂ variation was 10% and the average of washin EELV and washout EELV for each PEEP levels was recorded.

Variables were calculated using the following equations:

• Absolute inspiratory transpulmonary pressure (P_L,es) = P_plat − end-inspiratory esophageal pressure;

• Elastance-related transpulmonary pressure (P_L,EL) = P_plat × (lung elastance/respiratory system elastance) [18];

• P_Lexpi = total PEEP − end-expiratory esophageal pressure;

• Airway driving pressure (DP_aw) = P_plat − total PEEP;

• Transpulmonary driving pressure (DP_L) = DP_aw − (end-inspiratory − end-expiratory esophageal pressure);

• Elastance-related driving pressure = DP_aw × (lung elastance/respiratory system elastance).

• Respiratory system elastance = (P_plat − total PEEP)/V_T;

• Lung elastance = DP_L/V_T;

• Respiratory system elastance = Lung elastance + Chest wall elastance.

The following were also measured:

• Estimated recruitment volume (Vrec in ml) = (EELV at high PEEP − EELV at low PEEP) − ((V_T/(P_plat − low PEEP) × (high PEEP − low PEEP)). [19]

Statistical analysis

No statistical power calculation was conducted prior to the study; the sample size was based on our previous studies with this design of physiological crossover study with pairing. Data are expressed, respectively, as mean ± standard deviation (SD) and median [interquartile range] for variables normally and non-normally distributed. The outliers were evaluated, but no action was necessary. The categorical data were expressed as numbers (percentage of patients). Comparison of variables between three settings was performed by using one-way repeated measures analysis of variance (ANOVA) followed by post hoc Tukey’s test for multiple comparisons. Comparison between categorical variables was performed using the Chi-squared test. Correlations used Spearman’s test. All statistical tests were two-tailed, and a p value of less than 0.05 was considered significant. All statistical analysis was performed using NCSS2007 software (Statistical Solutions Ltd, Cork, Ireland) and Prism 6 (GraphPad Software, La Jolla, CA, USA).

Results

Nineteen patients were included; they were all enrolled in the study less than 48 h after intubation. The baseline characteristics of these patients are summarized in Table 1, and there were no missing data.

Table 1.

Baseline characteristics of the patients (n = 19)

Characteristic
Male, n (%)	13 (68.4)
Age (years)	72 ± 10
Body mass index (kg/m2)	28 ± 6
SAPS II score	65 ± 15
Etiology of ARDS, n (%)
Pneumonia/aspiration	16 (84.2)
Sepsis	2 (10.5)
Pancreatitis	1 (5.3)
Organ failure at baseline (SOFA), n (%)
Hemodynamic	18 (94.7)
Renal	9 (47.4)
Hepatic	0 (0)
Hematological	2 (10.5)
Arterial blood gas
PaO2/FiO2 ratio	92 ± 31
FiO2 (%)	80 ± 21
pH	7.31 ± 0.11
PaCO2 (mmHg)	45 ± 10
HCO3- (mmol/l)	22.4 ± 4.0
Base excess	− 3.4 ± 5.1
Lactates (mmol/l)	1.6 ± 1.0
Hemodynamic variables
Heart rate (beats/min)	99 ± 27
Systolic arterial pressure (mmHg)	127 ± 23
Diastolic arterial pressure (mmHg)	59 ± 12
Mean arterial pressure (mmHg)	82 ± 13
Respiratory mechanics
Minute ventilation (L/min)	9.6 ± 1.6
Tidal volume (ml/kg PBW)	6.1 ± 0.4
EELV (ml)	1319 ± 626
Aspect of ARDS, n (%)
Patchy	6 (31.6)
Diffuse	10 (52.6)
Focal	3 (15.8)
Mortality at Hospital discharge	10/19 (53%)

Results are expressed as number (%), or mean ± standard deviation

SAPS 2: Simplified Acute Physiology Score 2; ARDS: acute respiratory distress syndrome; PBW: predicted body weight. SOFA: sepsis-related organ failure assessment; EELV: end-expiratory lung volume (ml)

PEEP levels, oxygenation and alveolar recruitment

Respiratory mechanics according to each PEEP setting are summarized in Table 2. In comparison with PEEP_baseline, the Express and P_Lexpi protocols significantly increased PEEP and P_plat without any change in driving pressure (Table 2). These changes were associated with a significant improvement in oxygenation. Median PEEP value was not significantly different between the Express and P_Lexpi protocols. However, analysis of individual PEEP data according to each protocol shows that no patient had the same PEEP (Fig. 1) with a median of absolute difference of 5.0 [4.0–8.0] cmH₂O and 13 patients had higher PEEP with P_Lexpi protocol.

Table 2.

Measurements of respiratory function and hemodynamics (n = 19)

Protocols	PEEPbaseline	Express protocol	P Lexpi	p value
PEEP (cmH2O)	7.0 ± 1.8	14.2 ± 3.6*	16.7 (5.9)*	< 0.0001
Pplat (cmH2O)	20.8 ± 4.0	28.8 ± 2.0 *	33.9 ± 10.6*	< 0.0001
PL,es (cmH2O)	7.0 ± 5.9	11.9 ± 6.2*	15.5 ± 8.5*	0.0013
PL,EL (cmH2O)	15.3 ± 4.9)	20.5 ± 4.7*	24.3 ± 11.4*	0.0025
PLexpi (cmH2O)	− 2.6 ± 5.2	1.4 ± 5.1*	3.3 ± 1.6*	< 0.0001
EELV (ml)	1546 ± 634	2067 ± 924*	2287 ± 945*	0.001
DPaw (cmH2O)	13.0 ± 3.9	14.2 ± 5.0	16.4 ± 7.8	0.17
DPL (cmH2O)	9.9 ± 4.4	10.6 ± 5.6	12.3 ± 8.3	0.20
DPL,EL (cmH2O)	7.5 ± 4.3	8.1 ± 5.6	9.5 ± 8.1	0.30
Crs (ml/cmH2O)	33.3 ± 15.8	30.0 ± 10.7	28.3 ± 13.2	0.17
Ecw (cmH2O/l)	8.7 ± 2.7	9.6 ± 3.4*	10.9 ± 4.3*	0.03
EL (cmH2O/l)	26.0 ± 11.9	28.0 ± 15.9	33.2 ± 25.1	0.25
FiO2 (%)	80.0 ± 21.1	80.6 ± 21.2	81.1 ± 21.6	0.46
PaO2/FiO2	91.2 ± 31.2	134.0 ± 67.2*	152.7 ± 80.1*	0.01
pH	7.31 ± 0.11	7.30 ± 0.11	7.31 ± 0.12	0.08
PaCO2 (mmHg)	45.2 ± 10.4	46.5 ± 9.6	45.3 ± 11.0	0.26
MAP (mmHg)	82.0 ± 13.4	74.7 ± 12.9	75.7 ± 12.0	0.06
Heart rate (beats/min)	99 ± 27	102 ± 26	107 ± 28	0.19
Lactates (mmol/l)	1.6 ± 0.9	1.5 ± 0.8	1.5 ± 0.8	0.27

Results are expressed as mean ± standard deviation

P_plat: plateau pressure; P_Lexpi: end-expiratory transpulmonary pressure; DP_L: transpulmonary driving pressure; P_L,EL: relative end-expiratory pressure; P_L,es: absolute inspiratory transpulmonary pressure; DP_aw: airway driving pressure; DP_L: transpulmonary driving pressure, DP_L,EL: transpulmonary elastance-related driving pressure; E_L: lung elastance; EELV: end-expiratory lung volume; E_cw: elastance chest wall; Crs: compliance respiratory system; MAP: mean arterial pressure. p value refers to repeated measures ANOVA. *p < 0.05 of Express and P_Lexpi groups versus baseline group. ^§p < 0.05 of Express versus P_Lexpi groups

Fig. 1.

Individual PEEP levels according to the Express or P_Lexpi protocol. PEEP increased from baseline but is individually different for almost all patients with each protocol Express or P_Lexpi

EELV variation from baseline was significantly higher with P_Lexpi protocol 60 (58) % vs 36 (28) % with Express protocol, p = 0.025. Estimated Vrec was significantly higher with the P_Lexpi protocol than with Express, 298 [0 to 845] vs 222 [47 to 483] ml, respectively. Vrec and PaO₂/FiO₂ ratio changes were significantly correlated with the P_Lexpi protocol (R² = 0.45, p = 0.002). Arterial blood gases were not significantly different between the Express and P_Lexpi protocols.

Expiratory transpulmonary pressure

P_Lexpi increased with both protocols (Table 2, Fig. 2).

Fig. 2.

Individual P_Lexpi levels according to baseline, Express and P_Lexpi protocols. P_Lexpi = positive end-expiratory transpulmonary pressure. Dash line represents the limit of 0 cmH₂O; more patients had negative P_Lexpi with the Express protocol

With the Express protocol, six patients had negative P_Lexpi − 2.5 [− 7.8 to − 1.15] cmH₂O with a median PEEP of 14.0 [9.7 to 14.5] cmH₂O. These six patients had a significant lower respiratory system compliance (25.2 [15.8 to 29.0] vs. 30.7 [25.6 to 39.2] ml/cmH₂O, p = 0.027), and a significant lower EELV (1240 [835 to 2118] vs. 2019 [1700 to 3045] ml, p = 0.040). When these patients received the P_Lexpi protocol, median PEEP increased to 24.0 [18.0 to 26.5] cmH₂O, P_plat was 40.2 [33.1 to 51.0] cmH₂O, and PaO₂/FiO₂ increased by +31 [11 to 206] % (p = 0.062).

Inspiratory transpulmonary pressure

With the Express protocol, mean P_L,EL was 20 cmH₂O, and P_L,es was significantly lower than P_L,EL with a mean of difference of 8.5 cmH₂O (p < 0.0001) (Table 2). P_L,EL increased from baseline with the Express protocol (Table 2), one patient was > 25 cmH₂O, and the rest were below (Fig. 3), but 2 patients had P_L,es > 20 cmH₂O.

Fig. 3.

Individual P_L,EL with baseline, Express and P_Lexpi protocols. P_L,EL = elastance-derived calculation of relative end-inspiratory transpulmonary pressure. Dash line represents the limit of 25 cmH₂O; more patients had P_L,EL above 25 cmH₂O with the P_Lexpi protocol

With the P_Lexpi protocol, mean P_L,EL was 24 cmH₂O, and P_L,es was significantly lower than P_L,EL with a mean of difference of 8.7 cmH₂O (p < 0.0001) (Table 2). P_L,EL increased from baseline with the P_Lexpi protocol (Table 2), seven patients had P_L,EL > 25 cmH₂O (Fig. 3), and four of them had P_L,es > 20 cmH₂O.

With the P_Lexpi protocol, patients with P_L,EL > 25 cmH₂O had pH of 7.25 [7.17 to 7.42] with significantly lower respiratory system compliance, higher DP and PEEP, than those with P_L,EL ≤ 25 cmH₂O (17 [15 to 22] ml/cmH₂O, 23 [18 to 25] cmH₂O and 21[17 to 27] cmH₂O, respectively).

Airway, transpulmonary and elastance-related driving pressures were not different between groups (Table 2).

Elastance

In comparison with baseline, respiratory system elastance and lung elastance were not significantly modified by the increase in PEEP with the Express protocol; only chest wall elastance was statistically different (Table 2). PEEP increase from baseline with the Express protocol was significantly correlated with lung elastance (R² = 0.38, p = 0.008). Respiratory system and lung elastance were similar between Express and P_Lexpi protocols.

Complications

No episodes of pneumothorax were detected by chest X-Ray after each protocol implementation. Hemodynamic assessment was done before PEEP titration, and fluid was given when required. Cardiac frequency and mean arterial pressure remained relatively stable with each PEEP protocol (Table 2). Fifteen patients underwent transthoracic echocardiography (four had no transthoracic echocardiography window), and none of them had right heart failure with septal dyskinesia after PEEP titration.

Discussion

This study demonstrates heterogeneity of end-expiratory or end-inspiratory transpulmonary pressures during PEEP titration with each method in severe ARDS. PEEP titration with a target of positive P_Lexpi will suggest individually different levels of PEEP than with Express protocol in a large majority of patients (higher or lower PEEP). These two protocols are not interchangeable, as described previously with two other protocols based on expiratory P_L [20, 21].

The goal of increasing PEEP from baseline with a specific titration protocol using P_L is to improve alveolar recruitment and oxygenation with limited hyperinflation and morbi-mortality [4]. ARDS patients have a great variation in lung damage with a gravitational vertical gradient of alveolar injuries determining dependent and non-dependent regions [22]. Pleural pressure also has a vertical gradient in the supine position [23]. Interestingly, P_L,EL is close to direct measurement of pleural transpulmonary end-inspiratory pressure in the non-dependent lung region and might therefore limit the risk of ventilator-induced lung injury by over-distension [11]. Our main results demonstrate that this risk is probably reduced when PEEP is titrated according to P_plat (28–30 cmH₂O) instead of a moderate positive P_Lexpi. (0–5 cmH₂O).

Oxygenation and alveolar recruitment, according to P_Lexpi

In our study, when compared to baseline, the Express and P_Lexpi protocols increased PEEP, Vrec and oxygenation at the same time significantly. These two protocols based on respiratory mechanic proposed high PEEP level which might explain the small differences in recruitment. In the 2 EPVent trials, the difference in the results might come from the comparator group with empirical PEEP-FiO₂ strategies, resulting in significantly different P_Lexpi on protocol between groups. P_Lexpi protocol proposed individually a different level of PEEP than Express protocol. The corresponding increase of PEEP with P_Lexpi protocol, when compared from baseline, was correlated to oxygenation. Patients with protective ventilation who respond to increased PEEP by improved oxygenation might have a lower risk of death [3]. The P_Lexpi protocol had a better alveolar recruitment than Express protocol with a median P_Lexpi of 3.6 cmH₂O. Indeed, increasing PEEP in order to have a positive P_Lexpi of around 4.5 cmH₂O can significantly reduce the risk of atelectasis in the dependent lung, whereas a P_Lexpi of 0 cmH₂O might not be enough [23].

With the Express protocol, six patients had negative P_Lexpi, which meant that esophageal pressure was greater than airway pressure. This may occur when pressures in the thorax and abdomen are pathologically elevated [24]. These patients had lower respiratory system compliance and EELV. With the P_Lexpi protocol, these patients received higher levels of PEEP and a trend toward increased oxygenation. This protocol might improve alveolar recruitment and oxygenation, but over-distension has to be controlled at the same time [4].

Over-distension, according to P_L,EL

In order to limit over-distension, P_plat should remain < 32 cmH₂O and DP_aw < 15 cmH₂O [2, 25]. P_L,EL can also help to limit over-distension in animal study based on CT scan [26], and a limit of 25 cmH₂O has been proposed in ARDS patients [13]. We found that DP_aw remained unchanged and within a safer range below 15 cmH₂O with all protocols [25]. DP_aw and DP_L were highly correlated, and the mean difference was similar to previous data (approximately 4 cmH₂O) [27]. The EPVent trial 2 proposed stopping the PEEP increase if P_L,es was > 20 cmH₂O [13]. With the P_Lexpi protocol, four patients had P_L,es > 20 cmH₂O, but seven patients had P_L,EL > 25 cmH₂O. This can be explained by a significant difference between these two assessments of end-inspiratory transpulmonary pressure as described previously [9, 23]. With the Express protocol, PEEP was titrated on the basis of P_plat, with the expectation that it closely approximated P_L. In patients with normal chest wall elastance, P_plat is a reasonable surrogate for P_L and with Express protocol, we found a median P_L,EL of 20 cmH₂O which is lower than the target/limit of 25 cmH₂O proposed by Grasso et al. [11]; this limit was crossed by only one patient in our study.

With the P_Lexpi protocol, Vrec was slightly higher, but some patients had P_L,EL > 25 cmH₂O; these patients had lower respiratory system compliance with higher DP and respiratory acidosis. Thus, for some patients having both moderate positive P_Lexpi and limited P_L,EL is not possible, and moderate positive P_Lexpi between 0–5 cmH₂O does not prevent P_L,EL being > 25 cmH₂O. In these patients, P_L,EL may need to be reduced and V_T might be decreased below 6 ml kg⁻¹ PBW in order to benefit from PEEP-induced alveolar recruitment with less distension and DP. The use of the prone position could also be interesting [28], but assessment of pleural pressure by esophageal pressure in prone position requires further investigations.

Elastance

Lung elastance in our patients was similar to previous studies [13, 26]. When chest wall elastance is high, P_plat may be much higher than P_L. Indeed, a substantial portion of P_plat is dissipated in distending the chest wall. As the chest wall becomes stiffer, the proportion of P_plat that distends the lung (P_L) decreases progressively [29]. Chest wall elastance was within the same range as other data in ARDS patients [12, 13]. In the study of Grasso et al., patients improved by PEEP had a higher chest wall elastance with a mean of 17 cmH₂O/l. Chest wall elastance can be elevated in patients with acute respiratory failure for various reasons [30]. Increases in chest wall elastance can occur as a result of intra-abdominal hypertension, pleural effusion, massive ascites, thoracic trauma and edema of the intra-thoracic and intra-abdominal tissues as a result of fluid resuscitation [7]. We found a significant increase of E_cw with P_lexpi protocol. This has already been described by Mezidi et al. and might be explained by an upward shift of the chest wall pressure–volume curve with more EELV [31].

Severity and complications

In our cohort, patients were severely ill with high Simplified Acute Physiology Scores II (SAPS II) and PaO₂/FiO₂ ratio at baseline was lower than in most studies including the EPVent trials [12, 13], Express study [5] and ARMA study [2]. Titration of PEEP was achieved with the P_Lexpi and Express protocols in all patients without hemodynamic impairment.

Limits and perspectives

There are several limitations. First of all, it is a small physiological study of moderate to severe ARDS patients with the risk of underpowered statistical analysis. We assessed alveolar recruitment and the risk of over-distension only with bedside respiratory mechanics and not with a CT scan that is the gold standard. This study did not assess alveolar inflammation, and we did not assess any outcome according to a specific PEEP titration protocol. The majority of the patients had a direct insult of the lung with pneumoniae or aspiration so it was not possible to compare respiratory mechanic between pulmonary and extrapulmonary ARDS [32]. All patients had a risk of derecruitment with a short ventilation with no PEEP between each protocol. Some of these limits need further investigations.

Conclusions

Our study demonstrates that, in comparison with a protocol using P_plat to titrate PEEP, a positive level of P_Lexpi with PEEP might slightly improve alveolar recruitment and oxygenation but also increases P_L,EL above 25 cmH₂O and the risk of over-distension in the dependent lung in one-third of patients.

Authors’ contributions

MB, NF, HR were involved in study concept and design; MB, NF, DTV, TS, AG, BF, HR contributed to acquisition of data; MB, NF, TB, HR were involved in analysis and interpretation of data; MB, HR, AO helped in drafting of the manuscript. All authors read and approved the final manuscript.

Funding

Support was provided solely from institutional sources.

Availability of data and materials

If requested.

Ethics approval and consent to participate

The study was approved by the French South-West Ethical Committee on November 2015 (CPP: 2015/113 by Chairperson Dr. Berdai), and written informed consent was obtained from all patients in accordance with current regulations.

Consent for publication

From all authors.

Competing interests

The authors declare that they have no competing interests.

Prior presentation

This study was presented in ESICM Lives Forum 2018 in Madrid as best abstract.