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Dynamics of end expiratory lung volume after changing positive end-expiratory pressure in acute respiratory distress syndrome patients

Abstract

Introduction

Lung recruitment maneuvers followed by an individually titrated positive end-expiratory pressure (PEEP) are the key components of the open lung ventilation strategy in acute respiratory distress syndrome (ARDS). The staircase recruitment maneuver is a step-by-step increase in PEEP followed by a decremental PEEP trial. The duration of each step is usually 2 minutes without physiologic rationale.

Methods

In this prospective study, we measured the dynamic end-expiratory lung volume changes (ΔEELV) during an increase and decrease in PEEP to determine the optimal duration for each step. PEEP was progressively increased from 5 to 40 cmH2O and then decreased from 40 to 5 cmH2O in steps of 5 cmH2O every 2.5 minutes. The dynamic of ΔEELV was measured by direct spirometry as the difference between inspiratory and expiratory tidal volumes over 2.5 minutes following each increase and decrease in PEEP. ΔEELV was separated between the expected increased volume, calculated as the product of the respiratory system compliance by the change in PEEP, and the additional volume.

Results

Twenty-six early onset moderate or severe ARDS patients were included. Data are expressed as median [25th-75th quartiles]. During the increase in PEEP, the expected increased volume was achieved within 2[2-2] breaths. During the decrease in PEEP, the expected decreased volume was achieved within 1 [1–1] breath, and 95 % of the additional decreased volume was achieved within 8 [2–15] breaths. Completion of volume changes in 99 % of both increase and decrease in PEEP events required 29 breaths.

Conclusions

In early ARDS, most of the ΔEELV occurs within the first minute, and change is completed within 2 minutes, following an increase or decrease in PEEP.

Introduction

Recruitment maneuvers and positive end-expiratory pressure (PEEP) are the key components of the open lung ventilation strategy in acute respiratory distress syndrome (ARDS) [1]. Lung recruitment maneuvers aim to reaerate collapsed or non-aerated distal airways and alveoli, and PEEP prevents derecruitment to improve oxygenation and decrease the risk of ventilator-induced lung injury [2]. Applied properly and early in selected patients, lung recruitment may decrease ARDS mortality [3]. Several types of recruitment maneuvers have been described. Some use a rapid increase in pressure for a short period of time [4], whereas others use a more progressive increase in pressure. The staircase recruitment maneuver (SRM) is a step-by-step increase in PEEP with a constant driving pressure [58]. With each increase in PEEP, end-expiratory lung volume (EELV) increases as a result of distension of already aerated alveoli and recruitment of non-aerated lung units. However, at high levels of PEEP, there is a risk of hemodynamic compromise, especially if the step duration is prolonged. Each step length is usually 2 minutes without a strong physiologic rationale for such duration [58]. After the recruitment maneuver, an adequate level of PEEP is required to prevent derecruitment. The optimal PEEP setting can be determined by a decremental PEEP trial. PEEP is decreased step by step until part of the lung collapses again, which can be detected by a decrease in static compliance or transcutaneous oxygen saturation (SpO2) [710]. During the decremental PEEP trial, each step length is usually maintained for 3–5 minutes without a physiologic rationale for such duration [58].

The aim of the present study was to measure the dynamics of EELV changes (ΔEELV) after a step increase or decrease in PEEP (ΔPEEP) to determine the optimal duration of steps during a SRM and a decremental PEEP trial.

Material and methods

This study was the second part of an analysis of a prospective interventional study (ClinicalTrials.gov identifier: NCT01899560) conducted between March and November 2013 in the 16-bed medical-surgical adult intensive care unit of Hôpital Sainte Musse, Toulon, France [11]. The study was approved by the local ethical review committee (Comité de Protection des Personnes Sud Méditérannée V), and informed consent was obtained from all patients or their next of kin before inclusion.

Patients

Eligible participants were all adults 18 years of age or older who had early-onset (less than 24 h) moderate or severe ARDS according to the Berlin definition [12] and had been invasively ventilated for less than 72 h at the time of inclusion. Exclusion criteria were the following contraindications for a recruitment maneuver: bronchopleural fistula, emphysema, pneumothorax, antecedent of pneumothorax, increased intracranial pressure, pulmonary arterial hypertension with right heart failure as assessed by transthoracic echocardiography, hemodynamic instability with mean arterial pressure less than 65 mmHg, large pleural effusion as assessed by lung ultrasound, and pregnancy. Patients were mechanically ventilated using a Hamilton-S1 ventilator (Hamilton Medical, Bonaduz, Switzerland) in pressure control with 15 cmH2O of driving pressure, 15 breaths per minute, inspiratory/expiratory ratio of 0.33, and PEEP of 5 cmH2O [12]. The fraction of inspired oxygen (FiO2) was adjusted to target a SpO2 between 90 % and 94 %. A heated humidifier (MR850; Fisher & Paykel Healthcare, Auckland, New Zealand) was used for inspiratory gas conditioning. The patients were in a semirecumbent position with the head of the bed at a 45-degree angle, and they were sedated with midazolam and sufentanil to target a Richmond Agitation Sedation Scale score of −5. Cisatracurium was administered continuously [13] or in repeated injections during the procedure. The cuff of the endotracheal tube was transiently overinflated to 60 cmH2O before the start of the study protocol to prevent air leaks. Heart rate, invasive arterial pressure, and SpO2 were continuously monitored.

Study protocol

A SRM was performed as follows: PEEP was increased from 5 cmH2O to 40 cmH2O and then decreased from 40 cmH2O to 5 cmH2O in steps of 5 cmH2O every 2.5 minutes. At the end of each step, airway pressure at end inspiration (PPLAT) and end expiration (PEEPTOT) was measured using a 5-second end-inspiratory and end-expiratory occlusion, respectively. Respiratory system compliance (CRS) was calculated as the ratio between tidal volume (VT) and the difference between PPLAT and PEEPTOT: VT/(PPLAT − PEEPTOT). The increase in PEEP was stopped, and the decrease was started at any level of PEEP if the patient developed bradycardia less than 60 beats per minute (bpm), tachycardia more than 140 bpm, arrhythmia, hypotension (systolic arterial pressure <80 mmHg or mean arterial pressure [MAP] <55 mmHg), or hypoxemia (SpO2 <85 %).

Measurements and calculations

Flow and airway pressure (PAW) were measured with a proximal pneumotachograph (linear between −120 L/min and +120 L/min with ±5 % [SD], PN279331; Hamilton Medical) positioned at the Y-piece. Volumes were integrated from flow measurements. Flow, volumes, and PAW were continuously recorded using Study Recorder software (Hamilton Medical) at 50 Hz.

ΔEELV after a PEEP step was calculated by direct spirometry, which was shown to be a robust method compared with functional residual capacity measured by a washin/washout method with insoluble gases [14]. The difference between inspiratory and expiratory VT measured by direct spirometry was calculated for each breath following a PEEP step. This difference was corrected by the systematic difference, called VT offset, between inspired and expired VT, calculated from the last 30 seconds of the step, owing to humidity and temperature differences between inhaled and exhaled gas and oxygen consumption [15]. ΔEELV was calculated as the cumulative difference between inspiratory and expiratory VT, corrected by VT offset, measured over the 30 breaths following the PEEP step (Fig. 1). ΔEELV was partitioned between the expected volume (VEXP) to distend already open alveoli (calculated as the product of CRS of the previous PEEP level by ΔPEEP) and the additional increased volume (VADI) following the increase in PEEP. Thus, ΔEELV = VEXP + VADI for each level of PEEP. During the increase in PEEP, the number of breaths required to achieve VEXP to distend already open alveoli, as well as the number of breaths needed to achieve 95 % of the VADI, was calculated. The number of breaths required to ensure completion of the volume change in 99 % of the increase in PEEP events was measured. During the decrease in PEEP, the number of breaths needed to achieve the expected decrease in volume (VEXP), as well as the number of breaths required to achieve 95 % of the additional decreased volume (VADD), was calculated. Thus, ΔEELV = VEXP + VADD for each level of PEEP. The number of breaths required to ensure completion of volume change in 99 % of the decrease in PEEP change events was measured.

Fig. 1
figure 1

Measurement of the dynamics of the end-expiratory lung volume change (ΔEELV) after an increase in positive end-expiratory pressure (PEEP). Left panel displays the volume waveform for each breath following the increase in PEEP. The difference between inspired and expired tidal volumes (VT) was calculated and corrected by the volume offset. Right panel displays the dynamics of ΔEELV after the increase in PEEP. The difference between inspired and expired tidal volumes was reported breath by breath. The gray line is the expected increase in volume (VEXP) required to distend already open alveoli (calculated as the product of respiratory system compliance of the previous PEEP level by ΔPEEP), and the black line is the additional volume (VADI). The number of breaths needed to reach 95 % of VADI was measured

Statistical analysis

The distribution of the data was assessed by Kolmogorov-Smirnov test. Data with normal distribution are presented as mean±SD; others are expressed as median [25th–75th quartiles].

The numbers of breaths needed to achieve 95 % of the volume change during increase and decrease in PEEP were compared using Student’s t test. The number of breaths required to achieve 95 % of the additional volume according to each level of PEEP was tested using analysis of variance at both increase and decrease in PEEP. Statistic analyses were performed using SigmaStat version 3.5 and SigmaPlot version 11.0 software (Systat Software, San Jose, CA, USA).

Results

Twenty-six patients were analyzed. The characteristics of the population at inclusion and patient outcomes are presented in Table 1.

Table 1 Characteristics of the population at inclusion and patient outcomes

The increase in PEEP was stopped prematurely in eight patients because of hypotension with MAP less than 55 mmHg (one patient at 25 cmH2O, two patients at 30 cmH2O, and five patients at 35 cmH2O). Totals of 170 increases in PEEP and 170 decreases in PEEP were analyzed. Totals of 17 increases in PEEP and 11 decreases in PEEP were excluded owing to technical errors. Therefore, 153 increases in PEEP and 159 decreases in PEEP were reported.

During the increase in PEEP, VEXP to distend already open alveoli was achieved within 2 [2] breaths. Ninety-five percent of the VADI was achieved within 13 [616] breaths (52 [24–64] s) (Fig. 2). Detailed results are presented in Tables 2 and 3. During the increase in PEEP, the dynamics of ΔEELV were the same at all tested PEEP levels (p = 0.825) and were not correlated with VT (r2 = 0.002) or PaO2/FiO2 ratio on admission (r2 = 0.170). Completion of volume change in 99 % of the patients’ PEEP increase events required 29 breaths (1 min, 56 s) (Fig. 3).

Fig. 2
figure 2

Percentage of additional volume achieved according to the number of breaths. Box plot shows medians (25th–75th quartiles) for all patients at all positive end-expiratory (PEEP) levels. Left and right panels depict increases and decreases of PEEP, respectively. VADD additional decreased volume, VADI additional increased volume

Table 2 ΔEELV, VEXP, VAD, and VAD/ΔEELV ratios for each PEEP step when PEEP was increased and decreased
Table 3 ΔEELV and VAD at 1 and 2 minutes and ratio between 1 and 2 minutes during increase and decrease in PEEP
Fig. 3
figure 3

Percentage of patients’ positive end-expiratory pressure (PEEP) events that had completed volume change against the number of breaths needed to complete volume change. Left panel: Percentage of patients’ PEEP increase events that had completed volume change plotted against the number of breaths required to complete volume change. Right panel: Percentage of patients’ PEEP decrease events that had completed volume change plotted against the number of breaths needed to complete volume change

During the decrease in PEEP, the expected decrease in volume was achieved within 1 [1] breath. Ninety-five percent of the VADD was achieved within 8 [215] breaths (32 [8–60] s) (Fig. 2). Detailed results are presented in Tables 2 and 3. During the decrease in PEEP, the dynamic ΔEELV remained the same at all tested PEEP levels (p = 0.114) and were not correlated with VT (r 2 = 0.014) or PaO2/FiO2 ratio on admission (r 2 = 0.002). Completion of volume change in 99 % of the patient’s PEEP decrease events required 29 breaths (1 min, 56 s) (Fig. 3).

For completeness, the individual additional increased and decreased volumes are presented in Figs. 4 and 5, respectively. As shown, the single patient behavior is consistent with the median values in the majority of cases.

Fig. 4
figure 4

Individual additional increased volume after increase in positive end-expiratory pressure (PEEP). The expected increase in volume was subtracted

Fig. 5
figure 5

Individual additional decreased volume after decrease in positive end-expiratory pressure (PEEP). The expected decrease in volume was subtracted

The number of breaths needed to reach 95 % of the VADI was higher than the number of breaths required to reach 95 % of the VADD (p = 0.003).

Discussion

In the present study, most of the ΔEELV during increase or decrease in PEEP occurred within the first minute and required 2 minutes to be completed. Change in 95 % of the additional volume during an increase in PEEP required more breaths than during the decrease in PEEP. If VADI is assumed to be recruited volume following the increase in PEEP and VADD is assumed to be derecruited volume following the decrease in PEEP, these results demonstrate a longer time course for 95 % recruitment compared with 95 % derecruitment but the same time course (1 min, 56 s) for completion of volume change after a PEEP step. This supports the use of a 2-minute step following both PEEP increases and decreases during a SRM if completion of volume change after each step is sought. A shorter time after PEEP changes (1 min) could be used if 95 % of volume change in 75 % of PEEP change events is an acceptable endpoint.

In the present study, 95 % of VADI was achieved within 13 [616] breaths after an increase of PEEP. Katz et al. found that, in patients with mild ARDS, 90 % of ΔEELV was achieved after 4.6±1.4 breaths [14]. Lung recruitment depends on applied pressure - namely, the transpulmonary pressure - and time [16]. To compare different studies and methods of recruitment, the time of exposure at high pressure needed to achieve 95 % of recruitment was calculated as the product of the number of breaths by the inspiratory time (TI). In this study, TI was 1 second; therefore, 13 seconds of exposure at high pressure was required. In patients with severe ARDS, 14 seconds of exposure at high pressure was needed [17]. During a sustained inflation recruitment maneuver, the average time constant of the volume increase was 2.3±1.3 seconds; thus, 95 % of the recruitment occurred during the first 7 seconds [18]. The small difference between these results is due to the fact that this simple calculation considers not alveolar pressure but PAW. In pressure-controlled mode, alveolar pressure is equal to PAW only at the end of TI. However, the main finding is consistent among these studies: most of the recruitment (assessed by ΔEELV) occurs rapidly during a recruitment maneuver or after a PEEP increase. Small VADI occurred beyond 1 minute up to 2 minutes after the PEEP step. Using electrical impedance tomography, it was possible to detect volume increases several minutes after the increase of PEEP [19, 20]. These changes in volume are too small to be detected by direct spirometry. Interestingly, when PEEP is increased, most of the PaO2 change occurs within the first 5 minutes, but PaO2 still increases slowly so that the equilibrium is not achieved at 1 h after the PEEP change [10]. On one hand, a possible reason could be slow alveolar recruitment, a chest wall adaptation with a shift down of the diaphragm, an improvement in cardiac output, or a change in hypoxemic vascular constriction. On the other hand, static compliance change is achieved within 5 minutes. These results are in line with the mechanism of recruitment that is time–pressure dependent and thus a progressive phenomenon of a sequence of breaking liquid bridges [21].

After a decrease in PEEP, 95 % of the VADD was achieved within 8 [215] breaths. Katz et al. measured that 90 % of ΔEELV in patients with mild ARDS was achieved after 3.1±0.6 breaths [14]. In the same way, the required time of exposure at PEEP needed to achieve 95 % of derecruitment was calculated as the product of the number of breaths by the expiratory time (TE). In this study, TE was 3 seconds; therefore, 24 seconds was required. In patients with severe ARDS, 95 % of the volume change was achieved within 17 seconds of exposure at PEEP [17]. This calculation is probably overestimated because alveoli pressure reaches PEEP only at the end of TE. However, these results are consistent in that most of the mechanical derecruitment occurs rapidly after a decrease in PEEP. Interestingly, when PEEP is decreased, the equilibration time for arterial oxygenation is reached within 5 minutes [10]. These results support the mechanism of derecruitment as a passive phenomenon. The immediate collapse after decrease in PEEP is probably due to the gravity-dependent closure of small airways in the dependent part of the lung. Oxygenation-related variables could guide the decremental PEEP trial, but further investigations are necessary to determine the evolution of these variables during the five 5 minutes. If we consider that derecruitment increases the shunt fraction, decreases in PaO2 or SaO2 should occur rapidly after lung collapse. Conversely, static CRS takes longer to decrease and should not be very informative in tracking within the minutes following the PEEP step.

The number of breaths required to recruit seems to be more than the number of breaths needed to derecruit. Recruitment is an active, progressive phenomenon of a sequence of breaking liquid bridges whereas derecruitment is a passive phenomenon due to gravity.

This study has a number of important implications. Most patients have significant recruitment after most PEEP increases, from the lowest to the highest, with no clear critical recruitment level, suggesting that all patients should be taken to the highest PEEP level (40 cmH2O) to maximize their recruitment. Furthermore, there was a concept that decremental PEEP was needed to find the critical PEEP level where derecruitment started to select a PEEP level at or above that level for clinical use. But again, although equivalent derecruitment did occur at lower PEEP levels, this study shows that most patients have significant derecruitment after most PEEP reductions, with no clear critical derecruitment level. This implies that the derecruitment-determined PEEP level would have to be based on a specified percentage (e.g., 10 % or 20 %) of derecruitment, possibly depending on the hemodynamic and gas exchange consequences.

The main limitation of this study is that we do not know if the additional ΔEELV is recruited volume, volume that overdistends already aerated units with a long time constant, or viscoelastance and chest wall adaptation, as we did not use any imaging of the thorax. Second, the direct spirometry method is not accurate enough to detect a ΔEELV below 10 ml. Therefore, these results may represent most but not all of the ΔEELV. Third, in an animal study, the restitution of lung volume after suctioning was significantly slower during pressure-controlled ventilation than during volume-controlled ventilation [22]. As our patients were ventilated in pressure-controlled mode, our results might have been different in volume-controlled mode. However, the breathing patterns are probably more important to explaining such differences than the mode itself. Fourth, these results concern sedated and paralyzed patients with ARDS, the population of interest in performing a SRM and decremental PEEP trial. In a spontaneously breathing patient, the time course of recruitment and derecruitment may be very different, as the inspiratory effort has a strong recruitment effect. Finally, this study included mainly ARDS caused by direct lung injury (88 %), in particular gastric aspiration. This is due to the case mix of our intensive care unit, which receives a lot of patients with coma or drug overdose complicated by gastric aspiration. Application of the results should be limited to this subgroup of the population, as the potentially recruitable lung in ARDS caused by indirect lung injury may be different [23].

In practice, these results support the use of a short duration for the PEEP step during a SRM: 1 minute to achieve most of the ΔEELV and 2 minutes to achieve complete ΔEELV. For the decreasing PEEP trial, changes in ΔEELV were even faster but difficult to assess at the bedside, so clinicians had to track oxygenation changes. For the moment, 5 minutes may be appropriate until we have data concerning the SaO2 changes during the first 5 minutes.

Conclusions

In patients with early-onset moderate to severe ARDS, most of the ΔEELV occurs within the first minute and was completed within 2 minutes following an increase or decrease in PEEP. Dynamic EELV is faster after a decrease in PEEP than after an increase in PEEP. These results demonstrate that recruitment and derecruitment have different time courses and support the use of short duration (1–2 min) for the PEEP step during SRM and decremental PEEP trial.

Key messages

  • What is the key question? How long does it take to reach a new steady state in end-expiratory lung volume after an increase and a decrease in PEEP?

  • What is the bottom line? Most of the change in end-expiratory lung volume occurs within the first minute, and change is completed within 2 minutes following a PEEP increase or decrease.

  • Why read on? To determine the optimal duration of the PEEP step during a recruitment maneuver and decremental PEEP trial.

Abbreviations

ARDS:

acute respiratory distress syndrome

bpm:

beats per minute

CRS :

respiratory system compliance

EELV:

end-expiratory lung volume

FiO2 :

fraction of inspired oxygen

MAP:

mean arterial pressure

PaO2 :

partial pressure of oxygen

PAW :

airway pressure

PEEP:

positive end-expiratory pressure

PEEPTOT :

airway pressure at end expiration

PPLAT :

airway pressure at end inspiration

SAPS:

Simplified Acute Physiology Score

SpO2 :

oxygen saturation

SRM:

staircase recruitment maneuver

TE :

expiratory time

TI :

inspiratory time

VADD :

additional decreased volume

VADI :

additional increased volume

VEXP :

expected volume

VT :

tidal volume

References

  1. Caironi P, Cressoni M, Chiumello D, Ranieri M, Quintel M, Russo SG, et al. Lung opening and closing during ventilation of acute respiratory distress syndrome. Am J Respir Crit Care Med. 2010;181:578–86.

    Article  Google Scholar 

  2. Crotti S, Mascheroni D, Caironi P, Pelosi P, Ronzoni G, Mondino M, et al. Recruitment and derecruitment during acute respiratory failure: a clinical study. Am J Respir Crit Care Med. 2001;164:131–40.

    Article  CAS  Google Scholar 

  3. Suzumura EA, Figueiró M, Normilio-Silva K, Laranjeira L, Oliveira C, Buehler AM, et al. Effects of alveolar recruitment maneuvers on clinical outcomes in patients with acute respiratory distress syndrome: a systematic review and meta-analysis. Intensive Care Med. 2014;40:1227–40.

    Article  Google Scholar 

  4. Lapinsky SE, Aubin M, Mehta S, Boiteau P, Slutsky AS. Safety and efficacy of a sustained inflation for alveolar recruitment in adults with respiratory failure. Intensive Care Med. 1999;25:1297–301.

    Article  CAS  Google Scholar 

  5. de Matos GFJ, Stanzani F, Passos RH, Fontana MF, Albaladejo R, Caserta RE, et al. How large is the lung recruitability in early acute respiratory distress syndrome: a prospective case series of patients monitored by computed tomography. Crit Care. 2012;16:R4.

    Article  Google Scholar 

  6. Borges JB, Okamoto VN, Matos GFJ, Caramez MP, Arantes PR, Barros F, et al. Reversibility of lung collapse and hypoxemia in early acute respiratory distress syndrome. Am J Respir Crit Care Med. 2006;174:268–78.

    Article  Google Scholar 

  7. Hodgson CL, Tuxen DV, Davies AR, Bailey MJ, Higgins AM, Holland AE, et al. A randomised controlled trial of an open lung strategy with staircase recruitment, titrated PEEP and targeted low airway pressures in patients with acute respiratory distress syndrome. Crit Care. 2011;15:R133.

    Article  Google Scholar 

  8. Hodgson CL, Tuxen DV, Bailey MJ, Holland AE, Keating JL, Pilcher D, et al. A positive response to a recruitment maneuver with PEEP titration in patients with ARDS, regardless of transient oxygen desaturation during the maneuver. J Intensive Care Med. 2011;26:41–9.

    Article  Google Scholar 

  9. Maggiore SM, Jonson B, Richard JC, Jaber S, Lemaire F, Brochard L. Alveolar derecruitment at decremental positive end-expiratory pressure levels in acute lung injury: comparison with the lower inflection point, oxygenation, and compliance. Am J Respir Crit Care Med. 2001;164:795–801.

    Article  CAS  Google Scholar 

  10. Chiumello D, Coppola S, Froio S, Mietto C, Brazzi L, Carlesso E, et al. Time to reach a new steady state after changes of positive end expiratory pressure. Intensive Care Med. 2013;39:1377–85.

    Article  CAS  Google Scholar 

  11. Garnero A, Tuxen D, Ducros L, Demory D, Donati SY, Durand-Gasselin J, et al. Non-invasive assessment of lung elastance in patients with acute respiratory distress syndrome. Minerva Anestesiol. In press.

  12. The ARDS Definition Task Force. Acute respiratory distress syndrome: the Berlin Definition. JAMA. 2012;307:2526–33.

    Google Scholar 

  13. Papazian L, Forel JM, Gacouin A, Penot-Ragon C, Perrin G, Loundou A, et al. Neuromuscular blockers in early acute respiratory distress syndrome. N Engl J Med. 2010;363:1107–16.

    Article  CAS  Google Scholar 

  14. Katz JA, Ozanne GM, Zinn SE, Fairley HB. Time course and mechanisms of lung-volume increase with PEEP in acute pulmonary failure. Anesthesiology. 1981;54:9–16.

    Article  CAS  Google Scholar 

  15. Stahl CA, Möller K, Schumann S, Kuhlen R, Sydow M, Putensen C, et al. Dynamic versus static respiratory mechanics in acute lung injury and acute respiratory distress syndrome. Crit Care Med. 2006;34:2090–8.

    Article  Google Scholar 

  16. Bates JH, Irvin CG. Time dependence of recruitment and derecruitment in the lung: a theoretical model. J Appl Physiol. 2002;93:705–13.

    Article  Google Scholar 

  17. Fretschner R, Laubscher TP, Brunner JX. New aspects of pulmonary mechanics: “slowly” distensible compartments of the respiratory system, identified by a PEEP step maneuver. Intensive Care Med. 1996;22:1328–34.

    Article  CAS  Google Scholar 

  18. Arnal JM, Paquet J, Wysocki M, Demory D, Donati S, Granier I, et al. Optimal duration of a sustained inflation recruitment maneuver in ARDS patients. Intensive Care Med. 2011;37:1588–94.

    Article  Google Scholar 

  19. Wrigge H, Zinserling J, Muders T, Varelmann D, Günther U, von der Groeben C, et al. Electrical impedance tomography compared with thoracic computed tomography during a slow inflation maneuver in experimental models of lung injury. Crit Care Med. 2008;36:903–9.

    Article  Google Scholar 

  20. Grivans C, Lundin S, Stenqvist O, Lindgren S. Positive end-expiratory pressure-induced changes in end-expiratory lung volume measured by spirometry and electric impedance tomography. Acta Anaesthesiol Scand. 2011;55:1068–77.

    Article  CAS  Google Scholar 

  21. Brower RG. Editorial: Time to reach a new equilibrium after changes in PEEP in acute respiratory distress syndrome patients. Intensive Care Med. 2013;39:2053–5.

    Article  Google Scholar 

  22. Lindgren S, Odenstedt H, Olegård C, Söndergaard S, Lundin S, Stenqvist O. Regional lung derecruitment after endotracheal suction during volume- or pressure-controlled ventilation: a study using electric impedance tomography. Intensive Care Med. 2007;33:172–80.

    Article  Google Scholar 

  23. Gattinoni L, Pelosi P, Suter PM, Pedoto A, Vercesi P, Lissoni A. Acute respiratory distress syndrome caused by pulmonary and extrapulmonary disease: different syndromes? Am J Respir Crit Care Med. 1998;158:3–11.

    Article  CAS  Google Scholar 

  24. Garnero A, Tuxen D, Embriaco N, Demory D, Donati SY, Durand-Gasselin J, et al. Dynamics of end expiratory lung volume after changing PEEP in ARDS patients [abstract 004]. Intensive Care Med. 2014;40:1–2. http://react-profile.org/Download/ESICM2014_Abstract_Book_final_version.pdf. Accessed 2 September 2015.

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Acknowledgements

This study was promoted by the Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer. The work was supported by the Association pour l’Assistance Respiratoire à Domicile (APARD). It was performed at the Service de réanimation polyvalente, Hôpital Sainte Musse, Toulon, France. The results reported here were previously presented in abstract form at the 2014 European Society of Intensive Care Medicine annual meeting in Barcelona [24].

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Correspondence to Jean-Michel Arnal.

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Competing interests

JMA is working part-time as a medical research manager for Hamilton Medical. The other authors declare that they have no competing interests.

Authors’ contributions

AG designed the study, wrote the protocol, collected data, analyzed the results and drafted the manuscript. CG and JDG made substantial contributions to collecting the data and revising the manuscript. DT and CH made substantial contributions to interpreting the results and revising the manuscript. JMA made a substantial contribution to writing the protocol, collecting data, analyzing the results and drafting the manuscript. All authors read and approved the final manuscript.

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Garnero, A., Tuxen, D., Corno, G. et al. Dynamics of end expiratory lung volume after changing positive end-expiratory pressure in acute respiratory distress syndrome patients. Crit Care 19, 340 (2015). https://doi.org/10.1186/s13054-015-1044-0

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