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The effects of airway pressure release ventilation on respiratory mechanics in extrapulmonary lung injury



Lung injury is often studied without consideration for pathologic changes in the chest wall. In order to reduce the incidence of lung injury using preemptive mechanical ventilation, it is important to recognize the influence of altered chest wall mechanics on disease pathogenesis. In this study, we hypothesize that airway pressure release ventilation (APRV) may be able to reduce the chest wall elastance associated with an extrapulmonary lung injury model as compared with low tidal volume (LVt) ventilation.


Female Yorkshire pigs were anesthetized and instrumented. Fecal peritonitis was established, and the superior mesenteric artery was clamped for 30 min to induce an ischemia/reperfusion injury. Immediately following injury, pigs were randomized into (1) LVt (n = 3), positive end-expiratory pressure (PEEP) 5 cmH2O, V t 6 cc kg−1, FiO2 21 %, and guided by the ARDSnet protocol or (2) APRV (n = 3), P High 16–22 cmH2O, P Low 0 cmH2O, T High 4.5 s, T Low set to terminate the peak expiratory flow at 75 %, and FiO2 21 %. Pigs were monitored continuously for 48 h. Lung samples and bronchoalveolar lavage fluid were collected at necropsy.


LVt resulted in mild acute respiratory distress syndrome (ARDS) (PaO2/FiO2 = 226.2 ± 17.1 mmHg) whereas APRV prevented ARDS (PaO2/FiO2 = 465.7 ± 66.5 mmHg; p < 0.05). LVt had a reduced surfactant protein A concentration and increased histologic injury as compared with APRV. The plateau pressure in APRV (34.3 ± 0.9 cmH2O) was significantly greater than LVt (22.2 ± 2.0 cmH2O; p < 0.05) yet transpulmonary pressure between groups was similar (p > 0.05). This was because the pleural pressure was significantly lower in LVt (7.6 ± 0.5 cmH2O) as compared with APRV (17.4 ± 3.5 cmH2O; p < 0.05). Finally, the elastance of the lung, chest wall, and respiratory system were all significantly greater in LVt as compared with APRV (all p < 0.05).


APRV preserved surfactant and lung architecture and maintenance of oxygenation. Despite the greater plateau pressure and tidal volumes in the APRV group, the transpulmonary pressure was similar to that of LVt. Thus, the majority of the plateau pressure in the APRV group was distributed as pleural pressure in this extrapulmonary lung injury model. APRV maintained a normal lung elastance and an open, homogeneously ventilated lung without increasing lung stress.


Acute respiratory distress syndrome (ARDS) is a syndrome encompassing a broad range of phenotypes yet is often studied clinically as a single disease phenotype. ARDS can be broadly sub-classified into pulmonary versus extrapulmonary ARDS, the ultimate pathology of which may be similar; however, the etiology and physiology of the two subtypes are distinct [1]. Despite these physiologic differences, many of the randomized controlled trials evaluating the impact of ventilator strategies on the incidence and mortality of ARDS analyze patients with pulmonary and extrapulmonary ARDS combined, usually with a preponderance of pulmonary ARDS [28], and despite decades of study, the mortality associated with ARDS has not changed since 1994 [8]. Therefore, in order to establish strategies to improve ARDS incidence and mortality, it may be necessary to stratify patients according to ARDS physiology rather than generalizing ARDS as a single phenotype.

Patients with extrapulmonary ARDS are at particular risk for alterations in chest wall mechanics, whereas patients with pulmonary ARDS are less likely to have increases in chest wall elastance (E cw), with the majority of the pathology associated with increased lung elastance (E l). The mechanism of increased chest wall elastance in extrapulmonary ARDS is a combination of chest wall edema and increased intra-abdominal pressure (IAP). In patients with normal E cw, airway opening pressure closely resembles the lung-distending (transpulmonary) pressure, but in patients with an increase in E cw, a greater portion of the airway opening pressure is generated as pleural pressure, leading to a lower transpulmonary pressure [9]. Chest wall elastance represents only a small fraction of the respiratory system elastance (E rs) in patients with ARDS with normal chest wall elastance [9]; however, in patients with altered chest wall mechanics, the E cw to E rs ratio ranges from 20 to 80 % [10]. This great variability demonstrates the fallibility of targeting airway opening pressures without taking the E cw and transpulmonary pressure into consideration.

In previous animal studies of extrapulmonary ARDS, airway pressure release ventilation (APRV) was associated with higher tidal volumes and plateau pressures [11, 12], which has raised concern for APRV potentially placing undue stress on the lung. In this study, we use esophageal manometry to measure transpulmonary pressure between preemptive application of APRV and low tidal volume ventilation in our clinically applicable porcine extrapulmonary ARDS model. We demonstrate that the transpulmonary pressures are similar between the two ventilation strategies, despite the increased tidal volumes and plateau pressures in the APRV group, and that APRV was able to limit increases in chest wall elastance.


All experiments were performed in accordance with National Institutes of Health guidelines in the use of laboratory animals and approved by the SUNY Upstate Medical University Institutional Animal Care and Use Committee (IACUC). The study was terminated upon achieving statistical significance between the two groups, according to the IACUC guidelines and study protocol. Female Yorkshire pigs (32–36 kg) were anesthetized using a continuous infusion of ketamine/xylazine to maintain a surgical plane of anesthesia. Animals were continuously monitored by the investigators for the duration of the experiment. Under sterile conditions, animals underwent tracheostomy and arterial and venous catheterization. The animals were connected to a Drӓger (Evita Infinity V500, Lübeck, Germany) ventilator and ventilated initially with (V t) 10 cc kg−1, positive end-expiratory pressure (PEEP) of 5 cmH2O, respiratory rate (RR) of 12 breaths min−1, and FiO2 100 %.

A pulse index continuous cardiac output (PiCCO) catheter (Pulsion Medical Systems, Germany) was placed in the femoral artery with hourly injections to assess cardiac index and global end-diastolic index. A cystostomy was performed for continuous urine output and hourly IAP monitoring (ConvaTec Inc. NJ). Intra-abdominal hypertension was defined as sustained or repeated elevation in IAP (>12 mmHg) and abdominal compartment syndrome as repeated elevation in IAP (>20 mmHg) associated with new organ dysfunction according to consensus criteria [13]. The esophageal catheter was placed by first advancing the balloon into the stomach, where placement was confirmed by a transient increase in pressure during abdominal compression, then retracting it to the middle third of the esophagus with placement confirmed by noting cardiac oscillation and respiratory variation in the waveform [14]. Baseline (BL) measurements were taken after surgical preparation and prior to injury.

Extrapulmonary lung injury was induced using a previously established double-hit model of ischemia reperfusion and fecal peritonitis [11, 12, 15]. Briefly, the superior mesenteric artery was clamped for 30 min and released to induce intestinal ischemia. Peritoneal sepsis was induced by performing a cecotomy and mixing feces with blood to create a fecal clot, which was then implanted into the peritoneum. Time zero (T0) measurements were taken immediately after induction of the double-hit injury and upon closure of the abdomen. The animals were subsequently randomized into two groups: low tidal volume (LVt) ventilation or APRV.

LVt group (n = 3): Animals were transitioned from the baseline settings to low tidal volume settings of V t 6 cc kg−1, PEEP of 5 cmH2O, RR 12 breaths min−1, and FiO2 21 %. All ventilator adjustments were made in accordance with the ARDSnet guidelines with PEEP and FiO2 titrated according to SpO2 and PaO2 as outlined by the “Lower PEEP/higher FiO2 scale”. RR was titrated according to pH and PaCO2 and V t was reduced to accommodate the plateau pressure (P plat) if values exceed 30 cmH2O.

APRV group (n = 3): APRV was applied and guided using a previously described protocol by Habashi [16]. Animals were ventilated at an inspiratory pressure P High set at the P plat established during the volume cycle setting used for BL measurements (16–22 cmH2O) for a time (T High) of 4.0–4.5 s, which was set to occupy approximately 90 % of the total ventilator cycle time. The release pressure (P Low) was set at 0 cmH2O to minimize expiratory resistance and maximize the peak expiratory flow rate. P Low was applied for a time (T Low) to terminate the end-expiratory flow rate at 75 % of the peak expiratory flow rate, which was between 0.32 and 0.37 s. P High, T High, T Low, and FiO2 were titrated throughout the study according to pulmonary parameters, PaO2 and PaCO2.

Resuscitative protocol

Antibiotics, fluid, and vasopressor administration were guided by the Surviving Sepsis campaign [17]. Broad-spectrum antibiotics (vancomycin 1 g and piperacillin/tazobactam 3.375 g) were administered following abdominal closure and throughout the study every 12 and 8 h, respectively. Animals were provided with continuous maintenance intravenous fluid resuscitation and boluses as needed with Lactated Ringers to maintain a mean arterial pressure (MAP) >65 mmHg. Continuous infusion of norepinephrine was initiated when the animal was no longer fluid responsive, followed by vasopressin and epinephrine. Rocuronium was initiated if spontaneous respiratory effort was demonstrated in order to standardize animals across groups.

Physiologic measurements

Hemodynamics were monitored continuously (Intellivue MP-90, Phillips Healthcare, Irvine, CA) using Edwards transducers (Pressure Monitoring Kit, Edwards Lifesciences, Irvine, CA). Blood gases were measured every 1–3 h with a Roche blood gas analyzer (Cobas b221, Basel, Switzerland).

Pulmonary parameters

Pulmonary parameters were measured or calculated by the Drӓger ventilator. The end-expiratory pressure in APRV was taken to be the lowest value during the expiratory release phase after accounting for tracheal tube compensation. The respiratory system may be partitioned into the lung and the chest wall, and the plateau pressure (P plat) distributed across the respiratory system may also be divided into the corresponding transpulmonary pressure (P l) and pleural pressure (P pl) [18, 19].

$$ {P}_{\mathrm{pl}\mathrm{at}} = {P}_{\mathrm{l}} + {P}_{\mathrm{pl}} $$

Similarly, the sum of the lung (E l) and chest wall (E cw) elastance represents the elastance of the entire respiratory system (E rs) (Eq. 2) [18].

$$ {E}_{\mathrm{rs}} = {E}_{\mathrm{cw}} + {E}_{\mathrm{l}} $$

The elastance calculated by the ventilator (standardly reported as compliance on the monitor) represents the elastance of the respiratory system (Eq. 3) but does not distinguish lung from chest wall elastance.

$$ {E}_{\mathrm{rs}} = \left({P}_{\mathrm{plat}}\hbox{--}\ \mathrm{PEEP}\right)/{V}_{\mathrm{t}} $$

The use of esophageal manometry to determine the partitioning of respiratory system elastance into chest wall and lung elastance was first described in a thesis by Buytendijk in 1949 [20, 21] although several methods of direct [22, 23] and indirect [14, 24, 25] measurements have since been described. The change in P es between inspiration and expiration (ΔP Es) approximates the change in P pl [26, 27]; thus, the elastance of the chest wall may be calculated as follows [28]:

$$ \Delta {P}_{\mathrm{Es}}/{V}_{\mathrm{t}} = {E}_{\mathrm{cw}} $$

Therefore, the distribution of P aw to the lung (P l) and chest wall (P pl) can be calculated based on the ratios of lung elastance and chest wall elastance to the respiratory system elastance, respectively (Eqs. 5 and 6) [9, 18].

$$ {P}_{\mathrm{pl}} = {P}_{\mathrm{pl}\mathrm{at}} \cdot \left({E}_{\mathrm{cw}}/{E}_{\mathrm{rs}}\right) $$
$$ {P}_{\mathrm{l}} = {P}_{\mathrm{plat}} \cdot \left({E}_{\mathrm{l}}/{E}_{\mathrm{rs}}\right) $$


After 48 h, the experimental protocol was terminated. Animals were euthanized with Fatal-Plus (1 mL 10 lbs−1 intravenous), cardiac death confirmed, and necropsy performed. The lungs were removed and inflated to 25 cmH2O, using stepwise increases in PEEP to standardize lung volume history, and grossly photographed. The left lung was filled with 10 % formalin to a height of 25 cmH2O, clamped and submerged in formalin. The right middle lobe was lavaged with 60 mL of normal saline to collect bronchoalveolar lavage fluid (BALF). The concentrations of interleukin-6 and -8 (IL-6 and IL-8) were determined using enzyme-linked immunosorbent assay (ELISA) quantification according to manufacturer’s recommendations. Western blot analyses of surfactant protein A (SP-A) and B (SP-B) abundance as well as determination of total protein were performed as described previously [11].

Quantitative histology

The quantitative histological assessment of the lung was based on image analysis of 120 photomicrographs (10 per animal) made at high-dry magnification following a validated, blinded, systematic sampling protocol [15]. Each photomicrograph was scored using a 4-point scale for each of the five parameters: atelectasis, fibrinous deposits and blood in air space, vessel congestion, alveolar wall thickness, and leukocytes.


The study was terminated upon achieving statistical significance between the two groups, according to the IACUC guidelines to reduce the number of animals used for experimentation and the study protocol. Data are reported as mean ± SEM. Repeated measures ANOVA was used to compare differences within and between treatment groups for continuous parameters and post hoc Tukey’s tests if significance was found in the group*time effect. Categorical data were compared using an unpaired Student’s t test. Quantitative histological assessment was analyzed using Mann-Whitney U test after testing for normality. p values <0.05 were considered significant. Analyses were performed using JMP (version 10, Cary, NC).



Both LVt and APRV pigs had a precipitous decline in MAP in the hour following injury with a steady decline thereafter (Table 1). The MAP was similar in both groups and was maintained above 65 mmHg with fluid and vasopressor support (p > 0.05). The total volume of fluid infused over the course of the experiment was similar between LVt (36.0 ± 7.5 L) and APRV (47.8 ± 7.2 L; p > 0.05; Table 1). The cardiac index (LVt 3.3 ± 0.7 L min−1 m−2; APRV 2.0 ± 0.3 L min−1 m−2) and global end-diastolic index (LVt 563.7 ± 167.8 mL · min−2; APRV 314.0 ± 111.9 mL · min−2), as measured by the PiCCO catheter, were similar between groups (p > 0.05; Table 1).

Table 1 Hemodynamic data and organ injury in low tidal volume (LVt) versus airway pressure release ventilation (APRV)

Pulmonary data

The end-expiratory release pressure was significantly greater in APRV as compared with LVt (p < 0.05; Table 2), despite a P Low of 0 cmH2O, demonstrating the importance of setting the T Low appropriately to ensure the end-expiratory pressure never has the time to actually reach 0 cmH2O. Consistent with previous studies [11, 29], the tidal volumes in the APRV group (13.3. ± 0.6 cc kg−1) were significantly greater than those in the LVt group (5.6 ± 0.3 cc kg−1; p < 0.05; Table 2). In one LVt animal, the P plat became greater than 30 cmH2O at T43 (although the corresponding transpulmonary pressures was 23.9 cmH2O) and the V t was decreased to maintain P plat below 30 cmH2O as per the ARDSnet protocol [3]; however, this led to prompt desaturation (SpO2 <88 %) that ultimately required titrating PEEP and FiO2 upward (requiring an FiO2 of 50 % and a PEEP of 10 cmH2O to maintain adequate oxygen saturation by T48). By the study end, LVt animals had significantly greater FiO2 requirements (37.7 ± 6.7 %) as compared with the APRV pigs, all of which were maintained on an FiO2 of 21 % throughout the study (21.0 ± 0.0 %; p < 0.05; Table 2). Significant differences in the PaO2/FiO2 ratio between APRV and LVt were revealed by T30 and persisted until T48 with final PaO2/FiO2 ratio of 226.2 ± 17.1 in LVt and 465.7 ± 66.5 in APRV (p < 0.05) with all animals in the LVt group meeting the Berlin criteria for mild ARDS [30] by T36 (Table 2).

Table 2 Pulmonary data in low tidal volume (LVt) versus airway pressure release ventilation (APRV)

The plateau pressures in both groups increased steadily over the course of the study with a significantly lower plateau pressure in LVt (22.2 ± 2.0 cmH2O) as compared with APRV (34.3 ± 0.9 cmH2O; p < 0.05; Table 2). Over time, the P pl in APRV increased from 5.5 ± 1.0 cmH2O at T0 to 17.4 ± 3.5 cmH2O at T48 whereas the P pl in LVt remained relatively stable from 4.0 ± 1.3 to 7.6 ± 0.5 cmH2O leading to a significant difference between the two groups by T48 (p < 0.05; Fig. 1). The P l in the LVt group (14.6 ± 2.1cmH2O) was similar to that of the APRV group (17.3 ± 2.9 cmH2O; p > 0.05). In combination, these data suggest that the majority of the increased P plat in APRV was being distributed as P pl, directed towards the chest wall, rather than increasing lung stress. Finally, the elastance of the lung, chest wall, and respiratory system were all significantly greater in LVt as compared with APRV (all p < 0.05; Table 2). By the end of the 48-h study, the lung elastance increased by 154 ± 78 % in the LVt group but was reduced by 43.2 ± 5.2 % in the APRV group.

Fig. 1
figure 1

The plateau pressure (black line at top of the red area curve) in LVt (a) is significantly lower than that of APRV (b) yet the transpulmonary pressures (blue) are statistically similar between groups. This demonstrates that the increases in plateau pressure in APRV reflects and increase in pleural pressure (red)

Organ injury

Animals in the APRV group had an increase in IAP (21.8 ± 0.8 cmH2O) as compared with LVt (11.3 ± 5.0 cmH2O; p < 0.05; Table 1), consistent with the increase in P pl seen in APRV. Despite the measured increased IAP in APRV, there was no clinical evidence of reduced end-organ perfusion in either group and no animal required a decompressive laparotomy for abdominal compartment syndrome. Both groups had similar blood urea nitrogen levels, and the total urine output between the two groups was similar (p > 0.05; Table 1).

Gross pathology and quantitative histology

The lungs of the LVt group inflated heterogeneously with predominant basilar and dependent atelectasis; the majority of which could be recruited with persistent pressure (Fig. 2a). The cut surfaces of the LVt group were erythematous and had both interlobular septal edema and bronchial edema (Fig. 2b). The lungs of the APRV group were pink, light, and inflated homogeneously (Fig. 2c), and the cut surface of the lung demonstrated interlobular septal edema but little bronchial edema (Fig. 2d). Two of the three pigs in each group demonstrated small bowel dilatation consistent with ileus as well as bowel wall edema. All of the pigs in both groups demonstrated gastric ulceration ranging from hyperemia to gross hemorrhagic ulcers. The wet-dry weight for the LVt group (7.0 ± 0.3) was similar to the APRV group (7.6 ± 0.9; p > 0.05).

Fig. 2
figure 2

Low tidal volume ventilation lungs (a) inflated heterogeneously with prominent dependent and basilar atelectasis and the cut surface (b) revealing airway edema. Airway Pressure Release Ventilation gross lungs (c) and cut surface (d) were pink, light and inflated homogeneously without airway edema

The lungs in the LVt group demonstrated a significant increase in alveolar wall thickening as compared with APRV (p < 0.05; Fig. 3). There was also a significant increase in intra-alveolar hemorrhage in the LVt group as compared with APRV (p < 0.05), with the luminal erythrocytes noted to be intact with no signs of hemolysis. Although not statistically significant, LVt had a relative increase in vessel congestion (Fig. 3), atelectasis, and fibrinous deposits (p > 0.05).

Fig. 3
figure 3

Low tidal volume (LVt; left) demonstrated increased alveolar wall thickness (between arrows) and vessel congestion (arrowheads) as compared with Airway Pressure Release Ventilation (APRV; right)

Bronchoalveolar lavage

There was a trend towards an increase in total protein in the BALF in the LVt group (1271.5 ± 590.6 μg mL−1) as compared with APRV (300.9 ± 9.8 μg mL−1) although this did not reach statistical significance (p = 0.18). SP-A in the BALF was significantly reduced in the LVt group as compared with APRV (p < 0.05) although SP-B was not significantly different between the two groups (p = 0.09). The BALF concentrations of IL-8 were similar between LVt (145.8 ± 115.5 pg mL−1) and APRV (79.4 ± 56.6 pg mL−1; p > 0.05). The BALF concentrations of IL-6 was relatively greater in the LVt group (2677 ± 1060 pg mL−1) as compared with APRV (342.1 ± 146.9 pg mL−1; p > 0.05).


The transpulmonary pressure between APRV and LVt, however, was similar suggesting that the P plat and V t in APRV did not lead to increased lung stress. This is in spite of the fact that the APRV group was associated with an elevated P plat and greater V t, as compared with LVt, both of which are currently considered injurious [3]. Thus, the majority of the plateau pressure in the APRV group was being distributed as pleural pressure, applied to the chest wall, an important finding in this extrapulmonary lung injury model associated with increased chest wall elastance. In addition, APRV preserved surfactant protein-A concentrations and reduced epithelial permeability, as measured by BALF protein. APRV also preserved lung elastance and reduced lung injury by histopathologic scoring.

Intra-abdominal pressure and chest wall elastance

ARDS can be largely subdivided by its original etiology: pulmonary (i.e., pneumonia and aspiration) and extrapulmonary (i.e., sepsis, hemorrhage, peritonitis, systemic inflammatory response syndrome, and multi-organ trauma). Although the two ARDS phenotypes may have similar pathophysiologic outcomes, the pathogenesis and treatment are different [1]. Whereas increased lung and respiratory system elastance is found in both pulmonary and extrapulmonary ARDS, an increase in chest wall elastance is primarily associated with extrapulmonary ARDS [1]. The chest wall consists of the anterior and posterior thoracic cage and the diaphragm, which serves as a pliable separation between the abdominal and thoracic cavities [31]. Approximately half of the IAP is transmitted to the intrathoracic space [31, 32]; thus, increased IAP is one of the most common causes of increased chest wall elastance in extrapulmonary ARDS and has been associated with increased pulmonary edema, atelectasis, and lung neutrophil activation [19]. Body wall edema can further increase elastance of both the chest wall and abdomen [33].

Intra-abdominal hypertension has been observed in 54.4 % of medical and 65.0 % of surgically critically ill patients [18]. The IAP at end-inspiration has been shown to be approximately four times greater in the surgical ARDS groups as compared with the medical ARDS group [34]. An increase in IAP transmits stress to the thoracic cavity causing a decrease in functional residual capacity, ventilation-perfusion mismatching, a shift in the volume-pressure curve of the chest to the right, and compression atelectasis [31, 32, 34, 35]. The negative effects of increased IAP on the thoracic cavity can be attenuated by increasing the pleural pressure, effectually placing an opposing force on the IAP [36, 37]. Since pleural pressure and IAP have a linear relationship [1], the combination of a prolonged inspiratory time and increased pleural pressure in the APRV group further increased the measured IAP [38] and is likely the mechanism of decreased chest wall elastance in this group.

Despite the increase in IAP, APRV improved lung elastance while maintaining a physiologic PaO2/FiO2 ratio. The importance of delivering a pressure sufficient to shift the volume-pressure curve of the chest back to the left and increase diaphragm tension at end-expiration to prevent the negative effects of IAP transmission to the chest wall was established in a study of increasing PEEP [39]. In the current study, the extended time at the P plat in the APRV group similarly opposed the effects of increased IAP. Conversely, the lungs of the LVt pigs universally had bibasilar atelectasis suggesting that the PEEP scale guided by the ARDSnet protocol was insufficient to oppose the force of the IAP on the lower lung lobes. This is supported by the significant increase in lung elastance in the LVt group by 48 h, and the trend suggested that the lung elastance would have increased further had the animals not reached the termination point of the study.

Plateau pressure versus pleural pressure

As the IAP increases and the chest wall becomes stiffer, more of the P plat is generated as P pl rather than P l [19, 33, 40]. In patients with high E cw, limiting P plat could worsen oxygenation and enable lung derecruitment if the transpulmonary pressure is not considered, whereas an appropriately high plateau pressure could improve oxygenation and lung/chest wall elastance [40]. In a porcine model by Kubiak et al. [33], pneumoperitoneum was established and, as IAP increased, P plat and P pl increased but P l did not, whereas ventilating to similar P plat in a desufflated abdomen led to a significant increase in P l. Thus, that study demonstrates that in a patient population with a compromised chest wall, P plat is a poor surrogate for P l, and setting the upper limit for P aw at 30 cmH2O may not be realistic without considering the underlying chest wall mechanics [33].

In patients with influenza A (H1N1)-induced ARDS referred for extracorporeal membrane oxygenation (ECMO), Grasso et al. [41] determined that there was a subset of patients in whom the majority of pressure applied by the ventilator was being transmitted to the stiff chest wall rather than to recruiting the lung [41]. The authors determined that targeting end-inspiratory P l rather than the respiratory system P plat significantly improved patient oxygenation such that 50 % of patients that previously met ECMO criteria no longer did [41]. In this current study, the LVt pig that achieved a P plat greater than 30 cmH2O had a corresponding P l of 23.4 cmH2O and dropping the tidal volumes to accommodate the P plat led to prompt desaturation.

It has previously been demonstrated in an in vivo study that APRV, with an extended time at the P plat, improves alveolar recruitment and alveolar surface area, suggesting that these larger tidal volumes are being distributed over a greater number of open alveoli, reducing the dynamic strain on individual alveoli [42]. In a prospective study by Chiumello et al. [43], comparing control patients with those with acute lung injury or ARDS, increasing PEEP from 5 to 15 cmH2O led to a decrease in lung, chest wall, and respiratory system elastance. Additional time at a greater pressure (PEEP or plateau pressure) therefore allows for increased alveolar recruitment and distribution of the tidal volume over a larger surface area of alveoli, reducing overall lung stress. Protective mechanical ventilation should be instituted early and consideration given towards increasing PEEP or extending time at the P plat to optimize recruitment while limiting the potential negative effects of larger V t.


In this study, we have demonstrated that the early application of APRV improves oxygenation and maintains surfactant as compared with LVt applied immediately following injury. APRV had greater plateau pressures and tidal volumes as compared with LVt yet the transpulmonary pressures between the groups were similar. Thus, APRV represents a safe and effective ventilation mode in patients at risk for the development of extrapulmonary lung injury.



acute respiratory distress syndrome


airway pressure release ventilation

LVt :

low tidal volume ventilation

E cw :

chest wall elastance

E rs :

respiratory system elastance

E l :

lung elastance


Institutional Animal Care and Use Committee

V t :

tidal volume


positive end-expiratory pressure


respiratory rate


intra-abdominal pressure




time zero

P plat :

plateau pressure

P l :

transpulmonary pressure

P pl :

pleural pressure

P es :

change in esophageal pressure


bronchoalveolar lavage fluid


surfactant protein A


surfactant protein B


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Correspondence to Joshua Satalin.

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This project was supported by the Upstate Medical University HSC Foundation account. Voluntary donations were accepted into this fund. Donors waived rights to determine how and to which projects the funds were allocated. Donations were accepted under the condition that ownership of intellectual property rights was waived and donor approval not required for publication. These funds were not provided for goods or services.

Authors’ contributions

MKS drafted the manuscript and participated in data collection and interpretation. BE, JL, EP, VK, and GW participated in the data collection and interpretation. SVJ, JS, LAG, and GFN critically revised the manuscript and participated in the data collection and interpretation. PA helped to conceive, draft, and critically revise the manuscript and participated in the data collection and interpretation. WM critically revised the manuscript. NMH helped to conceive, draft, and critically revise the manuscript and participated in the data collection and interpretation. All authors read and approved the final manuscript.

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Kollisch-Singule, M., Emr, B., Jain, S.V. et al. The effects of airway pressure release ventilation on respiratory mechanics in extrapulmonary lung injury. ICMx 3, 35 (2015).

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