Spatial distribution of sequential ventilation during mechanical ventilation of the uninjured lung: an argument for cyclical airway collapse and expansion
© Sinclair et al; licensee BioMed Central Ltd. 2010
Received: 10 August 2009
Accepted: 5 May 2010
Published: 5 May 2010
Ventilator-induced lung injury (VILI) is a recognized complication of mechanical ventilation. Although the specific mechanism by which mechanical ventilation causes lung injury remains an active area of study, the application of positive end expiratory pressure (PEEP) reduces its severity. We have previously reported that VILI is spatially heterogeneous with the most severe injury in the dorsal-caudal lung. This regional injury heterogeneity was abolished by the application of PEEP = 8 cm H2O. We hypothesized that the spatial distribution of lung injury correlates with areas in which cyclical airway collapse and recruitment occurs.
To test this hypothesis, rabbits were mechanically ventilated in the supine posture, and regional ventilation distribution was measured under four conditions: tidal volumes (VT) of 6 and 12 ml/kg with PEEP levels of 0 and 8 cm H2O.
We found that relative ventilation was sequentially redistributed towards dorsal-caudal lung with increasing tidal volume. This sequential ventilation redistribution was abolished with the addition of PEEP.
These results suggest that cyclical airway collapse and recruitment is regionally heterogeneous and spatially correlated with areas most susceptible to VILI.
Lung injury and edema are well-documented consequences of mechanical ventilation with high distending pressures in multiple experimental models [1–3]. It has been observed that maintaining end-expiratory lung volume, at some level above functional residual capacity, with positive end-expiratory pressure (PEEP) can prevent/reduce this ventilator-induced lung injury (VILI). Multiple animal models employing high distending pressures and/or volumes have demonstrated marked reductions in lung injury when adequate PEEP is applied [1–5]. In a surfactant-depletion model, lung injury occurs in the absence of large tidal volumes and distending pressures if inadequate or absent PEEP is used . However, applying PEEP above the lower inflection point of the inspiratory pressure-volume curve protected against injury . The protective effect of PEEP has been attributed primarily to prevention of repeated airway collapse and expansion (RACE) [6, 7], and to a lesser extent limitation of tidal excursion, and reduced cardiac output . These observations, although not always directly translatable to the clinical management of humans with lung injury, shed light on how management of mechanical ventilatory support might potentially impact patient outcomes. It has recently been observed that outcomes can be improved in ARDS patients if distending pressures are limited by tidal volume reduction [9, 10]. Although improved outcomes in ARDS patients ventilated with PEEP set above the lower inflection point of the inspiratory pressure-volume curve has been reported , a recent multi-center trial failed to show a survival advantage with a high-PEEP ventilation strategy . Similar outcomes have been observed in two subsequent trials employing either oxygenation-based  or plateau pressure-based  PEEP protocols. However, another recent study documented significant heterogeneity in how patients with ALI/ARDS respond to higher PEEP levels . They identified two populations of patients: those with a significant recruitable lung volume, and those with negligible recruitable volume. These intra-patient differences may suggest that some patients and not others may benefit from higher PEEP. Additionally, a recent study by Talmor and colleagues  examined the effect of higher PEEP based on a trans-pulmonary pressure-based protocol and found a strong trend toward improved survival in the higher PEEP group.
The RACE hypothesis has been called into question recently, favoring the tidal movement of fluid and/or foam in the airways as an explanation for the mechanical behavior of the injured lung during positive pressure ventilation . Also, a recent model of saline lavage lung injury found that high tidal volume/low PEEP ventilation resulted in lung injury in the non-dependent lung regions in supine rats, suggesting atelectasis in the dependent lung zones shifts stretch-induced injury to the non-dependent lung and argues against repetitive collapse and expansion as a cause of VILI . The current technological limitations of available imaging modalities preclude accurate real-time imaging of all but the most peripheral alveoli, therefore whether alveoli open and close during mechanical ventilation remains a point of contention.
We have recently shown in a rabbit model of VILI that lung injury is greater and more spatially variable with a dorso-caudal gradient in the absence of PEEP. One potential mechanism for this finding is regional repeated airway collapse and expansion in dependent lung areas during tidal breathing promotes subsequent injury. We hypothesize that 1) cyclical airway closure and expansion or RACE occurs in the lungs of anesthetized rabbits mechanically ventilated in the supine posture without PEEP and 2) RACE would occur regionally in the dorso-caudal lung regions, spatially correlating with the previously reported regional distribution of VILI .
To test this hypothesis, we measured how relative ventilation regionally redistributes with increasing tidal volume in the lungs of mechanically ventilated rabbits by measuring the distribution of aerosolized fluorescent microspheres. This ventilation redistribution with increasing tidal expansion of the lungs is referred to as sequential ventilation and reflects dynamic regional changes in lung mechanics during inspiration. By measuring regional ventilation redistribution with increasing tidal volume under different PEEP conditions, we could infer whether dynamic regional changes in lung mechanics were related to changes in the lower part of the pressure-volume curve (i.e. cyclical airway closure at FRC followed by expansion and increased ventilation during inspiration) or to changes at the upper part of the pressure volume curve (i.e. alveolar overdistension and regionally reduced compliance resulting in decreased regional ventilation).
The University of Washington Animal Care Committee in accordance with National Institutes of Health guidelines approved all methods. New Zealand white rabbits (either sex, 2.4 to 2.8 kg) were sedated with intramuscular ketamine (30 mg/kg) and xylazine (7.5 mg/kg) to allow placement of a 20 ga catheter in each marginal ear vein. A surgical plane of anesthesia was then maintained with a continuous intravenous infusion of ketamine (0.05 mg/kg/hr) and xylazine (0.003 mg/kg/hr) for the remainder of the protocol. A 3.5 mm cuffless endotracheal tube was inserted via tracheotomy to allow positive pressure mechanical ventilation. Arterial catheters were placed in the left carotid (blood gas sampling and arterial pressure measurement) and right femoral (thermistor tipped catheter for thermodilution cardiac output) arteries. A catheter was inserted into the right internal jugular vein for pressure monitoring and administration of thermodilution injectate. Pancuronium bromide (0.15 to 0.2 mg/kg) was administered intravenously, after adequate anesthesia was established, to suppress spontaneous respiratory efforts. A 30-min stabilization period followed the completion of surgical preparation, after which baseline data were collected. During this period, animals were ventilated in pressure control mode (Servo 900 C; Semens-Elema, Stockholm, Sweden) with a 50% inspiratory time and no inspiratory pause. Tidal volume was set at 10 - 12 ml/kg, PEEP = 5 cm H2O and a respiratory rate to achieve PaCO2 = 35 - 45 mmHg.
Data were recorded using Powerlab data acquisition software (AD-Instruments Castle Hill, New South Wales, Australia). Blood pressures (systemic arterial and right ventricular), heart rate, duplicate thermodilution cardiac output (Baxter Edwards SAT-2 Oximeter/Cardiac Output Computer, Irvine, CA), arterial blood gases (Radiometer ABL 5, Copenhagen, Denmark) and ventilatory parameters were measured for each experimental condition after a 20-minute stabilization period.
An in-line spirometer (KORR RSS 100; Medical Technologies Research Spirometry System, Salt Lake City, UT) was used to measure airway pressures and tidal volume. Plateau pressure was measured as the pressure achieved at the end of a 5-second end-inspiratory hold maneuver.
Sequential Ventilation Measurement
Physiological Response to Varying Mechanical Ventilation Strategies
Heart rate (min-1)
214 ± 45
219 ± 26
211 ± 25
230 ± 31
63 ± 18
47 ± 7
65 ± 9
52 ± 7
Mean RVP (mmHg)
14 ± 2
14 ± 1
13 ± 2
15 ± 1
Cardiac output (L·min-1)
0.34 ± 0.02
0.23 ± 0.05†
0.31 ± 0.05
0.25 ± 0.06
Peak PAW (cmH2O)
8 ± 1
16 ± 2†
13 ± 1*
30 ± 5*†
Plateau PAW (cmH2O)
7 ± 1
15 ± 2†
12 ± 2*
27 ± 2*†
7.38 ± 0.10
7.38 ± 0.07
7.42 ± 0.04
7.43 ± 0.02
Arterial PO2 (torr)
69 ± 11
95 ± 6†
69 ± 12
94 ± 11†
Arterial PCO2 (torr)
42 ± 2
40 ± 5
41 ± 2
41 ± 1
19 ± 21
8 ± 9
25 ± 7
5 ± 8†
The order of the four conditions was varied across experiments. Prior to each condition change, two static inflations to 40 cmH20 were performed via the syringe technique and held for 20 seconds each to ensure a standard volume history between conditions. All animals were ventilated with room air throughout all experimental conditions and respiratory rate was adjusted at each condition to achieve PaCO2 of 35 to 45 mmHg.
Twenty minutes after each condition was established, physiologic data were recorded. Aerosolized 1-μm diameter fluorescent microspheres were administered over 5 min to measure regional ventilation for each condition as previously described . A total of 4 different fluorescent colors (yellow, orange, orange-red, and red) were used. Each colored microsphere aerosol marked ventilation under one of the four conditions. By using four different aerosols, we can determine spatial ventilation distribution post-mortem for each of the four different ventilation conditions in each animal.
At the conclusion of each experiment, a sternotomy was performed, the main pulmonary artery and left atrium were cannulated, and the pulmonary vasculature was flushed with a dextran solution by gravity feed. The lungs were dissected from the chest cavity and dried inflated at 25-cmH2O. The dried lungs were fixed in rapid-setting foam, sliced, mapped, and diced into cubes of 1.5-2.0-cm3. Each piece was weighed, visually scored for airway and blood content, and soaked for 2 days in 1.5 ml of 2-ethoxyethyl acetate to extract the fluorescent dyes. The fluorescent signals for the four colors were measured in each piece with a fluorimeter (LS50B, Perkin-Elmer), corrected for background and spillover from adjacent signals , and converted to weight-normalized, relative ventilation signals as previously described .
Data Analysis and Statistics
Measurement of sequential ventilation distribution
Five animals were studied using the sequential ventilation experimental protocol. Several of the hemodynamic parameters were similar among the four ventilation conditions, although both mean arterial pressure (MAP) and cardiac output were lower during ventilation with PEEP for both tidal volumes (p = 0.08 and 0.01 for PEEP effect on MAP and cardiac output, respectively, at 6 ml/kg). Airway pressures were higher both with larger tidal volumes and with the addition of PEEP (Table 1), including statistically significant differences for three out of four comparisons. Arterial oxygenation was statistically higher during ventilation with PEEP (Table 1) for both tidal volumes; there were no statistically significant differences in arterial pH or PCO2 among the four conditions.
In summary, animals ventilated in the supine posture without PEEP demonstrated sequential redistribution of ventilation towards dorsal-caudal lung regions as tidal volume increased suggesting increasing regional compliance in dorsal-caudal lung regions relative to ventral-cranial regions. This sequential redistribution of ventilation was attenuated with the application of PEEP. This finding further suggests that the mechanism for the change in relative regional compliance was recruitment and increased compliance in dorsal-caudal lung, rather than over-distension and decreased compliance in ventral-cranial lung.
A regional increase in relative ventilation with an increase in tidal volume implies that local compliance is increasing relative to other lung regions.
Local lung compliance is roughly constant between volumes associated with either atelectasis (lower inflection point on a pressure-volume curve) or full inflation (upper inflection point on a pressure-volume curve - Figure 3).
Regional lung compliance can increase relative to other lung regions either because of local recruitment and improved compliance (Figure 3A) or because of over distension and reduced compliance in remote lung regions (Figure 3B).
If recruitment of dependent alveoli, which collapse at FRC, is responsible for redistribution of ventilation to dorso-caudal lung with increasing tidal volume, then application of PEEP should reduce this redistribution. However, if over distension of non-dependent alveoli is responsible for ventilation redistribution to dorso-caudal lung, then application of PEEP should augment this redistribution.
Although we have not directly visualized RACE, which is not obviously feasible, our data support a spatial distribution of cyclical airway collapse and recruitment, which correlates with our previously reported spatial distribution of lung injury . Because RACE is implicated as one cause of ventilator-induced lung injury [6, 18, 21–23], these findings further support regional RACE in uninjured, supine rabbits undergoing mechanical ventilation. All non-invasive measurements of volume change or alveolar density are indirect estimates of regional ventilation subject to erroneous interpretation. Using dynamic measurement of regional ventilation by the novel method of labeled aerosol deposition, we have demonstrated for the first time that regional ventilation redistributes with increasing tidal volume, suggesting dynamic regional changes in lung mechanics. Furthermore, by measuring sequential ventilation at different PEEP levels, we have shown that RACE is the most likely explanation for these dynamic changes in regional lung mechanics.
We have previously reported a dramatic dorsal-ventral and cranial-caudal gradient of lung injury severity in a rabbit model of VILI with supine ventilation in the absence of PEEP. The region with the most severe injury was the dorsal-caudal lung. With the application of 8 cmH2O of PEEP however, no such gradient is observed, rather a less severe, more homogeneously distributed injury pattern occurs, despite identical end inspiratory pressures . The application of PEEP has been shown to ameliorate VILI in a number of experimental models [1, 3, 4, 6, 24–26]. One potential explanation for the protective effects of PEEP is the prevention of tidal collapse and re-expansion of distal lung units. In the supine posture, lower alveolar volumes at FRC may predispose dependent lung regions to cyclical collapse. Muscedere et. al.  demonstrated epithelial injury in distal airways and alveoli, even with low tidal volumes (6 ml/kg), when isolated, unperfused rat lungs were allowed to deflate to volumes below the lower inflection point of the pressure-volume curve during exhalation. Although compelling, these findings must be interpreted in the context of an ex vivo, unperfused model which will favor tidal airway collapse and minimize edema formation in comparison with an intact animal model .
Distal airways and alveoli are not generally felt to be at risk of tidal collapse and re-expansion in vivo in uninjured lungs. In the current study, we examined this during mechanical ventilation in the supine posture by demonstrating sequential distribution of ventilation to the dorsal-caudal lung regions with increasing tidal volume, which was abolished by the application of PEEP. In the supine posture, a reduction was seen in relative ventilation to the dorsal-caudal region. One potential explanation for this is that the FRC is below the closing volume in this region at end-exhalation, resulting in cyclical airway closure. This would result in sequential ventilation with no inspired gas going to this lung region during the initial phase of tidal breathing, followed by recruitment and ventilation in the latter phase of each breath. To test this, we subjected uninjured animals to small (6 ml/kg) and large (12 ml/kg) tidal volume ventilation and measured relative regional ventilation distribution with inhaled fluorescent microspheres. We found a relative increase in ventilation to the dorsal-caudal lung and decreased ventilation to the ventral-cranial lung with larger tidal volumes. Two likely explanations for this observation are 1) alveoli in the dorsal-caudal lung were recruited with increased tidal volume or 2) ventral-cranial regions were over-distended with increased tidal volume, became less compliant, and ventilation was re-distributed to the dorsal-caudal lung. The effect of PEEP on the distribution of ventilation favors the former explanation. The application of PEEP = 8 cm H2O eliminated the observed sequential ventilation in the dorsal-caudal lung, consistent with recruitment of alveoli in this region which allowed the same relative ventilation to be delivered independent of tidal volume.
There are several limitations to the current study. The tidal volume used to induce VILI in our previous study  as well as other studies of VILI were much greater than the tidal volumes used in the measurement of ventilation distribution. The lower tidal volumes were chosen to avoid inducing lung injury during the experiment because aerosol deposition is unlikely to reflect ventilation distribution in the presence of spatially heterogeneous pulmonary edema secondary to differences in particle deposition. We did not measure ventilation distributions in the prone posture to identify whether or not sequential ventilation distribution was diminished. However, we have previously shown in a porcine model that posture change from supine to prone increases dorsal-caudal ventilation consistent with reduced airway collapse in these regions . Additionally, reduced sequential ventilation and airway closure in the prone posture compared with supine posture has been previously shown in dogs with normal lungs by single breath washout test . We have also ventilated animals in the prone posture in an identical fashion to that previously reported in supine animals. With supine ventilation, the most severe injury occurred in the dorsal-caudal lung while less severe injury was seen in the cranial-ventral region. In contrast, prone ventilation produced a more modest and homogeneously distributed injury pattern . These results are similar to that of previous observations in both oleic acid injured  and normal dogs . One potential explanation for the protective effects of prone posture is the prevention of tidal collapse and re-expansion of distal lung units. In the supine posture, lower alveolar volumes at FRC may predispose dependent lung regions to cyclical collapse. The more uniform pleural pressure gradient along the dorsal-ventral axis, in the prone posture, results in higher regional FRC in dependent lung zones  which may limit tidal collapse and recruitment of airways, and thus reduce VILI.
We previously reported in a rabbit model of VILI that lung injury is greater and more spatially heterogeneous in the supine posture as compared with the prone posture. One potential mechanism for this finding is regional repeated airway collapse and expansion during tidal breathing. To evaluate whether or not this occurred in the absence of lung injury with supine positioning, we measured regional ventilation at different tidal volumes in the presence and absence of PEEP. We found evidence of sequential ventilation distribution towards dorsal-caudal lung and away from ventral-cranial lung with increasing tidal volume. This sequential ventilation pattern was attenuated with the addition of PEEP compatible with RACE. We speculate that RACE occurs in normal lung with supine ventilation and in the absence of PEEP and that this may contribute to the development of lung injury.
List of Abbreviations
Positive end expiratory pressure
Ventilator-induced lung injury
Repeated airways collapse and expansion
- PaCO2 :
Partial pressure of arterial carbon dioxide
- PaO2 :
Partial pressure of arterial oxygen
The authors thank Wayne Lamm and Dowon An for assistance in performing these experiments.
This work was supported by NIH grants HL71020 and HL004479.
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