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01.12.2018 | Research | Ausgabe 1/2018 Open Access

Critical Care 1/2018

High frequency percussive ventilation increases alveolar recruitment in early acute respiratory distress syndrome: an experimental, physiological and CT scan study

Zeitschrift:
Critical Care > Ausgabe 1/2018
Autoren:
Thomas Godet, Matthieu Jabaudon, Raïko Blondonnet, Aymeric Tremblay, Jules Audard, Benjamin Rieu, Bruno Pereira, Jean-Marc Garcier, Emmanuel Futier, Jean-Michel Constantin
Wichtige Hinweise

Electronic supplementary material

The online version of this article (doi:https://​doi.​org/​10.​1186/​s13054-017-1924-6) contains supplementary material, which is available to authorized users.
A comment to this article is available at https://​doi.​org/​10.​1186/​s13054-018-1982-4.
Abbreviations
ARDS
Acute respiratory distress syndrome
CMV
Conventional mechanical ventilation
CT
Computed tomography
EELV
End-expiratory lung volume
FiO2
Fraction of inspired oxygen
HFO
High frequency oscillation
HFPV
High frequency percussive ventilation
HU
Hounsfield unit
IBW
Ideal body weight
ICU
Intensive Care Unit
IQR
Inter-quartile range
MAP
Mean arterial pressure
OLV
Open lung ventilation
PaO2
Arterial oxygen tension
Paw
Upper airways pressure
PEEP
Positive end-expiratory pressure
RM
Recruitment manoeuver
SD
Standard deviation
VDR
Volumetric diffusive respirator
VI
Vasopressor index
VILI
Ventilator induced lung injury
Vt
Tidal volume

Background

Conventional mechanical ventilation (CMV) is a cornerstone treatment for acute respiratory distress syndrome (ARDS). However, although being life-saving, CMV can induce ventilator-induced lung injury (VILI) [ 1]. Open-lung ventilation (OLV) can be applied to improve gas exchange and decrease VILI. Different strategies can be used to perform OLV. Conventional ventilation, combining low tidal volume [ 2], tailored positive end-expiratory pressure (PEEP) [ 3], prone positioning [ 4] and recruitment maneuvers (RM) [ 5] currently comprise the regular approach. High frequency ventilation, including high frequency oscillatory ventilation (HFO), high frequency percussive ventilation (HFPV) and jet ventilation, have been used. Two recent large randomized controlled trials [ 6, 7] argued for withdrawal use of HFO in adult patients with ARDS. For technical and safety issues, jet ventilation is no longer used in the ICU. HFPV has been used in neonates [ 8], burn patients [ 912], trauma patients [ 13] and patients with chronic obstructive lung disease [ 14]. HFPV has also been used in ARDS [ 15], or as rescue therapy [ 16, 17]. Its theoretical properties include the delivery of low tidal volume ventilation with effective recruitment and enhanced secretion clearance [ 18].
Gases are administered through pulsatile Flow Ventilation TM Phasitron®, an open circuit device that is believed to adapt ventilation to patient lung volumes, regardless of compliance [ 19]. During HFPV, high frequency oscillatory diffusive ventilation is superimposed to conventional tidal volume convective ventilation, resulting in a rapid increase in arterial oxygenation [ 15, 18]. However, despite positive effects on lung alveolar recruitment [ 18], hyperinflation might be induced by HFPV during ARDS, thus possibly limiting its use only as a rescue therapy in severe ARDS. Therefore, we designed a study to determine changes in lung aeration assessed by CT scan. Moreover, monitoring of alveolar pressures and especially plateau pressure is not obtained from the HFPV Monitron®, since no end-inspiratory hold is possible. We conducted an animal experiment in a pig model of ARDS to monitor upper airway and pleural pressures, in order to investigate correlation between Monitron®-based and pressures recorded in vivo. Some of the results of this study have been previously reported in the form of an abstract [ 20].

Methods

Additional details are provided in Additional file  1.

Human studies

Ethical statements

Our institutional review board approved the protocol (CPP Sud-Est VI, approval number AU 1138). All participants, or their next-of-kin, provided written consent to participate in this study. The clinical trial is registered at http://​www.​clinicaltrials.​gov (NCT02510105).

Study design

Consecutive patients were enrolled in this prospective non-randomized monocentric study within 24 hours of moderate to severe ARDS onset [ 21]. CMV was optimized by the ICU physician, following the ExPress study settings aimed at increasing alveolar recruitment [ 3] (Engström Carestation, General Electrics Healthcare). HFPV settings were obtained following manufacturer’s recommendations and equivalent to previously published ones [ 13, 15]. Further information is in Additional file  1: Table S1, with a pressure waveform example.

CT protocol

Baseline lung CT was performed during CMV end-expiratory holds. Lung morphology was assessed following ARDS study group criteria for the CT scan [ 22]. Diffuse and patchy patterns were considered non-focal [ 23].
Patients were ventilated with HFPV for 1 hour using the stand-alone ventilator VDR-4 (Volumetric Diffusive Respirator, Percussionaire® Corporation), with a mandatory maximal mean pressure (30 cmH 2O) and a CMV equivalent mean PEEP. CT was performed during end-inspiratory and end-expiratory holds, by clamping the endotracheal tube. Arterial blood gases were obtained prior to inclusion (time 0 (T0)), every 10 minutes during HFPV (T10–T60) and 10 minutes after resuming CMV (T-after).

CT scan analyses

CT scans were computed to obtain 5-mm-thick contiguous sections (Advance Workstation, General Electrics Healthcare). Qualitative assessment of lung aeration, was obtained using the UCLA color-coding table ( http://​osirixfoundation​.​com/​, OsiriX, Switzerland) and digital post-processing to convert purple into white pixels ( http://​gimp.​org, GNU Image Manipulation Program, Version 2.8.20). Quantitative assessment was performed using dedicated software (Maluna 3.17, University Hospital of Göttingen, Germany). Regions of interest were drawn manually including only lung parenchyma and excluding large vessels and bronchi. Lung gas content, lung weight and aeration distribution were measured as previously reported [ 23]. Lung tissue aeration was divided into four compartments according to their Hounsfield Units (HU): hyperinflated (densities from −1000 to −900 HU), normally aerated (−900 to −500 HU), poorly aerated (−500 to −100 HU) and non-aerated tissue (−100 to 100 HU). Two ICU physicians (TG and JMC) and a senior radiologist (JMG) reviewed CT scans and manual drawings.
Recruitment was computed during both end-inspiratory and end-expiratory holds as the decrease in non-aerated lung volumes:
Alveolar recruitment (mL) = (CMV non-aerated lung volume (mL))–(HFPV non-aerated lung volume (mL)).
HFPV tidal volume was defined by volume difference between end-inspiratory and end-expiratory holds.

Animal experiments

This study was approved by the National Ethics Committee on animal research (approval number 01505.01), and was carried out in accordance with the International Guiding Principles for Biomedical Research Involving Animals [ 24].
Briefly, after general anesthesia induction, animals were equipped with right lateral thoracic surgical drainage (Seldinger Chest Drainage Kit, Portex®, Smith Medical), to monitor pleural pressure (Ppl). A rigid 30-cm-long catheter was inserted into the endotracheal tube (diameter 8) towards the distal lumen to monitor tracheal upper airways pressure (Paw). Injurious mechanical ventilation was completed with hydrochloric acid tracheal instillation to model severe ARDS as adapted from Ambrosio [ 25]. Animals were ventilated with VDR-4 with random pressure levels.

Statistical analysis

Categorical data were expressed as numbers and percentages, and quantitative data as mean (SD) or median (IQR). Distribution normality was tested using the Shapiro-Wilk test. Continuous variables analyses were performed using Student’s t test or the non-parametric Mann-Whitney U test. Changes in arterial blood gases and hemodynamic data were analyzed by longitudinal analysis using mixed models to take into account between-subject and within-subject variability (with patient as random effect). Spearman’s rank correlation coefficient was calculated to assess the relationship between HFPV-induced hyperinflation and CMV volumes, and animal pulmonary pressures monitoring. Monitored and measured pressure was compared by Bland and Altman analysis for multiple measurements. P < 0.05 (two-sided) was considered significant.

Results

Study patients

Between February and July 2015, eight patients with moderate to severe non-focal ARDS were enrolled within 24 hours of disease onset. Table  1 summarizes the baseline characteristics.
Table 1
Characteristics of patients
Patient number
Etiology
Comorbidity
IBW (kg)
ARDS onset (h)
FiO 2 (%)
PaO 2/FiO 2 (mmHg)
PEEP (cmH2O)
Tidal volume (mL/kg IBW)
Compliance (mL.cmH 2O -1)
Pplat (cmH2O)
ARDS phenotype
1
Infectious Pneumonia
Acute leukemia
63
18
50
154
8
7.6
20
33
NF
2
Infectious Pneumonia
Myelofibrosis
70
6
100
127
16
5.9
25
33
NF
3
Infectious Pneumonia
Acute leukemia
55
24
70
109
18
5.8
21
33
NF
4
Infectious Pneumonia
 
47
4
100
75
12
5.7
13
28
NF
5
Infectious Pneumonia
Acute leukemia
54
10
60
145
13
6.3
18
31
NF
6
Aspiration
Cardiac arrest
73
4
100
50
12
5 .8
17
30
NF
7
Aspiration
Gastrectomy
77
12
100
80
18
5.5
20
28
NF
8
Viral pneumonia
 
64
6
70
113
20
7.4
18
32
NF
Median
   
63.5
8.0
85
111
14.5
5.9
19.0
31.5
 
IQR
   
(55.0–70.8)
(5.5–13.5)
(68–100)
(79–132)
(12.0–18.0)
(5.8–6.6)
(17.8–20.3)
(29.5–33.0)
 
Data are presented as median (IQR). Abbreviations: ARDS acute respiratory distress syndrome, IBW ideal body weight (Lorentz formula), FiO 2 fraction of inspired oxygen, PaO 2 arterial oxygen tension, NF non-focal, PEEP positive end-expiratory pressure, Pplat plateau pressure
Prior to inclusion, mean CMV time, arterial oxygen tension (PaO 2)/fraction of inspired oxygen (FiO 2) ratio and tidal volume (Vt) were 8 (4.5–16.5) hours, 111 (76–141) mmHg and 5.9 (5.8–7.1) mL.kg -1 of ideal body weight (IBW), respectively. PEEP and plateau pressures were respectively 14.5 (12.0–18.0) and 31.5 (28.5–33.0) cmH 20. Lung static compliance was 20.5 (17.3–36.3) mL.cmH 2O -1. Lung morphology was exclusively non-focal. HFPV settings are presented in Additional file  1: Table S1.

Changes in hemodynamics and respiratory parameters

Arterial blood gases showed substantial increase in PaO 2/FiO 2 30 minutes after HFPV initiation (T30), which persisted while under HFPV (Fig.  1a). Oxygenation benefits disappeared after resuming CMV (Fig.  1a, T-after). No PaCO 2 change was observed (Fig.  1b).
Mean arterial pressure (MAP) increased significantly between T10 and T30 (Fig.  1c) while norepinephrine doses dropped from 0.34 (0.24–0.63) (T0) to 0.19 (0.08–0.32) μg.kg -1.min -1 (T60, Fig.  1d). Benefits disappeared after resuming CMV (0.26 (0.04–0.53) μg.kg -1.min -1, T-after, Fig.  1d). Vasopressor index (VI) and vasopressor dependency index [ 26] followed similar trends (Additional file  1: Figure S1).
A significant increase in lung compliance was observed (T-after, 28.5 (24.5–32.3) versus T0, 20.5 (17.8–28.8) mL.cmH 2O -1, P = 0.04), without any airway resistance change (13.5 (12.5–14.0) versus 14.5 (11.0–15.5) mL.cmH 2O -1, P = 0.58, T-after vs T0, respectively). (Additional file  1: Table S2).

CT scan analysis

Tidal volumes remained stable over treatment duration: 5.9 (5.8–7.1) versus 5.7 (1.1–8.1) versus 6.1 (5.8–6.2) mL.kg -1 ideal body weight (IBW) (T0 versus HFPV versus T-after, P = 0.90). Alveolar recruitment, defined as the change in non-aerated lung volumes, increased significantly between CMV and HFPV (12.0% (8.5–18.0), P = 0.05 and 12.5% (9.3–16.8), P = 0.003, end-expiratory and end-inspiratory holds, respectively, Additional file  1: Table S3). When recruitment was assessed as the change in non-aerated and poorly aerated lung volumes, no significant evolution was observed between CMV and HFPV (12.0% (5.0–18.0) with end-expiratory hold, P = 0.27 and 11.0% (6.0–22.0) with end-inspiratory hold, P = 0.10, Additional file  1: Table S3).
No significant change in hyperinflated lung volumes was observed: 2.0% (0.5–2.5) (CMV versus HFPV end-expiratory hold, P = 0.89) and 3.0% (2.5–4.00 (CMV versus HFPV end-inspiratory hold, P = 0.27) (Fig.  2 and Additional file  1: Table S3) . Complete changes in lung volumes and masses are presented in Additional file  1: Table S4. Global increases in end-expiratory lung volume (EELV), total lung volume and normally-aerated lung volumes were observed.
Evolution of lung volumes’ absolute ratios according to aeration status and West zone are presented in Additional file  1: Figures S2 and S3. End-expiratory non-aerated volumes significantly decreased especially in posterior (dependant) lung zones. Normally aerated lung volumes increased in posterior lung regions. Hyperinflated and poorly aerated lung volumes remained stable. HFPV end-expiratory hold hyperinflated lung volume was correlated with CMV normally aerated ( r = 0.79, P = 0.05) and hyperinflated ( r = 0.79, P = 0.05) lung volumes. HFPV end-inspiratory hold hyperinflated lung volume was correlated with CMV hyperinflated lung volumes ( r = 0.88, P = 0.01) (Additional file  1: Table S4).

Animal experiments

Additional file  1: Table S5 presents correlations and bias between Ppl or Paw and absolute values of Monitron®-derived PEEP, mean and peak pressures. Figure  3 presents graphic illustration of interactions between maximal end-inspiratory Ppl and Monitron®-derived mean pressure. When considering the 58 pairs of measurements, bias (lower to upper limits of agreement) between absolute values of maximal end-inspiratory Ppl and HFPV mean pressure was 6.1 (−7.3 to 19.5) cmH 2O, without any correlation ( r = 0.19, P = 0.16). Maximal end-inspiratory Ppl remained below 25cmH 2O despite elevated HFPV mean pressures. Further analyses and correlations are presented in Additional file  1.

Discussion

This study is, to our knowledge, the first to demonstrate HFPV effects on lung aeration and tidal volume. Significant alveolar recruitment and tidal volume close to 6 ml/kg IBW were observed in patients with early non-focal ARDS receiving short-term HFPV. This study is also the first to investigate in vivo correlation between Phasitron and transpulmonary pressures.

Alveolar recruitment

Alveolar recruitment was statistically significant. Under CMV, alveolar recruitment is induced either by PEEP incremental increases and tidal recruitment ( e-sigh) or transpulmonary pressure transient increase [ 27]. Although alveolar recruitment remains difficult to assess at the bedside [ 28], it can be measured by analysis of lung CT scans [ 22]. The effects of RM on lung morphology have already been reported [ 23], and alveolar recruitment (poorly aerated and non-aerated volumes decrease) [ 29] was effective in both focal and non-focal ARDS following an RM (40 cmH 2O, 40 seconds). Recruitment reached 6 ± 6% and 18 ± 8% in focal and non-focal ARDS ( P = 0.004) [ 23], whereas we observed recruitment gains in around 12% depending on alveolar recruitment definition and HFPV end-expiratory or end-inspiratory holds (Additional file  1: Table S3). High frequency mini-bursts may allow a progressive move from alveolar collapse to re-opening, through discrete jumps [ 30]. The pragmatic definition of lung recruitment that we used clearly depicts HFPV effects over CMV in terms of alveolar recruitment. Indeed, no significant change in poorly aerated volumes was observed (Fig.  4). Lung recruitment seems predominant in posterior zones where non-aerated volumes are observed. Of note, CMV preliminary optimization and absence of zero-PEEP end-expiratory CT scan may have conducted to lesser HFPV effects on alveolar recruitment.

Alveolar hyperinflation

Alveolar hyperinflation is often associated with alveolar recruitment since intra-thoracic pressure increase may preferentially inflate normally aerated (high compliance) more than non-aerated (low compliance) lung regions, if there is lung inhomogeneity. No difference was observed between HFPV-induced and CMV-induced hyperinflation, in line with a previous report [ 31]. Hyperinflation was significantly correlated with baseline normally aerated and hyperinflated lung volumes, whereas our group reported a single correlation with normally aerated ones [ 23]. Those results agree with previous observations from Terragni, who reported that tidal hyperinflation persists despite protective ventilation [ 32]. Of particular interest in focal ARDS, high PEEP levels might sustain hyperinflation of non-dependent lung regions [ 33], as observed. Moreover, tidal recruitment/de-recruitment might worsen the patient’s status by exposing lung regions to shear stress [ 34], as observed in focal ARDS. Those observations were negligible in non-focal ARDS. Early identification of lung morphology should be of the highest importance in adapting mechanical ventilation strategies [ 35]. HFPV was suggested to better adapt Vt and lung pressures to dynamic changes in gas distribution [ 36], thus hampering prediction of its pathophysiological effects.
In our study, hyperinflation remained stable within all three West zones. As previously reported [ 23, 35], low hyperinflated lung regions have been observed while performing an RM, when dealing with a non-focal ARDS phenotype (in comparison to focal ARDS).
Finally, HFPV use as RM and open-lung strategy surrogates remains uncertain. RM has been reported to increase hyperinflation by 8 ± 9% and 24 ± 14% in patients with non-focal and focal ARDS [ 23]. In our study, hyperinflation was negligible in non-focal ARDS, at 2.0% (1.0–4.0).

Tidal volume

The difference between end-inspiratory and end-expiratory volumes approximated the Vt. HFPV-induced Vt remained within recommended limits. This observation supports an HFPV lung-protective ventilation strategy. Vt measurement on CT scans might be affected by oxygen consumption and stress relaxation. However, acquisition lasted a few seconds and was similar between both holds.

Oxygenation

HFPV markedly improved oxygenation. HFPV-induced alveolar recruitment may improve gas exchange surface and decrease ventilation/perfusion mismatch. Also, effective gas volume administered does not only include Vt but also volume from high frequency mini-bursts. Lucangelo showed in a single compartment lung model, that Vt accounts for approximately 10–40% of total administered volume [ 36]. Diffusive ventilation may therefore allow large inflow and out-flow, thus increasing alveolar gas mixing (O 2 in and CO 2 out).

Hemodynamics

Hemodynamics improved significantly during HFPV, the effect remaining unclear. As compared to RM-induced transient increase in intra-thoracic pressure, HFPV treatments did not decrease arterial pressure or induce serious adverse hemodynamic events. HFPV may reduce shunts through improved alveolar recruitment, and enhance peripheral arterial vasoconstriction by improving arterial oxygenation [ 37, 38]. In addition, HFPV may rapidly increase alveolar recruitment, lung aeration and arterial oxygenation, thus improving pulmonary vascular function and facilitating right ventricle output.

Monitoring of pressure

Monitron® device monitored high pressure during HFPV. Phasitron®-delivered pressures (recorded before endotracheal tube) are higher and correlate with Ppl. Intra-thoracic and transpulmonary pressures evaluations [ 39, 40] are relevant tools in understanding HFPV effects. Careful measurement of Ppl through the pleural drain and Paw through the intra-tracheal catheter allowed useful comparisons. We found good correlation (despite large agreements limits) between the Monitron® and measured pressures. Of high interest, Ppl remained within the protective limits: alveolar pressure was always below 30 cmH 2O (and especially, below 25cmH 2O in our experiments) whatever the Monitron® pressure, even with apparently excessive pressure settings. This 30-cmH 20 pressure seems to limit the risk of distension-related lung injury as reported by Boussarsar [ 41] and Tobin [ 42]. A recent study elucidated pressure drops through endotracheal tubes [ 43]. During the mini-burst inspiratory phase, pressure drops were: 9.28 (4.95–12.93), 9.48 (5.05–13.47), and 10.04 (5.62–16.97) cmH 2O for diameters 8, 7.5 and 6.5, respectively [ 44]. Administered pressures are strongly dampered through the endotracheal tube and airways. This phenomenon might explain low measured Ppl, well below the Monitron®-specified ones.

Limitations

Our study has several limitations. First, only eight patients were enrolled. Results presented herein only reflect HPFV effects on the lungs of patients with non-focal early ARDS. This could limit generalizability and/or dampen the strength of current associations. Further studies on patients with focal ARDS are necessary. Nevertheless, we believe that our findings represent an important first step in vivo to elucidate HFPV effects on the lungs in early non-focal ARDS. Second, hemodynamic improvements remain unexplained since no specific monitoring was used in our study, and further investigations are warranted. Third, only patients with early ARDS were included and extrapolation to later phases of ARDS remains uncertain. Fourth, CMV was optimized following “open-lung” ventilation recommendations; to what extent ventilator settings may have influenced our results remains unknown. Indeed, the Express study ventilator settings and strategy are supposed to optimize alveolar recruitment. No comparison with RM strategies was conducted and alveolar recruitment maximization remains empirical. Finally, the absence of a zero end-expiratory CT scan could have underestimated patients at risk of tidal hyperinflation, but remains delicate to be proposed to severe-to-moderate ARDS patients.

Conclusions

This study elucidates HFPV morphological effects in patients with early non-focal ARDS. Besides impressive improvements in arterial oxygenation and hemodynamics, HFPV-induced alveolar recruitment was significant. Therefore, HFPV might be used as a rescue therapy in early non-focal ARDS patients when CMV fails to improve oxygenation and lung aeration. However, further investigations are needed to assess HFPV effects on patient outcomes during ARDS, with a special focus on focal and non-focal lung phenotypes.

Acknowledgements

The authors wish to thank the nurses of the ICU and the technicians and staff from the department of radiology at Hospital Estaing, Clermont-Ferrand University hospital. The CICE (Centre International de Chirurgie Endoscopique, Université Clermont-Auvergne, Clermont-Ferrand, France) is acknowledged for facility access during animal experiments.

Funding

Funding was exclusively institutional.

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Ethics approval and consent to participate

Our institutional review board approved the protocol (CPP Sud-Est VI, approval number AU 1138). All participants or their next-of-kin provided written consent to participate in this study. The clinical trial is registered at http://​www.​clinicaltrials.​gov (NCT 02510105).
This study was approved by the National Ethics Committee on animal research (approval number 01505.01), and was carried out in accordance with the International Guiding Principles for Biomedical Research Involving Animals.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

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