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Hypothermic total liquid ventilation after experimental aspiration-associated acute respiratory distress syndrome
Annals of Intensive Care volume 8, Article number: 57 (2018)
Ultrafast cooling by total liquid ventilation (TLV) provides potent cardio- and neuroprotection after experimental cardiac arrest. However, this was evaluated in animals with no initial lung injury, whereas out-of-hospital cardiac arrest is frequently associated with early-onset pneumonia, which may lead to acute respiratory distress syndrome (ARDS). Here, our objective was to determine whether hypothermic TLV could be safe or even beneficial in an aspiration-associated ARDS animal model.
ARDS was induced in anesthetized rabbits through a two-hits model including the intra-tracheal administration of a pH = 1 solution mimicking gastric content and subsequent gaseous non-protective ventilation during 90 min (tidal volume [Vt] = 10 ml/kg with positive end-expiration pressure [PEEP] = 0 cmH2O). After this initial period, animals either received lung protective gas ventilation (LPV; Vt = 8 ml/kg and PEEP = 5 cmH2O) under normothermic conditions, or hypothermic TLV (TLV; Vt = 8 ml/kg and end-expiratory volume = 15 ml/kg). Both strategies were applied for 120 min with a continuous monitoring of respiratory and cardiovascular parameters. Animals were then euthanized for pulmonary histological analyses.
Eight rabbits were included in each group. Before randomization, all animals elicited ARDS with arterial oxygen partial pressure over inhaled oxygen fraction ratios (PaO2/FiO2) below 100 mmHg, as well as decreased lung compliance. After randomization, body temperature rapidly decreased in TLV versus LPV group (32.6 ± 0.6 vs. 38.2 ± 0.4 °C after 15 min). Static lung compliance and gas exchanges were not significantly different in the TLV versus LPV group (PaO2/FiO2 = 62 ± 4 vs. 52 ± 8 mmHg at the end of the procedure, respectively). Mean arterial pressure and arterial bicarbonates levels were significantly higher in TLV versus LPV. Histological analysis also showed significantly lower inflammation in TLV versus LPV group (median histological score = 3 vs. 4.5/5, respectively; p = 0.03).
Hypothermic TLV can be safely induced in rabbits during aspiration-associated ARDS. It modified neither gas exchanges nor respiratory mechanics but reduced lung inflammation and hemodynamic failure in comparison with LPV. Since hypothermic TLV was previously shown to provide neuro- and cardio protective effects after cardiac arrest, these findings suggest a possible use of TLV in the settings of cardiac arrest-associated ARDS.
After out-of-hospital cardiac arrest and successful resuscitation, a post-cardiac arrest syndrome occurs and makes patients prone to infectious complications [1, 2]. Among them, early-onset pneumonia affects up to two-thirds of successfully resuscitated patients and are mainly related to aspiration. In this setting, aspiration pneumonia deteriorates pulmonary function and has negative impact on outcome [1,2,3]. More dramatically, aspiration pneumonia can culminate into acute respiratory distress syndrome (ARDS). For instance, around six percent of the patients resuscitated after out-of-hospital cardiac arrest present ARDS [4,5,6].
Hypothermic total liquid ventilation (TLV) could be an interesting alternative to conventional ventilation in the context of cardiac arrest-associated aspiration pneumonia since this technique has been previously shown to limit the post-cardiac arrest syndrome in animal studies [7,8,9,10,11]. During TLV, the lungs can be alternatively filled and emptied by perfluorocarbons, authorizing lung lavage as well as gas and thermal exchanges. This approach provides ultrafast cooling  and powerful neuro- and cardioprotection after cardiac arrest, as well as attenuation of multi-organ dysfunction after low perfusion states [7,8,9,10,11].
In the context of aspiration-associated ARDS, hypothermic TLV might also provide benefits per se through lung lavage or anti-inflammatory effects of liquid ventilation [13,14,15,16,17,18]. Conversely, one would also argue that TLV could increase the risk of ventilation-induced injury when initiated after such lung injury. Our previous reports with hypothermic TLV were indeed done in animal models of cardiac with very controlled conditions preventing accidental aspiration. Accordingly, the goal of the present study was to investigate whether TLV could be safely induced in a model of aspiration-associated ARDS and whether it modifies gas exchanges, respiratory mechanics, hemodynamic status or pulmonary inflammatory response in rabbits.
The animal instrumentation and the ensuing experiments were approved by the institutional review board for animal research (project 04585-04 evaluated by the “Ethical committee Anses-Enva-UPEC”).
Male New Zealand rabbits (2.5–3.5 kg) were anesthetized using zolazepam, tiletamine and pentobarbital (all 20–30 mg/kg i.v.). After intubation, they were artificially ventilated with inspired fraction of oxygen (FiO2) of 30% (SAR-830P, CWE Inc., Ardmore, USA). Tidal volume was set at 8 mL/kg and respiratory rate at 30 cycles/min. Positive end-expiratory pressure (PEEP) was set at 5 cmH2O. Peripheral catheters were inserted into the ear marginal vein and artery for blood sampling and pressure monitoring, respectively. Temperature probes were also inserted into the rectum and esophagus. Anesthesia was maintained with additional administration of pentobarbital (5 mg/kg/h i.v.).
After stabilization, rabbits were paralyzed by vecuronium bromide (0.4 mg/kg/h, i.v.). ARDS was induced with a two-hits injury including an intra-tracheal administration of 4 ml/kg of an aqueous solution at pH = 1 and a period of conventional non-protective gas ventilation. The acid solution was administered slowly into the tracheal tube, while animals were manipulated in order to improve lung distribution. Conventional non-protective ventilation consisted in mechanical ventilation with tidal volumes set at 10 ml/kg and PEEP at 0 cmH2O. Inhaled fraction of oxygen (FiO2) was increased to 100%. Conventional non-protective ventilation was maintained during 90 min according to preliminary experiments demonstrating an optimal balance between the occurrence of reproducible ARDS and the need for a sufficient survival and follow-up after group allocation. Body temperature was maintained around 38.5 °C throughout ARDS induction phase.
After the period of conventional ventilation, animals were randomly allocated to a group treated by lung protective gas ventilation (LPV) or TLV for 120 min (Fig. 1). In the LPV group, tidal volume was set at 8 ml/kg with PEEP = 5 cmH2O. Such tidal volumes used are slightly higher that the recommended volumes for humans with ARDS. However, lower tidal volumes are currently recommended in rabbits. Body temperature was maintained at 38.5 °C using heating pads in the LPV group. In the TLV group, animals were ventilated with a dedicated prototype of liquid ventilator continuously controlling liquid pressures and volumes (Inolivent-5, Université de Sherbrooke, QC, Canada) [16, 19]. They were submitted to hypothermia with a target temperature of 33 °C [7,8,9,10,11, 20, 21]. Lungs were initially filled with 13 ml/kg of perfluoro-n-octane (PFO, C8F18; F2-chemical®, Preston, Lancashire, UK). Tidal volume was set at 8-10 ml/kg and respiratory frequency at 9 cycles/min. The pulmonary end-expiratory volumes of PFO were increased to reach 15–20 ml/kg. The temperature of the liquid was initially set at 20 °C and progressively increased in order to maintain body core temperature at 33 °C. Static lung compliance was calculated by dividing tidal volume by the difference between airways pressures between end-inspiratory and end-expiratory pauses. Pause pressures were calculated after valve closures at the end of inspiration and expiration, respectively. Mean values were obtained with at least 3 cycles. After 120 min of LPV or TLV, animals were weaned back to conventional gas ventilation. Both groups were submitted to broncho-alveolar lavage at the end of the protocol for the further evaluation of albumin content. Immediately after broncho-alveolar lavage, animals were then euthanized using a lethal dose of pentobarbital (60 mg/kg iv). Lungs were collected, perfused and fixed with formaldehyde (4%) for histological analysis.
Throughout the procedure, heart rate and arterial blood pressure were continuously monitored (HEM version 4.2, Notocord, Croissy-sur-Seine, France), as well as esophagus and rectal temperatures. Arterial blood samples were withdrawn at baseline, after ARDS induction and 30 and 120 min after the onset of LPV or TLV for the evaluation of arterial pH, bicarbonates blood levels, partial pressures of oxygen (PaO2) and carbon dioxide (PaCO2). Blood levels of interleukin 1β were also evaluated (ELISA Kit for interleukin 1 beta, SEA563Rb, Cloud-Clone, Katy, TX, USA). Albumin concentration was evaluated in the broncho-alveolar lavage solution.
In addition, lungs were prepared for histological analysis, as previously described . The severity of ARDS lesions was assessed by a pathologist blinded to the experimental group. Two separate scores were attributed to each lung after the evaluation of all pulmonary lobes, i.e., one score for the magnitude of lung congestion and edema (0 = normal histological appearance; 5 = extensive congestion and edema in the entire lung) and one score for inflammatory lesions (0 = normal histological appearance; 5 = extensive leukocytic alveolitis with haline membranes), respectively.
Data were expressed as mean ± SEM. Hemodynamic, respiratory and biochemical variables were compared between groups using a two-way ANOVA for repeated measures followed by a post hoc Holm–Sidak test if necessary. In order to reduce the number of comparisons, post hoc comparisons were performed between groups for each time point but not between time points within the same group. Histological scores were compared between groups using a Mann–Whitney U test. Significant differences were determined at p value ≤ 0.05.
Baseline characteristics and ARDS induction
Eight rabbits were included in each LPV and TLV groups. As shown in Tables 1 and 2, no difference was observed at baseline among groups regarding body weight (3.1 ± 0.1 vs. 3.1 ± 0.1 kg, respectively), body temperature, hemodynamic or blood biochemical parameters. At the end of the conventional non-protective ventilation period, typical signs of ARDS were observed in both groups, including decreased lung compliance and decreased PaO2/FiO2 ratios with no difference between groups. The latter ratio achieved 41 ± 5 and 51 ± 9 mmHg at the end of the conventional ventilation period in LPV and TLV groups, as compared to 755 ± 97 and 730 ± 150 mmHg at baseline, respectively. FiO2 was maintained at 100% in all animals after ARDS induction.
Effect of TLV on gas exchanges, airways pressures, lung volumes and compliance
As shown in Table 2, blood oxygen saturation, pH, PaO2 and PaCO2 were not significantly different during TLV versus LPV. The PaO2/FiO2 ratio remained below 100 mmHg during the experimental protocol in both groups. This ratio achieved 52 ± 8 and 62 ± 4 mmHg in the LPV and TLV groups, evidencing similar severity of ARDS in both conditions.
As shown in Fig. 2, end-inspiratory and expiratory airway pressures tended to decrease during TLV as compared to LPV. This difference was not statistically different for end-inspiratory pressures (p = 0.08) but only for end-expiratory pressures (5.3 ± 0.6 vs. − 2.4 ± 1.6 cmH2O at the end of the procedure, p < 0.001). Lung compliance was not significantly different between these two groups (Table 1). In the TLV group, lung liquid volumes averaged 25–30 and 15–20 ml/kg at the end of expiratory and inspiratory period (Fig. 2), respectively.
Effect of hypothermic TLV on temperature, hemodynamic and bicarbonate blood levels
As shown in Table 1, body temperatures decreased very rapidly after TLV initiation as compared to LPV. This was associated with a decreased heart rate, as well as improved systemic arterial pressure. Mean arterial pressure achieved 74 ± 9 versus 56 ± 8 mmHg at the end of the procedure period in the TLV vs. LPV groups (p < 0.05), respectively. As shown in Table 2, the drop in bicarbonates arterial levels was also significantly attenuated by hypothermia in the TLV group as compared to LPV. Bicarbonates arterial levels achieved 31 ± 2 versus 24 ± 2 mmol/l in TLV versus LPV at the end of the protocol (p = 0.007).
Effect of hypothermic TLV on inflammatory response assessed by broncho-alveolar lavage and lung histology
At the end of the protocol, the protein content of the broncho-alveolar lavage solution was similar between groups (351 ± 11 vs. 334 ± 13 µg/ml in TLV vs. LPV groups, respectively). Conversely, the concentration in interleukin-1β tended to decrease in TLV versus LPV, but the difference was not significant (7.1 ± 0.7 vs. 11.2 ± 2.5 pg/ml; p = 0.08).
After completion of the protocol, typical signs of ARDS were observed in all animals at lung histology. As illustrated in Fig. 3a, we observed moderate to severe leukocytic alveolitis and intra-alveolar red blood cells infiltration in all animals in the LPV group. Two animals also presented alveolar hyaline membranes, evidencing major ARDS lesions in this group. In the TLV group, lungs showed normal appearance in one animal and mild to severe inflammation and congestion in others. As shown in Fig. 3e, the blindly attributed score of inflammation was significantly reduced in TLV versus LPV group (median score = 3 vs. 4.5, respectively; p = 0.03). Conversely, the score attributed for congestion severity was not significantly different among groups (median score = 1 vs. 2.5; p = 0.08).
In the present study, hypothermic TLV did not modify gas exchange and lung compliance but attenuated hemodynamic failure and lung inflammation in a model of experimental aspiration-associated ARDS in rabbits. These demonstrations were obtained with a last-generation liquid ventilator which accurately controls lung volumes and pressures during TLV . Importantly, the design of the study does not able to differentiate the effect of TLV from hypothermia since we investigated the effect of hypothermic TLV. Our ultimate goal is indeed to translate hypothermic TLV from the bench side to human practice for the treatment of the post-cardiac arrest syndrome [7,8,9,10,11].
Importantly, there are apparently conflicting results regarding the effect of liquid ventilation during ARDS in the literature. In 2006, Kacmarek et al.  demonstrated that partial liquid ventilation did not improve outcome as compared to conventional mechanical ventilation and recommended against its use in ARDS patients. In the latter study, partial liquid ventilation was performed after lung filling with 10 ml/kg or 20 ml/kg of perflubron, with high values of positive end-expiratory pressure (13 cmH2O) and relatively high tidal volumes for gas ventilation (≈ 8–10 ml/kg). In addition, patients were repeatedly derecruited by abrupt decreases in PEEP from 13 to 0 cmH20, with putative air trapping . Our strategy was completely different as we performed TLV rather than partial liquid ventilation, and we used the pressure and volume-control mode of the ventilator . This led to much lower and likely safer airways pressures, averaging 15 cmH2O at end-inspiration, which is approximately 2 times lower than previously observed during partial liquid ventilation in ARDS patients . In addition, hypothermic TLV is expected to be instituted for very short periods only to induce hypothermia after cardiac arrest, which makes it much easier to implement than prolonged liquid ventilation.
Beyond partial liquid ventilation, previous strategies of TLV were also tested in animal models of ARDS in the past. Most studies used much higher filling volume (20–30 ml/kg) and tidal volume (20–30 ml/kg) than we did in the present study [13, 17, 19]. For example, Pohlmann et al. improved gas exchanges in sheep after experimental ARDS using TLV with an initial filling with 30 ml/kg of perfluorocarbons, a frequency of 5 cycle per min and a tidal volume of 15–20 ml/kg during 24 h . In another report, Avoine et al. used similar TLV parameters which improved gas exchanges after meconium aspiration . However, such respiratory parameters during TLV were associated with high pulmonary pressures, e.g., 28–30 cmH2O for TLV peak pressures which might again be poorly tolerated on the longer term. In comparison, airways pressures were much lower in the present study. Lung volumes were also strongly reduced, i.e., below 15–20 ml/kg for expiratory residual volumes. Using such parameters, we were not able to improve gas exchanges as compared to LPV but a compromise should be made between the short-term need of gas exchanges improvement and the long-term hazards of lung trauma. In previous reports, we indeed demonstrated that low-volume TLV was much better tolerated regarding systemic and pulmonary hemodynamic . In addition, hypothermic TLV could be done with low tidal volumes with no significant impact on gas exchanges, due to the reduced oxygen demand and carbon dioxide production during hypothermia. This is another argument in the favor of hypothermic TLV which is likely easier to implement in patients for these reasons. In the context of hypothermic TLV for post-cardiac arrest treatment, we could therefore speculate that such procedure is safe in both healthy  and damaged lungs after aspiration.
Interestingly, we also observed that hypothermic TLV could exert anti-inflammatory effects in the present report regarding lung histology. Such findings were already demonstrated with perfluorocarbons  or after experimental ARDS with other TLV devices. As example, Wolfson et al.  demonstrated that TLV could limit inflammation after oleic acid-induced ARDS. This could also be related to the lavage properties of TLV in a pulmonary aspiration setting. Indeed, Avoine et al.  demonstrated potent lavage properties of TLV in an animal model of meconial aspiration. This could open perspective for the treatment of pure ARDS, beyond the management of the post-cardiac arrest syndrome. For instance, a recent clinical study reported possible benefits with 48 h of cooling at 34–36 °C in 8 ARDS patients receiving neuromuscular blockade agents . In neonates, a retrospective analysis also suggested consideration of therapeutic hypothermic as an adjunctive therapy during meconial aspiration syndrome .
Overall, the present study further supports that hypothermic TLV could be a supplementary tool in the armamentarium against post-cardiac arrest syndrome, acting on several facets of this dreadful syndrome. In previous studies, we demonstrated potent cardiac, neuro- and renal protection after experimental cardiac arrest after both shockable [8, 11, 29] and non-shockable rhythms . More broadly, we reported strong attenuation of clinical and biological manifestations of multi-organ failure after aortic cross-clamping in a severe model of multi-organ ischemia reperfusion mimicking low perfusion states. This converges toward potent organ protection with hypothermic TLV after cardiac arrest, targeting the main component of the post-cardiac arrest syndrome. The current study further shows that hypothermic TLV might also be safely used after lung impairment and aspiration pneumonia, which carries specific morbidity after cardiac arrest through increased mechanical ventilation duration and ICU length of stay [1, 2].
Finally, this study presents several limitations. The main one is related to the experimental model which demonstrated very severe ARDS. As example, gas exchanges were dramatically altered, even after the initiation of LPV or TLV. This could explain the lack of actual benefits of TLV on gas exchanges. However, this further emphasizes that this strategy could be instituted safely even after lung injury. Importantly, the severity of ARDS in this model was previously described in rabbits submitted to HCl-induced lung injury . In the latter study, PaO2/FiO2 ratio decreased below 100 mmHg after 105 min in control conditions with conventional mechanical ventilation . Another limitation is that we did not induce cardiac arrest in this model. This could have been relevant since our ultimate goal is to implement TLV in the post-resuscitation setting. The protective effect of hypothermic TLV could have been different after such global ischemia–reperfusion injury. However, since we previously tested the effect of hypothermic TLV after cardiac arrest from respiratory cause , we chose to focus the present study on the pulmonary effect of TLV. Finally, we did not investigate the proper effect of normothermic TLV in the present study, which could be of interest to decipher the effect of TLV by itself on inflammation and hemodynamic status, independently from the rapid temperature management induced by TLV. The investigation of another group with “slow” cooling using other methods could also be of interest to strengthen our conclusions. All these comparisons deserve further investigations.
In conclusions, we demonstrated that hypothermic TLV can be safely induced in rabbits during aspiration-associated ARDS. It does not improve gas exchange and lung compliance but improves hemodynamic parameters and attenuates lung inflammation. This deserves further investigation after cardiac arrest-associated ARDS.
acute respiratory distress syndrome
- PaO2 :
partial pressure of oxygen
- PaCO2 :
partial pressure of carbon dioxide
positive end-expiratory pressure
lung protective ventilation
total liquid ventilation
Mongardon N, Perbet S, Lemiale V, Dumas F, Poupet H, Charpentier J, et al. Infectious complications in out-of-hospital cardiac arrest patients in the therapeutic hypothermia era. Crit Care Med. 2011;39:1359–64.
Perbet S, Mongardon N, Dumas F, Bruel C, Lemiale V, Mourvillier B, et al. Early-onset pneumonia after cardiac arrest: characteristics, risk factors and influence on prognosis. Am J Respir Crit Care Med. 2011;184:1048–54.
Kakavas S, Mongardon N, Cariou A, Gulati A, Xanthos T. Early-onset pneumonia after out-of-hospital cardiac arrest. J Infect. 2015;70:553–62.
Esteban A, Frutos-Vivar F, Muriel A, Ferguson ND, Peñuelas O, Abraira V, et al. Evolution of mortality over time in patients receiving mechanical ventilation. Am J Respir Crit Care Med. 2013;188:220–30.
Esteban A, Anzueto A, Frutos F, Alía I, Brochard L, Stewart TE, et al. Characteristics and outcomes in adult patients receiving mechanical ventilation: a 28-day international study. JAMA. 2002;287:345–55.
Esteban A, Ferguson ND, Meade MO, Frutos-Vivar F, Apezteguia C, Brochard L, et al. Evolution of mechanical ventilation in response to clinical research. Am J Respir Crit Care Med. 2008;177:170–7.
Mongardon N, Kohlhauer M, Lidouren F, Hauet T, Giraud S, Hutin A, et al. A brief period of hypothermia induced by total liquid ventilation decreases end-organ damage and multiorgan failure induced by aortic cross-clamping. Anesth Analg. 2016;123:659–69.
Darbera L, Chenoune M, Lidouren F, Kohlhauer M, Adam C, Bruneval P, et al. Hypothermic liquid ventilation prevents early hemodynamic dysfunction and cardiovascular mortality after coronary artery occlusion complicated by cardiac arrest in rabbits. Crit Care Med. 2013;41:e457–65.
Kohlhauer M, Lidouren F, Remy-Jouet I, Mongardon N, Adam C, Bruneval P, et al. Hypothermic total liquid ventilation is highly protective through cerebral hemodynamic preservation and sepsis-like mitigation after asphyxial cardiac arrest. Crit Care Med. 2015;43:e420–30.
Kohlhauer M, Berdeaux A, Kerber RE, Micheau P, Ghaleh B, Tissier R. Liquid ventilation for the induction of ultrafast hypothermia in resuscitation sciences: a review. Ther Hypothermia Temp Manag. 2016;6:63–70.
Tissier R, Giraud S, Quellard N, Fernandez B, Lidouren F, Darbera L, et al. Kidney protection by hypothermic total liquid ventilation after cardiac arrest in rabbits. Anesthesiology. 2014;120:861–9.
Hutin A, Lidouren F, Kohlhauer M, Lotteau L, Seemann A, Mongardon N, et al. Total liquid ventilation offers ultra-fast and whole-body cooling in large animals in physiological conditions and during cardiac arrest. Resuscitation. 2015;93:69–73.
Wolfson MR, Hirschl RB, Jackson JC, Gauvin F, Foley DS, Lamm WJE, et al. Multicenter comparative study of conventional mechanical gas ventilation to tidal liquid ventilation in oleic acid injured sheep. ASAIO J Am Soc Artif Intern Organs. 1992;2008(54):256–69.
Jiang L, Feng H, Chen X, Liang K, Ni C. Low tidal volume reduces lung inflammation induced by liquid ventilation in piglets with severe lung injury. Artif Organs. 2017;41:440–5.
Merz U, Klosterhalfen B, Häusler M, Kellinghaus M, Peschgens T, Hörnchen H. Partial liquid ventilation reduces release of leukotriene B4 and interleukin-6 in bronchoalveolar lavage in surfactant-depleted newborn pigs. Pediatr Res. 2002;51:183–9.
Robert R, Micheau P, Avoine O, Beaudry B, Beaulieu A, Walti H. A regulator for pressure-controlled total-liquid ventilation. IEEE Trans Biomed Eng. 2010;57:2267–76.
Pohlmann JR, Brant DO, Daul MA, Reoma JL, Kim AC, Osterholzer KR, et al. Total liquid ventilation provides superior respiratory support to conventional mechanical ventilation in a large animal model of severe respiratory failure. ASAIO J Am Soc Artif Intern Organs. 1992;2011(57):1–8.
Foust R, Tran NN, Cox C, Miller TF, Greenspan JS, Wolfson MR, et al. Liquid assisted ventilation: an alternative ventilatory strategy for acute meconium aspiration injury. Pediatr Pulmonol. 1996;21:316–22.
Avoine O, Bossé D, Beaudry B, Beaulieu A, Albadine R, Praud J-P, et al. Total liquid ventilation efficacy in an ovine model of severe meconium aspiration syndrome. Crit Care Med. 2011;39:1097–103.
Nadeau M, Sage M, Kohlhauer M, Mousseau J, Vandamme J, Fortin-Pellerin E, et al. Optimal control of inspired perfluorocarbon temperature for ultrafast hypothermia induction by total liquid ventilation in adult patient model. IEEE Trans Biomed Eng. 2017;64:2760–70.
Nadeau M, Micheau P, Robert R, Avoine O, Tissier R, Germim PS, et al. Core body temperature control by total liquid ventilation using a virtual lung temperature sensor. IEEE Trans Biomed Eng. 2014;61:2859–68.
Kacmarek RM, Wiedemann HP, Lavin PT, Wedel MK, Tütüncü AS, Slutsky AS. Partial liquid ventilation in adult patients with acute respiratory distress syndrome. Am J Respir Crit Care Med. 2006;173:882–9.
Ricard J-D, Iserin F, Dreyfuss D, Saumon G. Perflubron dosing affects ventilator-induced lung injury in rats with previous lung injury. Crit Care Med. 2007;35:561–7.
Sage M, Nadeau M, Forand-Choinière C, Mousseau J, Vandamme J, Berger C, Tremblay-Roy JS, Tissier R, Micheau P, Fortin-Pellerin E. Assessing the impacts of total liquid ventilation on left ventricular diastolic function in a model of neonatal respiratory distress syndrome. PLoS ONE. 2018;13:e0191885.
Sage M, Nadeau M, Kohlhauer M, Praud J-P, Tissier R, Robert R, et al. Effect of ultra-fast mild hypothermia using total liquid ventilation on hemodynamics and respiratory mechanics. Cryobiology. 2016;73:99–101.
Rüdiger M, Wendt S, Köthe L, Burkhardt W, Wauer RR, Ochs M. Alterations of alveolar type II cells and intraalveolar surfactant after bronchoalveolar lavage and perfluorocarbon ventilation. An electron microscopical and stereological study in the rat lung. Respir Res. 2007;8:40.
Slack DF, Corwin DS, Shah NG, Shanholtz CB, Verceles AC, Netzer G, et al. Pilot feasibility study of therapeutic hypothermia for moderate to severe acute respiratory distress syndrome. Crit Care Med. 2017;45:1152–9.
De Luca D, Tingay DG, van Kaam A, Brunow de Carvalho W, Valverde E, Christoph Roehr C, et al. Hypothermia and meconium aspiration syndrome: international multicenter retrospective cohort study. Am J Respir Crit Care Med. 2016;194:381–4.
Chenoune M, Lidouren F, Adam C, Pons S, Darbera L, Bruneval P, et al. Ultrafast and whole-body cooling with total liquid ventilation induces favorable neurological and cardiac outcomes after cardiac arrest in rabbits. Circulation. 2011;124:901–11.
Brackenbury AM, Puligandla PS, McCaig LA, Nikore V, Yao LJ, Veldhuizen RA, Lewis JF. Evaluation of exogenous surfactant in HCL-induced lung injury. Am J Respir Crit Care Med. 2001;163:1135–42.
JR, MK, MN, EF, PM, JDR, AB, BG, HW, RT contributed to the design of the study. JR, FL, MS, MK, MN, LZ, MT, PB, HW, RT were involved in the conduct of the study. JR, FL, MN, PM, NM, JDR, PB, HW, RT analyzed the data. RT contributed to statistical analysis. All authors were involved in manuscript writing.
R Tissier and A. Berdeaux are named as inventors on a patent on cooling with liquid ventilation (US20120226337 A1). P Micheau, M Nadeau and H Walti declare owning the following patents attached to the submitted manuscript: method and apparatus for conducting total liquid ventilation with control of residual volume and ventilation cycle profile, US Patent # 7,726,311 delivered on June 1, 2010; and indirect measurement in a total liquid ventilation system, preliminary patent in USA No 61/838,896, filled on June 25, 2013.
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The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
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Ethics approval and consent to participate
As stated in the method section of the manuscript, animal instrumentation and ensuing experiments were approved by the institutional review board for animal research (project 04585-04 evaluated par the “Ethical committee Anses-Enva-UPEC”).
This study was supported by a Grant from the Region Ile-de France (CORDDIM), a Grant DBS20140930781 from the “Fondation pour la Recherche Médicale” (FRM) and a Grant from the “Agence Nationale pour la Recherche” (ANR, Coolivent grant).
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Rambaud, J., Lidouren, F., Sage, M. et al. Hypothermic total liquid ventilation after experimental aspiration-associated acute respiratory distress syndrome. Ann. Intensive Care 8, 57 (2018). https://doi.org/10.1186/s13613-018-0404-8
- Total liquid ventilation
- Cardiac arrest