Feasibility and safety of extracorporeal CO2 removal to enhance protective ventilation in acute respiratory distress syndrome: the SUPERNOVA study



We assessed feasibility and safety of extracorporeal carbon dioxide removal (ECCO2R) to facilitate ultra-protective ventilation (VT 4 mL/kg and PPLAT ≤ 25 cmH2O) in patients with moderate acute respiratory distress syndrome (ARDS).


Prospective multicenter international phase 2 study. Primary endpoint was the proportion of patients achieving ultra-protective ventilation with PaCO2 not increasing more than 20% from baseline, and arterial pH > 7.30. Severe adverse events (SAE) and ECCO2R-related adverse events (ECCO2R-AE) were reported to an independent data and safety monitoring board. We used lower CO2 extraction and higher CO2 extraction devices (membrane lung cross-sectional area 0.59 vs. 1.30 m2; flow 300–500 mL/min vs. 800–1000 mL/min, respectively).


Ninety-five patients were enrolled. The proportion of patients who achieved ultra-protective settings by 8 h and 24 h was 78% (74 out of 95 patients; 95% confidence interval 68–89%) and 82% (78 out of 95 patients; 95% confidence interval 76–88%), respectively. ECCO2R was maintained for 5 [3–8] days. Six SAEs were reported; two of them were attributed to ECCO2R (brain hemorrhage and pneumothorax). ECCO2R-AEs were reported in 39% of the patients. A total of 69 patients (73%) were alive at day 28. Fifty-nine patients (62%) were alive at hospital discharge.


Use of ECCO2R to facilitate ultra-protective ventilation was feasible. A randomized clinical trial is required to assess the overall benefits and harms.



FormalPara Take-home message
Use of ECCO2R to facilitate ultra-protective ventilation is feasible. A randomized clinical trial is required to assess the overall benefit and harm


Mechanical ventilation may cause a form of injury (ventilator-induced lung injury, VILI) that is clinically indistinguishable from the acute respiratory distress syndrome (ARDS) [1, 2]. The ARDSNet investigators demonstrated that limiting tidal volume (VT) to 6 mL/kg of predicted body weight (PBW) and end-inspiratory plateau pressure (PPLAT) to ≤ 30 cmH2O improves survival [3], but in some patients these settings may not be fully protective [4, 5]. Reduction of VT to 3–4 mL/kg and PPLAT ≤ 25 cmH2O has been proposed to further minimize the risk of VILI [6], but this entails a significant risk of severe respiratory acidosis [7].

Extracorporeal carbon dioxide removal (ECCO2R) can minimize this acidosis by clearing carbon dioxide (CO2). In this way, less CO2 has to be eliminated from the lungs enabling strategies that are more lung protective than the ARDSNet strategy. Such strategies might improve outcomes by (a) using VT as low as 3–4 mL/kg and further decreasing PPLAT below 30 cmH2O (often termed ultra-protective strategy [6, 8,9,10,11], (b) decreasing respiratory rates [12], and/or (c) minimizing driving pressures [13] or mechanical power [14].

Several ECCO2R devices have recently been made available utilizing blood flow rates ranging from about 450 mL/min to 1000 mL/min, but there is a lack of data demonstrating how effective these devices would be in eliminating CO2 and hence supporting any of these lung protective strategies [15]. We therefore performed a multicenter, international study in patients with moderate ARDS to determine the feasibility and safety of ECCO2R to inform the design of a future randomized clinical trial. The primary endpoint was the number of patients who successfully achieved a VT of 4 mL/kg PBW with PaCO2 not increasing more than 20% from baseline with a value of arterial pH > 7.30. Secondary endpoints included (a) assessment of physiological variables during ultra-protective strategy and (b) frequency of adverse events.


The study was approved by institutional review boards at each of the 23 study sites. Informed consent was obtained from patients or legally authorized surrogates. Patients with moderate ARDS (PaO2/FiO2 100–200 mmHg, with PEEP ≥ 5 cmH2O) [16], > 18 years old, and expected to receive invasive mechanical ventilation for > 24 h were included. Exclusion criteria were decompensated heart insufficiency or acute coronary syndrome; severe chronic obstructive pulmonary disease; major respiratory acidosis with PaCO2 > 60 mmHg; acute brain injury; severe liver insufficiency (Child–Pugh scores > 7) or fulminant hepatic failure; heparin-induced thrombocytopenia; contraindication for systemic anticoagulation; platelet < 50 G/L; patient moribund, decision to limit therapeutic interventions; catheter access to femoral vein or jugular vein impossible; pneumothorax; refused consent; inclusion in other trials (ClinicalTrials.Gov Identifier NCT02282657). Study protocol is available online.

We used the Hemolung Respiratory Assist System (ALung Technologies, Pittsburgh, USA), the iLA activve (Novalung, Heilbronn, Germany) and the Cardiohelp® HLS 5.0 (Getinge Cardiopulmonary Care, Rastatt, Germany) devices. The first device employs a membrane lung with a cross-sectional area of 0.59 m2 and is run at an extracorporeal blood flow between 300 and 500 mL/min (lower extraction). The other two devices employ membrane lungs of 1.30 m2 and blood flows to 800–1000 mL/minFootnote 1 (higher extraction). Each center was assigned one device for the purposes of the trial on the basis of that center’s previous experience with the specific devices.

After enrollment, sedation and neuromuscular blockade were administered for a minimum of 24 h. VT was set at 6 mL/kg PBW and positive end-expiratory pressure (PEEP) was adjusted to obtain a PPLAT between 28 and 30 cmH2O [17]. Percutaneous vascular access was provided using a double lumen catheter inserted in the internal jugular vein or in the femoral vein. Sweep gas flow was set to zero (baseline). Continuous infusion of unfractionated heparin was used to maintain values of activated partial thromboplastin time (aPTT) in the range 35–80 s.Footnote 2

VT was reduced to 4 mL/kg PBW in three steps (from 6.0 to 5.0, from 5.0 to 4.5, and from 4.5 to 4 mL/kg PBW). At each step, PEEP was titrated to a target PPLAT of 23–25 cmH2O [6, 8,9,10,11]. Sweep gas and blood flow were set to maintain a partial pressure of arterial CO2 (PaCO2) between 80% and 120% of the baseline value. If PaCO2 exceeded 75 mmHg and/or pH was < 7.30 despite optimal ECCO2R settings and a respiratory rate of 35 breaths/min, VT was increased to the last previously tolerated value.

ECCO2R and ultra-protective ventilation were continued, and data collected (baseline, 8 h, and 24 h). After completing the study protocol, the attending physician determined the ventilatory strategy and use of ECCO2R, and ECCO2R settings as well as physiological variables were recorded until ECCO2R discontinuation. Patients were monitored for adverse events until hospital discharge or day 28 after enrollment, whichever came first.

The primary outcome was the number of patients who successfully achieved a VT of 4 mL/kg PBW with PaCO2 not increasing more than 20% from baseline with a value of arterial pH > 7.30.Footnote 3 Duration of ECCO2R was recorded.

Secondary endpoints included (a) assessment of physiological variables and ECCO2R settings and (b) frequency of adverse events.

Severe adverse events (SAE) in the trial were defined as (1) any fatal or immediately life-threatening event, permanently disabling, severely incapacitating, or requiring prolonged hospitalization, or any event jeopardizing the patient and requiring medical or surgical intervention and that the attending physician perceived might be directly related to ECCO2R; (2) any clinically important untoward medical occurrence that was different from what is expected in the clinical course of ARDS. Investigators reported severe adverse events to the clinical coordinator. An independent data and safety monitoring board (DSMB) received a detailed written report and evaluated whether the SAE was attributable to ECCO2R. SAE were considered to be study-related if the event followed a reasonable sequence from a study procedure and could readily have been produced by the study procedure. SAE were not study related if they were thought to be primarily related to the underlying disease or to ARDS and its sequelae.

Other adverse events not fulfilling the above definition were recorded as ECCO2R-related adverse events (ECCO2R-AE) and classified as previously described [6, 8,9,10,11] as mechanical or clinical. Definitions of ECCO2R-AE are provided in the online supplement.

Length of invasive mechanical ventilation, survival at day 28, and survival at hospital discharge were also recorded.

Power and data analysis

On the basis of previous data [6, 8,9,10,11] we predicted that (a) PaCO2 with 6 mL/kg would be 40–60 mmHg; (b) the reduction of VT to 4 mmHg would increase PaCO2 to 65–85 mmHg. To demonstrate the ability of ECCO2R to re-establish PaCO2 values close to the ones observed with a VT of 6 mL/kg (± 20%) we estimated that a sample size of 90 patients would detect a proportion of patients who successfully achieved this condition with a two-sided 95% confidence interval of 70–90% when incidence is 80% and 54–75% when incidence is 65%. In both estimates, the width of confidence interval is 0.211. For calculation of two-sided confidence intervals for the single proportion, we used the Clopper–Pearson method. To take into consideration a possible 3% of dropout due to ECCO2R malfunction the sample size was increased to 100 patients.

To ensure quality control, (a) data were collected and checked for consistency before the analysis was finalized; (b) queries to confirm or correct outlier values were directly sent to local investigators; (c) analyses were performed by a researcher (TP) who did not participate in data collection and was not a member of the study steering committee.

Continuous variables are reported as mean ± standard deviation (SD) or median (interquartile range [IQR]) and categorical variables as count and proportion. Comparisons of proportions were made using Chi-square or Fisher exact tests, as appropriate. Data at different times during ECCO2R were compared by analysis of variance (ANOVA) for repeated measures. If significant (P ≤ 0.05), values obtained after 8 h and 24 h of ECCO2R were compared with those obtained at baseline by using paired Student t test adjusting P value using Bonferroni correction for multiple comparisons.

No assumptions were made for missing data. Statistical analyses were performed using R (version 3.5.1). All p values were two-sided and values < 0.05 were deemed significant. The statistical analysis plan is available online.


Of the 483 patients matching entry criteria, 95 patients were enrolled between October 2015 and June 2017 at 23 centers in Europe and Canada. Thirty-three patients were treated with the Hemolung device at five sites. Ten sites used the iLA activve device and treated 34 patients; eight sites used the Cardiohelp® HLS 5.0 device and treated 28 patients (Fig. 1). The centers enrolled a median of 3 [1–5] patients. Baseline characteristics and concomitant treatments at inclusion are shown in Table 1. No patient was lost to follow-up.

Fig. 1

Study flow chart

Table 1 Characteristics of patients at study inclusion

The proportion of patients who achieved ultra-protective settings by 8 h and 24 h was 78% (confidence interval 68–89%) (74 out of 95) and 82% (confidence interval 76–88%) (78 out of 95), respectively. ECCO2R was maintained for 5 [3–8] days.

Cannulation was performed through the internal jugular vein in 57% and through the femoral vein in 43% of patients. Catheter size was 15.5 Fr in patients on the Hemolung device and 18 [18–20] Fr in patients on the iLA activve and Cardiohelp® HLS 5.0 devices (p < 0.001). Operational characteristics of ECCO2R are shown in Table 2.

Table 2 Operational characteristics of extracorporeal CO2 removal

The time course of the respiratory variables in the first 24 h is reported in Fig. 2. VT, respiratory rate, minute ventilation, PPLAT, and ∆P were significantly lower at 8 h and 24 h compared to baseline (p = 0.001). Compared to baseline, PaCO2 and PaO2/FiO2 ratio remained stable, while pH significantly increased at 8 h (p < 0.05) and 24 h (p < 0.001). Trend of respiratory variables until ECCO2R discontinuation was consistent with the one observed in the first 24 h (Table 1_online supplement).

Six SAE were reported (massive right frontal parenchymal hematoma, severe hematemesis and melena, superior vena cava thrombosis; sudden death, severe hypoxemia, pneumothorax at cannula insertion in the internal jugular vein). Two SAEs (massive right frontal parenchymal hematoma and pneumothorax at cannula insertion in the internal jugular vein) were considered attributable to ECCO2R. ECCO2R-AE were reported in 37 patients (39%). Adverse events occurred in the first 24 h of ECCO2R in 26 patients (Table 3).

Table 3 Numbers of patients experiencing ECCO2R-related adverse events occurring between enrollment and day 28
Fig. 2

Time course of respiratory variables. VT tidal volume, RR respiratory rate, VE minute ventilation, PPLAT end-inspiratory plateau pressure, PEEP positive end-expiratory pressure, ∆P delta pressure (ΔP = PPLAT minus PEEP), PaCO2 partial pressure of arterial CO2, PaO2/FiO2 ratio of arterial-to-inspiratory oxygen fraction. #P < 0.05 vs baseline. *P < 0.001 vs baseline

Duration of invasive mechanical ventilation was 17 [11–29] days. A total of 69 patients (73%) were alive at day 28. Fifty-nine patients (62%) were alive at hospital discharge. Ventilator-free days were 11 [0–17] days.


This study shows that ECCO2R can be used to minimize respiratory acidosis while applying an ultra-protective ventilatory strategy in patients with moderate ARDS. However, the relatively high numbers of observed adverse events confirm the need for randomized clinical trial(s) to assess if benefits outweigh the risks.

A number of lung protective strategies such as decreasing PPLAT, driving pressure, power, respiratory rate, or tidal volume have been suggested to decrease VILI. These approaches are often associated with hypercapnia and respiratory acidosis [18]. Although hypercapnia may be well tolerated [19], there are a number of important side effects [20, 21], and recent data suggest an association between values of PaCO2 > 50 mmHg and increased mortality [22]. In the present study we tested the efficacy of ECCO2R to decrease tidal volume below 6 mL/kg because it is the variable most commonly associated with lung protective strategies, has a clear physiologic linkage to CO2 removal, and has been studied in previous studies [6, 8, 9, 11].

Recent data have demonstrated that there is no safe upper limit for PPLAT or ΔP [13, 23]. For example, the mortality rate in ARDS patients with ΔP values ≤ 14 cmH2O is still as high as 20% [13, 23]. Patient outcomes may therefore be improved by aggressively lowering ventilatory variables such as VT, PPLAT, or ΔP as facilitated by ECCO2R devices that remove CO2. In addition, ECCO2R might further decrease VILI by allowing lower respiratory rates, which have been shown to be lung protective [12], perhaps by decreasing mechanical power delivered to the lungs [14].

A few studies have examined the feasibility of ultra-protective ventilation facilitated by ECCO2R. Two studies were single-center studies and included small numbers of patients [6, 10]. Other multicenter observational [8, 9] or randomized [11] studies treated patients with a single device. A survey of 239 French intensive care units found that 15% of the units used ECCO2R at least once (total of 303 patients) from January 2010 to January 2015, and that the most frequent indication was ultra-protective ventilation for ARDS (54%) [15].

A major strength of this study is the relatively large number of patients, from multiple centers in Europe and Canada. At the same time, the following major limitations of the study should be acknowledged: First, analysis of ECCO2R safety may be somewhat underpowered in that we only studied 95 patients. Second, although originally planned as secondary endpoints (see ClinicalTrials.Gov Identifier NCT02282657) we were not able to quantify clearance and total amount of CO2 removed by ECCO2R. Recent experimental data show that these measurements are essential to assess effectiveness of CO2 removal capacity during ECCO2R [24]. Third, although sample size was inflated to take into consideration a possible 3% of dropout due to ECCO2R malfunction, we studied 95 out of the 100 patients planned as a result of lack of equipment during the final phase of the study period.

Assessment of safety in the context of a large international cohort of patients is of paramount importance for the clinical implementation of ECCO2R and to move to a phase III randomized clinical trial. Previous data on safety of ECCO2R to support ultra-protective ventilation are limited to three small case series all using lower extraction devices. In a single-center study, Terragni and coworkers reported only adverse mechanical events that occurred in 8 out of the 10 patients [6]. Fanelli and coworkers in a four-center study that included 15 patients reported bleeding in 7 patients, hemolysis in 1 patient, and catheter kinking in 1 patient [8]. Schmidt and coworkers in a five-center study that included 20 patients reported bleeding in 2 patients and membrane-lung clotting in 10 patients [9]. A randomized clinical trial that included 79 patients from eight sites and that used a pumpless arterial-venous ECCO2R device showed that the number of units of red blood cells transfused was significantly higher in the ECCO2R group compared with control (3.7 ± 2.4 vs. 1.5 ± 1.3%, p < 0.05) but the incidence of ECCO2R-related adverse events was low (3 patients; 7.5%) [11].

ECCO2R-AE were a priori defined and collected systematically. ECCO2R-AE were observed in 39% of patients; 70% of these patients experienced adverse events in the first 24 h of ECCO2R. Bleeding and hemolysis were the most common ECCO2R-AEs. An independent DSMB adjudicated SAEs as attributable or not to ECCO2R. Six SAEs were reported. The DSMB considered only two as attributable to ECCO2R: a massive right frontal parenchymal hematoma, and a pneumothorax secondary to cannula insertion in the internal jugular vein. With respect to bleeding episodes, events requiring administration of at least 1 unit of packed red cells were reported in 6% of patients.

These data strongly support the need for a well-designed randomized clinical trial to confirm that the clinical benefits of an ultra-protective strategy supported by ECCO2R would compensate for the serious side effects associated with ECCO2R. The REST trial (pRotective vEntilation with veno-venouS lung assisT in respiratory failure; NCT02654327) is currently ongoing and is randomly assigning adult patients with acute hypoxemic respiratory failure (PaO2/FiO2 < 150 mmHg) to either conventional lung protective ventilation or ECCO2R using a lower extraction device (Hemolung Respiratory Assist System; ALung Technologies, Pittsburgh, USA). Given the relatively high risk of adverse events, future trials might aim to enhance the ratio of benefit to risk by selecting patients likely to have the greatest clinically relevant physiological response, as suggested previously [25]. However, data of the present study outline the difficulties a prospective randomized clinical trial on ECCO2R may incur. First, only 12.6% of the patients admitted in the study period for moderate ARDS could be enrolled and treated with ECCO2R. Second, contraindications for systemic anticoagulation and bleeding disorders (heparin-induced thrombocytopenia; platelet < 50 G/L) were observed in 30% of patients, thus limiting a wider use of ECCO2R in the clinical settings. Third, although we included study centers with substantial experience in ECCO2R, only 3 [1–5] patients per site were enrolled during the 21-month study period. These data emphasize the importance of providing a learning curve for the use of ECCO2R to those centers that, although without specific experience, will have to be included in the study to allow the recruitment of a sufficiently large number of patients.

In conclusion, this study demonstrates that ultra-protective ventilation facilitated by ECCO2R is feasible, mitigating respiratory acidosis in patients with moderate ARDS. A randomized clinical trial is required to assess overall benefits and harms.


  1. 1.

    Blood flow with the iLA activve (Novalung) and Cardiohelp® HLS 5.0 (Getinge) can range between 0.5 and 4.5 L/min, but was limited by study protocol to 800–1000 mL/min.

  2. 2.

    The study protocol (see online supplement) originally said: “aPTT ratio is maintained at 1.5–2.0 × baseline”. However, the case report form did not ask for aPTT ratio but for absolute aPTT values (see online supplement). This inconsistency was communicated to investigators at the beginning of the study and readers at the moment of publication. For the sake of transparency, we left unchanged study protocol and statement on ClinicalTrials.Gov.

  3. 3.

    On ClinicalTrials.Gov (NCT02282657) and in the study protocol (see online supplement) the primary endpoint is formalized as: “achievement of VT reduction to 4 mL/kg while maintaining pH and PaCO2 to ± 20% of baseline values obtained at VT of 6 mL/kg”. This formulation contains an obvious error that is the phrase “maintaining pH to ± 20% of baseline values”. Such variability of pH in fact does not make sense, allowing pH values ranging between 5.92 and 8.88. To avoid confusion and bias we (a) clarified the issue on the protocol with investigators at the beginning of the study; (b) left unchanged the statement on ClinicalTrials.Gov informing the readers about the mistake at the moment of publication.


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The trial was made possible thanks to an unrestricted grant from Alung Technologies Inc, Maquet (Getinge Group), and Novalung (Xenios now part of Fresenius Medical). They supported the costs of the data monitoring and site visits, the insurance fees, the supply of the equipment and materials, the shipments and the fees per patient. The grants from the companies amounted to €171,000 and were made available to the European Society of Intensive Care Medicine that supported the costs of the development and running of the eCRF platform, the IT infrastructure, and the administrative costs related to legal matters and contracting (insurance contracts, data use agreements, and hospital contracts).

Members of the Data and Safety Monitoring Board:

Jukka Takala, Chair (University Hospital Bern, Switzerland); Lluis Blanch Torra (Institut Universitari Fundació Parc Taulí-Universitat Autònoma de Barcelona, Spain); Christian Mélot (Erasme University Hospital, Brussel, Belgium)

Investigators of the SUPERNOVA trial:

Belgium: Jacques Creteur, Alexandre Brasseur (Erasme Hospital, Brussel); Daniel de Backer (CHIREC Hospitals, Brussel); Eric Hoste, Filip de Somer, Luc de Crop (Ghent University Hospital); Bernard Lambermont (University Hospital Liège).

Canada: Martin Dres, Orla Smith (St. Michael’s Hospital, Toronto).

France: Nicolas Brechot (Hôpital Pitié-Salpêtrière, Paris); Caroline Fritz, Antoine Kimmoun (Centre Hospitalier Universitaire de Nancy); Nadia Aissaoui, Emmanuel Guerot (Hôpital Européen Georges Pompidou, Paris Hôpital Nord); Laurent Papazian, Jean-Marie Forel (AP-HM Hopital Nord Marseille); Francois Belocncle, Marc Pierrot (Centre Hospitalier Universitaire Angers); Lucie Vettoretti, Hadrien Winiszewski (Centre Hospitalier Universitaire de Besançon); Xavier Repesse, Cyril Charron (Hopital Ambroise Paré, Paris); Didier Dreyfuss, Stephane Gaudry (Hôpital Louis Mourier, Paris).

Germany: Stephan Strassmann, Michaela Merten (Kliniken der Stadt, Köln); Lars Oliver Harmisch (Universitätsmedizin, Göttinge).

Italy: Rosario Urbino, Andrea Costamagna, Chiara Bonetto (Città della Salute e della Scienza di Torino); Davide Eleuteri, Gennaro de Pascale (Università Cattolica-Policlinico Universitario A.Gemelli, Roma); Antonio Braschi, Giorgio Iotti (Fondazione IRCCS Policlinico San Matteo, Pavia); Francesco Pugliese, Guglielmo Tellan, Silvia Corradini (Policlinico Umberto I, Roma); Nicola Bottino, Chiara Abbruzzese (Fondazione IRCCS Ca’ Granda - Ospedale Maggiore Policlinico, Milano).

Netherlands: Jozef Kesecioglu, Marc Platenkamp, Diederik van Dijk (University Medical Center, Utrecht).

Spain: Jordi Riera del Brio, Eduard Argudo (Hospital Universitari Vall d’Hebron, Barcelona); Indalecio Moran Chorro, Francisco Parrilla Gomez (Hospital de la Santa Creu i Sant Pau, Barcelona)

The authors wish to thank Luciano Gattinoni, MD. His criticisms and comments on the present study made this work better but most importantly will influence how results of the present study will impact the future scientific development of ECCO2R in ARDS. The authors thank Claudia Filippini Ph.D. for the support in statistical analysis.

European Society of Intensive Care Medicine Trials Group and the “Strategy of Ultra-Protective lung ventilation with Extracorporeal CO2 Removal for New-Onset moderate to seVere ARDS” (SUPERNOVA) investigators:

Ewan C. Goligher3, Daniel Brodie5, Antonio Pesenti6, Richard Beale7, Laurent Brochard3, Jean-Daniel Chiche8, Eddy Fan9, Daniel de Backer10, Guy Francois11, Niall Ferguson9, John Laffey12, Alain Mercat13, Daniel F. Mc Auley14, Thomas Müller15, Michael Quintel16, Jean-Louis Vincent17, Fabio Silvio Taccone17, Harlinde Peperstraete18, Philippe Morimont19, Matthieu Schmidt1, Bruno Levy20, Jean-Luc Diehl21, Christophe Guervilly22, Gilles Capelier23, Antoine Vieillard-Baron24, Jonathan Messika25, Christian Karagiannidis26, Onnen Moerer16, Rosario Urbino2, Massimo Antonelli27, Francesco Mojoli28, Francesco Alessandri29, Giacomo Grasselli6, Dirk Donker30, Ricard Ferrer31, Jordi Mancebo32 Arthur S. Slutsky3

5Division of Pulmonary, Allergy, and Critical Care Medicine, College of Physicians and Surgeons, Columbia University, New York, New York; and New York–Presbyterian Hospital, New York, New York USA; 6Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, University of Milan, Milan, Italy; 7Guy’s and St. Thomas’ NHS Foundation Trust, London, UK; 8Hôpital Cochin, Université Paris Descartes, France; 9Toronto General Hospital, University of Toronto, Canada; 10Hôpital de Braine l’Alleud-Waterloo, Université Libre de Bruxelles, Belgium; 11European Society of Intensive Care Medicine, Brussels, Belgium; 12Galway University Hospitals and National University of Ireland, Galway, Ireland; 13Centre Hospitalier Universitaire, University of Angers, France; 14Centre for Experimental Medicine, Queen’s University Belfast and Regional Intensive Care Unit, Royal Victoria Hospital, Belfast, UK; 15University Hospital Regensburg, Regensburg, Germany; 16Universitätsmedizin Göttingen, Germany; 17Erasme University Hospital, Université Libre de Bruxelles, Belgium; 18Ghent University Hospital, Belgium; 19University Hospital Liège, Belgium; 20Service de Réanimation Médicale Brabois, CHRU Nancy, Pôle Cardio-Médico-Chirurgical, INSERM U1116, Faculté de Médecine, 54511 Vandoeuvre-les-Nancy, France; Université de Lorraine, Nancy, France; 21Hôpital Européen Georges Pompidou, Paris, France; 22AP-HM, Hôpital Nord, Service de médecine intensive-réanimation, Marseille, France; 23Centre Hospitalier Universitaire de Besançon, France; 24Hôpital Ambroise Paré, Paris, France; 25Hôpital Louis Mourier, Paris, France; 26Kliniken der Stadt Köln and University Witten/Herdecke, Köln, Germany; 27Fondazione Policlinico Universitario A.Gemelli IRCCS, Roma, Italy; 28Fondazione IRCCS Policlinico San Matteo, Pavia, Italy; 29Policlinico Umberto I, Roma, Italy; 30University Medical Center, Utrecht University Medical Center, Utrecht, Netherlands; 31Hospital Universitari Vall d’Hebron, Barcelona, Spain; 32Hospital de la Santa Creu i Sant Pau, Barcelona, Spain

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Correspondence to V. Marco Ranieri.

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Conflicts of interest

Dr. Goligher reports receiving personal fees and research support in the form of equipment from Getinge. Dr. Brodie receives research support from ALung Technologies; he was previously on their medical advisory board. He is currently on the medical advisory boards for Baxter and BREETHE. Dr. Ferguson reports receiving personal fees from Getinge, Baxter, and Sedana Medical. Dr. Slutsky reports receiving personal fees from Getinge, Baxter, and Novalung/Xenios.

Ethical approval

The study was approved by institutional review boards at each of the 23 study sites.

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Informed consent was obtained from patients or legally authorized surrogates.

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Sponsored by the European Society of Intensive Care Medicine (ESICM).

Endorsed by the International ECMO Network (ECMONet).

Members of the European Society of Intensive Care Medicine Trials Group and investigators of the SUPERNOVA trial are listed in the Acknowledgements.

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Combes, A., Fanelli, V., Pham, T. et al. Feasibility and safety of extracorporeal CO2 removal to enhance protective ventilation in acute respiratory distress syndrome: the SUPERNOVA study. Intensive Care Med 45, 592–600 (2019). https://doi.org/10.1007/s00134-019-05567-4

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  • Acute respiratory distress syndrome
  • Mechanical ventilation
  • Extracorporeal carbon dioxide removal
  • Ventilator-induced lung injury