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ECCO2R therapy in the ICU: consensus of a European round table meeting

Critical Care volume 24, Article number: 490 (2020) Cite this article

Abstract

Background

With recent advances in technology, patients with acute respiratory distress syndrome (ARDS) and severe acute exacerbations of chronic obstructive pulmonary disease (ae-COPD) could benefit from extracorporeal CO2 removal (ECCO2R). However, current evidence in these indications is limited. A European ECCO2R Expert Round Table Meeting was convened to further explore the potential for this treatment approach.

Methods

A modified Delphi-based method was used to collate European experts’ views to better understand how ECCO2R therapy is applied, identify how patients are selected and how treatment decisions are made, as well as to identify any points of consensus.

Results

Fourteen participants were selected based on known clinical expertise in critical care and in providing respiratory support with ECCO2R or extracorporeal membrane oxygenation. ARDS was considered the primary indication for ECCO2R therapy (n = 7), while 3 participants considered ae-COPD the primary indication. The group agreed that the primary treatment goal of ECCO2R therapy in patients with ARDS was to apply ultra-protective lung ventilation via managing CO2 levels. Driving pressure (≥ 14 cmH2O) followed by plateau pressure (Pplat; ≥ 25 cmH2O) was considered the most important criteria for ECCO2R initiation. Key treatment targets for patients with ARDS undergoing ECCO2R included pH (> 7.30), respiratory rate (< 25 or < 20 breaths/min), driving pressure (< 14 cmH2O) and Pplat (< 25 cmH2O). In ae-COPD, there was consensus that, in patients at risk of non-invasive ventilation (NIV) failure, no decrease in PaCO2 and no decrease in respiratory rate were key criteria for initiating ECCO2R therapy. Key treatment targets in ae-COPD were patient comfort, pH (> 7.30–7.35), respiratory rate (< 20–25 breaths/min), decrease of PaCO2 (by 10–20%), weaning from NIV, decrease in HCO3− and maintaining haemodynamic stability. Consensus was reached on weaning protocols for both indications. Anticoagulation with intravenous unfractionated heparin was the strategy preferred by the group.

Conclusions

Insights from this group of experienced physicians suggest that ECCO2R therapy may be an effective supportive treatment for adults with ARDS or ae-COPD. Further evidence from randomised clinical trials and/or high-quality prospective studies is needed to better guide decision making.

Background

Advances in technology to deliver extracorporeal carbon dioxide removal (ECCO2R) therapy have simplified this approach, making it easier to deploy for the management of adults with both hypoxaemic and hypercapnic acute respiratory failure (ARF) [1,2,3,4]. In patients with acute respiratory distress syndrome (ARDS), ECCO2R therapy may be used to allow ultra-protective lung ventilation (UPLV) and reduce ventilator-induced lung injury (VILI) by decreasing tidal volume (VT), both plateau (Pplat) and driving pressures and respiratory rate, while also controlling respiratory acidosis [5,6,7,8,9,10,11,12,13,14]. In patients with acute exacerbations of chronic obstructive pulmonary disease (ae-COPD) with severe respiratory acidosis and hypercapnic respiratory failure, ECCO2R therapy may be applied to prevent intubation in patients at risk of non-invasive ventilation (NIV) failure [15]. It may also be used to hasten weaning from mechanical ventilation (MV) and early extubation in those who require invasive ventilation [10, 15,16,17].

However, there is currently limited evidence regarding the use of ECCO2R therapy in these indications, with available data limited to the description of single cases or to case series that include a small number of patients [16, 18,19,20,21], as well as a few retrospective matched cohort studies [15, 22]. Additionally, questions remain on how best to implement a therapy that might be associated with serious side-effects [1]. Ongoing and published trials such as VENT-AVOID (NCT03255057), REST (NCT02654327) [2] and SUPERNOVA (NCT02282657) [11, 12, 23] are expected to provide valuable evidence to support decision making.

Given the potential of ECCO2R therapy to provide effective supportive treatment for a wide range of patient groups, we convened a European ECCO2R therapy Expert Round Table Meeting to better understand how ECCO2R therapy is applied in key diagnostic groups, e.g. patients with ARDS or ae-COPD, identify how patients are selected, understand how treatment decisions are made and delineate areas of consensus in the group.

Methods

Research questions and objectives

The ECCO2R therapy Expert Round Table Meeting was held in Brussels in July 2019 and was attended by 14 clinicians who regularly provide ECCO2R therapy in hospitals across Europe in order to provide a European perspective on ECCO2R therapy. Each attendee was a senior clinician/intensivist invited based on their experience delivering ECCO2R therapy, with and without continuous renal replacement therapy, using different devices. The attendees had direct clinical experience with a wide range of ECCO2R devices, including ALung, iLA, Prismalung and PALP (the later had been removed from the market at the time of the meeting due to loss of the distribution agreement). In addition, several of the attendees are principal investigators in recently completed or ongoing clinical trials, including randomised controlled trials such as REST and SUPERNOVA. Conflict of interest declarations for the attendees can be found at the end of the manuscript.

The meeting objectives were to better define and understand the application of ECCO2R therapy in key indications (ARDS and ae-COPD), to identify patient selection criteria and when to initiate and stop/wean patients from treatment and to determine points of consensus and differences in clinical practice in those centres represented at the meeting. A non-systematic search of MEDLINE, ClinicalTrials.gov and other sites was performed to identify key studies and trials to support the development of the questions and the content of the meeting.

Data collection and analysis

A modified Delphi-based method (Fig. 1) was used to collate the clinicians’ views in three rounds of questioning [24]. The meeting questions as well as the pre-meeting and post-meeting questionnaires were developed by JG and KH before being reviewed and approved by AC. JG and KH were present as Baxter employees and moderators, but were not permitted to provide answers or responses, either to the survey questions or during the meeting. Round 1 data were collected via an interactive PDF questionnaire circulated in advance of the meeting, and results were analysed anonymously. Round 2 data were collected during the meeting, attendees were divided into 4 subgroups and the questions were presented by an independent facilitator. Open questions were used to encourage freedom of response, and the meeting was designed to allow the attendees adequate time to consider and respond to the questions based on their experience. Attendees could respond to the questions either through anonymous electronic voting or by inputting responses into a microcomputer, with responses collected and discussed openly by the group. Round 3 was a second interactive PDF questionnaire, circulated post-meeting, designed to follow up on discussion points raised at the face-to-face meeting, with results analysed anonymously. Details on the process for information gathering and the questions are provided in Additional file 1.

Fig. 1
figure 1

Overview of the five-step Delphi method used in the Round Table Meeting. Each step was a distinct process that was completed before the following step was initiated. Results and discussions from each step were independently analysed and used to inform the direction and content of the following steps, e.g. if the group were split on a topic, then clarifying questions were crafted to guide the discussions in the following step(s) to identify and explore points of consensus or difference. GPP3, Good Publication Practice 3

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Target values for ventilation parameters of interest—criteria for initiation of ECCO2R therapy and treatment targets for ECCO2R therapy in both ARDS and ae-COPD—were collected during the three rounds of questioning. These values were subsequently evaluated for consensus. To facilitate the analysis of the responses for certain questions, a scoring system was employed. Participants were asked to score their responses in order of importance, giving them a score (e.g. from 1 to 8, depending on the number of variables). Scores were then combined to give a total score for each parameter, with higher scores indicating a higher perceived importance. To determine whether a consensus was reached or not based on participant responses to the questions, a threshold of ≥ 80% of participants in agreement was used to define if consensus was reached, a level that has been used in previous analyses [25]. Majority agreement indicates that ≥ 50% of participants agreed, but consensus level was not reached, and no agreement means that < 50% of participants agreed. The report was drafted by an independent medical writing company (SciMentum, Nucleus Global) and paid for by Baxter in line with Good Publication Practice 3. The various drafts were reviewed and approved by AC before being reviewed by the full author team. All authors provided their approval to submit and meet the ICMJE criteria for authorship.

Results

Attendee clinical experience

Twelve clinicians completed the pre-meeting survey: eight worked in Combined Surgical and Medical intensive care units (ICUs), while the others were employed in Medical ICUs (n = 2), Surgical ICUs (n = 2) and Cardiac Surgery ICUs (n = 2); respondents could be employed at more than one type of centre. ICUs had a median of 20 beds/unit and 400–2000 admissions/year. Extracorporeal membrane oxygenation (ECMO) experience of participants ranged from 0 to 80 veno-venous ECMO procedures/year and 0 to 220 veno-arterial ECMO procedures/year.

Indications and rationale for ECCO2R based on pre-meeting survey

Analysis of the Round 1 pre-meeting survey responses revealed that ARDS was considered the primary indication for ECCO2R therapy by 7 participants, while 3 participants considered ae-COPD to be the primary indication. Severe asthma was also mentioned as another potential ECCO2R indication, although less frequently. The median number of ARDS admissions (as per the Berlin definition [26]) was 60 patients per centre per year, with some centres admitting up to 500 patients per year. While the most common criteria stated in the pre-meeting responses for initiating ECCO2R therapy in patients with ARDS were to manage hypercapnia with acidosis, although specific criteria varied across the ICUs, likewise, weaning criteria shared at Round 1 varied significantly, with no clearly consistent management pattern being identified between centres. However, most participants (92%) indicated that they would place patients with ARDS in the prone position when using ECCO2R therapy. The number of ae-COPD admissions ranged from 0 to 250 patients per centre per year (median 50). Participants indicated that ECCO2R therapy was predominantly initiated to prevent intubation in patients at risk of NIV failure or to facilitate extubation in patients who had been intubated after NIV failure.

Use of ECCO2R therapy in patients with ARDS

During the Expert Round Table Meeting and post-meeting survey (Rounds 2 and 3, respectively), the group considered the ventilation parameters for implementation of a lung protective ventilation (LPV) strategy in all patients with ARDS and agreed upon the following targets: driving pressure, 10–14 cmH2O; positive end-expiratory pressure (PEEP), 10–14 cmH2O; Pplat, 25–29 cmH2O; and respiratory rate either 20–25 or 25–30 breaths/min, although most of the group would target a respiratory rate of 25 breaths/min. There was some variation in responses among the group when asked about target pH, with half of participants opting for a target pH value of 7.25–7.30, while others indicated the target should be > 7.30 (n = 4), < 7.25–7.30 (n = 2) or < 7.20 (n = 1). Finally, the panellists thought VT should be set at 6.0 mL/kg of predicted body weight (PBW), although 6.1–7.0 or 7.1–8.0 mL/kg PBW were also considered to be reasonable targets. When asked in the post-meeting survey (Round 3) about the preferred ventilation mode used for patients with ARDS undergoing LPV, the group were split with respect to pressure control (pressure assist) (n = 8) and flow control (volume assist) (n = 6) modes of ventilation. These recommendations agreed with the most recent guidelines for the ventilation management of patients with ARDS [27, 28].

There was consensus among the group (91% [2 participants were unavailable for this question, 11 of n = 12/14 voted in favour]) that the primary treatment goal of ECCO2R therapy for patients with ARDS was to apply UPLV via managing CO2 levels. For initiating ECCO2R therapy in patients with ARDS, driving pressure (≥ 14 cmH2O) followed by Pplat (≥ 25 cmH2O) was considered the most important criteria, and this was confirmed in the post-meeting survey (Tables 1 and 2). Additional key parameters included pH (< 7.25), reducing VT to < 6 mL/kg PBW, PaCO2 (> 60–80 mmHg), respiratory rate (≥ 25 to > 30 breaths/min), PaO2/FiO2 (100–200) and PEEP (combined findings from Rounds 2 and 3).

Table 1 ECCO2R treatment criteria for patients with ARDS
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Table 2 Typical characteristics for initiating ECCO2R for rescue therapy and to facilitate ultra-protective ventilation in ARDS
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Participants were evenly split during the meeting on the primary rationale for ECCO2R therapy, being rescue therapy in patients with ARDS undergoing injurious MV, i.e. those with very high plateau and driving pressures despite reduced VT and PEEP (n = 7), or to facilitate UPLV to prevent the deleterious effects of MV in patients already undergoing LPV (n = 7). Based on the results of the post-meeting survey, a consensus was reached among the group (12/14, 86% of participants) that ECCO2R was a strategy they would consider selecting for rescue in patients with ARDS. Typical characteristics for initiating ECCO2R in a rescue situation obtained as part of the post-meeting survey are summarised in Table 2. A majority (10/14, 71% of participants) indicated that they would select ECCO2R as a means of facilitating UPLV for patients with ARDS, and typical characteristics for selecting patients are summarised in Table 2.

For both potential indications, patients would not be considered suitable for an ECCO2R strategy if they met the indications for ECMO, such as severe or refractory ARDS [29] and presence of severe right heart failure (ECMO may be a more adequate treatment for these patients), in cases where anticoagulation is contraindicated and for those with major comorbidities and/or predicted survival of < 1 year.

The group considered treatment targets for their patients with ARDS undergoing ECCO2R. A consensus was reached regarding driving pressure (< 14 cmH2O) and respiratory rate (< 25 or < 20 breaths/min). There was majority agreement with respect to targets for Pplat (< 25 cmH2O), pH (> 7.30 [Rounds 2 and 3]), PaCO2 (< 50 or < 55 mmHg) and VT (≤ 6 mL/kg PBW). Other target parameters were not proposed by the group (Table 1). The expected average length of time patients with ARDS would remain on ECCO2R therapy was suggested to be 1–3 days (n = 5) and 4–6 days (n = 9).

Following discussion during the meeting on a protocol for weaning from ECCO2R in patients with ARDS, a protocol was proposed and reviewed as part of the post-meeting survey (Table 3). The group voted on each step and reached consensus (92% of participants, n = 13) that this proposal was a suitable weaning strategy.

Table 3 ECCO2R weaning protocol for patients with ARDS
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Use of ECCO2R therapy in patients with ae-COPD

There was consensus during the meeting that patients with ae-COPD who should receive ECCO2R therapy were those at risk of NIV failure, as well as patients recently initiated on MV after NIV failure to allow for early extubation within 24 h of initiating ECCO2R therapy. Other patient groups would be considered (e.g. patients on prolonged MV who require weaning from invasive ventilation and patients who are refusing intubation), but a consensus was not reached.

The group agreed that for patients with ae-COPD at risk of NIV failure, ‘no decrease in PaCO2’ and ‘no decrease in respiratory rate’ while on NIV were both key initiation criteria for ECCO2R therapy (Table 4). These criteria were considered indicative of NIV failure. Clinical signs of respiratory failure and pH (< 7.25 [n = 5] or 7.25–7.30 [n = 6]) would be considered as initiation criteria by most of the participants. Baseline PaCO2 and respiratory rate as main triggers were favoured by less than half of participants. For patients with ae-COPD who had already been intubated, criteria for initiating ECCO2R therapy varied (Table 4).

Table 4 ECCO2R treatment initiation criteria for patients with ae-COPD
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Factors for excluding patients with ae-COPD from ECCO2R typically included patients with end-stage disease (the group highlighted that markers for this include severe functional limitation and cachexia); contraindications to anticoagulation; problems with vascular access; patient’s wishes, e.g. refusal to be intubated, except in cases where ECCO2R therapy represented the last resource accepted by the patient; poor quality of life; and the patient not being a candidate for MV.

Treatment targets for patients with ae-COPD receiving ECCO2R therapy were, in order of perceived importance (Table 5), comfortable patient, pH (> 7.35/7.30; no consensus on specific pH), respiratory rate (< 20–25 breaths/min), decrease of PaCO2 by 10–20%, weaning from NIV, decrease in HCO3− and maintaining haemodynamic stability. Consensus on a weaning protocol for patients with ae-COPD was reached during the meeting (Table 5).

Table 5 ECCO2R treatment targets and weaning protocol for patients with ae-COPD
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Anticoagulation strategy for patients receiving ECCO2R

Responses obtained during Round 1 (pre-meeting survey) showed that heparin was the preferred choice of anticoagulant used during ECCO2R therapy (~ 80% of participants stated that heparin was their anticoagulant of choice). This was confirmed in the post-meeting survey, in which unfractionated heparin was the anticoagulant of choice for the majority (~ 90% of participants). The proposed heparin anticoagulation protocol agreed by the group is shown in Table 6. Lastly, argatroban was the group’s preferred anticoagulant in case of proven heparin-induced thrombocytopenia (HIT).

Table 6 Heparin anticoagulation strategy
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Discussion

The responses obtained from the Expert Round Table Meeting and accompanying pre- and post-meeting surveys have provided further insights into the use of ECCO2R therapy across Europe. During a typical Delphi process [24], 100% agreement is rare, and any consensus is the result of multiple rounds of voting and discussion that lead to a convergence of opinion. However, in areas where clinical evidence is limited, as is the case for ECCO2R therapy in patients with ARDS and ae-COPD, using a modified Delphi method may offer insight into the current practice of experienced users, which could help inform decision making in local clinical practice. Additionally, the use of the Delphi method to guide these discussions and reach points of consensus will be of potential benefit for the design of future trials. Specifically, the discussions provide insight relevant to inclusion criteria, guidance on the management of patients while receiving ECCO2R therapy and possible primary and secondary endpoints.

Key areas of consensus for the use of ECCO2R therapy in the treatment of patients with ARDS or ae-COPD were identified. There was consensus among the group that the primary treatment goal of ECCO2R therapy for patients with ARDS was to apply UPLV via managing CO2 levels; this is in agreement with the findings of a systematic literature review [30]. The group reached a consensus that, when initiating ECCO2R therapy in patients with ARDS, driving pressure (≥ 14 cmH2O) followed by Pplat (≥ 25 cmH2O) was the most important criteria to consider. Higher PEEP, lower peak and plateau pressures and lower respiratory rate have been shown to correlate with improved survival in patients with ARDS [7, 11, 31]. However, only the driving pressure was associated with increased mortality using a multilevel mediation analysis in a large retrospective cohort study of patients with ARDS [32]. It is therefore perhaps not surprising that the key treatment targets for ECCO2R in ARDS identified by the group were reductions in driving pressure and respiratory rate.

A pH of < 7.25 was also considered by most of the group to be a criterion for initiation of ECCO2R therapy in this patient group. Indeed, a lower pH was recently shown to be independently associated with ICU mortality in the large prospective LUNG SAFE registry [31]. Most of the group also agreed that ECCO2R should be initiated at PaCO2 levels > 60–80 mmHg. While it was suggested that permissive hypercapnia provided protection against lung injury in terms of lung permeability, oxygenation and lung mechanics [33], more recent data have shown a positive correlation between hypercapnic acidosis and mortality [34, 35]. Raising pH (> 7.30 or > 7.25) and decreasing PaCO2 levels were considered important treatment targets, indicating that there is a perception that ECCO2R is an important therapy for the management of respiratory acidosis.

The experts were evenly split on the primary rationale for ECCO2R therapy, either as a rescue therapy in patients with ARDS undergoing injurious MV, or to facilitate UPLV to prevent VILI. The results from the post-meeting survey highlighted that the group agreed that they would at least consider selecting ECCO2R as a strategy in both settings. Ongoing (NCT02654327) [11] randomised trials may help clarify the role of ECCO2R, allowing UPLV in patients with acute hypoxemic respiratory failure.

To the best of our knowledge, this is the first publication of a proposed weaning strategy for ECCO2R in patients with ARDS. The group reached a consensus regarding a strategy for weaning patients from ECCO2R in this setting. It was agreed that ECCO2R therapy should be applied for at least 48 h in patients with ARDS, and that a test for PaO2/FiO2 > 200 mmHg while maintaining a driving pressure < 14 cmH2O should be carried out to determine weaning possibility. It was also agreed that patients should be stable for a minimum of 12 h at the ventilation parameters outlined (see Table 3) before any weaning attempt takes place [11].

In a randomised study exploring the role of helium/oxygen in ae-COPD, the rate of patients failing on NIV and requiring MV was 15% [36]. Identifying the subgroup of patients with ae-COPD at high risk of NIV failure is indeed crucial to improve their outcomes by deploying effective preventive strategies. The panel identified ‘lack of decrease in PaCO2’ and ‘respiratory rate during NIV’ as important indicators of increased risk of NIV failure and an indication for ECCO2R initiation. The group also felt that it was important to allow enough time to show that NIV was ineffective before initiating ECCO2R therapy. Furthermore, there are numerous factors involved in NIV failure, and the benefit of ECCO2R for this patient group is still a matter of debate due to lack of data from randomised clinical trials [15, 22].

For patients with ae-COPD who are already intubated, the intended use of ECCO2R therapy is to rapidly allow extubation, to facilitate oral nutrition and early physiotherapy and to prevent muscle deconditioning [3]. Treatment targets identified by the group clearly fit in with the strategy of reducing the duration of MV and are in line with published data and wider views on the use of ECCO2R therapy [1, 19]. The VENT-AVOID trial (NCT03255057) is currently randomising patients to further investigate the benefits of ECCO2R therapy in patients at risk of NIV failure or who already have been intubated after NIV failure.

Anticoagulation with intravenous unfractionated heparin was the preferred strategy of the group. This reflects recent studies in the literature in which unfractionated heparin appears to be the anticoagulant most frequently used in this setting [10, 11]. The post-meeting survey highlighted that anticoagulant activity should be monitored using activated partial thromboplastin time (aPTT) and/or anti-Xa; the monitoring approach remains dependent on local practice. For patients with proven HIT, argatroban was the group’s preferred anticoagulant [37, 38].

Limitations

The findings presented here relate to the experiences of a relatively small number of physicians from centres across Europe; evidence from a larger group of intensivists from multiple regions of the world may be required to support these observations. Certain topics were not covered due to the scope of the meeting. Firstly, the questions covered current practice and did not explore if practices, e.g. inclusion policies of the respective centres, had changed over time. Secondly, certain rarer indications, e.g. lung transplant, were not covered, as the meeting focussed on the broader population of patients requiring ECCO2R therapy, e.g. patients with ARDS or ae-COPD. These questions could be covered as part of a follow-up meeting. Additionally, while the authors took every opportunity to ensure all relevant major articles were cited, the purpose of the meeting was to understand current practice as opposed to conducting a comprehensive literature analysis. Finally, the experiences outlined are the physicians’ respective personal experiences and are not a replacement for formal guidelines. The reader should consider their patients’ needs and local guidelines when performing ECCO2R therapy.

Conclusions

The insights from this group of experienced physicians suggested that ECCO2R therapy may be a useful and effective supportive treatment for adults in the ICU with both ARDS and ae-COPD. They have however highlighted an urgent need for further evidence in the form of randomised clinical trials and/or high-quality prospective studies to help guide decision making. Ongoing and published trials such as VENT-AVOID (NCT03255057), REST (NCT02654327) [2] and SUPERNOVA (NCT02282657) [11, 12, 23] should provide the data to support these guidelines.

Availability of data and materials

Not applicable.

Abbreviations

ae-COPD:

Acute exacerbations of chronic obstructive pulmonary disease

aPTT:

Activated partial thromboplastin time

ARDS:

Acute respiratory distress syndrome

ARF:

Acute respiratory failure

ECCO2R:

Extracorporeal carbon dioxide removal

ECMO:

Extracorporeal membrane oxygenation

FiO2 :

Fraction of inspired oxygen

HIT:

Heparin-induced thrombocytopenia

ICU:

Intensive care unit

LPV:

Lung protective ventilation

MV:

Mechanical ventilation

NIV:

Non-invasive ventilation

PaCO2 :

Partial pressure of carbon dioxide

PBW:

Predicted body weight

PEEP:

Positive end-expiratory pressure

P plat :

Plateau pressure

SpO2 :

Oxygen saturation

UPLV:

Ultra-protective lung ventilation

VILI:

Ventilator-induced lung injury

V T :

Tidal volume

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Acknowledgements

Supported by Baxter Inc. Medical writing support was provided by Daniel Johnson and Ruth Brown of SciMentum Inc. (Nucleus Global), funded by Baxter Inc., under the authors’ conceptual direction and based on feedback from the authors.

Funding

The meeting and associated expenses as well as the publication of this research was supported by Baxter Inc.

Author information

Author notes

  1. Georg Auzinger, Gilles Capellier, Damien du Cheyron, Ian Clement, Guglielmo Consales, Wojciech Dabrowski, David De Bels, Francisco Javier González de Molina Ortiz, Antje Gottschalk, Matthias P. Hilty, David Pestaña, Eduardo Sousa and Redmond Tully contributed equally to this work.

Authors and Affiliations

  1. Sorbonne Université, INSERM, UMRS_1166-ICAN, Institute of Cardiometabolism and Nutrition, 47, Boulevard de l’Hôpital, F-75013, Paris, France

    Alain Combes

  2. Service de Médecine Intensive-Réanimation, Institut de Cardiologie, APHP Hôpital Pitié–Salpêtrière, F-75013, Paris, France

    Alain Combes

  3. Department of Critical Care, King’s College Hospital, London, SE5 9RS, UK

    Georg Auzinger

  4. Department of Critical Care, Cleveland Clinic, London, SW1Y 7AW, UK

    Georg Auzinger

  5. Service de Médecine Intensive-Réanimation CHRU Besançon, EA 3920 University of Franche Comte, Besançon, France

    Gilles Capellier

  6. Australian and New Zealand Intensive Care Research Centre, Department of Epidemiology and Preventive Medicine, Monash University, Melbourne, Australia

    Gilles Capellier

  7. Service de Médecine Intensive-Réanimation, Caen University Hospital, 14000, Caen, France

    Damien du Cheyron

  8. Critical Care Unit, Royal Victoria Infirmary, Newcastle upon Tyne, NE1 4LP, UK

    Ian Clement

  9. Department Emergency and Critical Care, Prato Hospital, Azienda Toscana Centro, Prato, Italy

    Guglielmo Consales

  10. Department of Anaesthesiology and Intensive Care, Medical University of Lublin, Jaczewskiego Street 8, 20-954, Lublin, Poland

    Wojciech Dabrowski

  11. Service des Soins Intensifs Médico-chirurgicaux, CHU Brugmann, 4 Place A Van Gehuchten, 1020, Brussels, Belgium

    David De Bels

  12. Department of Critical Care, University Hospital Mútua Terrassa, Universitat de Barcelona, Terrassa, Barcelona, Spain

    Francisco Javier González de Molina Ortiz

  13. Department of Critical Care, University Hospital Quirón Dexeus, Universitat Autònoma de Barcelona, Barcelona, Spain

    Francisco Javier González de Molina Ortiz

  14. Department of Anaesthesiology, Intensive Care Medicine and Pain Medicine, University Hospital Münster, Münster, Germany

    Antje Gottschalk

  15. Institute of Intensive Care Medicine, University Hospital of Zürich, Rämistrasse 100, 8091, Zürich, Switzerland

    Matthias P. Hilty

  16. Department of Anesthesiology and Surgical Critical Care, Hospital Universitario Ramón y Cajal, IRYCIS, Carretera de Colmenar Viejo km 9, 28034, Madrid, Spain

    David Pestaña

  17. Universidad de Alcalá de Henares, Madrid, Spain

    David Pestaña

  18. Serviço de Medicina Intensiva, Centro Hospitalar e Universitário de Coimbra, Praceta Mota Pinto, 3000-075, Coimbra, Portugal

    Eduardo Sousa

  19. Department of Intensive Care, Royal Oldham Hospital, Northern Care Alliance, Oldham, OL1 2JH, UK

    Redmond Tully

  20. Baxter World Trade SPRL, Acute Therapies Global, Braine-l’Alleud, Belgium

    Jacques Goldstein

  21. Baxter, Baxter Deutschland GmbH, Unterschleissheim, Germany

    Kai Harenski

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  1. Alain Combes
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  2. Georg Auzinger
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  3. Gilles Capellier
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Contributions

All authors participated in the discussions in the Round Table Meeting as well as the questionnaire rounds, contributed data, critically reviewed the manuscript providing interpretation of the data and their implications and provided approval for the final version to be published.

Authors’ information

FJGDM: Member of the Acute Respiratory Failure Working Group and Chair of the Nephrological Intensive Care Working Group of the Spanish Society of Critical and Intensive Care Medicine and Coronary Units (Sociedad Española de Medicina Intensiva, Críticos y Unidades Coronarias [SEMICYUC]).

Corresponding author

Correspondence to Alain Combes.

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Competing interests

All authors received financial compensation from Baxter for travel and accommodation for attending the meeting. MPH has received financial compensation from Baxter for travel and accommodation in the past.

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Supplementary information

Additional file 1: Expanded methods.

Details on the process for information gathering and the questions.

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Combes, A., Auzinger, G., Capellier, G. et al. ECCO2R therapy in the ICU: consensus of a European round table meeting. Crit Care 24, 490 (2020). https://doi.org/10.1186/s13054-020-03210-z

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Keywords

Critical Care

ISSN: 1364-8535