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Annals of Intensive Care
Annals of Intensive Care Cover Image
  • Research
  • Open Access

Low-flow CO2 removal in combination with renal replacement therapy effectively reduces ventilation requirements in hypercapnic patients: a pilot study

  • 1,
  • 2,
  • 2,
  • 3,
  • 3 and
  • 1Email author
Annals of Intensive Care20199:3

https://doi.org/10.1186/s13613-019-0480-4

©  The Author(s) 2019

  • Received: 2 August 2018
  • Accepted: 2 January 2019
  • Published:

Abstract

Background

Lung-protective strategies are the cornerstone of mechanical ventilation in critically ill patients with both ARDS and other disorders. Extracorporeal CO2 removal (ECCO2R) may enhance lung protection by allowing even further reductions in tidal volumes and is effective in low-flow settings commonly used for renal replacement therapy. In this study, we describe for the first time the effects of a labeled and certified system combining ECCO2R and renal replacement therapy on pulmonary stress and strain in hypercapnic patients with renal failure.

Methods

Twenty patients were treated with the combined system which incorporates a membrane lung (0.32 m2) in a conventional renal replacement circuit. After changes in blood gases under ECCO2R were recorded, baseline hypercapnia was reestablished and the impact on ventilation parameters such as tidal volume and driving pressure was recorded.

Results

The system delivered ECCO2R at rate of 43.4 ± 14.1 ml/min, PaCO2 decreased from 68.3 ± 11.8 to 61.8 ± 11.5 mmHg (p < 0.05) and pH increased from 7.18 ± 0.09 to 7.22 ± 0.08 (p < 0.05). There was a significant reduction in ventilation requirements with a decrease in tidal volume from 6.2 ± 0.9 to 5.4 ± 1.1 ml/kg PBW (p < 0.05) corresponding to a decrease in plateau pressure from 30.6 ± 4.6 to 27.7 ± 4.1 cmH2O (p < 0.05) and a decrease in driving pressure from 18.3 ± 4.3 to 15.6 ± 3.9 cmH2O (p < 0.05), indicating reduced pulmonary stress and strain. No complications related to the procedure were observed.

Conclusions

The investigated low-flow ECCO2R and renal replacement system can ameliorate respiratory acidosis and decrease ventilation requirements in hypercapnic patients with concomitant renal failure.

Trial registration NCT02590575, registered 10/23/2015.

Keywords

  • Low-flow extracorporeal CO2 removal
  • Mechanical ventilation
  • Lung protection
  • Ventilator-induced lung injury
  • Acute kidney injury
  • Renal replacement therapy
  • Multi-organ support

Background

Lung-protective strategies are the mainstay of mechanical ventilation in patients with ARDS and other inflammatory pulmonary disorders, as the use of lower tidal volumes and plateau pressures improves survival rates by reducing pulmonary stress and strain [1, 2]. In addition, there is a growing body of evidence that a further reduction in the mechanical stress resulting from positive pressure ventilation by further decreasing tidal volumes may be even more “lung protective” [3–5]. Whereas low tidal volume ventilation has been shown to reduce pulmonary inflammation and consequently mortality, it is often accompanied by hypercapnic acidosis, which will even be more pronounced under “ultra-protective” ventilation strategies. Although elevated PaCO2 levels in this setting (“permissive hypercapnia”) are often well tolerated and deemed to be safe [1–3], the degree to which hypercapnia may be tolerable or even beneficial by directly supporting anti-inflammation remains unclear [6–9]. Very recent data have shown a positive correlation between hypercapnic acidosis and mortality [10, 11], thereby casting doubt on the uncritical toleration of hypercapnic acidosis under lung-protective mechanical ventilation. On the other hand, many patients with ARDS present with multi-organ failure, e.g., due to septic shock, and consequently exhibit massive metabolic acidosis in combination with severe cardiovascular instability. This may further limit the concept of permissive hypercapnia since an additional decrease in pH may be considered unsafe in such patients. This problem is even more pronounced when aiming for an additional reduction in the invasiveness of mechanical ventilation by further reducing tidal volumes.

Although there are no conclusive data showing a reduction in mortality, there is evidence that extracorporeal CO2 removal (ECCO2R) can effectively normalize severe hypercapnia and facilitate ultra-protective ventilation strategies [12–15]. Whereas extracorporeal membrane oxygenation (ECMO) is becoming more and more widespread in the therapy of patients with severe ARDS and provides total decarboxylation in addition to oxygenation, such high-flow systems require substantial resources and carry a considerable risk of complications and are therefore limited to patients with severe hypoxemia [16–22]. Total extracorporeal CO2 removal can be achieved with less invasive techniques such as pumpless extracorporeal lung assist (pECLA) and other mid-flow systems [23, 24], but these techniques still require specialized vascular access and are therefore invasive and expensive.

On the other hand, it has repeatedly been demonstrated that even low-flow systems adapted from conventional renal replacement platforms with blood flow rates under 500 ml/min can achieve significant CO2 elimination (“respiratory dialysis”) [25–27]. Extracorporeal CO2 removal based on renal replacement platforms may be especially useful in mechanically ventilated patients with multi-organ failure, since in one- to two-thirds of those patients there is an indication for renal replacement therapy [28, 29]. Furthermore, concomitant lung and kidney injury may exhibit significant detrimental interaction (“organ cross talk”) [30, 31], which may negatively affect outcome. Because no additional vascular access other than the dialysis catheter is required, the implementation of a hollow-fiber gas exchanger in the renal replacement circuit could be an attractive therapeutic option in such patients.

Though the use of such combinations of ECCO2R and continuous renal replacement therapy (CRRT) has been reported [27, 32, 33], until recently no certified combination therapy has been available. In this pilot study, we describe for the first time the effectiveness of a commercially available combination of ECCO2R and CRRT regarding decarboxylation and ventilation as well as other clinical parameters.

Methods

Aims of the study, inclusion and exclusion criteria

The main goals of this multicenter observational pilot study were (1) to determine the changes in blood gases under the combined renal replacement and decarboxylation therapy and (2) to record the reduction in plateau pressures and tidal volumes that can thus be achieved. Secondary measurements included changes in ventilator settings, systemic hemodynamics, membrane lung performance, running time and patency of the extracorporeal circuit as well as documentation of system-related complications. The study protocol was approved by the local ethics committees at all three participating centers. We aimed to analyze data from 20 critically ill patients with the following inclusion criteria: (1) mechanical ventilation according to ARDS Network criteria with a prospected duration of at least 24 h, (2) hypercapnic acidosis with a pH below 7.30 and a PaCO2 of at least 55 mmHg under a plateau pressure of at least 25 cmH2O and (3) indication for renal replacement therapy. The study was registered under NCT02590575.

Extracorporeal circuit

The Prismalung™ system (Baxter Gambro Renal, USA) consists of a 0.32-m2 membrane oxygenator that can be included in the Prismaflex™ organ support platform either in a stand-alone fashion or in combination with CRRT to provide low-flow CO2 removal. For this study, we utilized the combination therapy where the membrane oxygenator is inserted serially in the extracorporeal circuit downstream to the hemofilter. 100% oxygen was used as sweep gas. The Prismaflex™ system is equipped with a software extension; otherwise, there are no changes compared to the basic CRRT mode. Systemic anticoagulation with unfractioned heparin and a target aPTT (activated partial thromboplastin time) of 60 s was used to prevent clotting in the extracorporeal circuit. Temperature management was according to local practice standards using tube heating or optionally a conventional heat exchanger directly connected to the membrane oxygenator. Renal replacement therapy was provided according to local practice standards as continuous veno-venous hemofiltration (CVVHF) using bicarbonate-buffered replacement fluids. CRRT dose was calculated according to international guideline recommendations; approximately one-third of the dose was applied as pre-dilution.

Study protocol

Patients underwent a checklist-based screening for inclusion criteria. If inclusion criteria were met and no exclusion criteria were present, informed consent was obtained by the patient or legal guardian. After inclusion patients underwent a 2-h stabilization period to ensure stable cardiovascular and respiratory conditions before implementation of the extracorporeal circuit. Adequate analgosedation with a Richmond agitation and sedation scale (RASS) target of − 4 was provided, neuromuscular blockade was not mandatory. During this period, vascular access was obtained with a conventional 13.5 French Shaldon catheter (Bard Access Systems, USA) via an internal jugular (75% of patients, catheter length 20 cm) or femoral vein (25% of patients, catheter length 24 cm) and the system was primed. The stabilization period could be shortened if the immediate commencement of renal replacement therapy was deemed to be necessary. After connecting the patient to the circuit and before starting sweep gas flow, baseline parameters were collected. Then sweep gas was started at a flow rate of 8 l/min and remained unchanged throughout the study. After recording changes in blood gases after a running time of 30 min, ventilator settings were adapted (i.e., Pplat lowered) with the goal of reestablishing baseline PaCO2. Original PaCO2 was reinstated using end-tidal CO2 as guidance and confirmed through blood gas analysis. After another 30 min data were collected and again at 24, 48 and 72 h after implementation. Ventilator settings were left to the discretion of the treating physician as soon as the initial data collections (at 30 and 60 min) were completed. The study ended after 72 h or loss of the system due to clotting. In case of system loss within the first 24 h, a new system could be implemented and data collection continued.

Statistical analysis and ECCO2R calculation

Data were collected using paper-based case record forms, and a database was created with conventional spreadsheet software (Microsoft Excel 2010). Mean and median values as well as standard deviations were calculated and one-sided Student’s t test was used for statistical comparison assuming normally distributed data. Diagrams were created with SciDAVis open-source software (version 1.22). Blood gas analysis was performed using a conventional blood gas analyzer (ABL 800 Flex, Radiometer, Denmark), and ECCO2R rate was calculated from blood flow and the difference between blood CO2 content at the beginning and end of the extracorporeal circuit according to the following equation [34]:

CO2 removal rate = (CO2 arterial content−CO2 venous content) × blood flow = 24 × ((HCO3 arterial + 0.03 × PCO2 arterial)−(HCO3 venous + 0.03 × PCO2 venous)) × blood flow with arterial and venous referring to the arterial and venous lines of the extracorporeal circuit, respectively.

Results

Patient characteristics

Between January 2016 and February 2017, 26 critically ill patients in three centers were included in the study. Because of the wrong application of inclusion criteria and inconsistent baseline measurements, data of 20 patients were included in the final analysis. All patients were on pressure-controlled mechanical ventilator support, received an opiate-based analgosedation regime and were on vasopressor support. The leading indications for renal replacement therapy were sepsis in 9/20 patients and established chronic renal failure in 6/20 patients; other indications included shock and acute cardiorenal syndrome. One surgical patient was included; all other patients (19/20) were medical. Patient characteristics and parameters at inclusion are given in Tables 1 and 2, respectively.
Table 1

Patient characteristics

Age (years)

64 (43–82)

Male sex

12/20 (60%)

BMI (kg/m2)

29.4 (24.2–39.7)

SAPS II

57 (27–79)

Patient category

 Medical

19/20 (95%)

 Surgical

1/20 (5%)

SOFA

14 (8–18)

Main diagnoses

 Pneumonia

17/20 (85%)

 Septic shock

14/20 (70%)

 ARDS

8/20 (40%)

 COPD

7/20 (35%)

 CIHD

6/20 (30%)

Analgosedation

 Opiates

20/20 (100%)

 Sedation

19/20 (95%)

 NMBA

5/20 (25%)

Hemodynamic support

 Vasopressors

20/20 (100%)

 Inotropes

2/20 (10%)

BMI body mass index; SAPS Simplified Acute Physiology Score; SOFA Sequential Organ Failure Assessment; ARDS acute respiratory distress syndrome; COPD chronic obstructive pulmonary disease; CIHD chronic intermittent hemodialysis; NMBA neuromuscular blocking agent

Table 2

Parameters at inclusion

Parameter

Value ± SD

Range

pH

7.20 ± 0.08

7.02–7.31

PaCO2 (mmHg)

66.3 ± 8.7

56.1–84.4

HCO3 (mmol/l)

24.1 ± 3.9

17.1–34.3

CaCO2 (ml/l)

626 ± 93

457–881

SBE (mmol/l)

− 2.4 ± 4.8

− 11.7–11.9

SaO2 (%)

95 ± 2

88–98

P/F (mmHg)

159 ± 36

107–224

VT/PBW (ml/kg)

6.0 ± 0.7

4.5–7.9

RR (bpm)

25 ± 4

16–31

RMV (l/min)

9.6 ± 1.7

6.3–12.7

Pplat (cmH2O)

30 ± 4

25–38

PEEP (cmH2O)

12 ± 3

6–18

ΔP (cmH2O)

18 ± 4

11–26

Cdyn (ml/cmH2O)

27.5 ± 10.8

14.9–48.0

HR (bpm)

101 ± 20

70–150

MAP (mmHg)

72 ± 12

56–98

Norepinephrine dose (mg/h]

2.7 ± 2.2

0.4–9.0

RASS

− 4 ± 1

− 5 to − 3

PaCO2 arterial CO2 partial pressure; HCO3 bicarbonate concentration; CaCO2 arterial CO2 content; SBE standard base excess; SaO2 arterial O2 saturation; P/F oxygenation index; VT tidal volume; PBW predicted body weight; RR respiratory rate; RMV respiratory minute volume; Pplat plateau pressure; PEEP positive end-expiratory pressure; ΔP driving pressure; Cdyn dynamical compliance; HR heart rate; MAP mean arterial pressure; RASS Richmond agitation and sedation scale

ECCO2R, blood gases and CO2 transfer

The average overall ECCO2R rate of the combined system was 43.4 ± 14.1 ml/min with a maximum of 75.0 ml/min and remained above 40 ml/min during the course of the study (Fig. 1). The CO2 elimination rate of the membrane lung alone was slightly higher (45.4 ± 15.7 ml/min). The resulting decrease in the CO2 content of extracorporeal blood was 113 ml/l (640 ± 98 vs. 527 ± 103 p < 0.05) corresponding to a decrease in patient arterial CO2 of 6.5 mmHg (68.3 ± 11.8 vs. 61.8 ± 11.5, p < 0.05) and an increase in pH from 7.18 ± 0.09 to 7.22 ± 0.08 (p < 0.05) after 30 min (Table 3). No change in systemic oxygenation was observed at this point. During the remaining study period, a further normalization of blood gases was observed (Fig. 2). Passage of the membrane lung reduced extracorporeal blood CO2 content from 645 ± 94 to 527 ± 103 ml/l (− 18%), corresponding to a drop in PCO2 from 66.6 ± 12.6 to 32.3 ± 5.5 mmHg (− 52%).
Fig. 1
Fig. 1

Time course of ECCO2R over the study period. At baseline, the patient was connected to the extracorporeal circuit with the sweep gas flow over the membrane lung turned off

Table 3

Changes in arterial CO2 load, partial pressure and pH between baseline and at 0.5 h

 

Baseline

+ 0.5 h

Δ (%)

P-value

pH

7.18 ± 0.09

7.22 ± 0.08

+ 0.04

< 0.05

PaCO2 (mmHg)

68.3 ± 11.8

61.8 ± 11.5

− 6.5 (− 9.5)

< 0.05

CaCO2(ml/l)

623 ± 106

611 ± 98

− 12 (− 1.9)

< 0.05

PaCO2 arterial CO2 partial pressure; CaCO2 arterial CO2 content

Fig. 2
Fig. 2

Time course of a arterial CO2 partial pressure and b pH over the study period. After adjusting ventilation parameters to reestablish baseline PaCO2 at 1 h, a trend toward further normalization of hypercapnic acidosis was observed

Ventilation

After ventilator settings were adapted and baseline PaCO2 was reestablished, we recorded a decrease in respiratory minute ventilation from 9.9 ± 2.1 to 8.5 ± 2.1 l/min (− 1.4 l/min, p < 0.05), corresponding to a reduction in tidal volume from 6.2 ± 0.9 to 5.4 ± 1.1 ml/kg of predicted body weight (PBW) (− 0.8 ml/kg, p < 0.05). Plateau pressures decreased from 30.6 ± 4.6 to 27.7 ± 4.1 cmH2O (− 2.9 cmH2O, p < 0.05) and driving pressures from 18.3 ± 4.3 to 15.6 ± 3.9 cmH2O (− 2.7 cmH2O, p < 0.05), respectively (Table 4). Ventilatory parameters showed a trend toward baseline values over the remaining study period (Fig. 3). After reduction in ventilator settings, a lower PaO2 (91.8 ± 23.8 vs. 84.4 ± 18.7 mmHg, p < 0.05) corresponding to a lower oxygenation index (164 ± 38 vs. 151 ± 35 mmHg, p < 0.05) was observed (Table 4).
Table 4

Changes in ventilation and oxygenation parameters between baseline and after reduction in tidal volumes at 1 h

 

Baseline

+ 1 h

Δ (%)

P-value

VT/PBW (ml/kg)

6.2 ± 0.9

5.4 ± 1.1

− 0.8 (− 12.9)

< 0.05

RMV (l/min)

9.9 ± 2.1

8.5 ± 2.1

− 1.4 (− 14.1)

< 0.05

Pplat (cmH2O)

30.6 ± 4.6

27.7 ± 4.1

− 2.9 (− 9.5)

< 0.05

ΔP (cmH2O)

18.3 ± 4.3

15.6 ± 3.9

− 2.7 (− 14.8)

< 0.05

PaO2 (mmHg)

91.8 ± 23.8

84.4 ± 18.7

− 7.4 (− 8.1)

< 0.05

P/F (mmHg)

164 ± 38

151 ± 35

− 13 (− 7.9)

< 0.05

VT tidal volume; PBW predicted body weight; RMV respiratory minute volume; Pplat plateau pressure; ΔP driving pressure; PaO2 arterial O2 partial pressure; P/F oxygenation index

Fig. 3
Fig. 3

Changes in ventilation under ECCO2R over the study period showing a significant decrease in tidal volumes per predicted body weight (a) and respiratory minute ventilation (b) compared to baseline, corresponding to a significant decrease in plateau (c) and driving pressures (d)

Extracorporeal circuit

Out of 20 patients, 16 (80%) completed the 72-h study period. The total running time of the system was 95.8 ± 47.7 h (range 14.5 to 223.4 h). Altogether five systems were lost due to clotting, three of which were replaced and the study continued. There were no interruptions of the therapy due to patient transport. The average activated partial thromboplastin time (aPTT) was 62 ± 16 s after 24 h, 57 ± 19 s after 48 h and 59 ± 20 s after 72 h at an average continuous dose of unfractioned heparin of 1154 ± 556 IU/h, which corresponds to two times the reference range (25–34 s). The targeted blood flow rate of 400 ml/min was reached in 17/20 patients (85%). In the majority of patients (12/20), vascular access was via a jugular Shaldon catheter, whereas a femoral catheter was used in the remaining patients. In two out of three patients in whom the targeted blood flow rate could not be reached, vascular access was via a left jugular Shaldon catheter which was consequently changed. The recorded pressures in the arterial and venous line of the circuit were − 148 ± 27 mmHg and 164 ± 36 mmHg, respectively. Transmembranous pressures in the hemofilter increased continually over time from 46 ± 22 mmHg at baseline to 76 ± 21 mmHg at 72 h, whereas oxygenation performance of the membrane lung (∆PO2) decreased from 350 ± 62 to 311 ± 63 mmHg. Renal replacement was effected by conventional hemofiltration (CVVHF) using bicarbonate-buffered replacement fluids with an average dose of 2615 ± 470 ml/h of total effluent. Renal parameters as well as phosphate levels developed as expected, which resulted in a significant decrease in plasma creatinine (3.30 ± 2.59 vs. 1.42 ± 0.42 mg/dl) and urea (72 ± 50 vs. 31 ± 18 mg/dl) over the study period. Serum bicarbonate did not depart significantly from baseline values. A slight decrease in average thrombocyte count compared to baseline was observed after 24 h (164 ± 75 vs. 184 ± 89 nl−1), and thrombocytes reached baseline levels after 72 h (179 ± 94 nl−1).

Systemic hemodynamics

No adverse cardiovascular effects were observed following implementation of the extracorporeal circuit. Two patients died within 24 h after inclusion due to refractory septic shock. In the remaining patients, hemodynamic improvement with markedly reduced vasopressor requirements (norepinephrine dose 3.1 ± 2.9 vs. 2.4 ± 2.0 mg/h, p < 0.05) and heart rate (103 ± 18 vs. 91 ± 23 bpm, p < 0.05) was recorded after 24 h. Hemodynamics remained stable over the further study period.

Complications

Four patients received blood products during the study; altogether 11 units of packed red blood cells (RBC) and one unit of thrombocytes were transfused. The major part of those blood products (eight units of packed RBC and one unit of thrombocytes) was given to two patients who had previously undergone allogeneic stem cell transplantation, thus confounding transfusion requirements. No bleeding directly attributed to the extracorporeal circuit was reported and no other clinical relevant hematological abnormalities such as signs of hemolysis or hyperfibrinolysis were detected during the course of the study. No other adverse effects were reported.

Discussion

Using a standardized protocol of ventilation based on current ARDS Network recommendations, we were able to demonstrate that the investigated combination therapy was able to ameliorate respiratory acidosis and effectively reduce the invasiveness of mechanical ventilation in hypercapnic critically ill patients while providing efficient renal replacement therapy and exhibiting a positive effect on hemodynamics in terms of vasopressor requirements. While combinations of ECCO2R and CRRT have previously been reported, our study provides the first description of a certified and labeled combination therapy on a commercially available organ support platform. The system was able to eliminate CO2 at a rate between 40 and 50 ml/min, thereby reducing arterial PCO2 significantly by about 10%. The additional integration of a membrane lung into a renal replacement circuit has first been described by Forster et al. [32], who were able to show a reduction in acidosis and decreased vasopressor requirements in ten hypercapnic patients. This concept was taken one step further by Allardet-Servent et al. [33], who were able to realize an ultra-protective ventilation strategy in 11 patients with ARDS using a similar combination. In both of these studies, membrane lungs with surfaces of about 0.7 m2 were used, which resulted in a higher CO2 removal rate and more pronounced correction of acidosis compared to our system, which incorporated a significantly smaller membrane lung (0.32 m2). As has recently been shown by Karagiannidis et al. [35], in low-flow ECCO2R the effectiveness of CO2 extraction is mainly a function of the membrane size. Whereas smaller membrane lungs may have advantages with regard to costs and likelihood of clotting, membrane size must be considered the most important limiting factor of the presented system. Another factor pertaining to combinations of ECCO2R and CRRT is the relative position of membrane lung and hemofilter, which may affect CO2 removal. In [33], the incorporation of the membrane lung downstream of the hemofilter was significantly less effective than in an upstream position. In our study, the CO2 removal rate of the combined system was about 5% lower than the elimination rate of the membrane lung alone, hinting at the same effect. We suggest that the substitution of bicarbonate-rich replacement fluids as a consequence of renal replacement therapy leads to an increase in the CO2 content of extracorporeal blood, thereby counteracting the overall effectiveness of CO2 removal by “loading” the blood with CO2. It would be interesting to investigate whether the use of citrate-based solutions which could also provide effective anticoagulation is associated with a more pronounced CO2 removal effect. Due to the relatively high citrate dosing requirements at the investigated blood flow (400 ml/min), no such combination is currently available.

Though the resulting drop in PaCO2, as is expected in a low-flow setting, is not sufficient to completely correct respiratory acidosis, implementation of the system still allowed for a significant decrease both in tidal volume (− 0.8 ml/kg) and plateau pressure (− 2.9 cmH2O) and in driving pressure (− 2.7 cmH2O). Since the study protocol did not require neuromuscular blockade to prevent spontaneous breathing and consequently only a quarter of the patients received neuromuscular blocking agents at some point during the study, there was considerable heterogeneity in response to plateau pressure reduction following implementation of ECCO2R with some patients counteracting the decreased inspiratory pressures by actively increasing spontaneous breathing efforts, thus mitigating the effect on tidal volume reduction.

In a recent study on the efficacy and safety of low-flow ECCO2R using the same platform in patients without renal failure, a more pronounced reduction in tidal volume and plateau pressure was reported [36]. In that study, all patients were paralyzed, making tidal volume reductions more easy to achieve. Also, the severity of illness was significantly different with a mean SOFA score of 9 as compared to 14 in our study. It is important to note that patients with combined respiratory and renal failure may constitute a different target group for ECCO2R than patients with isolated respiratory failure. In established multi-organ failure with often severe concomitant metabolic acidosis, there is typically an indication for renal replacement therapy, making the integration of an additional gas exchanger in the circuit much less invasive since vascular access is already in place. Our data show that combining ECCO2R with CRRT in the setting multi-organ failure, while being less effective than stand-alone therapies, can still significantly enhance lung protection and may therefore have beneficial effects. In contrast to [36], this effect can be achieved without further raising PaCO2, thus providing much better control of pH. Interestingly, while the additional surface of the hemofilter might be expected to activate coagulation, incidence of circuit clotting was much lower in the combination therapy than in the stand-alone procedure.

As it has been concluded by Gattinoni et al., ventilator-associated lung injury essentially results from the application of mechanical power to the lungs in order to actively eliminate CO2 from the circulation [37, 38]. The components of this mechanical power are tidal volume, driving pressure, PEEP, flow and respiratory rate. Any additional CO2 elimination is therefore capable of reducing the power applied to the lungs and consequently should attenuate ventilator-associated lung injury. This is mirrored in our study by significantly decreased tidal volumes and driving pressures. Although this rationale may seem compelling and comparable strategies have been able to show reduced systemic and pulmonary inflammation in experimental [39, 40] as well as in clinical ARDS [14, 27], to date it has not been demonstrated that ultra-protective ventilation strategies per se can improve clinically relevant patient outcomes.

Although partial extracorporeal CO2 elimination must therefore still be regarded as experimental at this juncture, due to its easy implementation and management, the combination of low-flow ECCO2R and CRRT nevertheless constitutes a safe and effective add-on therapy for ventilated patients with renal failure. Since the procedure runs on an established renal replacement platform and therefore only requires integration of a small membrane lung as well as a moderate increase in blood flow without need for specialized vascular access, the potential for complications seems low. Under systemic anticoagulation, the combined system exhibited reasonable circuit lifetimes and we observed no procedure-related bleeding or other relevant adverse events. This is in marked contrast to ECMO or even mid-flow ECCO2R therapies where higher blood flows can provide total CO2 removal but require large-bore and often multiple vascular access which is associated with significant bleeding risk and other local as well as systemic complications [12–14, 16]. We therefore conclude that combined ECCO2R and CRRT with the investigated system is a feasible and safe approach. However, due to the limited running time of the hemofilter for renal replacement, the system has to be discarded after 72 h, leading potentially to higher costs in prolonged treatments.

Our study has several limitations. In order to keep interference with local practice standards at the three centers at a minimum, no explicit ventilation strategy other than compliance with ARDS Network recommendations was stipulated. After the initial data collections, ventilation strategy was left to the discretion of the treating physician leading to considerable heterogeneity among the study population. With a growing number of spontaneously breathing patients over the study period, the effect of ECCO2R on ventilation is blurred to a considerable degree. Since neuromuscular blockade was not required, even the initial data collections may be significantly influenced by spontaneous breathing efforts. As expected in combined lung and renal failure, metabolic acidosis significantly contributes to overall acid base status. Consequently, in a number of patients, while ECCO2R led to a significant drop in PaCO2, marked overall acidosis remained, preventing a reduction in ventilator settings by the treating physician. We therefore cannot exclude that the overall effect on ventilation is confounded to some degree in this study. Furthermore, the study included only patients who already exhibited severe hypercapnia. Our data therefore allow no statement on the efficiency of the system in a normocapnic or only mildly hypercapnic environment. Due to the limited running time of the system (72 h), we also cannot provide data on long-term clinical effects.

Conclusions

In this study, we present the first description of a combination of extracorporeal CO2 removal and renal replacement therapy on a commercially available organ support platform in mechanically ventilated hypercapnic patients with renal failure. The investigated combination therapy was able to ameliorate hypercapnic acidosis and allow for a decrease in ventilation pressures while providing adequate renal replacement therapy. The system was easy to implement and manage; no severe procedure-related adverse events were observed. Whether strategies aiming at correcting hypercapnia and/or providing ultra-protective ventilation are beneficial for patients with combined lung and renal failure in terms of outcome remains to be demonstrated in future investigations.

Abbreviations

CO2 : 

carbon dioxide

ARDS: 

acute respiratory distress syndrome

ECCO2R: 

extracorporeal CO2 removal

PaCO2 : 

arterial CO2 partial pressure

PBW: 

predicted body weight

ECMO: 

extracorporeal membrane oxygenation

pECLA: 

pumpless extracorporeal lung assist

CRRT: 

continuous renal replacement therapy

aPTT: 

activated partial thromboplastin time

CVVHF: 

continuous veno-venous hemofiltration

RASS: 

Richmond agitation and sedation scale

P plat : 

plateau pressure

BMI: 

body mass index

SAPS: 

Simplified Acute Physiology Score

SOFA: 

Sequential Organ Failure Assessment

COPD: 

chronic obstructive pulmonary disease

CIHD: 

chronic intermittent hemodialysis

NMBA: 

neuromuscular blocking agent

SD: 

standard deviation

HCO3 : 

bicarbonate

CaCO2 : 

arterial CO2 content

SBE: 

standard base excess

SaO2 : 

arterial oxygen saturation

P/F : 

oxygenation index

V T : 

tidal volume

RR: 

respiratory rate

RMV: 

respiratory minute ventilation

PEEP: 

positive end-expiratory pressure

ΔP : 

driving pressure

C dyn : 

dynamical compliance

HR: 

heart rate

MAP: 

mean arterial pressure

PCO2 : 

CO2 partial pressure

PaO2 : 

arterial O2 partial pressure

ΔPO2 : 

O2 partial pressure difference

RBC: 

red blood cells

Declarations

Authors’ contributions

JN, SK and SJ were involved in study protocol and ethics. JN, DW, SL and HM collected the data. JN and SJ prepared the data/statistics. JN, SK, HM and SJ wrote the manuscript. All authors read and approved the final manuscript.

Acknowledgements

Not applicable.

Competing interests

JN received honoraria from Baxter Healthcare Corporation, USA, for oral presentations. SJ received honoraria from Baxter Healthcare Corporation, USA, for oral presentations and is a member of a Medical Advisory Board organized by Baxter. DW received honoraria from Baxter Healthcare Corporation, USA, for oral presentations and is a member of a Medical Advisory Board organized by Baxter. SK is currently on the Medical Advisory Boards of Baxter, Fresenius and Xenios. HM received honoraria from Fresenius Medical Care, Germany, and SALVIA, Germany, for oral presentations.

Availability of data and materials

The datasets generated and analyzed during this study are available from the corresponding author on reasonable request.

Consent for publication

Not applicable.

Ethics Approval and consent to participate

The study was approved by the ethics committee of the Friedrich–Alexander University Erlangen–Nuremberg, Germany, under the reference number 213_14 B. The study has been performed in accordance with the ethical standards laid down in the 1964 Declaration of Helsinki and its later amendments.

Funding

The study was funded by a grant of Baxter Healthcare Corporation, USA. The funding body was not involved in the design of the study or the collection, analysis and interpretation of the data or in the writing of the manuscript.

Publisher’s Note

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Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

Authors’ Affiliations

(1)
Medical Intensive Care, Department of Cardiology, Klinikum Nuremberg, Paracelsus Medical University, Nuremberg, Germany
(2)
Department of Intensive Care Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany
(3)
Department of Anesthesia, Intensive Care Medicine and Pain Therapy, University Hospital Frankfurt, Frankfurt, Germany

References

  1. Acute Respiratory Distress Syndrome Network, Brower RG, Matthay MA, Morris A, Schoenfeld D, Thompson BT, Wheeler A. Ventilation with lower tidal volumes as compared with traditional tidal volumes for acute lung injury and the acute respiratory distress syndrome. N Engl J Med. 2000;342(18):1301–8.View ArticleGoogle Scholar
  2. Amato MB, Barbas CS, Medeiros DM, Magaldi RB, Schettino GP, Lorenzi-Filho G, Kairalla RA, Deheinzelin D, Munoz C, Oliveira R, Takagaki TY, Carvalho CR. Effect of a protective-ventilation strategy on mortality in the acute respiratory distress syndrome. N Engl J Med. 1998;338(6):347–54.View ArticleGoogle Scholar
  3. ARDS Definition Task Force, Ranieri VM, Rubenfeld GD, Thompson BT, Ferguson ND, Caldwell E, Fan E, Camporota L, Slutsky AS. Acute respiratory distress syndrome: the Berlin definition. JAMA. 2012;307(23):2526–33. https://doi.org/10.1001/jama.2012.5669.View ArticleGoogle Scholar
  4. Slutsky AS, Ranieri VM. Ventilator-induced lung injury. N Engl J Med. 2013;369(22):2126–36. https://doi.org/10.1056/NEJMra1208707.View ArticlePubMedGoogle Scholar
  5. Terragni PP, Rosboch G, Tealdi A, Corno E, Menaldo E, Davini O, Gandini G, Herrmann P, Mascia L, Quintel M, Slutsky AS, Gattinoni L, Ranieri VM. Tidal hyperinflation during low tidal volume ventilation in acute respiratory distress syndrome. Am J Respir Crit Care Med. 2007;175(2):160–6.View ArticleGoogle Scholar
  6. Curley G, Hayes M, Laffey JG. Can ‘permissive’ hypercapnia modulate the severity of sepsis-induced ALI/ARDS? Crit Care. 2011;15(2):212. https://doi.org/10.1186/cc9994.View ArticlePubMedPubMed CentralGoogle Scholar
  7. Ismaiel NM, Henzler D. Effects of hypercapnia and hypercapnic acidosis on attenuation of ventilator-associated lung injury. Minerva Anestesiol. 2011;77(7):723–33.PubMedGoogle Scholar
  8. Vadász I, Hubmayr RD, Nin N, Sporn PH, Sznajder JI. Hypercapnia: a nonpermissive environment for the lung. Am J Respir Cell Mol Biol. 2012;46(4):417–21. https://doi.org/10.1165/rcmb.2011-0395ps.View ArticlePubMedPubMed CentralGoogle Scholar
  9. Curley G, Contreras MM, Nichol AD, Higgins BD, Laffey JG. Hypercapnia and acidosis in sepsis: a double-edged sword? Anesthesiology. 2010;112(2):462–72. https://doi.org/10.1097/ALN.0b013e3181ca361f.View ArticlePubMedGoogle Scholar
  10. Nin N, Muriel A, Peñuelas O, Brochard L, Lorente JA, Ferguson ND, Raymondos K, Ríos F, Violi DA, Thille AW, González M, Villagomez AJ, Hurtado J, Davies AR, Du B, Maggiore SM, Soto L, D’Empaire G, Matamis D, Abroug F, Moreno RP, Soares MA, Arabi Y, Sandi F, Jibaja M, Amin P, Koh Y, Kuiper MA, Bülow HH, Zeggwagh AA, Anzueto A, Sznajder JI, Esteban A, VENTILA Group. Severe hypercapnia and outcome of mechanically ventilated patients with moderate or severe acute respiratory distress syndrome. Intensive Care Med. 2017;43(2):200–8. https://doi.org/10.1007/s00134-016-4611-1.View ArticlePubMedPubMed CentralGoogle Scholar
  11. Tiruvoipati R, Pilcher D, Buscher H, Botha J, Bailey M. Effects of hypercapnia and hypercapnic acidosis on hospital mortality in mechanically ventilated patients. Crit Care Med. 2017;45(7):e649–56. https://doi.org/10.1097/CCM.0000000000002332.View ArticlePubMedGoogle Scholar
  12. Kreppein U, Litterst P, Westhoff M. Hypercapnic respiratory failure. Pathophysiology, indications for mechanical ventilation and management. Med Klin Intensivmed Notfmed. 2016;111(3):196–201. https://doi.org/10.1007/s00063-016-0143-2.View ArticlePubMedGoogle Scholar
  13. Bein T, Zimmermann M, Hergeth K, Ramming M, Rupprecht L, Schlitt HJ, Slutsky AS. Pumpless extracorporeal removal of carbon dioxide combined with ventilation using low tidal volume and high positive end-expiratory pressure in a patient with severe acute respiratory distress syndrome. Anaesthesia. 2009;64(2):195–8. https://doi.org/10.1111/j.1365-2044.2008.05735.x.View ArticlePubMedGoogle Scholar
  14. Bein T, Weber-Carstens S, Goldmann A, Müller T, Staudinger T, Brederlau J, Muellenbach R, Dembinski R, Graf BM, Wewalka M, Philipp A, Wernecke KD, Lubnow M, Slutsky AS. Lower tidal volume strategy (≈ 3 ml/kg) combined with extracorporeal CO2 removal versus ‘conventional’ protective ventilation (6 ml/kg) in severe ARDS: the prospective randomized Xtravent-study. Intensive Care Med. 2013;39(5):847–56. https://doi.org/10.1007/s00134-012-2787-6.View ArticlePubMedPubMed CentralGoogle Scholar
  15. Gattinoni L, Kolobow T, Tomlinson T, White D, Pierce J. Control of intermittent positive pressure breathing (IPPB) by extracorporeal removal of carbon dioxide. Br J Anaesth. 1978;50(8):753–8.View ArticleGoogle Scholar
  16. Braune S, Sieweke A, Jarczak D, Kluge S. Extracorporeal lung support. Med Klin Intensivmed Notfmed. 2017;112(5):426–36. https://doi.org/10.1007/s00063-017-0304-y.View ArticlePubMedGoogle Scholar
  17. Mosier JM, Kelsey M, Raz Y, Gunnerson KJ, Meyer R, Hypes CD, Malo J, Whitmore SP, Spaite DW. Extracorporeal membrane oxygenation (ECMO) for critically ill adults in the emergency department: history, current applications, and future directions. Crit Care. 2015;17(19):431. https://doi.org/10.1186/s13054-015-1155-7.View ArticleGoogle Scholar
  18. Peek GJ, Mugford M, Tiruvoipati R, Wilson A, Allen E, Thalanany MM, Hibbert CL, Truesdale A, Clemens F, Cooper N, Firmin RK, Elbourne D. CESAR trial collaboration. Efficacy and economic assessment of conventional ventilatory support versus extracorporeal membrane oxygenation for severe adult respiratory failure (CESAR): a multicentre randomised controlled trial. Lancet. 2009;374(9698):1351–63. https://doi.org/10.1016/s0140-6736(09)61069-2.View ArticlePubMedGoogle Scholar
  19. Staudinger T. Extracorporeal membrane oxygenation: system selection, (contra)indications, and management. Med Klin Intensivmed Notfmed. 2017;112(4):295–302. https://doi.org/10.1007/s00063-017-0279-8.View ArticlePubMedGoogle Scholar
  20. Millar JE, Fanning JP, McDonald CI, McAuley DF, Fraser JF. The inflammatory response to extracorporeal membrane oxygenation (ECMO): a review of the pathophysiology. Crit Care. 2016;20(1):387.View ArticleGoogle Scholar
  21. Murphy DA, Hockings LE, Andrews RK, Aubron C, Gardiner EE, Pellegrino VA, Davis AK. Extracorporeal membrane oxygenation-hemostatic complications. Transfus Med Rev. 2015;29(2):90–101. https://doi.org/10.1016/j.tmrv.2014.12.001.View ArticlePubMedGoogle Scholar
  22. Zangrillo A, Landoni G, Biondi-Zoccai G, Greco M, Greco T, Frati G, Patroniti N, Antonelli M, Pesenti A, Pappalardo F. A meta-analysis of complications and mortality of extracorporeal membrane oxygenation. Crit Care Resusc. 2013;15(3):172–8.PubMedGoogle Scholar
  23. Braune S, Sieweke A, Brettner F, Staudinger T, Joannidis M, Verbrugge S, Frings D, Nierhaus A, Wegscheider K, Kluge S. The feasibility and safety of extracorporeal carbon dioxide removal to avoid intubation in patients with COPD unresponsive to noninvasive ventilation for acute hypercapnic respiratory failure (ECLAIR study): multicentre case-control study. Intensive Care Med. 2016;42(9):1437–44. https://doi.org/10.1007/s00134-016-4452-y.View ArticlePubMedGoogle Scholar
  24. Hermann A, Riss K, Schellongowski P, Bojic A, Wohlfarth P, Robak O, Sperr WR, Staudinger T. A novel pump-driven veno-venous gas exchange system during extracorporeal CO2-removal. Intensive Care Med. 2015;41(10):1773–80. https://doi.org/10.1007/s00134-015-3957-0.View ArticlePubMedGoogle Scholar
  25. Livigni S, Maio M, Ferretti E, Longobardo A, Potenza R, Rivalta L, Selvaggi P, Vergano M, Bertolini G. Efficacy and safety of a low-flow veno-venous carbon dioxide removal device: results of an experimental study in adult sheep. Crit Care. 2006;10(5):R151.View ArticleGoogle Scholar
  26. Batchinsky AI, Jordan BS, Regn D, Necsoiu C, Federspiel WJ, Morris MJ, Cancio LC. Respiratory dialysis: reduction in dependence on mechanical ventilation by venovenous extracorporeal CO2 removal. Crit Care Med. 2011;39(6):1382–7. https://doi.org/10.1097/CCM.0b013e31820eda45.View ArticlePubMedGoogle Scholar
  27. Terragni PP, Del Sorbo L, Mascia L, Urbino R, Martin EL, Birocco A, Faggiano C, Quintel M, Gattinoni L, Ranieri VM. Tidal volume lower than 6 ml/kg enhances lung protection: role of extracorporeal carbon dioxide removal. Anesthesiology. 2009;111(4):826–35. https://doi.org/10.1097/ALN.0b013e3181b764d2.View ArticlePubMedGoogle Scholar
  28. Esteban A, Alía I, Gordo F, de Pablo R, Suarez J, González G, Blanco J. Prospective randomized trial comparing pressure-controlled ventilation and volume-controlled ventilation in ARDS, For the Spanish Lung Failure Collaborative Group. Chest. 2000;117(6):1690–6.View ArticleGoogle Scholar
  29. Liu KD, Matthay MA. Advances in critical care for the nephrologist: acute lung injury/ARDS. Clin J Am Soc Nephrol. 2008;3(2):578–86. https://doi.org/10.2215/cjn.01630407.View ArticlePubMedGoogle Scholar
  30. Faubel S, Edelstein CL. Mechanisms and mediators of lung injury after acute kidney injury. Nat Rev Nephrol. 2016;12(1):48–60. https://doi.org/10.1038/nrneph.2015.158.View ArticlePubMedGoogle Scholar
  31. John S, Willam C. Lung and kidney failure. Pathogenesis, interactions, and therapy. Med Klin Intensivmed Notfmed. 2015;110(6):452–8. https://doi.org/10.1007/s00063-014-0404-x.View ArticlePubMedGoogle Scholar
  32. Forster C, Schriewer J, John S, Eckardt KU, Willam C. Low-flow CO2 removal integrated into a renal-replacement circuit can reduce acidosis and decrease vasopressor requirements. Crit Care. 2013;17(4):R154. https://doi.org/10.1186/cc12833.View ArticlePubMedPubMed CentralGoogle Scholar
  33. Allardet-Servent J, Castanier M, Signouret T, Soundaravelou R, Lepidi A, Seghboyan JM. Safety and efficacy of combined extracorporeal CO2 removal and renal replacement therapy in patients with acute respiratory distress syndrome and acute kidney injury: the pulmonary and renal support in acute respiratory distress syndrome study. Crit Care Med. 2015;43(12):2570–81. https://doi.org/10.1097/CCM.0000000000001296.View ArticlePubMedPubMed CentralGoogle Scholar
  34. Godet T, Combes A, Zogheib E, Jabaudon M, Futier E, Slutsky AS, Constantin JM. Novel CO2 removal device driven by a renal-replacement system without hemofilter. A first step experimental validation. Anaesth Crit Care Pain Med. 2015;34(3):135–40. https://doi.org/10.1016/j.accpm.2014.08.006.View ArticlePubMedGoogle Scholar
  35. Karagiannidis C, Strassmann S, Brodie D, Ritter P, Larsson A, Borchardt R, Windisch W. Impact of membrane lung surface area and blood flow on extracorporeal CO(2) removal during severe respiratory acidosis. Intensive Care Med Exp. 2017;5(1):34. https://doi.org/10.1186/s40635-017-0147-0.View ArticlePubMedPubMed CentralGoogle Scholar
  36. Schmidt M, Jaber S, Zogheib E, Godet T, Capellier G, Combes A. Feasibility and safety of low-flow extracorporeal CO(2) removal managed with a renal replacement platform to enhance lung-protective ventilation of patients with mild-to-moderate ARDS. Crit Care. 2018;22(1):122. https://doi.org/10.1186/s13054-018-2038-5.View ArticlePubMedPubMed CentralGoogle Scholar
  37. Gattinoni L, Tonetti T, Cressoni M, Cadringher P, Herrmann P, Moerer O, Protti A, Gotti M, Chiurazzi C, Carlesso E, Chiumello D, Quintel M. Ventilator-related causes of lung injury: the mechanical power. Intensive Care Med. 2016;42(10):1567–75. https://doi.org/10.1007/s00134-016-4505-2.View ArticlePubMedGoogle Scholar
  38. Gattinoni L, Marini JJ, Collino F, Maiolo G, Rapetti F, Tonetti T, Vasques F, Quintel M. The future of mechanical ventilation: lessons from the present and the past. Crit Care. 2017;21(1):183. https://doi.org/10.1186/s13054-017-1750-x.View ArticlePubMedPubMed CentralGoogle Scholar
  39. Grasso S, Stripoli T, Mazzone P, Pezzuto M, Lacitignola L, Centonze P, Guarracino A, Esposito C, Herrmann P, Quintel M, Trerotoli P, Bruno F, Crovace A, Staffieri F. Low respiratory rate plus minimally invasive extracorporeal Co2 removal decreases systemic and pulmonary inflammatory mediators in experimental acute respiratory distress syndrome. Crit Care Med. 2014;42(6):e451–60. https://doi.org/10.1097/CCM.0000000000000312.View ArticlePubMedGoogle Scholar
  40. Güldner A, Kiss T, Bluth T, Uhlig C, Braune A, Carvalho N, Quast T, Rentzsch I, Huhle R, Spieth P, Richter T, Saddy F, Rocco PR, Kasper M, Koch T, Pelosi P, de Abreu MG. Effects of ultraprotective ventilation, extracorporeal carbon dioxide removal, and spontaneous breathing on lung morphofunction and inflammation in experimental severe acute respiratory distress syndrome. Anesthesiology. 2015;122(3):631–46. https://doi.org/10.1097/ALN.0000000000000504.View ArticlePubMedGoogle Scholar

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© The Author(s) 2019

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