key: cord-010772-e7kfe87q
authors: Hospach, Ingeborg; Goldstein, Jacques; Harenski, Kai; Laffey, John G.; Pouchoulin, Dominique; Raible, Manuela; Votteler, Stefanie; Storr, Markus
title: In vitro characterization of PrismaLung+: a novel ECCO(2)R device
date: 2020-05-13
journal: Intensive Care Med Exp
DOI: 10.1186/s40635-020-00301-7
sha: 
doc_id: 10772
cord_uid: e7kfe87q

BACKGROUND: Invasive mechanical ventilation is lifesaving in the setting of severe acute respiratory failure but can cause ventilation-induced lung injury. Advances in extracorporeal CO(2) removal (ECCO(2)R) technologies may facilitate more protective lung ventilation in acute respiratory distress syndrome, and enable earlier weaning and/or avoid invasive mechanical ventilation entirely in chronic obstructive pulmonary disease exacerbations. We evaluated the in vitro CO(2) removal capacity of the novel PrismaLung+ ECCO(2)R device compared with two existing gas exchangers. METHODS: The in vitro CO(2) removal capacity of the PrismaLung+ (surface area 0.8 m(2), Baxter) was compared with the PrismaLung (surface area 0.35 m(2), Baxter) and A.L.ONE (surface area 1.35 m(2), Eurosets) devices, using a closed-loop bovine blood–perfused extracorporeal circuit. The efficacy of each device was measured at varying pCO(2) inlet (p(in)CO(2)) levels (45, 60, and 80 mmHg) and blood flow rates (Q(B)) of 200–450 mL/min; the PrismaLung+ and A.L.ONE devices were also tested at a Q(B) of 600 mL/min. The amount of CO(2) removed by each device was assessed by measurement of the CO(2) infused to maintain circuit equilibrium (CO(2) infusion method) and compared with measured CO(2) concentrations in the inlet and outlet of the CO(2) removal device (blood gas analysis method). RESULTS: The PrismaLung+ device performed similarly to the A.L.ONE device, with both devices demonstrating CO(2) removal rates ~ 50% greater than the PrismaLung device. CO(2) removal rates were 73 ± 4.0, 44 ± 2.5, and 72 ± 1.9 mL/min, for PrismaLung+, PrismaLung, and A.L.ONE, respectively, at Q(B) 300 mL/min and p(in)CO(2) 45 mmHg. A Bland–Altman plot demonstrated that the CO(2) infusion method was comparable to the blood gas analysis method for calculating CO(2) removal. The resistance to blood flow across the test device, as measured by pressure drop, varied as a function of blood flow rate, and was greatest for PrismaLung and lowest for the A.L.ONE device. CONCLUSIONS: The newly developed PrismaLung+ performed more effectively than PrismaLung, with performance of CO(2) removal comparable to A.L.ONE at the flow rates tested, despite the smaller membrane surface area of PrismaLung+ versus A.L.ONE. Clinical testing of PrismaLung+ is warranted to further characterize its performance.

Patients with severe acute hypoxemic and/or hypercapnic respiratory failure require invasive mechanical ventilation (IMV) to facilitate gas exchange and to support breathing. While IMV may be lifesaving in this setting, it is associated with significant short-and long-term side effects. Consequently, there is considerable interest in developing strategies such as extracorporeal CO 2 removal (ECCO 2 R), which can facilitate CO 2 removal [1] , or extracorporeal membrane oxygenation (ECMO), which, in addition, provides oxygenation in instances of severe hypoxemic respiratory failure [2] . These approaches may enable reductions in the intensity and/or the duration of IMV in these patients.

In patients with severe hypoxemia, particularly those with acute respiratory distress syndrome (ARDS), the loss of alveolar ventilation capacity due to alveolar consolidation, edema and/or collapse contributes to the need for ventilatory support [3] . The discovery that high tidal and minute ventilation strategies can cause harm-termed "ventilator-induced lung injury" (VILI ) [4] [5] [6] -has led to the use of lung "protective" ventilation (LPV) strategies, where low tidal volumes (4-8 mL/kg of per body weight [PBW ] [7] versus 10-15 mL/kg of PBW in conventional mechanical ventilation [MV ] [6] ) decrease lung stretch, reduce VILI [8] , and can potentially improve survival and reduce mortality in patients with acute lung injury and ARDS [6, 9] . Amato et al. showed that lower driving pressure was the physical variable that best correlated with survival in patients with ARDS [10] ; higher positive end-expiratory pressure (PEEP), lower peak and plateau pressures, and lower respiratory rate, may also be associated with improved survival [11, 12] .

The use of lower tidal and minute volumes with LPV strategies is limited by the resultant respiratory acidosis [13] [14] [15] . The rationale to integrate ECCO 2 R into the management of severe ARDS is to allow more protective ventilation, i.e., providing very low tidal volumes (V T ) (less than 6 mL/kg PBW) with conventional MV, while avoiding extreme levels of respiratory acidosis. Arterial CO 2 tensions are generally maintained in the range 45-60 mmHg rather than targeting normocapnia with this approach [16] . The potential for use of ECCO 2 R in patients with ARDS has been evidenced in a number of clinical studies [17] [18] [19] , indicating it may be an effective strategy in ARDS management and a viable option to further reduce tidal and minute volumes in these patients [15, 16] .

In patients with acute exacerbations of chronic obstructive pulmonary disease (aeCOPD), where hypercapnia is predominant, non-invasive positive pressure ventilation (NIV) is used as a first-line strategy in order to avoid MV [20] . Use of NIV has been reported to reduce mortality by approximately 70% [21] ; however, in some patients, additional assistance is required to prevent the need for intubation [22] . NIV fails in almost 40% of cases, and patients must undergo endotracheal intubation and IMV to restore adequate gas exchange [22] [23] [24] [25] . There is increasing clinical evidence supporting the use of low-flow, partial ECCO 2 R for patients experiencing aeCOPD who are failing support with NIV [22] , avoiding the need for IMV and/or decreasing the length of time on the ventilator [26] .

Advances in extracorporeal device technologies have made selective ECCO 2 R devices a less invasive and more feasible option than ECMO, with several devices clinically available that utilize blood flow rates between 180 mL/min and 1700 mL/ min [27] . However, these devices were historically designed for use as oxygenators for ECMO treatment in the neonatal or pediatric setting, rather than being optimized for CO 2 removal [28] . Here, we describe a newly developed ECCO 2 R device, the PrismaLung+ (Additional file 1: Figure S1 ), created specifically for CO 2 removal. We compared the in vitro CO 2 removal rates during low blood flow (Q B 200-450 mL/min) of three devices: PrismaLung+ (Baxter), PrismaLung (Baxter), and Eurosets A.L.ONE (Eurosets) , and during a Q B of 600 mL/min for the Prisma-Lung+ and A.L.ONE devices [29] [30] [31] . We hypothesized that PrismaLung+ with a membrane surface area of 0.8 m 2 provides significantly higher CO 2 removal rates than PrismaLung (surface area 0.35 m 2 ), whereas we expected similar performance for PrismaLung+ and the A.L.ONE device (surface area 1.35 m 2 ), since with increasing membrane surface area, the low blood flow rates limit CO 2 removal.

In vitro experimentation to determine CO 2 removal rates was performed using three different ECCO 2 R devices: PrismaLung+ (Baxter), PrismaLung (Baxter), and Eurosets A.L.ONE (Eurosets) ( Table 1) . The devices were selected as they had the same membrane composition, i.e., polymethylpentene hollow-fiber mats, in order to remove this potential source of variability from the experiments. Five test devices of each type were Test media bovine blood parameters were adjusted as listed in Table 2 . NaCl and NaHCO 3 solutions were used to adjust the required ranges of blood parameters. The experimental setup was a closed-loop circuit in which a continuous CO 2 infusion balanced the CO 2 removal from the test gas exchanger to establish a steady-state condition and allowing the CO 2 removal rate to be determined (Fig. 1 ). The total amount of blood used in the circuit was approximately 600-700 mL. The test setup comprised the following: blood reservoir, 250 ml Duran glass bottle (Schott AG, Germany) with a temperature sensor Pt100 (Technetics, Germany); tubing (Promedt, Germany) with inserted septum as sample port and valves; 2 × peristaltic blood pumps (made in-house, Baxter, Germany); datalogger for sensor read-out mikromec® logger (Technetics, Germany); control loop: gas exchanger for CO 2 input, PrismaLung (Baxter, Germany) (closed at gas outlet with plugs), a Thermax blood warmer bag (Baxter, France) inside an in-house made holder, and water bath with thermostat EH (Julabo, Germany); CO 2 gas bottle ≥ 99.5% purity (Linde, Germany) including pressure regulator and gas tubing; CO 2 mass flow regulator GSC-A9TA-BB22 (Vögtlin, Switzerland); 2 × pressure sensor, PE2 bar (Technetics, Germany); Test loop: sweep gas mass flow regulator GSC-C9TA-BB12 (Vögtlin, Switzerland); 3 × pressure sensor, PE1 bar (Technetics, Germany); syringe pump 540270 (TSE Systems, Germany); compressed air as sweep gas (in-house) including pressure regulator and tubing. Blood samples were analyzed with an ABL 90 blood gas analyzer (Radiometer, Germany) .

Before use, an integrity test of the CO 2 infusion circuit was performed, after which the whole test setup, including test devices, was primed with saline or dialysate solution (e.g., Prismasol 2, Baxter) to remove all air. The setup was then filled with bovine blood and all saline or dialysate solution was replaced. The test circuit comprised a central reservoir filled with 200-300 mL of blood as well as two loops. The control loop had a gas exchanger connected to a CO 2 supply, which was used to achieve the targeted p in CO 2 levels. In addition, a blood warming system, where the blood warmer bag was submerged in a water bath, was used to maintain blood pool temperature at 37 ± 1°C. The control loop was fed through the central reservoir then connected to the test loop in which the test device was attached, and CO 2 removal was determined. Loss of water due to evaporation through the membrane and into the sweep gas was balanced by infusion of reverse osmosis water. The sodium concentration was kept constant throughout experimentation, as analyzed by the blood gas analyzer, to maintain a constant water flow.

When the test was initiated, the blood flow of the control loop was set to 500 mL/ min and the sweep gas flow was set at the targeted rate. The CO 2 inlet flow was adjusted in a stepwise fashion to maintain p in CO 2 at the targeted value and to reach steady-state conditions (constant values for p in CO 2 , CO 2 inflow rate, CO 2 removal rate). The pCO 2 value was measured by blood gas analysis, after samples were taken at the blood inlet of the test device. Following an equilibration time of at least 13 minutes, during which CO 2 removal from the test circuit was demonstrated to be balanced by CO 2 addition to the control loop, CO 2 removal rate was determined based on the CO 2 inflow rate. If blood samples were taken, a syringe with a volume of 0.5-1 mL was used. On average, no more than 2-3 blood sample measurements were necessary to confirm a steady state, which is below 0.5% of the total circuit blood volume. For each test device, at all requested test parameters (9 settings of varying Q B and p in CO 2 , Table 3 in the Appendix), measurements were taken at the inlet and outlet, with samples taken in triplicate. PO 2 inlet values (160-183 mmHg) indicated that the blood used in this study was oxygen saturated. All devices were tested at Q B 200, 300, and 450 mL/min, with additional testing of the PrismaLung+ and A.L.ONE devices at Q B 600 mL/min and p in CO 2 45 mmHg. Test conditions are outlined in Table 2 .

The primary method utilized for measuring CO 2 removal was the infusion method, which was validated using the blood gas analysis method. In the infusion method, normalized CO 2 removal rate (JCO 2(inf) ) was determined based on the CO 2 input flow rate at equilibrium, controlled by sample taking and analysis at the inlet. The blood gas analysis method utilized the same setup as the infusion method, but blood samples were taken additionally after the test device, at the outlet. Only samples, where measured pCO 2 and/or pH were inside the reportable range (i.e., pCO 2 > 12 mmHg, pH < 7.85) were used to validate the data from the infusion method.

Prior to the series of experiments, the suitability of the analyzer, with respect to its intended use, was verified through the measurement principles of the blood gas analyzer [32, 33] , to ensure that the device was able to measure bovine parameters. Furthermore, the same device was used for all replicates. Measurements taken included the analysis of ctHb (g/dL), pH, pCO 2 (mmHg), pO 2 (mmHg), and FMetHb (%) ( Table  3 in the Appendix). Following experimentation, an integrity test of the circuit was again performed to confirm its CO 2 gas integrity.

Mean values were determined from triplicate measurements.

In the infusion method, JCO 2(inf) was determined based on CO 2 input flow rate, using the following equation:

where QCO 2 is the CO 2 input flow within the control loop, p in CO 2(ref) is the target inlet pCO 2 of 45, 60, or 80 mmHg, and p in CO 2(inlet) is the actual partial pressure of CO 2 in the blood reservoir or gas exchanger inlet. p in CO 2 was normalized to reduce variability in measurements resulting from small deviations from target p in CO 2 values (± 10%). QCO 2 values are referred to in mL/min under normal conditions (0°C, 1013 mbar) and are re-calculated where appropriate, applying the ideal gas equation:

where Q (T) is the volumetric flow at a defined temperature (T, in°C). The temperatures used for calculation ranged from 0 to 37°C. Note: the atmospheric pressure is assumed to be constant at 1013 mbar. In addition, using the more commonly utilized blood gas analysis method, the normalized CO 2 removal rate (JCO 2(BGA) ) was determined according to the following equation: 

where V m is the temperature-dependent molar volume; Q B is the blood flow within the test loop; ctCO 2 is the total blood concentration of CO 2 (given by the blood gas analyzer, derived from pH, pCO 2 , saturation of oxygen sO 2 , and hemoglobin concentration); p in CO 2(ref) is the target inlet pCO 2 of 45, 60, or 80 mmHg; and p in CO 2(inlet) is the partial pressure of CO 2 in blood. CO 2 removal rates were additionally calculated in units of mmol/min to remove any dependency of reported values upon pressure and reference temperature.

A total of 5 test runs were performed for each device and parameter settings. Data are expressed as mean ± SD and the normal distribution of the data sets was assessed using the Kolmogrov-Smirnov Test (α = 0.05). CO 2 removal performance results were compared using an ANOVA test with p values of < 0.05 considered as indicating a significant difference. Bland-Altman analysis was used to compare the two different performance test methods, generated using Sigmaplot software [34, 35] . A linear regression comparing both methods was additionally used. A paired t test was used to compare data obtained via the infusion and blood gas analysis methods.

The CO 2 removal rates of the different devices were analyzed using the infusion method at p in CO 2 levels (45, 60, and 80 mmHg) and Q B (200, 300, and 450 mL/min), at 37°C (Fig. 2 a-c, Table 4 in the Appendix). The A.L.ONE and PrismaLung+ devices provided comparable CO 2 removal rates across the range of different test conditions (p > 0.05, not significant). For both devices, removal rates were significantly higher than those observed with the PrismaLung device (p < 0.05). CO 2 removal rates at an increased blood flow rate of 600 mL/min were additionally evaluated for the PrismaLung+ and A.L.ONE devices only and were comparable for both devices (p > 0.05) (Additional file 2: Figure S2 ). At a p in CO 2 of 45 mmHg, at 37°C, the mean CO 2 removal rates at a blood flow rate of 600 mL/min were 106 ± 3.8 mL/min and 106 ± 5.8 mL/min for the PrismaLung+ and A.L.ONE devices, respectively.

As the volume flow of gases, i.e., the CO 2 removal rate, is temperature-and pressure-dependent, data were calculated at standard reference conditions, 0°C and 25°C (STP as defined by IUPAC), in addition to the physiological conditions, 37°C, for the PrismaLung+ device at a p in CO2 of 45 mmHg and Q B range of 200-450 mL/min (Fig. 3a) . Results illustrate the dependence of CO 2 removal on the chosen reference temperature. By definition, calculation of CO 2 removal rates in mmol/min across Q B 200-450 mL/min, at a p in CO 2 of 45 mmHg, is independent from any reference temperature (Fig. 3b) .

To examine the blood flow resistance for each device, pressure drop was analyzed at the blood side, for all p in CO 2 levels (45, 60, and 80 mmHg). Pressure drop was observed to be largest for the PrismaLung, and lowest for the A. 

The CO 2 removal performances were analyzed using the infusion and blood gas analysis methods. However, at the lower blood flow rates, many of the outlet samples were below the measuring range of pCO 2 , among others, using the blood gas analyzer method. A comparison of the two methods using a Bland-Altman analysis (Fig. 5a) and linear regression analysis (Fig. 5b) across the different p in CO 2 levels (45, 60, and 80 mmHg) and blood flow rates (200, 300, and 450 mL/min), using valid data within the reportable range of the blood gas analyzer used, indicated a linear relationship between the data obtained by the two methods, suggesting comparability. Statistical analysis revealed that CO 2 removal performance values obtained with the infusion method were, on average, 4.2 mL greater than the values obtained with blood gas analysis (p < 0.05). In addition, the difference was shown to be independent of the test conditions and a constant offset between the two methods. The infusion method was used for the analysis of the full data set as the two methods are similar in terms of validity. 

In this in vitro study, the CO 2 removal performance of the new PrismaLung+ device was comparable to the A.L.ONE device, with both devices demonstrating CO 2 removal rates~50% greater than the PrismaLung device. The performance of the three devices was consistent over a range of blood p in CO 2 levels and at flow rates from 200 to 450 mL/min, with both the PrismaLung+ and A.L.ONE devices also performing comparably at the higher flow rate of 600 mL/min. CO 2 removal data obtained with the CO 2 infusion method were comparable to those obtained with the blood gas analysis method. The resistance to blood flow across the test device, as measured by pressure drop, varied as a function of blood flow rate, being greatest for the PrismaLung, intermediate for the PrismaLung+, and lowest for the A.L.ONE device, most likely driven by the differences in the surface areas. Taken together with prior clinical studies of ECCO 2 R devices [17] [18] [19] 22] , these findings suggest that the PrismaLung+ may be an effective device and further testing in the clinical setting is warranted.

Rationale for CO 2 removal ECCO 2 R technologies may have important roles in the management of patients with ARDS and patients with aeCOPD. ECCO 2 R can help facilitate lung-protective strategies by enabling very low V T (< 6 mL/kg PBW) ventilation [36, 37] . The safety and feasibility of ECCO 2 R has been demonstrated in multiple studies [16, 18, 19] of patients with ARDS, with reduced lung injury and benefits in terms of pulmonary inflammation with low V T ventilation [17] . Several studies also support the use of ECCO 2 R in patients with aeCOPD requiring ventilatory support [38] [39] [40] [41] [42] .

Devices with reduced blood flow requirements will, by design, be less efficient at removing CO 2 than higher flow devices, but they do have several advantages. The PrismaLung+ device in this study has a design tailored to specifically remove CO 2 . The lack of a need for a heat exchanger inside the device allows for reduced size and weight, given that a heat exchanger is available for use next to the machine during treatment. The new PrismaLung+ device has the lowest ratio of blood volume to membrane surface of the tested devices reducing the risks associated with large extracorporeal blood volumes. The removal of the heater also allows for a streamlined design, which should reduce the potential for pooling and low flows of blood within the device. Further aspects of the device design, including the fluid path and dimensional parameters, have been developed to enable an intended operating blood flow of 200 to 450 mL/min. Namely blood flow velocity distribution was calculated to avoid stagnant areas or areas with very low blood flow velocity and to ensure that channeling of the blood did not occur. The residual volume space is smaller than other devices, minimizing the space for blood to clot. The ratio of CO 2 removal rate to blood volume of the PrismaLung+ device allows for optimized performance at these flow rates. It has been shown that an extracorporeal CO 2 removal rate of 51 ± 26 mL/min was associated with an increase in PaCO 2 from 43 ± 8 to 53 ± 9 mmHg when applying low tidal volume ventilation (V T = 4 mL/kg) in patients with mild-to-moderate ARDS [43] . Whereas a mean CO 2 removal of 81 ± 9 mL/min enabled a reduction in V T to 4.29 ± 9 mL/min without an increase in PaCO 2 of more than 10% [19] . Therefore, larger CO 2 removal rates are desirable to allow ultraprotective ventilation in ARDS patients without a significant increase in PaCO 2 . Furthermore, it is assumed that a reduced interaction between blood and foreign material, i.e., a preferably small device, may potentially support biocompatibility [44] . The streamlined design of Prismalung+ might require less anticoagulation, which entails a lower risk of bleeding complications in patients, as there is less potential for pooling and low flows of blood within the device. This hypothesis needs to be investigated in future studies. An advantage of lower flow ECCO 2 R devices is that smaller bore catheters can be used. A second advantage is that they may be integrated with other organ support strategies familiar to critical care physicians and nurses, such as continuous renal replacement therapy (CRRT), making these approaches much more feasible in the busy critical care environment. The potential to integrate ECCO 2 R into continuous renal replacement circuits may improve the risk/benefit ratio for hypercapnic patients with acute kidney injury (AKI) [45] . If effective, such devices could also be used in patients that do not have AKI, given the familiarity of the critical care team with this equipment. A feasibility study demonstrated that the use of a low-flow ECCO 2 R device managed with an RRT platform easily and safely enabled very-low-tidal-volume ventilation with moderate increase in PaCO 2 in patients with mild-to-moderate ARDS [43] .

In this study, the new PrismaLung+ device performed similarly to the A.L.ONE device, with both devices demonstrating CO 2 removal rates~50% greater than the PrismaLung device. While the increase in CO 2 removal observed with PrismaLung+ compared with PrismaLung can, at least in part, be explained by an increase in membrane surface area from 0.35 m 2 to 0.8 m 2 , the similarities observed for Pris-maLung+ and A.L.ONE occurred despite an increase in surface area, suggesting a more complex explanation. Recent data from Karagiannidis and colleagues suggest that the capability of different ECCO 2 R devices to eliminate CO 2 is dependent upon a dynamic interplay within the device between the surface area available for gas exchange and the blood flow rate [44] . Devices with gas exchange membrane surface areas ranging from 0.35 m 2 (e.g., PrismaLung) up to 1.3 m 2 (e.g., A.L.ONE) are currently used in clinical practice [19, 22, 26, [46] [47] [48] . Furthermore, recent in vitro and in silico studies suggest that CO 2 removal rate can increase with increasing blood flow rate [49, 50] , in line with the observations we report here. Our study also confirms the findings from Karagiannidis and colleagues [44] , as both surface area and blood flow rates govern the rate of CO 2 removal; however, an increase in the surface area above a certain threshold has limited impact on CO 2 removal when low blood flows are applied, as is the case with the A.L.ONE device. Larger membrane surface areas are thought to result in greater levels of CO 2 removal at higher blood flow rates, with a smaller pressure drop across the gas exchanger [44] . In our in vitro study, pressure drop values across the three devices were relatively low, with levels of up to 25 mmHg with PrismaLung+ (surface area 0.8 m 2 ) at a blood flow rate of 450 mL/min. Some challenges do exist for devices with larger membrane surface areas and those that require larger priming volumes, as they may have increased thrombotic potential due to increased interaction with an artificial surface [44] . A lower blood flow rate combined with a larger surface area may lead to more clotting events due to the increased time blood spends passing through the membrane [43, 51] . Furthermore, in the clinic, larger priming volumes can negatively affect exposure time and the hemolysis index [51] , potentially resulting in increased blood loss due to clotting events and the device having to be replaced. We did not observe clotting events; however, this was not a focus of the study and would require investigation in the clinic.

These findings highlight the potential for lower flow devices with higher surface areas to remove CO 2 from blood. The data also demonstrate the restrictions of conventional diffusive CO 2 removal determined by blood flow rates. To further enhance CO 2 removal at low blood flow rates novel systems, such as approaches involving acidification of bloo d [52] or bicarbonate dialysi s [53] , need to be investigated.

We used the infusion analysis rather than the more commonly accepted blood gas analysis method to determine the CO 2 removal rates. This was done because of the limitations of the blood gas analysis method, because test conditions utilizing lower blood flow produced CO 2 results below the reportable range of the analyzer. The blood gas analysis method was used to determine CO 2 removal rates when test results where within the reportable range of the blood gas analyzer. The results obtained with the blood gas analysis method demonstrated the validity of the infusion method. The comparison of the valid data obtained by blood gas analysis versus the infusion method by slope analysis indicated that these two data sets are comparable (Fig. 5) . It is important to note that the comparative data indicated that a small amount of gas loss from the test setup was likely, as for example, if the reservoir and/or tubing are not fully gas-tight. This is demonstrated by the data being slightly off the line of identity, the offset of the mean, as shown in the Bland-Altman diagram (4.2 mL/min) and the paired t test.

The general suitability of the blood gas analyzer, with respect to its intended use, was verified through the measurement principles of the analyzer [32, 33] , to ensure that the ABL90 device used here could measure bovine blood parameters. In addition, the ABL devices from Radiometer have been routinely used to perform experiments on blood from different species [54] [55] [56] [57] .

We used a flow rate that would be achievable by a monitor that the PrismaLung+ device is intended to be used on in the clinic, namely 200 to 450 mL/min, allowing us to characterize the device in conditions comparable to mild-to-moderate hypercapnia where the device would be used. The A.L.ONE device is designed to run at higher blood flow rates than the flow rates used in this study; therefore, conditions perhaps did not favor the CO 2 removal rate of the device, despite the high surface area in comparison with PrismaLung+ [31] .

Further methodological limitations to consider include the use of bovine blood for experimentation, as it is easier to obtain than human blood and well-accepted for use in in vitro studies. It should be noted that as the blood was obtained from healthy animals, levels of blood components will be different from those for ICU patients; however, levels were consistent across experiments. Furthermore, a high dose (5 U/mL) of heparin was used that is higher than that routinely used in the clinic; this dose was selected to ensure no clotting occurred during transportation from the slaughterhouse and during the in vitro experiment and is not expected to impact CO 2 removal. Given the in vitro nature of the data, caution should be exercised when translating these data to the clinical setting, and further studies are needed to explore coagulation in the clinic.

Here, and in similar studies, the CO 2 removal rates are stated in units of mL/ min, with dependency upon pressure and chosen reference temperature. To remove the dependency upon these parameters, units of mmol/min would be more appropriate and comparable when reporting CO 2 removal rates. Despite this, the units of mmol/min are not standard and are not used in the clinical setting . ECCO 2 R uses similar gas-exchange principles as ECMO, but the main goal is to remove CO 2 in those with sufficient oxygenation and at lower blood flow rates than ECMO [58] . Oxygenation and O 2 transfer rates were not a focus in this study. In the clinical setting, venous sO 2 levels are expected to be around 70% and therefore the testing of fully oxygen-saturated blood in this setting may slightly underestimate CO 2 removal performance. This will require further experimental confirmation.

In summary, at the flow rates tested, PrismaLung+ performed more effectively than PrismaLung for CO 2 removal, with comparable performance to A.L.ONE, despite the smaller surface area. The PrismaLung+ may be an effective device for reducing CO 2 levels, and further testing in the clinical setting is warranted. 

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A Proof of concept study, demonstrating extracorporeal carbon dioxide removal using hemodialysis with a low bicarbonate dialysate

Evaluation of the i-STAT analyzer for determination of ionized calcium concentrations in bovine blood

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Editorial support for the development of this manuscript was provided by Daniel Johnson PhD, Ailsa Bennett PhD, Ruth Brown PhD, and Siobhán Ahern PhD, SciMentum (Nucleus Global), with funding provided by Baxter.

Supplementary information accompanies this paper at https://doi.org/10.1186/s40635-020-00301-7.Additional file 1: Figure S1 . Cross section of the PrismaLung+ device Additional file 2: Figure S2 . CO 2 removal rates for the PrismaLung+ and A.L.ONE devices. Assessed at 37°C, Q B 600 mL, and a p in CO 2 of 45 mmHg. p in CO 2 , partial pressure of carbon dioxide at the inlet; Q B , blood flow rate. Data are plotted as mean values ± SD. p > 0. 05 

This study was sponsored by Baxter.

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.Ethics approval and consent to participate Not applicable.

Not applicable.

The authors declare that they have no competing interests. IH, JG, MS, KH, DP, MR, SV are full-time employees of Baxter International. J.L. has received consulting fees from Baxter International.

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