- Open Access
Respiratory and metabolic acidosis correction with the ADVanced Organ Support system
Intensive Care Medicine Experimental volume 7, Article number: 56 (2019)
The lung, the kidney, and the liver are major regulators of acid-base balance. Acidosis due to the dysfunction of one or more organs can increase mortality, especially in critically ill patients. Supporting compensation by increasing ventilation or infusing bicarbonate is often ineffective. Therefore, direct removal of acid may represent a novel therapeutic approach. This can be achieved with the ADVanced Organ Support (ADVOS) system, an enhanced renal support therapy based on albumin dialysis. Here, we demonstrate proof of concept for this technology.
An ex vivo model of either hypercapnic (i.e., continuous CO2 supply) or lactic acidosis (i.e., lactic acid infusion) using porcine blood was subjected to hemodialysis with ADVOS. A variety of operational parameters including blood and dialysate flows, different dialysate pH settings, and acid and base concentrate compositions were tested. Comparisons with standard continuous veno-venous hemofiltration (CVVH) using high bicarbonate substitution fluid and continuous veno-venous hemodialysis (CVVHD) were also performed.
Sixty-one milliliters per minute (2.7 mmol/min) of CO2 was removed using a blood flow of 400 ml/min and a dialysate pH of 10 without altering blood pCO2 and HCO3− (36 mmHg and 20 mmol/l, respectively). Up to 142 ml/min (6.3 mmol/min) of CO2 was eliminated if elevated pCO2 (117 mmHg) and HCO3− (63 mmol/l) were allowed. During continuous lactic acid infusion, an acid load of up to 3 mmol/min was compensated. When acidosis was triggered, ADVOS multi normalized pH and bicarbonate levels within 1 h, while neither CVVH nor CVVHD could. The major determinants to correct blood pH were blood flow, dialysate composition, and initial acid-base status.
In conclusion, ADVOS was able to remove more than 50% of the amount of CO2 typically produced by an adult human. Blood pH was maintained stable within the physiological range through compensation of a metabolic acid load by albumin dialysate. These in vitro results will require confirmation in patients.
Lung, kidney, and hepatic dysfunction are common in the critically ill, and acid-base regulation is frequently compromised in these patients. Acidosis is commonly associated with high mortality rates in critically ill and injured patients. Recently, a strong correlation was found between hypercapnic acidosis and increased hospital mortality in mechanically ventilated patients, compared to compensated hypercapnia or normocapnia . Indeed, a delayed pH normalization is associated with increased mortality in the intensive care unit (ICU), reaching 57% in cases of severe metabolic or mixed acidemia . If accompanied by hyperlactatemia, these values could go above 80% [3, 4].
While acidosis is well tolerated in healthy humans, acidosis leads to a myriad of physiologic effects that can be deleterious and thus contribute to morbidity and mortality in patients . In fact, an interaction exists between acidosis and inflammation, which is specifically relevant in critically ill patients [6, 7]. Acidosis can impair several immune response mechanisms, including lymphocyte cytotoxicity, complement activation, or antibody binding to leukocytes . Since some of these findings have been already reported in patients , acid-base imbalances should be considered in the context of a host response to an aggression, and not as an isolated insult. Moreover, pH might also influence normal physiology, among others, modulating oxygen affinity to hemoglobin [9, 10], promoting vasoconstriction in the lungs , altering potassium and calcium levels, reducing glomerular filtration rate , reducing intestinal mobility , impairing coagulation , or depressing myocardial contractility .
The ADVanced Organ Support (ADVOS) system (ADVITOS GmbH, Munich, Germany—previously, Hepa Wash GmbH) is an albumin-based hemodialysis device initially designed to support the liver and kidney of ICU patients. As a hemodialysis system, it removes water-soluble substances, while the albumin dialysate allows to remove protein-bound toxins too [15,16,17]. The ADVOS system consists of three circuits: an extracorporeal blood, a dialysate, and an ADVOS multi circuit with an acidic and an alkaline path (Fig. 1). Briefly, the dialysate’s albumin binds protein-bound substances that diffuse from blood into the dialysate through a semi-permeable membrane in the extracorporeal circuit. Differently to conventional single pass albumin dialysis (SPAD), in the ADVOS system, the dialysate is not systematically discarded and recirculates then through the dialysate circuit into the ADVOS multi circuit. There, dialysate albumin is recycled by systematically modifying the tertiary structure of albumin through temperature and pH changes. This facilitates the release of toxins from albumin (cationic—e.g., copper—and anionic—e.g., bilirubin—substances in the acidic and alkaline paths, respectively) and makes it ready for further binding. pH changes are possible by the addition of an acidic and an alkaline concentrate, whose customizable mixing relation forms a dialysate with a variable composition. This includes modifiable carbonate, sodium, or chloride concentrations that allow to achieve a customizable dialysate with a pH from 7.2 to 10.0. Consequently, this latter feature enables a continuous control and adjustment of dialysate acid-base properties, which in turn corrects deviations in blood pH (e.g., acidosis) by means of altering blood pCO2, strong ion difference, or both .
In the present study, the ability of ADVOS to eliminate CO2 and to correct blood pH was investigated in an ex vivo model of either lactic or hypercapnic acidosis, using porcine blood and a continuous supply of lactic acid and/or CO2, respectively. A variety of operational parameters, including blood and dialysate flows as well as different dialysate pH settings and acid and base concentrate compositions, were tested. In addition, comparisons with standard continuous veno-venous hemofiltration (CVVH) using high bicarbonate substitution fluid and continuous veno-venous hemodialysis (CVVHD) were performed. Finally, an analysis of the mechanism of action regarding classic and modern acid-base balance approaches is provided.
Material and methods
Ex vivo model
For all the experiments, an ex vivo model comprising 5 l fresh porcine blood connected to an extracorporeal support device (either ADVOS multi, CVVH, or CVVHD) was employed. For experiments with ADVOS multi or CVVHD, an additional continuous CO2 supply was added. Small modifications comprising the administration of different solutions were performed for each specific experiment (Fig. 1).
Fresh porcine blood was obtained from the local slaughterhouse (Münchner Schlachthof Betriebs GmbH, Munich, Germany) and prepared following a standard operation procedure (SOP) diluting it with modified Ringer’s solution (100 mmol/l NaCl, 3 mmol/l KCl, 1 mmol/l MgSO4.7H2O, 1.75 mmol/l CaCl2, 1200 mg/dl glucose) to a hematocrit of 36%, standard electrolyte concentrations, and normal blood gas values. 100,000 IU of heparin (Ratiopharm, Ulm, Germany) prevented coagulation. Blood was maintained at a constant temperature of 37 °C using a bath heater while stirring it at 130–180 rpm.
For the ADVOS system (ADVITOS GmbH, Munich, Germany), two SURELYZER PES-190 DH dialyzers (Nipro D.Med Germany GmbH, Hamburg, Germany) with blood and dialysate flowing co-currently were employed in the extracorporeal circuit. Blood flow can be adjusted between 100 and 400 ml/min. A dialysate flow of 800 ml/min was used throughout the study, which refers to the amount of fluid per minute being recirculated and detoxified in the ADVOS multi circuit by means of pH adjustments and filtration, instead of being discarded after a single pass. Variations of pH and composition are achieved using acidic and basic concentrates (see below). The concentrate flow (160 or 320 ml/min) determines the quantity of dialysate cleaned by convective transport in the ADVOS multi circuit. Toxins released from albumin or water-soluble toxins are separated from the albumin dialysate through two ELISIO-13H filters (Nipro D.Med Germany GmbH. Hamburg, Germany). Additionally, the concentrate flow refers to the amount of new fresh concentrate (i.e., mix of water and acidic and alkaline concentrates) pumped into the system.
CO2 administration for ADVOS multi and CVVHD experiments
For this ex vivo model, CO2 was continuously infused into the blood pool via an additional SURELYZER PES-190 DH dialyzer (Nipro D.Med Germany GmbH, Hamburg, Germany) connected to a CO2 gas supply (Linde AG, Munich, Germany). Contrary to a standard dialyzer setup, in the CO2 dialyzer, blood was circulated through the external side to reduce the pressure within the blood circuit. CO2 was supplied to the inner side of the CO2 dialyzer in a countercurrent flow via a pressure reducer (FMD 202, Linde AG, Munich, Germany) and a mass flow meter FMA-1618A (OMEGA Engineering, Deckenpfronn, Germany). The bottom outlet of the CO2 dialyzer was closed to avoid CO2 losses while the semipermeable membrane allowed the gas to diffuse freely into the blood.
Dialysate for ADVOS multi
In contrast to other hemodialysis methods, the ADVOS system does not use a fixed dialysate composition. Instead, two concentrates (acid and base) are automatically mixed in a specifically designed reservoir throughout the treatment depending on the desired dialysate pH (range 7.20–10.00). A higher dialysate pH setting means a higher basic/acidic concentrate ratio and thus higher sodium and lower chloride levels. Two 100 ml bottles of albumin 20% (Human Albumin 200 g/l, Baxter, Vienna, Austria) are added to the above dialysate mix via a specific port in the ADVOS multi device. The dialysate is furthermore supplemented with 40% glucose at an infusion rate of 70 ml/h to maintain glucose levels around 100 mg/dl in blood.
Acidic concentrate (AC) included H+, Na+, Cl−, HPO42−, Mg2+, and Ca2+ while basic concentrate (BC) consisted primarily of OH−, Na+, and K+. Two versions of BC were employed. BC-Bic20 contained Na2CO3, while BC-Bic0 did not.
Continuous veno-venous hemodialysis
The NIKKISO DBB-03 dialysis system (NIKKISO Europe GmbH, Langenhagen, Germany) consisted of a blood and dialysate circuit working as a single pass process without recirculating the dialysate. The dialysate flow (350 ml/min) determined the amount of dialysate being supplied and discarded. It was equipped with one SUREFLUX-25UX dialyzer (Nipro D.Med Germany GmbH, Hamburg, Germany) working with a countercurrent flow. Constant HCO3− and Na+ concentrations in the dialysate were maintained by an integrated sodium bicarbonate cartridge (B. Braun Melsungen AG, Melsungen, Germany). Additionally, glucose (1 g/l), potassium (2 mmol/l), and calcium (1.5 mmol/l) were infused into the reservoir.
Continuous veno-venous hemofiltration
Sartorius Haemoprocessor 40040
For standard CVVH system, the Haemoprocessor 40040 and its specific Plasma Line (Meise Medizintechnik GmbH, Schalksmühle, Germany) were connected to one SURELYZER PES-190 DH dialyzer (Nipro D.Med Germany GmbH, Hamburg, Germany). The multiPlus-CRRT solution containing 35 mmol/l of bicarbonate (Fresenius Medical Care, Bad Homburg, Germany) was employed as substitution solution in post-dilution mode. A blood flow of 200 ml/min was used for all experiments. The ultrafiltration and substitution flow rates were automatically adjusted by the device being always around 15 ml/min and 65 ml/min, respectively.
Experiments were divided into three groups. First, blood was titrated with CO2 or lactic acid to achieve a blood pH range of 7.35–7.45 while being treated with ADVOS multi using different settings (set 1 and 2, respectively). Second, using a fixed CO2 or lactic acid supply, the performance of ADVOS multi vs. hemodialysis (CVVHD) or hemofiltration (CVVH) was compared (set 3 and set 4, respectively). Third, a hypercapnic acidosis was triggered in blood and further treated with ADVOS multi until recovery of normal blood gas values. Details for each of the experimental sets are summarized in Table 1.
Set 1: Influence of ADVOS multi operational settings on CO2 removal
In order to determine the influence of blood flow and dialysate composition on CO2 removal ability of the ADVOS system, different settings were tested during a continuous CO2 supply (Fig. 1). Briefly, 5 l of blood at physiological levels of pH (7.35–7.45), HCO3− (22–28 mmol/l), and pCO2 (35–45 mmHg) was treated with ADVOS multi at experimental blood flows (Qb) of 100, 200, or 400 ml/min with co-currently recirculating dialysate at flows of 800 ml/min. At each Qb, dialysate pH was set to 7.5, 8.0, 8.5, and 9.0 using a concentrate flow (Qc) of 160 ml/min. At the highest Qb of 400 ml/min, additional tests were carried out with a Qc of 320 ml/min. All these experiments were carried out using the concentrates AC and BC-Bic20.
With the intention to test if different bicarbonate concentrations of the dialysate might affect CO2 removal, additional experiments with BC-Bic0 (without bicarbonate) instead of BC-Bic20 were carried out setting dialysate pH to 10.00.
Prior to blood hemodialysis, every dialyzer was primed with a 0.9% NaCl solution removing air before blood contact. The CO2 dialyzer was flushed with gas prior to and during NaCl and blood perfusion to create a positive pressure gradient which prevented liquids from entering the capillaries. Every test consisted of a 20-min stabilization period during which CO2 supply was adjusted such that blood pH remained between 7.35 and 7.45. This was followed by a 1-h treatment phase during which samples from the inlet (pre-dialyzer) and outlet (post-dialyzer) were analyzed by the blood gas analyzer GEM Premier 4000 (Instrumentation Laboratory, Munich, Germany) every 20 min. In addition, pH was measured by an InPro 3253 pH probe inserted into the blood container and M300 displayed it continuously (both Mettler Toledo, Greifersee, Switzerland).
To quantify CO2 removal in milliliters per minute, post-dialyzer TCO2 values in millimoles per liter were subtracted from pre-dialyzer values and this difference multiplied by the corresponding blood flow (Qb) and by the molar volume (Vm) of CO2 at STP (22.4 ml/mmol) (Eq. 1). The fraction of TCO2 excreted as dissolved CO2 or HCO3− was calculated likewise .
Set 2: Influence of ADVOS multi operational settings on blood pH during continuous acid load
The same experimental design as for set 1 was performed to determine the influence of ADVOS parameters, with small modifications. Briefly, a continuous 2% lactic acid solution was used to titrate blood pH to 7.35–7.45. CO2, instead, was continuously infused on demand to maintain pCO2 levels between 35 and 45 mmHg. These experiments were only carried out with Qc of 320 ml/min and with BC-Bic20.
For each experiment, the maximal combined acid supply resulting from lactic acid infusion and CO2 influx supply was calculated from the infusion rate of the pump (Volumat MC Agilia. Fresenius Kabi, Bad Homburg, Germany) and reading of the mass flow meter FMA-1618A (OMEGA Engineering, Deckenpfronn, Germany), respectively.
Set 3: ADVOS multi vs. CVVHD during continuous maximal CO2 supply
The maximum CO2 supply was determined previously in set 1 to be 110 ml/min (Additional file 1: Table S1). Blood was treated for 4 h with either the ADVOS multi or the CVVHD device NIKKISO DBB-03. The settings for each device are detailed in Table 1. Blood gas analysis was performed every 15 min.
Set 4: ADVOS multi vs. CVVH for the treatment of lactic acidosis in vitro
First, 5 l of fresh swine blood was subjected to CVVH with a substitution fluid with 10 mmol/l bicarbonate. Simultaneously, a 2% lactic acid solution was infused in order to reach a pH < 7.15, a pCO2 between 35 and 45 mmHg, HCO3− levels between 12 and 14 mmol/l, and lactate of 5–6 mmol/l, which simulated a severe lactic acidosis. Blood was then treated with either ADVOS multi or CVVH for 1 h. Lactic acid infusion was maintained during the treatment phase. Blood was analyzed as described above.
Set 5: Treatment of hypercapnic acidosis in vitro with ADVOS multi
In this case, a hypercapnic acidosis was triggered first. Briefly, 27 ml/min CO2 was infused while a blood flow of 100 ml/min and a dialysate pH of 7.8 were set. During this phase, AC was combined with BC-Bic20. Once a pH < 7.15, a pCO2 > 60 mmHg, and HCO3− levels >32 mmol/l were reached, both the settings and the BC were changed, and the treatment phase started. Blood was then treated with ADVOS multi until normal values of pH (7.35–7.45), pCO2 (35–45 mmHg), and HCO3− (22–26 mmol/l) were detected. Blood values were analyzed as described above. CO2 was continuously supplied with the same flow of 27 ml/min.
Acid-base balance according to Stewart
We obtained blood samples both at the inlet and the outlet of the dialyzers from experimental sets 1 and 2. The analysis of these data provides an understanding of pH variations attending to pCO2 and SID changes. In order to better understand this physicochemical method proposed by Stewart , several authors have tried to calculate specific values for the total concentration and the effective dissociation constant for plasma nonvolatile buffers. Constable suggested that “at normal pH (7.40), a 1-meq/l increase in SID will increase pH by 0.016, a 1-Torr increase in pCO2 will decrease pH by 0.009, and a 1 g/dl increase in total protein will decrease pH by 0.039” . It is assumed that no variation on total protein content occurs in our setting as it cannot be lost in the dialyzer. Therefore, variations in [Atot] (i.e., total protein) are not considered within the equation that was employed to predict the resulting outlet pH.
Experiments were performed at different settings between 3 and 6 times each covering a wide range of operational parameters. Student’s t test for paired samples was used to compare CO2 removal and acid supply between different ADVOS settings for experimental sets 1 and 2, respectively. A two-tailed p value lower than 0.05 was considered to indicate statistical significance. For correlations assessment, Pearson’s coefficient was employed. Data were documented and analyzed using Microsoft Excel and IBM SPSS 24.0 for Windows®, respectively. Data are presented as mean ± standard deviation (SD)
Influence of ADVOS multi operational settings on CO2 removal
In this experimental design, where blood was titrated with CO2 to maintain a blood pH between 7.35 and 7.45, CO2 removal with ADVOS multi depended on three variables: (1) the amount of CO2 being supplied, (2) the blood flow, and (3) the dialysate composition (i.e., according to carbonate concentration and dialysate pH setting) (Fig. 2 and Additional file 1: Table S1). During experiments with BC-Bic20 and Qc of 160 ml/min, higher Qb resulted in higher CO2 elimination with an average of 77 ± 22 ml/min at Qb 400 ml/min with a dialysate of pH 9.0. With the same dialysate pH, 35 and 19 ml/min of CO2 were removed at Qb 200 and 100 ml/min, respectively. A lower dialysate pH setting (i.e., lower sodium and higher chloride) resulted in lower CO2 removal, independently of any other setting. In fact, the dialysate composition (i.e., the presence of albumin and sodium and chloride concentrations) together with the dialysate pH (but not dialysate pH alone) is responsible for blood pH correction.
At a Qc of 160 ml/min compared to 320 ml/min, setting dialysate pH to 9.0 resulted in significantly higher blood HCO3− (57.0 ± 10.2 vs. 38.5 ± 2.8 mmol/l) and pCO2 (103 ± 17 vs. 74 ± 4 mmHg), which is correlated with the higher amount of CO2 removed (Additional file 1: Table S1).
Increasing the Qc from 160 ml/min to 320 ml/min means doubling the convective transport, which results in faster removal of substances diffused from blood (e.g., bicarbonate). Therefore, at higher concentrate flows, a more efficient concentration gradient between blood and dialysate is available, resulting, in this case, in lower blood baseline levels of HCO3− with a Qc of 320 ml/min in comparison to a Qc of 160 ml/min. Lower blood HCO3− can buffer less acid in blood (i.e., less CO2 can be supplied without altering blood pH), which, due to the lower total CO2 concentration in blood (i.e., lower pCO2 at the inlet of the dialyzer), it was translated in a lower CO2 removal in our experimental setting. Nevertheless, this is an artefactual result caused by the experimental design as not Qc, but Qb, CO2 supply, and dialysate pH setting affect the CO2 removal capacity.
In line with these results, using a carbonate-free dialysate BC-Bic0 with dialysate pH set to 10, a maximum removal of 142 ml/min CO2 was achieved during ADVOS treatment with Qb of 400 ml/min and Qc of 160 ml/min. However, with this setting, pCO2 and HCO3− were extremely above physiological levels (117 ± 5 mmHg and 62.8 ± 3.4 mmol/l, respectively). Thus, blood was then titrated with CO2 only as long as every blood gas value was maintained within a physiological range (including pCO2 and HCO3−). This setting allowed a CO2 removal of 61 ml/min using a Qb of 400 ml/min and a Qc of 320 ml/min. This was only possible with a basic concentrate without carbonate. In fact, similar CO2 removal rates were achieved with the same flows and with dialysate pH 9 with the BC-Bic20 concentrate (58 ml/min), but blood gas levels were above physiological values in this case (Fig. 2 and Additional file 1: Table S1).
Variations between the inlet (pre) and the outlet (post) of the dialyzers for SID, pCO2, HCO3−, and pH are shown in Additional file 1: Table S1.
Influence of ADVOS multi operational settings on blood pH during continuous acid load
Experiments with ADVOS multi employing different operational settings showed that higher blood flows and dialysate pH settings were able to allow higher acid loads. The influence of each parameter is shown in Fig. 3. These results show a low level of CO2 removal needed (< 1 mmol/min or 22.5 ml/min) to maintain pCO2 stable (35–45 mmHg) in those cases where CO2 elimination is not required.
Variations between the inlet (pre) and the outlet (post) of the dialyzers for SID, pCO2, HCO3−, and pH are shown in Additional file 1: Table S2.
ADVOS multi vs. CVVHD during continuous maximal CO2 supply
Using a carbonate-free dialysate with a pH of 10, ADVOS multi removed 79 ± 1 ml/min TCO2 on average during 4 h of continuous supply of 110 ml/min CO2. Blood pCO2 (66 ± 9 mmHg) and HCO3− (33.1 ± 0.1 mmol/l) levels were stable throughout the experiments. The ADVOS device was able to maintain pH stable and within the physiological range (Fig. 4) while post-dialyzer pH remained always below 8.
In contrast, despite identical CO2 influx, blood pH dropped already 15 min after circulating blood through the NIKKISO renal dialysis device reaching a constant pH of around 6.60 after 1 h. Post-dialyzer pH remained below 7 during the experiment.
Treatment of metabolic acidosis in vitro: ADVOS multi vs. CVVH
Once metabolic acidosis was triggered (minute 40, Fig. 5), bicarbonate therapy during CVVH was able to normalize HCO3− levels. However, as expected, due to the lack of ventilation, pCO2 was correspondingly elevated (> 90 mmHg) resulting in an even lower pH (< 7.00) after the treatment. Conversely, ADVOS multi normalized pH and bicarbonate levels in less than 1 h. Due to the high CO2 removal ability of the ADVOS system when dialysate pH is set to 9.0, even 15 ml/min of CO2 was additionally provided during the treatment with ADVOS multi to maintain blood pH between 7.35 and 7.45.
Treatment of hypercapnic acidosis in vitro with ADVOS multi
Using a basic concentrate without Na2CO3 (BC-Bic 0), ADVOS multi was able to restore a hypercapnic acidosis in vitro in less than 30 min using a Qb of 200 ml/min, a Qc of 160 ml/min, and dialysate pH set to 9.0 during a continuous supply of 27 ml/min of CO2. After changing the settings (dialysate pH 7.8 vs. 9.0) and the basic concentrate (BC-Bic 20 vs. BC-Bic 0), values of pH (7.12 vs. 7.35), pCO2 (99 vs. 40 mmHg), and HCO3− (32.7 vs. 22.6 mmol/l) returned to physiological standards (Fig. 6).
Acid-base balance according to Stewart
As shown in Additional file 1: Tables S1 and S2, the higher the pCO2 reduction, the higher the pH increase that can be achieved in blood, describing a direct correlation for more than 200 blood samples in both experimental sets 1 and 2 (Additional file 2: Figure S1 r2 = 0.812 and Additional file 2:Figure S2 r2 = 0.935, respectively).
To note, to increase the dialysate pH, the ratio “basic concentrate/acidic concentrate” increases. Attending to the composition of these solutions, an increase in the basic/acidic concentrate ratio results in a dialysate with higher sodium and lower chloride concentrations. Indeed, an increase in SID was observed for set 1 (Additional file 1: Table S1), but not for set 2 due to the lactate addition (Additional file 1: Table S2).
Finally, we were able to predict pH variations solely by measuring SID and pCO2 changes (Additional file 2: Figures S1 and S2; Additional file 3: Figures S3 and S4; Additional file 4: Figures S5 and S6). The calculated values correlated perfectly with measured values (r2 = 0.98). Variations in total protein are not expected since no albumin loss occurs in the dialyzer.
In the present study, the ability of an albumin hemodialysis system (ADVOS multi) to correct hypercapnic and lactic acidosis in vitro has been demonstrated. Different settings can be varied in this device (blood flow, concentrate flow, carbonate content, and dialysate pH), allowing different rates of CO2 removal or acid load. This is only possible due to the presence of albumin in the dialysate, which permits to alter the composition of the dialysate (including the strong ion difference and the CO2 content). A concentrate gradient between blood and dialysate for electrolytes or bicarbonate is then possible, allowing the correction of acidosis from hypercapnic or metabolic origin.
Lung support through CO2 removal
The lung removes CO2 directly, thanks to the fast transformation of H+ + HCO3− through carbonic anhydrase into CO2 gas and water. However, in blood, CO2 is mainly found as HCO3−. ADVOS reduces pCO2 through the removal of HCO3− by forming a concentration gradient between blood and dialysate. Additionally, the high dialysate pH helps to reduce the H+ concentration in blood and thus increase the pH. This is possible due to the presence of albumin in the dialysate. Albumin increases the buffer capacity via a protonation of its imidazole side chain , which contains several buffering residues of histidine [23, 24]. Preliminary in-house studies indicate that a dialysate of pH 9 containing two 100 ml bottles of albumin 20% increased the buffer capacity by 35% compared to the same dialysate without albumin (Additional file 5: Figure S7).
Bearing this in mind, first, a higher blood flow may account for a higher HCO3− concentration gradient between blood and dialysate (i.e., 400 ml/min). Second, a higher dialysate pH (with a higher SID) allows a higher decrease in H+ concentration (i.e., dialysate pH 10). Third, lower (or none) dialysate carbonate levels permit a more effective convective transport in the ADVOS multi circuit (Fig. 1). Finally, this convective transport will be faster insofar a higher concentrate flow is set (i.e., 320 ml/min) (Fig. 2 and Additional file 1: Table S1). Even at lower blood and concentrate flows (200 and 160 ml/min, respectively) and with dialysate pH set to 9, the use of a dialysate without carbonate allowed a correction of hypercapnic acidosis in vitro in less than 1 h (Fig. 6).
Kidney support through HCO3 − generation
The renal compensatory mechanism during a respiratory acidosis tries to increase the acid excretion into urine and the HCO3− resorption into blood . When using a bicarbonate containing dialysate with high pH, this mechanism is mimicked by ADVOS.
This can be explained following the CO2 equilibrium in Eq. 3. Carbonic acid, or CO2 in its gas form, is converted to HCO3− and H+. The reduction of H+ concentration in blood forces the equilibrium to the right of the equation, increasing HCO3− even as it is removed from blood, and consequently, CO2 is transferred down its concentration gradient from the intracellular space (i.e., correcting intracellular acidosis) into the blood and into the dialysate in the form of HCO3−. This means that in the absence of adequate ventilation, as simulated in our ex vivo model through elevated CO2 supply without additional oxygenation, ADVOS multi could “imitate” the renal compensatory mechanism for acidemia control .
In the case of ADVOS, the higher the dialysate pH setting, the higher the H+ concentration reduction is achieved (Fig. 2). This results into HCO3− generation, which helps to correct HCO3− levels during metabolic acidosis (Fig. 5). This is only possible if a concomitant pCO2 reduction is achieved, which does not occur during conventional renal replacement therapy or bicarbonate infusion. In fact, in the absence of adequate ventilation (i.e., CO2 removal), a metabolic acidosis can turn into a hypercapnic acidosis (Fig. 5), which cannot be corrected with conventional CVVHD (Fig. 4).
The Stewart model to explain acid-base balance with the ADVOS system
We analyzed if the observed changes could also be explained by the mathematical model proposed by Stewart  and its revision by others [27,28,29], who showed that three independent variables are responsible for determining the pH in plasma: PaCO2, plasma weak acids (i.e., phosphate and albumin), and the SID as the difference between fully dissociated plasma anions and cations. Therefore, neither the H+ movement nor the buffering effect of HCO3− is necessary or sufficient to explain acid-base regulation. In any case, our data can be also explained using this model, as shown in Additional files.
Taking into account the conclusions obtained by Constable , blood pH could be predicted solely by changes in total protein, pCO2, and SID. Applying this to our data demonstrated a perfect correlation between the measured and the calculated pH in the outlet of the dialyzer (Additional file 2: Figures S1 and S2; Additional file 3: Figures S3 and S4; Additional file 4: Figures S5 and S6). Indeed, SID variations were correlated with dialysate pH variations, specifically at high values of 10.0. To reach such a dialysate pH, a higher rate of basic/acidic concentrate is needed, which provides higher Na+ and lower Cl−, and can therefore result into SID reductions in blood through the dialyzer. Moreover, the presence of albumin as a weak acid facilitates this process.
Although SID and pCO2 are considered independent variables by Stewart, it has been suggested that an interdependency between both values might exist . Langer et al. observed that the greater the variation in pCO2, the greater the reduction in plasma SID. We might reach the same conclusion when, as this group did, quartiles of pCO2 variations are analyzed and plotted against the corresponding SID variations (r2 = 0.991; Additional file 6: Figure S8). However, if raw data are drawn, no correlation is observed (r2 = 0.190; Additional file 7: Figure S9).
Rationale for multi organ support with ADVOS during acidosis
Using either the classical or the modern approach, this work should serve as a proof of concept of the ability of the ADVOS therapy to correct acid-base disturbances. As described above, the lungs (i.e., CO2) and kidneys (i.e., NH4+, HCO3−, for the classic approach or Na+, Cl− for the Stewart model) are usually defined to be responsible for acid-base control. However, the liver plays also an important role (i.e., metabolism of organic acid anions like citrate and certain amino acids) [31, 32] and can also be supported by ADVOS. Indeed, acidemia and metabolic acidosis are associated with poor outcome in cirrhosis patients, as demonstrated by Drolz and colleagues in a cohort of 178 critically ill patients with liver cirrhosis and acute on chronic liver failure .Therefore, attention should not only be paid to a specific organ. In addition, the majority of the cases of acidosis reflect a mixed nature, involving both a metabolic and a respiratory component . In view of this, a multiple organ approach seems to be needed while facing acidosis, where the variety of adjustable parameters of the ADVOS multi might play an important role.
Limitations and justification of the ex vivo model
Although our results are encouraging, our work is limited by its in vitro nature, the selection of parameters, and the number of experiments performed. Nevertheless, so as to serve as a proof of concept, this experimental setting is adequate based on the following: (1) the different parameters analyzed and varied (i.e., pCO2, HCO3−, lactate) to resemble different types of acidosis, (2) the possibility to control the concrete amount of acid load (i.e., CO2 and/or lactic acid) being supplied, and (3) the analysis of inlet and outlet measurements to describe the course of blood values along the dialyzer. These encouraging results need now to be confirmed in the clinical setting.
In conclusion, the ADVOS albumin hemodialysis system was able to remove 61 ml/min while maintaining blood gas values in the physiological range or up to 142 ml/min CO2 in hypercapnic conditions at low blood flow without the need of a gas phase. Blood pH was maintained stable within the physiological range of 7.35–7.45 by the albumin-containing dialysate. Moreover, during continuous lactic acid addition, up to 3 mmol/min of acid load was compensated. The major determinants to stabilize blood pH were blood flow, dialysate composition, and blood bicarbonate levels. The mechanism of action of ADVOS multi can be explained using either the classical acid-base balance model or the newer Stewart approach. This feature in combination with the previously demonstrated ability to eliminate water-soluble and protein-bound toxins may be of valuable help in the management of critically ill patients with multiple organ failure.
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
ADVanced Organ Support
Acute kidney injury
Acute respiratory distress syndrome
- CO2 :
Chronic obstructive pulmonary disease
- HCO3 :
Intensive care unit
Multiple organ failure
Multiple organ support therapy
- Na2CO3 :
- NaHCO3 :
- PaCO2 :
Arterial partial pressure of carbon dioxide
- pCO2 :
Partial pressure of carbon dioxide
- Qb :
- Qc :
Strong ion difference
Sepsis-related organ failure assessment
Standard operating procedure
- TCO2 :
Total content of CO2
Tiruvoipati R, Pilcher D, Buscher H, Botha J, Bailey M (2017) Effects of hypercapnia and hypercapnic acidosis on hospital mortality in mechanically ventilated patients. Crit Care Med. 45:e649–e656. https://doi.org/10.1097/CCM.0000000000002332
Jung B, Rimmele T, Le Goff C, Chanques G, Corne P, Jonquet O et al (2011) Severe metabolic or mixed acidemia on intensive care unit admission: incidence, prognosis and administration of buffer therapy. A prospective, multiple-center study. Crit Care. 15:R238. https://doi.org/10.1186/cc10487
Kim HJ, Son YK, An WS (2013) Effect of sodium bicarbonate administration on mortality in patients with lactic acidosis: a retrospective analysis. PLoS One. 8:e65283. https://doi.org/10.1371/journal.pone.0065283
Kluge S, de HG, Jarczak D, Nierhaus A, Fuhrmann V (2018) Lactic acidosis - update 2018. Dtsch Med Wochenschr. 143:1082–1085. https://doi.org/10.1055/a-0585-7986
Critical care nephrology: Springer; 1998.
Kellum JA, Song M, Li J (2004) Science review: Extracellular acidosis and the immune response: clinical and physiologic implications. Crit Care. 8:331–336. https://doi.org/10.1186/cc2900
Zampieri FG, Kellum JA, Park M, Ranzani OT, Barbeiro HV, de SHP et al (2014) Relationship between acid-base status and inflammation in the critically ill. Crit Care. 18:R154. https://doi.org/10.1186/cc13993
Lardner A (2001) The effects of extracellular pH on immune function. J Leukoc Biol. 69:522–530
Mitchell JH, Wildenthal K, Johnson RL (1972) JR. The effects of acid-base disturbances on cardiovascular and pulmonary function. Kidney Int. 1:375–389
Stringer W, Wasserman K, Casaburi R, Porszasz J, Maehara K, French W (1994) Lactic acidosis as a facilitator of oxyhemoglobin dissociation during exercise. J Appl Physiol (1985). 76:1462–1467. https://doi.org/10.1152/jappl.19184.108.40.2062
Lejeune P, Brimioulle S, Leeman M, Hallemans R, Melot C, Naeije R (1990) Enhancement of hypoxic pulmonary vasoconstriction by metabolic acidosis in dogs. Anesthesiology. 73:256–264
Farber MO, Szwed JJ, Dowell AR, Strawbridge RA (1976) The acute effects of respiratory and metabolic acidosis on renal function in the dog. Clin Sci Mol Med. 50:165–169
Tournadre JP, Allaouchiche B, Malbert CH, Chassard D (2000) Metabolic acidosis and respiratory acidosis impair gastro-pyloric motility in anesthetized pigs. Anesth Analg. 90:74–79
Engstrom M, Schott U, Romner B, Reinstrup P (2006) Acidosis impairs the coagulation: a thromboelastographic study. J Trauma. 61:624–628. https://doi.org/10.1097/01.ta.0000226739.30655.75
Al-Chalabi A, Matevossian E, V Thaden A-K, Luppa P, Neiss A, Schuster T et al (2013) Evaluation of the Hepa Wash(R) treatment in pigs with acute liver failure. BMC Gastroenterol. 13:83. https://doi.org/10.1186/1471-230X-13-83
Al-Chalabi A, Matevossian E, von Thaden A, Schreiber C, Radermacher P, Huber W et al (2017) Evaluation of an ADVanced Organ Support (ADVOS) system in a two-hit porcine model of liver failure plus endotoxemia. Intensive Care Med Exp. 5:31. https://doi.org/10.1186/s40635-017-0144-3
Huber W, Henschel B, Schmid R, Al-Chalabi A (2017) First clinical experience in 14 patients treated with ADVOS: a study on feasibility, safety and efficacy of a new type of albumin dialysis. BMC Gastroenterol. 17:32. https://doi.org/10.1186/s12876-017-0569-x
Fuhrmann VH, Jarczak D, Boenisch O, Kluge S (2018) ADVOS reduces liver and kidney disease markers and corrects acidosis: the Hamburg experience. Critical Care. 22:82
May AG, Sen A, Cove ME, Kellum JA, Federspiel WJ (2017) Extracorporeal CO2 removal by hemodialysis: in vitro model and feasibility. Intensive Care Med Exp. 5:20. https://doi.org/10.1186/s40635-017-0132-7
Stewart PA (1983) Modern quantitative acid-base chemistry. Can J Physiol Pharmacol. 61:1444–1461
Constable PD (2001) Total weak acid concentration and effective dissociation constant of nonvolatile buffers in human plasma. J Appl Physiol (1985). 91:1364–1371. https://doi.org/10.1152/jappl.2001.91.3.1364
Kaneko K, Chuang VTG, Minomo A, Yamasaki K, Bhagavan NV, Maruyama T, Otagiri M (2011) Histidine146 of human serum albumin plays a prominent role at the interface of subdomains IA and IIA in allosteric ligand binding. IUBMB Life. 63:277–285. https://doi.org/10.1002/iub.457
Abe H (2000) Role of histidine-related compounds as intracellular proton buffering constituents in vertebrate muscle. Biochemistry (Mosc). 65:757–765
Szebedinszky C, Gilmour KM (2002) The buffering power of plasma in brown bullhead (Ameiurus nebulosus). Comp Biochem Physiol B Biochem Mol Biol. 131:171–183
Skelton LA, Boron WF, Zhou Y. Acid-base transport by the renal proximal tubule. J Nephrol. 2010;23 Suppl 16:S4-18.
Dorman PJ, Sullivan WJ, Pitts RF (1954) The renal response to acute respiratory acidosis. J Clin Invest. 33:82–90. https://doi.org/10.1172/JCI102874
Figge J, Mydosh T, Fencl V (1992) Serum proteins and acid-base equilibria: a follow-up. J Lab Clin Med. 120:713–719
Figge J, Rossing TH, Fencl V (1991) The role of serum proteins in acid-base equilibria. J Lab Clin Med. 117:453–467
Kellum JA (2009) In: Paul WG, WG EP (eds) Stewart’s textbook of acid-base, 2nd edn. United States of America, Lulu.com
Langer T, Scotti E, Carlesso E, Protti A, Zani L, Chierichetti M et al (2015) Electrolyte shifts across the artificial lung in patients on extracorporeal membrane oxygenation: Interdependence between partial pressure of carbon dioxide and strong ion difference. J Crit Care. 30:2–6. https://doi.org/10.1016/j.jcrc.2014.09.013
Scheiner B, Lindner G, Reiberger T, Schneeweiss B, Trauner M, Zauner C, Funk G-C (2017) Acid-base disorders in liver disease. J Hepatol. 67:1062–1073. https://doi.org/10.1016/j.jhep.2017.06.023
Gullo A, Häussinger D (1998) The role of the liver in acid-base regulation: anaesthesia, pain, intensive care and emergency medicine - A. Springer Milan, P.I.C.E
Drolz A, Horvatits T, Roedl K, Rutter K, Brunner R, Zauner C et al (2018) Acid-base status and its clinical implications in critically ill patients with cirrhosis, acute-on-chronic liver failure and without liver disease. Ann Intensive Care. 8:48. https://doi.org/10.1186/s13613-018-0391-9
Funding information is not applicable.
Ethics approval and consent to participate
Consent for publication
BK is the Chief Executive Officer (CEO) of the company ADVITOS GmbH and owns stocks in the company. AP is employed by ADVITOS GmbH. JK has a consulting arrangement with ADVITOS GmbH. The other authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Additional file 1: Table S1. Results from blood gas analysis obtained after hemodialysis of swine blood under different treatment settings with ADVOS and different CO2 supply during experimental Set 1. Samples were taken in the inlet and outlet of the dialyzer at the same time. Mean ± S.D. Table S2. Results from blood gas analysis obtained after hemodialysis of swine blood under different treatment settings with ADVOS and different lactic acid supply during experimental Set 2. Samples were taken in the inlet and outlet of the dialyzer at the same time. Mean ± S.D.
Additional file 2: Figure S1 and S2. Correlation between variations of inlet and outlet pCO2 with measured or calculated variations in blood pH during experimental Set 1 and Set 2, respectively. The black line shows values obtained from BGA. The green line shows values calculated according to the Equation 2 (see methods 2.7). According to these data, the removal of CO2 and the corresponding decrease on pCO2 accounts for the elevation of blood pH. The higher the CO2 removal, the higher the pH increase in blood that can be achieved.
Additional file 3: Figure S3 and S4. Representation of all the BGA tests performed during the experiments from Set 1 and Set 2, respectively. The black line shows values obtained from blood. The green line shows calculated values considering variations (inlet – outlet) from pCO2 and SID according Equation 2 (see methods 2.7). It is assumed that no variation on total protein content occurs as it cannot be lost in the dialyzer. Therefore, variations in [Atot] are not considered within the equation. These results show, that taking into account variations in pCO2 and SID along the dialyzer, the resulting pH at the outlet can be predicted following the calculations suggested by Stewart .
Additional file 4: Figure S5 and S6. Correlation of the measured and calculated pH variations between the inlet and the outlet of the dialyzer (ΔpH = pHoutlet – pHinlet) during experimental Set 1 and 2, respectively. Measured values were obtained from BGA while calculated values were obtained according to the Equation 2. Each line accounts for a combination of different ADVOS settings (blood flow/concentrate flow). As demonstrated for Supplementary Figure 3 and 4, for each of the settings, there is a correlation between measured and calculated values according to the Stewart approach.
Additional file 5: Figure S7. Buffer capacity of a dialysate containing 20 mmol/l sodium bicarbonate with or without albumin (2 g/dl). The buffer capacity (β) is defined as the moles of an acid or base necessary to change the pH of a solution by 1, divided by the pH change and the volume of buffer in liters.
Additional file 7: Figure S9. Correlation between SID variations (outlet – inlet) and pCO2 variation (outlet – inlet) using raw data. These data show, that in our experiments there is no interdependence between SID and pCO2 variation, contrary to what is described in . Using quartiles for pCO2 variation as shown in Supp. Figure 8, an artefactual correlation might be created.
About this article
Cite this article
Perez Ruiz de Garibay, A., Kellum, J.A., Honigschnabel, J. et al. Respiratory and metabolic acidosis correction with the ADVanced Organ Support system. ICMx 7, 56 (2019) doi:10.1186/s40635-019-0269-7
- Multiple organ failure
- Respiratory hemodialysis
- Extracorporeal carbon dioxide removal
- Respiratory acidosis
- Metabolic acidosis
- Lactic acidosis
- Albumin dialysis
- Extracorporeal organ support