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Open Access

Peer-reviewed

Research Article

Middle molecule clearance with high cut-off dialyzer versus high-flux dialyzer using continuous veno-venous hemodialysis with regional citrate anticoagulation: A prospective randomized controlled trial

  • Lorenz Weidhase ,

    Roles Conceptualization, Formal analysis, Funding acquisition, Investigation, Methodology, Project administration, Resources, Writing – original draft

    lorenz.weidhase@medizin.uni-leipzig.de

    Affiliation Medical Intensive Care Unit, University Hospital Leipzig, Leipzig, Saxony, Germany

    ⨯
  • Elena Haussig,

    Roles Conceptualization, Data curation, Formal analysis, Investigation, Project administration, Writing – review & editing

    Affiliation Medical Intensive Care Unit, University Hospital Leipzig, Leipzig, Saxony, Germany

    ⨯
  • Stephan Haussig,

    Roles Data curation, Formal analysis, Supervision, Validation, Visualization, Writing – review & editing

    Affiliation Department of Internal Medicine/Cardiology, University of Dresden, Heart Center Dresden, Dresden, Saxony, Germany

    ⨯
  • Thorsten Kaiser,

    Roles Resources, Supervision, Validation, Writing – review & editing

    Affiliation Institute for Laboratory Medicine, Clinical Chemistry and Molecular Diagnostics, University Hospital Leipzig, Leipzig, Saxony, Germany

    ⨯
  • Jonathan de Fallois,

    Roles Data curation, Investigation, Writing – review & editing

    Affiliation Medical Intensive Care Unit, University Hospital Leipzig, Leipzig, Saxony, Germany

    ⨯
  • Sirak Petros

    Roles Conceptualization, Supervision, Writing – review & editing

    Affiliation Medical Intensive Care Unit, University Hospital Leipzig, Leipzig, Saxony, Germany

    ⨯

Abstract

Background

Regional anticoagulation with citrate during renal replacement therapy (RRT) reduces the risk of bleeding, extends dialyzer lifespan and is cost-effective. Therefore, current guidelines recommend its use if patients are not anticoagulated for another reason and if there are no contraindications against citrate. RRT with regional citrate anticoagulation has been established in critically ill patients as continuous veno-venous hemodialysis (CVVHD) to reduce citrate load. However, CVVHD is inferior regarding middle molecule clearance compared to continuous veno-venous hemofiltration (CVVH). The use of a high cut-off dialyzer in CVVHD may thus present an option for middle molecule clearance similar to CVVH. This may allow combining the advantages of both techniques.

Methods

In this prospective, randomized, single-blinded single-center-trial, sixty patients with acute renal failure and established indication for renal replacement therapy were randomized 1:1 into two groups. The control group was put on CVVHD using regional citrate anticoagulation and a high-flux dialyzer, while the intervention group was on CVVHD using regional citrate anticoagulation and a high-cut-off dialyzer. The concentrations of urea, creatinine, β2-microglobulin, myoglobin, interleukin 6 and albumin were measured pre- and post-dialyzer 1, 6, 12, 24 and 48 hours after initiating CVVHD.

Results

Mean plasma clearance for β2-microglobulin was 19.6±5.8 ml/min in the intervention group vs. 12.2±3.6 ml/min in the control group (p<0.001). For myoglobin (8.0±4.5 ml/min vs. 0.2±3.6 ml/min, p<0.001) and IL-6 (1.5±4.3 vs. -2.5±3.5 ml/min, p = 0.002) a higher mean plasma clearance using high-cut-off dialyzer could be detected too, but no difference for urea, creatinine and albumin could be observed concerning this parameter between the two groups.

Conclusion

CVVHD using a high cut-off dialyzer results in more effective middle molecule clearance than that with high-flux dialyzer.

Trial registration

German Clinical Trials Register (DRKS00005254, registered 26th November 2013)

Citation: Weidhase L, Haussig E, Haussig S, Kaiser T, de Fallois J, Petros S (2019) Middle molecule clearance with high cut-off dialyzer versus high-flux dialyzer using continuous veno-venous hemodialysis with regional citrate anticoagulation: A prospective randomized controlled trial. PLoS ONE 14(4): e0215823. https://doi.org/10.1371/journal.pone.0215823

Editor: Yoshitaka Isaka, Osake University Graduate School Of Medicine, JAPAN

Received: October 23, 2018; Accepted: April 9, 2019; Published: April 26, 2019

Copyright: © 2019 Weidhase et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Data Availability: Data underlying the findings are available in Supporting Information in SPSS und EXCEL format.

Funding: Laboratory analyses, medical disposables and additional costs of material were funded by Fresenius Medical Care Deutschland GmbH, Else-Kröner-Straße 1, D-61352 Bad Homburg v.d.H. This is an investigator initiated trial. Design of the study, collection, analysis and interpretation of data as well as writing the manuscript were not influenced by the funding body and are the work of the authors alone. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Competing interests: Laboratory analyses, medical disposables and additional costs were funded by Fresenius Medical Care Deutschland GmbH, Else-Kröner-Straße 1, D-61352 Bad Homburg v.d.H. This is an investigator initiated trial. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. There is no relation of authors to the funder concerning employment, consultancy, patents, products in development and marketed products. This does not alter our adherence to PLOS ONE policies on sharing data and materials.

Introduction

Acute kidney injury requiring renal replacement therapy (RRT) is associated with a high mortality [1, 2] and represents an independent risk factor besides the severity of the underlying disease [3]. Continuous renal replacement therapy (CRRT) offers better hemodynamic stability and gentle removal of solutes and fluids [4]. Nevertheless, a better survival could not be demonstrated with CRRT compared to intermittent hemodialysis (IHD) [5, 6]. Furthermore, there is a lack of evidence concerning optimal dose [7, 8, 4, 9, 10] and the best time point to start RRT [11, 12].

Anticoagulation during CRRT is necessary to avoid blood clotting in the extracorporeal circuit. Systemic anticoagulation poses a risk, particularly in patients with a high risk of bleeding, such as the critical care patient population. Regional citrate anticoagulation has already been implemented in clinical practice during the last years and it has been proved feasible and safe [13]. It reduces the risk of bleeding [14, 15], extends dialyzer lifespan [15, 16] and it is cost-effective [16]. However, a definite survival advantage has not yet been demonstrated [17, 18]. Current international guidelines recommend regional citrate anticoagulation if patients are not anticoagulated for another reason and if there are no contraindications against citrate [19]. Citrate has to be metabolized in the intermediary metabolism to bicarbonate. Thus, its metabolism may be seriously impaired in patients with severe liver dysfunction [20].

A lower extracorporeal circuit blood flow is required in diffusion-based RRT techniques compared to convection-based ones. Therefore, continuous veno-venous hemodialysis (CVVHD) enables reducing citrate load in critical care patients [21]. However, CVVHD is inferior regarding middle molecule clearance compared to continuous veno-venous hemofiltration (CVVH) [22]. Using high cut off (HCO) membranes with a pore size larger than 0.01 μm in CVVHD could be a solution for this problem [23, 24]. One of such dialyzers is the Ultraflux EMiC2 (Fresenius Medical Care, Bad Homburg, Germany). Clinical data concerning this dialyzer are limited.

The aim of this prospective randomized trial was to evaluate the middle molecule clearance with citrate anticoagulated CVVHD using a HCO-dialyzer compared to CVVHD with the standard high-flux dialyzer.

Material and methods

This study is a prospective, randomized, single-blinded single-center trial in a 28-bed medical intensive care unit (ICU) at the University Hospital Leipzig, Germany. The study was approved by the local ethics committee (University of Leipzig, reference number: 447-12-24092012), conducted in accordance with the German medical product law and registered in the German Clinical Trials Register (DRKS00005254, registered 26 November 2013). Informed consent was obtained from all participating subjects. Eligible patients were enrolled after informed consent by the patients themselves or their legal guardians. The trial was conducted between May 2014 and May 2015.

Subjects

Eligible patients were critically ill patients with acute renal failure and indication for RRT based on the recommendations of the Kidney Disease: Improving Global Outcomes [19]. Exclusion criteria were anticoagulation therapy for other reasons, high risk for citrate accumulation (e.g. liver failure), contraindications for renal replacement therapy (e.g. advanced malignant disease), moribund patients, pregnancy and lactation, age lower than 18 years, rejection of renal replacement therapy at all or refusal to participate in the study. 26 patients per group had been calculated to show a difference in plasma clearance of 8 ml/min (two-tailed power 90%, p = 0.05) based on findings by Ricci et al. [22]. Thus, sixty consecutive patients were randomized 1:1 into the intervention and control groups. An unrestricted randomization was carried out using sequentially numbered, opaque sealed envelopes as described by Doig et al. [25]. Recruitment flow chart is illustrated in Fig 1.

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Fig 1. Recruitment flow chart.

https://doi.org/10.1371/journal.pone.0215823.g001

The following clinical data were collected in all patients: age, sex, body height, body weight, APACHE II score, SAPS II, SOFA score, the need for mechanical ventilation and vasopressor treatment.

Intervention

The control group was managed with CVVHD using the high-flux-dialyzer Ultraflux AV 1000S (Fresenius Medical Care, Bad Homburg, Germany), while CVVHD with the HCO-dialyzer Ultraflux EMiC2 (Fresenius Medical Care, Bad Homburg, Germany) was performed in the intervention group. Both dialyzers have the same effective surface area (1.8 m2), consist of identical material (polysulfone), exhibit a similar wall thickness (35μm) and differ only in pore size.

Regional citrate anticoagulation was used in both groups. Sodium citrate infusion (citrate: 136 mmol/l) was adjusted based on the concentration of post-dialyzer ionized calcium (target: 0.25–0.34 mmol/l). Calcium chloride solution (calcium: 83 mmol/l) was added to the extracorporeal circuit closer to the vascular access of the patient to keep systemic ionized calcium between 1.12–1.20 mmol/l. The vascular access was in all cases a double-lumen high-flow catheter. RRT was performed with the dialysis machine multiFiltrate (Fresenius Medical Care, Bad Homburg, Germany). A bicarbonate buffered dialysate (Ci-Ca Dialysate K4, Fresenius Medical Care, Bad Homburg, Germany) was used in all cases, at a dose of 25 ml/kg/h after adjusting for body weight. Ideal body weight was calculated using the Hamwi equation (for males: 48 kg for the first 152 cm + 1.1 kg for each additional cm; for females 45 kg for the first 152 cm +0.9 kg for each additional cm; [26]). The quotient of current body weight to ideal body weight was then computed. If this quotient was more than 1.3, the adjusted body weight was used for calculation of dialysate flow (for males: (current body weight-ideal body weight) x 0.38 + ideal body weight; for females: (current body weight-ideal body weight) x 0.32 + ideal body weight; [27]). Blood flow (QB) in the extracorporeal circuit was adjusted threefold of the dialysate flow. Duration of the extracorporeal circuit was limited to 72 hours (h) according to manufacturer`s instructions.

Endpoints and calculations

The concentrations of urea (60 Dalton (Da)), creatinine (113 Da), β2-microglobulin (11800 Da), myoglobin (17053 Da), interleukin 6 (IL-6, 26000 Da) and albumin (66470 Da) were measured pre-and post-dialyzer 1, 6, 12, 24 and 48 h after initiating CVVHD.

Plasma flow in the extracorporeal circuit (Qp) was calculated using the patient’s hematocrit level (Hct) at the time of clearance sampling:

Substance-specific plasma clearance (Clp) at the sampling time points was estimated using the following equation:

[28]

The primary outcome was plasma clearance of β2-microglobulin, which is considered to represent middle molecules. Secondary endpoints were the plasma clearance of urea, creatinine, myoglobin, IL-6, albumin. For estimating the total clearance (Cltotal), the integral for substance-specific elimination between the first and the forty-eighth hour was calculated using the following formula:

The period between starting RRT and the first measurement after 1 h was not considered because of equilibration processes. Mean plasma clearance (Clmean) was determined as follows:

The mean ultrafiltration rate (UFRmean) to achieve negative fluid balance was calculated similar mean plasma clearance:

Laboratory analyses

Blood samples were sent for analysis immediately after the draw. Laboratory analyses were performed using Cobas 8000 (Roche, Mannheim, Germany) according to the manufacturer´s instructions.

The following methods had been used:

  • urea: kinetic test with urease and glutamate dehydrogenase
  • creatinine: enzymatic method with creatinase
  • β2-microglobulin: am c701 immunological test for turbidity
  • myoglobin: ElektroChemiLumineszenzImmunoAssay (ECLIA)
  • IL-6: ECLIA
  • albumin: color test with bromocresol green

Statistical analyses

Data were analyzed using the IBM SPSS 24. Categorical variables were tested by chi-square (two-sided). The Kolmogorov-Smirnov test was performed to test for normal distribution of continuous variables. Normally distributed variables were analyzed by the Student’s t-test and presented as mean with standard deviation and confidence interval (CI). Not normally distributed variables were assessed by Mann-Whitney U test and presented as median with25th and75th quantiles in brackets. A p value <0.05 was considered statistically significant.

Results

Baseline characteristics of the study groups are shown in Table 1, with no significant difference between the control group and the intervention group.(Table 1)

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Table 1. Baseline characteristics.

https://doi.org/10.1371/journal.pone.0215823.t001

The calculated median dialysate flow (control group: 1800 ml/h (1500,2000); intervention group:1800 ml/h (1538,2000) and mean blood flow (control group: 103.6±19.0 ml/min; intervention group: 94.6±18.0 ml/min) did not differ significantly between the treatment groups. Based on this, a dialysate flow of 1800 ml/h (1500,2000) and blood flow of 98 ml/min (90,102.5) in the control group and a dialysate flow of 1900 ml/h (1663,2000) and blood flow of 90 ml/min (80.0,100.0) ml/min in the intervention group were realized without significant differences. The median dialyzer lifespan in the extracorporeal circuit was 69.3h (47.8,73.6) in the control group and 62.8h (49.6,70.1) in the intervention group (p = 0.40). Sodium citrate and calcium chloride infusion rates did not differ between Ultraflux AV 1000S and Ultraflux EMiC2 study arm (Table in S1 Table, Table in S2 Table).

Data for plasma clearance of β2-microglobulin are given in Table 2 and Figure in S1 Fig, showing a significant difference between the two groups at all study time points.

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Table 2. β2-microglobulin plasma clearance (ml/min).

https://doi.org/10.1371/journal.pone.0215823.t002

The mean plasma clearance was 12.2±3.6 ml/min (CI: 10.5–13.9) in the control group and 19.6±5.8 ml/min (CI: 17.0–22.1) in the intervention group (p<0.001).

Concerning secondary endpointsa significantly better elimination of myoglobin and IL-6 could be observed in the intervention group, but there was no significant difference for mean urea, creatinine and albumin clearance between the two groups. Mean plasma clearance data are given in Table 3 and Figure in S2 Fig.

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Table 3. Mean plasma clearance (ml/min), n = 42.

https://doi.org/10.1371/journal.pone.0215823.t003

The median ultrafiltration rate to achieve negative fluid balance showed no significant differences (control group: 50.0 ml/h (0.0, 99.5); intervention group: 12.8 ml/h (0.0, 62.5)). The ratio of β2-microglobulin plasma clearance between 1h and 48h to estimate dialyzer performance for middle molecules over time was 1.31 (1.07,1.70) in control group and 1.19 (0.54,1.61) in intervention group without significant differences.

Discussion

This prospective randomized trial compared the application of two different dialyzers during CVVHD with regional citrate anticoagulation in critically ill patients. A significantly better plasma clearance of middle molecules could be demonstrated with the high cut-off dialyzer compared with the standard high-flux dialyzer. Since both dialyzers are made of the same membrane surface and material, the differences in the plasma clearance of the investigated substances can be explained only by the difference in pore sizes. β2-microglobulin is a surrogate parameter for middle molecular uremic toxins. Elevated serum levels of this protein are associated with increased mortality and development of amyloidosis [29, 30, 31, 32]. A few reports showed that reduction in β2-microglobulin levels may have mortality benefit in end stage renal disease [29, 30]. Hemodialysis using high cut-off dialyzers was shown to effectively lower plasma β2-microglobulin levels [33]. A cross-over study in a small study population using sustained low efficiency daily dialysis (SLEDD) [28] demonstrated a superior elimination of β2-microglobulin using the high cut-off Ultraflux EMiC2 dialyzer than with the high-flux dialyzer Ultraflux AV 1000S (plasma clearance: 52 ± 1,7 ml/min vs. 41.7 ± 1.5 ml/min, p<0.001). The higher clearance rate in that study compared to ours is due to the higher volume exchange per time with SLEDD. Similar to that study, our trial also showed that there is no relevant albumin loss with the high cut-off dialyzer. Another investigation showed an enhanced elimination of glutamine and serine with the high cut-off Ultraflux EMiC2 [34], while circulating microRNAs were not eliminated by this dialyzer [35]. A recent study demonstrated a higher clearance of IL-6 and interleukin 10 using Ultraflux EMiC2 compared with AV 1000S in CVVHD with citrate anticoagulation [36]. Another recent trial revealed no differences in removing β2-microglobulin between continuous veno-venous hemodiafiltration (CVVHDF) using Ultraflux AV 1000S and CVVHD using Ultraflux EMiC2. However, the dialysis dose was in the CVVHDFgroup (36±4 ml/kg/h) much higher than in the CVVHD group (21±6 ml/kg/h) [37]. In summary, the available data indicate that Ultraflux EMiC2 allows an effective elimination of molecules up to a molecular weight of 40 kDa [38].

Clinical trials with other high cut-off membranes with a maximum cut-off at 50 kDa are limited [39]. An older study on 16 patients with sepsis-related multiple organ failure using an intermittent high permeability hemofiltration over five days for 12 h per day alternated with conventional hemofiltration showed that IL-6 could be eliminated effectively by high cut-off membranes. However, an albumin loss was detected, particularly at the beginning of the RRT, while antithrombin, protein C, protein S, thrombin, coagulation factor V and VIII were not affected [40]. The decline in albumin loss during further RRT could be explained by formation of a new layer at the membrane surface, known as membrane fouling [39]. Our trial showed a significant clearance in IL-6 without albumin loss. This result agrees with the findings of a recent publication [36]. A good dialyzer performance for β2-microglobulin over time could be demonstrated in our investigation, which can be explained by a lower membrane fouling and protein cake formation with regional citrate anticoagulation [41].

Several other studies showed that high cut-off dialyzers allow a diffusive removal of cytokines [42, 43, 44]. Therefore, hemodialysis with high cut-off membranes and sufficient dialysate flow seems to be effective in the elimination of inflammatory mediators and safer than high permeability hemofiltration without any relevant albumin loss [39].

A case report on a patient with rhabdomyolysis showed a decline in serum myoglobin levels by 50% within 4 hours using high cut-off intermittent hemodialysis, while myoglobin levels even increased using standard high-flux dialysis [45]. A case series demonstrated that CVVHD and SLEDD with high cut-off dialyzers allow a considerable removal of myoglobin [46]. The present trial found a significantly better elimination of myoglobin in the intervention group. Therefore, patients suffering from rhabdomyolysis and increased risk of bleeding could be treated effectively by citrate anticoagulated CVVHD using the high cut-off Ultraflux EMiC2 dialyzer. Further clinical investigations are required to validate this conclusion.

Other middle molecule toxic proteins may also be removed using the HCO dialyzer. Two case series in patients with multiple myeloma showed a significant removal of free light chains by HCO dialyzer [47, 48]. A case report using the Ultraflux EMiC2 dialyzer showed similar results [38].

There are limitations to our trial. It is a monocentric, single-blinded trial. The study was designed and powered to analyze substance-related elimination in critical care patients. Therefore, the sample size is not adequate to evaluate hard clinical endpoints such as mortality. Furthermore, the dialyzer life span exceeded 48 hours in only 42 of our patients, so that mean plasma clearance calculation was limited to this group. Nevertheless, our study provides a solid background to generate hypotheses and design clinical trials.

Conclusions

There is an effective elimination of β2-microglobulin in citrate anticoagulated CVVHD using the HCO-dialyzer Ultraflux EMiC2 in critical care patients. A significant removal of myoglobin and IL-6 also seems to be possible. Therefore this procedure could be useful in patients suffering from rhabdomyolysis and increased risk of bleeding as well as those with severe inflammation.

Acknowledgments

We thank the following colleagues for their continuous support during the trial: Martin Grimm, Jan Halbritter, Anna-Maria Keilitz, Katrin Knoll, Kevin Kunz, Konstanze Lichtenberger, Tom Lindner, Frank Meineke, Bastian Pasieka, Alexander Peschka, Gero Schulze, Frank Seidel.

References

  1. 1. Uchino S, Kellum JA, Bellomo R, Doig GS, Morimatsu H, Morgera S et al. Beginning and Ending Supportive Therapy for the Kidney (BEST Kidney) Investigators. Acute renal failure in critically ill patients: a multinational, multicenter study. JAMA. 2005 Aug 17;294(7):813–8.
  2. 2. Hoste EA, Bagshaw SM, Bellomo R, Cely CM, Colman R, Cruz DN et al. Epidemiology of acute kidney injury in critically ill patients: the multinational AKI-EPI study. Intensive Care Med. 2015 Aug;41(8):1411–23. pmid:26162677
  3. 3. Levy EM, Viscoli CM, Horwitz RI. The effect of acute renal failure on mortality. A cohort analysis. JAMA. 1996 May 15;275(19):1489–94. pmid:8622223
  4. 4. Palevsky PM. Dialysis modality and dosing strategy in acute renal failure. Semin Dial. 2006 Mar-Apr;19(2):165–70. pmid:16551296
  5. 5. Bagshaw SM, Berthiaume LR, Delaney A, Bellomo R. Continuous versus intermittent renal replacement therapy for critically ill patients with acute kidney injury: a meta-analysis. Crit Care Med. 2008 Feb;36(2):610–7. pmid:18216610
  6. 6. Truche AS, Darmon M, Bailly S, Clec’h C, Dupuis C, Misset B et al. OUTCOMEREA Study Group. Continuous renal replacement therapy versus intermittent hemodialysis in intensive care patients: impact on mortality and renal recovery. Intensive Care Med. 2016 Sep;42(9):1408–17. pmid:27260258
  7. 7. Ronco C, Bellomo R, Homel P, Brendolan A, Dan M, Piccinni P et al. Effects of different doses in continuous veno-venous haemofiltration on outcomes of acute renal failure: a prospective randomised trial. Lancet. 2000 Jul 1;356(9223):26–30. pmid:10892761
  8. 8. Saudan P, Niederberger M, De Seigneux S, Romand J, Pugin J, Perneger T et al. Adding a dialysis dose to continuous hemofiltration increases survival in patients with acute renal failure. Kidney Int. 2006 Oct;70(7):1312–7. pmid:16850022
  9. 9. VA/NIH Acute Renal Failure Trial Network, Palevsky PM, Zhang JH, O'Connor TZ, Chertow GM, Crowley ST, Choudhury D et al. Intensity of renal support in critically ill patients with acute kidney injury. N Engl J Med. 2008 Jul 3;359(1):7–20. pmid:18492867
  10. 10. RENAL Replacement Therapy Study Investigators, Bellomo R, Cass A, Cole L, Finfer S, Gallagher M, Lo S et al. Intensity of continuous renal-replacement therapy in critically ill patients. N Engl J Med. 2009 Oct 22;361(17):1627–38. pmid:19846848
  11. 11. Gaudry S, Hajage D, Schortgen F, Martin-Lefevre L, Pons B, Boulet E et al. AKIKI Study Group. Initiation Strategies for Renal-Replacement Therapy in the Intensive Care Unit. N Engl J Med. 2016 Jul 14;375(2):122–33. pmid:27181456
  12. 12. Zarbock A, Kellum JA, Schmidt C, Van Aken H, Wempe C, Pavenstädt H et al. Effect of Early vs Delayed Initiation of Renal Replacement Therapy on Mortality in Critically Ill Patients With Acute Kidney Injury: The ELAIN Randomized Clinical Trial. JAMA. 2016 May 24–31;315(20):2190–9. pmid:27209269
  13. 13. Morgera S, Haase M, Ruckert M, Krieg H, Kastrup M, Krausch D et al. Regional citrate anticoagulation in continuous hemodialysis—acid-base and electrolyte balance at an increased dose of dialysis. Nephron Clin Pract. 2005;101(4):c211–9 pmid:16155399
  14. 14. Oudemans-van Straaten HM, Bosman RJ, Koopmans M, van der Voort PH, Wester JP, van der Spoel JI et al. Citrate anticoagulation for continuous venovenous hemofiltration. Crit Care Med. 2009 Feb;37(2):545–52. pmid:19114912
  15. 15. Hetzel GR, Schmitz M, Wissing H, Ries W, Schott G, Heering PJ et al. Regional citrate versus systemic heparin for anticoagulation in critically ill patients on continuous venovenous haemofiltration: a prospective randomized multicentre trial. Nephrol Dial Transplant. 2011 Jan;26(1):232–9. pmid:20876598
  16. 16. Schilder L, Nurmohamed SA, Bosch FH, Purmer IM, den Boer SS, Kleppe CG et al. CASH study group. Citrate anticoagulation versus systemic heparinisation in continuous venovenous hemofiltration in critically ill patients with acute kidney injury: a multi-center randomized clinical trial. Crit Care. 2014 Aug 16;18(4):472. pmid:25128022
  17. 17. Bai M, Zhou M, He L, Ma F, Li Y, Yu Y et al. Citrate versus heparin anticoagulation for continuous renal replacement therapy: an updated meta-analysis of RCTs. Intensive Care Med. 2015 Dec;41(12):2098–110. pmid:26482411
  18. 18. Liu C, Mao Z, Kang H, Hu J, Zhou F. Regional citrate versus heparin anticoagulation for continuous renal replacement therapy in critically ill patients: a meta-analysis with trial sequential analysis of randomized controlled trials. Crit Care. 2016 May 13;20(1):144. pmid:27176622
  19. 19. Kidney Disease: Improving Global Outcomes (Kdigo) Acute Kidney Injury Work Group (2012) KDIGO clinical practice guideline for acute kidney injury. Kidney Int 2(1):1–138.
  20. 20. Kramer L, Bauer E, Joukhadar C, Strobl W, Gendo A, Madl C et al. Citrate pharmacokinetics and metabolism in cirrhotic and noncirrhotic critically ill patients. Crit Care Med. 2003 Oct;31(10):2450–5. pmid:14530750
  21. 21. Morgera S, Scholle C, Voss G, Haase M, Vargas-Hein O, Krausch D et al. Metabolic complications during regional citrate anticoagulation in continuous venovenous hemodialysis: single-center experience. Nephron Clin Pract. 2004;97(4):c131–6. pmid:15331942
  22. 22. Ricci Z, Ronco C, Bachetoni A, D'amico G, Rossi S, Alessandri E et al. Solute removal during continuous renal replacement therapy in critically ill patients: convection versus diffusion. Crit Care. 2006;10(2):R67. pmid:16646985
  23. 23. Naka T, Haase M, Bellomo R. 'Super high-flux’ or ’high cut-off’ hemofiltration and hemodialysis. Contrib Nephrol. 2010;166:181–9. pmid:20473007
  24. 24. Villa G, Zaragoza JJ, Sharma A, Neri M, De Gaudio AR, Ronco C. Cytokine removal with high cut-off membrane: review of literature. Blood Purif. 2014;38(3–4):167–73. pmid:25471681
  25. 25. Doig GS, Simpson F. Randomization and allocation concealment: a practical guide for researchers. J Crit Care. 2005 Jun;20(2):187–91 pmid:16139163
  26. 26. Glynn CC, Greene GW, Winkler MF, Albina JE. Predictive versus measured energy expenditure using limits-of-agreement analysis in hospitalized, obese patients. JPEN J Parenter Enteral Nutr. 1999 May-Jun;23(3):147–54. pmid:10338222
  27. 27. Krenitsky J. Adjusted body weight, pro: evidence to support the use of adjusted body weight in calculating calorie requirements. Nutr Clin Pract. 2005 Aug;20(4):468–73. pmid:16207686
  28. 28. Schmidt JJ, Hafer C, Clajus C, Hadem J, Beutel G, Schmidt BM et al. New high-cutoff dialyzer allows improved middle molecule clearance without an increase in albumin loss: a clinical crossover comparison in extended dialysis. Blood Purif. 2012;34(3–4):246–52. pmid:23171639
  29. 29. Roumelioti ME, Nolin T, Unruh ML, Argyropoulos C. Revisiting the Middle Molecule Hypothesis of Uremic Toxicity. A Systematic Review of Beta 2 Microglobulin Population Kinetics and Large Scale Modeling of Hemodialysis Trials In Silico. PLoS One. 2016 Apr 7;11(4):e0153157. pmid:27055286
  30. 30. Cheung AK, Greene T, Leypoldt JK, Yan G, Allon M, Delmez J et al. HEMO Study Group. Association between serum 2-microglobulin level and infectious mortality in hemodialysis patients. Clin J Am Soc Nephrol. 2008 Jan;3(1):69–77. Epub 2007 Dec 5. pmid:18057309
  31. 31. Okuno S, Ishimura E, Kohno K, Fujino-Katoh Y, Maeno Y, Yamakawa T et al. Serum beta2-microglobulin level is a significant predictor of mortality in maintenance haemodialysis patients. Nephrol Dial Transplant. 2009 Feb;24(2):571–7. pmid:18799606
  32. 32. Liabeuf S, Lenglet A, Desjardins L, Neirynck N, Glorieux G, Lemke HD et al. European Uremic Toxin Work Group (EUTox). Plasma beta-2 microglobulin is associated with cardiovascular disease in uremic patients. Kidney Int. 2012 Dec;82(12):1297–303. pmid:22895515
  33. 33. Pellicano R, Polkinghorne KR, Kerr PG. Reduction in beta2-microglobulin with super-flux versus high-flux dialysis membranes: results of a 6-week, randomized, double-blind, crossover trial. Am J Kidney Dis. 2008 Jul;52(1):93–101. pmid:18423807
  34. 34. Schmidt JJ, Hafer C, Spielmann J, Hadem J, Schönenberger E, Schmidt BM et al. Removal characteristics and total dialysate content of glutamine and other amino acids in critically ill patients with acute kidney injury undergoing extended dialysis. Nephron Clin Pract. 2014;126(1):62–6. pmid:24577340
  35. 35. Martino F, Lorenzen J, Schmidt J, Schmidt M, Broll M, Görzig Y et al. Circulating microRNAs are not eliminated by hemodialysis. PLoS One. 2012;7(6):e38269. pmid:22715378
  36. 36. Eichhorn T, Hartmann J, Harm S, Linsberger I, König F, Valicek G et al. Clearance of Selected Plasma Cytokines with Continuous Veno-Venous Hemodialysis Using Ultraflux EMiC2 versus Ultraflux AV1000S. Blood Purif. 2017 Oct 7;44(4):260–266 pmid:28988232
  37. 37. Balgobin S, Morena M, Brunot V, Besnard N, Daubin D, Platon L et al. Continuous Veno-Venous High Cut-Off Hemodialysis Compared to Continuous Veno-Venous Hemodiafiltration in Intensive Care Unit Acute Kidney Injury Patients. Blood Purif. 2018;46(3):248–256. pmid:29972818
  38. 38. Jayaballa M, Bose B, Gangadharan Komala M, Fischer ER, Taper J, Sud K. Effective Removal of κ-Free Light Chains with Hemodialysis Using Fresenius Ultraflux EMiC2 Dialyser in a Patient with Myeloma Cast Nephropathy, with Associated Cost Savings. Blood Purif. 2016;42(2):158–9. pmid:27270690
  39. 39. Villa G, Zaragoza JJ, Sharma A, Neri M, De Gaudio AR, Ronco C. Cytokine removal with high cut-off membrane: review of literature. Blood Purif. 2014;38(3–4):167–73. pmid:25471681
  40. 40. Morgera S, Rocktäschel J, Haase M, Lehmann C, von Heymann C, Ziemer S et al. Intermittent high permeability hemofiltration in septic patients with acute renal failure. Intensive Care Med. 2003 Nov;29(11):1989–95. Epub 2003 Sep 3. pmid:12955174
  41. 41. Fischer KG. Essentials of anticoagulation in hemodialysis. Hemodial Int. 2007 Apr;11(2):178–89. Review. pmid:17403168
  42. 42. Haase M, Bellomo R, Baldwin I, Haase-Fielitz A, Fealy N, Davenport P et al. Hemodialysis membrane with a high-molecular-weight cutoff and cytokine levels in sepsis complicated by acute renal failure: a phase 1 randomized trial. Am J Kidney Dis. 2007 Aug;50(2):296–304. pmid:17660031
  43. 43. Kade G, Lubas A, Rzeszotarska A, Korsak J, Niemczyk S. Effectiveness of High Cut-Off Hemofilters in the Removal of Selected Cytokines in Patients During Septic Shock Accompanied by Acute Kidney Injury-Preliminary Study. Med Sci Monit. 2016 Nov 13 [revised 2016 Nov 14];22:4338–4344. pmid:27840404
  44. 44. Chelazzi C, Villa G, D'Alfonso MG, Mancinelli P, Consales G, Berardi M et al. Hemodialysis with High Cut-Off Hemodialyzers in Patients with Multi-Drug Resistant Gram-Negative Sepsis and Acute Kidney Injury: A Retrospective, Case-Control Study. Blood Purif. 2016;42(3):186–93. pmid:27352068
  45. 45. Albert C, Haase M, Bellomo R, Mertens PR. High cut-off and high-flux membrane haemodialysis in a patient with rhabdomyolysis-associated acute kidney injury. Crit Care Resusc. 2012 Jun;14(2):159–62. pmid:22697626
  46. 46. Heyne N, Guthoff M, Krieger J, Haap M, Häring HU. High cut-off renal replacement therapy for removal of myoglobin in severe rhabdomyolysis and acute kidney injury: a case series. Nephron Clin Pract. 2012;121(3–4):c159–64 pmid:23327834
  47. 47. Martín-Reyes G, Toledo-Rojas R, Torres-de Rueda Á, Sola-Moyano E, Blanca-Martos L, Fuentes-Sánchez L et al. Haemodialysis using high cut-off dialysers for treating acute renal failure in multiple myeloma. Nefrologia. 2012;32(1):35–43. pmid:22294003
  48. 48. Heyne N, Denecke B, Guthoff M, Oehrlein K, Kanz L, Häring HU et al. Extracorporeal light chain elimination: high cut-off (HCO) hemodialysis parallel to chemotherapy allows for a high proportion of renal recovery in multiple myeloma patients with dialysis-dependent acute kidney injury. Ann Hematol. 2012 May;91(5):729–735. pmid:22170517