Pharmacokinetics and pharmacodynamics of danaparoid during continuous venovenous hemofiltration: a pilot study
© de Pont et al.; licensee BioMed Central Ltd. 2007
Received: 22 June 2007
Accepted: 13 September 2007
Published: 13 September 2007
In patients with suspected heparin-induced thrombocytopenia (HIT) who need renal replacement therapy, a nonheparin anticoagulant has to be chosen to prevent thrombosis in the extracorporeal circuit. Danaparoid, a low-molecular-weight heparinoid consisting of heparan sulphate, dermatan sulphate, and chondroitin sulphate, is recommended for systemic anticoagulation in patients with HIT. However, there are few data on the use of danaparoid in patients with acute renal failure, especially in patients dependent on renal replacement therapy such as continuous venovenous hemofiltration (CVVH). In the present study, we analyzed the pharmacokinetics and pharmacodynamics of danaparoid during CVVH in patients with suspected HIT.
Based on a mathematical model, a dosing scheme for danaparoid was designed, aiming at anti-Xa levels of 0.5 to 0.7 U/mL, with a maximum of 1.0 U/mL. This dosing scheme was prospectively tested in the first CVVH run of a cohort of five patients with suspected HIT. CVVH with a blood flow rate of 150 mL/minute and a substitution rate of 2,000 mL/hour was performed with a cellulose triacetate membrane. Danaparoid was administered as a continuous infusion of 100 anti-Xa-U/hour after a loading dose of 3,500 anti-Xa-U. Serial measurements of anti-Xa activity and prothrombin fragment F1+2 were performed at baseline, at t = 5, 15, and 30 minutes, and at t = 1, 2, 4, 8, 16, and 24 hours after the danaparoid loading dose.
The median anti-Xa activity reached a maximum of 1.02 (0.66 to 1.31) anti-Xa-U/mL after 15 minutes and gradually declined to 0.40 (0.15 to 0.58) anti-Xa-U/mL over the span of 24 hours. Target anti-Xa levels were reached from 2 to 12 hours after the loading dose. Median prothrombin fragment F1+2 gradually decreased from 432 (200 to 768) to 262 (248 to 317) pmol/L after 24 hours. No bleeding or thromboembolic events occurred throughout the described treatment period.
Danaparoid administered by a continuous infusion of 100 anti-Xa-U/hour after a loading dose of 3,500 anti-Xa-U elicited target anti-Xa levels from 2 to 12 hours after the loading dose, without bleeding or thromboembolic events during the described CVVH treatment in patients with suspected HIT.
During continuous venovenous hemofiltration (CVVH), anticoagulation with unfractionated heparin is commonly used to prevent thrombosis in the extracorporeal circuit. However, in patients with suspected heparin-induced thrombocytopenia (HIT), another anticoagulant has to be chosen. Because patients with HIT have a 25% to 50% risk of symptomatic thrombosis, systemic anticoagulation is indicated . In the American College of Chest Physicians guidelines for recognition, prevention, and treatment of HIT, direct thrombin inhibitors and danaparoid are recommended for systemic anticoagulation in patients with HIT . Danaparoid is a low-molecular-weight heparinoid consisting of a mixture of heparan sulphate (84%), dermatan sulphate (12%), and small amounts of chondroitin sulphate (4%). Its pharmacological effect is exerted primarily by the inhibition of factors Xa and IIa at a ratio greater than that of unfractionated heparin .
Although extensive experience with danaparoid has been gained in the clinical setting, there are few data on its use in patients with acute renal failure, especially in patients dependent on CVVH. Under normal conditions, the elimination of danaparoid is predominantly renal, with an elimination half-life of 25 hours. During CVVH, danaparoid can be removed only by means of a polyarylethersulphone membrane, with a sieving coefficient of 0.78 ± 0.03 . Therefore, treatment with a continuous infusion of danaparoid carries the risk of accumulation in patients with acute renal failure dependent on CVVH. Because an antidote is lacking, this accumulation may entail an increased risk of bleeding. The recommended dose for anticoagulation with danaparoid in HIT patients requiring CVVH is an intravenous (IV) loading dose of 2,250 anti-Xa-U followed by a continuous infusion of 600 anti-Xa-U/hour for the first 4 hours, 400 anti-Xa-U/hour for the next 4 hours, and then 200 to 400 anti-Xa-U/hour adjusted by anti-Xa level . A therapeutic anti-Xa level is 0.5 to 0.7 anti-Xa-U/mL, with a maximum of 1.0 anti-Xa-U/mL. However, using the recommended dosing scheme, our patients frequently experienced bleeding, especially when peak anti-Xa levels exceeded 1.0 anti-Xa-U/mL. In a retrospective analysis, we found a linear relationship between the peak anti-Xa level and the need of red blood cell transfusions in patients with a peak anti-Xa level of greater than 0.7 anti-Xa-U/mL (r2 = 0.55; p = 0.02) (ACJM de Pont, JJH Hofstra, DR Pik, JCM Meijers, MJ Schultz, unpublished data). Therefore, we decided to design a safer dosing scheme for danaparoid, based on a mathematical model aiming at a peak anti-Xa level of less than 1.0 and a maintenance level of between 0.5 and 0.7 anti-Xa-U/mL. Lindhoff-Last and colleagues  have suggested that a loading dose of 750 anti-Xa-U IV followed by a maintenance dose of 50 to 150 anti-Xa-U/hour might be sufficient to maintain a safe and effective level of anticoagulation. However, serial pharmacokinetic measurements to confirm this hypothesis have never been published. The aim of the present study was to determine the pharmacokinetic and pharmacodynamic properties of danaparoid in patients with suspected HIT treated with CVVH, using a new dosing scheme based on a mathematical model.
Materials and methods
Patients and study design
The observations in this study were made in the context of standardized protocol for routine patient care. Our institutional review board waived a formal approval procedure for the study. Eligible patients were suspected of HIT and had acute renal failure necessitating CVVH. Suspicion of HIT was based on the 4T score: (a) a more than 50% decrease in platelet count after exposure to heparin, (b) timing of the decrease in platelet count compatible with HIT, (c) a new thrombosis, skin necrosis, or an acute systemic reaction after heparin administration, and (d) absence of other causes of thrombocytopenia . In addition, antibodies against heparin/platelet factor 4 (PF4) complex were detected by means of enzyme-linked immunosorbent assay (ELISA). The exclusion criterion was overt bleeding or a manifest clotting disorder defined as a prothrombin time or an activated partial thromboplastin time of more than 1.5 times the upper limit of normal. Enrolled patients were studied for the duration of the first CVVH run in which danaparoid was used as an anticoagulant.
Vascular access was obtained by insertion of a double-lumen catheter (Duo-Flow 400XL, 14F × 6 inches (15 cm); Medcomp, Harleysville, PA, USA) into a large vein (femoral, subclavian, or internal jugular vein). CVVH was performed using a Diapact hemofiltration machine (B. Braun Melsungen AG, 34212 Melsungen, Germany) and a cellulose triacetate hemofilter (CT-190G; Baxter Healthcare Corp., Deerfield, IL, USA). The ultrafiltration rate was set at 2,000 mL/hour, and a bicarbonate-buffered substitution fluid was administered in predilution mode with a flow of 2,000 mL/hour. The blood flow was set at 150 mL/minute, and a negative fluid balance was allowed. Circuit survival time was defined as the time elapsed from starting CVVH until clotting of the extracorporeal circuit.
where α = 21/25. Ideally, the plasma concentration should be between 0.5 and 0.7 anti-Xa-U/mL. Thus, the value D is obtained by taking time to infinity, which yields D = 0.7 × 3.500 × (α - 1) anti-Xa-U, and consequently the loading dose B can be found as the maximal value for which the concentration does not exceed the value of 1.0 anti-Xa-U/mL.
The extracorporeal circuit was not primed with any anticoagulant. Based on the mathematical model, the danaparoid loading dose B was calculated to be 3,500 anti-Xa-U and the continuous dose D to be 100 anti-Xa-U/hour. The CVVH procedure was started immediately after administration of the danaparoid loading dose of 3,500 anti-Xa-U followed by a continuous danaparoid infusion of 100 anti-Xa-U/hour.
Blood collection, laboratory assays, and statistical analysis
Blood was collected in citrated vacutainer tubes at baseline, at t = 5, 15, and 30 minutes, and at t = 1, 2, 4, 8, 16, and 24 hours after the danaparoid loading dose and was processed immediately. Plasma was prepared by centrifugation at 2,500 g twice for 20 minutes at 16°C followed by storage at -80°C until assays were performed. Antibodies against heparin/PF4 complex were detected by ELISA (GTI PF4 HAT 45; Diagast, Loos, France). Anti-Xa activity was determined with Berichrom Heparin on a Behring Coagulation System (both from Dade Behring Marburg GmbH, Marburg, Germany). To assess the process of thrombin generation during CVVH, prothrombin fragments F1+2 (F1+2) were measured by ELISA (Enzygnost F1+2 [monoclonal]; Dade Behring Marburg GmbH). Normal values for F1+2 range from 300 to 1,600 pmol/L. Data are reported as median and range. Changes in coagulation parameters over time were compared by means of a paired Student's t test. Circuit survival times were compared with those previously published in the literature by means of Student's t test. A p value of less than 0.05 was considered significant.
Characteristics of the enrolled patients
Body weight (kg)
Etiology of ARF
Type of ARF
APACHE II score
Circuit survival time (hours)
Post-CABG × 5
Post-CABG × 3
Post-CABG × 5
Pharmacokinetics and pharmacodynamics of danaparoid during continuous venovenous hemofiltration
No clinically important bleeding events or thromboembolic complications occurred in any of the five patients during the described CVVH treatment.
Circuit survival times
The individual circuit survival times reached with danaparoid as an anticoagulant during CVVH are reported in Table 1. A median circuit survival time of 50.2 (20 to 89) hours was achieved.
In this small prospective cohort study, we demonstrated that using danaparoid in a loading dose of 3,500 anti-Xa-U IV followed by a continuous infusion of 100 anti-Xa-U/hour, the median peak anti-Xa level reached was slightly too high, whereas the median anti-Xa level fell below the target range of 0.5 to 0.7 U/mL after 12 hours. Thrombin generation remained within the normal range during the first 6 hours. To our knowledge, this is the first time the pharmacokinetics and pharmacodynamics of danaparoid have been studied during CVVH. A limitation of this study is that we used an ultrafiltration rate of 2 L/hour, which is lower than the 35 mL/kg per hour proven by Ronco and colleagues  to be most effective. Additional studies are needed to determine the optimal danaparoid dosing scheme during CVVH with an ultrafiltration rate of 35 mL/kg per hour or more.
Although in our cohort the median anti-Xa activity dropped below 0.5 U/mL after 12 hours, we achieved median circuit survival times similar to those reported by Lindhoff-Last and colleagues : 50.2 (20 to 89) hours versus 36 (24 to 70) hours (p value not significant). However, their mean circuit survival time was achieved with a lower loading dose (or no loading dose at all) followed by a continuous infusion varying from 90 to 225 anti-Xa-U/hour, reaching a mean anti-Xa activity varying from 0.33 to 0.89 U/mL. In addition, Lindhoff-Last and colleagues reported that with continuous venovenous hemodialysis, an even lower dose of danaparoid was effective: with a loading dose of 750 anti-Xa-U IV followed by a continuous infusion varying from 64 ± 10 to 315 ± 163 anti-Xa-U/hour, an anti-Xa activity of 0.23 ± 0.13 to 0.53 ± 0.17 U/mL was reached. Unfortunately, the circuit survival times achieved with this dose were not reported. However, in a study on anticoagulation with low-molecular-weight heparins during CVVH, we did not find a relationship between anti-Xa activity and circuit survival time: with a maximum anti-Xa activity of 0.46 ± 0.14 U/mL gradually declining over the span of 24 hours, a circuit survival time of 15.4 ± 7.4 hours was reached . This finding confirmed an earlier finding by Journois and colleagues , who did not find a relationship between anti-Xa levels and circuit survival times either. A recent randomized controlled crossover study among 40 critically ill patients also failed to establish a correlation between anti-Xa levels and filter survival .
Because bleeding complications are related to the anti-Xa activity reached , it is important to use the lowest possible dose of danaparoid that is still effective during CVVH. As can be calculated by our proposed formula, this might be achieved by lowering the loading dose, the level of continuous infusion, or both. Given that a loading dose of 3,500 anti-Xa-U IV led to a median maximum anti-Xa activity of 1.02 (0.66 to 1.31) U/mL, lowering the loading dose is recommended. Continuous infusion of 100 IU/hour was effective, as anti-Xa activities remained within the target range during the first 12 hours, leading to acceptable circuit survival times. Additional studies are needed to determine the lowest danaparoid dose for both loading and continuous infusion necessary to keep the circuit open.
This study demonstrated that danaparoid in a loading dose of 3,500 IU IV followed by a continuous infusion of 100 IU/hour was effective at keeping the extracorporeal circuit open, with median anti-Xa activities within the therapeutic range from 2 to 12 hours after the loading dose and without any bleeding or thomboembolic complications during the described treatment period.
When danaparoid was used as an anticoagulant during continuous venovenous hemofiltration, a loading dose of 3,500 IU IV followed by a continuous infusion of 100 IU/hour led to target anti-Xa levels of 0.5 to 0.7 U/mL from 2 to 12 hours after the loading dose.
To reach a peak anti-Xa level within the target range, the loading dose should be lowered according to the mathematical formula, aiming at a peak anti-Xa level of 0.5 to 0.7 U/mL.
When danaparoid was administered as a continuous infusion of 100 IU/hour after a loading dose of 3,500 IU, a median circuit survival time of 50.2 hours was reached, while no clinically important bleeding events or thromboembolic complications occurred during the particular hemofiltration run.
continuous venovenous hemofiltration
enzyme-linked immunosorbent assay
prothrombin fragment F1+2
platelet factor 4.
- Warkentin TE, Greinacher A: Heparin-induced thrombocytopenia: recognition, treatment and prevention. The seventh ACCP Conference on antithrombotic and thrombolytic therapy. Chest 2004, 126: 311S-337S. 10.1378/chest.126.3_suppl.311SView ArticlePubMedGoogle Scholar
- Acostamadiedo JM, Iyer UG, Owen J: Danaparoid sodium. Expert Opin Pharmacother 2000, 1: 803-814. 10.1517/146565126.96.36.1993View ArticlePubMedGoogle Scholar
- Schneider KS: Elimination of danaparoid by means of filtration – determination of the elimination technique in saline, human albumin and human whole blood. Elimination von Danaparoid mittels Filtration – Bestimmung der Eliminationstechnik in physiologischer Kochsalzlösung, Humanalbumin und humanem Vollblut. PhD thesis. Medizinische Fakultät, Albert-Ludwigs-Universität, Freiburg im Breisgau 2004.Google Scholar
- Hassell K: The management of patients with heparin-induced thrombocytopenia who require anticoagulant therapy. Chest 2005,127(2 Suppl):1S-8S. 10.1378/chest.127.2_suppl.1SView ArticlePubMedGoogle Scholar
- Lindhoff-Last E, Betz C, Bauersachs R: Use of a low molecular weight heparinoid (danaparoid sodium) for continuous renal replacement therapy in intensive care patients. Clin Appl Thromb Haemost 2001, 7: 300-304.View ArticleGoogle Scholar
- Lo GK, Juhl D, Warkentin TE, Sigouin CS, Eichler P, Greinacher A: Evaluation of pretest clinical score (4T's) for the diagnosis of heparin-induced thrombocytopenia in two clinical settings. J Thromb Haemost 2006, 4: 759-765. 10.1111/j.1538-7836.2006.01787.xView ArticlePubMedGoogle Scholar
- Ronco C, Bellomo R, Homel P, Brendolan A, Dan M, Piccinni P, La Greca G: Effects of different doses in continuous veno-venous haemofiltration on outcomes of acute renal failure: a prospective, randomised trial. Lancet 2000, 356: 26-30. 10.1016/S0140-6736(00)02430-2View ArticlePubMedGoogle Scholar
- de Pont AC, Oudemans-van Straaten HM, Roozendaal KJ, Zandstra DF: Nadroparin versus dalteparin anticoagulation in high-volume continuous venovenous hemofiltration: a double-blind, randomized, crossover study. Crit Care Med 2000, 28: 421-425. 10.1097/00003246-200002000-00022View ArticlePubMedGoogle Scholar
- Journois D, Safran D, Castelain MH, Chanu D, Drevillon C, Barrier G: Comparison of the antithrombotic effects of heparin, enoxaparin and prostacycline in continuous hemofiltration. [Comparaison des effets antithrombotiques de l'héparine, l'enoxaparine et la prostacycline au cours de l'hémofiltration continue]. Ann Fr Anesth Reanim 1990, 9: 331-337.View ArticlePubMedGoogle Scholar
- Joannidis M, Kountchev J, Rauchenzauner M, Schusterschitz N, Ulmer H, Mayr A, Bellmann R: Enoxaparin vs. unfractionated heparin for anticoagulation during continuous veno-venous hemofiltration: a randomized controlled crossover study. Intensive Care Med 2007, 33: 1571-1579. 10.1007/s00134-007-0719-7View ArticlePubMedGoogle Scholar
- Hirsh J, Warkentin TE, Shaughnessy SG, Anand SS, Halperin JL, Raschke R, Granger C, Ohman EM, Dalen JE: Heparin and low-molecular-weight heparin: mechanisms of action, pharmacokinetics, dosing, monitoring, efficacy, and safety. Chest 2001, 119: 64S-94S. 10.1378/chest.119.1_suppl.64SView ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.