Tirofiban preserves platelet loss during continuous renal replacement therapy in a randomised prospective open-blinded pilot study
© Link et al.; licensee BioMed Central Ltd. 2008
Received: 8 April 2008
Accepted: 29 August 2008
Published: 29 August 2008
Approximately one third of all patients with cardiogenic shock suffer from acute kidney injury. Percutaneous coronary intervention, intra-aortic balloon pump, and continuous renal replacement therapy (CRRT) require effective antiplatelet therapy and anticoagulation, resulting in a high risk for platelet loss and bleeding events. The reversible platelet glycoprotein IIb/IIIa receptor inhibitor tirofiban was investigated to preserve platelet number and activation in a prospective open-blinded endpoint evaluation study.
Forty patients with cardiogenic shock and acute kidney injury requiring CRRT were randomly assigned to two groups receiving unfractioned heparin (UFH) (n = 20) or a combined anticoagulation with UFH and tirofiban (n = 20). The primary endpoint was platelet loss during CRRT. Secondary endpoints were urea reduction, haemofilter life span, bleeding events, and necessity for platelet transfusions.
In UFH-treated patients, the percentage of platelet-monocyte aggregates significantly increased (P < 0.001) and consecutively platelet cell count significantly decreased (P < 0.001). In contrast, combined treatment with UFH and tirofiban significantly decreased platelet-monocyte aggregates and platelet numbers (P < 0.001).
This pilot study provides evidence that the use of tirofiban in addition to UFH prevents platelet loss and preserves platelet function in patients with cardiogenic shock and acute kidney injury requiring CRRT. The pathophysiological inhibition of platelet aggregation and platelet-monocyte interaction appears to be causally involved.
Approximately one third of all patients with cardiogenic shock suffer from acute kidney injury. This increases in-hospital mortality from 53% to 87% . Early revascularisation, intra-aortic balloon pump (IABP), and antithrombotic therapy improve outcomes in cardiogenic shock . In cases of acute kidney injury with necessity for continuous renal replacement therapy (CRRT), effective anticoagulation is required. However, excessive anticoagulation in critically ill patients receiving CRRT may cause changes in platelet function, platelet loss, and bleeding events [3, 4].
The contact of blood with surfaces of the extracorporeal membrane circuits and different anticoagulants leads to platelet and leukocyte activation [5, 6] and platelet-leukocyte coaggregation [7, 8]. All of these interactions result in glycoprotein (GP) IIb/IIIa receptor activation that becomes capable of binding soluble fibrinogen . GP IIb/IIIa receptor antagonists primarily act on the platelet surface by inhibition of fibrinogen binding that is essential for platelet bridging and aggregate formation .
Tirofiban is a reversible short-acting inhibitor of platelet GP IIb/IIIa receptors used in acute coronary syndromes and cardiac interventions . The hypothesis that tirofiban preserves platelet number and function and shortens postoperative bleeding times was first described in baboons  and in patients with heparin-induced thrombocytopenia type II (HIT-II) during cardiopulmonary bypass surgery [13, 14]. The aim of this study was to prove the efficacy of tirofiban on platelet protection and safety in critically ill patients with cardiogenic shock and necessity for CRRT receiving either conventional therapy with unfractionated heparin (UFH) or additional tirofiban.
Materials and methods
CRRT was performed as continuous veno-venous haemodialysis, using a pump system (ADM; Fresenius, Bad Homburg, Germany) and capillary polysulfone haemofilters (Ultraflux® AV 1000S; Fresenius). Blood flow ranged from 100 to 120 mL/hour. Dialysis flow was, on average, 2,000 mL/hour. The ultrafiltration rate was adjusted to patient hydratation and haemodynamic status. Haemofilters and tubing were changed routinely every 24 hours according to the manufacturer's recommendations. Therefore, blood was reinfused to the patient and the entire set of single-use tubes was changed together with the haemofilter. Blood products were administered during a CRRT pause if necessary when haemofilters were changed. The efficacy of CRRT was measured by mean treatment dose and steady-state BUN during CRRT . The study drugs standard unfractioned heparin (UFH) and tirofiban were administered into the extracorporeal circuit as a prefilter infusion. All patients received UFH (Heparin-Natrium-ratiopharm®; ratiopharm GmbH, Ulm, Germany) by intravenous bolus application of 80 IU/kg followed by a continuous infusion with 18 IU/kg per hour. For UFH dose titration, plasma activated partial thromboplastin time (aPTT) was measured every hour until a two- to three-fold aPTT was reached. In cases of a steady state, CRRT was started and aPTT was measured twice daily. The short-acting reversible GP IIb/IIIa inhibitor tirofiban (Aggrastat®; MSD Sharp & Dohme GmbH, Haar, Germany) has a protein binding of 65% and an elimination half-life of 1.5 to 2 hours predominantly achieved via the renal pathway. According to the manufacturer's recommendations for severe renal insufficiency (creatinine clearance of less than 30 mL/minute), patients of the tirofiban group received, in addition to UFH, tirofiban by intravenous bolus application of 0.2 μg/kg per minute over 30 minutes followed by a continuous infusion with 0.05 μg/kg per minute. According to clinical guidelines, prophylactic platelet transfusions are recommended beyond a platelet count of less than 10 × 109/L . Because of the off-label use of tirofiban, the threshold level for prophylactic platelet transfusion was changed to 20 × 109/L.
To determine changes in haemostasis during the passage of blood through the extracorporeal circuit, blood was sampled in citrate tubes from the efferent line of the extracorporeal circulation (postfilter). All tests were performed in duplicate. Blood samples for analysis of full clinical chemistry, haematology, and platelet-monocyte aggregates were taken before starting CRRT and the following 4 days after starting treatment. The bleeding time was measured by the standardised Ivy method . Other causes of platelet loss were excluded by HIT-II screening tests using the particle gel immunoassay (ID-HPF-4; DiaMed, Cressier, Switzerland) for rapid detection and the enzyme-linked immunosorbent assay for discovering antibodies (IgG, IgA, and IgM) to heparin-platelet factor-4 complexes. Both HIT-II tests were done for all patients. Flow cytometry is a sensitive technique that permits the use of whole blood to assess platelet function in a physiological manner although the interaction of blood with the endothelium is excluded . Staining platelets with antibodies was performed immediately after blood collection, avoiding artificial platelet activation and aggregation. Platelets were identified by monoclonal anti-human antibodies directed against CD41 (clone HIP8, phycoerythrin-conjugated; BD Pharmingen, Heidelberg, Germany), the activated form of GP IIb/IIIa receptors by PAC-1 (clone PAC-1, fluorescein isothiocyanate-conjugated; BD Pharmingen), and monocytes by CD14 (clone RMO52, phycoerythrin-cyanin [PECy5]-conjugated; Beckman Coulter, Krefeld, Germany). Increases in PAC-1 have been shown to be directly correlated with the activation of GP IIb/IIIa binding to fibrinogen and/or monocytes. Measurements were performed by flow cytometer (FACSCalibur; Becton Dickinson, Heidelberg, Germany) and the Cellquest software system (Becton Dickinson, Heidelberg, Germany). Monocytes were selectively gated for analysis by forward scatter, side scatter, and CD14-PECy5. The percentages of PAC-1+/CD41a+/CD14+ platelet-monocyte aggregates were measured. Nonspecific immunofluorescence was determined using unspecific control monoclonal antibodies.
The sample size calculation was performed by the software of the Survey System (Creative Research Systems, Petaluma, CA, USA). The sample size was calculated by the following acceptations: a platelet loss of more than 50% to baseline and a variability of platelet counts of 15%. To detect platelet loss with a power of 95%, a sample size of at least 20 patients in each study group was required. To compare the two treatment regimens, the Mann-Whitney U test and analysis of variance were used. Data were given as mean ± standard deviation. Differences were considered significant if the P value was less than 0.05. Observed-to-expected (O/E) mortality ratios were reported for each group using the observed-to-SAPS II (Simplified Acute Physiology Score) expected rates per group. Ninety-five percent confidence intervals were calculated.
Demographic and baseline clinical characteristics of patients
UFH (n = 20)
UFH + tirofiban (n = 20)
Age in years, median (range)
71 (44, 85)
70 (52, 81)
Severity of illness scores
APACHE II score, median (range)
27 (18, 34)
28 (18, 34)
SAPS II, median (range)
46 (31, 66)
48 (30, 64)
Cardiogenic shock: reasons and haemodynamics at admission
Acute coronary syndromes, number
Acute decompensation of CHF, number
Left ventricular ejection fraction as a percentage, median (range)
31 (20, 57)
30 (18, 54)
Cardiac index in L/minute per square metre, median (range)
2 (1.4, 2.4)
2 (1.6, 2.4)
Renal failure: reasons and parameters at admission
Acute kidney injury, number
Acute decompensation of CRI, number
Creatinine in mg/dL, mean ± SD
2.9 ± 0.3
2.5 ± 0.2
Blood urea nitrogen in mg/dL, mean ± SD
72 ± 23.3
70 ± 24.1
Platelet count, × 109/L, mean ± SD
216 ± 64.3
194 ± 39.5
Monocyte count, × 106/L, mean ± SD
1,059 ± 85.4
981 ± 103
Platelet-monocyte aggregates as a percentage, mean ± SD
20.2 ± 5.9
20.8 ± 6.1
The influence of IABP treatment on platelet count is shown in Figure 2. At day 2, which is the mean IABP duration, there was no significant difference in platelet count between the UFH groups with or without IABP. In the same way, no significant differences could be observed in the tirofiban groups with or without IABP. Similarly, no differences in platelet count in patients with or without IABP were detected on days 3 and 4. After discontinuation of IABP, no significant increase in platelet count was observed for either the UFH or the tirofiban group until the end of the study period.
UFH (n = 20)
UFH + tirofiban (n = 20)
Coronary angiography, number
Percutaneous coronary intervention, number
Intra-aortic balloon pump, number
Intra-aortic balloon pump duration in hours, mean ± SD
48 ± 14.4
50 ± 12.5
Treatment dose in mL/kg per hour, mean ± SD
28 ± 2.5
28 ± 2.9
Blood urea nitrogen (BUN)
Pretreatment BUN in mg/dL, mean ± SD
72 ± 23.3
70 ± 24.1
Steady-state BUN during CRRT in mg/dL, mean ± SD
32 ± 18.1
31 ± 22.1
Antiplatelet therapy and anticoagulation
No antiplatelets, number
Acetylsalicylic acid alone, number
Acetylsalicylic acid and thienopyridine, number
UFH, number (dose in IU/kg per hour, mean ± SD)
20 (18.4 ± 0.6)
20 (18.2 ± 0.8)
Activated partial thromboplastin time in seconds, mean ± SD
64 ± 13.2
62 ± 11.8
Ivy bleeding time in seconds, mean ± SD
422 ± 58.1
599 ± 118.1
Further concomitant therapy
Dobutamine, number (dose in μg/kg per minute, mean ± SD)
18 (6 ± 2.8)
19 (6 ± 3.2)
Norepinephrine, number (dose in μg/kg per minute, mean ± SD)
14 (0.2 ± 0.1)
13 (0.2 ± 0.15)
Opioids and benzodiazepins, number
Mechanical ventilation, number
The efficacy of CRRT was estimated by mean treatment dose, steady-state BUN during CRRT, and haemofilter life span. The calculated mean treatment dose was 25 to 30 mL/kg per hour in both anticoagulation regimens and confirmed by an acceptable steady-state BUN during CRRT (Table 2).
Primary and secondary endpoints
UFH (n = 20)
UFH + tirofiban (n = 20)
Platelet/Monocyte counts at the end of CRRT
Platelet count, × 109/L, mean ± SD
87 ± 41.1
158 ± 45.3
Monocyte count, × 106/L, mean ± SD
945 ± 77.3
1,394 ± 151
Platelet-monocyte aggregates as a percentage, mean ± SD
27.5 ± 9.3
3.9 ± 2.1
Bleeding events during CRRT
Minor bleeding, number
Major bleeding, number
Platelet transfusions during CRRT
Platelet units per patient per day, mean ± SD
0.05 ± 0.02
Intensive care unit mortality rate, number (percentage)
Hospital mortality rate, number (percentage)
SAPS II predicted mortality rate as a percentage
Observed-to-expected mortality ratio
95% confidence interval for the observed-to-expected mortality ratio
The study was not powered for mortality. The in-hospital mortality rates were 35% in the UFH + tirofiban group and 40% in the UFH group. ICU mortality, hospital mortality, O/E mortality ratios, and 95% confidence intervals were calculated (Table 3).
In a pilot study, we investigated the possible use and effectiveness of the reversible platelet GP IIb/IIIa receptor inhibitor tirofiban to preserve platelet number and function during CRRT in patients with cardiogenic shock. Tirofiban additional to UFH for anticoagulation apparently prevented platelet loss over a period of 96 hours of CRRT. Furthermore, the inhibition of the activated platelet fibrinogen receptor GP IIb/IIIa (PAC-1) by tirofiban results in an inhibition of platelet-leukocyte interaction and aggregation [7, 8, 21]. We examined changes in platelet loss and platelet-monocyte coaggregates by analysing the platelet-specific CD41a and PAC-1 antigen on monocytes using three-color flow cytometry as whole-blood technique. The percentage of platelet-monocyte coaggregates showed a highly significant decrease by combined anticoagulation with UFH and tirofiban. Platelet-monocyte aggregates were shown to promote monocyte adhesion to endothelium and to induce proinflammation [22–25]. Our findings suggest that the combined anticoagulation with UFH and tirofiban during CRRT inhibits platelet activation and platelet-monocyte interactions with consequences for platelet protection and antithrombotic and anti-inflammatory effects. In contrast, the treatment with UFH alone increased platelet-monocyte binding.
Platelet loss under CRRT in the UFH group was marked. This may be related to the critically ill patients with cardiogenic shock combined with acute kidney injury. Our results are comparable to other examinations of critically ill patients with multiple organ dysfunction syndrome and acute kidney injuries . Neither the concomitant treatment with intra-aortic counterpulsation nor the antiplatelet therapy with acetylsalicylic acid and thienopyridine had an effect on the platelet loss between these subgroups.
The efficacy of CRRT assessed by mean treatment doses and steady-state BUN during CRRT was comparable in the two treatment groups. Despite the different anticoagulation regimens and the higher potency of anticoagulation within the tirofiban + UFH group, this therapy was not associated with an increased number of bleeding events. To minimise the risk of bleeding, tirofiban and UFH were administered into the extracorporeal circuit as a prefilter infusion. The study was not focused on bleeding events and therefore an analysis regarding bleeding events would be totally underpowered. But as a result, no clinically important bleedings were detected and no transfusions of red blood cells or platelet units were necessary in patients treated with the combined tirofiban + UFH anticoagulation. Nevertheless, further studies are warranted to ascertain the safety of an anticoagulation regimen with tirofiban + UFH during long-term CRRT.
One might argue that the study could be limited by (a) the open-label character of its design, (b) the small number of patients, (c) the lack of a specific antidote for tirofiban, and (d) missing data on long-term efficacy and bleeding events of tirofiban during CRRT. Because of the pilot-study character and the off-label use of tirofiban during CRRT, the physicians were not blinded. However, clinical evaluation and determination of primary endpoints were done separately by clinical and experimental investigators, the latter of which were blinded to the clinical data of the patients. As there is no specific antidote for tirofiban in cases of bleeding events, donor platelets should be transfused and haemofiltration is suggested for extracorporeal elimination of tirofiban . A recent development of a rapid whole-blood point-of-care platelet function assay, the rapid platelet function assay, now allows for the bedside monitoring of platelet inhibition by GP IIb/IIIa receptor antagonists . Further investigations with larger numbers of patients are necessary for the determination of haemofilter run times, long-term efficacy, and bleeding events of tirofiban during CRRT.
The GP IIb/IIIa receptor antagonist tirofiban inhibits platelet activation and platelet-monocyte interaction. Its use in addition to UFH during CRRT prevents platelet loss and preserves platelet function.
The glycoprotein IIb/IIIa receptor antagonist tirofiban inhibits platelet activation and platelet-monocyte interaction.
The use of tirofiban during continuous renal replacement therapy prevents platelet loss and preserves platelet function.
activated partial thromboplastin time
blood urea nitrogen
continuous renal replacement therapy
heparin-induced thrombocytopenia type II
intra-aortic balloon pump
intensive care unit
activated platelet fibrinogen receptor glycoprotein IIb/IIIa
We would like to thank all of the people who were involved in the study.
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