Tranexamic acid (TXA) reduces bleeding by inhibiting the enzymatic breakdown of fibrin blood clots (fibrinolysis) . Plasminogen produced by the liver is converted into the fibrinolytic enzyme plasmin by tissue plasminogen activator (tPA). Plasminogen and tPA bind to C-terminal lysine residues on fibrin leading to localized plasmin formation and fibrin cleavage . TXA is a molecular analogue of lysine that inhibits fibrinolysis by competing with fibrin for the lysine-binding sites in plasminogen. TXA inhibits the capacity of plasminogen and plasmin to bind to fibrin, hence preserving blood clots from plasmin-mediated lysis .
Intravenous administration of TXA safely reduces death because of bleeding in patients with trauma and postpartum haemorrhage (PPH) [3–5]. In both situations, most deaths occur soon after bleeding onset and treatment delay reduces the survival benefit . It is imperative that patients are treated urgently. TXA is inexpensive, widely available, and heat stable. It is cost effective in sub-Saharan Africa and Southern Asia, where most haemorrhagic deaths occur . Nevertheless, because of long distances to healthcare facilities and a lack of emergency transport many patients are not treated soon enough.
One of the barriers to rapid treatment is the need for an intravenous injection. Health workers able to insert intravenous lines may be unavailable in rural areas and even when they are, securing intravenous access can be difficult in shocked patients with collapsed veins. Although TXA is available for oral and intravenous use, there has been little research into different routes of administration. Intramuscular injection would be easier and would require less training than IV use.
To determine the minimal plasma level of TXA needed to inhibit fibrinolysis, and hence identify whether oral or intramuscular injection would be a viable treatment option, we conducted a systematic review of pharmacodynamics studies. We reviewed in-vivo and in-vitro studies reporting both the concentration of TXA in blood or plasma and its effects on any reliable measure of fibrinolysis. This work will inform future studies into the bioavailability of TXA after oral, intramuscular, and subcutaneous administration.
The systematic review methods were published in advance of data collection on the PROSPERO register (protocol number CRD42017079646). The review is reported in accordance with PRISMA guidelines .
Types of studies: In-vitro and in-vivo studies reporting the effects of TXA on fibrinolysis in human blood, plasma, or simulated clotting models.
Methods to measure TXA in the blood and plasma include HPLC, liquid chromatography–mass spectrometry, gas chromatography, or paper electrophoresis [9–11].
Eligible fibrinolysis assays included:
Whole blood tests. These assess fibrinolysis in the presence of platelets and blood cells.
Thromboelastography (TEG) and rotational thromboelastometry (ROTEM) measure the viscoelastic properties of blood during clot formation and fibrinolysis in vitro. Comparisons with biochemical assays (e.g., plasmin–antiplasmin complexes) suggest that they may be insensitive to low-grade hyperfibrinolysis [12,13].
The halo assay is a high throughput method that involves forming halo-shaped, tissue factor-induced blood clots in 96 well plates and measuring fibrinolysis using a spectrophotometer .
Global fibrinolytic capacity involves measuring fibrin degradation products by ELISA in clotted-lysing blood. Global fibrinolytic capacity is estimated after correcting for background fibrin degradation products in parallel blood samples incubated with the direct plasmin inhibitor, aprotinin. Because no activators are used, endogenous fibrinolysis is assessed [15,16].
Plasma tests: A limitation of these tests is that platelets, cells, and some proteins are absent .
The overall fibrinolytic potential and global fibrinolytic potential of plasma is assessed by measuring plasma turbidity in a spectrophotometer after addition of tPA . The initiation of coagulation and subsequent fibrinolysis change the optical density of the plasma. Other optical assays include the clot formation and lysis (CloFAL) assay [16,17] and the clot lysis assay (for example, as described by Niego et al.).
ELISA and other immunoassays measure specific fibrinolytic markers such as D-dimer [17,19]. D-dimer can be measured by ELISA (quantitative), whole blood agglutination (qualitative), or latex bead agglutination (quantitative or qualitative). Results from different assays are not comparable and false positives can result from other factors influencing D-dimer levels [17,19].
To facilitate comparisons, concentrations of tPA were converted to ng/ml using the following formula: 10 000 IU/ml = 20 000 ng/ml = 300 nM . Similarly, urokinase-type plasminogen activator (uPA) concentrations were converted to ng/ml with the following formula: 3200 IU/ml = 20 000 ng/ml = 380 nM .
Types of participants
Studies on blood from healthy volunteers or patients. Animal studies were excluded because the concentration needed to inhibit fibrinolysis may be different from humans [22,23]. Animal (e.g., murine) plasma clots are known to be more resistant to lysis with human tPA .
Types of interventions
TXA is added to blood, plasma, or clotting models in vitro or given by any route (in vivo).
Types of outcomes
Concentration of TXA (mg/l) needed to reduce fibrinolytic activity to a clinically significant level, for example, 80% reduction in activity , or 95% maximal effective concentration (EC95) .
We searched MEDLINE, EMBASE, OviSP, and the ISI Web of Science from the date of database inception to 6 November 2017 using the following terms and keywords:
TXA, amino methyl carboxylic acid, amino methyl cyclohexane acid, cyklokapron, pharmacodynamics, pharmacokinetics, blood, plasma, human, fibrinolysis, fibrin, fibrinogen, antifibrinolytic, antifibrinolysis, clot, lysis, turbidity, immunoassay, immunochemistry, TEG, ROTEM, intravenous, oral, intramuscular, dose, dosing, concentration, and haemorrhage (see Appendix for detailed search strategy, http://links.lww.com/BCF/A58). Truncation symbols were used with the text words, when appropriate, to capture variations in spelling and word endings. We also examined the references of systematic reviews located during the search and performed a forward search with the eligible studies to identify further potential articles.
Two reviewers independently assessed records to determine whether they met the inclusion criteria. Titles and abstracts were screened and the full texts of any potentially relevant reports were assessed for inclusion. Two reviewers independently assessed the full texts to confirm eligibility. Disagreements between reviewers were resolved by consensus.
Data were extracted into a prespecified table including: method to detect TXA in blood or plasma, protocol for TXA administration or addition, fibrinolytic assay used, outcome of fibrinolysis assay, and TXA concentration that achieved a significant reduction of fibrinolysis.
The results of each study were described with no mathematical synthesis of results. We examined graphically the relationship between the concentration of tPA used to stimulate fibrinolysis and the minimal inhibitory TXA concentration (80% inhibition of fibrinolysis) and calculated a regression line with 95% confidence intervals (95% CI). The regression was calculated with Stata statistical software: Release 15 (College Station, Texas, USA).
We found 369 potentially eligible records. After screening titles and abstracts we reviewed the full text of 35 records. We found 21 studies meeting the inclusion criteria (Fig. 1), one of which was unpublished [personal communication]. The first study was published in 1968. All studies were published in English.
The results are shown in Tables 1 and 2. We found 20 in-vitro and one in-vivo study. There were 16 in-vitro studies in which TXA was added to blood or plasma drawn from healthy volunteers or commercial sources, and four studies using clotting models or fibrin plates. One clinical trial measured TXA levels and fibrinolysis in blood from surgical patients.
In most studies, fibrinolysis was stimulated with tPA (Table 1).
Andersson et al. incubated fibrin plates with tissue homogenates containing tPAs and measured the effect of TXA concentrations up to 100 mg/l. Fibrinolysis (lysed area on plate) was reduced by 98% with 100 mg/l TXA, 90% with 25 mg/l TXA and 80% with 10 mg/l TXA.
Dai et al. used tPA to stimulate fibrinolysis in plasma from haemophilia patients who had factor VIII antibodies. Clot lysis time was measured using optical methods. Clot lysis time increased from 6 to 16 min with TXA at 5 mg/l and from 6 to 37 min using 10 mg/l.
Dietrich et al. stimulated fibrinolysis in blood (tPA at 200 ng/ml) from healthy volunteers and used ROTEM (LY60, defined as percentage decrease in clot amplitude at 60 min after maximal amplitude) to assess the effect of TXA on fibrinolysis. Fifty percentage inhibition [IC50, median (25th; 75th percentile)] was achieved with TXA 0.43 mg/l (0.29, 0.51) and complete inhibition with TXA 1.57 mg/l. The authors stimulated fibrinolysis in plasma (tPA 100 ng/ml) and studied the decrease in optical density 45 min after maximum optical density. Fifty percentage inhibition (IC50) was achieved with TXA 0.66 mg/l (0.48, 0.67). TXA 1.57 mg/l decreased fibrinolysis to less than 10%.
Dirkman et al. stimulated fibrinolysis in blood with tPA (100 ng/ml) and evaluated the effect of a single dose of TXA (330 mg/l) corresponding to 2 g/75 kg body weight using ROTEM. TXA reduced clot lysis at 45 and 60 min [clot lysis index (CLI45) and CLI60]. CLI60 (median, 25th/75th percentile) increased from 21% (7%/59%) without TXA to 90% (89%/92%) with TXA. TXA 330 mg/l increased CLI45 from 64% (48/80) to 94% (93/98) in conditions of moderate acidosis and from 49% (26/71) to 92% (86.5/94) in severe acidosis .
Fears et al. stimulated fibrinolysis in plasma with anisoylated lys-plasminogen streptokinase activator complex or tPA and measured the lysis time of iodine-radiolabelled fibrin clots. TXA at 10 mg/l reduced anisoylated lys-plasminogen streptokinase activator complex -induced fibrinolysis by 80%. TXA at 157.2 mg/l completely inhibited tPA-induced initiation of fibrinolysis. TXA at 40 mg/l caused 80% inhibition at 4 h, TXA at 10 mg/l caused 70% inhibition at 1 h and 30% inhibition at 4 h. TXA at 10 and 40 mg/l inhibited 34% of ongoing tPA-induced fibrinogenolysis.
Fletcher et al. used tPA-stimulated plasma and TEG to calculate the estimated percentage lysis 30 min after maximum clot amplitude. The TXA concentration needed to inhibit fibrinolysis was 14.7 mg/l (95% CI 13.7–15.6).
Godier et al. spiked blood samples with 67 ng/ml, 267 ng/ml, and 1333 ng/ml tPA and studied the effect of TXA on fibrinolysis using TEG. 67 ng/ml tPA did not affect the TEG traces but there was a significant effect with 267 and 1333 ng/ml. With 267 ng/ml tPA, a concentration of 3 mg/l TXA partially corrected TEG parameters, whereas 300 mg/l TXA corrected most parameters. With 1333 ng/ml tPA, a concentration of 3 mg/l TXA was ineffective, but 300 mg/l TXA corrected LY60 and estimated percentage lysis. The effect of 30 mg/l TXA was similar to that of 300 mg/l TXA at all tPA concentrations (Table 1). TXA also inhibited fibrinogenolysis (based on the drop in fibrinogen level after tPA addition). Addition of 67 ng/ml tPA did not cause fibrinogenolysis. However, tPA resulted in a concentration-dependent fall in fibrinogen levels at 267 and 1333 ng/ml tPA. This fall was partly prevented by the addition of 3 mg/l TXA and almost fully prevented at a concentration of 30 mg/l or higher.
He et al. spiked normal commercial plasma with tPA in the presence of a thrombin inhibitor or a factor Xa inhibitor to mimic an antithrombotic therapy. TXA at 0.4 mg/l prolonged the clot lysis time from 40 to 50 min with a thrombin inhibitor and from 25 to 50 min with a factor Xa inhibitor. TXA at 9.5 mg/l abolished fibrinolysis in both cases.
Hoylaerts  used tPA in an in-vitro system where wells of tissue culture plates were coated with iodine-radiolabelled fibrin. Plasminogen was preincubated with several TXA concentrations and added to the wells. The radioactivity released into the solution was the product of the solubilization of fibrin and was measured for up to 200 min. The time required to solubilize 50% of fibrin was calculated. The solubilization time increased from 100 min in the controls to 200 min with 2 mg/l of TXA.
Kostousov et al. used tPA to induce moderate fibrinolysis in blood diluted with Ringer's lactate (Hospira, Lake Forest, Illinois, USA) and severe fibrinolysis in blood diluted with Ringer's lactate and Voluven (Hospira, Lake Forest, Illinois, USA). In moderate fibrinolysis, TXA at 1 and 2 mg/l inhibited TEG clot lysis. In severe fibrinolysis, TXA 3 mg/l decreased LY30 to less than 8%.
Lijnen et al. induced fibrinolysis in plasma with staphylokinase 30 nM or streptokinase 100 nM. Lysis time of iodine-radiolabelled fibrin clots was measured. The concentrations of TXA needed to reduce clot lysis to 50% of the value measured without TXA after 2 h were 0.63 mg/l with staphylokinase and 3.14 mg/l with streptokinase. In other experiments, TXA was added 30 min after the addition of staphylokinase or 15 min after streptokinase. TXA needed to reduce fibrinolysis to 50% after 90 min was 2.36 mg/l with staphylokinase and 11 mg/l with streptokinase.
Longstaff  prepared fibrin clots by mixing fibrinogen and α-thrombin. Plasmin was added when maximal optical density was reached and clot lysis measured for 5 h. Lysis decreased with increasing TXA concentration (Table 1). Plasminogen activation was also assessed in a solution with fibrinogen, thrombin, plasminogen, and tPA. Plasminogen activation dropped to 40% with 7.86 mg/l TXA and 20% with 15.72 mg/l of TXA. TXA between 8 and 15 mg/l reduced clot lysis (75 and 45% lysis rate, respectively) and inhibited plasminogen activation (40 and 20% activation rate, respectively).
Longstaff [unpublished] used ROTEM (maximum clot firmness, clot lysis index) to measure tPA and uPA-induced fibrinolysis. TXA 1.57 mg/l inhibited fibrinolysis almost as efficiently as TXA 157.21 mg/l with both tPA and uPA. Longstaff also used the halo assay  with whole blood or plasma. In both cases, 40 mg/l of TXA almost completely inhibited tPA-induced clot lysis and a concentration almost an order of magnitude lower inhibited uPA-induced lysis (Table 1).
Niego et al. stimulated fibrinolysis in commercial human plasma with tPA and measured clot turbidity for 100 min. TXA at 15.7 mg/l completely inhibited fibrinolysis.
Okamoto et al. incubated fibrin plates and tested the inhibitory activity of TXA on fibrinolysis caused by the human plasma activator of plasminogen. They showed that 0.16 mg/l of TXA inhibited 50% of fibrinolysis, 1.6 mg/l inhibited about 90% of fibrinolysis, and 15.7 mg/l inhibited fibrinolysis almost completely.
Rozen et al. used ROTEM to study the effect of TXA on fibrinolysis in blood from children (aged 1–10 years) undergoing cardiac catheterization for congenital heart disease (10 cyanotic and 10 noncyanotic) and blood from healthy adult volunteers. Fibrinolysis was induced with tPA and the effect of TXA on lysis index at 30 min was assessed. The efficacy concentration 50% (EC50) in adults was 6.8 mg/l (95% CI, 6.4–7.2), and the EC95 was 11.3 mg/l (95%CI, 10.6–12.9). In children, EC50 was 2.8 mg/l (95%CI, 2.6–3.0) and EC95 was 8.6 mg/l (95%CI, 6.9–14.9).
Sperzel and Huetter  spiked plasma with tPA and assessed fibrinolysis by measuring plasma turbidity in a spectrophotometer following the addition of tPA. TXA concentrations ranged from 0.47 to 471.63 mg/l. TXA inhibited fibrinolysis with an IC50 of 3.79 ± 0.17 mg/l.
Takada et al. added either 1250 or 6250 ng/ml of urokinase to plasma and assessed a single dose of TXA (157.2 mg/l) by measuring fibrin and fibrinogen degradation products. For both concentrations of urokinase, TXA inhibited fibrinolysis and fibrinogenolysis. TXA was also tested in a system with plasminogen, thrombin, fibrinogen, and urokinase (6250 ng/ml). TXA completely inhibited fibrinolysis and reduced fibrinogenolysis by about 50%.
Yee et al. added tPA to adult plasma and plasma from cord blood collected at caesarean deliveries of 23 full-term (38–42 weeks) singleton live births. The effect of TXA on fibrinolysis was determined with TEG (LY30). The minimum dose of TXA needed to completely inhibit fibrinolysis was 6.54 mg/l (95% CI, 5.19–7.91) in neonatal plasma and 17.5 mg/l (95% CI, 14.59–20.41) in adult plasma.
Figure 2 shows the relationship between the tPA concentration used to induce fibrinolysis and the minimal concentration of TXA needed to inhibit at least 80% of fibrinolysis. The TXA concentration required increased by 0.004 mg/l for every 1 ng/ml of tPA used to stimulate fibrinolysis (95% CI 0.001–0.008, R2 = 47.26%).
Couturier et al. compared the effect of two TXA dosing schemes with a no TXA group in children undergoing surgery with cardiopulmonary bypass (CPB) (Table 2). The dosing schemes included a continuous administration of TXA (10 mg/kg bolus dose followed with a continuous 1 mg/kg/h infusion until completion of surgery, and then 10 mg/kg dose in the CPB prime), and a discontinuous administration (10 mg/kg bolus dose, then a 10 mg/kg dose in the CPB prime, and 10 mg/kg dose at the end of CPB). They measured TXA, D-dimer, and fibrinogen. TXA levels ranged between 28.0 ± 2.3 and 59.9 ± 7.5 mg/l (mean ± SEM) during surgery. TXA inhibited the bypass-induced D-dimer increase which peaked at 393 ± 93 ng/ml in the discontinuous group and 562 ± 165 ng/ml in the continuous group compared with the no TXA group (2274 ± 474 ng/ml).
Although TXA may have other biological effects, this systematic review aimed to determine the minimum concentration of TXA necessary to inhibit fibrinolysis [42,43]. Our results suggest that TXA concentrations between 10 and 15 mg/l provide near maximal inhibition of fibrinolysis, although concentrations between 5 and 10 mg/l provide significant inhibition (e.g., 18, 32). The minimum TXA concentration might be lower in children .
Despite an extensive search for all eligible studies, published or unpublished, it is possible that some studies were missed. Although less is known about the impact of publication bias in systematic reviews of pharmacodynamics studies, than in reviews of clinical trials, selective reporting has been documented and is a potential threat to validity [45,46]. Furthermore, many pharmacodynamics studies fail to report aspects of study methodology (e.g., blinding) that may have a bearing on the results. Because the rate of fibrinolysis in normal blood or plasma is slow, fibrinolytic activators are added to speed up the process. Although differences in the potency of fibrinolytic activators make direct comparisons difficult, our results suggest that the tPA concentration used to stimulate fibrinolysis influences the results. Indeed, the wide range of tPA concentrations used may explain the heterogeneity in inhibitory concentrations. Another potential limitation is the diversity of the methods used to measure fibrinolysis. The validation and standardization of methods to measure fibrinolysis has progressed more slowly than for coagulation testing and widely accepted assays are unavailable.
Can results from in-vitro studies be used to guide the target TXA concentration for patients with trauma and PPH? Cohort studies in patients with major trauma show that plasma tPA concentrations are highest in patients with hypotension and acidosis. Nevertheless, the tPA concentrations seen in even the most severely injured patients are lower than those used to stimulate fibrinolysis in vitro. Indeed, tPA levels in trauma patients are generally below 100 ng/ml [47–50]. This suggests that results from in-vitro studies may overestimate the concentration of TXA needed to inhibit fibrinolysis in vivo.
In most of the included in-vitro studies, TXA was added either before tPA was added or at the same time. The experimental protocol therefore differs from clinical situations. Only one publication  reported the effect of TXA on ongoing fibrinolysis, adding TXA 15–30 min after stimulating fibrinolysis, but very high doses of fibrinolysis activators were used (e.g., 80 nM of tPA, corresponding roughly to more than 5000 ng/ml). For this reason, the extent to which in-vitro results can be applied to the clinical practice is open to question.
Urokinase is a fibrinolytic activator sometimes used in in-vitro experiments. However, clinical studies show that tPA is involved in the early activation of fibrinolysis with levels reaching a peak at about 3 h after injury. uPA levels increase after tPA levels begin to decrease . It is unlikely that uPA plays a major role in fibrinolysis during the early stage of trauma or PPH, when TXA is known to be life saving.
In conclusion, this systematic review suggests that TXA concentrations in the range of 10–15 mg/l result in substantial inhibition of fibrinolysis. These results will inform pharmacokinetic studies to examine the bioavailability of TXA after oral, intramuscular, and subcutaneous administration. If therapeutic levels of TXA can be achieved in a timely manner via these alternative routes, this could have important implications for the prehospital management of patients with trauma and postpartum haemorrhage.
We thank Ms Sarah Dawson, Senior Research Associate in Information Retrieval at the Bristol Medical School (University of Bristol, UK), for designing and performing the literature search. We thank Dr Stanislas Grassin-Delyle and Dr Colin Longstaff for their helpful comments on the manuscript and thank Dr Colin Longstaff for sharing unpublished data.
This study was funded by Wellcome (grant number WT208870/Z/17/Z) and the Bill & Melinda Gates Foundation (grant number OPP1176150) as part of the WOMAN-2 program.
Role of the sponsor: Wellcome and the Bill & Melinda Gates Foundation did not play a role in the design and conduct of the study, collection, analysis, and interpretation of the data, preparation, review, or approval of the manuscript.
Conflicts of interest
There are no conflicts of interest.
1. McCormack PL. Tranexamic acid
: a review of its use in the treatment of hyperfibrinolysis. Drugs
2. Okamoto S, Okamoto U. Amino-methyl-cyclohexane-carboxylic acid: AMCHA a new potent inhibitor of the fibrinolysis
. Keio J Med
3. Roberts I, Shakur H, Afolabi A, Brohi K, Coats T, Dewan Y, et al. CRASH-2 Collaborators. The importance of early treatment with tranexamic acid
in bleeding trauma patients: an exploratory analysis of the CRASH-2 randomised controlled trial. Lancet
4. Shakur H, Roberts I, Bautista R, Caballero J, Coats T, Dewan Y, et al. CRASH-2 Trial Collaborators. Effects of tranexamic acid
on death, vascular occlusive events, and blood transfusion in trauma patients with significant haemorrhage (CRASH-2): a randomised, placebo-controlled trial. Lancet
5. WOMAN Trial Collaborators. Effect of early tranexamic acid
administration on mortality, hysterectomy, and other morbidities in women with postpartum haemorrhage (WOMAN): an international, randomised, double-blind, placebo-controlled trial. Lancet
6. Gayet-Ageron A, Prieto-Merino D, Ker K, Shakur H, Ageron FX, Roberts I. Antifibrinolytic Trials Collaboration. Effect of treatment delay on the effectiveness and safety of antifibrinolytics in acute severe haemorrhage: a meta-analysis of individual patient-level data from 40 138 bleeding patients. Lancet
7. Guerriero C, Cairns J, Perel P, Shakur H, Roberts I. CRASH 2 Trial Collaborators. Cost-effectiveness analysis of administering tranexamic acid
to bleeding trauma patients using evidence from the CRASH-2 trial. PLoS One
8. Liberati A, Altman DG, Tetzlaff J, Mulrow C, Gotzsche PC, Ioannidis JP, et al. The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate healthcare interventions: explanation and elaboration. BMJ
9. Andersson L, Nilsoon IM, Colleen S, Granstrand B, Melander B. Role of urokinase and tissue activator in sustaining bleeding and the management thereof with EACA and AMCA. Ann N Y Acad Sci
10. Nilsson IM. Clinical pharmacology of aminocaproic and tranexamic acids. J Clin Pathol Suppl (R Coll Pathol)
11. Pilbrant A, Schannong M, Vessman J. Pharmacokinetics and bioavailability of tranexamic acid
. Eur J Clin Pharmacol
12. Larsen OH, Fenger-Eriksen C, Ingerslev J, Sorensen B. Improved point-of-care identification of hyperfibrinolysis is needed. Thromb Res
13. Raza I, Davenport R, Rourke C, Platton S, Manson J, Spoors C, et al. The incidence and magnitude of fibrinolytic activation in trauma patients. J Thromb Haemost
14. Bonnard T, Law LS, Tennant Z, Hagemeyer CE. Development and validation of a high throughput whole blood thrombolysis plate assay. Sci Rep
15. Rijken DC, Hoegee-De Nobel E, Jie AF, Atsma DE, Schalij MJ, Nieuwenhuizen W. Development of a new test for the global fibrinolytic capacity in whole blood. J Thromb Haemost
16. Ilich A, Bokarev I, Key NS. Global assays of fibrinolysis
. Int J Lab Hematol
17. Pepperell D, Morel-Kopp MC, Ward C. Kolev K. Clinical Application of Fibrinolytic Assays. Fibrinolysis and thrombolysis
. Rijeka: InTech; 2014; Chapter 06.
18. Niego B, Horvath A, Coughlin PB, Pugsley MK, Medcalf RL. Desmoteplase-mediated plasminogen activation and clot lysis are inhibited by the lysine analogue tranexamic acid
. Blood Coagul Fibrinolysis
2008; 19:322–324. https://dx.doi.org/10.1097/MBC.0b013e3282f54568
19. Gorog DA. Prognostic value of plasma fibrinolysis
activation markers in cardiovascular disease. J Am Coll Cardiol
21. Longstaff C, Thelwell C, Rigsby P. SSC Fibirinolysis Subcommittee. An international collaborative study to establish the WHO 2nd International Standard for HIGH MOLECULAR WEIGHT UROKINASE: communication from SSC of the ISTH. J Thromb Haemost
22. Fletcher DJ, Blackstock KJ, Epstein K, Brainard BM. Evaluation of tranexamic acid
and epsilon-aminocaproic acid concentrations required to inhibit fibrinolysis
in plasma of dogs and humans. Am J Vet Res
2014; 75:731–738. https://dx.doi.org/10.2460/ajvr.75.8.731
23. Fletcher DJ, Brainard BM, Epstein K, Radcliffe R, Divers T. Therapeutic plasma concentrations of epsilon aminocaproic acid and tranexamic acid
in horses. J Vet Intern Med
24. Lijnen HR, van Hoef B, Beelen V, Collen D. Characterization of the murine plasma fibrinolytic system. Eur J Biochem
25. Rozen L, Faraoni D, Sanchez Torres C, Willems A, Noubouossie DC, Barglazan D, et al. Effective tranexamic acid
concentration for 95% inhibition of tissue-type plasminogen activator induced hyperfibrinolysis in children with congenital heart disease: a prospective, controlled, in-vitro study. Eur J Anaesthesiol
2015; 32:844–850. https://dx.doi.org/10.1097/EJA.0000000000000316
26. Dai L, Bevan D, Rangarajan S, Sorensen B, Mitchell M. Stabilization of fibrin clots by activated prothrombin complex concentrate and tranexamic acid
in FVIII inhibitor plasma. Haemophilia
27. Dietrich W, Nicklisch S, Koster A, Spannagl M, Giersiefen H, van de Locht A. CU-2010: a novel small molecule protease inhibitor with antifibrinolytic and anticoagulant properties. Anesthesiology
28. Dirkmann D, Gorlinger K, Gisbertz C, Dusse F, Peters J. Factor XIII and tranexamic acid
but not recombinant factor VIIa attenuate tissue plasminogen activator
-induced hyperfibrinolysis in human whole blood. Anesth Analg
2012; 114:1182–1188. https://dx.doi.org/10.1213/ANE.0b013e31823b6683
29. Dirkmann D, Radu-Berlemann J, Gorlinger K, Peters J. Recombinant tissue-type plasminogen activator-evoked hyperfibrinolysis is enhanced by acidosis and inhibited by hypothermia but still can be blocked by tranexamic acid
. J Trauma Acute Care Surg
2013; 74:482–488. http://dx.doi.org/10.1097/TA.0b013e318280dec1
30. Fears R, Greenwood H, Hearn J, Howard B, Humphreys S, Morrow G, Standring R. Inhibition of the fibrinolytic and fibrinogenolytic activity of plasminogen activators in vitro by the antidotes epsilon-aminocaproic acid, tranexamic acid
and aprotinin. Fibrinolysis
1992; 6:79–86. http://dx.doi.org/10.1016/0268-9499%2892%2990064-O
32. He S, Johnsson H, Zabczyk M, Hultenby K, Cao H, Blomback M. A fibrinogen concentrate Haemocomplettan (Riastap) or a Factor XIII concentrate Fibrogammin combined with a mini dose of tranexamic acid
can reverse the fibrin instability to fibrinolysis
induced by thrombin or FXa-inhibitor. Br J Haematol
2013; 160:806–816. https://dx.doi.org/10.1111/bjh.12189
33. Hoylaerts M, Lijnen HR, Collen D. Studies on the mechanism of the antifibrinolytic action of tranexamic acid
. Biochim Biophys Acta
34. Kostousov V, Wang YW, Cotton BA, Wade CE, Holcomb JB, Matijevic N. Influence of resuscitation fluids, fresh frozen plasma and antifibrinolytics on fibrinolysis
in a thrombelastography-based, in-vitro, whole-blood model. Blood Coagul Fibrinolysis
2013; 24:489–497. https://dx.doi.org/10.1097/MBC.0b013e32835e4246
35. Lijnen HR, Stassen JM, Collen D. Differential inhibition with antifibrinolytic agents of staphylokinase and streptokinase induced clot lysis. Thromb Haemost
36. Longstaff C. Studies on the mechanisms of action of aprotinin and tranexamic acid
as plasmin inhibitors and antifibrinolytic agents. Blood Coagul Fibrinolysis
37. Okamoto S, Oshiba S, Mihara H, Okamoto U. Synthetic inhibitors of fibrinolysis
: in vitro and in vivo mode of action. Ann N Y Acad Sci
38. Sperzel M, Huetter J. Evaluation of aprotinin and tranexamic acid
in different in vitro and in vivo models of fibrinolysis
, coagulation and thrombus formation. J Thromb Haemost
2007; 5:2113–2118. http://dx.doi.org/10.1111/j.1538-7836.2007.02717.x
39. Takada A, Makino Y, Takada Y. Effects of tranexamic acid
, fibrinogenolysis and amidolysis. Thromb Res
40. Yee BE, Wissler RN, Zanghi CN, Feng C, Eaton MP. The effective concentration of tranexamic acid
for inhibition of fibrinolysis
in neonatal plasma in vitro. Anesth Analg
2013; 117:767–772. http://dx.doi.org/10.1213/ANE.0b013e3182a22258
41. Couturier R, Rubatti M, Credico C, Louvain-Quintard V, Anerkian V, Doubine S, et al. Continuous or discontinuous tranexamic acid
effectively inhibits fibrinolysis
in children undergoing cardiac surgery with cardiopulmonary bypass. Blood Coagul Fibrinolysis
2014; 25:259–265. http://dx.doi.org/10.1097/MBC.0000000000000051
42. Draxler DF, Medcalf RL. The fibrinolytic system: more than fibrinolysis
? Transfus Med Rev
43. Sigaut S, Tremey B, Ouattara A, Couturier R, Taberlet C, Grassin-Delyle S, et al. Comparison of two doses of tranexamic acid
in adults undergoing cardiac surgery with cardiopulmonary bypass. Anesthesiology
44. Couturier R, Grassin-Delyle S. Tranexamic acid
: more than inhibition of fibrinolysis
? Anesth Analg
45. Freeman GA, Kimmelman J, Dancey J, Monzon JG. Reporting practices of pharmacodynamic studies involving invasive research procedures in cancer trials. Br J Cancer
46. Freeman GA, Kimmelman J. Publication and reporting conduct for pharmacodynamic analyses of tumor tissue in early-phase oncology trials. Clin Cancer Res
47. Cardenas JC, Matijevic N, Baer LA, Holcomb JB, Cotton BA, Wade CE. Elevated tissue plasminogen activator
and reduced plasminogen activator inhibitor promote hyperfibrinolysis in trauma patients. Shock
48. Chapman MP, Moore EE, Moore HB, Gonzalez E, Gamboni F, Chandler JG, et al. Overwhelming tPA release, not PAI-1 degradation, is responsible for hyperfibrinolysis in severely injured trauma patients. J Trauma Acute Care Surg
49. Engelman DT, Gabram SG, Allen L, Ens GE, Jacobs LM. Hypercoagulability following multiple trauma. World J Surg
50. Moore HB, Moore EE, Gonzalez E, Chapman MP, Chin TL, Silliman CC, et al. Hyperfibrinolysis, physiologic fibrinolysis
, and fibrinolysis
shutdown: the spectrum of postinjury fibrinolysis
and relevance to antifibrinolytic therapy. J Trauma Acute Care Surg
51. Medcalf RL. The traumatic side of fibrinolysis
52. Tanswell P, Seifried E, Su PC, Feuerer W, Rijken DC. Pharmacokinetics and systemic effects of tissue-type plasminogen activator in normal subjects. Clin Pharmacol Ther