Wiener klinische Wochenschrift

, Volume 125, Issue 21–22, pp 721–729 | Cite as

Management of dabigatran-induced bleeding: expert statement

  • Dietmar Fries
  • Alexander Giurea
  • Manfred Gütl
  • Walter-Michael Halbmayer
  • Sibylle Kozek-Langenecker
  • Andreas Pachucki
  • Franz Roithinger
  • Barbara Steinlechner
  • Heinrich Thaler
  • Ansgar Weltermann
Open Access
consensus report


The interdisciplinary group of experts has compiled a clinical guidance for manifest dabigatran-induced haemorrhage and envisaged invasive interventions on patients under dabigatran. It recommends an escalation of treatment measures as summarized in a pocket guide (see electronic supplementary material online and insert in the print issue).


Thrombin time Ccarin clotting time Patient blood management Haemodialysis Prothrombincomplex concentrate Recombinant factor VIIa 

Management bei Dabigatran-induzierter Blutung - Expertenempfehlung


Die interdisziplinäre Expertengruppe hat einen klinischen Leitfaden für das Vorgehen bei manifester Dabigatran-induzierter Blutung und bei anstehenden invasiven Eingriffen bei Patienten unter Dabigatran zusammengestellt. Es wird ein eskalierendes Vorgehen vorgeschlagen und in einer Karte für die Manteltasche zusammengefasst (siehe “Electronic supplementary material” online und Beilage in der Print-Ausgabe).


Thrombinzeit Ecarin clotting time Patient Blood Management Hämodialyse Prothrombinkomplexkonzentrat rekombinanter Faktor VIIa 


Not least on account of demographic developments, the number of patients receiving oral anticoagulants is constantly increasing [1]. Accordingly, in case of elective and semi-elective surgery, there is an increasing need for a perioperative risk benefit assessment of whether anticoagulation should be continued, discontinued, or “bridged” parenterally. In case of continued oral anticoagulation perioperatively and in case of acute surgery severe bleeding episodes may require rapid inhibition of the biological action of the anticoagulant (reversal). Emergency reversal may also be indicated after injuries and spontaneous non-surgical bleeding. Such measures should be taken in due consideration of the situation, i.e. depending on the severity of the (risk of) haemorrhage, and balancing the risks of haemorrhage and thrombosis in view of the pre-existing indication for chronic anticoagulation. For Vitamin K antagonists, long-standing experience is available, although at a low level of scientific evidence [2, 3]. Such experience and evidence on perioperative management and practical clinical bleeding management is, however, still lacking for the new oral anticoagulants (NOACs; more recently also referred to as direct oral anticoagulants, DOACs). Dabigatran etexilate is the longest-standing NOAC registered for chronic application. Accordingly, the management of dabigatran-induced haemorrhagic complications is currently a frequent clinical and interdisciplinary challenge.

Currently available expert statements permit only an incomplete insight into the complexity of the management of dabigatran-induced haemorrhages, particularly in terms of the classification of haemorrhages according to acuity and severity, as well as the escalating indication for multi-modal therapies and the availability of therapy monitoring methods [4]. Therefore, the objective of the present interdisciplinary group of experts was to prepare recommendations for the management of dabigatran-induced bleeding in the course of day-to-day clinical work. The resulting expert opinion reflects the medical knowledge, specific experience, evaluations and opinions of the authors. As with all expert statements, each of these recommendations will have to be revised over time as new evidence and experience is gained. It should also be noted that use of the proposed recommendations will not guarantee therapeutic success or the absence of complications.

The present expert recommendation does not focus on presenting fundamental knowledge of the pharmacology of dabigatran and the research required for registration since such reviews are readily available [4, 5, 6, 7, 8]. For this reason, we merely recapitulate the facts relevant for prophylactic and therapeutic management of bleeding.

Background information on dabigatran

Action mechanism and pharmacology

Dabigatran is an oral, reversible direct thrombin inhibitor (DTI) that inhibits both free and fibrin-bound thrombin and thrombin-induced platelet aggregation [5, 6]. After adsorption, non-specific plasma esterases transform the inactive prodrug dabigatran etexilate into the active substance in both plasma and liver. Its mean terminal half-life has been stated to be 14–17 h but may be longer postoperatively [9]. As the drug is primarily eliminated by the kidneys, the half-life is significantly prolonged in patients with renal insufficiency [10]. For this reason, renal function should be monitored at regular intervals (e.g. twice a year) whenever dabigatran is used for long-term therapy [11]. Contraindications against the use of dabigatran are a creatinine clearance <  30 ml/min, artificial heart valves, allergies, haemorrhages, liver disease affecting survival, spontaneous or pharmacologically induced impairment of haemostasis. A dose reduction of Pradaxa® (from 2 × 150 mg to 2 × 110 mg per os or from 220 mg to 150 mg per os) is indicated in patients with a creatinine clearance of 30–50 ml/min, concomitant administration of verapamil, in the presence of thrombopathy/thrombopenia, gastroesophageal reflux disease and in patients aged 80 years or older.

On account of its low tendency to bind to plasma proteins, 62–68 % of the active substance can be eliminated by haemodialysis within 2–4 h [4]. It may be assumed that dabigatran can also be removed by haemofiltration and haemodiafiltration, though elimination times are likely to be longer ( >  4 h).

Efficacy and approval

The randomised phase-III study RELY relevant for regulatory approval investigated the efficacy of dabigatran (2 × 110 mg/2 × 150 mg) vs. warfarin in preventing stroke and systemic embolism in 18,113 patients suffering from atrial fibrillation in combination with at least one additional risk factor for stroke [12], with the occurrence of stroke or embolism serving as primary endpoint. At the higher dosage level, the administration of dabigatran resulted in a significantly lower incidence of haemorragic and ischaemic strokes as compared with warfarin, and the incidence of cardiovascular deaths was also significantly lower. Dabigatran at 2 × 150 mg is so far the only direct oral anticoagulant causing a significant reduction of ischaemic strokes, which is numerically the most relevant threat. However, no significant difference was found with regard to overall mortality. As far as patient safety was concerned, it should be noted that life-threatening haemorrhages, most importantly intracranial haemorrhage, occurred significantly less often in patients receiving dabigatran at either dosage level than in those treated with warfarin [12].

In Austria, dabigatran has been approved under the trade name Pradaxa® for primary prevention of venous thromboembolic events in adult patients following elective surgery for hip or knee joint replacement at a dosage level of 220 mg 1x a day or 150 mg 1x a day, as well as for the prevention of strokes or embolisms in non-valvular atrial fibrillation at a level of 150 mg 2x a day or 110 mg 2x a day. Dabigatran is recommended as a ‘first-line’ therapy for this chronic indication [13].

Coagulation tests

No laboratory analyses are required for routine monitoring during dabigatran therapy [6]. Under certain clinical conditions, however, it may be advisable to test for the new anticoagulants, for instance in cases of suspected accidental overdosing, acute bleeding complications, invasive emergency interventions, drug interaction, renal insufficiency, critically ill patients, advanced age and to check compliance.

Routine coagulation tests

Depending on the dosage administered and the time between the last administration and blood sampling, dabigatran may significantly affect the results of all conventional coagulation tests [14]. Accordingly, the diagnostic acuity of routine coagulation tests is impaired when preoperative patients treated with dabigatran are tested for other hereditary or acquired coagulopathies. Prolonged routine lab tests will not provide specific and quantitative information on the causation or level of dabigatran and could also be due to other haemostatic disorders or substances [14].

A combination of a highly pathological prothrombin time (INR >  2) and a highly pathological activated partial thromboplastin time (aPTT >  90 s) at the trough level may suggest (but cannot prove) possible overdosing of dabigatran [15]. According to the manufacturer (SMPC, January 2013), a double or triple prolongation of the aPTT values dabigatran at trough level may be associated with an increased bleeding risk. The thrombin time (TT) is prolonged even at low dabigatran plasma levels, thus a normal TT can be assumed to rule out a clinically relevant dabigatran level.

The least influence on routine coagulation tests can be expected at the trough level of dabigatran 12 h after the last or immediately before the next administration. To avoid misinterpretations and possibly wrong therapeutic decisions it is therefore imperative, when requesting routine coagulation tests for patients treated with dabigatran, to inform the laboratory of the last time the drug was administered.

Dabigatran-sensitive tests

Dabigatran-sensitive coagulation tests performed shortly before surgery could best provide information on the extent of the residual pharmacological coagulation inhibition caused by dabigatran [4]. In principle, this information could be obtained by means of the adapted thrombin time (e.g. the Hemoclot® Test) or the ecarin clotting time (ECT). The determination of the adapted TT is based on the inhibition of a defined constant thrombin concentration in diluted plasma samples. On account of their linear dose-effect relation the adapted thrombin time and ECT permit, when calibrated in line with CE standards, a quantitative determination of the effect of dabigatran, whereas the correlation of these dabigatran-sensitive tests with the clinical outcome parameters of haemorrhages is yet unclear. According to the manufacturer (SMPC, January 2013), a double or triple prolongation of the aPTT values dabigatran at trough level may ≥ 200 ng/ml in the Hemoclot® Test may be associated with an increased bleeding risk in non-surgical patients. Most importantly, a threshold limit value for the Hemoclot® Test, which predicts a low perioperative bleeding risk, has not yet been established.

Individual risk of thromboembolism and haemorrhage

Individual risks vary with the magnitude and nature of surgery (expositional risk factors) and individual (dispositional) risk factors. The bleeding risk of non-surgical patients can be assessed by means of the HAS-BLED Score, with a score of ≥ 3 being generally seen as indicative of an increased risk of haemorrhage [16]. Post-operative bleeding risk and possible strategies to control bleeding will also depend on the experience of the medical care personnel and on locally available resources.

One well-established approach to the stratification of the risks of thromboembolism and stroke is the use of the CHADS2 Score and the CHA2DS2-VASc Score [17]. In cases of atrial fibrillation with a fairly low CHA2DS2-VASc Score (≤ 4) and a negative history concerning a thromboembolic event anticoagulation with dabigatran may be discontinued for up to 1 week without causing a clinically relevant increase in the thromboembolism rate.

With pending indications for the use of dabigatran in patients with deep vein thrombosis or pulmonary embolism [18, 19], bleeding complications may and will occur in this cohort as well. Nevertheless, the longer treatment and the higher dosage will, in general, always be applied to patients with atrial fibrillation. Therefore, the risks of haemorrhage may possibly be extrapolated to these new indications.

Management of bleeding in patients receiving dabigatran

Strategies recommended for the management of manifest bleeding in patients receiving dabigatran have been summarised in Fig. 1.

Fig. 1

Management of manifest bleeding under dabigatran

Mild bleeding


The term mild bleeding (e.g. superficial bleeding, diverticular bleeding) describes haemorrhages that do not require transfusions, are haemodynamically irrelevant and can be staunched easily.

Basic measures

Basic measures comprise general clinical observation of the haemorrhagic patient including haemodynamic monitoring and local haemostasis. The latter can be achieved by such means as mechanical compression or sclerotherapy on condition that the area of bleeding is accessible. Other basic measures are the avoidance of arterial pressure peaks, hypothermia, etc.

Administration of dabigatran

Until haemostasis has been achieved, patients may require skipping of one or more dosages of dabigatran—all on condition that the increased risk of thrombosis does not outweigh the current risk of bleeding. If anticoagulation with dabigatran has been discontinued, it can be resumed within 72 h once haemostasis has been achieved, in particular if the relapse risk is considered to be low and that of thromboembolism high.

Laboratory tests

A blood count analysis (including a platelet count) or, if the same is not readily available, the determination of the haematocrit/haemoglobin values by blood gas analysis may be used to exclude haemorrhages requiring blood transfusion. A renal function test (determination of creatinine clearance by the Cockroft-Gault formula, glomerular filtration rate eGFR using the MDRD formula) may be useful to estimate the risk of dabigatran accumulation. Before resuming dabigatran therapy in patients with renal insufficiency care should be taken to modify, if necessary, the dosage and/or review the indication for dabigatran.

In the case of spontaneous minor bleeding it does not appear imperative to routinely perform laboratory coagulation tests. Excessively prolonged coagulation times may, however, be seen as an indicator of possible overdosing requiring further diagnostic (dabigatran level determination, exploration of other coagulopathies) and therapeutic action (review of dabigatran dosage and its indication).

Strategies not recommended

On the basis of a risk/benefit assessment in cases of mild bleeding it is not advisable to use coagulation factor concentrates in an attempt to reverse dabigatran action. The use of tranexamic acid for mild haemorrhages does not appear useful in the absence of any association with the pathomechanism of dabigatran-induced bleeding.

In view of the fact that mild bleeding complications can usually be managed by other means, general measures to reduce dabigatran resorption and stimulating elimination are not recommended.

Severe bleeding


Severe bleeding is defined as haemorrhages that require transfusion but, in terms of their haemodynamic relevance, do not appear to require catecholamines and are not deemed immediately life-threatening or organ-threatening.

Basic measures

In the case of heavy bleeding (e.g. psoas muscle bleeding) it is recommended to control symptoms by individualised volume replacement for the purpose of achieving haemodynamic stabilisation and to transfuse erythrocyte concentrates on the basis of individualised transfusion triggers. Mostly the transfusion trigger should not exceed 9 g/dl nor be lower than 7 g/dl [20]. Depending on the extent of bleeding, invasive haemostatic methods, e.g. surgical or radiologic/endovascular interventions, should be considered. As a basic principle, it is advisable to avoid hypothermia, acidosis and hypocalcaemia. Correction of secondarily acquired coagulopathies (e.g. hyperfibrinolysis by antifibrinolytics, factor deficits by coagulation factor concentrates) may be undertaken in line with current trauma guidelines [21, 22].

Administration of dabigatran

In the case of severe bleeding dabigatran should be discontinued until haemostasis has been achieved; once this is the case, anticoagulation with dabigatran can be resumed with an appropriate safety window of 3 days to 2 weeks.

In the case of recent oral dabigatran intake (within the last 2 h) enteral administration of activated coal (1 g/kg BW) is recommended, which will bind the substance and reduce resorption [23]. Moreover, dabigatran can be eliminated by haemodialysis.

Laboratory tests

A blood count analysis (including a platelet count) or, if the same is not readily available, the determination of the haematocrit/haemoglobin values by blood gas analysis is recommended, since it will allow targeted erythrocyte transfusion and avoid transfusion in excess of the individual transfusion triggers.

In the case of severe bleeding requiring transfusion it is recommended to perform routine coagulation tests (with blood samples preferably at dabigatran trough level) in order to rule out (not yet) evaluated hereditary or acquired coagulation disorders if the bleeding was not (or not exclusively) caused by dabigatran. Prolonged thrombin times may lead to evaluation of dabigatran levels (e.g. Hemoclot® Test).

A renal function test (eGFR, creatinine clearance) will permit conclusions regarding possible accumulations that will help adapt the dosage once haemostasis has been achieved. The indication for dabigatran therapy should be checked before administration is resumed.

Strategies not recommended

In the case of severe bleeding that is not life-threatening and does not jeopardise an organ function, emergency dabigatran reversal by means of coagulation factor concentrates is not recommended because this might, without further benefit for the patient, compound the manifest risk of haemorrhage with an additional risk of a thromboembolic event.

Life-threatening or organ-threatening bleeding


The borderline between massive and life-threatening haemorrhages is blurred but can be arbitrarily defined by the need for transfusion with ≥ 4 erythrocyte concentrates and the administration of exogenous catecholamins (noradrenalin, adrenalin, dobutamine) for the purpose of haemodynamic stabilisation. Diagnosis of an organ-threatening haemorrhage depends also on the localisation of the lesion, e.g intracerebral, intraspinal or intraocular and the risk of the intervention(s) to achieve local haemostasis.

Basic measures, administration of dabigatran and laboratory tests

Cases of life-threatening or organ-threatening bleeding should be managed in the same way as severe bleeding (see severe bleeding section above); in addition, the feasibility of emergency measures to offset dabigatran action (emergency reversal) should be considered. In the absence of clinical evidence for emergency reversal of dabigatran only few experimental studies and pharmacological data are available and suggest that the action of dabigatran might, at least partially, be offset by activated prothrombin complex concentrate (e.g. factor eight bypassing activity FEIBA) or recombinant factor VIIa [23, 24, 25, 26, 27, 28]. To date no dose-finding studies have been published for this indication. Should reversal be planned, an initial dose of at least 25 U/kg BW FEIBA or at least 50 µg/kg BW rFVIIa (NovoSeven®) could be considered, possibly with a repeated administration. Considering the strong increase in thrombin generation induced by these activated coagulation factor concentrates they should be used only after careful benefit/risk assessment. Cost-effectiveness of FEIBA and rFVIIa for the reversal of dabigatran has not yet been proven. Furthermore, FEIBA and rVIIa, or experience with their use, are not available in all hospitals.

Conventional prothrombin complex concentrate (PCC) (Beriplex® 50 U/kg BW) stopped bleeding in an animal experiment [26] but heparin-free PCC (Cofact® 50 U/kg BW) could not reverse clotting times in six volunteers after 2.5 days dabigatran intake [27]. Clinical outcome parameters of bleeding were not assessed in this volunteer trial [27]. PCC is listed in monodisciplinary recommendations as a reversing agent [7]. National data recorded by the NOAC Line ( suggest favourable results with PCC, so that an attempted reversal with PCC may be seen as a possible therapeutical option if bleeding is deemed life-threatening or organ-threatening.

Measures not recommended

In view of the limited efficacy of fresh frozen plasma (FFP) to correct perioperative bleeding [29] and abnormal laboratory coagulation test results [30] the administration of FFP to reverse dabigatran-induced haemorrhages cannot be recommended.

Perioperative management of dabigatran-treated patients

Recommended strategies are summarised in Fig. 2.

Fig. 2

Management of patients under dabigatran during surgical interventions

Elective interventions

Surgical interventions should be classified in terms of their bleeding risk.

Minor interventions

In the case of minor interventions with a low bleeding risk it is recommended to continue administration of vitamin K antagonists [2, 3]. Analogously, dabigatran can also be continued in such cases [3]. During the intervention the theatre staff should make full use of available measures to ensure effective haemostasis and thus avoid excessive blood transfusions. The ward staff should be made fully aware of the risk of postoperative complications (haemorrhages) to ensure rapid recognition and correction.

Major interventions

In major interventions the bleeding risk is either due to the extent of foreseeable haemorrhage or its critical location (e.g. intracranial). Normal coagulation during major surgery and the early postoperative phase is seen as an important factor of patient safety. Accordingly, discontinuation of vitamin K antagonists and, where necessary, bridging with low-molecular-weight heparins is recommended [2, 3]. Similarly, dabigatran may be discontinued. Whether bridging with heparins should be performed in the case of NOACs is still controversial. The authors of the present recommendations do not recommend bridging when NOACs are discontinued for the periods stipulated in the MAA documentation to prevent a possible increase in perioperative bleeding risk. However, if the thromboembolic risk is higher (CHADS2-Vasc Score ≥ 4) and surgery requires discontinuation of dabigatran for more than 5 days, a bridging therapy with low-molecular-weight heparin may be an option [11].

At what time dabigatran should be discontinued pre-operatively will depend on the patient’s current renal function [31]. In patients with a normal renal elimination facing a low-risk intervention a 2-day interval may be sufficient to preclude a clinically relevant residual effect of dabigatran during surgery. In the case of patients with a reduced renal elimination (creatinine clearance <  50 ml/min) and a high-risk intervention dabigatran should be suspended for at least 4 days to prevent the intraoperative risk of residual anticoagulation.

Particularly in the case of major interventions the theatre staff should make full use of available measures to ensure effective haemostasis and thus avoid excessive blood transfusions. The ward staff should be made fully aware of the risk of postoperative complications (haemorrhages or thromboses) to ensure rapid recognition and correction.

Laboratory tests

Pre-operative renal function tests (creatinine clearance according to the Cockroft-Gault formula or calculating the glomerular filtration rate according to the MDRD formula) help determine the necessary interval before discontinuation of dabigatran administration.

Pre-operative blood counts or haemoglobin/haematocrit assays may detect the presence of anaemia, and a subsequent differential diagnosis and correction may enhance tolerance to perioperative bleeding [3]. This recommendation is in line with the concept of patient blood management [32]. An intra-operative and post-operative blood count analysis (including a platelet count) or, if the same is not readily available, the determination of haemoglobin/haematocrit values by means of blood gas analysis is recommended since it may serve as an indication for erythrocyte transfusion and can help avoid transfusions as soon as the individual transfusion trigger is exceeded.

The success of discontinuing vitamin K antagonists can be checked by means of the target value of INR (preoperatively mostly <  1.4). Analogously, it would be desirable to obtain direct evidence that a safe plasma level has been reached or that the biological anticoagulatory effects of dabigatran have been eliminated. A dabigatran-sensitive coagulation test shortly prior to surgery might provide information on the extent of residual pharmacological anticoagulation [4]. The residual effect of dabigatran cannot be quantified by means of routine coagulation tests (global tests such as aPTT, PT, INR).

Strategies not recommended

Prophylactic administration of coagulation factor concentrates is not recommended for elective interventions since the operative trauma would compound the pre-existing risks of thromboembolism and acute-phase reaction with yet another prothrombotic stimulus in the form of the concentrates. Our recommendation, as described above in the context of acute bleeding, is to consider the administration of coagulation factor concentrates only in cases of severe intra-operative or post-operative haemorrhage.

Elective interventions under regional anaesthesia

Dabigatran for postoperative thrombosis prevention has only been approved for elective hip and knee joint replacement. In these cases the intervention may be performed under neuraxial regional anaesthesia: The epidural catheter is put in place prior to starting the postoperative administration of the prophylactic dose of dabigatran (110 mg Praxada® 2–4 h postoperatively, followed by 1 × 220 mm Praxada® per day). Dabigatran should only be administered after removal of the catheter, in the interest of patient safety with a delay of at least 2 h. According to the current recommendations based on pharmacokinetics the catheter may also be removed after a dabigatran withdrawal interval of 26 h, and the next dose of dabigatran should be given, at the earliest, 4–6 h after removal of the catheter [33, 34]. In the absence of study data, locoregional anaesthesia or the neuraxial catheter technique should not be used in patients for whom a rapid resumption of the administration of therapeutic doses of dabigatran (2 × 150 mg or 2 × 110 mg Praxada® per day) has been envisaged.

Acute and urgent major interventions (within 24 h)

Administration of dabigatran

In the case of acute or urgent (semi-elective) major surgery with a relevant risk of bleeding (e.g. fractures near the hip, revision of septic joints, urgent tumour surgery) it is imperative to establish exactly when dabigatran was last administered: If the time interval recommended for elective major surgery cannot be respected on account of the urgency of the intervention, dabigatran therapy should at least be interrupted as soon as the indication for surgery has been established. If dabigatran was last given within the last 1 or 2 h, reduction of resorption by means of oral activated coal may be attempted. Prior to high-bleeding-risk interventions it might be reasonable to reduce dabigatran by means of haemodialysis for >  4 h.

Basic measures

Patient monitoring should comply with the measures outlined in the severe bleeding section above.

Symptomatic treatment of slight, massive, life-threatening and organ-threatening haemorrhages should be in line with the severe bleeding and life-threatening or organ-threatening bleeding section above.

Administration of coagulation factor concentrates should only be considered individually in the case of massive bleeding.

Laboratory tests

TT can be used to determine whether a residual dabigatran effect is still to be expected immediately before or in the course of an urgent or acute surgical intervention. Normal TT values may exclude the presence of a clinically relevant residual dabigatran effect. It is advisable to measure TT at two points in time to assess possible variations in the findings. If the TT is prolonged, a dabigatran-sensitive test should be performed as outlined in the mild bleeding section above: adapted thrombin time (e.g. Hemoclot®Test) or ecarin clotting time (ECT).

Particularly in the case of massive bleeding repeated blood counts are recommended to ensure targeted transfusion. Routine coagulation tests, and possibly also complementary rotational thromboelastometry/thromboelastography (especially for the diagnosis of hyperfibrinolysis) should be performed repeatedly to permit targeted correction of (especially) secondarily acquired coagulopathies [3, 22, 35].

Emergency interventions

Administration of dabigatran

In the case of peracute interventions that cannot be delayed and carry a high bleeding risk in terms of extent and location (e.g. ruptured hollow organs or vessels, traumatic brain injury, polytrauma) no further dose of dabigatran should be administered once the need for surgery has been established. In principle, emergency interventions on patients receiving dabigatran should be delayed as long as it is medically acceptable.

Basic measures

Patient monitoring should comply with the measures outlined in the severe bleeding section above.

Symptomatic treatment of slight, massive, life-threatening and organ-threatening haemorrhages should be in line with the severe bleeding and life-threatening or organ-threatening bleeding sections above. As soon as the first clinical symptoms of severe bleeding become apparent, reversal by FEIBA, rFVIIa or PCC should be considered in line with life-threatening or organ-threatening bleeding section. Forced elimination by haemodialysis (or haemo(dia)filtration, in which case both the effectiveness and the necessary duration of application are still in doubt) might be difficult under emergency surgery conditions and, in the case of polytrauma, in patients undergoing diagnostic imaging. As a matter of principle, emergency interventions should not be delayed on account of forced dabigatran elimination or reversal measures.

If the gastrointestinal tract is intact, dabigatran adsorption may be reduced without major delay by administering activated coal via a stomach tube in place. In patients whose history taken in an emergency situation fails to reveal the circumstances and time of dabigatran intake, external sources of information (statements of relatives etc.) may be significant.

Laboratory tests

The recommendations given in the acute and urgent major interventions section apply.

As regards the collective of trauma patients under dabigatran, physicians should refer to the European and Austrian Guidelines [21, 22].

Final comment.

Randomised clinical trials are highly warranted to prove the suggested treatment options above and, finally, to define safe and efficacious therapeutic interventions and indicative laboratory testing in patients with or at risk for dabigatran-induced bleeding. Until this evidence is available registries may help us to establish patient-oriented care. The ‘NOAC line’ at offers an electronic database to which anonymised cases of NOAC-induced bleeding and its management can be added, irrespective of the success or failure of the measures taken.

Conflict of interest

Sibylle Kozek-Langenecker received honoraria for lectures and travel reimbursement from Baxter, Boehringer Ingelheim, Biotest, CSL Behring, Novo Nordisk, Octapharma, TEM Innovations. Walter-Michael Halbmayer received honoraria for lectures or consultation from Bayer, Boehringer-Ingelheim, Pfizer Corporation, Roche Diagnostics, Siemens Healthcare, Stago.


Open Access

This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.

Supplementary material

508_2013_430_MOESM1_ESM.pdf (66 kb)
(PDF 66kb)


  1. 1.
    Fugate JE, Rabinstein AA, McBane RD, Lanzino G. Dabigatran: a primer for neurosurgeons. World Neurosurg. 2012 Jun 19. doi:pii:S1878–8750(12)00639-0. 10.1016/j.wneu.2012.06.019 (Epub ahead of print).Google Scholar
  2. 2.
    Guyatt GH, Akl EA, Crowther M, Gutterman DD, Schuünemann HJ, American college of chest physicians antithrombotic therapy and prevention of thrombosis panel. Executive summary: antithrombotic therapy and prevention of thrombosis, 9th ed: american college of chest physicians evidence-based clinical practice guidelines. Chest. 2012;141(Suppl 2):7S–47S.PubMedCrossRefGoogle Scholar
  3. 3.
    Kozek-Langenecker S, Afshari S, Albaladejo P, Santullano CA, De Robertis E, Filipescu D, Fries D, Görlinger K, Haas T, Imberger G, Jacob M, Lancé M, Llau J, Mallett S, Meier J, Rahe-Meyer N, Samama CM, Smith A, Solomon C, Van der Linden P, Wikkelsø A, Wouters P, Wyffels P. Guidelines on the management of severe perioperative bleeding. Eur J Anaesthesiol. 2013;30(6):270–382.PubMedCrossRefGoogle Scholar
  4. 4.
    Weltermann A, Brodmann M, Domanovits H, Eber B, Gottsauner-Wolf M, Halbmayer WM, Hiesmayr JM, Kyrle PA, Längle F, Roithinger FX, Watzke H, Windhager R, Wolf C, Zweiker R. Dabigatran in patients with atrial fibrillation: perioperative and periinterventional management. Wien Klin Wochenschr. 2012;124(9–10):340–7.PubMedCrossRefGoogle Scholar
  5. 5.
    Cheng JW, Vu H. Dabigatran etexilate: an oral direct thrombin inhibitor for the management of thromboembolic disorders. Clin Ther. 2012;34(4):766–87.PubMedCrossRefGoogle Scholar
  6. 6.
    Kreutz R. Pharmakologie neuer oraler Antikoagulantien. Grundlage für rationale Entscheidungen. Klinikarzt. 2012;41(S1):10–5.Google Scholar
  7. 7.
    Spannagl M, Bauersachs E, Debus ES, Gawaz M, Gerlach H, Haas S, Hach-Wunderle V, Lindhoff-Last E, Riess H, Schellong S, Schinzel H, Bode C. Therapie mit Dabigatran—Periinterventionelles Management und Interpretation von Gerinnungstests. Hämostaseologie. 2012;32:294–305.PubMedCrossRefGoogle Scholar
  8. 8.; Leitfaden der Arzneimittelkommission der deutschen Ärzteschaft. Orale Antikoagulation bei nicht valvulärem Vorhofflimmern. Empfehlungen zum Einsatz der neuen Antikoagulantien Dabigatran (Pradaxa) und Rivaroxaban (Xarelto). Version 1.0, September 2012.
  9. 9.
    Samama CM. New anticoagulants: pharmacology and clinical studies. Wien Med Wochenschr. 2011;161(3–4):54–7.PubMedCrossRefGoogle Scholar
  10. 10.
    Stangier J, Rathgen K, Stähle H, Gansser D, Roth W. The pharmacokinetics, pharmacodynamics and tolerability of dabigatran etexilate, a new oral 2 thrombin inhibitor, in healthy male subjects. Br J Clin Pharmacol. 2007;64(3):292–303.PubMedCrossRefGoogle Scholar
  11. 11.
    Sauer H, Wankmüller H, Leschke M. Blutungsmanagement, perioperatives und periprozedurales Bridging: Vorschlag praktischer Strategien für die neuen oralen Antikoagulantien. Klinikarzt. 2012;41:26–32.CrossRefGoogle Scholar
  12. 12.
    Connolly SJ, Ezekowitz MD, Yusuf S, Eikelboom J, Oldgren J, Parekh A, Pogue J, Reilly PA, Themeles E, Varrone J, Wang S, Alings M, Xavier D, Zhu J, Diaz R, Lewis BS, Darius H, Diener HC, Joyner CD, Wallentin L, RE-LY steering committee and investigators. Dabigatran versus warfarin in patients with atrial fibrillation. N Engl J Med. 2009;361(12):1139–51.PubMedCrossRefGoogle Scholar
  13. 13.
    Camm AJ, Lip GY, De Caterina R, Savelieva I, Atar D, Hohnloser SH, Hindricks G, Kirchhof P, ESC Committee for Practice Guidelines (CPG), Bax JJ, Baumgartner H, Ceconi C, Dean V, Deaton C, Fagard R, Funck-Brentano C, Hasdai D, Hoes A, Kirchhof P, Knuuti J, Kolh P, McDonagh T, Moulin C, Popescu BA, Reiner Z, Sechtem U, Sirnes PA, Tendera M, Torbicki A, Vahanian A, Windecker S, Document Reviewers, Vardas P, Al-Attar N, Alfieri O, Angelini A, Blömstrom-Lundqvist C, Colonna P, De Sutter J, Ernst S, Goette A, Gorenek B, Hatala R, Heidbüchel H, Heldal M, Kristensen SD, Kolh P, Le Heuzey JY, Mavrakis H, Mont L, Filardi PP, Ponikowski P, Prendergast B, Rutten FH, Schotten U, van Gelder IC, Verheugt FW. 2012 focused update of the ESC guidelines for the management of atrial fibrillation: an update of the 2010 ESC guidelines for the management of atrial fibrillation. Developed with the special contribution of the European Heart Rhythm Association. Eur Heart J. 2012;33(21):2719–47.PubMedCrossRefGoogle Scholar
  14. 14.
    Halbmayer WM, Weigel G, Quehenberger P, et al. Interference of the new oral anticoagulant dabigatran with frequently used coagulation tests. Clin Chem Lab Med. 2012;50(9):1601–5. doi:10.1515/cclm-2011–0888.PubMedCrossRefGoogle Scholar
  15. 15.
    Lindahl TL, Baghaei F, Blixter IF, Gustafsson KM, Stigendal L, Sten-Linder M, Strandberg K, Hillarp A, Expert group on coagulation of the external quality assurance in Laboratory Medicine in Sweden. Effects of the oral, direct thrombin inhibitor dabigatran on five common coagulation assays. Thromb Haemost. 2011;105(2):371–8.PubMedCrossRefGoogle Scholar
  16. 16.
    Omran H, Bauersachs R, Rübenacker S, Goss F, Hammerstingl C. The HAS-BLED score predicts bleedings during bridging of 2 oral anticoagulation. Results from the national multicentre BNK Online bridging registry (BORDER). Thromb Haemost. 2012;108(1):65–73.PubMedCrossRefGoogle Scholar
  17. 17.
    Lip GY, Nieuwlaat R, Pisters R, Lane DA, Crijns HJ. Refining clinical risk stratification for predicting stroke and thromboembolism in atrial fibrillation using a novel risk factor-based approach: the euro heart survey on atrial fibrillation. Chest. 2010;137(2):263–72.PubMedCrossRefGoogle Scholar
  18. 18.
    Schulman S, Kearon C, Kakkar AK, et al. Extended use of dabigatran, warfarin, or placebo in venous thromboembolism. N Engl J Med. 2013;368(8):709–18.PubMedCrossRefGoogle Scholar
  19. 19.
    Schulman S, Kearon C, Kakkar AK, et al. Dabigatran versus warfarin in the treatment of acute venous thromboembolism. N Engl J Med. 2009;361:2342–52.PubMedCrossRefGoogle Scholar
  20. 20.
    Hébert PC, Wells G, Blajchman MA, Marshall J, Martin C, Pagliarello G, Tweeddale M, Schweitzer I, Yetisir E. A multicenter, randomized, controlled clinical trial of transfusion requirements 2 critical care. Transfusion requirements in critical care investigators, canadian critical care trials group. N Engl J Med. 1999;340(6):409–17.PubMedCrossRefGoogle Scholar
  21. 21.
    Rossaint R, Bouillon B, Cerny V, Coats TJ, Duranteau J, Fernández-Mondéjar E, Hunt BJ, Komadina R, Nardi G, Neugebauer E, Ozier Y, Riddez L, Schultz A, Stahel PF, Vincent JL, Spahn DR, Task force for advanced bleeding care in trauma. Management of bleeding following major trauma: an updated European guideline. Crit Care. 2010;14(2):R52.PubMedCrossRefGoogle Scholar
  22. 22.
    Fries D, Innerhofer P, Perger P, Gütl M, Hofmann N, Kneifel W, Neuner L, Pernerstorfer T, Pfanner G, Schöchl H, Ziegler B, Kölblinger C, Kozek-Langenecker SA. Gerinnungsmanagement bei traumatisch bedingter Massivblutung. AINS. 2010;45:552–61.PubMedGoogle Scholar
  23. 23.
    Cotton BA, McCarthy JJ, Holcomb JB. Acutely injured patients on dabigatran. N Eng J Med. 2011;365:2038–40.CrossRefGoogle Scholar
  24. 24.
    Weitz JI, Quinlan DJ, Eikelboom JW. Periprocedural management and approach to bleeding in patients taking dabigatran. Circulation. 2012;126(20):2428–32.PubMedCrossRefGoogle Scholar
  25. 25.
    Pezborn E, Trabandt A, Selbach K, Tinel H. Prothrombin complex concentrate reverses the effects of high-dose rivaroxaban in rats (Abstract). Pathophysiol Haemost Thromb. 2010;37:A10–OC251.Google Scholar
  26. 26.
    van Ryn J, Stangier J, Haertter S, Liesenfeld KH, Wienen W, Feuring M, Clemens A. Dabigatran etexilate—a novel, reversible. oral direct thrombin inhibitor: interpretation of coagulation assays and reversal of anticoagulant activity. Thromb Haemost. 2010;103(6):1116–27.PubMedCrossRefGoogle Scholar
  27. 27.
    Eerenberg ES. Reversal of rivaroxaban and dabigatran by prothrombin complex concentrate. Circulation. 2011;124:1573–9.PubMedCrossRefGoogle Scholar
  28. 28.
    Baron TH, Kamath PS, McBane RD. Management of anithrombotic therapy in patients undergoing invasive procedures. N Engl J Med. 2013;368:2113–24.PubMedCrossRefGoogle Scholar
  29. 29.
    Kozek-Langenecker S, Sorensen B, Hess J, Spahn DR. Clinical effectiveness of fresh frozen plasma compared with fibrinogen concentrate: a systematic review. Critical Care. 2011;15:R239.PubMedCrossRefGoogle Scholar
  30. 30.
    Abdel-Wahab O, Healy B, Dzik W. Effect of fresh frozen plasma transfusion on prothrombin time and bleeding in patients with mild coagulation abnormalities. Transfusion. 2006;46:1279–85.PubMedCrossRefGoogle Scholar
  31. 31.
    Ortel TL. Perioperative management of patients on chronic antithrombotic therapy. Hematology Am Soc Hematol Educ Program. 2012;2012:529–35.PubMedGoogle Scholar
  32. 32.
    Goodnough LT, Shander A. Special article: current status of pharmacologic therapies. Anesth Analg. 2013;116:15–34.PubMedCrossRefGoogle Scholar
  33. 33.
    Regionalanästhesie unter gerinnungshemmender Medikation. Empfehlungen der Arbeitsgruppe perioperative Gerinnung der ÖGARI.ästhesie%20und%20Gerinnungshemmer%202013.pdf. Last access 24 Sep 2013.
  34. 34.
    Gogarten W, Vandermeulen E, Van Aken H, Kozek S, Llau J, Samama M. Regional anaesthesia and antithrombotic agents: recommendations of the European Society of Anaesthesiology. Eur J Anaesthesiol. 2010;27:999–1015.PubMedCrossRefGoogle Scholar
  35. 35.
    Afshari A, Wikkelsø A, Brok J, Møller AM, Wetterslev J. Thrombelastography (TEG) or thromboelastometry (ROTEM) to monitor haemotherapy versus usual care in patients with massive transfusion. Cochrane Database Syst Rev. 2011;(3):CD007871. doi:10.1002/14651858.CD007871.Google Scholar

Copyright information

© The Author(s) 2013

Authors and Affiliations

  • Dietmar Fries
    • 1
  • Alexander Giurea
    • 2
  • Manfred Gütl
    • 3
  • Walter-Michael Halbmayer
    • 4
  • Sibylle Kozek-Langenecker
    • 5
  • Andreas Pachucki
    • 6
  • Franz Roithinger
    • 7
  • Barbara Steinlechner
    • 8
  • Heinrich Thaler
    • 9
  • Ansgar Weltermann
    • 10
  1. 1.Department of Anesthesia and Intensive CareMedical University InnsbruckInnsbruckAustria
  2. 2.Department of OrthopedicsMedical University of ViennaViennaAustria
  3. 3.Department of Anesthesiology and Intensive CareMedical University GrazGrazAustria
  4. 4.Institute of Laboratory MedicineKrankenhaus HietzingViennaAustria
  5. 5.Department of Anesthesia and Intensive CareEvangelical Hospital ViennaWienAustria
  6. 6.Department of Trauma SurgeryLandesklinikum AmstettenAmstettenAustria
  7. 7.Department of Internal MedicineLandesklinikum MödlingMödlingAustria
  8. 8.Department of Anesthesia, General Intensive Care and Pain ManagementMedical University of ViennaViennaAustria
  9. 9.Trauma Centre Meidling, Division of Internal MedicineAUVA-Unfallkrankenhaus MeidlingViennaAustria
  10. 10.Department of Internal MedicineKrankenhaus ElisabethinenLinzAustria

Personalised recommendations