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Anestezjologia Intensywna Terapia
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Use of direct oral anticoagulants in ICU patients. Part I – Applied pharmacology

Abdul Wahab
1
,
Rupali Patnaik
2
,
Mohan Gurjar
2

  1. University of Iowa Hospitals and Clinics, Iowa City, United States
  2. Sanjay Gandhi Postgraduate Institute of Medical Sciences (SGPGIMS), Lucknow, Uttar Pradesh, India
Anestezjologia Intensywna Terapia 2021; 53, 5: 430–440
Data publikacji online: 2021/12/30
Plik artykułu:
- Use of direct.pdf  [0.17 MB]
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In general, critically ill patients are susceptible to vascular thrombosis and have a higher risk of bleeding compared to non-critically ill medical or surgical patients. The advent of direct oral anticoagulants (DOACs) is a revolution in medicine. Unfortunately, clinical trials of the use of DOACs in the intensive care unit (ICU) are lacking. Over the last decade, the utilization of DOACs has increased, and critical care clinicians can come across patients with known and unknown use of DOACs [1]. Pivotal phase III DOAC trials did not include patients requiring ICU management, patients with acute kidney injury, patients with major bleeding, or patients in need of urgent surgical interventions [2–6]. This narrative review covers current evidence on the use of DOAC in indicated conditions and anticoagulant management of medical or surgical patients receiving DOAC before ICU admission. This article is the second part of the narrative review. Pharmacology, including indications and dosing, has been covered in the first part: “Use of direct oral anticoagulants in ICU patients. Part I – Applied pharmacology”.

Search strategy and selection criteria

This is a non-structured narrative review to provide current clinical evidence about the use of DOACs in ICU patients. The review was conducted by a search on the PubMed, Embase, Medline, Google Scholar, and Cinicaltrials.gov databases. The search included publications from 1994 to 2020, using the terms “dabigatran”, “rivaroxaban”, “apixaban”, “edoxaban”, or “betrixaban”, “oral anticoagulants use in critically ill patients”, “DOACs/NOACs use in the intensive care unit”, “oral anticoagulants in sepsis, shock, and acute kidney injury”, and “oral anticoagulant mana­gement in the perioperative period” to identify rele­vant papers, including randomized clinical trials, meta-analyses, observation studies, case series, and guidelines.

Current evidence for use of DOAC

Atrial fibrillation

Warfarin (vitamin K antagonist) remains the anti­coagulant of choice for patients with valvular atrial fibrillation (AF), secondary to mechanical valves and moderate to severe rheumatic mitral valve stenosis, due to the exclusion of such patients from phase III DOAC trials and evidence of thrombotic and bleeding risks in these patients [7–10]. Current guidelines recommend using DOACs in patients with non-valvular AF (NVAF) because DOACs are non-inferior to warfarin in stroke prevention in this population [11, 12]. Due to the lack of evidence and pragmatism, the consensus opinion is to switch a DOAC to a parenteral anticoagulant if such patients are admitted to the ICU either due to AF, AF-associated complications (e.g. stroke), the need for an invasive procedure, or sepsis/shock [13, 14]. In patients with new-onset NVAF of > 48 hours, who need urgent cardioversion, DOACs can be started 4 hours before transoesophageal echocardiogram and cardioversion, if there are no other concerns related to the use of DOACs (e.g. sepsis, stroke, acute kidney injury) [11, 15]. Patients with NVAF of < 48-hour duration who need urgent cardioversion can receive DOACs as soon as possible before or immediately after cardioversion [11, 12, 15]. Patients with bio-prosthetic valves were also excluded or minimally included in DOAC trials [3–6]. Current guidelines are not clear about using DOACs for stroke prevention in patients with AF and bio-prosthetic valves; such patients could be eligible for DOACs after 3 months of surgery [11]. But, as per the manufacturers of DOACs, such use is considered off-label and is not recommended [16–18].

Acute coronary syndrome

Patients already on a DOAC/ Patients with a new indication for anticoagulation Parenteral anticoagulants (unfractionated or low-molecular-weight heparin, bivalirudin, fondaparinux) are the recommended agents during the management of acute coronary syndrome (ACS) [19, 20]. For patients already taking DOACs, who present with ACS, DOACs should be stopped on admission [13]. For ST-segment elevation myocardial infarction (STEMI) patients undergoing percutaneous coronary intervention (PCI), parenteral anticoagulation is initiated as soon as possible, regardless of the timing of the last dose of DOAC [14, 20]. Fibrinolysis can be considered if PCI is not available and fibrinolysis is the only option, and if the plasma level of a specific DOAC is below the reference range and DOAC-related coagulation parameters are normal (as discussed in part 1 of this review) [14]. For non-STEMI patients who are not in urgent need of reperfusion, parenteral anticoagulation can be delayed to dissipate the anticoagulant effect of the DOAC [11]. After management of ACS, DOAC should be resumed combined with dual antiplatelet therapy (DAPT) at least in the immediate period [11]. For patients who have a new indication for anticoagulation (atrial fibrillation, venous thromboembolism), DOAC can be started in combination with DAPT as soon as there is no further indication of parenteral anticoagulants. The total duration of triple therapy should be individualized based on the specific indication, risk of a recurrent ischaemic event, stent thrombosis, and bleeding risk [14, 21]. See Figure 1 for the practical approach.

DOAC use in ACS patients not undergoing PCI and without other indications for anticoagulation

ACS patients who do not undergo PCI are at high risk of recurrence of symptoms due to thrombus persistence, increased platelet reactivity, and elevated thrombin generation, which provides the rationale for chronic anticoagulation in such patients [22]. Rivaroxaban is the only DOAC that has been shown to reduce the risk of recurrent ischae­mic events and mortality when added to DAPT in ACS patients who have not received PCI and do not have other indications for anticoagulation (e.g., AF or VTE) [23, 24]. Rivaroxaban was used at a much lower dose (2.5 mg or 5 mg twice daily) compared to its dose for AF patients (20 mg once daily), and it was noted that a 5 mg dose did not show a survival benefit [24]. Based on the phase III ATLAS ACS TIMI 51 trial (Anti-Xa Therapy to Lower Cardiovascular Events in Addition to Aspirin With or Without Thie­nopyridine Therapy in Subjects with Acute Coronary Syndrome–Thrombolysis in Myocardial Infarction 51), rivaroxaban was recommended in combination with aspirin or aspirin plus clopidogrel (or ticlopidine) in certain ACS patients with a low bleeding risk [21, 24]. Dabigatran or apixaban combined with DAPT led to increased bleeding risk without reducing ischae­mic events [23, 25]. Importantly, randomized trials are ongoing to assess the safety and efficacy of DOACs when used in combination with antiplatelets [26, 27].

Post cardiac valve replacement

Warfarin remains the anticoagulant of choice in patients with mechanical valves [11, 12]. In the recent past, there has been a shift from mechanical to bioprosthetic valves [28]. Even though bioprosthetic valves are less thrombogenic than mechanical valves, the true incidence of bio-prosthetic valve thrombosis is more than previously thought [28]. Recommendations regarding antithrombotic prophylaxis following bioprosthetic valve implantation remain controversial regarding the adequacy of antiplatelet therapy alone versus the addition of either warfarin or a DOAC, especially in the early post-procedure period. Warfarin is also the agent of choice for bio-prosthetic mitral valve and mitral valvuloplasty [15]. Patients who undergo transcatheter aortic valve replacement and have AF could use DOACs after 3 months of the procedure as per the European Society of Cardiology [11]. However, the American Heart Association (AHA) and DOAC manufacturers do not recommend such use [15–18].

Venous thromboembolism treatment (deep venous thrombosis and pulmonary embolism)

DOACs have been approved for the treatment of venous thromboembolism (VTE) [29]. DOACs are non-inferior to low-molecular-weight heparin (LMWH) and warfarin to prevent recurrent VTE [30–32]. Patients with haemodynamic compromise or those with the anticipated need for invasive intervention should be treated with unfractionated hepa­rin during the critical phase. DOACs can be started as soon as there is no need for invasive intervention and patients are haemodynamically stable [29]. Patients on DOACs can have a recurrent VTE [33, 34]. In such cases, an incorrect dose of DOAC, noncompliance, and any drug interactions should be excluded. Such cases can be managed by switching to full-dose LMWH for at least 1 month [34, 35]. There is a lack of data to guide clinicians whether to use thrombolysis in patients who develop pulmonary embolism (PE) while taking a DOAC and require thrombolysis due to haemodynamic compromise. It may be reasonable to consider thrombolysis in cases of arrest or peri-arrest due to PE in the setting of concomitant DOAC use [1]. Endovascular intervention could be an option in patients with intermediate to high risk [1].

Venous thromboembolism prevention

VTE incidence has been reported to be as high as 40% in critically ill patients who do not receive thromboprophylaxis [36]. Trials have evaluated the use of DOACs for VTE prevention in hospitalized patients with acute medical illness, but not in ICU patients [13]. Betrixaban is the only DOAC approved with an extended duration of prophylaxis against VTE in medically ill hospitalized patients, but current guidelines do not recommend extended duration thromboprophylaxis [37, 38].

Acute ischaemic stroke

Data on the safety and efficacy of intravenous (iv) thrombolysis in ischaemic stroke patients taking DOACs is minimal [39]. The American Heart Association (AHA), American Stroke Association (ASA), and European Heart Rhythm Association (EHRA) discourage the use of IV thrombolytics in patients presenting with acute ischaemic stroke who are on DOACs [14, 40]. As per AHA/ASA/EHRA, IV thrombolytics may be considered if the DOAC plasma level is below the detection limit and DOAC-related coagulation parameters are normal, or if the last dose of DOAC was > 48 hours before presentation in a patient with normal renal parameters [14, 40]. Endovascular therapy may be considered for patients who are not candidates for IV thrombolysis due to the use of DOACs [11]. Current evidence is not sufficient to guide with certainty when to resume or initiate DOACs (in the setting of AF) after ischaemic stroke [3–6]. So far, only prospective observational studies and 2 small, randomized trials have assessed the timing, efficacy, and safety of DOACs following a cardioembolic stroke [41–44]. These studies have reported that early DOAC administration (with a median of 3–5 days) in mild to moderate AF-associated ischae­mic stroke did not increase symptomatic or radiographic haemorrhage, but delayed administration was associated with increased frequency of recurrent ischaemic stroke [41–44]. AHA and ASA recommend starting anticoagulation after 4–14 days of ischaemic stroke in the setting of AF [45]. EHRA suggests a timeline to resume or initiate anticoagulants based on the severity of stroke/neurologic deficit. DOAC can be resumed or started 1 day after a transient ischaemic attack, ≥ 3 days after mild ischaemic stroke, ≥ 6–8 days after moderate stroke, and ≥ 12–14 days after severe stroke [14]. In patients with moderate and severe stroke, haemorrhagic transformation should be excluded before starting an anticoagulant [14]. See Figure 2 for a practical approach.

Heparin-induced thrombocytopaenia

In vitro analyses have demonstrated that DOACs do not activate platelet aggregation in the presence of antiplatelet factor 4/heparin antibodies [46]. Current evidence evaluating the use of DOACs to manage heparin-induced thrombocytopaenia (HIT) is limited to small retrospective studies. The acuity of the studied population, if reported, was low, which prohibits the application of results to critically ill patients [47, 48]. Based on current evidence, the American Society of Hematology 2018 guidelines included conditional recommendations to use DOACs in the acute phase of HIT, but only in clinically stable patients with an average risk of bleeding [49].

Cerebral venous thrombosis

Due to the significantly reduced risk of intracranial haemorrhage compared to warfarin, DOACs are an attractive option for the long-term treatment of cerebral venous thrombosis (CVT) [50, 51]. A multi­centre prospective observational study by Wasay et al. [52] found that using a DOAC (rivaroxaban or dabigatran) for the long-term treatment of CVT is safe and as effective as warfarin. In this study, patients were treated with UFH or LMWH during the acute phase, and an oral anticoagulant (either DOAC or warfarin) for the long-term treatment was started within a median of 7 days of diagnosis of CVT. Recently published results of the RE-SPECT CVT trial (Rationale, design, and protocol of a randomized controlled trial of the safety and efficacy of dabigatran etexilate versus dose-adjusted warfarin in patients with cerebral venous thrombosis) showed that dabigatran is non-inferior to warfarin in treating CVT, and with fewer bleeding events [53]. Currently, warfarin is being used for the long-term treatment of CVT [54].

DOAC use during concurrent acute medical conditions

Sepsis

Sepsis is commonly encountered among hospitalized patients and is associated with coagulation abnormalities [55]. Patients with sepsis are at high risk of multiorgan dysfunction and poor outcomes as sepsis is associated with microvascular thrombosis or bleeding due to depletion of coagulation factors and platelets [56]. Sepsis increases the risk of AF and VTE [57]. Observational data have shown that the use of warfarin in patients with AF during critical illness is associated with an increased risk of bleeding [57, 58]. Unfortunately, there are no safety and efficacy data for the use of DOACs in patients with sepsis if they need therapeutic anticoagulation [3–6]. For patients who are already on DOACs and need ICU admission due to sepsis, it is suggested to switch DOAC to UFH or LMWH [13].

Acute kidney injury

As discussed in Part I of this review series (“Use of direct oral anticoagulant in ICU patients. Part I – Applied pharmacology”), all DOACs are dependent on renal excretions to some extent. Renal impairment, either acute or chronic, affects the clearance of the DOACs [59]. In the case series by Singh et al. [60], all 5 cases of dabigatran-associated acute bleeding had an acute decline in the renal functions, and all of them were on a stable dose of DOAC before the critical events. Unfortunately, so far, there are no safety and efficacy data on DOACs in acute kidney injury patients. Switching DOACs to alternative anticoagulants is suggested for patients with acute kidney injury [14].

Perioperative management of patients on DOAC

Emergency surgery

Idarucizumab and andexanet alfa are the 2 agents approved by the Food and Drug Administration (FDA) to reverse the anticoagulant effect of dabigatran and factor-Xa-inhibitors, respectively. The RE-VERSE AD (Reversal Effects of Idarucizumab on Active Dabigatran) trial evaluated outcomes in patients who received idarucizumab in the setting of urgent surgical interventions or bleeding [61]. Unfortunately, the ANNEXA-4 (Andexanet Alfa for Acute Major Bleeding Associated with Factor Xa Inhibitors) trial evaluated patients who had factor-Xa-inhibitor-associated bleeding and did not include patients in need of urgent surgical intervention [62]. Based on the urgency and bleeding risk of the procedure, idarucizumab and andexanet alfa can be considered to prevent bleeding complications [11, 14, 61]. If specific reversal agents are not available and surgical intervention is associated with increased risk of bleeding, prothrombin complex concentrates (unactivated or activated) and antifibrinolytics (e.g., tranexamic acid) can be considered to reduce bleeding [63–65].

Elective surgery

Outcomes in patients on DOACs and the need for elective procedures have been examined according to the bleeding risk of the surgery [66, 67]. Most dermatologic, dental, and ophthalmologic procedures can be performed without interruption of systemic anticoagulation, usually 24 hours after the last dose [11, 68, 69]. For other procedures, pre-procedure cessation of anticoagulants is gene­rally recommended, which depends on the risk of bleeding, clinical impact of holding the anticoagulant, and renal clearance of the DOAC [11, 68, 69]. Commonly, DOACs are held 1–4 days before the procedure. In patients with creatinine clearance (CrCl) < 50 mL min–1, dabigatran should be discontinued at least 4 days and factor-Xa-inhibitors at least 2 days before the procedure [14, 68–70] (see Figure 3). Due to the quick onset of action and short half-life of DOACs, peri-procedural bridging is not recom­mended [11, 71]. Post-procedure resumption of DOACs is based on post-procedure bleeding risks and consultation with the clinician who did the procedure. The expert opinion is to hold the DOAC for the same number of days after the procedure as before the procedure [13, 70].

Patients undergoing cardiac device implantation

Uninterrupted use of warfarin has shown better outcomes than bridging with parenteral anticoagulation in patients who need cardiac device implantation [72, 73]. Interrupted or continuous DOAC therapy during device implantation remains a matter of debate [74]. Most clinicians discontinue DOACs before device implantation based on the half-life of the DOAC and CrCl. Usually, dabigatran is stopped 24 hours before device implantation in those with CrCl > 80 mL min–1, 36 hours before in those with CrCl 50–79 mL min–1, and 48 hours earlier in those with CrCl < 50 mL min–1. Patients on apixaban, edoxaban, or rivaroxaban are advised to hold the DOAC 24 hours before the procedure [72, 74]. After device implantation, DOACs can be resumed 24 hours after the procedure in patients with high thromboembolic risk and after 3–5 days in those with increased bleeding risks [72, 74].

Managing bleeding in patients taking DOAC

Better outcomes have been reported in patients on DOACs and suffering from intracranial haemorrhage or major traumatic bleeding compared to patients who take warfarin [51, 75]. For the mana­gement of confirmed or suspected DOAC-induced bleeding, the basic principles remain the same as for any other bleeding case [76]. If possible, specific DOAC, the timing of the last dose, and the indication for DOAC use should be identified. Laboratory tests, including renal function, tests of anticoagulation (aPTT, PT), anti-factor-Xa activity for factor Xa-inhibitors, and diluted thrombin time (dTT) for dabigatran should be performed [77]. Idarucizu­mab can be used to reverse the anticoagulant effect of dabigatran, and andexanet alfa or 4-factor prothrombin complex concentrates are the available options for factor Xa-inhibitors associated bleeding [11, 32, 61–64]. If the last dose of DOAC was recent enough, oral activated charcoal could decrease the absorption of the unabsorbed drug [78]. Haemo­dialysis can be considered to remove dabigatran from circulation [60, 79] (see Table 1). Scoring systems such as CHA2DS2-VASc and HAS-BLED can help decide whether to resume anti­coagulant or not. DOACs may be resumed 4–8 weeks after the intracranial bleed if the underlying aetiology and bleeding risks have been managed ade­quately [14].

Ongoing important trials

Continued extensive research has led to the increasing use of DOACs during the last decade. Still, the safety and efficacy related to DOACs use in critically ill patients requiring ICU admission are unanswered. Several clinical trials are underway to answer some of the essential clinical queries [80] (Table 2).

Coronavirus disease 2019 (COVID-19) and use of DOAC

In the recent COVID-19 pandemic, SARS-CoV-2 (severe acute respiratory syndrome coronavirus-2)-infected critically ill patients demonstrated dysre­gulated inflammation and higher thrombotic complications (up to 45% in ICU patients) [81]. Direct factor Xa inhibitors have shown beneficial effects in COVID-19 patients, with anticoagulant, anti- inflammatory, and anti-viral properties [82]. Despite multiple potential benefits of direct factor Xa inhibitors in patients with COVID-19, good clinical evidence is scarce in terms of risk benefit at present. The longer half-life of these drugs can be detrimental when urgent invasive procedures are planned in critically ill hospitalized patients or in the event of rapid worsening of renal or hepatic function. At present (updated May 2021), no major guidelines recommend the use of DOAC, either as a prophylactic or therapeutic, in COVID-19 patients admitted to the ICU (Table 3). Only a few guidelines recommend the use of direct factor Xa inhibitors in COVID-19 patients in specific situations like non-ICU settings for extended prophylaxis, post-discharge prophylaxis in high-risk populations, and post-discharge extended therapy in confirmed VTE patients (Table 3) [83–87].

Conclusions

In the near future, it will not be uncommon for critical care physicians to have more and more patients who are already taking DOACs for various clinical conditions, due to its ever-increasing popularity because of their fixed dosing with minimal monitoring and the availability of specific reversal agents. At present, there is little evidence about the safety of continuing DOACs in critically ill patients after admission in the ICU, even if anticoagulation is indicated. In these patients, the anticoagulant effect is preferably achieved by switching to heparin (LMWH or UFH). Some studies also evaluated DOAC use for VTE prevention in hospitalized patients with acute medical illness but not ICU patients. Hopefully, ongoing and future trials will provide strong evidence for the use of DOACs in ICU patients.

ACKNOWLEDGEMENTS

1. Financial support and sponsorship: none.
2. Conflict of interest: none.

References

1. Lefevre E, Wondergem M, ten Tusscher B. Direct oral anticoagulants and critical care: a review of literature and current opinion. Neth J Crit Care 2018; 26: 174-179.
2. Cohen AT, Harrington R, Goldhaber SZ, et al. The design and rationale for the Acute Medically Ill Venous Thromboembolism Prevention with Extended Duration Betrixaban (APEX) study. Am Heart J 2014; 167: 335-341. doi: 10.1016/j.ahj.2013.11.006.
3. Connolly SJ, Ezekowitz MD, Yusuf S, et al. Dabigatran versus warfarin in patients with atrial fibrillation. N Engl J Med 2009; 361: 1139-1151. doi: 10.1056/NEJMoa0905561.
4. Giugliano RP, Ruff CT, Braunwald E, et al. Edoxaban versus warfarin in patients with atrial fibrillation. N Engl J Med 2013; 369: 2093. doi: 10.1056/NEJMoa1310907.
5. Granger CB, Alexander JH, McMurray JJV, et al. Apixaban versus warfarin in patients with atrial fibrillation. N Engl J Med 2011; 365: 981-992. doi: 10.1056/NEJMoa1107039.
6. Patel MR, Mahaffey KW, Garg J, et al. Rivaroxaban versus warfarin in nonvalvular atrial fibrillation. N Engl J Med 2011; 365: 883-891. doi: 10.1056/NEJMoa1009638.
7. Avezum A, Lopes RD, Schulte PJ, et al. Apixaban in comparison with warfarin in patients with atrial fibrillation and valvular heart disease: findings from the Apixaban for Reduction in Stroke and Other Thromboembolic Events in Atrial Fibrillation (ARISTOTLE) trial. Circulation 2015; 132: 624-632. doi: 10.1161/CIRCULATIONAHA.­ 114.014807.
8. Breithardt G, Baumgartner H, Berkowitz SD, et al. Clinical characteristics and outcomes with rivaroxaban vs. warfarin in patients with non-valvular atrial fibrillation but underlying native mitral and aortic valve disease participating in the ROCKET AF trial. Eur Heart J 2014; 35: 3377-3385. doi: 10.1093/eurheartj/ehu305.
9. De Caterina R, Renda G, Carnicelli AP, et al. Valvular heart disease patients on edoxaban or warfarin in the ENGAGE AF-TIMI 48 trial. J Am Coll Cardiol 2017; 69: 1372-1382. doi: 10.1016/j.jacc.2016. 12.031.
10. Ezekowitz DM, Nagarakanti AR, Noack JH, et al. Comparison of dabi­gatran versus warfarin in patients with atrial fibrillation and valvular heart disease: the RE-LY trial. Circulation 2016; 134. doi: 10.1161/ CIRCULATIONAHA.115.020950.
11. Heidbuchel H, Verhamme P, Alings M, et al. Updated European Heart Rhythm Association practical guide on the use of non-vitamin-K antagonist anticoagulants in patients with non-valvular atrial fibrillation: executive summary. Eur Heart J 2017; 38: 2137-2149. doi: 10.1093/eurheartj/ehw058.
12. January TC, Wann SL, Calkins YH, et al. 2019 AHA/ACC/HRS focused update of the 2014 AHA/ACC/HRS guideline for the management of patients with atrial fibrillation: a report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines and the Heart Rhythm Society in Collaboration with the Society of Thoracic Surgeons. Circulation 2019; 140: e125-e151. doi: 10.1161/CIR.0000000000000665.
13. Rali P, Gangemi A, Moores A, Mohrien K, Moores L. Direct acting oral anticoagulants (DOACs) in critically ill patients. Chest 2019; 156: 604-618.
14. Steffel J, Verhamme P, Potpara TS, et al. The 2018 European Heart Rhythm Association practical guide on the use of non-vitamin K antagonist oral anticoagulants in patients with atrial fibrillation. Eur Heart J 2018; 39: 1330-1393.
15. Nishimura AR, Otto MC, Bonow OR, et al. 2017 AHA/ACC focused update of the 2014 AHA/ACC guideline for the management of patients with valvular heart disease: a report of the American College of Cardiology/American Heart Association Task Force on clinical practice guidelines. Circulation 2017; 135: e1159-e1195. doi: 10.1161/CIR.0000000000000503.
16. Bayer Pharma A. Xarelto (rivaroxaban) prescribing information 2011. Available from: http://www.janssenlabels.com/package-insert/product-monograph/prescribing-information/XARELTO-pi.pdf.
17. Boehringer Ingelheim Pharmaceuticals I. Pradaxa (dabigatran) prescribing information 2010. Available from: https://www.pradaxa.com/.
18. Bristol-Myers Squibb Company. Eliquis (apixaban) prescribing information 2012. Available from: https://www.eliquis.bmscustomerconnect.com/?cid=sem_679499&ovl=isi.
19. Amsterdam AE, Wenger KN, Brindis GR, et al. 2014 AHA/ACC Guideline for the management of patients with non–st-elevation acute coronary syndromes: executive summary: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines. Circulation 2014; 130: 2354-2394. doi: 10.1161/CIR.0000000000000133.
20. O’Gara PT, Kushner FG, Ascheim DD, et al. 2013 ACCF/AHA guideline for the management of ST-elevation myocardial infarction: executive summary. J Am Coll Cardiol 2013; 61: 485. doi: 10.1016/ j.jacc. 2012.11.018.
21. Roffi M, Patrono C, Collet JP, et al. 2015 ESC guidelines for the mana­gement of acute coronary syndromes in patients presenting without persistent ST-segment elevation. Eur Heart J 2016; 37: 267-315. doi: 10.1093/eurheartj/ehv320.
22. Bassand JP. Novel oral anticoagulants in acute coronary syndrome: re-evaluating the thrombin hypothesis. EuroIntervention 2014; 9: 1333-1341. doi: 10.4244/EIJV9I11A224.
23. Khan SU, Arshad A, Riaz IB, Talluri S, Nasir F, Kaluski E. Meta-analysis of the safety and efficacy of the oral anticoagulant agents (apixaban, rivaroxaban, dabigatran) in patients with acute coronary syndrome. Am J Cardiol 2018; 121: 301-307. doi: 10.1016/j.amjcard. 2017.10.035.
24. Mega JL, Braunwald E, Wiviott SD, et al. Rivaroxaban in patients with a recent acute coronary syndrome. N Engl J Med 2012; 366: 9-19. doi: 10.1056/NEJMoa1112277.
25. Oldgren J, Budaj A, Granger CB, et al. Dabigatran vs. placebo in patients with acute coronary syndromes on dual antiplatelet therapy: a randomized, double-blind, phase II trial. Eur Heart J 2011; 32: 2781-2789. doi: 10.1093/eurheartj/ehr113.
26. Gibson CM, Mehran R, Bode C, et al. An open-label, randomized, controlled, multicenter study exploring two treatment strategies of rivaroxaban and a dose-adjusted oral vitamin k antagonist treatment strategy in subjects with atrial fibrillation who undergo percutaneous coronary intervention (PIONEER AF-PCI). Am Heart J 2015; 169: 472-478.e5. doi: 10.1016/j.ahj.2014.12.006.
27. Hoshi T, Sato A, Nogami A, Gosho M, Aonuma K. Rationale and design of the SAFE-A study: SAFety and Effectiveness trial of Apixaban use in association with dual antiplatelet therapy in patients with atrial fibrillation undergoing percutaneous coronary intervention. J Cardiol 2017; 69: 648-651. doi: 10.1016/j.jjcc.2016.06.007.
28. Puri R, Auffret V, Rodés-Cabau J. Bioprosthetic valve thrombosis. J Am Coll Cardiol 2017; 69: 2193-2211. doi: 10.1016/j.jacc.2017.02.051.
29. Mazzolai L, Aboyans V, Ageno W, et al. Diagnosis and management of acute deep vein thrombosis: a joint consensus document from the European Society of Cardiology working groups of aorta and peripheral vascular diseases and pulmonary circulation and right ventricular function. Eur Heart J 2018; 39: 4208-4218. doi: 10.1093/eurheartj/ehx003.
30. Agnelli G, Buller HR, Cohen A, et al. Oral apixaban for the treatment of acute venous thromboembolism. N Engl J Med 2013; 369: 799-808. doi: 10.1056/NEJMoa1302507.
31. Büller HR, Prins MH, Lensin AWA, et al. Oral rivaroxaban for the treatment of symptomatic pulmonary embolism. N Engl J Med 2012; 366: 1287-1297. doi: 10.1056/NEJMoa1113572.
32. Schulman KS, Kakkar ZA, Goldhaber VS, et al. Treatment of acute venous thromboembolism with dabigatran or warfarin and pooled analysis. Circulation 2014; 129: 764-772. doi: 10.1161/CIRCULATIONAHA.113.004450.
33. Heit JA, Mohr DN, Silverstein MD, Petterson TM, O’Fallon WM, Melton LJ. Predictors of recurrence after deep vein thrombosis and pulmonary embolism: a population-based cohort study. Arch Intern Med 2000; 160: 761-768. doi: 10.1001/archinte.160.6.761.
34. Rodger MA, Miranda S, Delluc A, Carrier M. Management of suspected and confirmed recurrent venous thrombosis while on anticoagulant therapy. What next? Thromb Res 2019; 180: 105-109. doi: 10.1016/j.thromres.2019.06.017.
35. Kearon C, Akl EA, Ornelas J, et al. Antithrombotic therapy for VTE disease. Chest 2016; 149: 315-352. doi: 10.1016/j.chest.2015.11.026.
36. Todd JL, Tapson VF. Thrombolytic therapy for acute pulmonary embolism. Chest 2009; 135: 1321-1329. doi: 10.1378/chest.08-2125.
37. Cohen AT, Harrington RA, Goldhaber SZ, et al. Extended thromboprophylaxis with betrixaban in acutely ill medical patients. N Engl J Med 2016; 375: 534-544. doi: 10.1056/NEJMoa1601747.
38. Kahn SR, Lim W, Dunn AS, et al. Prevention of VTE in nonsurgical patients. Chest 2012; 141: e195S-e226S. doi: 10.1378/chest.11-2296.
39. Xian Y, Hernandez AF, Harding T, et al. Acute management of stroke patients taking non-vitamin K antagonist oral anticoagulants Addressing Real-world Anticoagulant Management Issues in Stroke (ARAMIS) Registry: design and rationale. Am Heart J 2016; 182: 28-35. doi: 10.1016/j.ahj.2016.07.023.
40. Powers WJ, Rabinstein AA, Ackerson T, et al. Guidelines for the early management of patients with acute ischemic stroke: 2019 update to the 2018 guidelines for the early management of acute ischemic stroke: a guideline for healthcare professionals from the American Heart Association/American Stroke Association. Stroke 2019; 50: e344-e418. doi: 10.1161/STR.0000000000000211.
41. Arihiro S, Todo K, Koga M, et al. Three-month risk-benefit profile of anticoagulation after stroke with atrial fibrillation: The SAMURAI- Nonvalvular Atrial Fibrillation (NVAF) study. Int J Stroke 2016; 11: 565-574. doi: 10.1177/1747493016632239.
42. Hong KS, Kwon S, Lee S, et al. Rivaroxaban vs warfarin sodium in the ultra-early period after atrial fibrillation-related mild ischemic stroke a randomized clinical trial. JAMA Neurol 2017; 74: 1206-1215. doi: 10.1001/jamaneurol.2017.2161.
43. Ng KH, Sharma M, Benavente O, et al. Dabigatran following acute transient ischemic attack and minor stroke II (DATAS II). Int J Stroke 2017; 12: 910-914. doi: 10.1177/1747493017711947.
44. Paciaroni M, Agnelli G, Falocci N, et al. Early recurrence and major bleeding in patients with acute ischemic stroke and atrial fibrillation treated with non–vitamin‐K oral anticoagulants (RAF‐ NOACs) Study. J Am Heart Assoc 2017; 6: e007034. doi: 10.1161/JAHA.117.007034.
45. Powers JW, Rabinstein AA, Ackerson MT, et al. 2018 guidelines for the early management of patients with acute ischemic stroke: a guideline for healthcare professionals from the American Heart Association/American Stroke Association. Stroke 2018; 49: e46-e110. doi: 10.1161/STR.0000000000000158.
46. Krauel K, Hackbarth C, Fürll B, Greinacher A. Heparin-induced thrombocytopenia: in vitro studies on the interaction of dabigatran, rivaroxaban, and low-sulfated heparin, with platelet factor 4 and anti-PF4/heparin antibodies. Blood 2012; 119: 1248-1255. doi: 10.1182/blood-2011-05-353391.
47. Davis KA, Davis DO. Direct acting oral anticoagulants for the treatment of suspected heparin‐induced thrombocytopenia. Eur J Haematol 2017; 99: 332-335. doi: 10.1111/ejh.12921.
48. Warkentin TE, Pai M, Linkins LA. Direct oral anticoagulants for treatment of HIT: update of Hamilton experience and literature review. Blood 2017; 130: 1104-1113. doi: 10.1182/blood-2017-04-778993.
49. Cuker A, Arepally GM, Chong BH, et al. American Society of Hematology 2018 guidelines for management of venous thromboembolism: heparin-induced thrombocytopenia. Blood Adv 2018; 2: 3360-3392. doi: 10.1182/bloodadvances.2018024489.
50. Mendonca MD, Barbosa R, Cruz-e-Silva V, Calado S, Viana-Baptista M. Oral direct thrombin inhibitor as an alternative in the management of cerebral venous thrombosis: a series of 15 patients. Int J Stroke 2015; 10: 1115-1118. doi: 10.1111/ijs.12462.
51. Tsivgoulis HG, Lioutas KVA, Varelas WP, et al. Direct oral anticoagulant– vs vitamin K antagonist-related nontraumatic intracerebral hemorrhage. Neurology 2017; 89: 1142-1151. doi: 10.1212/WNL. 0000000000004362.
52. Wasay M, Khan M, Rajput HM, et al. New oral anticoagulants versus warfarin for cerebral venous thrombosis: a multi-center, observational study. J Stroke 2019; 21: 220-223. doi: 10.5853/jos.2019.00150.
53. Ferro JM, Dentali F, Coutinho JM, et al. Rationale, design, and protocol of a randomized controlled trial of the safety and efficacy of dabigatran etexilate versus dose-adjusted warfarin in patients with cerebral venous thrombosis. Int J Stroke 2018; 13: 766-770. doi: 10.1177/1747493018778125.
54. Saposnik G, Barinagarrementeria F, Brown RD, et al. Diagnosis and management of cerebral venous thrombosis: a statement for healthcare professionals from the American Heart Association/American Stroke Association. Stroke 2011; 42: 1158-1192. doi: 10.1161/STR. 0b013e31820a8364.
55. Angus DC, van der Poll T. Severe sepsis and septic shock. N Engl J Med 2013; 369: 840-851. doi: 10.1056/NEJMra1208623.
56. Darwish OS, Strube S, Nguyen HM, Tanios MA. Challenges of anticoagulation for atrial fibrillation in patients with severe sepsis. Ann Pharmacother 2013; 47: 1266-1271. doi: 10.1177/1060028013 500938.
57. Walkey AJ, Greiner MA, Heckbert SR, et al. Atrial fibrillation among Medicare beneficiaries hospitalized with sepsis: incidence and risk factors. Am Heart J 2013; 165: 949-955.e3. doi: 10.1016/j.ahj. 2013.03.020.
58. Søgaard M, Skjøth F, Kjældgaard JN, Lip GYH, Larsen TB. Bleeding complications in anticoagulated patients with atrial fibrillation and sepsis: a propensity‐weighted cohort study. J Am Heart Assoc 2017; 6: e007453. doi: 10.1161/JAHA.117.007453.
59. Chan KE, Giugliano RP, Patel MR, et al. Nonvitamin K anticoagulant agents in patients with advanced chronic kidney disease or on dialysis with AF. J Am Coll Cardiol 2016; 67: 2888-2899. doi: 10.1016/j.jacc. 2016.02.082.
60. Singh T, Maw TT, Henry BL, et al. Extracorporeal therapy for dabigatran removal in the treatment of acute bleeding: a single center experience. Clin J Am Soc Nephrol 2013; 8: 1533-1539. doi: 10.2215/CJN.01570213.
61. Pollack CV, Reilly PA, van Ryn J, et al. Idarucizumab for dabigatran reversal – full cohort analysis. N Engl J Med 2017; 377: 431-441. doi: 10.1056/NEJMoa1707278.
62. Connolly SJ, Crowther M, Eikelboom JW, et al. Full study report of andexanet alfa for bleeding associated with factor Xa inhibitors. N Engl J Med 2019; 380: 1326-1335. doi: 10.1056/NEJMoa1814051.
63. Eerenberg SE, Kamphuisen WP, Sijpkens KM, Meijers CJ, Buller RH, Levi RM. Reversal of rivaroxaban and dabigatran by prothrombin complex concentrate: a randomized, placebo-controlled, crossover study in healthy subjects. Circulation 2011; 124: 1573-1579. doi: 10.1161/CIRCULATIONAHA.111.029017.
64. Santibanez M, Lesch CA, Lin L, Berger K. Tolerability and effectiveness of 4-factor prothrombin complex concentrate (4F-PCC) for warfarin and non-warfarin reversals. J Crit Care 2018; 48: 183-190. doi: 10.1016/j.jcrc.2018.08.031.
65. Schulman S, Gross P, Ritchie B, et al. Prothrombin complex concentrate for major bleeding on factor Xa inhibitors: a prospective cohort study. Thromb Haemost 2018; 118: 842-851. doi: 10.1055/s-0038-1636541.
66. Garcia D, Alexander JH, Wallentin L, et al. Management and clinical outcomes in patients treated with apixaban versus warfarin undergoing procedures. Blood 2014; 124: 3692-3698. doi: 10.1182/blood- 2014-08-595496.
67. Jeff SH, John E, James D, et al. Periprocedural bleeding and thromboembolic events with dabigatran compared with warfarin: results from the randomized evaluation of long-term anticoagulation therapy (RE-LY) randomized trial. Circulation 2012; 126: 343-348. doi: 10.1161/CIRCULATIONAHA.111.090464.
68. Dubois V, Dincq AS, Douxfils J, et al. Perioperative management of patients on direct oral anticoagulants. Thromb J 2017; 15: 14. doi: 10.1186/s12959-017-0137-1.
69. Hornor MA, Duane TM, Ehlers AP, et al. American College of Surgeons’ guidelines for the perioperative management of antithrombotic medication. J Am Coll Surg 2018; 227: 521-536.e1. doi: 10.1016/ j.jamcollsurg.2018.08.183.
70. Tafur A, Douketis J. Perioperative management of anticoagulant and antiplatelet therapy. Heart 2018; 104: 1461. doi: 10.1136/heartjnl- 2016-310581.
71. Doherty J, Gluckman T, Hucker W, et al. 2017 ACC expert consensus decision pathway for periprocedural management of anticoagulation in patients with nonvalvular atrial fibrillation. J Am Coll Cardiol 2017; 69: 871-898. doi: 10.1016/j.jacc.2016.11.024.
72. Birnie HD, Healey SJ, Essebag SV. Management of anticoagulation around pacemaker and defibrillator surgery. Circulation 2014; 129: 2062-2065. doi: 10.1161/CIRCULATIONAHA.113.006027.
73. Cheng A, Nazarian S, Brinker JA, et al. Continuation of warfarin during pacemaker or implantable cardioverter-defibrillator implantation: a randomized clinical trial. Heart Rhythm 2011; 8: 536-540. doi: 10.1016/j.hrthm.2010.12.016.
74. Nascimento T, Birnie DH, Healey JS, et al. Managing novel oral anticoagulants in patients with atrial fibrillation undergoing device surgery: Canadian survey. Can J Cardiol 2014; 30: 231-236. doi: 10.1016/j.cjca. 2013.11.027.
75. Feeney MJ, Santone CE, Difiori CM, Kis CL, Jayaraman CV, Montgomery CS. Compared to warfarin, direct oral anticoagulants are associated with lower mortality in patients with blunt traumatic intracranial hemorrhage: a TQIP study. J Trauma 2016; 81: 843-848. doi: 10.1097/TA.0000000000001245.
76. Teruya J (ed.). Management of Bleeding Patients. 1st ed. Cham: Springer International Publishing; 2016.
77. Lindahl T, Baghaei F, Fagerberg Blixter I, et al. Effects of the oral, direct thrombin inhibitor dabigatran on five common coagulation assays. Thromb Haemost 2011; 105: 371-378. doi: 10.1160/TH10-06-0342.
78. Exner T, Ahuja M, Ellwood L. Effect of an activated charcoal pro­duct (DOAC Stop) intended for extracting DOACs on various other APTT-prolonging anticoagulants. Clin Chem Lab Med 2019; 57: 690-696. doi: 10.1515/cclm-2018-0967.
79. Chang DN, Dager WE, Chin AI. Removal of dabigatran by hemodia­lysis. Am J Kidney Dis 2013; 61: 487-489. doi: 10.1053/j.ajkd.2012. 08.047.
80. https://clinicaltrials.gov/ct2/results?cond=Direct+oral+anticoagulants&term=&cntry=&state=&city=&dist=.
81. Nopp S, Moik F, Jilma B, Pabinger I, Ay C. Risk of venous thromboembolism in patients with COVID-19: a systematic review and meta-analysis. Res Pract Thromb Haemost 2020; 4: 1178-1191. doi: 10.1002/ rth2.12439.
82. Al-Horani RA. Potential therapeutic roles for direct factor Xa inhibitors in coronavirus infections. Am J Cardiovasc Drugs 2020; 20: 525-533. doi: 10.1007/s40256-020-00438-6.
83. Moores LK, Tritschler T, Brosnahan S, et al. Prevention, diagnosis, and treatment of VTE in patients with coronavirus disease 2019: CHEST guideline and expert panel report. Chest 2020; 158: 1143-1163. doi: 10.1016/j.chest.2020.05.559.
84. Spyropoulos AC, Levy JH, Ageno W, et al. Scientific and standardization committee communication: clinical guidance on the diagnosis, prevention, and treatment of venous thromboembolism in hospitalized patients with COVID-19. J Thromb Haemost 2020; 18: 1859-1865. doi: 10.1111/jth.14929.
85. World Health Organization. COVID-19 clinical managment: living guidance 2021, January 25. Available from: https://www.who.int/publications/i/item/WHO-2019-nCoV-clinical-2021-1.
86. Cuker A, Tseng EK, Nieuwlaat R, et al. American Society of Hemato­logy 2021 guidelines on the use of anticoagulation for thromboprophylaxis in patients with COVID-19. Blood Adv 2021; 5: 872-888. doi: 10.1182/bloodadvances.2020003763.
87. National Institutes of Health. Coronavirus disease 2019 (COVID-19) treatment guidelines 2021, May 27. Available from: https://www.covid19treatmentguidelines.nih.gov.
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