DIrect Oral Anticoagulation and Bioprothesis Aortic Valve

Official title

DIrect Oral Anticoagulant for Antithrombotic Management Of Aortic Bioprothesis Valve implaNted Patients for Valvular Heart Disease Study

Overview

DIAMOND study is a national, multicentre, randomized, parallel-group, open label study in patients (aged ≥18 years) with aortic bioprosthesis (excluding TAVI) at least 7 days after cardiac surgery. Experimental group: Patients treated with apixaban 5 mg twice daily (BID) Active Comparator group: Aspirin 75 to 100mg once a day The primary objective is to demonstrate that antithrombotic treatment with apixaban is superior to aspirin in patients with recent surgical bioprosthetic aortic valve replacement for the primary composite efficacy endpoint of death from any cause, myocardial infarction, stroke, systemic embolism, deep vein thrombosis, or pulmonary embolism and valve thrombosis after 105 days of follow-up.

Detailed description

Early antithrombotic management of patients who have undergone aortic valve replacement using a bioprosthesis remains a source of medical concern. The optimal antithrombotic strategy early after surgery remains controversial due to lack of high-quality evidence. Some observational studies support the use of vitamin K antagonists (VKAs) compared to aspirin (ASA) to significantly reduce the risk of thromboembolism but suffer from major source of bias inherent to retrospective analyses of observational data. A small, randomized trial found that VKA for 3 months significantly increased major bleeding compared with ASA, without reducing the rate of deaths or thromboembolic events but this study was underpowered for ischemic events. There is therefore a lack of evidence demonstrating the superiority of anticoagulant treatment compared to aspirin early after bioprosthetic aortic valve surgery. Current ESC guidelines recommend that ASA or VKA should be considered for 3 months after surgical implantation of an aortic bioprosthesis. At the opposite, current AHA/ACC guidelines recommend that anticoagulation with VKA to achieve an INR of 2.5 is reasonable for at least 3 months and for as long as 6 months for patients at low risk of bleeding (IIa, level B). However, anticoagulation by VKAs is currently underused and guideline recommendations are not followed by most clinicians as VKAs have major drawbacks: narrow therapeutic window, variable dose-response in individuals, interaction with several foods and drugs.

Despite their superiority to reduce bleeding in patients with non-valvular atrial fibrillation compared to VKAs, direct oral anticoagulants (DOACs) including apixaban have not been well evaluated in the first 3 months after surgical bioprosthetic valve implantation. A small, randomized trial found that edoxaban was non-inferior to warfarin for preventing thromboembolism and the occurrence of major bleeding in the first 3 months after aortic or mitral surgical bioprosthetic valve implantation. DOAC(s) are effective in patients with atrial fibrillation and bioprosthetic valve implanted after 3 months.

Finally, there is an unmet clinical need for an alternative to ASA or VKAs, such as an anti-Xa DOAC like apixaban, as anticoagulation in patients in the first 3 months after surgical bioprosthetic valve implantation.

The purpose of this study is to compare the efficacy of apixaban and aspirin on ischemic endpoints during the first 3 months after aortic surgical bioprosthetic valve implantation excluding TAVI.

Interventions

• Drug Apixaban 5 MG Oral Tablet
  Patients treated with apixaban 5 mg twice daily (BID)
• Drug Aspirin 75 to 100mg once a day
  Patients treated with Aspirin 75 to 100mg once a day

Primary outcome measures

• Major Adverse Clinical Events (MACE) [Time frame: Up to 3.5 months]

Secondary outcome measures (12)

• Bleeding [Time frame: Up to 3.5 months]
• Death [Time frame: Up to 3.5 months]
• Myocardial infarction [Time frame: Up to 3.5 months]
• Stroke [Time frame: Up to 3.5 months]
• Systemic embolism [Time frame: Up to 3.5 months]
• Deep vein thrombosis or pulmonary embolism [Time frame: Up to 3.5 months]
• Valve thrombosis [Time frame: Up to 3.5 months]
• Bleeding [Time frame: Up to 3.5 months]
• Echographic parameter of aortic valve [Time frame: Up to 3.5 months]
• Assessment of coagulation [Time frame: Up to 3.5 months]
• To evaluate platelet activation (sP-selectin) in a subgroup population (n = 216) [Time frame: Up to 3.5 months]
• To build a population PK/PD in the experimental group [Time frame: Up to 3.5 months]

Eligibility criteria

Inclusion criteria

• Male or female ≥18 years of age
• Prior implantation of a surgical bioprosthesis in the aortic position at least 7 days and before hospital discharge (excluding TAVI)
• Participants currently not requiring chronic anticoagulation for another reason (atrial fibrillation, pulmonary embolism or any other condition)
• Patients affiliated to social security
• Patient able to give free, informed and written consent

Exclusion criteria

• Any cardiac surgery less than 7 days prior to enrollment or more than 1 month
• Mechanical valve in any position or combined valve surgery (mitral or tricuspid).
• Any major bleeding in the three months (90 days) prior to enrollment.
• Active bleeding or high risk of bleeding after cardiac surgery (i.e. hemopericardium) or lesion or condition considered as a significant risk factor for major bleeding according to investigator
• Atrial fibrillation requiring chronic anticoagulation
• Need to be on dual antiplatelet therapy (aspirin >100 mg daily and a P2Y12 inhibitor, i.e. clopidogrel, ticagrelor, prasugrel) or requiring chronic anticoagulation whatever the treatment (oral or injection).
• Known hypersensitivity or other contraindications to apixaban (hepatic disease associated with coagulopathy and clinically relevant bleeding risk).
• Creatinine clearance <40 mL/min (Cockcroft) or patients requiring apixaban dose reduction.
• Known hypersensitivity or other contraindications to aspirin (Hypersensitivity to aspirin or any of the excipients, history of asthma induced by the administration of salicylates, ongoing peptic ulcer, constitutional or acquired hemorrhagic disease including gastrointestinal bleeding, history of hemorrhagic stroke and thrombocytopenia, pregnancy after 24 weeks of gestation, risk of bleeding, severe renal failure, severe hepatic impairment, uncontrolled severe heart failure
• Known hypersensitivity or other contraindications to heparin or low molecular weight heparin (history of heparin-induced thrombocytopenia, hypersensitivity to any of the excipients…)
• Ischemic stroke within 1 month or intracranial hemorrhage
• Active endocarditis at the time of screening for enrollment.
• Women of childbearing potential without efficient contraception, pregnant or breastfeeding women.
• Concomitant combined strong P-gp and CYP3A4 inducers or inhibitors.
• History of non-compliance
• Participation in another interventional study
• Active cancer or life expectancy less than 1 year
• Persons deprived of their liberty by judicial or administrative decision

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation

Randomized

Model

Parallel assignment

Masking

Open label

Primary purpose

Treatment

Study locations

France · 1 center

• Service de Cardiologie Hôpital Lariboisière — Paris

Identifiers

NCT: NCT05687448 · 2024-516643-64-00

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗