Apixaban in Adults With Congenital Heart Disease and Atrial Arrhythmias: the PROTECT-AR Study

Completed

• Conditions: Anticoagulants Causing Adverse Effects in Therapeutic Use; Congenital Heart Disease; Atrial Arrhythmia; Thromboembolism

• Registration Number: NCT03854149
• Lead Sponsor: AHEPA University Hospital

Brief Summary

The purpose of this study is to evaluate the safety and efficacy of apixaban for the prevention of thromboembolism in adult patients with congenital heart disease (CHD) and non-valvular atrial arrhythmias (AA)

Detailed Description

Adult patients with congenital heart disease (ACHD) represent a rapidly growing population due to the progress of surgical techniques and optimal medical management. Non-valvular atrial arrhythmias (AA) carries a significant burden for long-term morbidity and potentially mortality in ACHD patients. AA occur three times more frequently in ACHD compared to the general population. When complicating ACHD, AA convey a twofold increase in the risk for stroke, contributing to an up to 100-fold higher prevalence of stroke in the ACHD population compared to age-matched healthy controls. At present, the European Society of Cardiology (ESC) Guidelines suggest oral anticoagulation (OAC) in all adult patients with AA and intracardiac repair, cyanosis, Fontan palliation, or systemic right ventricle. In the remaining ACHD patients with AA, OAC is suggested if CHA2DS2-Vasc (congestive heart failure, hypertension, age ≥75 years, diabetes mellitus, stroke/transient ischemic attack, vascular disease, age 65 to 74 years, sex category) score is ≥1 (Class of recommendation IIa, level of evidence C).

Non-vitamin K oral anticoagulants (NOACs) are increasingly preferred over vitamin-K antagonists (VKAs) in most clinical scenarios due to improved safety (with regard to intracranial and other major bleeding) and efficacy (prevention of embolic stroke or systemic embolism) along with the convenience they offer for patients and physicians (fixed dose, no food and drug interactions, no INR monitoring). On the other hand, scarce data is available on the use of NOAC in ACHD.

In order to address this gap in evidence, we propose a prospective multicenter single arm, observational cohort trial, which will provide data on the efficacy and safety of apixaban used for the prevention of thromboembolism in ACHD patients with AA.

Study Timeline

• Study First Submitted: 2019-02-23
• Study First Submitted QC: 2019-02-23
• Study First Posted: 2019-02-26
• Study Start: 2019-07-01
• Primary Completion: 2023-04-30
• Study Completion: 2023-05-30
• Status Verified: 2023-06
• Last Update Submitted: 2023-06-20
• Last Update Posted: 2023-06-22

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 218

Inclusion Criteria

1. Male or female patients aged ≥18 years.
2. Presence of congenital heart disease (intracardiac repair, cyanosis, Fontan palliation, or systemic right ventricle or other congenital heart disease).
3. Non-Valvular Atrial Arrhythmia (including at least one electrocardiographically documented episode).
4. Signed written informed consent by the patient for participation in the study and agreement to comply with the medication and the follow-up schedule.

Exclusion Criteria

1. moderate-to-severe mitral stenosis or mechanical valves
2. patient unwilling or unable to complete follow-up procedures

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Stroke, systemic or pulmonary arterial thromboembolism and intracardiac thrombosis.	up to 58 months	The composite endpoint of all-cause stroke, systemic and pulmonary embolism and intracardiac thrombosis
Major bleeding	up to 58 months	Defined as clinically overt bleeding that is associated with: * A fall in hemoglobin of 2 g/dL or more; * A transfusion of ≥2 units of packed red blood cells or whole blood; * Bleeding in a critical site: intracranial, intraspinal, intraocular, pericardial, intraarticular, intramuscular with compartment syndrome, retroperitoneal; * Death (fatal bleeding)

Secondary Outcome Measures

Name	Time	Method
Transient ischemic attack	up to 58 months	Defined as new neurologic symptoms or deficit lasting less than 24 hours with no new infarction on neuroimaging (if available).
Myocardial infarction	up to 58 months	Defined as the detection of a significant rise/fall of Troponin in association with symptoms of ischemia, ECG changes, proof of ischemia on imaging or intracoronary thrombus at angiography. \[Fourth definition of myocardial infarction; European Society of Cardiology (ESC) 2018\]
Τhe composite of stroke, systemic or pulmonary arterial thromboembolism and intracardiac thrombosis, transient ischemic attack, myocardial infarction, or cardiovascular death	up to 58 months
Death from cardiovascular causes	up to 58 months	Cardiovascular deaths were classified as deaths due to: ischemic stroke, hemorrhagic stroke, systemic or pulmonary embolism, other cardiovascular (i.e., myocardial infarction, sudden death, heart failure) and unobserved deaths.
Τhe composite of major and clinically relevant nonmajor bleeding	up to 58 months	Clinically relevant nonmajor bleeding bleeding=bleeding that is clinically overt, that satisfies none of the additional criteria required for the event to be adjudicated as a major bleeding event, that led to either hospital admission for bleeding, physician-guided medical or surgical treatment for bleeding, or a change in antithrombotic therapy.

Trial Locations

Locations (4)

AHEPA University Hospital; 🇬🇷 Thessaloníki, Greece

Onassis Cardiac Surgery Centre; 🇬🇷 Athens, Greece

Attikon University Hospital; 🇬🇷 Athens, Greece

Mitera Children's Hospital; 🇬🇷 Athens, Greece