The DanAblate-HF trial will investigate whether early catheter ablation treatment for atrial fibrillation in patients with heart failure is superior to standard treatment.
Atrial fibrillation (AF) is the most common arrhythmia in patients with heart failure (HF), with rates ranging between 20-65%, depending on age, severity of HF, subtypes of HF and duration of HF. The two conditions have an intricate and often overlapping pathophysiology, with each condition leading to development of the other, as well as progression of disease. Studies have shown that the presence of AF in HF patients is associated with increased morbidity and mortality, deterioration in HF, exacerbated HF symptoms, and reduced quality of life. The optimal treatment of AF in the presence of HF remains unknown. Currently, there is a pull towards catheter ablation as first-line therapy for AF in HF patients. However, there is no solid scientific evidence to support this approach. Furthermore, it is unknown whether early rhythm control by catheter ablation in HF patients is beneficial. The investigators aim to conduct a pragmatic, randomized clinical trial designed to evaluate the efficacy and safety of early catheter ablation for AF in patients with HF compared with standard treatment. Eligible patients with HF and AF will be prospectively screened from all Danish hospitals and randomized 1:1 to early catheter ablation with pulmonary vein isolation (within 6 weeks) or standard guideline directed treatment for AF. Patients with reversible causes for AF, conditions that preclude the use of catheter ablation or previous catheter ablation for AF will be excluded from the study. Randomization and follow-up will be conducted at six specialized sites in Denmark. There will be one scheduled on-site 12-months follow-up visit after randomization. All clinical follow-up will be conducted at the patient's local hospital, according to standard practice and out of trial setting. Information regarding hospital visits/admissions, events, adverse events, changes in medication, cross-over, heart rhythm and rate, and results of relevant blood-work will be ascertained through systematic patient chart-review at pre-specified time-points. The results from this trial will mold future treatment of AF in HF patients. The investigators hypothesize that early catheter ablation reduces the risk of HF hospitalizations and mortality when compared with standard treatment, thereby significantly improving the clinical prognosis for patients with HF and AF.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
1,616
Catheter ablation with pulmonary vein isolation will be the study intervention. Patients randomized to the intervention arm will undergo catheter ablation within six weeks of randomization. In the waiting-time for ablation, patients will receive standard treatment for AF and HF, as per current guideline recommendations. Catheter ablation will be performed at one of six high-volume ablation centers in Denmark. Mode of catheter ablation will be at the discretion of the operator. Radiofrequency ablation, cryo-balloon ablation and pulsed-field ablation will be utilized. The treating physician should ensure successful pulmonary vein isolation after ablation with either post-procedural mapping or pacing, as per current standards. Only pulmonary vein isolation will be performed during the ablation procedure.
Aalborg University Hospital, Department of Cardiology
Aalborg, Denmark
RECRUITINGAarhus University Hospital
Aarhus, Denmark
NOT_YET_RECRUITINGDepartment of Cardiology, Rigshospitalet
Copenhagen, Denmark
Time to hospitalization for worsening HF or cardiovascular death
The primary outcome of the trial is defined as the time from randomization to the composite of one the following, whichever comes first * Hospitalization for worsening HF * Cardiovascular (CV) mortality Hospitalization for worsening HF will be defined as hospital admission primarily for HF (as deemed so by the event adjudication committee) with a duration of at least 24 hours and requiring intensification of diuretic treatment. CV mortality will be defined as all deaths resulting from one or more of the following: HF, stroke, acute myocardial infarction, CV procedural deaths, CV hemorrhage, arrythmia, sudden cardiac death, death due to other CV causes and death of undetermined cause.
Time frame: From baseline to study completion, with a minimum of 1 year
Time to cardiovascular death
Time from randomization to cardiovascular death. Cardiovascular death will be defined as in the primary endpoint.
Time frame: From baseline to study completion, with a minimum of 1 year
Time to all-cause mortality
Time from randomization to all-cause mortality
Time frame: From baseline to study completion, with a minimum of 1 year
Time to first heart failure hospitalization
Time from randomization to first hospitalization for heart failure, as defined in the primary endpoint
Time frame: From baseline to study completion, with a minimum of 1 year
Time to first-time AF hospitalization
Time from randomization to first hospitalization for AF
Time frame: From baseline to study completion, with a minimum of 1 year
Time to primary outcome stratified by age
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Department of Cardiology, Herlev-Gentofte University Hospital
Hellerup, Denmark
RECRUITINGDepartment of Cardiology, Odense University Hospital
Odense, Denmark
NOT_YET_RECRUITINGDepartment of Cardiology, Zealand University Hospital
Roskilde, Denmark
NOT_YET_RECRUITINGTime from randomization to trial primary outcome stratified by median age at baseline
Time frame: From baseline to study completion, with a minimum of 1 year
Time to primary outcome stratified by sex
Time from randomization to trial primary outcome stratified by sex
Time frame: From baseline to study completion, with a minimum of 1 year
Time to primary outcome stratified by symptomatic and asymptomatic AF
Time from randomization to trial primary outcome stratified by whether patients have symptomatic or asymptomatic AF at baseline
Time frame: From baseline to study completion, with a minimum of 1 year
Time to primary outcome stratified by paroxysmal or persistent AF
Time from randomization to trial primary outcome stratified by paroxysmal or persistent AF at baseline
Time frame: From baseline to study completion, with a minimum of 1 year
Time to primary outcome stratified by left ventricular ejection fraction (LVEF)
Time from randomization to trial primary outcome stratified by LVEF \<=40% and LVEF\>40% at baseline
Time frame: From baseline to study completion, with a minimum of 1 year
Change in Quality of Life
Change in Quality of Life will be assessed through Kansas City Cardiomyopathy Questionnaire (KCCQ-23) at baseline and 12 months. The KCCQ-23 quantifies physical function/limitations, symptoms, quality of life, social function/limitations and self-efficacy. Scores are generated for each domain and scaled from 0 to 100, with higher scores reflecting better health outcome.
Time frame: From baseline to 12 months
Change in self-assessed health
Change in self-assessed health will be assessed through short form-36 (SF-36) questionnaire at baseline and 12 months. The SF-36 questionnaire consists of 8 domains: Physical functioning, limitions due to physical health, limitations due to emotional problems, fatigue, emotional well-being, social functioning, general bodily pain and general health. Each domain is scored from 0 to 100, with higher scores reflecting better self-assessed health.
Time frame: From baseline to 12 months
Change in New York Heart Association (NYHA) class
Change in NYHA class assessed at baseline and 12 months visit
Time frame: From baseline to 12 months
Change in European Heart Rhythm Association score of atrial fibrillation (EHRA class)
Change in EHRA class assessed at baseline and 12 months visit
Time frame: From baseline to 12 months