Abstract

BackgroundAtrial fibrillation is the commonest arrhythmia which raises the risk of heart failure, thromboembolic stroke, morbidity and death. Pharmacological treatments of this condition are focused on heart rate control, rhythm control and reduction in risk of stroke. Selective ablation of cardiac tissues resulting in isolation of areas causing atrial fibrillation is another treatment strategy which can be delivered by two minimally invasive interventions: percutaneous catheter ablation and thoracoscopic surgical ablation. The main purpose of this trial is to compare the effectiveness and safety of these two interventions.Methods/designCatheter Ablation versus Thoracoscopic Surgical Ablation in Long Standing Persistent Atrial Fibrillation (CASA-AF) is a prospective, multi-centre, randomised controlled trial within three NHS tertiary cardiovascular centres specialising in treatment of atrial fibrillation. Eligible adults (n = 120) with symptomatic, long-standing, persistent atrial fibrillation will be randomly allocated to either catheter ablation or thoracoscopic ablation in a 1:1 ratio. Pre-determined lesion sets will be delivered in each treatment arm with confirmation of appropriate conduction block. All patients will have an implantable loop recorder (ILR) inserted subcutaneously immediately following ablation to enable continuous heart rhythm monitoring for at least 12 months. The devices will be programmed to detect episodes of atrial fibrillation and atrial tachycardia ≥ 30 s in duration. The patients will be followed for 12 months, completing appropriate clinical assessments and questionnaires every 3 months. The ILR data will be wirelessly transmitted daily and evaluated every month for the duration of the follow-up. The primary endpoint in the study is freedom from atrial fibrillation and atrial tachycardia at the end of the follow-up period.DiscussionThe CASA-AF Trial is a National Institute for Health Research-funded study that will provide first-class evidence on the comparative efficacy, safety and cost-effectiveness of thoracoscopic surgical ablation and conventional percutaneous catheter ablation for long-standing persistent atrial fibrillation. In addition, the results of the trial will provide information on the effects on patients’ quality of life.Trial registrationISRCTN Registry, ISRCTN18250790. Registered on 24 April 2015.

Highlights

  • Atrial fibrillation is the commonest arrhythmia which raises the risk of heart failure, thromboembolic stroke, morbidity and death

  • Any surgical procedure carries a risk of morbidity and complications, but risks associated with thoracoscopic surgical ablation have not been directly compared with catheter ablation

  • This protocol follows the guidance of Standard Protocol Items: Recommendations for Interventional Trials (SPIRIT) 2013 statement [37, 38], and it includes the schedule of enrolment and relevant assessments (Figs. 1 and 2) based on the SPIRIT figure template

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Summary

Discussion

The use of traditional pharmacological agents to treat LSPAF is not satisfactory, owing to their serious side effects and need for lifelong treatment. On the basis of the encouraging results of thoracoscopic surgical ablation in several cohort studies of subjects with persistent AF and LSPAF and our pilot study [45, 87, 88], we have designed this trial to compare the two ablative treatments and provide first-class evidence of their efficacy, safety and cost-effectiveness. Trial status The trial was open to recruitment on 1 August 2015 and currently is actively recruiting at two three NHS specialist care centres (Royal Brompton and Harefield NHS Foundation Trust, Brighton and Sussex University Hospitals NHS Trust and Liverpool Heart and Chest NHS Foundation Trust). Author details 1Royal Brompton and Harefield NHS Trust, London, UK.

Background
Ablation procedures
Findings
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