Catheter ablation vs. thoracoscopic surgical ablation in long-standing persistent atrial fibrillation: CASA-AF randomized controlled trial

Author:

Haldar Shouvik12ORCID,Khan Habib Rehman23ORCID,Boyalla Vennela12,Kralj-Hans Ines1ORCID,Jones Simon4,Lord Joanne5ORCID,Onyimadu Oluchukwu5,Satishkumar Anitha1,Bahrami Toufan1,De Souza Anthony1,Clague Jonathan R1,Francis Darrel P2ORCID,Hussain Wajid1ORCID,Jarman Julian W1ORCID,Jones David Gareth12,Chen Zhong1,Mediratta Neeraj6,Hyde Jonathan7,Lewis Michael7,Mohiaddin Raad12ORCID,Salukhe Tushar V12ORCID,Murphy Caroline8,Kelly Joanna8,Khattar Rajdeep S1ORCID,Toff William D9ORCID,Markides Vias12ORCID,McCready James7,Gupta Dhiraj6ORCID,Wong Tom12ORCID

Affiliation:

1. Royal Brompton & Harefield NHS Foundation Trust, Sydney Street, London SW3 6NP, UK

2. National Heart and Lung Institute, Imperial College London, Cale Street, London SW3 6LY, UK

3. London Health Sciences Centre, University of Western Ontario, 800 Commissioners Rd E, London ON N6A 5W9, Canada

4. New York University, Langone Health, 227 East 30th Street, New York, NY 10016, USA

5. Southampton Health Technology Assessment Centre, University of Southampton, University Road, Southampton SO17 1BJ, UK

6. Liverpool Heart and Chest Hospital, Thomas Dr, Liverpool L14 3PE, UK

7. Brighton and Sussex University Hospitals NHS Trust, Royal Alexandra Children’s Hospital, Eastern Road, Brighton BN2 5BE, UK

8. Clinical Trials Unit, Kings College London, Institute of Psychiatry, 16 De Crespigny Park, London SE5 8A, UK

9. Department of Cardiovascular Sciences, University of Leicester and NIHR Leicester Biomedical Research Centre, Glenfield Hospital, Groby Road, Leicester LE3 9QP, UK

Abstract

Abstract Aims  Long-standing persistent atrial fibrillation (LSPAF) is challenging to treat with suboptimal catheter ablation (CA) outcomes. Thoracoscopic surgical ablation (SA) has shown promising efficacy in atrial fibrillation (AF). This multicentre randomized controlled trial tested whether SA was superior to CA as the first interventional strategy in de novo LSPAF. Methods and results  We randomized 120 LSPAF patients to SA or CA. All patients underwent predetermined lesion sets and implantable loop recorder insertion. Primary outcome was single procedure freedom from AF/atrial tachycardia (AT) ≥30 s without anti-arrhythmic drugs at 12 months. Secondary outcomes included clinical success (≥75% reduction in AF/AT burden); procedure-related serious adverse events; changes in patients’ symptoms and quality-of-life scores; and cost-effectiveness. At 12 months, freedom from AF/AT was recorded in 26% (14/54) of patients in SA vs. 28% (17/60) in the CA group [OR 1.128, 95% CI (0.46–2.83), P = 0.83]. Reduction in AF/AT burden ≥75% was recorded in 67% (36/54) vs. 77% (46/60) [OR 1.13, 95% CI (0.67–4.08), P = 0.3] in SA and CA groups, respectively. Procedure-related serious adverse events within 30 days of intervention were reported in 15% (8/55) of patients in SA vs. 10% (6/60) in CA, P = 0.46. One death was reported after SA. Improvements in AF symptoms were greater following CA. Over 12 months, SA was more expensive and provided fewer quality-adjusted life-years (QALYs) compared with CA (0.78 vs. 0.85, P = 0.02). Conclusion  Single procedure thoracoscopic SA is not superior to CA in treating LSPAF. Catheter ablation provided greater improvements in symptoms and accrued significantly more QALYs during follow-up than SA. Clinical Trial Registration ISRCTN18250790 and ClinicalTrials.gov: NCT02755688

Funder

Efficacy and Mechanism Evaluation

Programme, a Medical Research Council

National Institute for Health Research

NIHR

MRC

Department of Health and Social Care

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine

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