Investigating the efficacy of chest pressure for direct current cardioversion in atrial fibrillation: a randomised control trial protocol (Pressure-AF)
David Ferreira,
Nicholas Collins,
Andrew Boyle,
Thomas Ford,
Nicholas Jackson,
Aaron Sverdlov,
James Leitch,
Philo Mikhail,
Michael McGee,
Maged William,
Malcolm Barlow,
Bradley Wilsmore
Affiliations
David Ferreira
School of Medicine and Public Health, The University of Newcastle, Callaghan, New South Wales, Australia
Nicholas Collins
Department of Cardiology, John Hunter Hospital, New Lambton Heights, New South Wales, Australia
Andrew Boyle
Wellcome-Wolfson Institute for Experimental Medicine, Queens University Belfast, Belfast, UK
Thomas Ford
School of Medicine and Public Health, The University of Newcastle, Callaghan, New South Wales, Australia
Nicholas Jackson
Department of Cardiology, John Hunter Hospital, New Lambton Heights, New South Wales, Australia
Aaron Sverdlov
Department of Cardiology, John Hunter Hospital, New Lambton Heights, New South Wales, Australia
James Leitch
Department of Cardiology, John Hunter Hospital, New Lambton Heights, New South Wales, Australia
Philo Mikhail
Department of Cardiology, Gosford Hospital, Gosford, New South Wales, Australia
Michael McGee
School of Medicine and Public Health, The University of Newcastle, Callaghan, New South Wales, Australia
Maged William
Department of Cardiology, Gosford Hospital, Gosford, New South Wales, Australia
Malcolm Barlow
Department of Cardiology, John Hunter Hospital, New Lambton Heights, New South Wales, Australia
Bradley Wilsmore
Department of Cardiology, John Hunter Hospital, New Lambton Heights, New South Wales, Australia
Introduction Atrial fibrillation (AF) is the most common sustained arrhythmia worldwide. Direct current cardioversion is commonly used to restore sinus rhythm in patients with AF. Chest pressure may improve cardioversion success through decreasing transthoracic impedance and increasing cardiac energy delivery. We aim to assess the efficacy and safety of routine chest pressure with direct current cardioversion for AF.Methods and analysis Multicentre, double blind (patient and outcome assessment), randomised clinical trial based in New South Wales, Australia. Patients will be randomised 1:1 to control and interventional arms. The control group will receive four sequential biphasic shocks of 150 J, 200 J, 360 J and 360 J with chest pressure on the last shock, until cardioversion success. The intervention group will receive the same shocks with chest pressure from the first defibrillation. Pads will be placed in an anteroposterior position. Success of cardioversion will be defined as sinus rhythm at 1 min after shock. The primary outcome will be total energy provided. Secondary outcomes will be success of first shock to achieve cardioversion, transthoracic impedance and sinus rhythm at post cardioversion ECG.Ethics and dissemination Ethics approval has been confirmed at all participating sites via the Research Ethics Governance Information System. The trial has been registered on the Australia New Zealand Clinical Trials Registry (ACTRN12620001028998). De-identified patient level data will be available to reputable researchers who provide sound analysis proposals.