Emanuela Falaschetti
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Recent Grants
Grant: Open
A novel reliever strategy for children with asthma: CARE-UK: Children's Anti-Inflammatory Reliever Study
Open Date: 2023-06-01
Close Date: 2027-02-28
Grant: Close
Dietary nitrate supplementation to enhance daily physical activity in hypoxic COPD: a randomised controlled trial
Open Date: 2022-06-01
Close Date:
Grant: Close
AV optimisation delivered with direct His bundle pacing, in patients with heart failure, long PR without left bundle branch block: randomised multi-centre clinical outcome study 'The His Optimised Pacing Evaluated for Heart Failure Trial (HOPE-HF)'
Open Date: 2016-01-01
Close Date: 2019-08-31
Grant: Close
A randomized controlled trial of a duodenal sleeve bypass device (Endobarrier) compared with standard medical therapy for the management of obese subjects with type 2 diabetes
Open Date: 2014-05-01
Close Date: 2019-04-30
Grant: Close
REducing Microvascular dysfunction in patients with angina, ischaemia and unobstructED coronarY arteries – a pilot study (REMEDY-Pilot)
Open Date:
Close Date:
Articles (11)
Year:
2024
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2024
Year:
2024
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2024
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2024
Year:
2023
Year:
2022
Year:
2022
Aims There is rising healthcare utilization related to the increasing incidence and prevalence of atrial fibrillation (AF) worldwide. Simplifying therapy and reducing hospital episodes would be a valuable development. The efficacy of a streamlined AF ablation approach was compared to drug therapy and a conventional catheter ablation technique for symptom control in paroxysmal AF. Methods and results We recruited 321 patients with symptomatic paroxysmal AF to a prospective randomized, multi-centre, open label trial at 13 UK hospitals. Patients were randomized 1:1:1 to cryo-balloon ablation without electrical mapping with patients discharged same day [Ablation Versus Anti-arrhythmic Therapy for Reducing All Hospital Episodes from Recurrent (AVATAR) protocol]; optimization of drug therapy; or cryo-balloon ablation with confirmation of pulmonary vein isolation and overnight hospitalization. The primary endpoint was time to any hospital episode related to treatment for atrial arrhythmia. Secondary endpoints included complications of treatment and quality-of-life measures. The hazard ratio (HR) for a primary endpoint event occurring when comparing AVATAR protocol arm to drug therapy was 0.156 (95% CI, 0.097–0.250; P < 0.0001 by Cox regression). Twenty-three patients (21%) recorded an endpoint event in the AVATAR arm compared to 76 patients (74%) within the drug therapy arm. Comparing AVATAR and conventional ablation arms resulted in a non-significant HR of 1.173 (95% CI, 0.639–2.154; P = 0.61 by Cox regression) with 23 patients (21%) and 19 patients (18%), respectively, recording primary endpoint events (P = 0.61 by log-rank test). Conclusion The AVATAR protocol was superior to drug therapy for avoiding hospital episodes related to AF treatment, but conventional cryoablation was not superior to the AVATAR protocol. This could have wide-ranging implications on how demand for AF symptom control is met. Trial registration Clinical Trials Registration: NCT02459574.
Year:
2022
Year:
2021
Year:
2021
Collaborators (14)
Joseph Tomson
Honorary Associate Clinical Professor
University College London
Werd Al-Najim
Dublin City University
Pedro Ferreira
Imperial College London
Manuela Funke
Chief physician
Inselspital Universitätsspital Bern
Daniel Hammersley
Imperial College London
Francesco Lombardi
Università Cattolica del Sacro Cuore Facoltà di Medicina e Chirurgia
Dan Stieper Karbing
Aalborg University
Neil Poulter
Imperial College London
Laura Fabbri
Imperial College London
Kerri Johannson
Associate Professor
University of Calgary
John Frater
University of Oxford
Duncan Richards
University of Oxford
Helena Fisk
Lecturer in nutrition and dietetics (0.2FTE)
University of Winchester
Ming Jie Lee
Imperial College London
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