Atrial Fibrillation
Conditions
Keywords
Ganglionated plexi
Brief summary
This study evaluates the effect of catheter ablation of ganglionated plexi (GP) for the treatment of adult patients with atrial fibrillation heart arrhythmias. The location of GP will be demonstrated by a novel nuclear imaging cardiac camera. 3D images from the cardiac camera will guide the GP ablation procedure.
Detailed description
Catheter ablation procedures are nowadays routine procedures in patients with drug-refractory atrial fibrillation (AF). However, ablation success for patients even in the early stages of AF is currently only around 70% and may require multiple procedures. The intrinsic cardiac autonomic nervous system (ANS), which forms a neural network, has been shown to be a critical element responsible for the initiation and maintenance of AF. Autonomic inputs to the heart converge at several locations; these convergence points are typically embedded in the epicardial fat pads and form ganglionated plexi (GP) that contain autonomic ganglia and nerves. In human hearts, there are at least 7 GP and the 4 major left atrial GP are located around the antrum of the pulmonary veins (PVs). High-frequency stimulation (HFS; 20 Hz, 10-150 V and pulse width 1-10 ms) can localize GP during an invasive electrophysiology (EP) study. A novel dedicated cardiac nuclear imaging camera with solid-state detectors (D-SPECT, Spectrum Dynamics) has demonstrated significantly improved sensitivity and image resolution and can provide novel imaging information on previously 'invisible' structures like the GP. Using this 3D image information to guide GP ablation could significantly facilitate AF ablation and result in improved ablation outcomes.
Interventions
PROCEDUREImage guided GP ablation
3D imaging data from the D-SPECT system will be used to visualise the GP and guide the location of catheter ablation sites during the electrophysiology procedure.
DEVICED-SPECT dedicated cardiac nuclear camera
Sponsors
Spectrum Dynamics
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
19 Years to 80 Years
Healthy volunteers
No
Inclusion criteria
* Paroxysmal or early persistent atrial fibrillation with ongoing AF for less than 1 week * Able to give written informed consent * Age \>18 years old and ≤ 80 years * Fulfil established clinical criteria for catheter ablation of atrial fibrillation * Normal left ventricular (LV) ejection fraction and no evidence of significant structural heart disease
Exclusion criteria
* Reversible cause of atrial fibrillation * Recent cardiovascular event including transient ischaemic attack (TIA) * Intolerance or unwillingness to oral anticoagulation with Warfarin * Bleeding disorder * Contraindication to computed tomography (CT) scan * Presence of intracardiac thrombus * Vascular disorder preventing access to femoral veins * Cardiac congenital abnormality * Severe, life threatening non cardiac disease * Active malignant disease or recent (\<5 years) malignant disease * Presence of atrial septal defect (ASD) or patent foramen ovale (PFO) closure device * Unable or unwilling to comply with follow-up requirements * Patients on amiodarone until less than 3 months prior to the screening visit * Left atrium size \> 5.5 cm on parasternal diameter in transthoracic echocardiography (TTE) * Renal impairment * Pregnancy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Termination of atrial fibrillation during image guided ablation | At the time of the ablation procedure. |
| Freedom from atrial fibrillation/flutter/tachycardia (>30 seconds) off antiarrhythmic medication at the end of 12 months following the index ablation procedure. | 12 months post the index ablation procedure. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Time to first recurrence of atrial fibrillation/flutter/tachycardia (>30 seconds) | Up to 12 months from the index ablation procedure | — |
| Freedom from atrial fibrillation on previously failed antiarrhythmic medication | 12 months from the index ablation procedure. | — |
| Atrial fibrillation/flutter/tachycardia (>30 seconds) burden at 12 months post the index ablation procedure. | 12 months from the index ablation procedure. | AF/flutter/tachycardia burden will be modelled as a continuous variable with the number of episodes recorded. |
| Left atrial transport function | 6 months and 12 months post the index ablation procedure | Left atrial transport function will be assessed by echo as a categorical variable with 3 categories; poor, moderately impaired and normal. |
Countries
United Kingdom
Outcome results
None listed