Atrial Fibrillation Clinical Trial
Official title:
EP Study at >1 Year to Evaluate the Presence of Conduction Block Across the Cinch Line in Patients Who Have Received Left Atrial Ablation Using High Intensity Focused Ultrasound(HIFU)
The purpose of this study is to check if at 1 year after surgical ablation the electrical
impulses that cause atrial fibrillation (AF) are still blocked from being able to get into
the heart.
Hypothesis Conduction block and ganglionic destruction are required for freedom from AF.
Atrial fibrillation (AF) is an increasing common disease. It ranges from being asymptomatic
to a highly disabling condition with a severe impact on quality of life. It is termed
paroxysmal (PAF) when an episode lasts less than 7 days, persistent (PerAF) when it lasts
more than 7 days and needs intervention and permanent (PermAF) when it is accepted as the
long term rhythm. Treatment is based on symptom control and the prevention of complications
such as stroke. When an attempt is made to restore normal sinus rhythm (NSR), this is termed
'rhythm control'.
Treatments for rhythm control of AF can be broadly divided into pharmacological and ablative.
Ablative techniques1 are typically performed percutaneously using catheter-based technology
(minimally invasive), though some surgical techniques also exist. They work on the principle
that performing a series of 'burns' (scar) in appropriate places can prevent abnormal
electrical signals forming and propagating within the heart.
The problem of atrial fibrillation is vast. Prevalence ranges from 0.2% in the 45-54 age
group, rising to 8% in the over 75s. Though the majority of patients can be satisfactorily
treated medically, in a not insignificant portion, the drugs are either poorly tolerated or
are ineffective. For these patients, the United Kingdom (UK) NICE guidelines recommend
consideration of an ablation procedure. In Derriford hospital alone we see approximately 14
patients suitable for AF ablation in a typical month.
The electrophysiological consequences of ablation are unclear. It is not known whether
complete bidirectional electrical block across the ablation lines isolating the pulmonary
antral region from the rest of the left atrium is a prerequisite for long-term cure of Atrial
Fibrillation (AF). Studies in canine models of atrial fibrillation have suggested that
incomplete lines of block can be as effective in reducing AF burden as complete lines,
however the limited number of follow up studies in humans that have assessed both patients
with recurrent AF and also asymptomatic patients who appear to have been cured by catheter
ablation have suggested that complete electrical isolation of the pulmonary veins is
necessary for a cure. Advocates for ablation without assessing electrical block argue success
rates in humans are similar whether circumferential electrical isolation of the pulmonary
veins is achieved or not. Assessing freedom from AF and correlating it with the presence or
absence of complete bidirectional electrical block, intra-operatively and at post one-year
follow-up, will allow a further understanding of the mechanisms determining the success or
failure of AF ablation therapies. This will be very important in knowing how to treat
patients in whom AF still occurs and will guide the approach to subsequent interventions.
Though there is a small risk involved in this study, the question it addresses will have a
significant impact on the development of future AF ablation techniques. Within this group,
over 300 separate ablation procedures have been performed with no deaths or significant
complications. Previous groups have published trans-septal observational studies in humans
demonstrating that previous ethics committees have appreciated the importance of such work.
The 2012 Heart Rhythm Society (HRS)/European Heart Rhythm Association (EHRA)/European Cardiac
Arrhythmia Society (ECAS) consensus statement on catheter and surgical ablation for AF has
recently highlighted the need for novel trial designs demonstrating 'durability of pulmonary
vein isolation' with a repeat diagnostic electrophysiological study.
This trial will therefore increase our understanding of the electrophysiological properties
associated with successful ablation and how Atrial Fibrillation ablation and the HIFU
procedure work.
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