Ventricular tachycardia (VT) is an abnormal rapid heartbeat which occurs after a heart attack and can cause sudden death. Patients at risk of this rhythm disturbance usually receive an implantable cardioverter defibrillator (ICD) that can prevent death by returning the heart's rhythm back to normal by electrically stimulating the heart but in doing so gives the patient painful and debilitating shocks. The first ICD shock after implantation appears to be a powerful predictor of subsequent shock therapy as well as being a predictor of of increased mortality in patients with primary prevention ICDs. In patients who receive repeated shocks VT ablation is performed to 'burn' the abnormal area of the heart that causes the problem. However, it is often only performed as a last resort as it is technically challenging. We believe that performing VT ablation using the robotic system early after the first episode of VT after ICD implantation, may reduce the number of painful shocks received by the patient and possibly increase life expectancy and quality of life. 200 patients from 5 european countries will be recruited in a prospective, open, randomised trial. Eligible, consenting patients who have experienced their first episode of VT since ICD implantation, will be randomised in a 1:1 manner into treatment arms of either VT ablation or standard 'conventional' therapy and followed-up every 4 months over two years to assess the number of subsequent ICD shocks, hospitalisation, mortality and quality of life.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
51
Robotic VT Ablation
Review of ICD programming to ensure that detection and therapy will occur appropriately
St Bartholomew's Hospital
London, United Kingdom
Hammersmith Hospital, Imperial College Healthcare
London, United Kingdom
John Radcliffe Hospital
Oxford, United Kingdom
Any appropriate ICD therapy
Time frame: 24 months post randomisation
Treatment Failures defined as either2 ICD shocks or 5 ATP episodes
Time frame: 24 months post randomisation
Total therapy rate
Time frame: 24 months post randomisation
Mortality
Time frame: 24 months post randomisation
All cause hospitalisation
Time frame: 24 months post randomisation
Quality of Life
Time frame: 12 months post randomisation
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