Description

OBJECTIVE

Primary

• Evaluate the efficacy of bilateral sympathectomy in the reduction of VT episodes in patients with Chagas cardiomyopathy.

Secondary

• To compare the efficacy of bilateral sympathectomy against VT ablation and against optimal medical therapy.
• To evaluate the density of ventricular premature beats 24-hour Holter and monitor the events recorded by the ICD and the impact of the treatment performed.
• To evaluate the length of the hospital stay according to the type of intervention.
• To evaluate the rate of clinical complications according to the type of intervention.
• To evaluate the impact of treatment on left ventricular function.

Follow up

Outcomes Assessment in six months and one year

• Recurrence rate of appropriate therapies;
• Density of ventricular ectopies;
• Complication rates per type of intervention;
• Number of in-hospital days per type of intervention;
• Assessment of LV function;

METHODS

This is a pilot, single-centre, open-label, randomized trial in patients with Chagas disease and multiple appropriate ICD therapies. This study consists of three groups: (1) medical treatment, (2) catheter ablation and (3) bilateral sympathectomy, being included 15 patients in each group.

Inclusion Criteria:

• Patients with Chagas Disease Cardiomyopathy having an ICD
• At least four appropriate ICD therapies in the past six months, documented by device interrogation or medical records;
• Use of amiodarone and beta blockers in an optimized fashion;
• Life expectancy of more than one year
• Conditions for following the plan of clinical follow-up of the study.

Exclusion criteria:

• Presence of an absolute contraindication to receive any of the possible treatments of the study;
• Pregnant Woman;
• Less than 18 years-old;
• Renal insufficiency with creatinine >2.5 mg/dL (221 umol/L);
• Mobile thrombus in the left ventricle;
• Left Ventricle Ejection fraction < 10%;
• Unstable angina;
• Severe aortic stenosis
• Primary severe mitral insufficiency;
• New York Heart Association (NYHA) functional class IV;
• Previous cardiac surgery or scheduled.

The patients will be recruited consecutively in the outpatient clinic of Cardiac Pacing Unit, or in outpatient clinic of Arrhythmias Clinical Unit or in the Emergency Clinical Unit.

Group 1 - Medical Treatment: patients allocated to this group will receive amiodarone reimpregnation, incremental dose of beta-blocker and if possible ICD reprogramming.

Group 2 - Catheter ablation: patients allocated to this group will undergo epicardial and endocardial catheter ablation with the use of an irrigated contact sensor tip catheter. Voltage electroanatomical mapping using Carto System will be performed in all cases and if hemodynamically stable VT is induced, activation mapping will also be performed. The aim of the ablation is to eliminate the clinical VT additionally to substrate modification. The result of ablation will be defined as (1) complete success (all VTs non-inducible); (2) partial success (clinical VT non inducible, but other morphologies still inducible) and (3) failure (clinical VT still inducible).

Group 3 - Bilateral sympathectomy - bilateral sympathectomy will be performed using video assisted thoracoscopy using the Ethicon Ultracision device. The denervation consists of lower 1/3 stellate ganglion and T3- T4 thoracic interspinal space videothoracoscopic cutting, isolating the whole sympathetic chain between these two points using ultracision device on the nerve branches. The cephalic portion of the stellate ganglion will be preserved to avoid Horner's syndrome and the electrocautery use will also be avoided for the same reason. Hemodynamic and echocardiographic behaviors will be continuously monitored during these surgical maneuvers. After the application, 10 ml of 0.25% bupivacaine solution will be injected along the site of the pleural dissection for postoperative analgesia. The lung will be reinflated under direct vision and a small tube will be inserted to remove the air through the upper incision, which will be removed at the end of the operation if possible. The two port sites will be closed primarily with absorbable stitches.

The study conformed to the principles outlined in the Declaration of Helsinki and was approved by the ethics committee and institutional review board of our hospital. All patients will provide written informed consent before randomization.