scholarly journals Stereotactic radioablation for the treatment of ventricular tachycardia: preliminary data and insights from the STRA-MI-VT phase Ib/II study

Author(s):  
Corrado Carbucicchio ◽  
Daniele Andreini ◽  
Gaia Piperno ◽  
Valentina Catto ◽  
Edoardo Conte ◽  
...  

Abstract Purpose We present the preliminary results of the STRA-MI-VT Study (NCT04066517), a spontaneous, phase Ib/II study, designed to prospectively test the safety and efficacy of stereotactic body radiotherapy (SBRT) in patientswith advanced cardiac disease and intractable ventricular tachycardia (VT). Methods Cardiac computed tomography (CT) integrated by electroanatomical mapping was used for substrate identification and merged with dedicated CT scans for treatment plan preparation. A single 25-Gy radioablation dose was delivered by a LINAC-based volumetric modulated arc therapy technique in a non-invasive matter. The primary safety endpoint was treatment-related adverse effects during acute and long-term follow-up (FU), obtained by regular in-hospital controls and implantable cardioverter defibrillator (ICD) remote monitoring. The primary efficacy endpoint was the reduction at 3 and 6 months of VT episodes and ICD shocks. Results Seven out of eight patients (men; age, 70 ± 7 years; ejection fraction, 27 ± 11%; 3 ischemic, 4 non-ischemic cardiomyopathies) underwent SBRT. At a median 8-month FU, no treatment-related serious adverse event occurred. Three patients died from non-SBRT-related causes. Four patients completed the 6-month FU: the number of VT decreased from 29 ± 33 to 11 ± 9 (p = .05) and 2 ± 2 (p = .08), at 3 and 6 months, respectively; shocks decreased from 11 to 0 and 2, respectively. At 6 months, all patients. showed a significant reduction of VT episodes and no electrical storm recurrence, with the complete regression of iterative VTs in 2/2 patients. Conclusion The STRA-MI-VT Study suggests that SBRT can be considered an alternative option for the treatment of VT in patients with structural heart disease and highlights the need for further clinical investigation addressing safety and efficacy.

EP Europace ◽  
2018 ◽  
Vol 20 (suppl_1) ◽  
pp. i42-i42
Author(s):  
S Mathew ◽  
T Maurer ◽  
C Lemes ◽  
C Heeger ◽  
B Reissmann ◽  
...  

2015 ◽  
Vol 156 (25) ◽  
pp. 995-1002
Author(s):  
Attila Mihálcz ◽  
Tamás Szili-Török ◽  
Kálmán Tóth

Catheter ablation of ventricular tachycardias emerged significantly as standard therapy in the past 20 years. In this review recent advances in catheter ablation of ventricular tachycardias are discussed. The authors first present in details the technical aspects of ablation strategies, main indications and contraindications of ventricular tachycardia ablation and the necessary pre- and postinterventional diagnostic tests. Outcome is also discussed in different forms of ventricular tachycardias in detail. The authors summarize the safety and efficacy of catheter ablation of ventricular arrhythmias. They recommend that ablation of ventricular tachycardias should be considered earlier in patients with and without structural heart disease. Orv. Hetil., 2015, 156(25), 995–1002.


2020 ◽  
Author(s):  
Rodrigo Melo Kulchetscki ◽  
Felipe Kalil Beirão Alexandre ◽  
Marina Pereira Mayrink ◽  
Carina A. Hardy ◽  
Sissy L. de Melo ◽  
...  

2011 ◽  
Vol 27 (Supplement) ◽  
pp. OP06_3
Author(s):  
Hiroshi Furushima ◽  
Masaomi Chinushi ◽  
Keiko Sonoda ◽  
Kanae Hasegawa ◽  
Nobue Yagihara ◽  
...  

2015 ◽  
Vol 1 (1-2) ◽  
pp. 52-58 ◽  
Author(s):  
Jackson J. Liang ◽  
Shaan Khurshid ◽  
Robert D. Schaller ◽  
Pasquale Santangeli ◽  
Francis E. Marchlinski ◽  
...  

PLoS ONE ◽  
2017 ◽  
Vol 12 (2) ◽  
pp. e0171830 ◽  
Author(s):  
Bashar Aldhoon ◽  
Dan Wichterle ◽  
Petr Peichl ◽  
Robert Čihák ◽  
Josef Kautzner

Author(s):  
Granitz Christina ◽  
Jirak Peter ◽  
Strohmer Bernhard ◽  
Pölzl Gerhard

Abstract Background  Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a severe genetic arrhythmogenic disorder characterized by adrenergically induced ventricular tachycardia manifesting as stress-induced syncope and sudden cardiac death. While CPVT is not associated with dilated cardiomyopathy (DCM) in most cases, the combination of both disease entities poses a major diagnostic and therapeutic challenge. Case summary  We present the case of a young woman with CPVT. The clinical course since childhood was characterized by repetitive episodes of exercise-induced ventricular arrhythmias and a brady-tachy syndrome due to rapid paroxysmal atrial fibrillation and sinus bradycardia. Medical treatment included propranolol and flecainide until echocardiography showed a dilated left ventricle with severely depressed ejection fraction when the patient was 32 years old. Cardiac magnetic resonance imaging revealed non-specific late gadolinium enhancement. Myocardial inflammation, however, was excluded by subsequent endomyocardial biopsy. Genetic analysis confirmed a mutation in the cardiac ryanodine receptor but no pathogenetic variant associated with DCM. Guideline-directed medical therapy for HFrEF was limited due to symptomatic hypotension. Over the next months, the patient developed progressive heart failure symptoms that were finally managed by heart transplantation. Discussion  Management in patients with CPVT and DCM is challenging, as Class I antiarrhythmic drugs are not recommended in structural heart disease and prophylactic internal cardioverter-defibrillator implantation without adjuvant antiarrhythmic therapy can be detrimental. Regular echocardiographic screening for DCM is recommendable in patients with CPVT. A multidisciplinary team of heart failure specialists, electrophysiologists, geneticists, and imaging specialists is needed to collaborate in the delivery of clinical care.


Heart Rhythm ◽  
2014 ◽  
Vol 11 (4) ◽  
pp. 541-546 ◽  
Author(s):  
Benjamin F. Remo ◽  
Mark Preminger ◽  
Jason Bradfield ◽  
Suneet Mittal ◽  
Noel Boyle ◽  
...  

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