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Myocardial perfusion images of regional viable (A) and non-viable myocardium (B) at the postero-lateral LV lead position in the standard 20-segment model. 

Myocardial perfusion images of regional viable (A) and non-viable myocardium (B) at the postero-lateral LV lead position in the standard 20-segment model. 

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The presence of myocardial fibrosis is associated with ventricular tachyarrhythmia (VT) occurrence irrespective of cardiomyopathy etiology. The aim of our study was to evaluate the impact of global and regional viability on VTs in patients undergoing cardiac resynchronization therapy (CRT). Fifty-seven patients with advanced heart failure (age 62.3...

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... without VTs had more viable segments (17.6 ± 2.35 vs 14.2 ± 4.0; P = .002) and higher via- bility of the corresponding segments at LV lead position (66.1% ± 10.3% vs 54.8% ± 11.4% of tracer activity; P = .001). Distribution of non-viable segments (tracer uptake \ 50% of normal myocardium) according to 20- segments model is presented in Table 1. In VTs group, more patients had non-viable segments in antero-lateral, infero-lateral, inferior and also in apical region of LV. In addition, the example of two patients with viable and non-viable segments in the LV pacing lead area was also noted in Figure 3. All segments at the LV lead were viable in only two patients (11.1%) with registered VTs and in 26 patients (66.7%) without VTs (P \ .001). In addition, among patients with registered VTs, the extent of regional viability is also related to the number of malignant tachyarrhythmias. Patients with more than two appropriate device therapies had lower regional viability [52.3% (46.5-54.5) vs 66.5% (55.0-68.0); P = .013]. VTs, Ventricular tachyarrhythmias; CRT, cardiac resynchronization therapy; NYHA class, New York Heart Association class; CABG, coronary artery bypass grafting; PCI, percutaneous coronary intervention; MPI, myocardial perfusion imaging; LVEF, left ventricular ejection fraction; LVESV, left ventricular end systolic volume; LVEDV, left ventricular end diastolic volume; 6-MWT, 6-minute walking distance test; BNP, brain natriuretic peptide; AF, atrial fibrillation; LV, left ventricle; ACE-i, angiotensin-converting enzyme inhibitors; ARB, angiotensin II receptor blockers; VAD, ventricular assist device. * Location of non-viable segments (tracer uptake \ 50% of normal myocardium) according to 20-segment model (Figure 2): segments 1, 7, 13 presented anterior; segments 6, 12, 18 antero-lateral; segments 5, 11, 17 infero-lateral; segments 4, 10, 16 inferior; segments 3, 9, 15 infero-septal; segments 2, 8, 14 antero-septal part of the left ventricle and segments 19, 20 were ...

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... In addition to reducing the chances of CRT response, the presence of LV scar has also been implicated in increased arrhythmia risk and ventricular tachycardia (VT) in the CRT population (24). A study of 57 consecutive patients undergoing CRT placement who had SPECT MPI reported that decreased global viability, as well as decreased local viability at the location of the LV lead had increased the risks of post-implantation VT (25). The utility of combining echocardiography with speckle tracking strain and nuclear SPECT imaging was evaluated in a randomized controlled trial of 182 patients (26). ...
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Cardiac electrophysiology procedures have evolved to provide improvement in morbidity and mortality for many patients. Cardiac resynchronization therapy (CRT), implantable cardioverter/defibrillator (ICD) placement and lead extraction procedures are proven procedures, associated with significant reductions in patient morbidity and mortality as well as improved quality of life. The applications and optimization of these therapies are an evolving field. The optimal use and outcomes of cardiac electrophysiology procedures require a multidisciplinary approach to patient selection, device selection, and procedural planning. Cardiac imaging using echocardiography plays a key role in selection of patients for CRT therapy, for guidance of left ventricular (LV) lead placement, and for optimization of atrioventricular pacing delays in patients with CRT. Cardiac computed tomography (CT) is an important tool in assessment of lead perforation, as well as assessing risk of lead extraction and procedural planning. Cardiac magnetic resonance imaging (MRI) is an important adjunct to transthoracic echocardiography for patient selection and risk stratification for defibrillator therapy for multiple disease states including ischemic cardiomyopathy, hypertrophic cardiomyopathy, cardiac sarcoidosis, and arrhythmogenic right ventricular cardiomyopathy (ARVC). Cardiac positron emission tomography (PET) is a useful adjunct to the diagnosis of device infections as well as inflammatory conditions including cardiac sarcoidosis. Our review attempts to summarize the contemporary roles of multimodality imaging in CRT therapy, ICD therapy and lead extraction therapy.
... A high LV pacing threshold (PT) at resynchronization device implantation may be a contributing factor to the adverse CRT outcome and could indicate a regional myocardial scar [10]. In addition, our previous study demonstrated that lower regional viability in the vicinity of the LV lead pacing site could be associated with increased risk of malignant tachyarrhythmias [11]. ...
... On the other hand, in a study with ischemic CRT patients, regional scar and reversible ischemia adjacent to LV pacing site were independent predictors of HF hospitalization and death [8]. Furthermore, in our previous study we showed that lower regional LV viability could be associated with increased risk of malignant tachyarrhythmias [11]. In addition, a substudy of MADIT-CRT (multicentre automatic defibrillator implantation trial with cardiac resynchronization therapy) trial demonstrated that patients with anterior LV lead position and prior adjacent myocardial infarction had an increased risk of malignant arrhythmias [20]. ...
... Higher LVPT is an issue of substantial importance, not just in terms of increased battery drain and potentially diminished echocardiographic response [6][7][8]10], but also in view of the current controversy regarding the need of implantable defibrillator backup. Patients with increased scar burden should be considered for CRT-D as they could pose a higher risk of VA occurrence [9,11]. However, localization of scar requires specialized imaging techniques and personnel that may not be promptly available before CRT device implantation. ...
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... However, the effect of CRT on arrhythmia susceptibility has not been definitively established and data regarding the risk of ventricular arrhythmias (VA) with CRT has been limited and conflicting. Case reports have provided anecdotal evidence of CRT precipitating ventricular tachycardia [3,4]; moreover the presence of scarred myocardium has been associated with an increased risk of arrhythmia in CRT [5,6]. Multiple mechanisms have been proposed for this phenomenon. ...
... Multiple mechanisms have been proposed for this phenomenon. Epicardial pacing results in a reversal of the normal physiologic myocardial activation sequence, which prolongs the QT interval and produces a substrate and the trigger for reentrant arrhythmias in both canine and human subjects [5,7]. The CRT non-responders also experience an increase in ventricular arrhythmia burden [8]. ...
... Diminishing of intraventricular conduction delay, and prevention of pause-dependent tachyarrhythmias, as seen with CRT, may contribute to this phenomenon as well [18]. All these effects could be dependent on LV location [19] and proximity to the scar [5]. Neither the LV lead position, the pacing polarity nor LV lead sensed voltage (a surrogate of scar proximity) affected the change in VA in our population. ...
... Furthermore, it has been shown to increase the risk for ventricular arrhythmias. 20 Therefore, as computer simulations suggest, the optimal LV lead position should be a compromise between a position distant from the scar and from the septum, 21 while the concept of early activation for potential scar unloading remains to be demonstrated in vivo. ...
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