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Dive into the research topics where Elias Sevaptsidis is active.

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Featured researches published by Elias Sevaptsidis.


Pacing and Clinical Electrophysiology | 1991

A Three-Dimensional Display for Cardiac Activation Mapping

Stephane Masse; Elias Sevaptsidis; Ian Parson; Eugene Downar

A three‐dimensional display is described that allows activation sequences from the epicardium and endocardium to be shown simultaneously on the same image. Three electrode arrays (epicardial sock, left ventricular balloon, right ventricular balloon) are represented in a three‐dimensional perspective by an array of dots that are intensified when activated. This arrangement requires fewer calculations and is easier to interpret than siiced‐isochronal maps but cannot represent a complete heart cycle in one image. The three‐dimensional display eliminates the distortion caused by two‐dimensional diagrams and facilitates activation correlation between electrode arrays. A standard, low cost microcomputer has been used to implement the activation display.


Pacing and Clinical Electrophysiology | 1996

A comparison of unipolar and bipolar electrodes during cardiac mapping studies.

S. Kimber; Eugene Downar; Stephane Masse; Elias Sevaptsidis; Tom W. W. Chen; Lynda L. Mickleborough; Ian Parsons

Controversy exists as to whether the unipolar or bipolar electrode configuration is superior in detecting local activations during cardiac mapping studies. However, the strengths and weaknesses of each mode suggest that they may provide complementary information. To examine therelative merits of unipolar and bipolar electrode configurations, recordings by each were simultaneously acquired during episodes of ventricular tachycardia in eight consecutive patients undergoing map guided arrhythmia surgery. Unipolar electrograms were classified as either unambiguous or ambiguous according to whether or not they were polyphasic in nature. The activation times from the unambiguous electrograms were compared with activation times from the corresponding bipolar signals where local activation was measured both at the signals peak amplitude (BI‐PK), and at the point at which the waveforms first major, rapid transient crossed baseline (BI‐TRN). Occurrences of discrete diastolic activations were also quantified from the unipolar and bipolar tracings. From a total of 415 unipolar electrograms, 301 unambiguous signals were identified as suitable for comparison with the bipolar signals. Both BI‐PK and BI‐TRN criteria for the determination of local activation were highly correlated with and not significantly different from the local activation from the unipolar electrogram. From 85 ambiguous unipolar electrograms, it was possible to determine local activation from the corresponding bipolar signal in 33% of the occurrences. From the eight patients, 64 diastolic potentials were recorded of which 42 were seen only in bipolar mode, 7 in only unipolar mode, and 15 were evident in both tracings. The prevalence of diastolic potentials was significantly greater in recordings made using bipolar mode. The results demonstrate that complementary information regarding local activations and diastolic potentials can be derived from unipolar and bipolar recordings and suggest that both electrode configurations should be used in multichannel cardiac mapping systems.


IEEE Transactions on Biomedical Engineering | 2009

Spatiotemporal Frequency Analysis of Ventricular Fibrillation in Explanted Human Hearts

Karthikeyan Umapathy; Stephane Masse; Elias Sevaptsidis; John Asta; Sridhar Sri Krishnan; Kumaraswamy Nanthakumar

Ventricular fibrillation (VF) is a medical condition that occurs due to rapid and irregular electrical activity of heart. If undiagnosed or untreated, VF leads to sudden cardiac death. VF has been studied by researchers for over 100 years to elucidate the mechanism that maintains VF, and thus to arrive at therapeutic options. VF is a nonstationary process, and it manifests into variations in the waveform morphology, phase, and frequency dynamics of the surface electrograms. Dominant frequency analysis (DF maps) and phase maps are two widely used complementary approaches in assessing the evolution of VF process. These techniques are applied to electrograms or fluorescence signals obtained with voltage-sensitive dyes. In spite of VF being a nonstationary process, most of the existing literature limits frequency analysis to a segmented, time-averaged spectral analysis, where valuable information on the instantaneous temporal evolution of the spectral characteristics is lost. In order to resolve this issue, in this paper, we present a joint time-frequency approach that is suited for VF analysis and demonstrate the application of instantaneous mean frequency (IMF) in interpreting VF episodes. Human VF sources are rarely anatomically stable and are migratory. Traditional DF techniques fail in tracking this migratory behavior. IMF, on the other hand, can deal with these migratory sources and conduction blocks better than DF approaches. Results of the analysis using the electrograms of 204 VF segments obtained from 13 isolated human hearts (explanted during cardiac transplantation) indicate that in 81% of the VF segments, there were significant changes in the spatiotemporal evolution of the frequency, suggesting that IMF provides better mechanistic insight of these signals. The IMF tool presented in this paper demonstrates potential for applications in tracking frequency patterns, conduction blocks, and arriving at newer therapies to modulate VF.


Canadian Medical Association Journal | 2008

Cardiac stimulation with high voltage discharge from stun guns

Kumaraswamy Nanthakumar; Stephane Masse; Karthikeyan Umapathy; Paul Dorian; Elias Sevaptsidis; Menashe B. Waxman

The ability of an electrical discharge to stimulate the heart depends on the duration of the pulse, the voltage and the current density that reaches the heart. Stun guns deliver very short electrical pulses with minimal amount of current at high voltages. We discuss external stimulation of the heart by high voltage discharges and review studies that have evaluated the potential of stun guns to stimulate cardiac muscle. Despite theoretical analyses and animal studies which suggest that stun guns cannot and do not affect the heart, 3 independent investigators have shown cardiac stimulation by stun guns. Additional research studies involving people are needed to resolve the conflicting theoretical and experimental findings and to aid in the design of stun guns that are unable to stimulate the heart.


American Journal of Physiology-heart and Circulatory Physiology | 2009

Effect of global ischemia and reperfusion during ventricular fibrillation in myopathic human hearts

Stephane Masse; Talha Farid; Paul Dorian; Karthikeyan Umapathy; Krishnakumar Nair; John Asta; Heather J. Ross; Vivek Rao; Elias Sevaptsidis; Kumaraswamy Nanthakumar

The effect of lack of global coronary perfusion on myocardial activation rate, wavebreak, and its temporal progression during human ventricular fibrillation (VF) is not known. We tested the hypothesis that global myocardial ischemia decreases activation rate and spatiotemporal organization during VF in myopathic human hearts, while increasing wavebreak, and that a short duration of reperfusion can restore these spatiotemporal changes to baseline levels. The electrograms were acquired during VF in a human Langendorff model using global mapping consisting of two 112-electrode arrays placed on the epicardium and endocardium simultaneously. We found that global myocardial ischemia results in slowing of the global activation rate (combined endo and epi), from 4.89+/-0.04 Hz. to 3.60+/-0.04 Hz. during the 200 s of global ischemia (no coronary flow) (P<0.01) in eight myopathic hearts. Two minutes of reperfusion contributed to reversal of the slowing with activation rate value increasing close to VF onset (4.72+/-0.04 Hz). In addition, during the period of ischemia, an activation rate gradient between the endocardium (3.76+/-0.06 Hz) and epicardium (3.45+/-0.06 Hz) was observed (P<0.01). There was a concomitant difference in wavebreak index (that provides a normalized parameterization of phase singularities) between the epicardium (11.29+/-2.7) and endocardium (3.25+/-2.7) during the 200 s of ischemia (P=0.02). The activation rate, gradient, and wavebreak changes were reversed by short duration (2 min) of reperfusion. Global myocardial ischemia of 3 min leads to complex spatiotemporal changes during VF in myopathic human hearts; these changes can be reversed by a short duration of reperfusion.


Journal of Interventional Cardiac Electrophysiology | 1998

Characteristics of Local Electrograms with Diastolic Potentials: Identification of Different Components of Return Pathways in Ventricular Tachycardia

J. Saito; Eugene Downar; J. C. Doig; Stephane Masse; Elias Sevaptsidis; M.-H. Shi; T. C. K. Chen; S. Kimber; Louise Harris; Lynda L. Mickleborough

Background:Diastolic potentials are often sought as a possible site for catheter ablation in post-infarct ventricular tachycardia. However, delivery of energy at such sites is often unsuccessful. The purpose of this study was to determine the characteristics of local electrograms with diastolic potentials and to identify activation pattern which might indicate the critical portion of the return path of the ventricular tachycardia reentry circuit.Methods: In 17 patients with post-myocardial infarction ventricular tachycardia, 30 ventricular tachycardias were mapped with an 112 bipolar endocardial balloon at the time of surgery. Diastolic mapping of the return tract in ventricular tachycardia was performed. Four activation patterns were observed (15 figure 8 patterns, 2 circular patterns, 2 biregional patterns and 11 monoregional patterns). Of 3,360 local electrograms, 207 (6.2%) demonstrated a diastolic potential in ventricular tachycardia. They were classified into following four categories, based on the appearance and timing of the systolic component. Type A-1 electrogram: systolic activation was of low amplitude (<2 mV) and was prolonged (≤100 msec), but preceded the onset of the surface QRS in ventricular tachycardia. Type A-2 electrogram: systolic activation was of low amplitude, was prolonged, but followed the onset of the surface QRS. Type B electrogram: systolic electrogram was fractionated, but relatively normal amplitude (2.0–3.6 mV). Type C electrogram: systolic electrogram was almost normal.Results: Of all electrograms with diastolic potentials, three type A-1 electrograms (1.4%) were located at the exit of the return pathway, 11 type A-1 electrograms (5.3%) were located at the pre-exit site. No type A-1 was found at an entrance/bystander area. 21 type A-2 electrograms (10.1%) were at the pre-exit and 83 type A-2 electrograms (40.2%) were located at the entrance/bystander area, but such electrograms were never found at the exit site. 71 type B electrograms (34.3%) and 18 type C electrograms (8.7%) were located at the entrance/bystander area. To distinguish the type A-2 electrograms at the pre-exit site from those at the entrance/bystander area, the diastolic potential to QRS interval was measured. This interval at the pre-exit was significantly shorter than that at the entrance/bystander area (−47.2 ± 10.7 vs −96.3 ± 31.3 msec, p = 0.0001).Conclusion: Type A-1 electrograms indicated the exit or pre-exit site of return pathway. Type A-2 electrograms with diastolic potential to QRS interval <−50 msec indicated the pre-exit site. However, the other types of local electrograms with diastolic potential did not indicate the critical portion of the ventricular tachycardia circuit. These observations may be helpful during catheter mapping and ablation of patients with post-infarct ventricular tachycardia.Condensed Abstract. Diastolic potentials are often sought to direct catheter ablation in post-infarct ventricular tachycardia. We investigated the characteristics of local electrograms showing diastolic activity in an attempt to determine whether critical portions of the ventricular tachycardia circuit could be identified by a typical “signature.” In 17 patients with a remote myocardial infarction, 30 ventricular tachycardias were mapped with 112 bipolar endocardial balloon at the time of surgery. Diastolic potentials in association with low amplitude (<2 mV) and prolonged (≤100 msec) systolic electrograms preceding the onset of QRS were found at the exit site and pre-exit site of return pathway. A similar systolic electrogram occurring after QRS onset with a diastolic potential to QRS interval of <−50 msec was found at the pre-exit site. However, other local electrograms with diastolic activity were at sites remote from the exit or pre-exit of the return pathway. These observations may be helpful during catheter mapping and ablation in patients with ventricular tachycardia.


Pacing and Clinical Electrophysiology | 1992

Simultaneous Unipolar and Bipolar Recording of Cardiac Electrical Activity

Elias Sevaptsidis; Stephane Masse; Ian Parson; Eugene Downar; Shane Kimber

An analog mapping system using a true bipolar left ventricular balloon electrode array is described, which enables simultaneous unipolar and bipolar recordings. It is an adaptation of a previous clinical analog mapping system used in the investigation of ventricular arrhythmias. The bipolar balloon array consists of 112 electrode pairs, each having a 2‐mm separation. The signals from the electrodes are sensed in parallel by separate unipolar and bipolar amplifier units, which then drive a common multiplexer bus. The bipolar recording unit consists of high quality instrumentation amplifiers with adjustable gain and exhibits a full bandwidth minimum common mode rejection of 78 dB. Using this combination, it is possible to record local cardiac micropotentials while still retaining the advantages of unipolar electrograms to track overall cardiac activation.


American Journal of Physiology-heart and Circulatory Physiology | 2012

Studying semblances of a true killer: experimental model of human ventricular fibrillation

Krishnakumar Nair; Talha Farid; Stephane Masse; Karthikeyan Umapathy; Sheila Watkins; Kwaku Poku; John Asta; M. Kusha; Elias Sevaptsidis; Jeku Jacob; John S. Floras; Kumaraswamy Nanthakumar

It is unknown whether ventricular fibrillation (VF) studied in experimental models represents in vivo human VF. First, we examined closed chest in vivo VF induced at defibrillation threshold testing (DFT) in four patients with ischemic cardiomyopathy pretransplantation. We examined VF in these same four hearts in an ex vivo human Langendorff posttransplantation. VF from DFT was compared with VF from the electrodes from a similar region in the right ventricular endocardium in the Langendorff using two parameters: the scale distribution width (extracted from continuous wavelet transform) and VF mean cycle length (CL). In a second substudy group where multielectrode phase mapping could be performed, we examined early VF intraoperatively (in vivo open chest condition) in three patients with left ventricular cardiomyopathy. We investigated early VF in the hearts of three patients in an ex vivo Langendorff and compared findings with intraoperative VF using two metrics: dominant frequency (DF) assessed by the Welch periodogram and the number of phase singularities (lasting >480 ms). Wavelet analysis (P = 0.9) and VF CL were similar between the Langendorff and the DFT groups (225 ± 13, 218 ± 24 ms; P = 0.9), indicating that wave characteristics and activation rate of VF was comparable between the two models. Intraoperative DF was slower but comparable with the Langendorff DF over the endocardium (4.6 ± 0.1, 5.0 ± 0.4 Hz; P = 0.9) and the epicardium (4.5 ± 0.2, 5.2 ± 0.4 Hz; P = 0.9). Endocardial phase singularity number (9.6 ± 5, 12.1 ± 1; P = 0.6) was lesser in number but comparable between in vivo and ex vivo VF. VF dynamics in the limited experimental human studies approximates human in vivo VF.


international conference of the ieee engineering in medicine and biology society | 2013

Analysis of reliability metrics and quality enhancement measures in current density imaging

Farbod Hosseyndoust Foomany; M. Beheshti; Karl Magtibay; Stephane Masse; Warren D. Foltz; Elias Sevaptsidis; Patrick F.H. Lai; David A. Jaffray; Sridhar Sri Krishnan; Kumaraswamy Nanthakumar; Karthikeyan Umapathy

Low frequency current density imaging (LFCDI) is a magnetic resonance imaging (MRI) technique which enables calculation of current pathways within the medium of study. The induced current produces a magnetic flux which presents itself in phase images obtained through MRI scanning. A class of LFCDI challenges arises from the subject rotation requirement, which calls for reliability analysis metrics and specific image registration techniques. In this study these challenges are formulated and in light of proposed discussions, the reliability analysis of calculation of current pathways in a designed phantom and a pig heart is presented. The current passed is measured with less than 5% error for phantom, using CDI method. It is shown that Gausss law for magnetism can be treated as reliability metric in matching the images in two orientations. For the phantom and pig heart the usefulness of image registration for mitigation of rotation errors is demonstrated. The reliability metric provides a good representation of the degree of correspondence between images in two orientations for phantom and pig heart. In our CDI experiments this metric produced values of 95% and 26%, for phantom, and 88% and 75% for pig heart, for mismatch rotations of 0 and 20 degrees respectively.


international conference of the ieee engineering in medicine and biology society | 2001

Electro-anatomical four-dimensional mapping of ventricular tachycardia

Dorin Panescu; Mansoon Nasir; Stephan Masse; Elias Sevaptsidis; Eugene Downar

The objectives of this study were: 1) to reconstruct the ventricular 3-D geometry by processing intracardiac echo (ICE) images, 2) to reconstruct the nesting position and orientation of the mapping catheters inside the ventricle, 3) integrate the geometrical information with the cardiac activity data recorded with the catheter and 4) to provide anatomic localization of electrical events during clinical ventricular tachycardia (VT). We employed commercially available 64-electrode mapping catheters, ICE equipment, a custom designed EP recording system and custom reconstruction software. In vitro, the positions of basket catheter electrodes were identified correctly. During clinical use, the basket electrode positions were not identified reliably by ICE. However, the nesting position of the basket was identified correctly. The custom software integrated the geometrical information and cardiac activity data off line, during the procedure. Electrical events occurring during VT were correctly displayed on the reconstructed geometry.

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Stephane Masse

University Health Network

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John Asta

Toronto General Hospital

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Eugene Downar

University Health Network

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Talha Farid

Toronto General Hospital

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Heather J. Ross

University Health Network

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