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Results for “Body Surface Potential Mapping”

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At least 253 records · Page 14Linked to original sources

PubMed2006

Atrial repolarization as observable during the PQ interval.

OBJECTIVE: We aimed to study the involvement of atrial repolarization in body surface potentials. METHODS: Electrocardiograms of healthy subjects were recorded using a 64-lead system. The data analysis focused on the PQ intervals while devoting special attention to the low-amplitude signals during the PQ segment: the segment from the end of the P wave until onset QRS. The data were analyzed by inspecting body surface potential maps and the XYZ signals of the vectorcardiogram. RESULTS: Standard P-wave features exhibited normal values. The local potential extremes were found at positions not sampled by the standard leads. The PQ segment was found to be not isoelectric, the time course of the potential distribution being very similar to that during the P wave but for a reversed polarity and about 3-fold lower magnitudes. CONCLUSION: The results demonstrate a significant involvement of atrial repolarization during the PQ interval and essentially discordant "atrial T waves," suggesting a small dispersion of atrial action potential durations.

Atrial Function↗

PubMed1999

Bioelectromagnetic localization of a pacing catheter in the heart.

The accuracy of localizing source currents within the human heart by non-invasive magneto- and electrocardiographic methods was investigated in 10 patients. A non-magnetic stimulation catheter inside the heart served as a reference current source. Biplane fluoroscopic imaging with lead ball markers was used to record the catheter position. Simultaneous multichannel magnetocardiographic (MCG) and body surface potential mapping (BSPM) recordings were performed during catheter pacing. Equivalent current dipole localizations were computed from MCG and BSPM data, employing standard and patient-specific boundary element torso models. Using individual models with the lungs included, the average MCG localization error was 7+/-3 mm, whereas the average BSPM localization error was 25+/-4 mm. In the simplified case of a single homogeneous standard torso model, an average error of 9+/-3 mm was obtained from MCG recordings. The MCG localization accuracies obtained in this study imply that the capability of multichannel MCG to locate dipolar sources is sufficient for clinical purposes, even without constructing individual torso models from x-ray or from magnetic resonance images.

Body Surface Potential Mapping↗

PubMedDate not supplied

[Multi-electrode mapping from thoracic surface in patients with Wolff-Parkinson-White syndrome].

Body surface potentials mapping is a new method of heart electric phenomena visualisation. Attempts of accessory conduction pathways localisation in 9 patients with overt and in 1 with concealed WPW syndrome are presented. In 4 pts the preexcitation with QRS complex > 120 ms was clearly seen, in next 4 individuals that symptom was less evident and in one case the retrograde conduction through the accessory pathway was hardly noticed. The isopotential maps allowed precise localisation of the accessory pathways ventricular insertion in all patients with QRS > 120 ms and in one with QRS < 120 ms. After successful dissection of accessory pathways, isopotential maps became normal. In patients with slight signs of preexcitation, noninvasive (transesophageal) or invasive atrial stimulation could improve the visibility of accessory pathways localisation.

Action Potentials↗

PubMed1994

Enhanced glucose oxidation in exercise-induced myocardial ischemia.

BACKGROUND: In animal models, dichloroacetate (DCA) facilitates recovery from severe myocardial ischemia by stimulating glucose oxidation. OBJECTIVE: To evaluate the acute efficacy of DCA as a metabolic anti-ischemic intervention in patients with coronary artery disease (CAD) and exercise-induced myocardial ischemia in a clinical trial. METHODS: Double-blind, randomized, crossover comparison of single dose (50 mg/kg intravenously) DCA versus placebo on clinical and electrocardiographic variables in seven patients with single vessel CAD and 34 patients with multiple vessel CAD during standard dynamic exercise testing. RESULTS: Blood pressure did not differ with placebo or DCA but mean heart rate was higher with DCA at rest (62 versus 59, P < 0.004) and at 5 mins of recovery (78 versus 75, P < 0.02). Exercise duration averaged 538 s with DCA and 534 s with placebo (not significant). Chest pain occurred in 14 patients in both tests, clinical ST depression occurred, in 34 placebo tests and 37 DCA tests (not significant). Body surface potential maps (BSPM) of the decrease in the area under the ST curve from rest to peak exercise averaged -5096 microV's with DCA and -5159 microV's with placebo (not significant). BSPM at 1 and 5 mins postexercise also showed no differences in rate of ST integral recovery. CONCLUSIONS: In the transient regional model of human myocardial ischemia induced by dynamic exercise, the acute administration of the pyruvate dehydrogenase agonist DCA was not associated with clinical or electrocardiographic moderation of, nor accelerated recovery from, ischemia. Whether DCA or metabolically similar agents that enhance oxidative metabolism are beneficial in other ischemic settings, such as the no-flow states of acute ST elevation myocardial infarction or angioplasty, requires further systematic evaluation.

Adult↗

PubMed2001

Electrocardiographic imaging: II. Effect of torso inhomogeneities on noninvasive reconstruction of epicardial potentials, electrograms, and isochrones.

INTRODUCTION: Noninvasive electrocardiographic imaging (ECGI) involves inverse reconstruction of epicardial potentials, electrograms (EGMs), and isochrones from body surface potential maps (BSPMs). The heart lies in a volume conductor that includes lungs, blood, bone, muscle, and fluid. We investigate the effects of these torso inhomogeneities on reconstructed epicardial potentials, EGMs, and isochrones to address the issue of whether they should be included in clinical ECGI methodology. METHODS AND RESULTS: Potential data were obtained for different pacing protocols from a dog heart suspended in a human-shaped torso tank. Accurate geometry of torso inhomogeneities was digitized from the Visual Human Project and appropriately introduced into a computer model of the torso. Three models were used: accurate inhomogeneous torso, homogeneous torso, and a torso with stylized lungs (to generate an approximate model). The inhomogeneous model was used to compute BSPMs from the measured epicardial potentials. These BSPMs were the starting point for inverse computations in the different torso models. Epicardial potential maps, EGMs, and isochrones were computed. The homogeneous model produced slightly less accurate epicardial potential reconstructions than the inhomogeneous model and stylized lung model, but epicardial potential patterns, EGMs, isochrones, and locations of pacing sites were reconstructed with comparable accuracy when torso inhomogeneities were ignored. CONCLUSION: The results demonstrate that, in the clinical application, it is not necessary to include torso inhomogeneities for noninvasive reconstructions of epicardial potentials, EGMs, and activation sequences.

Animals↗

PubMed2006

Body surface ECG signal shape dispersion.

The spatial distribution of the shape of the electrocardiography (ECG) waves obtained by body surface potential mapping (BSPM) is studied, using a 64-channel high-resolution ECG system. The index associated to each lead is the shape difference between its ECG wave and a reference computed taking into account all the leads on the same column. The reference is either a selected real wave or a synthetic signal computed by integral shape averaging (ISA). Better results are obtained with the ISA signal using the distribution function method (DFM) for computing the shape difference. The spatial dispersion of ECG waves is showed to allow the separation of patients after myocardial infarction (MI) from healthy subjects. In addition, the reference signal position for each column is computed. The path linking these positions appears as an invariant, i.e., it is independent of the subject and the ECG wave.

Algorithms↗

PubMed2003

Noninvasive imaging of cardiac transmembrane potentials within three-dimensional myocardium by means of a realistic geometry anisotropic heart model.

We have developed a new approach for imaging cardiac transmembrane potentials (TMPs) within the three-dimensional (3-D) myocardium by means of an anisotropic heart model. The cardiac TMP distribution is estimated from body surface electrocardiograms by minimizing objective functions of the "measured" body surface potential maps (BSPMs) and the heart-model-generated BSPMs. Computer simulation studies have been conducted to evaluate the present 3-D TMP imaging approach using pacing protocols. Simulations of single-site pacing at 24 sites throughout the ventricles, as well as dual-site pacing at 12 pairs of sites in the vicinity of atrio-ventricular ring were performed. The present simulation results show that the correlation coefficient (CC) and relative error (RE) between the "true" and inversely estimated TMP distributions were 0.9915 +/- 0.0041 and 0.1266 +/- 0.0326, for single-site pacing, and 0.9889 +/- 0.0034 and 0.1473 +/- 0.0237 for dual-site pacing, respectively, when 10 microV Gaussian white noise (GWN) was added to the BSPMs. The effects of heart and torso geometry uncertainty were also evaluated by shifting the heart position by 10 mm and altering the torso size by 10%. The CC between the "true" and inversely estimated TMP distributions was above 0.97 when these geometry uncertainties were considered. The present simulation results demonstrate the feasibility of noninvasive estimation of TMP distribution throughout the ventricles from body surface electrocardiographic measurements, and suggest that the present method may become a useful alternative in noninvasive imaging of distributed cardiac electrophysiological processes within the 3-D myocardium.

Body Surface Potential Mapping↗

PubMed1999

Paradoxical QRST integral changes with ventricular repolarization dispersion.

Body surface QRST integral (QRSTI) maps have been shown theoretically to reflect disparity of intrinsic repolarization properties and have been experimentally linked to increased arrhythmia susceptibility. Paradoxically, a lower magnitude of QRSTI in patients with heart disease and at risk for arrhythmias has been reported. We hypothesized that this paradoxical reduction in QRST magnitude is a consequence of increased heterogeneity of repolarization gradients in normal hearts. We generated QRSTI using a previously published heart model to compare QRSTI for aligned and random repolarization gradients. The heart model consisted of 50,000 cubic units in an anatomically correct arrangement that included parameters to simulate anisotropic conduction and inhomogeneous distribution of refractoriness. Body surface potential maps (BSPMs) were generated on a torso surface assuming a homogeneous torso and using the boundary element method for normal alignment of repolarization gradients and spatially reassigned repolarization values that randomized repolarization directions. QT duration was measured by the subtraction of Q onset time from T offset time on the BSPM. T offset was defined as the last potential to be detected at intervals of 3 ms that was above the threshold of 0.1 mV during recovery. The time of T offset showed a consistent tendency to shift to the left posterior and to split. When slow conduction velocities were assigned, BSPMs showed delayed propagation and multiple extrema. QRSTI showed systematic magnitude decrease with increasing randomness of repolarization gradient direction. Ventricular fibrillation (VF) could be induced by successive extrastimuli under the conditions of over 70% deviation and slow conduction of 0.5 m/s for the longitudinal direction. In conclusion, a possible explanation for the paradoxical reduction in QRSTI in the presence of constant repolarization disparity is the change in alignment of repolarization gradients.

Body Surface Potential Mapping↗

PubMed2003

Plasma levels of dosulepine and heart electric field.

Antidepressants, particularly tricyclic (TCA) antidepressants, may have cardiotoxic effects, such as cardiac arrhythmias, especially in patients with cardiovascular diseases. For most of TCA, no exact correlation between dosage, plasma levels and changes of ECG parameters of standard ECG has been found. So far, no relationship between dosulepine plasma levels and heart electric field parameters has been studied. We selected 18 female outpatient subjects diagnosed with recurrent depressive disorders, currently in the remission phase (HAMD < 10), without any cardiovascular disease. Patients were treated with daily dosulepine doses of 25-125 mg for 4-8 weeks. 30 heart electric field parameters were analyzed by Cardiag 128.1 diagnostic system as part of BSPM (Body Surface Potential Mapping). Acquired data were correlated with dosulepine plasma levels by means of Spearman's rank order correlation test. Four ECG parameters showed a significant correlation with dosulepine plasma levels: QRS axis deviation in frontal plane (p=0.01), DIAM 40 max (p<0.05), QRS-STT angle in transversal and left sagittal plane (p<0.05). The demonstrated changes confirmed dosulepine influence on the early myocardium depolarization phase and the correlation of this effect with dosulepine dose (its plasma concentration). The higher the dosulepine level, the more marked are the changes of the QRS-STT angle in transversal and sagittal planes and the changes in the QRS axis deviation in frontal plane. Repeatedly recorded changes in the heart electric field were dosulepine-specific and dependent on its plasma levels.

Adult↗

PubMed2006

Cardiac anisotropy: is it negligible regarding noninvasive activation time imaging?

The aim of this study was to quantify the effect of cardiac anisotropy in the activation-based inverse problem of electrocardiography. Differences of the patterns of simulated body surface potential maps for isotropic and anisotropic conditions were investigated with regard to activation time (AT) imaging of ventricular depolarization. AT maps were estimated by solving the nonlinear inverse ill-posed problem employing spatio-temporal regularization. Four different reference AT maps (sinus rhythm, right-ventricular and septal pacing, accessory pathway) were calculated with a bidomain theory based anisotropic finite-element heart model in combination with a cellular automaton. In this heart model a realistic fiber architecture and conduction system was implemented. Although the anisotropy has some effects on forward solutions, effects on inverse solutions are small indicating that cardiac anisotropy might be negligible for some clinical applications (e.g., imaging of focal events) of our AT imaging approach. The main characteristic events of the AT maps were estimated despite neglected electrical anisotropy in the inverse formulation. The worst correlation coefficient of the estimated AT maps was 0.810 in case of sinus rhythm. However, all characteristic events of the activation pattern were found. The results of this study confirm our clinical validation studies of noninvasive AT imaging in which cardiac anisotropy was neglected.

Action Potentials↗

PubMed1996

[Can permanent sinus arrhythmia in conscious dogs be suppressed with anesthesia?].

OBJECTIVE: Large prospective studies in dogs with healed myocardial infarction (MI) recently show a positive relation between heart rate variability (HRV) and sudden cardiac death. METHODS: We have done similar experiments in dogs and we studied HRV, ECG and body surface potential maps (BSPM) in 26 normal mongrel dogs (10-15 kg) and 12 dogs with an experimental MI (ligation of LAD). A two-channel 8 hours lasting ECG recording was performed in all conscious dogs. The 2nd recording was done in Penthobarbital anaesthesia (30 mg/kg). RESULTS: We have found sinus arrhythmia (SA) in all 26 conscious dogs. The anaesthesia suppressed the sinus arrhythmia and HRV via compensatory tachycardia and alterations in baroreflexes. The suppression of arrhythmia was also present in dogs with myocardial infarction. CONCLUSIONS: It is suggested, that HRV and SA in dogs depend on conscious state and anaesthesia. On the basis of our results we can anticipate that the most important for HRV is the present status of the sympathetic nerve. We suggest, that our results are an important finding for experimental arrhythmology. (Fig. 4, Ref. 24.)

Anesthesia↗

PubMed1999

Changes in autonomic activity and ventricular repolarization.

An increase in sympathetic activity, manifested by shortening of RR intervals (RRi) and changes in RRi variability, precedes and possibly triggers ventricular tachyarrhythmias (VTAs) by altering repolarization. We examined the effects of autonomic activity on the projection of repolarization as detected by body surface potential maps (BSPMs). We recorded 32 lead/192-point BSPMs during passive head-up tilt, tilt + infusion of isoproterenol, rapid atrial pacing, and atrial pacing + infusion of isoproterenol. Changes in QT; recovery time; activation-recovery interval (ARi); T-wave amplitude; and QT, QRST, and ST integrals and their dispersion were analyzed. Autonomic effects on sinus node were inferred from the Fourier transform-derived low and high frequency powers of RRi variability. Patients were divided into those with (SHD) and without structural heart disease (NSHD). Heart rate increased, whereas QT interval and ARi declined with tilt in both groups. RRi variability indices of sympathetic activity increased in NSHD but did not change in SHD. T-wave amplitudes declined in NSHD but did not change in SHD, suggesting altered responsiveness of ventricular repolarization to autonomic stimulation. Tilt and rapid atrial pacing during infusion of isoproterenol resulted in a paradoxical increase in T-wave amplitudes in some patients, similar to that observed before the onset of spontaneous arrhythmias. We conclude that altering autonomic activity by head-up tilt and/or infusion of sympathomimetic agents results in significant changes in the body surface projection of cardiac repolarization, which differ in patients with SHD from those without SHD. Similar paradoxical changes in the T-wave amplitude have been observed before the onset of spontaneous VTA, suggesting that abnormal response of repolarization to autonomic stimulation predisposes to arrhythmogenesis.

Adult↗

PubMed1997

The ventricular gradient and altered ventricular activation patterns.

The ventricular gradient vector was determined in normal persons and in cases with left and right bundle branch block (BBB) by means of the best fit method from body surface potential mapping data. Similar measurements were also made in cases with artificial ventricular pacing and the G vector during sinus rhythm was compared with that of the paced beats. Results indicated that the magnitude of the G vector in cases with BBB was smaller than in normal persons. The directional change in the G vector was found to be along the direction of the QRS change in the majority of cases with left BBB. In right BBB, the direction of the G change was variable but the angle between the QRS change was less than 90 degrees on average. Following right ventricular pacing a small increase of the G magnitude was observed acutely, which was opposite in direction to the QRS change. Possible mechanisms are discussed. The G changes in left and right BBB are considered to be based on certain chronic processes, different from those involved in the acute immediate effect of altered activation.

Adult↗

PubMed2006

Noninvasive reconstruction of three-dimensional ventricular activation sequence from the inverse solution of distributed equivalent current density.

We propose a new electrocardiographic (ECG) inverse approach for imaging the three-dimensional (3-D) ventricular activation sequence based on the modeling and estimation of the equivalent current density throughout the entire volume of the ventricular myocardium. The spatio-temporal coherence of the ventricular excitation process has been utilized to derive the activation time from the estimated time course of the equivalent current density. In the present study, we explored four different linear inverse algorithms (the minimum norm and weighted minimum norm estimates in combination with two regularization schemes: the instant-by-instant regularization and the isotropy method) to estimate the current density at each time instant during the ventricular depolarization. The activation time at any given location within the ventricular myocardium was determined as the time point with the occurrence of the maximum local current density estimate. Computer simulations were performed to evaluate this approach using single- and dual-site pacing protocols in a physiologically realistic cellular automaton heart model. The performance and stability of the proposed approach was evaluated with respect to the various levels of measurement noise (0, 5, 10, 20, 40, and 60 microV), the various numbers of ECG electrodes and the modeling errors on the torso geometry and heart position. The simulation results demonstrate that: 1) the single-site paced 3-D activation sequence can be well reconstructed from 200-channel body surface potential maps with additive Gaussian white noise of 20 microV (correlation coefficient = 0.90, relative error = 0.19, and localization error = 5.49 mm); 2) a higher imaging accuracy can be obtained when the activation is initiated from the left/right ventricle (LV/RV) compared to from the septum; 3) the isotropy method gives rise to a better performance than the conventional instant-by-instant regularization; 4) a decreased imaging accuracy results from a larger noise level, a fewer number of electrodes, or the volume conductor modeling errors; however, a reasonable imaging accuracy can still be obtained with a 60 microV noise level, 64 electrodes, or mild errors on both the torso geometry and heart position, respectively; 5) the dual-site paced 3-D activation sequence can be imaged when the two sites are paced either simultaneously or with a time delay of 20 ms; 6) two pacing sites can be resolved and localized in the imaged 3-D activation sequence when they are located at the contralateral sides of ventricles or at the ventricular lateral wall and the apex, respectively.

Body Surface Potential Mapping↗

PubMed2001

Current-density estimation of exercise-induced ischemia in patients with multivessel coronary artery disease.

Magnetocardiographic and body surface potential mapping data measured in 6 patients with multivessel coronary artery disease were used in equivalent current-density estimation (CDE). Patient-specific boundary-element torso models were acquired from magnetic resonance images. Positron emission tomography data registrated with anatomical magnetic resonance imaging data provided the gold standard. Discrete current-density estimation values were computed on the epicardial surface of the left ventricle from difference (stress-rest) ST-segment maps. The ill-posed inverse problem was regularized with 3 different methods (Tikhonov regularization with an identity or a surface Laplacian operator and a maximum a posteriori estimator). Comparisons with positron emission tomography studies showed that the maximum a posteriori estimator is superior to other regularizations, provided that a suitable a priori information is available. In general, good correspondence was found for segments of high and low amplitude in current-density estimations, and the viable and scar areas in positron emission tomography, respectively.

Body Surface Potential Mapping↗

PubMed2005

Spatial repolarization abnormalities in old myocardial infarction.

Conventional electrocardiogram criteria for myocardial infarction (MI) rely on QRS features, but ST-T segment is also affected. We recorded body surface potential mapping in 24 patients with prior MI and in 24 controls. T-wave maximum amplitude and QRS and ST-T integrals were automatically determined. Old MI was verified by magnetic resonance imaging. ST-T integral and T-wave maximum amplitude outperformed QRS integral in detecting MI, with area under receiver operating characteristic curve of 94%, 95%, and 83%, respectively. ST-T integral performed better in non-Q-wave than Q-wave MI, with area under receiver operating characteristic curve of 97% and 92%, respectively. QRS integral correlated negatively with ST-T integral in patients with MI (r = -0.58, P < .001) and positively in controls (r = 0.45, P < .001). In conclusion, ST-T integral proved equal to QRS integral in old MI detection. Inclusion of ventricular repolarization phase and development of electrocardiographic analysis over larger chest area may improve the QRS-based diagnosis of old myocardial infarction.

Adult↗

PubMed2002

Direct mechanical stimulation of brainstem modulates cardiac rhythm and repolarization in humans.

Natural mechanical stimulation of the brainstem area by the blood pressure waves propagating in the adjacent arteries plays an important role in the homeostasis of the brainstem centers of cardiovascular control. However, effects of direct mechanical stimulation of this area on the cardiac elecrophysiology have never been studied in humans. In 12 patients (age: 54 +/- 13 years, 5 females) undergoing microvascular decompression, the left (9 patients) or the right (3 patients) side of the ventro-lateral surface of the medulla oblongata was exposed during the surgery, and a mechanical stimulation (duration: 1 min, frequency: 1-2 Hz) of the roots of the cranial nerves and the surface of the brainstem was performed at 3-7 sites using a 2-mm metallic ball. Spatial changes in cardiac repolarization were examined using the 32-lead/192 site electrocardiographic body surface potential maps. Blood pressure was monitored using intra-arterial line. The intervals between the onset of the Q-wave and the offset of the T-wave (QTe) and between the onset of the Q-wave and the peak of the T-wave (QTp), the activation-recovery intervals (ARi), the peak T-wave amplitude, and the QRS and STT integrals were measured using custom software. During the stimulation between the caudal rootlets of the 10th nerve, the peak T-wave amplitude decreased 22% (range: 6-50%) and RR-intervals decreased from 923 +/- 190 to 794 +/- 111 ms compared to the recordings obtained before the stimulation (P =.025 and.063, respectively), whereas QTe, QTp, Ari, and the QRS- and the STT-integrals did not change. Decreased T-wave amplitudes and unchanged QT-intervals suggest that brainstem stimulation might evoke spatially inhomogenious repolarization changes. Stimulation of a localized region surrounding the caudal rootlets of the 10th nerve elicits pronounced effects on cardiac rhythm and repolarization.

Blood Pressure↗

PubMed2002

The effect of volume currents due to myocardial anisotropy on body surface potentials.

Changes in anterior and posterior body surface potential maps (BSPMs) due to myocardial anisotropy were examined using a highly heterogeneous finite element model of an adult male subject constructed from segmented magnetic resonance images. A total of 23 different tissue types were identified in the whole torso. The myocardial fibre orientations in the human heart wall were mapped from the fibre orientations of a canine heart which are available in the literature using deformable mapping techniques. The current and potential distributions in the whole torso were computed using dipolar sources in the septum, apical area, left ventricular wall or right ventricular wall. For each dipole x, y, z orientations were studied. An adaptive finite element solver was used to compute currents and potential distributions in the whole torso with an element size of 0.78 x 0.78 x 3 mm in the myocardium and larger elements in other parts of the torso. For each dipole position two cases were studied. In one case the myocardium was isotropic and in the other it was anisotropic. It was found that BSPMs showed a very notable difference between the isotropic and the anisotropic myocardium for all dipole positions with the largest difference for the apical dipoles. The correlation coefficients for the BSPMs between the isotropic and anisotropic cases ranged from 0.83 for an apical dipole to 0.99 for an RV wall dipole. These results suggest that myocardial fibre anisotropy plays an important role in determining the body surface potentials.

Adult↗