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R S MacLeod

Publications and source records attributed to R S MacLeod.

34 records · Page 2Linked to original sources

Temporal and spatial analysis of potential maps via multiresolution decompositions.

Cardiac potentials recorded on the epicardium or the body surface by an array of electrodes are usually analyzed either as spatial distributions or temporal waveforms. Thus, the analysis often involves temporal descriptors (eg. max dV/dt) or spatial descriptors (eg. location of local extrema) only. The best known transform technique that has been applied to these data that combines both spatial and temporal characteristics is the Karhunen-Loeve transform, a global transform applied to temporal and/or spatial bases obtained by statistical analysis of a database. As an alternative, multiresolution decompositions and related wavelet-type transforms have recently seen great development in signal processing and related fields. They offer flexibility, employing transformations onto local (rather than global) and fixed (rather than data-dependent) databases, and allow transformation of distributions, waveforms, or both, as desired. The utility of this method as applied to temporal and spatial segmentation and analysis of map data from both epicardial plaques and body surface potentials recorded during percutaneous transluminal coronary angioplasty is illustrated.

Body Surface Potential Mapping↗

Evaluation of novel measurement methods for detecting heterogeneous repolarization.

There exists a well-documented link between heterogeneity of cardiac recovery characteristics and vulnerability to arrhythmia; however, electrocardiographic detection of this heterogeneity remains problematic. The only modalities suitable for measuring variation of repolarization are electrophysiologic in nature, with action potential duration in single cells the most direct method and QT intervals from the body surface electrocardiogram the most common clinical approach. The authors have shown previously, however, that the QT interval is a poor measure of regional change in repolarization, especially when shortening occurs. Here, the authors discuss an experimental preparation based on an isolated canine heart suspended in a human-shaped, instrumented, electrolytic tank and describe a method of applying cold to create local, transient changes in recovery characteristics. The authors have simultaneously recorded epicardial and torso tank surface potentials before, during, and after intervention, and from them have generated isopotential and isointegral maps and computed activation-recovery intervals (ARIs). In all cases, epicardial potentials revealed changes in recovery associated with localized heating and cooling. The changes were visible from tank surface potential distributions in some, but not all, cases. The results also suggest that epicardial ARIs are sensitive to changes in recovery and that, at least for a subset of tank surface leads, ARIs can be used to create noninvasive indices of disparity of repolarization characteristics.

Animals↗

Estimating ECG distributions from small numbers of leads.

The utility of body surface potential mapping to improve interpretation of electrocardiographic information lies in the presentation of thoracic surface distributions to characterize underlying electrophysiology less ambiguously than that afforded by conventional electrocardiography. Localized cardiac disease or abnormal electrophysiology presents itself electrocardiographically on the body surface in a manner in which pattern plays an important role for identifying or characterizing these abnormalities. Thus, in myocardial infarction, transient myocardial ischemia, Wolff-Parkinson-White syndrome, or ventricular ectopy, observation of electrocardiographic potential patterns, their extrema, and their magnitudes permits localization and quantization of the abnormal activity. Conventional electrocardiography assesses pattern information incompletely and does not use information of distribution extrema locations or magnitudes. Thus, increases or decreases in the magnitudes of electrocardiographic features (ST-segment potential displacement, amplitude, or morphology of Q, R, S, or T waves) associated with changes in cardiac sources (ischemia, infarction, conduction abnormalities, etc.) as measured from fixed leads have a high likelihood of being misinterpreted if the distribution itself is changing. In this study, the authors demonstrate the utility of estimating distributions from small numbers of optimally selected leads, including conventional leads, to reduce uncertainty in the interpretation of electrocardiographic information. This issue is highly relevant when thresholds are used to detect significance of potential levels (exercise testing, detection of myocardial infarction, and continuous monitoring to assess ST-segment changes). Significance of this work lies in improved detection and characterization of abnormal electrophysiology using conventional or enhanced leadsets and methods to estimate thoracic potential distributions.

Angioplasty, Balloon, Coronary↗

Errors in ECG parameter estimation from standard leadsets.

With the availability of low-cost, high-speed computers with (relatively) vast amounts of storage has come something of an explosion in the application of "quantitative electrocardiography." A search of the Medline medical reference database on the subject string "quantitative AND electrocardiography" reveals no less than 509 citations, suggesting that the term has gained widespread acceptance. However, while quantitative techniques are, in general, to be welcomed to clinical medicine and research, their use as a diagnostic or patient monitoring tool begs a careful examination of just what is being counted and how it is being linked to physiology. In this study, the authors focus on the use of standard electrocardiographic lead systems as the basis for quantitative patient evaluation and attempt to highlight some limitations in the ability to extract meaningful parameters with such a limited sampling of human thoracic electrical activity.

Angioplasty, Balloon, Coronary↗

Map representation and diagnostic performance of the standard 12-lead ECG.

The diagnostic information contained in the standard 12-lead electrocardiogram was assessed by comparing the classification results produced by the standard leads for various clinical settings, such as normal versus myocardial infarction or versus left ventricular hypertrophy to those achieved by 120-lead data or body surface potential maps (BSPMs). Separately, optimal signal leads were extracted from the BSPM by ranking all leads in function of their capability of reconstructing the BSPM. Ranking was achieved by deriving eigenvalues from the covariance matrix calculated from all leads and corresponding measurements. Thus, while comparing the results from the standard leads (diagnostic leads) to those from the original raw map data, a comparison was also performed with respect to the best signal leads, namely the four best and the eight best. From the results observed for all bi- and multigroup classifications, it appeared that the diagnostic yield of the 12 standard leads matched those obtained with a number of signal leads lying between 4 and 8. This indicated that a large overlap still existed between the leads composing the 12-lead ECG (in fact, only 8 independent leads). Another interesting observation resulted from this investigation: although classifiers (discriminating variables) used for classification were identical, whether they originated from the raw standard leads (derived from the raw maps) or from standard leads reconstructed with four or eight signal leads, reconstructed measurements performed better than original measurements. This paradox can be explained by looking at the respective F values. Indeed, since increased F values result from higher ratios between the difference of group means and the composite variance from the pooled groups, higher differences and/or smaller variances produce larger ratios and hence, better group separations.

Body Surface Potential Mapping↗

Application of an electrocardiographic inverse solution to localize ischemia during coronary angioplasty.

Localization of Ischemia. This study demonstrates the utility of an electrocardiographic inverse solution, coupled with body surface potential mapping (BSPM), in localizing acute ischemia in patients undergoing percutaneous transluminal coronary angioplasty (PTCA). PTCA balloon inflations produce complete occlusion and acute transient ischemia, which can be detected electrocardiographically with BSPM. Comparisons between maps recorded both during and before the inflation of the PTCA balloon allow patient- and artery-specific characterizations of the resulting ischemia. Knowledge of the patient's coronary anatomy and the location of the occlusion site by coronary angiography permit an estimation based on cardiac hemodynamics of the region of myocardium most likely to suffer from PTCA-induced ischemia. Electrocardiographic inverse solutions provide a means of predicting cardiac potentials from body surface maps. In this study, we describe an inverse solution we have developed to localize the transient ischemia produced by PTCA. To validate the procedure, we compared the locations of predicted ischemia in seven patients with a qualitative estimate of the perfusion region based on fluoroscopic examination of each patient's coronary anatomy and PTCA balloon location. In each case, the region of ischemia predicted by the model included the perfusion zone determined fluoroscopically. These results suggest that electrical changes induced by acute ischemia can be localized with an electrocardiographic inverse solution.

Angioplasty, Balloon, Coronary↗

Analysis of PTCA-induced ischemia using an ECG inverse solution or the wavelet transform.

In patients without significant collaterals, percutaneous transluminal coronary angioplasty (PTCA) produces acute transient ischemia that is detectable in both standard electrocardiograms (ECG) and body surface potential maps (BSPMs). Control recordings made before or between inflations provide personalized baselines, which isolate the effects of ischemia from interpatient differences, such as torso shape and electrode location. In this study, two methods of evaluating PTCA-induced ischemia from BSPM recordings are presented. In the first method, an ECG inverse solution that estimates epicardial potentials from body surface signals using a realistic model of torso geometry is applied. The strength of this method lies in its potential ability to localize areas of cardiac ischemia on the epicardial surface. In the second approach, wavelet transforms were used to perform a multiresolution decomposition of the BSPM data into different frequency bands. The basis functions of the wavelet transform are time-limited and narrow band and hence can be expected to be sensitive to features of the BSPM that originate in discrete electrophysiologic events, such as intrusion of the activation front onto regions of ischemia or arrhythmias due to local conduction abnormalities. The method also offers a means of temporal and frequency localization of cardiac events related to the initiation of injury currents and abnormal conduction due to PTCA-induced ischemia. The inverse solution and the wavelet transform each offer new views of the spatial and temporal courses of acute ischemia potentially leading to new diagnostic insights in ECG patient examination.

Angioplasty, Balloon, Coronary↗

Assessment of spatial and temporal characteristics of ventricular repolarization.

Measurement of dynamics and spatial characteristics of ventricular repolarization is of interest in assessing patients with ischemic heart disease, particularly in relation to the detection and characterization of ischemic events, identification of patients at risk of ventricular arrhythmias, or determination of the efficacy of drugs intended to alter repolarization. The QT interval (QTI) has been the index of choice for assessing repolarization abnormalities. It is a general measure of repolarization duration but lacks the power to assess the spatial aspects of repolarization and the ability to detect localized shortening in the setting of global prolongation. For direct cardiac surface measurement, QRST integrals and activation recovery intervals (ARIs) were used to assess repolarization and its disparity. The use of similar measurements from the body surface was proposed to provide better characterization of repolarization, its disparity, and its dynamics than is possible using the QTI. In one open-chest experiment using an intact canine heart and two experiments using isolated canine hearts suspended in a torso-shaped electrolytic tank, 64 epicardial electrograms and 192 torso surface electrocardiograms were measured simultaneously. Ventricular repolarization was globally altered by varying pacing cycle lengths or tank temperature. Atrial and ventricular pacing were used to assess sensitivity of repolarization indices to activation sequence. At the cardiac surface, (1) QTI tracks global repolarization changes but is affected by activation sequence and insensitive to localized shortening of repolarization; (2) distribution of QRST integrals reflects disparity of repolarization and is largely independent of activation sequence; and (3) ARI measures local repolarization duration and is only weakly affected by activation sequence.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

QRST changes during and after percutaneous transluminal coronary angioplasty.

This study reports preliminary results on 45 patients who underwent percutaneous transluminal coronary angioplasty (PTCA); 120-lead data (including the 12-lead standard electrocardiogram [ECG]) were recorded before, during, and after balloon inflation. Twenty-one patients underwent PTCA for left anterior descending coronary disease, 13 for right coronary artery disease, and 10 for left circumflex; 1 patient had combined left anterior descending and right coronary artery disease. In each patient, voltage data recorded during the various phases of the procedure were compared with the patient's own baseline data. In 18 patients, 120 leads were also recorded 24 hours after PTCA. In this study, the usefulness of the standard 12-lead ECG was investigated in locating the coronary artery being occluded, in elucidating the mechanisms of the QRS changes, and in identifying changes occurring 24 hours after completion of the procedure. Results indicate that the observation of ST elevation in the 12-lead ECG may lead to ambiguous interpretation. Also, limiting observation to ST-T patterns alone instead of including QRS changes further hampers correct identification of the involved vessel. QRS modifications during inflation are interpreted as conduction disturbances, although other mechanisms are evoked: study of surface maps may contribute to the understanding of these mechanisms. Changes present 24 hours later are visible in the standard leads, but again, in the absence of the thoracic potential distribution, these are difficult to interpret. These changes were different from those observed after cessation of inflation at the end of the procedure. It is hypothesized that next-day changes may reflect reperfusion injury and/or represent myocardial stunning. Presence of injury and reversibility of changes require further investigation. Also, biochemical markers such as creatine kinase-MB mass, creatine kinase-MB activity, myoglobin, and troponin-T may help elucidate the significance of these findings.

Angioplasty, Balloon, Coronary↗

A computer model for the study of electrical current flow in the human thorax.

Electrocardiography has played an important role in the detection and characterization of heart function, both in normal and abnormal states. In this paper we present an inhomogeneous, anisotropic computer model of the human thorax for use in electrocardiography with emphasis on the calculation of transthoracic potential and current distributions. Knowledge of the current pathways in the thorax has many applications in electrocardiography and has direct utility in studies pertaining to cardiac defibrillation, forward and inverse problems, impedance tomography, and electrode placement in electrocardiography.

Computer Simulation↗

Persistent changes in the body surface electrocardiogram following successful coronary angioplasty.

One hundred twenty-lead body surface potential maps (BSPMs) were recorded immediately before and 24 hours after coronary angioplasty (PTCA) in 24 patients with symptomatic coronary artery disease (single-vessel in 21 and two-vessel in 3). All PTCAs were uncomplicated and successful. The modified Gensini score decreased in every patient and the mean score fell from 43 +/- 36 to 21 +/- 28 (p less than 0.001). Resting spatial patterns of QRS, ST-segment, and T wave integral distributions over the torso surface were unchanged from before to after PTCA. Quantitative temporal subtraction maps, however, revealed a large precordial area of decreased T wave integral values after PTCA. The sum (sigma) positive T wave integrals fell from 20,501 +/- 10,544 microV.s before PTCA to 17,647 +/- 10,310 microV.s after PTCA (p less than 0.02). In contrast, the sigma positive QRS (10,115 +/- 4,848 microV.s before PTCA vs. 9,656 +/- 4,556 microV.s after PTCA) and the sigma negative ST integrals (-2,489 +/- 1,467 microV.s before PTCA vs. -2,359 +/- 1,505 microV.s after PTCA) were unchanged (NS). Thus, successful PTCA does not produce any persistent change in depolarization or early repolarization electrocardiographic variables but is associated with a decrease in late repolarization potentials that persists for at least 24 hours after the procedure. The pathophysiology of this persistent change is speculative, but myocardial ischemia during the PTCA procedure is a likely possibility. The clinical significance, including predictive value for subsequent stenosis, and the natural history of T wave effect remain incompletely defined. These data suggest that measures to decrease myocardial ischemia during PTCA are warranted.

Adult↗

Different effects of calcium-antagonists on automaticity in single pacemaker cells and in synchronized networks of cultured embryonic heart muscle cells.

The inhibitory effects of the calcium antagonists D-600 and diltiazem on impulse formation of pacemaker cells were studied in embryonic chick heart cells, cultured either as single cells or as synchronized multicellular networks. Our findings show that D-600 and diltiazem inhibit the spontaneous action potentials of the cultured cells in a potential- and use-dependent way. However, a marked reduction of the beat frequency could not be found during inactivation of the spontaneous action potentials in the single cells. Only in synchronized multicellular networks cultured under the same conditions was the beat frequency clearly reduced, probably due to the ability of Ca-antagonists to inactivate the most quickly discharging cells first. Thus, the dominant pacemaker cell in a synchronized multicellular network will fade out first and the subsequent negative chronotropic effect is the outcome of a shift in the pacemaker center to cells with a lower intrinsic frequency. These findings indicate that Ca-antagonists predominantly inhibit excitability and impulse conduction. The velocity of slow diastolic depolarization of the single pacemaker cell is not markedly decreased and, therefore, cannot be used to explain the process behind the negative chronotropic effects seen in multicellular systems.

Action Potentials↗

Three-dimensional activation mapping in ventricular muscle: interpolation and approximation of activation times.

Interpolation plays an important role in analyzing or visualizing any scalar field because it provides a means to estimate field values between measured sites. A specific example is the measurement of the electrical activity of the heart, either on its surface or within the muscle, a technique known as cardiac mapping, which is widely used in research. While three-dimensional measurement of cardiac fields by means of multielectrode needles is relatively common, the interpolation methods used to analyze these measurements have rarely been studied systematically. The present study addressed this need by applying three trivariate techniques to cardiac mapping and evaluating their accuracy in estimating activation times at unmeasured locations. The techniques were tetrahedron-based linear interpolation, Hardy's interpolation, and least-square quadratic approximation. The test conditions included activation times from both high-resolution simulations and measurements from canine experiments. All three techniques performed satisfactorily at measurement spacing < or = 2 mm. At the larger interelectrode spacings typical in cardiac mapping (1 cm), Hardy's interpolation proved superior both in terms of statistical measures and qualitative reconstruction of field details. This paper provides extensive comparisons among the methods and descriptions of expected errors for each method at a variety of sampling intervals and conditions.

Animals↗

A novel interpolation method for electric potential fields in the heart during excitation.

In mapping the electrical activity of the heart, interpolation of electric potentials plays two important roles. First, it permits the estimation of potentials in regions that could not be sampled or where signal quality was poor, and second, it supports the construction of isopotential lines and surfaces for visualization. The difficulty in developing robust interpolation techniques for cardiac applications lies in the abrupt change in potential in the vicinity of the activation wave front. Despite the resulting nonlinearities in spatial potential distributions, simple linear interpolation methods are the current standard and the resulting errors due to aliasing can be large if electrode spacing does not lie on the order of 0.5-2 mm--the thickness of the activation wave front. We have developed a novel interpolation method that is based on two observations specific to the spread of excitation in the heart: (1) that propagation velocity changes smoothly within a region large enough to contain several measurement electrodes and (2) that electrogram morphology varies very little in the neighborhood of each sample point except for a time shift in the potential wave forms. The resulting interpolation scheme breaks the interpolation of one highly nonlinear variable--extracellular potential--into two separate interpolations of variables with much less drastic spatial variation--activation time and electrogram morphology. We have applied this method to potentials originally recorded at 1.5 mm spacing and then subsampled at a range of densities for testing of the interpolation. The results based both on reconstruction of isopotential contour maps and statistical comparison showed significant improvement of this novel approach over standard linear techniques. The applications of the new method include improved determination of electrophysiological parameters such as spatial gradients of potential and the path of cardiac activation and recovery, estimation of electrograms at desired locations, and visualization of electric potential distributions.

Algorithms↗

An admissible solution approach to inverse electrocardiography.

The goal of the inverse problem of electrocardiography is noninvasive discrimination and characterization of normal/abnormal cardiac electrical activity from measurements of body surface potentials. Smoothing and attenuation in the torso volume conductor cause the problem to be ill posed. Standard regularized solutions employ an a priori constraint to achieve reliability and may be biased by the constraint chosen as well as the regularization parameter used to weight it. In this paper, we describe an approach that reformulates this inverse problem as the search for a solution that is a member of an admissible solution set; admissibility is defined in terms of the available constraints. In principle, this approach can utilize as many constraints as may be available, unlike standard techniques which do not easily permit the use of multiple constraints. No regularization parameter is required; instead, we need to choose the nature and size of the constraint sets. Constraints described include several spatial constraints, weighted constraints, and temporal constraints. We describe a solution approach based on iterative convex optimization, and the algorithm--the ellipsoid algorithm--which we have used. Accuracy and feasibility of the method are illustrated with simulation results using dipole sources and measured epicardial potentials.

Algorithms↗