An integrated system for intraoperative cardiac activation mapping.
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Biomedical subjects
Publications and source records attributed to R Guardo.
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Body surface potential mapping (BSPM) was used to study the spatial distribution of late ventricular potentials. In a group of 15 normals and 21 patients with documented ventricular tachycardia (VT), BSPM performed with 63 averaged and high-pass filtered ECG leads (LP-BSPM) showed that late potentials have a mostly dipolar distribution and that they can be reasonably well detected with only three orthogonal leads. In a group of 17 VT patients who also had BSPM performed during induced VT (VT-BSPM), six patients had LP-BSPM similar to one of the VT-BSPM, suggesting that the locations and orientations of both types of sources are similar. In a group of 12 VT patients who had epi-endo VT mapping at surgery, LP-BSPM showed close extrema (reflecting antero-apical delay) for patients with anterior or apical VT sites, suggesting that VT originates in delayed regions. BSPM thus provides useful information about the detection and significance of late potentials.
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Low-level activity at the end of the QRS complex was analyzed from 63 thoracic leads in 15 normal subjects and in 21 patients with ventricular tachycardia (VT). The latter had old myocardial infarction and no conduction disturbances and had not been receiving antiarrhythmic drugs. In both normal subjects and patients with VT, isopotential maps of the time-averaged and filtered (25 Hz high-pass) electrocardiograms during the terminal portion of the QRS were dipolar, i.e., they showed single positive and negative regions. For patients with VT, the extrema were either distant, with one over the precordial area and the other over the back, or close together in the precordial region. In 10 patients, maps recorded after administration of antiarrhythmic drugs remained the same while QRS duration was prolonged. In six patients, maps recorded before antiarrhythmic surgery showed distant extrema for septal or posterobasal VT sites of origin and close extrema for anterior or posteroapical sites. Generally, QRS duration was reduced and maps were modified after surgery. Late potentials can be well detected with only three orthogonal leads because their distributions are dipolar, but maps provide additional information about their distribution, which may be related to conduction delay sites and possibly to VT sites of origin. Sources near the torso surface would produce close extrema, whereas deeper sources would produce distant extrema.
Isolated cells can be kept in steady-state conditions for very long periods of time when inserted into dialysis microfibers and perifused with a nutrient-containing solution. Using this system, stable 31P NMR spectra have been obtained on dog kidney tubules for a period of 13 h.
A simulation study was performed to evaluate different recovery procedures for computing the multipole components of the cardiac electrical activity. A series of dipolar potential distributions was first generated on a realistic numerical model of the human torso. Then, different procedures based on surface integration (SI) and least-squares (LS) minimization were used to compute the multipole components. The parameters of a single moving dipole (SMD) computed from the estimated multipoles were compared with those of the original dipole source. For a finite and homogeneous simulation as well as recovery medium, the results showed that SI employing the potentials over all 1216 surface elements of the torso model was not affected by the various numerical approximations used to perform the integration (e.g., rms error for the SMD position, p = 0.7 mm). By integrating the potentials with truncated capping surfaces at the neck and the waist, the recovery errors increased (p = 2.1 mm). Sampling the potentials at 63 sites, followed by interpolation over the rest of the torso surface, severely affected the SI results for the SMD (p = 6.4 mm), as compared with LS minimization using also 63 values (p = 0.9 mm). With lungs and intraventricular blood masses in the simulation medium but a finite and homogeneous recovery medium, SI was less effective (p = 10.8 mm) than LS (p = 8.6 mm). Adequate compensation for the effects of lungs was obtained by including regions of lower electrical conductivity in the recovery medium for LS, and by a correction matrix for SI. In general, LS gave better results than SI, but with a higher initial computation time.
The accuracy of different computation techniques for the non-invasive localization of cardiac ectopic activity was evaluated. Body surface potentials were recorded from 63 leads in 14 patients with implanted pacemakers. The location, orientation and magnitude of a single moving dipole (SMD) were computed from the first eight terms of a truncated multipole expansion estimated from the body surface potentials. The SMD trajectories obtained during the QRS complex were plotted along with the heart outlines and pacing leads obtained independently from chest x-rays. The origin of the SMD trajectories was compared to the position of the pacing lead to evaluate the accuracy of the SMD. The optimum computation technique used a least-squares (LS) estimation of the multipole expansion truncated at 15 multipoles, in conjunction with a torso model that included regions of lower conductivity representing the lungs. With this method, the SMD trajectories originated near the pacing lead (25 +/- 12 mm) and adequately represented the progression of the ectopic wavefront across the entire heart silhouette. With the LS techniques using 8 or 24 multipoles, the spans of the trajectories were respectively too short, or too long to cover the heart, and the average distance between the SMD at QRS onset and the pacing lead was larger. With a surface integration technique, the SMD-pacing lead distances were similar, both for a finite homogeneous torso model with a fixed geometry, as well as for torso models adapted to the torso geometry of each patient. The SMD was found adequate to represent the progression of an ectopic wavefront, and to localize its origin in man.
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A cardiac stimulator is described which combines the ease of operation required in clinical investigations, particularly endocavitary studies of cardiac arrhythmias, and the versatility needed in a research context. This instrument uses a microcomputer to control two independent optically-isolated stimulation ports which can be addressed either independently or jointly to stimulate at two different sites. The main software module operates as a cascade of ten real time pulse generators with individually presettable parameters: amplitude, duration, period, initial delay, periodic and cyclic modifiers, triggering mode, etc. A simple interactive procedure allows the operator to define a stimulation protocol either by accessing the generator structure directly, or by calling any of five pre-programmed stimulation protocols. With this combination, the instrument can provide a large variety of pulse patterns. The operator can intervene at any time during stimulation to change parameter values or modify the pulse pattern. Concurrently with stimulation, the instrument generates time-codes to help relate cardiac responses recorded on paper chart and magnetic tape, and reference them to specific events. The instrument can be readily expanded by the addition of parallel microprocessor modules; other real time tasks such as acquisition and processing of cardiac responses can thus be incorporated.
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A direct image reconstruction method of electrical impedance tomography (EIT) is evaluated using three-dimensional (3-D) finite element models of cylindrical and torso-shaped volume conductors. The cylindrical model is used to examine the effect of electrode configurations and the sensitivity to off-plane objects and to noise in the measured data. It is also used to validate the modeling procedures by comparison with experimental data acquired from a similar cylindrical tank filled with saline. Simulation results show only minor differences in performance between the various electrode configurations. In the second part, a realistic human thorax model constructed from CT images is used to evaluate monitoring of pulmonary edema by EIT. The conductivity, volume, and vertical position of an abnormal region in the lungs are varied to simulate the progress of edema. Dynamic EIT images are reconstructed from data computed for the inhomogeneous thorax (heart and lungs) as the reference set and a realistic amount of noise is added to reproduce the conditions in which the technique would be used in practice. Simulation results show that a 10 ml edema region with a conductivity equal to that of blood can be detected at a 40 dB signal-to-noise ratio (SNR). Detection of a smaller volume, in the order of 2 ml, should be possible by improving either the instrumentation to achieve 60 dB SNR or the performance of reconstruction algorithms.