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Biomedical subjects

S M Blanchard

Publications and source records attributed to S M Blanchard.

18 recordsLinked to original sources

Intermittent biotelemetric monitoring of electrocardiograms and temperature in male broilers at risk for sudden death syndrome.

Biotelemetry was used to acquire electrocardiograms (ECG) and temperature measurements in a study of male broilers at risk for sudden death syndrome (SDS), a fatal condition that may have underlying cardiovascular mechanisms. Day-old (Day 1) Arbor Acres x Arbor Acres male chicks were randomly assigned to two different diets: control (Diet A) and one that contained elements that contribute to SDS (Diet B). The heaviest birds in each group on Day 13 underwent surgery on Day 15 to have transmitters with temperature sensors and ECG electrodes implanted. After surgery, three controls and three implanted birds from each diet group were kept in individual cages and exposed to 23 h of light and 1 h of darkness during each 24-h cycle. Implantation did not affect weight gain between Days 13 and 22 (P = 0.396). Temperature measurements and 1-min ECG were taken every 15 min. Heart rate and heart rate variability were measured from three 2-s segments in two dark and two light period samples during Days 17 to 19. Diet B decreased weight gain (P = 0.045), lowered heart rate (P < 0.0001), and increased internal temperature (P < 0.0001). Heart rate variability was lower during dark versus light periods (P = 0.004), which indicates that the birds rested during the dark periods, but was not affected by diet (P = 0.651). Thus, biotelemetry provided a useful method for intermittent physiological monitoring of poultry on different diets and under changing environmental conditions.

Animals↗

Using an artificial neural network to detect activations during ventricular fibrillation.

Ventricular fibrillation is a cardiac arrhythmia that can result in sudden death. Understanding and treatment of this disorder would be improved if patterns of electrical activation could be accurately identified and studied during fibrillation. A feedforward artificial neural network using backpropagation was trained with the Rule-Based Method and the Current Source Density Method to identify cardiac tissue activation during fibrillation. Another feedforward artificial neural network that used backpropagation was trained with data preprocessed by those methods and the Transmembrane Current Method. Staged training, a new method that uses different sets of training examples in different stages, was used to improve the ability of the artificial neural networks to detect activation. Both artificial neural networks were able to correctly classify more than 92% of new test examples. The performance of both artificial neural networks improved when staged training was used. Thus, artificial neural networks may beuseful for identifying activation during ventricular fibrillation.

Diagnosis, Computer-Assisted↗

Biomedical information technology: medicine and health care in the digital future.

Advancements in medicine and health care are being significantly influenced by the exploding information technology developments. The IEEE Transactions on Information Technology in Biomedicine will address the applications and the infrastructure innovations that would harness biomedical and health care programs in the 21st century.

Biomedical Engineering↗

The World Wide Web--a new tool for biomedical engineering education.

An ever-increasing variety of materials (text, images, videos, and sound) are available through the World Wide Web (WWW). While textbooks, which are often outdated by the time they are published, are usually limited to black and white text and images, many supplemental materials can be found on the WWW. The WWW also provides many resources for student projects. In BAE 465: Biomedical Engineering Applications, student teams developed WWW-based term projects on biomedical topics, e.g. biomaterials, MRI, and medical ultrasound. After the projects were completed and edited by the instructor, they were placed on-line for world-wide access if permission for this had been granted by the student authors. Projects from three classes have been used to form the basis for an electronic textbook which is available at http:@www.eos.ncsu.edu/bae/research/blanchard /www/465/textbook/. This electronic textbook also includes instructional objectives and sample tests for specific topic areas. Student projects have been linked to the appropriate topic areas within the electronic textbook. Links to relevant sites have been included within the electronic textbook as well as within the individual projects. Students were required to link to images and other materials they wanted to include in their project in order to avoid copyright issues. The drawback to this approach to copyright protection is that addresses can change making links unavailable. In BAE 465 and in BAE 235: Engineering Biology, the WWW has also been used to distribute instructional objectives, the syllabi and class policies, homework problems, and abbreviated lecture notes. This has made maintaining course-related material easier and has reduced the amount of paper used by both the students and the instructor. Goals for the electronic textbook include the addition of instructional simulation programs that can be run from remote sites. In the future, biomedical engineering may be taught in a virtual classroom with participation by an instructor and students from many different parts of the world.

Biomedical Engineering↗

An automated technique for identification and analysis of activation fronts in a two-dimensional electrogram array.

Cardiac activation sequences are normally determined by (i) the detection and timing of local activations in cardiac electrograms, (ii) the grouping together of activations in different electrodes that are generated by the same activation fronts, and (iii) the construction by interpolation of isochronal maps showing the pathways of the activation fronts. This process is typically carried out by manual or semiautomated methods. These methods are usually adequate for stable, repeatable rhythms in normal hearts. However, in situations in which the electrograms are distorted, as in those recorded from abnormal myocardium, or the mapped rhythms are rapidly changing, as in ventricular fibrillation, they are tedious and time-consuming and yield results that are subjective and not repeatable from one investigator to another. Therefore, we developed a computer-based method for automating the identification and analysis of activation fronts recorded from a large array of electrodes. The electrodes are closely spaced (1 mm) so that interpolation is not required. Electrodes are identified as recording an activation when the temporal derivative of the potential is more negative than a user-specified value. Activations occurring less than a user-specified distance apart in time and space are identified as part of the same activation front. Characteristics of the activation fronts, such as their number, size, and the presence of reentry or collision, are then quantified. The differences between the results obtained by this automated method and those obtained by four human investigators was no greater than the differences in results among the four investigators themselves. Because the method is automated and algorithmic, it is both rapid and repeatable.

Algorithms↗

Mechanisms of electrical defibrillation: impact of new experimental defibrillator waveforms.

Six possible explanations for why some biphasic waveforms have lower defibrillation thresholds than monophasic waveforms of the same duration are as follows: (1) the impedance for the second phase of the biphasic shock is very low because electrode polarization develops during the first phase; (2) the large change in voltage between the first and second phases of a biphasic waveform is responsible for the increased defibrillation efficacy; (3) biphasic waveforms cause less severe detrimental effects in regions of high potential gradient; (4) the first phase of the biphasic waveform restores activity of the sodium channels, which makes defibrillation easier for the second phase; (5) the potential gradient required for defibrillation is less for biphasic waveforms than for monophasic waveforms; and (6) biphasic waveforms are better able to stimulate the myocardium to induce new action potentials or to cause refractory period prolongation. Evidence shows that, while a few of these proposed mechanisms are incorrect, several of the others may together contribute to the general superiority of biphasic waveforms.

Action Potentials↗

Why is catheter ablation less successful than surgery for treating ventricular tachycardia that results from coronary artery disease?

Nearly 80% of patients with coronary artery disease who have map-directed surgery for control of ventricular tachycardias require no drug therapy to prevent recurrences, while fewer than 50% of patients undergoing catheter ablation have similar outcomes. Catheter ablation will fail if arrhythmogenic sites are incompletely ablated by lesions that are too small or too far away from the reentrant pathway or if all arrhythmogenic sites are not identified. The underlying assumptions used to guide site selection are that: (a) ventricular tachycardias arise from reentrant mechanisms; (b) monomorphic ventricular tachycardias with similar QRS morphologies arise from the same pathway; (c) the ventricular tachycardia initiated during the procedure represents the patient's spontaneous arrhythmia; (d) the endocardial site that should be ablated can be identified from cardiac activation maps produced during induced ventricular tachycardia or from ancillary techniques; and (e) the patient has only one or two reentrant pathways. Relying on incorrect assumptions may account for the difference in success rates. Patients may have similar appearing ventricular tachycardias that arise from different pathways, and the entire thin layer of viable tissue between the infarct and the endocardium may contain many reentrant pathways. Some ventricular tachycardias may arise from the myocardium away from the endocardium, while others may arise from the epicardium. Small lesions may not be large enough to eliminate all possible reentrant pathways. Catheter ablation may be less successful because the lesions are inadequate, the assumptions guiding the selection of arrhythmogenic tissue are incorrect, or all arrhythmogenic sites are not identified. The primary reason catheter ablation is less successful than surgery in the treatment of ventricular tachycardias is that catheter ablation does not ablate as much tissue as is removed by surgery. The success rate of catheter ablation probably can be improved if the amount of tissue ablated is increased.

Catheter Ablation↗

Effects of peroneal nerve stimulation on hypothalamic stimulation-induced ventricular arrhythmias in rabbits.

We tested the hypothesis that peripheral afferent nerve stimulation decreases the incidence of ventricular arrhythmias induced by central nervous system stimulation. The hypothalamus in each of 24 anesthetized rabbits (12 with anterior myocardial ischemia) was electrically stimulated for 10 s with 10-min intervals between each of six consecutive stimulation episodes. The left peroneal nerves were electrically stimulated for 15 min beginning 5 min after the second hypothalamic stimulation episode in six ischemic and six nonischemic rabbits. Cardiac rhythm was monitored with the electrocardiogram lead I and atrial and ventricular electrograms. Hypothalamic stimulation alone induced ventricular arrhythmias [mean no. of arrhythmic beats occurring during 3rd and 4th hypothalamic stimulation episodes: nonischemic animals, 20 +/- 8; ischemic animals, 62 +/- 41 (P < 0.05 by unpaired t-test)]. Peroneal nerve stimulation reduced the number of arrhythmic beats induced by hypothalamic stimulation in nonischemic animals (6 +/- 5; P < 0.05 vs. without peroneal stimulation) and prevented an increase in arrhythmic beats during ischemia (21 +/- 16). Thus peripheral nerve stimulation decreased the number of ventricular arrhythmic beats induced by repeated hypothalamic stimulation in both ischemic and normal rabbit hearts and may be important in the prevention of arrhythmias in patients.

Afferent Pathways↗

Accelerated transmural gradients of energy compound metabolism resulting from left ventricular hypertrophy.

Eighteen dogs underwent transmural left ventricular biopsies for adenosine triphosphate and suturing of the noncoronary cusp, creating valvular aortic stenosis. Three months after aortic stenosis and the subsequent development of left ventricular hypertrophy, animals underwent repeat transmural left ventricular biopsies followed by total myocardial ischemia at 37 degrees C. Left ventricular tissue samples for adenosine triphosphate and lactate levels were determined at 15-minute intervals and compared with 15 control animals. No significant difference between subendocardial and subepicardial adenosine triphosphate levels was found between left ventricular samples taken before left ventricular hypertrophy and 3 months after left ventricular hypertrophy. Significant differences in adenosine triphosphate utilization occurred between subendocardial and subepicardial layers in control and left ventricular hypertrophy myocardium, however. The gradient between the subendocardium and the subepicardium was significantly increased by left ventricular hypertrophy (p less than 0.05). Significant differences also occurred within the same layer when left ventricular hypertrophy and control groups were compared. During total ischemia, lactate concentration was significantly greater within the subendocardium than within the subepicardium in left ventricular hypertrophy. The onset of ischemic contracture was 48.2 +/- 2.1 minutes in left ventricular hypertrophy versus 62.3 +/- 1.8 minutes in control hearts (p less than 0.01). Subendocardial intramyocardial pressure increased significantly earlier than subepicardial in both left ventricular hypertrophy and control hearts. Adenosine triphosphate was used, and lactate accumulated more rapidly in animals with a more pronounced hemodynamic gradient. These data show that after left ventricular hypertrophy, adenosine triphosphate stores in the subendocardium and the subepicardium are unchanged from control values, yet the rates of adenosine triphosphate utilization and lactate accumulation during total ischemia are significantly increased. Furthermore, the subendocardial to subepicardial gradient of adenosine triphosphate utilization during ischemia found in normal hearts is markedly increased by left ventricular hypertrophy.

Adenosine Triphosphate↗

Cocaine-mediated impairment of cardiac conduction in the dog: a potential mechanism for sudden death after cocaine.

Deaths from cocaine abuse continue to increase, while the mechanism of lethality remains unclear. Previous investigations have focused on potential ventricular dysrhythmias and myocardial ischemic events from enhanced autonomic tone or seizure activity from central stimulation. However, cocaine is a local anesthetic and may impair cardiac conduction. To evaluate this, 16 conscious dogs received i.v. cocaine over 30 sec to mimic "recreational" use in doses of 3 mg/kg (n = 6), 5 mg/kg (n = 6) or 7 mg/kg (n = 4). Another group of anesthetized dogs (n = 6) received two infusions of cocaine (5 mg/kg) 1 hr apart. Plasma cocaine levels and His bundle electrograms were obtained at control and at 0.5, 1.0, 1.5, 2.0, 3.0, 4.0, 5.0, 10 and 15 min after cocaine administration. At 0.5 min, plasma cocaine reached peak levels of 30.0, 45.0 and 59.6 micrograms/ml with increasing dose. Cocaine rapidly produced severe prolongation of His to ventricle interval and widening of the R wave. Slowing of conduction was dose-dependent, with maximal increases in His to venticle interval of 37 to 56% (P = .0299) and R wave duration of 34 to 77% (P less than .025). Furthermore, significant conduction impairment developed at cocaine levels that did not produce seizures. Conduction effects were equally pronounced during repeated administration of cocaine. These data indicate that cocaine causes marked conduction slowing, which could play an important role in cocaine death.

Animals↗

Four digital algorithms for activation detection from unipolar epicardial electrograms.

The reproducibility of activation detection by each of four algorithms used to calculate maximum derivatives was tested on two sequential paced beats of right ventricular unipolar epicardial electrograms which represented either local activation of the right ventricle alone or synchronous activation of both ventricles. The methods were evaluated by comparing the shape of the two beats aligned on their selected activation times, i.e., the time at which the maximum negative deflection occurred, the differences in activation intervals for the two beats, and the effect on the activation time of superimposing distant events on local activation. The 17-point second-order data fit algorithm performed slightly better than the first-order difference, three-point Lagrange derivative, and five-point second-order data fit algorithms except that activation time selection by the 17-point technique was slightly, but significantly, delayed by the superposition of distant potentials. The 17-point second-order data fit technique is therefore recommended for use in detecting activation unless computation time is a major consideration. In that case, the five-point second-order data fit technique, which uses only four data values for each computation, can be used with only slight decreases in accuracy.

Algorithms↗

Interpolating unipolar epicardial potentials from electrodes separated by increasing distances.

In cardiac mapping, potentials for unexplored areas are estimated by interpolating values from nearest neighbor electrodes regardless of distances between these sites or wave front orientation. The effects of these variables on interpolated unipolar electrograms were analyzed two ways: with a computer model and with electrograms recorded 9.9 and 14.1 mm apart. For the model, wave fronts (n = 39) were generated from electrograms recorded during right ventricular (RV) activation in five dogs following the RV isolation procedure. Each wave front was assumed to propagate radially at 0.5 m/sec from a site 30 mm from the center of a square array with electrodes located at the center and corners. Each wave front crossed the array with its tangent at an angle of 0 degrees, 45 degrees, or 90 degrees to the diagonal line connecting opposite corner electrodes. Potentials for all five sites were generated from each wave front and were interpolated for the center site from the generated corner potentials. Generated and interpolated center site potentials were compared using correlation coefficients (r) and percent root mean square differences (%RMSD). Mean r values fell below 0.90 for interelectrode distances of 15.6 mm, 2.8 mm, and 1.4 mm at 0 degrees, 45 degrees, and 90 degrees wave front orientations, respectively. For experimentally measured potentials recorded 9.9 mm apart, results from interpolated electrograms were similar to results from the model at 0 degrees propagation. Electrograms interpolated from potentials measured 14.1 mm apart had poorer r and %RMS values than those from the computer model. Thus, with linear interpolation unipolar electrograms can be inaccurately interpolated from electrodes less than 3 mm apart or correctly interpolated from electrodes more than 14 mm apart depending upon wave front orientation.

Action Potentials↗

The assumptions of isochronal cardiac mapping.

Isochronal maps of cardiac activation are commonly used to study the mechanisms and to guide the ablative therapies of arrhythmias. Little has been written about the assumptions implicit in the construction and use of isochronal cardiac maps. These assumptions include the following: (1) the location of the recording electrodes is known with sufficient accuracy to determine the mechanism of an arrhythmia or to guide therapy; (2) a single, discrete activation time can be assigned to each recording electrode location; (3) the presence or absence of activation at an electrode site can be reliable ascertained, and when activation is present, the time of activation can be determined with sufficient accuracy to specify the mechanism of an arrhythmia or to guide therapy; and (4) the recording electrodes are close enough together that the activation sequence can be estimated with sufficient accuracy to determine the mechanism of an arrhythmia or to guide therapy. The manuscript reviews evidence that these assumptions may not always be true, and when they are not, the isochronal map may be misleading.

Arrhythmias, Cardiac↗

Effects of distant potentials on unipolar electrograms in an animal model utilizing the right ventricular isolation procedure.

The effects of distant potentials on local epicardial unipolar electrograms were examined utilizing a model that enabled both ventricles to be paced independently in five dogs. The right ventricular isolation procedure electrically isolates the right from the left ventricle. Right ventricular electrograms were separated into their local (right ventricular) and distant (left ventricular) components by altering the left-right ventricular pacing interval. Waveform configuration, peak to peak amplitude, magnitude of the slope and timing of the fastest downstroke were carefully evaluated at each electrode site, both with and without the presence of distant left ventricular potentials. Except for the timing of the fastest downstroke, all of these variables were significantly altered by distant potentials. Although the slope of the fastest downstroke was significantly affected by distant potentials, it remained a sensitive indicator of local versus distant activation. All electrograms of local right ventricular activation had a slope magnitude greater than 2.5 mV/2 ms whereas none of the right ventricular electrograms containing only distant left ventricular activity had a magnitude greater than 2.5 mV/2 ms. Computer-generated electrograms were calculated by digitally summing the recorded local right and distant left ventricular components. The simulated electrograms correlated well with the recorded electrograms during synchronous ventricular pacing. Thus, the configuration, amplitude and slope of unipolar electrodes were profoundly influenced by distant potentials. The timing of the fastest downstroke is largely independent of the effect of distant potentials and most closely represents local activation. The magnitude of the slope of the recorded electrogram accurately distinguishes local from distant activation.

Action Potentials↗

SAPA-2 is the Fan.

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Electrocardiography↗