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Protection from cyclopropane-adrenalin tachycardia by various drugsAllen, Charles Robert. January 1941 (has links)
Thesis (Ph. D.)--University of Wisconsin, 1941. / Typescript (carbon copy). Includes bibliographical references.
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Novel insight into the mechanisms and treatment of ventricular tachyarrhythmiasLiu, Yuan, 刘媛 January 2011 (has links)
Progressive heart failure (HF) post myocardial infarction (MI) remains the leading cause of morbidity and mortality worldwide. Non-pharmacological interventions, including stem cell therapy and spinal cord stimulation (SCS), are emerging novel therapeutic approach to prevent or treat HF. Nevertheless, the potential impact of these interventions on the susceptibility for ventricular tachyarrhythmias (VT/VF), which are the most common cause of sudden death in HF patients remains unknown.
For stem cell therapy, sympathetic hyperinnervation as reflected by nerve spouting, lack of gap junction and immature electrophysiological phenotypes of the transplanted cells are potentially trigger and/or substrate for VT/VF after transplantation. Previous studies suggested that stem cell transplantation post-MI may induce cardiac nerve sprouting but their effects on gap junction expression are unclear. Furthermore, the effects of stem cell transplantation on cardiac nerve spouting and gap junction expression in chronic myocardial ischemia have not been addressed. In Chapter 3, we investigated bone marrow (BM) derived mononuclear cells (MNCs) and endothelial progenitor cells (EPCs) via direct intramyocardial transplantation in a porcine model of chronic myocardial ischemia. Our results showed that BM-MNCs or BM-EPCs transplantation was not associated with increased cardiac nerve sprouting, which might account for their low risk of proarrhythmias observed in clinical and experimental studies. In Chapter 4, we investigated the susceptibility to develop VT/VF after embryonic stem cells (ESCs) and their derived cardiomyocytes (ESC-CMs) transplantation in a murine model of MI. Moreover, the potential application of bioengineered ESC-CMs with over-expression of Kir 2.1 to reduce their susceptibility to induce VT/VF was also studied. Our results showed that transplantation of ESC or ESC-CMs reduced cardiac nerve sprouting and increased gap junction expression in the infarcted regions when compared with MI alone. The inducibility of VT/VF after ESC-CM transplantation was significantly higher than ESC transplantation or MI alone. On the other hand, over-expression of Kir2.1 improved the electrical maturation of ESC-CMs which significantly attenuated their vulnerability for VT/VF. These results suggested that the immature electrical phenotypes of ESC-CMs, rather than cardiac nerve spouting and changes in gap junction expression, plays an important role for proarrhythmias after stem cells transplantation, which can be eliminated by bioengineering of ESC-CMs.
Dysregulation of the autonomic nervous system with increased sympathetic tone and decreased parasympathetic tone has been well documented in HF progression, and is proposed to play an important role in arrhythmogenesis. In Chapter 5, we performed acute thoracic SCS at T1-T2 level in an animal model of ischemic HF (MI+HF) induced by MI and rapid ventricular pacing. Our results showed that acute SCS significantly increased left ventricular (LV) contractile function as determined by echocardiographic measurement of LV ejection fraction (LVEF) and invasive hemodynamic assessment of +dP/dt. Furthermore, myocardial oxygen consumption also significantly decreased during SCS without any change in serum norepinephrine level. Nevertheless, acute SCS failed to prevent spontaneous VT/VF provoked by prolonged (>2 minutes) acute myocardial ischemia.
Taken together, our results provide important insights into the potential mechanisms of proarrhythmias after stem cell transplantation as well as the acute beneficial effects SCS in ischemic HF. / published_or_final_version / Medicine / Doctoral / Doctor of Philosophy
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Can the real-time measurement of intracardiac impedance discriminate haemodynamically stable from unstable arrhythmias?Arthur, Wayne R. January 2003 (has links)
No description available.
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Mechanisms and mapping of ventricular arrhythmias in cardiomyopathyHaqqani, Haris M. January 2009 (has links)
Heart failure due to ischemic and dilated cardiomyopathy is a large and expanding public health problem, and ventricular arrhythmias are a common and potentially fatal complication of this condition. Despite extensive investigation, the mechanisms of ventricular arrhythmias in cardiomyopathy remain incompletely understood. This thesis examines these mechanisms, particularly with reference to the potential role of the underlying electrophysiologic substrate. It also evaluates the validity and utility of some of the tools commonly used to assist in the mapping and catheter ablation of ventricular arrhythmias. / The central rationale of this thesis is that the mechanisms of ventricular arrhythmogenesis in cardiomyopathy are optimally studied by comparing ischemic and dilated cardiomyopathy patients with spontaneous (rather than inducible) ventricular tachycardia to otherwise similar heart failure patients who have never developed clinical arrhythmias. This has been done in the two largest projects herein. In the setting of ischemic cardiomyopathy, it is demonstrated that there are large differences in the electrophysiologic substrate between the groups such that patients with clinical ventricular tachycardia have substantially greater endocardial scarring as inferred by the presence of low-voltage zones and scar-related electrograms compared to control cardiomyopathy patients with no spontaneous arrhythmias. Furthermore, there appear to be fundamental differences in the nature of the scarring process with ventricular tachycardia patients having more abnormal electrograms per unit area of low-voltage and more scar-related putative conducting channels (which may form critical diastolic isthmuses in tachycardia). / This was accompanied by a lower rate of ventricular tachycardia inducibility in the control patients. Taken together these findings point to a major role for the electrophysiologic substrate in ventricular arrhythmogenesis in the setting of ischemic cardiomyopathy. The situation in dilated cardiomyopathy is more complicated and although significant endocardial substrate differences were again seen in this context, there was marked heterogeneity in the group with ventricular tachycardia with some patients having extensive low-voltage zones and others having normal endocardial voltage. As the pericardium could not be accessed for ethical reasons in control patients with no clinical arrhythmia, the precise role of an abnormal epicardial substrate was not able to be defined in this study. Another project in this thesis examines potential improvements (in the form of a multielectrode mapping catheter) to a widely used electroanatomic mapping system that can assist in mapping ventricular tachycardia circuits and the substrates underlying them. A further project compares magnetic resonance imaging and electroanatomic substrate mapping in defining ventricular scarring in the context of cardiomyopathy. And finally, electroanatomic mapping is used to look at endocardial activation patterns and electrical dyssynchrony in cardiomyopathy patients with and without left bundle branch block. The demonstrated variability in these factors may underlie the significant non-response rates to cardiac resynchronization therapy. / In summary, it is apparent from this work that the electrophysiologic substrate plays a crucial role in mechanism of the ventricular arrhythmias seen in heart failure patients with ischemic and dilated cardiomyopathy. An improved understanding of these mechanisms may in turn lead to better diagnosis, risk stratification and ultimately management of heart failure patients suffering from, or at risk of developing these potentially lethal arrhythmias.
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Mechanisms and mapping of ventricular arrhythmias in cardiomyopathy /Haqqani, Haris M. January 2009 (has links)
Thesis (Ph.D.)--University of Melbourne, Dept. of Medicine, The Royal Melbourne Hospital, 2010. / Typescript. Includes bibliographical references (leaves 164-202)
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Nocturnal vs. diurnal ventricular dysrhythmias in acute anterior wall myocardial infarction a research report /Reed, Pamela Sue. Boyle, Mary Jo. January 1988 (has links)
Thesis (M.S.)--University of Michigan, 1988.
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Nocturnal vs. diurnal ventricular dysrhythmias in acute anterior wall myocardial infarction a research report /Reed, Pamela Sue. Boyle, Mary Jo. January 1988 (has links)
Thesis (M.S.)--University of Michigan, 1988.
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Interactions between trains of premature stimuli and anatomically anchored reentrant wavefronts implications for antitachycardia pacing /Byrd, Israel A. January 2006 (has links) (PDF)
Thesis (Ph. D.)--University of Alabama at Birmingham, 2006. / Description based on information viewed Oct. 3, 2006; title from title screen. Includes bibliographical references (p. 87-90).
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Experience With Moricizine HCl in Children With Supraventricular TachycardiaMehta, Ashok V., Subrahmanyam, Arumughakumari B., Long, J. Blake, Kanter, Ronald J. 15 November 1996 (has links)
Eight children, age between 4.5 and 19 years were treated with moricizine for supraventricular tachycardia during the last 3 years. The tachycardia was documented by surface electrocardiogram (EGG), and/or by ambulatory ECG in all the children and the mechanism of tachycardia was determined by previously published surface ECG and electrophysiologic criteria in all but one child. Of the eight children, three had atrial ectopic tachycardia, three had automatic junctional ectopic tachycardia, one had atrioventricular (AV) nodal reentry tachycardia and one had atrial reentry. All the children except one had failed trial of two or more antiarrhythmic drugs prior to moricizine therapy. The duration of moricizine therapy ranged from 4 days to 25 months. In three of the eight children (patients 3, 5 and 7), who presented with AV nodal reentrant tachycardia, automatic junctional ectopic tachycardia and atrial ectopic tachycardia, respectively, moricizine therapy was effective in restoring sinus rhythm and controlling the clinical tachycardia. Only one child (patient 1) developed proarrhythmia, an episode of fast, narrow-QRS supraventricular tachycardia lasting for 30 s, on the third day of therapy. This was subsequently confirmed by electrophysiologic study to be AV nodal reentrant tachycardia. The other side effects noted were non-cardiac, not dose-dependant and did not require discontinuation of therapy. Based on our small series and those of others, moricizine, a newer class I anti-arrhythmic agent, has a limited but useful role in the management of recalcitrant type of supraventricular tachycardia, such as ectopic atrial and junctional tachycardia in children.
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A sensitive method for measuring plasma catecholamines and its application on the study of the effect of alfentanil and esmolol onintra-operative hypertension蕭德成, Siu, Tak-shing. January 1998 (has links)
published_or_final_version / abstract / toc / Anaesthesiology / Master / Master of Philosophy
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