1.Extreme septal hypertrophy in an adolescent with congenital familial hypertrophic cardiomyopathy.
Byoung Won PARK ; Min Ho LEE ; Duk Won BANG ; Min Su HYON
The Korean Journal of Internal Medicine 2015;30(6):940-941
		                        		
		                        			
		                        			No abstract available.
		                        		
		                        		
		                        		
		                        			Adolescent
		                        			;
		                        		
		                        			Adrenergic beta-Antagonists/therapeutic use
		                        			;
		                        		
		                        			Calcium Channel Blockers/therapeutic use
		                        			;
		                        		
		                        			Cardiomyopathy, Hypertrophic, Familial/complications/genetics/*pathology/physiopathology/therapy
		                        			;
		                        		
		                        			Electric Countershock
		                        			;
		                        		
		                        			Electrocardiography
		                        			;
		                        		
		                        			Female
		                        			;
		                        		
		                        			Genetic Predisposition to Disease
		                        			;
		                        		
		                        			Heart Failure/etiology/therapy
		                        			;
		                        		
		                        			Heart Septum/drug effects/*pathology/physiopathology/ultrasonography
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Magnetic Resonance Imaging
		                        			;
		                        		
		                        			Male
		                        			;
		                        		
		                        			Middle Aged
		                        			;
		                        		
		                        			Pedigree
		                        			;
		                        		
		                        			Phenotype
		                        			;
		                        		
		                        			Tachycardia, Ventricular/etiology/therapy
		                        			;
		                        		
		                        			Treatment Outcome
		                        			;
		                        		
		                        			Ventricular Outflow Obstruction/etiology
		                        			
		                        		
		                        	
3.Complication Rate of Transfemoral Endomyocardial Biopsy with Fluoroscopic and Two-dimensional Echocardiographic Guidance: A 10-Year Experience of 228 Consecutive Procedures.
Se Yong JANG ; Yongkeun CHO ; Joon Hyuck SONG ; Sang Soo CHEON ; Sun Hee PARK ; Myung Hwan BAE ; Jang Hoon LEE ; Dong Heon YANG ; Hun Sik PARK ; Shung Chull CHAE
Journal of Korean Medical Science 2013;28(9):1323-1328
		                        		
		                        			
		                        			Endomyocardial biopsy (EMB) is one of the reliable methods for the diagnosis of various cardiac diseases. However, EMB can cause various complications. The purpose of this study is to evaluate the complication of transfemoral EMB with both fluoroscopic and two-dimensional (2-D) echocardiographic guidance. A total of 228 patients (148 men; 46.0+/-14.6 yr-old) who underwent EMB at Kyungpook National University Hospital from January 2002 to June 2012 were included. EMB was performed via the right femoral approach with the guidance of both echocardiography and fluoroscopy. Overall, EMB-related complications occurred in 21 patients (9.2%) including one case (0.4%) with cardiac tamponade requiring emergent pericardiocentesis, four cases (1.8%) with small pericardial effusion without pericardiocentesis, two cases (0.9%) with hemodynamically unstable ventricular tachycardia (VT), one case (0.4%) with nonsustained VT, one case (0.4%) with tricuspid regurgitation, twelve cases (5.3%) with right bundle branch block. There was no occurrence of either EMB-related death or cardiac surgery. Left ventricular ejection fraction was significantly lower (32.0+/-18.7% vs 42.0+/-19.1%, P=0.023) and left ventricular end-diastolic dimension was larger (60.0+/-10.0 mm vs 54.2+/-10.2 mm, P=0.013) in patients with EMB related complications than in those without. It is concluded that transfemoral EMB with fluoroscopic and 2-D echocardiographic guidance is a safe procedure with low complication rate.
		                        		
		                        		
		                        		
		                        			Adult
		                        			;
		                        		
		                        			Biopsy/*adverse effects
		                        			;
		                        		
		                        			Cardiac Tamponade/etiology
		                        			;
		                        		
		                        			Echocardiography/*adverse effects
		                        			;
		                        		
		                        			Endocardium/*ultrasonography
		                        			;
		                        		
		                        			Female
		                        			;
		                        		
		                        			Fluoroscopy/*adverse effects
		                        			;
		                        		
		                        			Heart Diseases/*pathology
		                        			;
		                        		
		                        			Heart Ventricles/metabolism
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Male
		                        			;
		                        		
		                        			Middle Aged
		                        			;
		                        		
		                        			Pericardial Effusion/etiology
		                        			;
		                        		
		                        			Tachycardia, Ventricular/etiology
		                        			;
		                        		
		                        			Ventricular Function
		                        			
		                        		
		                        	
4.Time-dependent expression of vascular endothelial growth factor after acute myocardial ischemia in rats.
Rui-ming MAO ; Zhong-bo DU ; Wei-min GAO ; Li MI ; Bao-li ZHU
Journal of Forensic Medicine 2012;28(3):179-184
		                        		
		                        			OBJECTIVE:
		                        			To investigate the immunohistochemical distributions and expressions of vascular endothelial growth factor (VEGF) in the model of rat myocardial ischemia.
		                        		
		                        			METHODS:
		                        			The model of myocardial ischemia was established by ligating the left anterior descending (LAD) coronary artery of rats. The changes of VEGF expression were detected by immunohistochemistry and Western blot at time points after myocardial ischemia. The electrocardiographic changes were evaluated uninterruptedly.
		                        		
		                        			RESULTS:
		                        			The expression of VEGF was not be found in control group. Fifteen minutes after LAD ligation, weak positive expression of VEGF were found in the ischemic myocardium. The expression of VEGF reached the peak at 3 hours after ligation. The VEGF distribution was mainly localized in the ischemic and peri-ischemic regions. Six hours after LAD ligation, the expression of VEGF decreased comparing with 3 hours and showed a relatively higher level. Fatal arrhythmia was found in nine rats by the electrocardiograph.
		                        		
		                        			CONCLUSION
		                        			The immunohistochemical staining of VEGF could be helpful for investigating the location and severity of acute myocardial ischemia. Fatal arrhythmia may be secondary to myocardial ischemia.
		                        		
		                        		
		                        		
		                        			Acute Disease
		                        			;
		                        		
		                        			Animals
		                        			;
		                        		
		                        			Blotting, Western
		                        			;
		                        		
		                        			Disease Models, Animal
		                        			;
		                        		
		                        			Electrocardiography
		                        			;
		                        		
		                        			Forensic Pathology
		                        			;
		                        		
		                        			Immunohistochemistry
		                        			;
		                        		
		                        			Male
		                        			;
		                        		
		                        			Myocardial Ischemia/pathology*
		                        			;
		                        		
		                        			Myocardium/pathology*
		                        			;
		                        		
		                        			Myocytes, Cardiac/metabolism*
		                        			;
		                        		
		                        			Rats
		                        			;
		                        		
		                        			Rats, Sprague-Dawley
		                        			;
		                        		
		                        			Tachycardia, Ventricular/mortality*
		                        			;
		                        		
		                        			Time Factors
		                        			;
		                        		
		                        			Vascular Endothelial Growth Factor A/metabolism*
		                        			
		                        		
		                        	
5.Nifekalant hydrochloride terminating sustained ventricular tachycardia accompanied with QT dispersion prolongation.
Jing WANG ; Wei HUA ; Jun ZHU ; Yan-Min YANG ; Fang-Zheng WANG ; Jie-Lin PU ; Ke-Ping CHEN ; Shu ZHANG
Chinese Medical Journal 2010;123(15):2028-2033
BACKGROUNDVentricular tachycardia (VT) and ventricular fibrillation are the main reasons causing sudden cardiac death. This study aimed to investigate the effects of nifekalant hydrochloride (NIF) on QT dispersion (QTd) in treating VT.
METHODSA total of 16 consecutive patients suffered sustained VT was included and then randomly divided into two groups according to the administration duration of NIF. In long-time group (group L), patients were injected with NIF continuously for at least 12 hours after a bolus dose. The patients in short-time group (group S) were injected with NIF just for 1 hour.
RESULTSThere were 7 of all 10 episodes of VT which were terminated by NIF, including 4 episodes in group L were stopped over 1 hour after continuous infusion of NIF. One patient suffered from torsade de pointes. Electrocardiography analysis indicated that QTd was significantly decreased 12 hours after stopping of infusing NIF compared with that when VT stopped ((45.4 +/- 22.1) ms vs. (73.4 +/- 33.2) ms, P < 0.01), and the corrected QTd (QTcd) decreased too ((47.8 +/- 22.9) ms vs. (78.3 +/- 36.5) ms, P < 0.01). There was a positive correlation between the increase in QTd and dose of administrating NIF (P < 0.01), so was QTcd (P < 0.01).
CONCLUSIONSMore administration of NIF indicates higher terminating rate of VT and more QTd prolongation. However, the safety is acceptable if several important issues were noticed in using NIF, such as serum potassium concentration, stopping side-effect related agents, and carefully observing clinical responses.
Adult ; Anti-Arrhythmia Agents ; therapeutic use ; Electrocardiography ; Female ; Humans ; Long QT Syndrome ; drug therapy ; pathology ; Male ; Middle Aged ; Pyrimidinones ; therapeutic use ; Tachycardia, Ventricular ; drug therapy ; pathology ; Treatment Outcome
6.Postmortem genetic testing in sudden cardiac death due to ion channelopathies.
Journal of Forensic Medicine 2010;26(2):120-127
		                        		
		                        			
		                        			Sudden cardiac death accounts for majority of deaths in human. Evident cardiac lesions that may explain the cause of death can be detected in comprehensive postmortem investigation in most sudden cardiac death. However, no cardiac morphological abnormality is found in a considerable number of cases although the death is highly suspected from cardiac anomaly. With the advances in the modern molecular biology techniques, it has been discovered that many of these sudden deaths are caused by congenital ion channelopathies in myocardial cell, i.e., Brugada syndrome, long QT syndrome, catecholaminergic polymorphic ventricular tachycardia, and short QT syndrome, etc. This article presents the molecular genetics, electrocardiographic abnormalities, clinical manifestations, and mechanisms leading to sudden cardiac death with emphasis on the role of postmortem genetic testing in certification of cause of death. It may provide helpful information in investigating sudden cardiac death due to ion channelopathies in medico-legal practice.
		                        		
		                        		
		                        		
		                        			Arrhythmias, Cardiac/genetics*
		                        			;
		                        		
		                        			Autopsy/methods*
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		                        			Brugada Syndrome/genetics*
		                        			;
		                        		
		                        			Cause of Death
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		                        			Channelopathies/genetics*
		                        			;
		                        		
		                        			Death, Sudden, Cardiac/pathology*
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		                        			Electrocardiography
		                        			;
		                        		
		                        			Forensic Pathology
		                        			;
		                        		
		                        			Genetic Testing
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		                        			Heart Conduction System/physiopathology*
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		                        			Humans
		                        			;
		                        		
		                        			Ion Channels/genetics*
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		                        			Long QT Syndrome/genetics*
		                        			;
		                        		
		                        			Mutation
		                        			;
		                        		
		                        			Tachycardia, Ventricular/genetics*
		                        			
		                        		
		                        	
7.Coronary-Subclavian Steal Syndrome Presenting with Ventricular Tachycardia.
Hurkan KURSAKLIOGLU ; Sedat KOSE ; Atila IYISOY ; Basri AMASYALI ; Turgay CELIK ; Kudret AYTEMIR ; Ersoy ISIK
Yonsei Medical Journal 2009;50(6):852-855
		                        		
		                        			
		                        			Coronary-subclavian steal through the left internal mammary graft is a rare cause of myocardial ischemia in patients who have had a coronary bypass surgery. We report a 70-year-old man who presented with sustained monomorphic ventricular tachycardia 5 years after the surgical creation of a left internal mammary to the left anterior descending artery. Cardiac catheterization illustrated that the left subclavian artery was occluded proximally and that the distal course was visualized by retrograde filling through the left internal mammary graft. Clinical ventricular tachycardia was reproducibly induced with a single ventricular extrastimulus, and antitachycardia pacing terminated the tachycardia. Restoration of blood flow by way of a Dacron graft placed between the descending aorta and the subclavian artery resulted in the total relief of symptoms. Ventricular tachycardia could not be induced during the control electrophysiologic study after surgical revascularization.
		                        		
		                        		
		                        		
		                        			Aged
		                        			;
		                        		
		                        			Coronary Artery Bypass/adverse effects
		                        			;
		                        		
		                        			Coronary Artery Disease/*diagnosis/etiology/*pathology
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Male
		                        			;
		                        		
		                        			Postoperative Complications/diagnosis/etiology
		                        			;
		                        		
		                        			Subclavian Steal Syndrome/*diagnosis/etiology/*pathology
		                        			;
		                        		
		                        			Tachycardia, Ventricular/*pathology
		                        			
		                        		
		                        	
8.A Case of Catecholaminergic Polymorphic Ventricular Tachycardia.
Seung Yul LEE ; Jin Bae KIM ; Eui IM ; Woo In YANG ; Boyoung JOUNG ; Moon Hyoung LEE ; Sung Soon KIM
Yonsei Medical Journal 2009;50(3):448-451
		                        		
		                        			
		                        			Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a familial cardiac arrhythmia that is related to RYR2 or CASQ2 gene mutation. It occurs in patients with structurally normal heart and causes exercise-emotion-triggered syncope and sudden cardiac death. We experienced a case of CPVT in an 11 year-old female patient who was admitted for sudden cardiovascular collapse. The initial electrocardiogram (ECG) on emergency department revealed ventricular fibrillation. After multiple defibrillations, sinus rhythm was restored. However, recurrent ventricular fibrillation occurred during insertion of nasogastric tube without sedation in coronary care unit. On ECG monitoring, bidirectional ventricular tachycardia occurred with sinus tachycardia and then degenerated into ventricular fibrillation. To our knowledge, there has been no previous case report of CPVT triggered by sinus tachycardia in Korea. Therefore, we report the case as well as a review of the literature.
		                        		
		                        		
		                        		
		                        			Catecholamines/*metabolism
		                        			;
		                        		
		                        			Child
		                        			;
		                        		
		                        			Electrocardiography
		                        			;
		                        		
		                        			Female
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Tachycardia, Ventricular/*diagnosis/genetics/pathology
		                        			
		                        		
		                        	
9.Repetitive monomorphic ventricular tachycardia arising from left His-Purkinje system.
Ming-Long CHEN ; Bing YANG ; Wei-Zhu JU
Chinese Journal of Cardiology 2008;36(1):77-79
		                        		
		                        		
		                        		
		                        			Adolescent
		                        			;
		                        		
		                        			Adult
		                        			;
		                        		
		                        			Bundle of His
		                        			;
		                        		
		                        			pathology
		                        			;
		                        		
		                        			physiopathology
		                        			;
		                        		
		                        			Child
		                        			;
		                        		
		                        			Female
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Male
		                        			;
		                        		
		                        			Purkinje Fibers
		                        			;
		                        		
		                        			pathology
		                        			;
		                        		
		                        			physiopathology
		                        			;
		                        		
		                        			Tachycardia, Ventricular
		                        			;
		                        		
		                        			pathology
		                        			;
		                        		
		                        			physiopathology
		                        			
		                        		
		                        	
10.Clinical features of idiopathic ventricular tachycardia of various types and their radiofrequency ablation therapy.
Jian PENG ; Fa-hui RUAN ; Rong-hai YANG ; Shao-dong YI ; Ying-kai CUI ; Xiao-bao HUANG ; Man-ying JIA ; Su-rong MENG
Journal of Southern Medical University 2006;26(8):1152-1162
OBJECTIVETo analyze the clinical features idiopathic ventricular tachycardia (IVT) and evaluate the effect of radiofrequency ablation therapy for their management.
METHODSAn retrospective analysis was conducted in 165 IVT patients who received radiofrequency ablation therapy. IVT was classified into 3 types according to the site of origin, namely the right ventricular outflow tract (RVOT-IVT, 86 cases), left ventricular septum (LV-IVT, 75 cases), and left Valsalva sinus (4 cases).
RESULTS AND CONCLUSIONRVOT-IVT was more frequent in female patients than in male patients (60 vs 26, M/F ratio of 0.43). In LV-IVT, male patients prevailed (54 vs 21, M/F ratio of 2.57), suggesting a gender difference in the incidence of IVT. IVT occurred mainly in young and middle-age patients. Most RVOT-IVT occurred in the third to fourth decade of life (mean 36-/+12 years), and LV-IVT occurred at a younger age than did RVOT-IVT (mean 26-/+15 years, P<0.01). Twelve-lead ECGs revealed left bundle branch block morphology in RVOT-IVT, and most of them presented with frequent premature ventricular contraction and/or non-sustained ventricular tachycardia. All the RVOT-IVT patients were successfully ablated by radiofrequency energy in pace mapping. LV-IVT patients with right bundle branch block morphology presented sustained ventricular tachycardia for most of the time, and 97% of the patients were successfully managed with radiofrequency ablation in activation mapping. Four IVT patients were characterized by atypical bundle branch block, an inferior axis, and an R/S ratio >1 in lead V3 or V2, and their tachycardia was ablated successfully in the left sinus of Valsalva using pace mapping. Radiofrequency ablation is currently an effective procedure for IVT management.
Adult ; Aged ; Angioplasty, Laser ; methods ; Catheter Ablation ; methods ; Female ; Humans ; Male ; Middle Aged ; Retrospective Studies ; Tachycardia, Ventricular ; pathology ; therapy ; Treatment Outcome
            
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