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Pediatric Right Bundle Branch Block

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[Clinical observation on six children of left bundle branch area pacing].

C C Dai, W L Dai, B J Guo,

Objective: To explore the safety and effectiveness of left bundle branch area pacing (LBBAP) in children. Methods: Clinical data, pacing electrocardiogram and parameters of 6 patients (5 females and 1 male) who underwent permanent pacemaker implantation and LBBAP from January to June 2019 in the Department of Pediatric Cardiology of ... Read more >>

Zhonghua Er Ke Za Zhi (Zhonghua er ke za zhi = Chinese journal of pediatrics)
[2020, 58(2):107-112]

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Selective left bundle branch pacing for pediatric complete heart block.

Shunmuga Sundaram Ponnusamy, Giridhar Muthu, Dasarath Bopanna,

Traditionally Right Ventricle has been the preferred site of pacing for the management of symptomatic brady-arrhythmias. The deleterious effect of chronic RV pacing has been shown by several studies. This has generated interest into a novel pacing strategy called physiological pacing wherein the His bundle or the left bundle is ... Read more >>

Indian Pacing Electrophysiol J (Indian pacing and electrophysiology journal)
[2020, 20(2):78-80]

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Rare Association Between Atrioventricular Septal Defect and Partial Anomalous Pulmonary Venous Connection.

Alexandre Noboru Murakami, Gabriela Guimarães Baston, Mariana Ribeiro Rodero Cardoso, Carlos Henrique De Marchi, Ulisses Alexandre Croti,

CLINICAL DATA:Infant, 7 months, female, referred to our department at one month of age, suspecting of congenital heart disease for further investigation. CHEST RADIOGRAPHY:Demonstrates cardiomegaly and prominent pulmonary vascular markings. ELECTROCARDIOGRAPHY:Shows right ventricular hypertrophy and left anterior fascicular block. ECHOCARDIOGRAPHY:Evidenced common atrioventricular valve with two orifices and the left superior ... Read more >>

Braz J Cardiovasc Surg (Brazilian journal of cardiovascular surgery)
[2020, 34(6):765-768]

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Transcatheter Device Closure of Perimembranous Ventricular Septal Defect in Pediatric Patients: Long-Term Outcomes.

Jayal Hasmukhbhai Shah, Sanket Pravinchandra Saraiya, Tushar Sudhakarrao Nikam, Mukesh Jitendra Jha,

Aims:The aim of this study is to evaluate the safety and efficacy of transcatheter device closure of perimembranous ventricular septal defects in pediatric patients at long-term follow-up. Materials and Methods:We prospectively studied 376 patients with perimembranous VSDs between September 2008 and December 2015 who underwent percutaneous closure at our center. ... Read more >>

Heart Views (Heart views : the official journal of the Gulf Heart Association)
[2020, 21(1):17-21]

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Italian recommendations for the management of pediatric patients under twelve years of age with suspected or manifest Brugada syndrome.

Fabrizio Drago, Raffaella Bloise, Gabriele Bronzetti, Loira Leoni, Giulio Porcedda, Berardo Sarubbi, Paolo De Filippo, Simone Gulletta, Marco Scaglione, ,

Minerva Pediatr. (Minerva pediatrica)
[2020, 72(1):1-13]

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Visualization and quantification of the atrioventricular conduction axis in hearts with ventricular septal defect using phase contrast computed tomography.

Shuichi Yoshitake, Yukihiro Kaneko, Kiyozo Morita, Masato Hoshino, Yoshihiro Oshima, Masashi Takahashi, Robert H Anderson, ,

OBJECTIVE:To visualize and quantify the atrioventricular conduction axis in the setting of ventricular septal defect using phase contrast computed tomography. METHODS:We used the SPring-8 synchrotron radiation facility in Hyogo prefecture in Japan, processing and reconstructing the data with 3-dimensional software. RESULTS:We studied 8 hearts obtained from patients known to have ... Read more >>

J. Thorac. Cardiovasc. Surg. (The Journal of thoracic and cardiovascular surgery)
[2020, :]

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Can the 12-lead ECG distinguish RVOT from aortic cusp PVCs in pediatric patients?

Bradley C Clark, Scott R Ceresnak, Robert H Pass, Lynn Nappo, Kohei Sumihara, Anne M Dubin, Kara Motonaga, Jeffrey P Moak,

BACKGROUND:The ability to differentiate right ventricular outflow tract (RVOT) from coronary cusp (CC) site of origin (SOO) by 12-lead ECG in pediatric patients may impact efficacy and procedural time. The objective of this study was to predict RVOT versus CC SOO by ECG in pediatric patients. METHODS:Pediatric patients (<21 years) ... Read more >>

Pacing Clin Electrophysiol (Pacing and clinical electrophysiology : PACE)
[2020, 43(3):308-313]

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Transcatheter Closure of Perimembranous Ventricular Septal Defects Using Different Generations of Amplatzer Devices: Multicenter Experience.

Roberto Mijangos-Vázquez, Amal El-Sisi, Juan P Sandoval Jones, José A García-Montes, Rogelio Hernández-Reyes, Rodina Sobhy, Antoine Abdelmassih, Mohammed M Soliman, Safaa Ali, Tatiana Molina-Sánchez, Carlos Zabal,

Objectives:To demonstrate safety and efficacy of using different generations of softer Amplatzer™ devices for ventricular septal defect (VSD) closure to avoid serious complications at follow-up. Background:Transcatheter closure of perimembranous ventricular septal defects (PmVSD) is a well-established procedure; however, it is associated with unacceptable incidence of complete heart block. Great advantages ... Read more >>

J Interv Cardiol (Journal of Interventional Cardiology)
[2020, 2020:8948249]

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Clinical Profile and Long-Term Follow-Up of Children with Brugada Syndrome.

Ibrahim El-Battrawy, Gretje Roterberg, Kim Schlentrich, Volker Liebe, Siegfried Lang, Boris Rudic, Erol Tülümen, Xiaobo Zhou, Martin Borggrefe, Ibrahim Akin,

Brugada syndrome (BrS) is a rare channelopathy associated with sudden cardiac death (SCD). Although outcome data of adult cohorts are well known, information on children are lacking. The aim of the present study was to analyze the clinical profile, treatment approach and long-term outcome of children affected with BrS. After ... Read more >>

Pediatr Cardiol (Pediatric cardiology)
[2020, 41(2):290-296]

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Risk factors for development of ventricular tachycardia in patients with ventricular premature contraction with a structurally normal heart.

Yuichi Nomura, Syunji Seki, Daisuke Hazeki, Kentaro Ueno, Yuji Tanaka, Kiminori Masuda, Makoto Nishibatake, Masao Yoshinaga,

Background:We examined risk factors for development of ventricular tachycardia (VT) in pediatric patients with ventricular premature contractions (VPCs) and a structurally normal heart. Methods:The subjects were 81 844 first graders and 88 244 seventh graders of Kagoshima City School-based cardiovascular screening (SCV-screening) between 2001 and 2015. We retrospectively reviewed the clinical data ... Read more >>

J Arrhythm (Journal of arrhythmia)
[2020, 36(1):127-133]

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A proposed approach to the asymptomatic pediatric patient with Wolff-Parkinson-White pattern.

Henry Chubb, Scott R Ceresnak,

HeartRhythm Case Rep (HeartRhythm case reports)
[2020, 6(1):2-7]

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Successful right anteroseptal manifest accessory pathway cryoablation in a six-month infant with dyssynchrony-induced dilated cardiomyopathy.

Pelin Köşger, Fatma Sevinç Şengül, Hasan Candaş Kafalı, Birsen Uçar, Yakup Ergül,

Anatol J Cardiol (Anatolian journal of cardiology)
[2019, 22(5):272-275]

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Pediatrics and GUCHs.

J Arrhythm (Journal of Arrhythmia)
[2019, 35(Suppl 1):693-711]

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Post-operative Brugada electrocardiographic pattern, polymorphic ventricular tachycardia, and sudden death in a child after administration of propofol anaesthesia.

Duygu Uzun, Nimra Hassan, Utkarsh Kohli,

A 9-year-old African-American girl presented with sudden cardiac arrest a few hours after adenotonsillectomy. She received anaesthesia which included propofol during the procedure. Her electrocardiogram (EKG) showed type 1 Brugada pattern, and genetic testing revealed a variant of unknown significance in desmoplakin (DSP) gene. We discuss the association between propofol, ... Read more >>

Cardiol Young (Cardiology in the young)
[2020, :1-4]

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Is right ventricular resynchronization the key to both right and left ventricular remodeling?

Franziska Markel, Christian Paech, Roman Antonin Gebauer,

HeartRhythm Case Rep (HeartRhythm case reports)
[2020, 6(1):20-22]

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Exercise-induced syncope and Brugada syndrome.

Anjan S Batra, Rachel Watson, Anthony C McCanta,

Brugada syndrome (BrS) is a hereditary condition that is characterized by ST elevation, ventricular tachycardia or fibrillation, and sudden cardiac death in otherwise healthy patients. Life-threatening arrhythmias generally occur, while at rest, with fever or during vagotonic states. Exercise is generally not considered a trigger for ventricular arrhythmias or syncope ... Read more >>

Ann Pediatr Cardiol (Annals of pediatric cardiology)
[2019, 12(3):292-294]

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Simultaneous dual AV node antegrade conduction (2 for 1) and lower common pathway (2-1) block illustrate AVNRT physiology.

Balaram Krishna Hanumanthu, Andrew Krummerman, Michael Grushko,

We report a rare case of spontaneous initiation of Atrioventricular nodal reentry tachycardia (AVNRT) via 2 for 1 phenomenon, into a 2:1 AV block due to lower common pathway block and finally transition to 1:1 tachycardia. The premature atrial p wave traverses down both the fast and slow pathway simultaneously ... Read more >>

Indian Pacing Electrophysiol J (Indian pacing and electrophysiology journal)
[2020, 20(2):70-72]

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Abnormal myocardial expression of SAP97 is associated with arrhythmogenic risk.

Hassan Musa, Cherisse A Marcou, Todd J Herron, Michael Makara, David J Tester, Ryan O'Connell, Brad Rosinski, Guadalupe Guerrero-Serna, Michelle L Milstein, Andre Monteiro Da Rocha, Dan Ye, Lia Crotti, Vladislav V Nesterenko, Silvia Castelletti, Margherita Torchio, Maria-Christina Kotta, Federica Dagradi, Charles Antzelevitch, Peter J Mohler, Peter J Schwartz, Michael J Ackerman, Justus M B Anumonwo,

Background Synapse-associated protein 97 (SAP97) is a scaffolding protein crucial for the functional expression of several cardiac ion channels and therefore proper cardiac excitability. Alterations in the functional expression of SAP97 can modify the ionic currents underlying the cardiac action potential and consequently confer susceptibility for arrhythmogenesis. In this study, ... Read more >>

Am. J. Physiol. Heart Circ. Physiol. (American journal of physiology. Heart and circulatory physiology)
[2020, :]

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Prospective Evaluation of the Utility of Whole Exome Sequencing in Dilated Cardiomyopathy.

Jay Ramchand, Mathew Wallis, Ivan Macciocca, Elly Lynch, Omar Farouque, Melissa Martyn, Dean Phelan, Belinda Chong, Siobhan Lockwood, Robert Weintraub, Tina Thompson, Alison Trainer, Dominica Zentner, Jitendra Vohra, Michael Chetrit, David L Hare, Paul James,

Background Dilated cardiomyopathy may be heritable but shows extensive genetic heterogeneity. The utility of whole exome sequencing as a first-line genetic test for patients with dilated cardiomyopathy in a contemporary "real-world" setting has not been specifically established. Using whole exome sequencing with rigorous, evidence-based variant interpretation, we aimed to identify ... Read more >>

J Am Heart Assoc (Journal of the American Heart Association)
[2020, 9(2):e013346]

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Neonatal supraventricular tachycardia.

Chandra Srinivasan, Seshadri Balaji,

Supraventricular tachycardia (SVT) is one of the most common conditions requiring emergency cardiac care in neonates. Atrioventricular reentrant tachycardia utilizing an atrioventricular bypass tract is the most common form of SVT presenting in the neonatal period. There is high likelihood for spontaneous resolution for most of the common arrhythmia substrates ... Read more >>

Indian Pacing Electrophysiol J (Indian pacing and electrophysiology journal)
[2019, 19(6):222-231]

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Pearson marrow-pancreas syndrome with cardiac conduction abnormality necessitating prophylactic pacemaker implantation.

Mats Steffi Jennifer, Daniel Cortez,

Pearson marrow-pancreas syndrome (PS), an exceedingly rare mitochondrial disorder, involves multiple systems including hematologic system and pancreas. Other mitochondrial disorders have been associated with progressive infrahisian block but this has not yet been described as a major feature of PS. We report a 7-year-old girl with classical features of PS ... Read more >>

Ann Noninvasive Electrocardiol (Annals of Noninvasive Electrocardiology : The Official Journal of the International Society for Holter and Noninvasive Electrocardiology, Inc)
[2020, 25(1):e12681]

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[Analysis of 30 cases of inherited cardiac arrhythmia syndrome in children].

Z L Li, S Y Zeng, D P Liang, T Liu, S S Wang, Z W Zhang,

Objective: To analyze and summarize the diagnosis and treatment experience of common inherited cardiac arrhythmia syndrome in pediatric patients, and explore the most appropriate therapy. Methods: A retrospective review identified 30 pediatric cases (19 males, 11 females) diagnosed with long QT syndrome (LQTS), Brugada syndrome (BrS), catecholaminergic polymorphic ventricular tachycardia ... Read more >>

Zhonghua Er Ke Za Zhi (Zhonghua er ke za zhi = Chinese journal of pediatrics)
[2019, 57(9):700-704]

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2019 HRS/EHRA/APHRS/LAHRS expert consensus statement on catheter ablation of ventricular arrhythmias: Executive summary.

Edmond M Cronin, Frank M Bogun, Philippe Maury, Petr Peichl, Minglong Chen, Narayanan Namboodiri, Luis Aguinaga, Luiz Roberto Leite, Sana M Al-Khatib, Elad Anter, Antonio Berruezo, David J Callans, Mina K Chung, Phillip Cuculich, Andre d'Avila, Barbara J Deal, Paolo Della Bella, Thomas Deneke, Timm-Michael Dickfeld, Claudio Hadid, Haris M Haqqani, G Neal Kay, Rakesh Latchamsetty, Francis Marchlinski, John M Miller, Akihiko Nogami, Akash R Patel, Rajeev Kumar Pathak, Luis C Saenz Morales, Pasquale Santangeli, John L Sapp, Andrea Sarkozy, Kyoko Soejima, William G Stevenson, Usha B Tedrow, Wendy S Tzou, Niraj Varma, Katja Zeppenfeld,

Ventricular arrhythmias are an important cause of morbidity and mortality and come in a variety of forms, from single premature ventricular complexes to sustained ventricular tachycardia and fibrillation. Rapid developments have taken place over the past decade in our understanding of these arrhythmias and in our ability to diagnose and ... Read more >>

J Arrhythm (Journal of arrhythmia)
[2020, 36(1):1-58]

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Balloon pulmonary valvuloplasty in neonates with critical pulmonary stenosis: Jugular or femoral.

Erick Hoetama, Radityo Prakoso, Poppy Surwianti Roebiono, Indriwanto Sakidjan, Yovi Kurniawati, Sisca Natalia Siagian, Olfi Lelya, Anna Ulfah Rahajoe, Ganesja Moelia Harimurti, Oktavia Lilyasari,

Background:Critical pulmonary stenosis (PS) is one of the life-threatening congenital heart diseases which present during the neonatal period with cyanosis. Surgical valvotomy was once the procedure of choice for critical PS; however, balloon pulmonary valvuloplasty (BPV) has now become the standard treatment. Although the procedure is usually simple, crossing the ... Read more >>

Ann Pediatr Cardiol (Annals of pediatric cardiology)
[2020, 13(1):11-15]

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DSP p.(Thr2104Glnfs*12) variant presents variably with early onset severe arrhythmias and left ventricular cardiomyopathy.

Krista Heliö, Tiia Kangas-Kontio, Sini Weckström, Sari U M Vanninen, Katriina Aalto-Setälä, Tero-Pekka Alastalo, Samuel Myllykangas, Tiina M Heliö, Juha W Koskenvuo,

BACKGROUND:Dilated cardiomyopathy (DCM) is a condition characterized by dilatation and systolic dysfunction of the left ventricle in the absence of severe coronary artery disease or abnormal loading conditions. Mutations in the titin (TTN) and lamin A/C (LMNA) genes are the two most significant contributors in familial DCM. Previously mutations in ... Read more >>

BMC Med. Genet. (BMC medical genetics)
[2020, 21(1):19]

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