Results 41 to 50 of about 357,919 (156)

Successful Treatment With Ivabradine for Junctional Ectopic Tachycardia–Induced Cardiomyopathy With Hypoplastic Left Heart Syndrome

Journal of Arrhythmia, Volume 41, Issue 6, December 2025.
A patient with hypoplastic left heart syndrome developed heart failure due to tachycardia‐induced cardiomyopathy from junctional ectopic tachycardia. Conventional antiarrhythmic therapy was ineffective, but ivabradine successfully controlled the arrhythmia and improved both ventricular function and heart failure.
Yuto Fukuda, Hisaaki Aoki, Kiyohiro Takigiku, Noboru Inamura   +3 more
wiley   +1 more source

Parent’s involvement in decisions when their child is admitted to hospital with suspected shunt malfunction: study protocol [PDF]

, 2009
Aim.  This paper outlines the protocol for a study aimed at exploring parent’s involvement during professional–parent interactions and decisions about their child’s care in the context of suspected shunt malfunction. Background.
Smith, Joanna, Bekker, Hilary, Chatwin, John, Cheater, Francine, Bekker, H, Chatwin, J, Smith, J, Cheater, F   +7 more
core   +1 more source

Assessment of Double Outlet Left Ventricle in Pediatrics Using Transthoracic Echocardiography and Computed Tomographic Angiography

Pediatric Discovery, Volume 3, Issue 4, December 2025.
The clinical manifestation of DOLV was atypical. TTE has a relatively high diagnostic accuracy for DOLV in pediatric, which is very valuable for its early detection. ABSTRACT Double outlet left ventricle (DOLV) is a rare congenital cardiac anomaly in which both great arteries originate entirely or predominantly from the morphologic left ventricle.
Xu Zhu, Guangyi Zhong, Xiaojuan Ji, Xue Xiang, Min Zheng, Huina Yan, Rui Li   +6 more
wiley   +1 more source

Ductus arteriosus banding to regulate excessive pulmonary blood flow in a neonate with necrotizing enterocolitis and complex congenital heart disease, including pulmonary atresia and total anomalous pulmonary venous return: a case report

Journal of Cardiothoracic Surgery, 2022
Background Patients with right isomerism have accompanying complex congenital heart disease, which is characterized by pulmonary atresia and total anomalous pulmonary venous return.
Takayoshi Oyasu, Mineji Hayakawa, Noriyoshi Ebuoka, Junichi Oba   +3 more
doaj   +1 more source

Tricuspid Atresia and Transposition of the Great Arteries in a Neonate With Successful Surgical Correction: A Case Report

Clinical Case Reports, Volume 13, Issue 8, August 2025.
ABSTRACT Tricuspid atresia (TA) with transposition of the great arteries (TGA) without pulmonary obstruction is a rare type of TA that delays diagnosis due to late onset of cyanosis, which delays surgery, as timely surgical interventions have contributed to converting the high mortality rate into a high survival rate.
William Borghol, Saja Karaja, Saleh Takkem   +2 more
wiley   +1 more source

Isolated chylopericardium: A rare complication postpediatric cardiac surgery: A case report

Journal of Pediatric Critical Care
Common complications following congenital cardiac surgery include pleural effusion, excessive bleeding, cardiac arrest, and systemic infections. Chylopericardium, however, is very rare. Our patient experienced exertional dyspnea, 1 month after undergoing
Aayush Sharma, Veeresh Manvi, Gananjay Salve, Nidhi Manvi   +3 more
doaj   +1 more source

Aretrospective analysis of Fontan procedure and its sequence in tertiary care teaching hospital in southern India [PDF]

Perspectives In Medical Research, 2015
Introduction: The Fontan operation is usually the final palliative procedure in patients with univentricular heart. The objectives of this study were firstly to describe the clinical and hemodynamic characteristics of a group of patients with ...
1 2 3 4 Abhishek Prabhu , Mahadev DamodarDixit , Mohan Dattatraya Gan ,Veeresh Manvi
doaj  

Clinical and Imaging Predictors of Poor Prognosis in Ebstein Anomaly

CJC Pediatric &Congenital Heart Disease, Volume 4, Issue 4, Page 203-212, August 2025.
Abstract Ebstein anomaly is a rare congenital heart condition characterized by the partial or complete absence of tricuspid valve delamination, a variable degree of “atrialization” of the right ventricle, and a redundant anterior leaflet with fenestrations.
Nabil Dib, Laura Vidales, Juva Benseba, Paul Khairy, François‐Pierre Mongeon, Annie Dore, Nancy Poirier, Blandine Mondésert, Stéphanie Tan, Marie‐A. Chaix   +9 more
wiley   +1 more source

Half a Century's Experience With the Superior Cavopulmonary (Classic Glenn) Shunt

, 2016
Five decades after its introduction, the Glenn shunt remains an integral step for patients undergoing single-ventricle palliation. We performed a longitudinal follow-up of the original cohort of patients who underwent Glenn shunt.
Steele, Margaret M, Kirshbom, Paul M, Karimi, Mohsen, Zahr, Riad Abou, Kopf, Gary S, Elder, Robert W, Sainathan, Sandeep   +6 more
core   +1 more source

Optimization of the Assisted Bidirectional Glenn Procedure for First Stage Single Ventricle Repair

, 2018
Background: First-stage single-ventricle palliation is challenging to manage, and significant interstage morbidity and mortality remain. Prior computational and in vitro studies of the assisted bidirectional Glenn (ABG), a novel first-stage procedure ...
Jessica Shang, Jeffrey A. Feinstein, Alison L. Marsden, Tain-Yen Hsia, Aekaansh Verma, Mahdi Esmaily, Richard Figliola   +6 more
core   +1 more source