Filed (PHiled). Greater than 1-2 years since publication

Williams Syndrome and Neonatal Cardiac Surgery for Congenital Single Ventricle

Taylor E. Katt, Robert L. Spicer, Anji T. Yetman, Ali N. Ibrahimiye, James M. Hammel, Jeffrey A. RobinsonUniversity of Nebraska Medical Center and Children’s Hospital and Medical Center.United States Journal of the American College of Cardiology Case ReportsJACC Case Rep 2020; 2: 1716-1719DOI: 10.1016/j.jaccas.2020.05.098 AbstractWilliams syndrome (WS) is an arteriopathic derangement associated with supravalvular aortic stenosis […]

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Echocardiographic Predictors of Ductal Tissue-Related Branch Pulmonary Artery Stenosis in Pulmonary Atresia

Marisha McClean, Deliwe Ngwezi, Timothy Colen, Kandice Mah, Mohammed Al-Aklabi, Lisa HornbergerStollery Children’s Hospital and University of Alberta. Children’s Hospital LHSC and Western University. Canada Pediatric CardiologyPediatr Cardiol 2022; 43: 878-886DOI: 10.1007/s00246-021-02799-4 AbstractBranch pulmonary artery (PA) stenosis due to ductus arteriosus (DA) tissue (DA-PS) contributes to the morbidity associated with pulmonary atresia (PAtr). We sought to

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Preoperative Computed Tomographic Angiography Can Predict Need for Branch Pulmonary Artery Intervention in Patients With Ductal-Dependent Pulmonary Blood Flow

Kirsten Graff, Anthony M. Hlavacek, Nicholas Aizcorbe, Scott M. Bradley, Shahryar M. ChowdhuryMedical University of South Carolina.United States World Journal of Pediatric and Congenital Heart SurgeryWorld J Pediatr Congenit Heart Surg 2023; 14: 275-281DOI: 10.1177/21501351221151050 AbstractBackground: Neonates with ductal-dependent pulmonary blood flow (DD-PBF) are at risk for pulmonary artery (PA) stenosis. The objective of this study was

Preoperative Computed Tomographic Angiography Can Predict Need for Branch Pulmonary Artery Intervention in Patients With Ductal-Dependent Pulmonary Blood Flow Read More »

Transcatheter management of combined patent ductus arteriosus and left pulmonary artery stenosis in congenital rubella syndrome: A series of three patients and an insight into case selection for intervention

Mahua Roy, Debasree Gangopadhyay, Noopur Goyel, Amitabha Chattopadhyay, Biswajit BandyopadhyayNH RTIICS and NSH.India Annals of Pediatric CardiologyAnn Pediatr Cardiol 2022; 15: 164-168DOI: 10.4103/apc.apc_232_20 AbstractTranscatheter closure of patent ductus arteriosus (PDA) is now the standard of care with some exceptions. Best treatment for peripheral pulmonary artery (PA) stenosis in small children is still debatable. Surgical augmentation, balloon

Transcatheter management of combined patent ductus arteriosus and left pulmonary artery stenosis in congenital rubella syndrome: A series of three patients and an insight into case selection for intervention Read More »

Erosion of Pulmonary Artery Banding into the Cardiovascular System: A First Case Report

Manouchehr Hekmat, Hamid Ghaderi, Zahra Ansari Aval, Seyedeh Adeleh Mirjafari, Mandana HekmatShahid Beheshti University of Medical Sciences. Ali-Asghar Children’s Hospital and Iran University of Medical Sciences.Iran ARYA AtherosclerosisARYA Ateroscler 2023; 19: 63-68 DOI: 10.48305/arya.2023.31062.2714 AbstractThere have been very rare reports on the migration of foreign bodies that are left or implanted in the body, and so

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The multisystem nature of isomerism: left isomerism complicated by Abernethy malformation and portopulmonary hypertension

Megan L. Ringle, Rohit Loomba, John C. Dykes, Danyal Khan, David Schidlow, Gil WernovskyLucile Packard Children’s Hospital and Stanford University School of Medicine. Advocate Children’s Hospital and Chicago Medical School. Nicklaus Children’s Hospital. Boston Children’s Hospital and Harvard Medical School. Children’s National Hospital.United States Cardiology in the YoungCardiol Young 2021; 31: 532-540DOI: 10.1017/S1047951121000809 AbstractIsomerism, also referred

The multisystem nature of isomerism: left isomerism complicated by Abernethy malformation and portopulmonary hypertension Read More »

Echocardiographic assessment of cardiac function abnormalities and related risk factors in Thai overweight and obese children

Darunwan Nimpum, Worawan JitthamNaresuan University.Thailand Annals of Pediatric CardiologyAnn Pediatr Cardiol 2023; 16: 413-421DOI: 10.4103/apc.apc_134_23 AbstractBackground: Childhood obesity has become a global concern, with its prevalence steadily increasing over the past decade. This condition negatively impacts the cardiovascular system, increasing the risk of morbidity and mortality in adulthood. This study aimed to identify cardiac function abnormalities and

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Incidence, Risk Factors and Effective Treatment Strategies for Chylothorax After Pediatric Heart Surgeries: Retrospective Analysis of Large Database in Single Institution

Muhammad Shahzada, Yasser A. Alheraish, Reem M. E. Beheri, Bushra Algethami, Patricia Machado, Gamal Mohamed, Fared Khouqeer, Zohair Al HaleesKing Faisal Specialist Hospital and Research Center.Saudi Arabia Journal of the Saudi Heart AssociationJ Saudi Heart Assoc 2023; 35: 169-176DOI: 10.37616/2212-5043.1341 AbstractBackground: Risk factors for postoperative chylothorax in children who had cardiothoracic procedures are not always clear. Due

Incidence, Risk Factors and Effective Treatment Strategies for Chylothorax After Pediatric Heart Surgeries: Retrospective Analysis of Large Database in Single Institution Read More »

Case report of generalized lymphatic dysplasia with PIEZO1 mutation and review of the literature

Wedad Alhazmia, Afnan Qurbana, Essa AlrashidiMaternity and Children Hospital in Makkah. King Saud Medical City in Riyadh.Saudi Arabia Respiratory Medicine Case ReportsRespir Med Case Rep 2023; 44:DOI: 10.1016/j.rmcr.2023.101872 AbstractBackground: The newborn malformation of primary lymphatic dysplasia (PLD), developed primarily due to PIEZO1 gene autosomal recessive mutation, is known to hinder with the lymphatic system action, causing chyle or lymph

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Resolution of Protein-Losing Enteropathy after Congenital Heart Disease Repair by Selective Lymphatic Embolization

Ranjit I. Kylat, Marlys H. Witte, Brent J. Barber, Yoav Dori, Fayez K. GhishanUniversity of Arizona College of Medicine. Children’s Hospital of Philadelphia. United States Pediatric Gastroenterology Hepatology and NutritionPediatr Gaestroenterol Hepatol Nutr 2019; 22: 594-600DOI: 10.5223/pghn.2019.22.6.594 AbstractWith improving survival of children with complex congenital heart disease (CCHD), postoperative complications, like protein-losing enteropathy (PLE) are increasingly

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