Pediatric Pulmonary Vascular Disease

Invasive haemodynamics predict outcomes in paediatric pulmonary artery hypertension

Rupesh Kumar Natarajan, Nathan Rodgers, Shanti Narasimhan, Matthew Ambrose, Abraham Rothman, Michael Shyne, Michael Evans, Varun AggarwalUniversity of Minnesota. University of Nevada, Las Vegas School of Medicine.United States Cardiology in the YoungCardiol Young 2024;DOI: 10.1017/S1047951124000647 AbstractBackground: Invasive haemodynamics are often performed for initiating and guiding pulmonary artery hypertension therapy. Little is known about the predictive value of […]

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Patent Ductus Arteriosus and Lung MRI Phenotype in Moderate and Severe Bronchopulmonary Dysplasia-Pulmonary Hypertension

Kurt R. Bjorkman, Kimberley G. Miles, Laura E. Bellew, Kristin A. Schneider, S. Melissa Magness, Nara S. Higano, Nicholas J. Ollberding, X. Hoyos Cordon, Russel M. Hirsch, Erik B. Hysinger, Jason C. Woods, Paul J. CritserCincinnati Children’s Hospital Medical Center and University of Cincinnati.United States American Journal of Respiratory and Critical Care MedicineAm J Respir

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Host Factor Vulnerability and Development of Progressive Intraluminal Pulmonary Vein Stenosis after Congenital Heart Disease Surgery

Donna A. Goff, Kimberlee Gauvreau, Pedro J. del Nido, Mark W. Kieran, Stephen J. Roth, Kathy J. JenkinsChildren’s Hospital Boston and Harvard Medical School. Lucille Packard Children’s Hospital and Stanford University.United States Congenital Heart DiseaseCongenit Heart Dis 2009; 4: 86–90DOI: https://doi.org/10.1111/j.1747-0803.2009.00272.x AbstractObjective. The aim of this study is to explore the risk factors for progressive intraluminal

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Anomalous pulmonary venous connections and related anomalies: nomenclature, embryology, anatomy, and morphology

Michael J. Walsh, Ross M. Ungerleider, Vera D. Aiello, Diane Spicer, Jorge M. GiroudBrenner Children’s Hospital and Wake Forest University Medical Center. Universidade de São Paulo. Johns Hopkins All Children’s Hospital.United States and Brazil World Journal of Pediatric and Congenital Heart SurgeryWorls J Pediatr Congenit Heart Surg 2013; 4: 30-43DOI: 10.1177/2150135112458439 AbstractThis article combines material from

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Single-Cell RNA Sequencing Reveals Repair Features of Human Umbilical Cord Mesenchymal Stromal Cells

Chanéle Cyr-Depauw, David P. Cook, Ivana Mizik, Flore Legase, Arul Vadivel, Laurent Renesme, Yupu Deng, Shumei Zhong, Pauline Bardin, Liqun Xu, Marius A. Möbius, Jenny Marzahn, Daniel Freund, Duncan J. Stewart, Barbara C. Vanderhyden, Mario Rüdiger, Bernard ThébaudOttawa Hospital Research Institute. University of Ottawa. Universitätsklinikum Carl Gustav Carus. Technische Universität Dresden. Children’s Hospital of Eastern

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Mixed type of total anomalous pulmonary venous connection with hemi-pulmonary vein atresia

Yasuhisa Shimazaki, Susumu Nakano, Hiroshi Kato, Shigeaki Ohtake, Seiichiro Ikawa, Takuya Miura, Tetuya Sano, Jun Arisawa, Hikaru MatsudaOsaka University Medical School.Japan Annals of Thoracic SurgeryAnn Thorac Surg 1993; 56: 1399-1401DOI: 10.1016/0003-4975(93)90694-d AbstractThis reports a successfully corrected case of an 8-day-old baby who had a rare mixed type of total anomalous pulmonary venous connection in which the

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Common pulmonary vein atresia: a successfully corrected case

Yasuhisa Shimazaki, T. Yagihara, T. Nakada, O. Hirose, H. SugimotoOsaka University Medical School.Japan Journal of Cardiovascular SurgeryJ Cardiovasc Surg 1987; 28: 395-397DOI: Not Available AbstractCommon pulmonary vein atresia is a rare congenital cardiac anomaly in which there is no communication between the confluence of the pulmonary veins and the heart or the major systemic venous

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Spontaneous pneumothorax in common pulmonary vein atresia

Joan K. Sharda, Lawrence E. Kurlandsky, Samuel L. Lacina, Leonard L. RadeckiButterworth Hospital.United States Journal of PerinatologyJ Perinatol 1990; 10: 70-74DOI: Not Available AbstractCommon pulmonary vein atresia is a rare congenital anomaly that is rapidly fatal unless immediately recognized and corrected by surgical intervention. This article describes three neonates who died with the diagnosis soon

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Atresia of the common pulmonary vein

Youcef Sadou, Matteo Ciuffreda, Giancarlo CrupiOspedali Riuniti di Bergamo.Italy Cardiology in the YoungCardiol Young 2006; 16: 398-400DOI: 10.1017/S1047951106000199 AbstractA newborn girl with atresia of the common pulmonary vein, presented immediately after birth with severe cyanosis and acidosis. The diagnosis of totally obstructed total pulmonary venous return was made by cross-sectional echocardiography. Subsequent cardiac catheterization failed to

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Common pulmonary vein atresia: a diagnostic and therapeutic challenge

Carlos Mas, Andrew Cochrane, Samuel Menahem, Brodie KnightRoyal Children’s Hospital. Women’s and Children’s Hospital.Australia Pediatric CardiologyPediatr Cardiol 2000; 21: 490-492DOI: 10.1007/s002460010119 AbstractFollowing Doppler echocardiographic evaluation, a 16 hour-old infant underwent successful surgical repair of common pulmonary vein atresia. Investigations for prolonged postoperative ventilatory assistance, including cardiac catheterization and computerized tomography, led to a clinical diagnosis of

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