Pediatric Pulmonary Vascular Disease

Unusual Malformation of the Heart

Robert J. Probyn-WilliamsGeneral Lying-in Hospital.Great Britain Journal of Anatomy and PhysiologyJ Anat Physiol 1894; 28: 305-308DOI: Not Available AbstractAbstract Not Available CategorySegmental Pulmonary Venous Disease. Without a Focus on Pulmonary HypertensionPulmonary Vascular Pathology Age Focus: Pediatric Fresh or Filed Publication: Filed (PHiled). Greater than 1-2 years since publication Article AccessFree PDF File or Full Text Article […]

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Lung biopsies in infants and children in critical care situation

Yaül Levy, Lauren Bitton, Chiara Sileo, Jérome Rambaud, Yohan Soreze, Camille Louvrier, Hubert Ducou le Pointe, Harriet Corvol, Erik Hervieux, Sabine Irtan, Pierre-Louis Leger, Blandine Prévost, Aurore Coulomb, L’Herminé, Nadia NathanArmand Trousseau Hospital and Sorbonne University. Centre de recherche Saint Antoine. France Pediatric PulmonologyPediatr Pulmonol 2023;DOI: 10.1002/ppul.26845 AbstractIntroduction: Lung biopsy is considered as the last step investigation

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Predischarge death or lung transplantation in tracheostomy and ventilator dependent grade 3 bronchopulmonary dysplasia

Roy Maynard, Madeline Armstrong, Katrin O’Grady, Brooke Moore, Stephen Kurachek, George B. Mallory, William WheelerChildren’s Minnesota. Pediatric Home Service. Johns Hopkins University. Texas Children’s Hospital and Baylor College of Medicine. United States Pediatric PulmonologyPediatr Pulmonol 2024;DOI: 10.1002/ppul.26837 AbstractBackground: Premature infants surviving beyond a postmenstrual age (PMA) of 36 weeks with severe or grade 3 bronchopulmonary dysplasia (sBPD)

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Sutureless Repair of Extracardiac Univentricular Total Anomalous Pulmonary Venous Connection

Takeaki Harada, Toshihide Nakano, Yuseke Ando, Joji HashimotoFukuoka Children’s Hospital.Japan Annals of Thoracic SurgeryAnn Thorac Surg 2023;DOI: 10.1016/j.athoracsur.2023.05.010 AbstractBackground: This study aimed to evaluate the results of sutureless repair of extracardiac total anomalous pulmonary venous connection (TAPVC) with a functional single ventricle at a single institution, including changes in the anastomotic site over time.Methods: The database contained 98

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Surgical results of total anomalous pulmonary venous connection repair in 256 patients

Takeaki Harada, Toshihide Nakano, Shinichiro Oda, Hideaki KadoFukuoka Children’s Hospital.Japan Interactive CardioVascular and Thoracic SurgeryInteract Cardiovasc Thorac Surg 2019; 8: 421-426DOI: 10.1093/icvts/ivy267 AbstractObjectives: This study was performed to analyse the surgical results of total anomalous pulmonary venous connection (TAPVC) repair at a single institution and to identify trends and variables associated with mortality and morbidity, particularly predictors

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Total anomalous pulmonary venous connection: results of surgical repair of 100 patients at a single institution

Angela M. Kelle, Carl L. Backer, Jeffrey G. Gossett, Sunjay Kaushal, Constantine MavroudisNorthwestern University Feinberg School of Medicine and Children’s Memorial Hospital.United States Journal of Thoracic and Cardiovascular SurgeryJ Thorac Cardiovasc Surg 2010; 139: 1387-1394DOI: 10.1016/j.jtcvs.2010.02.024 AbstractObjective: Surgical repair of total anomalous pulmonary venous connection is associated with significant mortality and morbidity, especially in patients with single-ventricle

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Left-side pulmonary vein obstruction after arterial switch operation in infants with D-transposition of the great arteries

Mathias Emmel, I. Bauer, M. Plug, Sabine Schickendantz, U. MennickenUniversity of Cologne. Germany Pediatric CardiologyPediatr Cardiol 1997; 18: 306-308 DOI: 10.1007/s002469900180 AbstractWe describe two cases of left-side pulmonary vein obstruction observed after the arterial switch operation (Jatene) for D-transposition of the great arteries. This appears to be related to left-sided pulmonary vein obstruction occurring coincidently with

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Congenital unilateral pulmonary vein stenosis complicating transposition of the great arteries

Michael Vogel, Judith Ash, Richard D. Rowe, George A. Trusler, Marlene RabinovitchHospital for Sick Children and University of Toronto.Canada American Journal of CardiologyAm J Cardiol 1984; 54: 166-171DOI:https://doi.org/10.1016/0002-9149(84)90323-0 AbstractFour patients with transposition of the great arteries and unilateral pulmonary vein (PV) stenosis, all left-sided, were studied. Two patients had an intact ventricular septum (1 with

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Management of total anomalous pulmonary venous drainage in early infancy

Welton M. Gersony, Frederick O. Bowman Jr, Carl N. Steeg, Constance J. Hayes, Mary Jane Jesse, James R. MalmColumbia University College of Physicians & Surgeons and Presbyterian Hospital.United States CirculationCirculation 1971; 43: I19-I24DOI: 10.1161/01.cir.43.5s1.i-19 AbstractTen consecutive babies ranging in age from two weeks to five months, with total anomalous pulmonary venous drainage and pulmonary artery hypertension,

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[Budd-Chiari syndrome with hepatopulmonary syndrome: a case report and literature review]

Tian Fengyan, Dong Xiao, Hou Xiaohan, Yuan Ruyue, Pan Yuanwei, Zhang DaFirst Affiliated Hospital of Zhengzhou University. China Zhonghua Er Ke Za Zhi 2024; 62: 71-75DOI: 10.3760/cma.j.cn112140-20230828-00139 AbstractObjective: To summarize the clinical features and prognosis of Budd-Chiari syndrome with hepatopulmonary syndrome (HPS) in children. Methods: The clinical data of a child who had Budd-Chiari syndrome with HPS treated at the Department of Pediatrics of the

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