Pediatric Pulmonary Vascular Disease

Absent left pulmonary vein without anomalous connection: diagnosis and management in the newborn

Ashok V. Mehta, Balasubrahmanyam ChidambaramJames H. Quillen College of Medicine.United States American Heart JournalAm Heart J 1992; 124: 804-806DOI: 10.1016/0002-8703(92)90302-c AbstractAbstract Not Available CategorySegmental Pulmonary Venous Disease. Without a Focus on Pulmonary HypertensionDiagnostic Testing for Pulmonary Vascular Disease. Invasive Testing Age Focus: Pediatric Pulmonary Vascular Disease Fresh or Filed Publication: Filed (PHiled). Greater than 1-2 years […]

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Pulsed wave and color Doppler findings in congenital pulmonary vein stenosis

Steven A. Webber, Eustace de Souza, Michael W. H. PattersonBritish Columbia Children’s Hospital and University of British Columbia.Canada Pediatric CardiologyPediatr Cardiol 1992; 13: 112-115DOI: 10.1007/BF00798218 AbstractA premature infant presented at 8 weeks of age with respiratory failure and pulmonary hypertension. Two-dimensional echocardiography was not diagnostic but color flow imaging and pulsed Doppler examination revealed turbulent and

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[Surgical treatment of total anomalous pulmonary venous connection Darling type Ib using pedicled right atrial flap]

S. Nemoto, Y. Imai, S. Hoshino, K. Ishihara, K. Sawatari, H. Misumi, M. Terada, T. Hiramatsu, H. HikawaTokyo Women’s Medical College.Japan Kyobu Geka (Japanese Journal of Thoracic SurgeryKyobu Geka 1992; 45: 878-882DOI: Not Available AbstractA one-month-old baby with total anomalous pulmonary venous connection (TAPVC) type Ib underwent a total correction with a pedicled right atrial

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Common pulmonary vein atresia: the role of extracorporeal membrane oxygenation

Golde G. Dudell, Marva L. Evans, Henry F. Krous, Robert L. Spicer, John J. LambertiChildren’s Hospital, San Diego.United States PediatricsPediatrics 1993; 91: 403-410DOI: Not Available AbstractCommon pulmonary vein atresia is a rare form of cyanotic congenital heart disease in which the pulmonary veins join to form a blind confluence that does not communicate with the

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Intraoperative and percutaneous stenting of congenital pulmonary artery and vein stenosis

Alan M. Mendelsohn, Edward L. Bove, Flavian M. Lupinetti, Dennis C. Crowley, Thomas R. Lloyd, Raymond T. Fedderly, Robert H. Beekman IIIUniversity of Michigan Medical Center.United States CirculationCirculation 1993; 88: II210-II217DOI: Not Available AbstractBackground: Conventional surgical or balloon dilation therapy for pulmonary artery or vein stenosis has been unsatisfactory in many patients. Balloon-expandable stents offer a

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Hybrid approach to pulmonary vein stenting after Fontan palliation

Daniel R. Critchfield, Reid C. Chamberlain, Joseph W. Turek, Gregory A. FlemingDuke University Medical Center.United States Catheterization and Cardiovascular InterventionsCatheter Cardiovasc Interv 2023; DOI: 10.1002/ccd.30831 AbstractPulmonary vein stenosis is poorly tolerated in patients who have undergone Fontan palliation and typically requires surgical or transcatheter intervention. Percutaneous transcatheter approaches to intervention can be technically difficult due to

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Recurrent fibrovascular granulation on PhotoFix® bovine pericardium causing systemic and pulmonary venous obstruction after repair of scimitar syndrome

Nikki Taylor, Zsofia Long, Michael Ma, Alisa ArunamataStanford University School of Medicine.United States Cardiology in the YoungCardiol Young 2021; 31: 829-830 DOI: 10.1017/S1047951121000822 AbstractA young adult with late diagnosis of scimitar syndrome underwent infradiaphragmatic baffling of the scimitar vein to left atrium through an intra-atrial tunnel using PhotoFix® bovine pericardium with recurrent extensive fibrovascular granulation of

Recurrent fibrovascular granulation on PhotoFix® bovine pericardium causing systemic and pulmonary venous obstruction after repair of scimitar syndrome Read More »

Essential role of cardiac computed tomography for surgical decision making in children with total anomalous pulmonary venous connection and single ventricle

Ana L. Vasquez Choy, Dilachew A. Adebo, Sheba John, Christopher E. Greenleaf, Jorge D. Salazar, Antonio F. KornoChildren’s Heart Institute, Memorial Hermann Hospital and University of Texas Medical School at Houston. United States Journal of Cardiac SurgeryJ Card Surg 2022; 37: 1544-1549DOI: 10.1111/jocs.16427 AbstractBackground: Total anomalous pulmonary venous connection (TAPVC) is a major risk factor in infants

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Outcomes of total anomalous pulmonary venous drainage repair in neonates and the impact of pulmonary hypertension on survival

Antonia Schulz, Damien M. Wu, Shuta Ishigami, Edward Buratto, Duncan MacGregor, Matthew S. Yong, Yaroslav Ivanov, Roberto Chiletti, Christian P. Brizard, Igor E. KonstantinovRoyal Children’s Hospital. University of Melbourne. Murdoch Children’s Research Institute.Australia Journal of Thoracic and Cardiovascular Surgery OpenJTCVS Open 2022; 12: 335-343DOI: 10.1016/j.xjon.2022.09.008 AbstractBackground: Mortality after repair of total anomalous pulmonary venous drainage (TAPVD) in

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Modified Warden Operation With the Use of Femoral Vein Homograft for Repair of a Variant of Right-Sided Partial Anomalous Pulmonary Venous Connection

Josue Chery, Karthik Ramakrishnan, Russel Cross, Richard A. JonasVirginia Commonwealth University. Children’s National Health System and George Washington University School of Medicine and Health Sciences.United States World Journal for Pediatric and Congenital Heart SurgeryWorld J Pediatr Congenit Heart Surg 2020; 11: 217-219DOI: 10.1177/2150135119888219 AbstractSurgical repair of right-sided partial anomalous pulmonary venous return (PAPVR) involves baffling the

Modified Warden Operation With the Use of Femoral Vein Homograft for Repair of a Variant of Right-Sided Partial Anomalous Pulmonary Venous Connection Read More »

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