Surgical and Catheter-mediated Interventions for Pulmonary Vascular Disease

Extracorporeal membrane oxygenation support for balloon atrial septostomy in a BMPR2 variant-associated pulmonary arterial hypertension

Shoji Fukuoka, Noriyuki Kaku, Hazumu Nagata, Yusaku Nagatomo, Kanako Higashi, Daisuke Toyomura, Yuichiro Hirata, Keiichi Hirono, Kenichiro Yamamura, Shouichi OhgaKyushu University. University of Toyama.Japan Pediatric PulmonologyPediatr Pulmonol 2024; DOI: 10.1002/ppul.26973 AbstractAbstract Not Available CategoryClass I. Heritable Pulmonary HypertensionSurgical and Catheter-mediated Interventions for Pulmonary Vascular Disease Age Focus: Pediatric Pulmonary Vascular Disease Fresh or Filed Publication: Fresh […]

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Virtual Transcatheter Interventions for Peripheral Pulmonary Artery Stenosis in Williams and Alagille Syndromes

Ingrid S. Lan, R. Thomas Collins, II, Weiguang Yang, Jeffrey A. Feinstein, Michael Ma, Jacqueline Kreutzer, Gregory T. Adamson, Alison L. MarsdenStanford University. University of Pittsburgh.United States Journal of the American Heart AssociationJ Am Heart Assoc 2022; 11:DOI: 10.1161/JAHA.121.023532 AbstractBackground: Despite favorable outcomes of surgical pulmonary artery (PA) reconstruction, isolated proximal stenting of the central PAs

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Analysis of risk factors associated with extracorporeal membrane oxygenation after surgical repair of peripheral pulmonary artery stenoses

L. Mac Felmly, Richard D. Mainwaring, Claudia Algaze, Elisabeth Martin, Michael Ma, Frank L. HanleyStanford University School of Medicine and Lucile Packard Children’s Hospital.United States Journal of Thoracic and Cardiovascular Surgery OpenJTCVS Open 2023; 13: 344-356DOI: 10.1016/j.xjon.2023.01.011 AbstractObjective: Acute lung injury is a known complication of pulmonary artery reconstruction for peripheral pulmonary artery stenosis. Severe cases may

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Surgical Experience With Crossed and Anomalous Origin of the Pulmonary Arteries From the Pulmonary Trunk: A Single Center Report of 24 Cases

Sameh M. Said, Eric Hoggard, Shanti NarasimhanMaria Fareri Children’s Hospital and Westchester Medical Center. Alexandria University. University of Minnesota and Masonic Children’s Hospital.United States and Eygpt World Journal of Pediatric and Congenital Heart SurgeryWorld J Pediatr Congenit Heart Surg 2023; 14: 185-193DOI: 10.1177/21501351221139833 AbstractBackground: Anomalies of the pulmonary origin of the pulmonary arteries are uncommon; however, the

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Nonhepatic Alagille Syndrome Associated With Predominant Cardioskeletal Anomalies: A Rare Case

Vishal V. Bhende, Hardil P. Majmudar, Tanishq S. Sharma, Sohilkhan R. Pathan, Deepakkumar V. MehtaShree Krishna Hospital. Pramukhswami Medical College. Bhaikaka University.India CureusCureus 2021; 13:DOI: 10.7759/cureus.17429 AbstractAlagille syndrome (ALGS) is a rare autosomal dominant genetic disorder with multisystem involvement including the liver, heart, skeleton, eyes, kidneys, and other organ systems, along with characteristic facial abnormalities. Some

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Tailoring stents to fit the anatomy of unique vascular stenoses in congenital heart disease

Patrick M. Sullivan, Aimee Liou, Cheryl Takao, Henri Justino, Christopher J. Petit, Jorge D. Salazar, Frank F. IngChildren’s Hospital Los Angeles and University of Southern California Keck School of Medicine. Texas Children’s Hospital and Baylor College of Medicine. Children’s Healthcare of Atlanta and Emory University School of Medicine. Children’s Hospital Boston, Harvard Medical SchoolUnited States

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Comparison of fusion imaging and two-dimensional angiography to guide percutaneous pulmonary vein interventions

Sebastian Góreczny, Gareth J. Morgan, Daniel McLennan, Rizwan Rehman, Jenny E. ZablahUniversity Children’s Hospital and Jagiellonian University Medical College. Children’s Hospital of Colorado and University of Colorado. Birmingham Children’s Hospital.Poland, United States and United Kingdom Kardiologia Polska (Polish Heart Journal)Kardiol Pol (Polish Heart J) 2022; 80: 476-478DOI: 10.33963/KP.a2021.0197 AbstractAbstract Not Available CategorySegmental Pulmonary Venous Disease. Without

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Fusion imaging for guidance of pulmonary arteriovenous malformation embolisation with minimal radiation and contrast exposure

Catalina Vargas-Acevedo, Ernesto Mejia, Jenny E. Zablah, Gareth J. MorganUniversity of Colorado and Children’s Hospital Colorado.United States Cardiology in the YoungCardiol Young 2024; DOI: 10.1017/S1047951124000349 AbstractHereditary haemorrhagic telangiectasia is an inherited disorder characterised by vascular dysplasia that leads to the development of arteriovenous malformations. Pulmonary arteriovenous malformations occur in approximately 30% of patients with haemorrhagic telangiectasia.

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Pulmonary flow-study can predict in-hospital prognosis of unifocalization and corrective repair of pulmonary atresia/ventricular septal defect with major aortopulmonary collateral arteries

Xiaofeng Wang, Zhiyuan Zhu, Zhongyuan Lu, Wenlong Wang, Xu WangFuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College.China HeliyonHeliyon 2024; 10:DOI: 10.1016/j.heliyon.2024.e27109 AbstractObjectives: With the development of perioperative treatment, the results of the unifocalization and corrective repair of pulmonary atresia/ventricular septal defect with major aortopulmonary collateral arteries have been significantly improved. However, the in-hospital

Pulmonary flow-study can predict in-hospital prognosis of unifocalization and corrective repair of pulmonary atresia/ventricular septal defect with major aortopulmonary collateral arteries Read More »

Surgical management of congenital and acquired pulmonary vein stenosis

Thomas L. Spray, Nancy D. BridgesThe Children’s Hospital of Philadelphia.United States Seminars in Thoracic and Cardiovascular Surgery Pediatric Cardiac Surgery AnnualSemin Thorac Cardiovasc Surg Pediatr Card Surg Ann 1999; 2: 177-188DOI: 10.1016/s1092-9126(99)70015-3 AbstractPulmonary vein stenosis describes a variety of entities with a variable clinical course. The basic pathologic process appears to be fibrous intimal thickening, which

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