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

Individual pulmonary vein size and survival in infants with totally anomalous pulmonary venous connection

Kathy J. Jenkins, Stephen P. Sanders, E. John Orav, Elizabeth A. Coleman, John E. Mayer Jr., Steven D. ColanChildren’s Hospital, Boston.United States Journal of the American College of CardiologyJ Am Coll Cardiol 1993; 22: 201-206DOI: 10.1016/0735-1097(93)90835-o AbstractObjectives: We investigated whether mortality in totally anomalous pulmonary venous connection could be predicted from preoperative individual pulmonary vein size.Background: Some infants with this anomaly die with or without surgical repair because […]

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Total anomalous pulmonary venous connection. Long-term results following repair in infancy

Christopher M. Whight, Brian G. Barratt-Boyes, A. Louise Calder, John M. Neutze, Peter W. BrandtGreen Lane Hospital.New Zealand Journal of Thoracic and Cardiovascular SurgeryJ Thorac Cardiovasc Surg 1978; 75: 52-63DOI: Not Available AbstractTwenty-three infants, aged 5 days to 10 months, underwent repair of total anomalous pulmonary venous connection (TAPVC). Coronary sinus drainage was unusually common,

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Total anomalous pulmonary venous drainage

Shunji Sano, William J. Brawn, Roger B. MeeRoyal Children’s Hospital.Australia Journal of Thoracic and Cardiovascular SurgeryJ Thorac Cardiovasc Surg 1989; 97: 886-992DOI: Not Available AbstractForty-four patients with total anomalous pulmonary venous drainage underwent repair between 1979 and 1987. The anomalous drainage was supracardiac in 16, cardiac in 12, and infracardiac in 16. Median age at

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Surgical repair of neonatal total anomalous pulmonary venous connection: A single institutional experience with 241 cases

Jin Shentu, Guocheng Shi, Qian Zhang, Chen Wen, Hao Zhang, Zhongqun Zhu, Huiwen ChenShanghai Children’s Medical Center and Shanghai Jiao Tong University.China Journal of Thoracic and Cardiovascular Surgery OpenJ Thorac Cardiovasc Surg Open 2023; 16: 739-754DOI: 10.1016/j.xjon.2023.07.021 AbstractObjective: Challenges persist in surgery for neonatal total anomalous pulmonary venous connection (neoTAPVC), with the high mortality risk not mitigated

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Fetal MRI-Based Mediastinal Shift Angle (MSA) and Percentage Area of Left Ventricle (pALV) as Prognostic Parameters for Congenital Diaphragmatic Hernia

Greta Thater, Lara Angermann, Silviu-Viorel Virlan, Christel Weiss, Neysan Rafat, Michael Boettcher, Julia Elrod, Tom Bayer, Oliver Nowak, Stefan O. Schönberg, Meike WeisUniversity Medical Center Mannheim. Hospital Stuttgart. Germany Journal of Clinical MedicineJ Clin Med 2024; 13:DOI: 10.3390/jcm13010268 AbstractObjective: Fetal magnetic resonance imaging (MRI) is broadly used as a method for assessing prognosis in congenital diaphragmatic hernia

Fetal MRI-Based Mediastinal Shift Angle (MSA) and Percentage Area of Left Ventricle (pALV) as Prognostic Parameters for Congenital Diaphragmatic Hernia Read More »

Allele-specific control of rodent and human lncRNA KMT2E-AS1 promotes hypoxic endothelial pathology in pulmonary hypertension

Yi- Yin Tai, Qiujun Yu, Ying Tang, Wei Sun, Neil J. Kelly, Satoshi Okawa, Jingsi Zhao, Tae- Hwi Schwantes-An, Caroline Lacoux, Stephanie Torrino, Yassmin Al Aaraj, Wadih El Khoury, Vinny Negi, Mingjun Liu, Catherine G. Corey, Frances Belmonte, Sara O. Vargas, Brian Schwartz, Bal Bhat, B. Nelson Chau, Jason H. Karnes, Taijyu Satoh, Robert J.

Allele-specific control of rodent and human lncRNA KMT2E-AS1 promotes hypoxic endothelial pathology in pulmonary hypertension Read More »

Total anomalous pulmonary venous connection: an analysis of current management strategies in a single institution

Camille L. Hancock Friesen, David Zurakowski, Ravi R. Thiagarajan, Joseph M. Forbess, Pedro J. del Nido, John E. Mayer, Richard A. JonasChildren’s Hospital Boston and Harvard Medical School.United States Annals of Thoracic SurgeryAnn Thorac Surg 1999; 79: 596-606DOI: 10.1016/j.athoracsur.2004.07.005 AbstractBackground: Repair of total anomalous pulmonary venous connection (TAPVC) continues to be associated with significant mortality. We reviewed

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Prognostic and diagnostic utility of interleukin-6 in pediatric pulmonary arterial hypertension – a case-control study

Mohamed Abdallah Abd El Megied, Mohammed Ahmed Abouelhassan, Eman Saad Abd El Salam HadwaCairo University.Egypt European Journal of PediatricsEur J Pediatr 2024;DOI: 10.1007/s00431-023-05413-2 AbstractPulmonary arterial hypertension (PAH) in pediatrics is a progressive disease with significant vascular remodeling, right sided heart failure, and death if left untreated. Elevated interleukin-6 (IL-6) level in PAH patients is taken as

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Total anomalous pulmonary venous connection: factors associated with mortality and recurrent pulmonary venous obstruction

S. Adil Husain, Elaine Maldonado, Debbie Rasch, Joel Michalek, Richard Taylor, Christopher Curzon, Steve Neish, John H. CalhoonUniversity of Texas Health Sciences Center-San Antonio. United States Annals of Thoracic SurgeryAnn Thorac Surg 2012; 94: 825-831DOI: 10.1016/j.athoracsur.2012.04.026 AbstractBackground: Surgical repair of total anomalous pulmonary venous connection (TAPVC) is associated with high rates of mortality and need for reintervention.

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Computed tomographic findings in TBX4 mutation: a common cause of severe pulmonary artery hypertension in children

Helio V. Neves da Silva, Jason P. Weinman, Erin K. Englund, Robin R. Deterding, D. Dunbar Ivy, Lorna P. BrowneChildren’s Hospital Colorado and University of Colorado School of Medicine, Anschutz Medical Campus. Highland Hospital. United States Pediatric RadiologyPediatr Radiol 2024;DOI: 10.1007/s00247-023-05848-7 AbstractBackground: Mutations in the T-Box 4 (TBX4) gene are a lesser-known cause of heritable pulmonary arterial

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