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

Sutureless pericardial repair of total anomalous pulmonary venous connection in patients with right atrial isomerism

Naoki Yoshimura, Yoshihiro Oshima, Roland Henaine, Hironori MatsuhisaUniversity of Toyama.Japan Interactive CardioVascular and Thoracic SurgeryInteract Cardiovasc Thorac Surg 2010; 10: 675-678DOI: 10.1510/icvts.2009.221440 AbstractSurgical repair of total anomalous pulmonary venous connection (TAPVC) in patients with right atrial isomerism is associated with a significant risk of recurrent pulmonary venous obstruction (PVO). We evaluate the effect of sutureless repair […]

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Tumor Necrosis Factor-α-Induced Protein-8-like 2 Transfected Adipose-Derived Stem Cells Regulated the Dysfunction of Monocrotaline Pyrrole-Induced Pulmonary Arterial Smooth Muscle Cells and Pulmonary Arterial Endothelial Cells

Jing Li, Xin He, Feng Liu, Kinglong Zheng, Jing JiangFirst Affiliated Hospital of Xi’an Jiaotong University. Fourth Military Medical University.China Journal of Cardiovascular PharmacologyJ Cardiovasc Pharmacol 2024; 83:73-85DOI: 10.1097/FJC.0000000000001505 AbstractPulmonary arterial hypertension (PAH) is characterized by pulmonary arterial endothelial cell (PAEC) dysfunction and pulmonary arterial smooth muscle cell (PASMC) activation. For decades, the therapies for PAH

Tumor Necrosis Factor-α-Induced Protein-8-like 2 Transfected Adipose-Derived Stem Cells Regulated the Dysfunction of Monocrotaline Pyrrole-Induced Pulmonary Arterial Smooth Muscle Cells and Pulmonary Arterial Endothelial Cells Read More »

Postnatal treatment and evolution patterns of giant fetal hepatic hemangioma: a case series of 29 patients

Lu-lu Xie, Yan-bing Huang, Kui-ran Dong, Shao-bo Yang, Chun Shen, Yang-yang MaShanghai Institute of Infectious Disease and Biosecurity. Children’s Hospital of Fudan University. Fujian Medical University. China BioMed Central PediatricsBMC Pediatr 2024; 24:DOI: 10.1186/s12887-023-04476-2 AbstractObjectives: To explore the clinical characteristics, postnatal treatment and prognosis of giant fetal hepatic hemangioma (GFHH).Method: Retrospective analysis was performed on children with giant

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Reversible severe pulmonary hypertension related to scurvy in children

Marin Satawiriya, Apichai Khongphatthanayothin, Alisa LimsuwanFaculty of Medicine Ramathibodi Hospital and Mahidol University. Bangkok Heart Hospital. Chulalongkorn University. Thailand BioMed Central Cardiovascular DisordersBMC Cardiovasc Disord 2024; 24:DOI: 10.1186/s12872-023-03629-6 AbstractBackground: Severe pulmonary hypertension (PH) in childhood is rare and can manifest as a life-threatening episode. We present 2 children with restrictive dietary habits with severe pulmonary hypertension secondary

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Preoperative pulmonary venous obstruction affects long-term outcome for survivors of total anomalous pulmonary venous connection repair

Paul M. Kirshbom, Richard J. Myung, J. William Gaynor, Richard F. Ittenbach, Stephen M. Paridon, William M. DeCampli, Tom R. Karl, Thomas L. SprayChildren’s Hospital of Philadelphia.United States Annals of Thoracic SurgeryAnn thorac Surg 2002; 74: 1616-1620DOI: 10.1016/s0003-4975(02)03935-8 AbstractBackground: Early outcomes after repair of total anomalous pulmonary venous connection continue to improve; however, little information is available

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Outcomes of surgery for simple total anomalous pulmonary venous drainage in neonates

Matthew S. Yong, Yves d’Udekem, Terry Robertson, Stephen Horton, Mithilesh Dronavalli, Christian Brizard, Robert Weintraub, Frank Shann, Michael Cheung, Igor E. KonstantinovRoyal Children’s Hospital and University of Melbourne.Australia Annals of Thoracic SurgeryAnn Thorac Surg 2011; 91: 1921-1927DOI: 10.1016/j.athoracsur.2010.12.069 AbstractBackground: Repair of total anomalous pulmonary venous drainage (TAPVD) in neonates remains a challenge as it is often associated

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Heterotaxy patients with total anomalous pulmonary venous return: improving surgical results

David L. S. Morales, Brandi E. Braud, Justin H. Booth, Daniel E. Graves, Jeffrey S. Heinle, E. Dean McKenzie, Charles D. FraserBaylor College of Medicine and Texas Children’s Hospital.United States Annals of Thoracic SurgeryAnn Thorac Surg 2006; 82: 1621-1627DOI: 10.1016/j.athoracsur.2006.05.053 AbstractBackground: Survival after repair of total anomalous pulmonary venous return in patients with heterotaxy syndrome has consistently

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Total anomalous pulmonary venous return: report of 201 patients treated surgically

Michael J. Reardon, Denton A. Cooley, Luiz Kubrusly, David A. Ott, William Johnson, Gregory L. Kay, Michael S. SweeneyTexas Heart Institute, St. Luke’s Episcopal Hospital and Texas Children’s Hospital.United States Texas Heart Institute JournalTex Heart Inst J 1985; 12: 131-141DOI: Not Available AbstractBetween 1956 and June 1984, 201 patients with uncomplicated total anomalous pulmonary venous

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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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Total anomalous pulmonary return; an analysis of thirty cases

Vincent L. Gott, Richard G. Lester, C. Walton Lillehei, Richard L. VarcoUniversity of MinnesotaUnited States CirculationCirculation 1956; 13: 543-552DOI: 10.1161/01.cir.13.4.543 AbstractThirty cases of total anomalous pulmonary return have been collected and analyzed. The pathways of drainage and their embryologic development are discussed. The cardiac catheterization, electrocardiographic and radiologic findings are also presented. These laboratory data accompanied

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