Incidence or Prevalence of Disease

Primary sutureless repair for infants with mixed total anomalous pulmonary venous drainage

Osami Honjo, Cori R. Atlin, Barbara C. S. Hamilton, Osman Al-Radi, Nicola Viola, John G. Coles, Glen S. Van Arsdell, Christopher A. Caldarone Hospital for Sick Children.Canada Annals of Thoracic SurgeryAnn Thorac Surg 2010; 90: 862-868DOI: 10.1016/j.athoracsur.2010.05.007 AbstractBackground: Mixed type total anomalous pulmonary venous drainage (TAPVD) poses technical challenges and high mortality owing to diminutive size and […]

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Outcomes after surgical treatment of children with partial anomalous pulmonary venous connection

Bahaaldin Alsoufi, Sally Cai, Glen S. Van Arsdell, William G. Williams, Christopher A. Caldarone, John G. Coles Hospital for Sick Children and University of Toronto.Canada Annals of Thoracic SurgeryAnn Thorac Surg 2007; 84: 2020-2026DOI: 10.1016/j.athoracsur.2007.05.046 AbstractBackground: We explore early results and time-related morbidity after surgical repair of partial anomalous pulmonary venous connection (PAPVC) at our institution.Methods: Between 1982

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Factors associated with mortality and reoperation in 377 children with total anomalous pulmonary venous connection

Tara Karamlou, Rebecca Gurofsky, Eisar Al Sukhni, John G. Coles, William G. Williams, Christopher A. Caldarone, Glen S. Van Arsdell, Brian W. McCrindle University of Toronto and Hospital for Sick Children.Canada CirculationCirculation 2007; 115: 1591-1598DOI: 10.1161/CIRCULATIONAHA.106.635441 AbstractBackground: We sought to determine era-specific changes in the incidence of mortality and reoperation in children with total anomalous pulmonary venous

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Conventional and sutureless techniques for management of the pulmonary veins: Evolution of indications from postrepair pulmonary vein stenosis to primary pulmonary vein anomalies

Tae-Jin Yun, John G. Coles, Igor E. Konstantinov, Osman O. Al-Radi, Rachel M. Wald, Vitor Guerra, Nilto C. de Oliveira, Glen S. Van Arsdell, William G. Williams, Jeffrey Smallhorn, Christopher A. Caldarone Hospital for Sick Children and University of Toronto.Canada Journal of Thoracic and Cardiovascular SurgeryJ Thorac Cardiovasc Surg 2005; 129: 167-174DOI: 10.1016/j.jtcvs.2004.08.043 AbstractObjective: We have previously

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Total anomalous pulmonary venous drainage. Seventeen-year surgical experience

R. K. Lamb, S. A. Qureshi, J. L. Wilkinson, R. Arnold, C. R. West, D. I. Hamilton Royal Liverpool Children’s Hospital.United Kingdom Journal of Thoracic and Cardiovascular SurgeryJ Thorac Cardiovasc Surg 1988; 96: 368-375DOI: Not Available AbstractBetween 1968 and 1985, 80 children underwent correction of total anomalous pulmonary venous drainage. There were 47 boys and

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Surgical management of total anomalous pulmonary venous connection. Thirty-year trends

Ko Bando, Mark W. Turrentine, Gregory J. Ensing, K. Sun, Thomas G. Sharp Y. Sekine, Donald A. Girod, John W. Brown James W. Riley Hospital for Children.United States CirculationCirculation 1996; 94(9 Suppl): II12-II16DOI: Not Available AbstractBackground: Reports of surgical correction of total anomalous pulmonary venous connection (TAPVC) over the past 30 years indicate a general improvement

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Long-term outcomes of total correction for isolated total anomalous pulmonary venous connection: lessons from 50-years’ experience

Takahiko Sakamoto, Mitsugi Nagashima, Kentarou Umezu, Ryogo Houki, Jin Ikarashi, Junko Katagiri, Kenji Yamazaki The Heart Institute of Japan and Tokyo Women’s Medical University.Japan Interactive Cardiovascular and Thoracic SurgeryInteract Cardiovasc Thorac Surg 2018; 27: 20-26DOI: 10.1093/icvts/ivy034 AbstractObjectives: Isolated total anomalous pulmonary venous connection (TAPVC) is a relatively rare congenital cardiac defect, while pulmonary venous obstruction (PVO) is

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Correction of total anomalous pulmonary venous connection of the cardiac type

R. Aeba, T. Katogi, S. Takeuchi, S. Kawada Keio University.Japan Cardiovascular SurgeryCardiovasc Surg 1998; 6: 50-57DOI: 10.1016/s0967-2109(97)00112-9 AbstractSurgical treatment of the cardiac type of total anomalous pulmonary venous connection requires special techniques. The treatment and outcome in 17 consecutive patients who had undergone primary repairs of the cardiac type between 1965 and 1996 were reviewed. The

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Outcome predictors and implications for management of scimitar syndrome

Susan M. Dusenbery, Tal Geva, Anna Seale, Anne Marie Valente, Jing Zhou, Laureen Sena, Robert L. Geggel Boston Children’s Hospital.United States American Heart JournalAm Heart J 2013; 165: 770-777DOI: 10.1016/j.ahj.2013.01.016 AbstractBackground: Scimitar syndrome is a rare congenital anomaly. We evaluated risk factors for postoperative pulmonary vein stenosis or death and predictive factors for survival without scimitar vein surgery in patients with scimitar syndrome.Methods: The records of patients with scimitar

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