Segmental Pulmonary Venous Disease. Without a Focus on Pulmonary Hypertension

Alberto Cabrera, Carlos Vazquez, Iñaki LekuonaHospital Infantil, Bilbao.Spain International Journal of CardiologyInt J Cardiol 1985; 7: 298-302DOI: 10.1016/0167-5273(85)90055-5 AbstractFour cases of congenital isolated atresia of the left pulmonary veins were observed over a 12-year period. The diagnosis was established through radionuclide pulmonary perfusion studies together with cardiac catheterization and pulmonary arteriography. Both procedures showed an elevated […]

Edward S. Yee, Kevin Turley, Wen R. Hsieh, Paul A. EbertUniversity of California, San Francisco.United States CirculationCirculation 1987; 76 (3 Pt 2): III83-III87DOI: Not Available AbstractThe surgical experience in 75 patients with total anomalous pulmonary venous connection (TAPVC) between 1975 and 1986 was reviewed. Most of these patients underwent operation at less than 1 month

Serafin Y. DeLeon, Samuel S. Gidding, Michel N. Ilbawi, Farouk S. Idriss, Alexander J. Muster, Roger B. Cole, Milton H. PaulNorthwestern University Medical School. Children’s Memorial Hospital.United States Annals of Thoracic SurgeryAnn Thorac Surg 1987; 43: 207-211DOI: 10.1016/s0003-4975(10)60398-0 AbstractEight infants with complex cardiac anomalies and pulmonary stenosis or atresia were noted to have obstructed total anomalous

William H. Fleming, Edward B. Clark, Kenneth J. Dooley, Philip J. Hofschire, Roger N. Ruckman, Alan R. Hopeman, Lynne Sarafian, Paul K. MooringUniversity of Nebraska Medical Center and Henrietta Egleston Hospital for Children.United States Annals of Thoracic SurgeryAnn Thorac Surg 1979; 27: 435-439DOI: 10.1016/s0003-4975(10)63342-5 AbstractBetween May, 1975, and June, 1977, we surgically repaired an infracardiac total

Hellmut Oelert, Hans-J. Schafers, Thomas Stegmann, Hans-C. Kallfelz, Hans G. BorstHannover Medical School.Germany Annals of Thoracic SurgeryAnn Thorac Surg 1986; 41: 392-394DOI: 10.1016/s0003-4975(10)62693-8 AbstractFrom January, 1973, to August, 1984, 53 infants with total anomalous pulmonary venous drainage (TAPVD) underwent a corrective operation in our unit. TAPVD was of the supracardiac type in 41% of the patients,

D. F. Dickinson, K. M. Parimelazhagan, M. C. Tweedie, C. R. West, G. P. Piccoli, F. Musumeci, D. I. HamiltonRoyal Liverpool Children’s Hospital.United Kingdom British Heart JournalBrit Heart J 1982; 48: 249-254DOI: 10.1136/hrt.48.3.249 AbstractForty-four consecutive infants aged from 3 days to 10 months underwent repair of total anomalous pulmonary venous connection using deep hypothermia with circulatory

Kevin Turley, William Y. Tucker, Daniel J. Ullyot. Paul A. EbertUniversity of California, San FranciscoUnited States American Journal of CardiologyAm J Cardiol 1980; 45: 92-97DOI: 10.1016/0002-9149(80)90225-8 AbstractThe factor of age has been proposed as the major determinant of survival after correction of total anomalous pulmonary venous connection; consequently, operation may be postponed and the infant’s clinical