Pediatric Pulmonary Vascular Disease

Anomalies of Venous Return

H. A. Snellen, C. Bruins University of LeidenNetherlands In Watson, H. Editor: Pediatric Cardiology 1968; 427-428C. V. Mosby CompanyDOI: Not Available AbstractAbstract Not Available CategorySegmental Pulmonary Venous Disease. Without a Focus on Pulmonary Hypertension Age Focus: Pediatric Pulmonary Vascular Disease Fresh or Filed Publication: Filed (PHiled). Greater than 1-2 years since publication Article Access Free […]

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Successful preoperative diagnosis and surgical repair of pulmonary vein stenosis

Sang C. Park, William H. Neches, Cora C. Lenox, James R. Zuberbuhler, Ralph D. Siewers, Henry T. BahnsonUniversity of Pittsburgh School of Medicine and Children’s Hospital of Pittsburgh.United States CirculationCirculation 1973; 48 (Supplement IV): 33DOI: Not Available AbstractNot Available CategorySegmental Pulmonary Venous Disease. Without a Focus on Pulmonary HypertensionDiagnostic Testing for Pulmonary Vascular Disease. Non-invasive TestingSurgical

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Congenital pulmonary vein stenosis

Roberta M. Bini, David C. Cleveland, Ricardo Ceballos, Lionel M. Bargeron, Albert D. Pacifico, John W. KirklinUniversity of Alabama BirminghamUnited States American Journal of CardiologyAm J Cardiol 1984; 54: 369-375DOI: 10.1016/0002-9149(84)90199-1 AbstractCongenital pulmonary vein stenosis is a rare and serious form of congenital heart disease. Between 1969 and 1982 10 patients with this lesion were studied.

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Anatomical and functional evaluation of pulmonary veins in children by magnetic resonance imaging

Lars Grosse-Wortmann, Abdulmajeed Al-Otay, Hyun Woo Goo, Christopher K. Macgowan, John G. Coles, Leland N. Benson, Andrew N. Redington, Shi-Joon YooHospital for Sick Children and The University of Toronto.Canada Journal of the American College of CardiologyJ Am Coll Cardiol 2007; 49: 993-1002DOI: 10.1016/j.jacc.2006.09.052 AbstractPulmonary vein pathologies often present a diagnostic challenge. Among the different imaging modalities

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Two-dimensional and pulsed Doppler echocardiography in the postoperative evaluation of total anomalous pulmonary venous connection

Jeffrey F. Smallhorn, Patricia Burroughs, G. Wilson, John Coles, David L. Gilday, Robert M. FreedomHospital for Sick Children.Canada CirculationCirculation 1987; 76: 298-305DOI: 10.1161/01.cir.76.2.298 AbstractThe role of combined two-dimensional and pulsed Doppler echocardiography in the postoperative assessment of patients with total anomalous pulmonary venous connection was evaluated. Twenty-two cases with a median age of 9.5 weeks at

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Longitudinal follow-up of mixed connective tissue disease and overlapping autoimmune diseases of childhood onset in the Afro-descendant population of the French West Indies

Arthur Felix, Lindsay Osei, Frederique Delion, Benoit Suzon, Aurore Abel, Moustapha Drame, Yves Hatchuel, Christophe Deligny, Fabienne Louis‑SidneyUniversity of the French West Indies and Martinique University Hospital. CHU de la Martinique La Meynard. Andrée Rosemon Hospital. Guadeloupe University Hospital. France Pediatric Rheumatology Online JournalPediatr Rheumatol Online J 2024; 22:DOI: 10.1186/s12969-023-00951-3 AbstractIntroduction: Overlap autoimmune syndromes (OAS) and mixed

Longitudinal follow-up of mixed connective tissue disease and overlapping autoimmune diseases of childhood onset in the Afro-descendant population of the French West Indies Read More »

Vasopressin in newborns with refractory acute pulmonary hypertension

Simon Ouellet, Christine Drolet, Genevéve Morissette, Annie Pellerin, Audrey HébertCHU de Québec, Université Laval. Canada Pediatric ResearchPediatr Res 2024;DOI: 10.1038/s41390-023-02995-3 AbstractBackground: Acute pulmonary hypertension (aPH) in newborns can be life threatening and challenging to manage. In newborns with refractory aPH, there is currently limited therapeutic agents.Methods: Retrospective single-center cohort study in newborns less than one month old who

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Total anomalous pulmonary venous return. Prenatal damage to pulmonary vascular bed and extrapulmonary veins

Sheila G. HaworthInstitute of Child Health.United Kingdom British Heart JournalBrit Heart J 1982; 48: 513-524DOI: 10.1136/hrt.48.6.513 AbstractTo investigate the possibility that pulmonary vascular disease may be present at birth in children presenting with obstructed total anomalous pulmonary venous return in the neonatal period, pulmonary vascular structure was analysed in the lungs of six babies who died

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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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