The effects of systemic-pulmonary artery shunts on growth, body composition, and adipose tissue were studied in 29 children, aged 2 to 16 years, with cyanotic congenital heart disease. Of these, 16 received surgical shunts and 13 were unoperated. Postoperatively, all patients who received shunts were better oxygenated (systemic oxygen saturation 69 +/- 11% preoperatively and 84 +/- 4% postoperatively; mean +/- standard error of the mean) and were symptomatically improved. However, the groups were not significantly different in height, weight, lean body mass, total body fat, lean/fat ratio, cellular lipid content, or total number of lipid-containing fat cells. Age at operation did not seem to influence the effects of surgery. These observations suggest that growth and certain measurements of tissue development were unaffected by surgical systemic-pulmonary artery shunts despite increased oxygenation and symptomatic improvement after operation.
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http://dx.doi.org/10.1016/0002-9149(83)90137-6 | DOI Listing |
J Clin Med
October 2024
Department of Obstetrics and Prenatal Medicine, University Hospital Bonn, Venusberg Campus 1, 53127 Bonn, Germany.
: Truncus arteriosus communis (TAC) is a rare congenital heart defect characterized by a single arterial trunk that supplies systemic, pulmonary, and coronary circulations. This defect, constituting approximately 1-4% of congenital heart diseases, poses significant challenges in prenatal diagnosis, management, and postnatal outcomes. : A retrospective analysis was conducted at the local tertiary referral center on cases of TAC diagnosed prenatally between 2019 and 2024.
View Article and Find Full Text PDFPediatr Cardiol
September 2024
Intermountain Primary Children's Hospital, Salt Lake City, UT, USA.
Int J Cardiol
November 2024
KU Leuven, Department of Cardiovascular Sciences, Leuven, Belgium; UZ Leuven, Congenital and Structural Cardiology, Leuven, Belgium. Electronic address:
Background: Pulmonary Atresia, Ventricular Deptal Defect, and Major Aortopulmonary Collateral Arteries (PA-VSD-MAPCAs) is a congenital cyanotic heart defect with poor prognosis. Due to its complex and highly variable anatomy, the best treatment plan is not clear. We aimed (1) to investigate the survival of PA-VSD-MAPCAs patients according to the underlying original anatomy and treatment strategy, and (2) to evaluate life expectancy between patients with or without severe hypoplastic native pulmonary arteries (NPAs) after surgical versus non-surgical treatment.
View Article and Find Full Text PDFInterdiscip Cardiovasc Thorac Surg
August 2024
Department of Translational Medical Sciences, Unit of Cardiac Surgery, Monaldi Hospital, University of Campania "L. Vanvitelli", Naples, Italy.
J Clin Ultrasound
October 2024
Neonatology Clinic, University Hospital of Obstetrics and Gynecology Maichin Dom, Sofia, Bulgaria.
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