One hundred-five patients (median age 14 months) in whom a PTFE prosthesis was used to create a systemic-pulmonary artery shunt were studied between 1978 and 1980. The prosthesis was mainly used to create a modified Blalock-Taussig anastomosis. Nine patients died in hospital (8.5%, 70% confidence limits: 5.7% to 12.3%). The clinical condition did not appear to be an incremental risk factor, while the young age and the underlying type of disease accounted for the hospital mortality to a large extent. All 96 survivals were available for follow-up information. One graft, which was damaged intraoperatively, occluded 3 months later. The remaining patients have a patent graft 3 months to 36 months (mean 24 months) postoperatively. In 6 patients the patency was assessed angiographically and no damages of the pulmonary artery were observed, therefore this type of palliation is advisable for any patient, particularly in the first year of life.
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http://dx.doi.org/10.1055/s-2007-1023464 | 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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