Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Matthew Buelow"'
Publikováno v:
Congenital Heart Disease. 13:919-926
BACKGROUND Single ventricle heart disease with aortic arch hypoplasia has high morbidity and mortality, with the greatest risk after stage 1 palliation. Residual lesions often require catheter-based or surgical reintervention to minimize risk. We sou
Autor:
Emily Reinhardt, Scott Cohen, Salil Ginde, Chana L. Bushee, Michael G. Earing, Matthew Buelow
Publikováno v:
Progress in Pediatric Cardiology. 62:101343
Background Transition programs educate patients on the importance of continued congenital heart disease specialized care. Objective The aim of this study was to evaluate changes in the rate of unplanned cardiac hospitalizations after the implementati
Autor:
Ruta Brazauskas, Jennifer Dixon, Katie E. Cohen, Scott Cohen, Matthew Buelow, Michael G. Earing, Salil Ginde
Publikováno v:
Progress in Pediatric Cardiology. 46:51-55
Autor:
Katie E. Cohen, Ruta Brazauskas, Scott Cohen, Matthew Buelow, Salil Ginde, Jennifer Dixon, Michael G. Earing
Publikováno v:
Congenital Heart Disease. 12:435-440
Objective Abnormal lung function characterized by a reduced forced vital capacity (FVC) is common in adults with repaired tetralogy of Fallot (TOF) and is associated with previous thoracotomies and sternotomies. The impact of abnormal lung function o
Publikováno v:
Pediatric Cardiology. 38:893-901
It is unclear if neonatal tetralogy of Fallot repair offers better outcomes compared to repair later in infancy. We therefore conducted a meta-analysis comparing outcomes of neonatal and non-neonatal repair. Manuscripts were identified and reviewed f
Publikováno v:
Indian Journal of Critical Care Medicine : Peer-reviewed, Official Publication of Indian Society of Critical Care Medicine
Introduction: Adults with congenital heart disease (ACHD) represent a population with unique health-care needs. Many patients require cardiac surgery, with some requiring postoperative extracorporeal membrane oxygenation (ECMO). This study aimed to i
Autor:
Rohit Arora, Karan Nijhawan, Rohit Loomba, Navdeep Gupta, Saurabh Aggarwal, Venkata M. Alla, Matthew Buelow
Publikováno v:
Congenital Heart Disease. 11:548-553
Introduction Children born with congenital malformations of the heart are increasingly surviving into adulthood. This population of patients possesses lesion-specific complication risks while still being at risk for common illnesses. Bodily isomerism
Publikováno v:
World Journal for Pediatric and Congenital Heart Surgery. 7:385-388
The surgical palliation of several congenital heart defects requires the use of a conduit, particularly between the right ventricle and the pulmonary artery. Contegra, a valved bovine vein conduit, is a conduit frequently used. Pseudoaneurysms, aneur
Publikováno v:
Pediatrics. 146:629-629