8 results match your criteria: "From the The Heart Institute.[Affiliation]"
ASAIO J
September 2024
From the The Heart Institute, Division of Cardiothoracic Surgery, Cincinnati Children's Hospital Medical Center, and The University of Cincinnati College of Medicine, Cincinnati Ohio.
Extracorporeal membrane oxygenation (ECMO) is often associated with disturbances in acid/base status that can be triggered by the underlying pathology or the ECMO circuit itself. Extracorporeal membrane oxygenation is known to cause hypocapnia, but the impact of reduced partial pressure of carbon dioxide (pCO 2 ) on biomarkers of tissue perfusion during veno-arterial (VA)-ECMO has not been evaluated. To study the impact of low pCO 2 on perfusion indices in VA-ECMO, we placed Sprague-Dawley rats on an established VA-ECMO circuit using either an oxygen/carbon dioxide mixture (O 2 95%, CO 2 5%) or 100% O 2 delivered through the oxygenator (n = 5 per cohort).
View Article and Find Full Text PDFThe mechanisms driving the pathologic state created by extracorporeal membrane oxygenation (ECMO) remain poorly defined. We developed the first complete blood-primed murine model of veno-arterial ECMO capable of maintaining oxygenation and perfusion, allowing molecular studies that are unavailable in larger animal models. Fifteen C57BL/6 mice underwent ECMO by cannulating the left common carotid artery and the right external jugular vein.
View Article and Find Full Text PDFASAIO J
December 2021
From the The Heart Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
A 15 year old female with hypoplastic left heart syndrome status post Norwood with Sano modification, bidirectional Glenn and extracardiac conduit Fontan developed severe right ventricular (RV) systolic dysfunction. Due to symptomatic heart failure, she underwent assessment for ventricular assist device (VAD) placement as a bridge-to-cardiac transplantation strategy. To evaluate her atypical anatomy, a chest computed tomography (CT) was uploaded into an EchoPixel True3D (Santa Clara, CA) view portal along with an accurately scaled 3D surface model of the HeartMate III (HM3) device.
View Article and Find Full Text PDFASAIO J
February 2018
From the *The Heart Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, OH; and †Department of Family Medicine, University of Oklahoma, Tulsa, OK.
Ventricular assist devices (VADs) are increasingly used to support children to heart transplant, however, it is unclear whether this trend is broadly applicable across the age/size spectrum. Children (≤18 years) listed for transplant were identified from the United Network of Organ Sharing (UNOS) database between January 2006 and May 2014. Patients were stratified by era (Early: 2006-2010, Current: 2011-2014), size (<25, 25-50, and >50 kg), and device type.
View Article and Find Full Text PDFASAIO J
February 2018
From the *The Heart Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio; and †Cedars-Sinai Heart Institute, Los Angeles, California.
Individual centers have documented the use of the Syncardia Total Artificial Heart (TAH) in adolescents with heart failure; however, the number of patients at any given center is small. Herein, we describe the worldwide experience for all patients ≤21 years old supported with the TAH between May 2005 and May 2015 (n = 43). The number of patients experiencing a positive outcome at 60, 90, and 120 days were 30 (70%), 27 (63%), and 25 (58%), respectively.
View Article and Find Full Text PDFCirc Cardiovasc Imaging
August 2016
From the The Heart Institute, Cedars-Sinai, Los Angeles, CA.
Circ Arrhythm Electrophysiol
April 2016
From the The Heart Institute, Cedars-Sinai Medical Center, Los Angeles, CA
ASAIO J
October 2014
From the *The Heart Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio; †Division of Pulmonary Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio; and ‡Division of Neurology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Duchenne muscular dystrophy (DMD) is an X-linked recessive disorder affecting 1 in 3,500 males, characterized by progressive skeletal muscle weakness and death secondary to cardiac or respiratory failure in the 2nd or 3rd decade. Being a progressive disease, patients are rarely candidates for cardiac transplantation and death from dilated cardiomyopathy (DCM) is common. Implantation of left ventricular assist device (LVAD) offers the potential to alter clinical trajectory by alleviating heart failure symptoms.
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