Carol A. Wittlieb-Weber
University of Rochester Medical Center
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Publication
Featured researches published by Carol A. Wittlieb-Weber.
Cardiology in The Young | 2015
Carol A. Wittlieb-Weber; Matthew A. Harris; Joseph W. Rossano
We describe a case of influenza A myocarditis and transient left ventricular wall thickening in a 14-year-old girl presenting with acute heart failure. Admission echocardiogram revealed significant left ventricular hypertrophy with depressed left ventricular systolic function. The aetiology of the ventricular thickening was demonstrated to be myocardial oedema using cardiac magnetic resonance imaging. The natural course of this unusual clinical presentation of acute myocarditis and the importance of cardiac magnetic resonance imaging in this challenging clinical setting are discussed.
World Journal for Pediatric and Congenital Heart Surgery | 2018
Rachel L. Bounds; Joseph D. Kuebler; Jill M. Cholette; George M. Alfieris; Sitaram M. Emani; Carol A. Wittlieb-Weber
A 2-month-old male with dysmorphic facies, neonatal thrombocytopenia, left congenital cataract, and long bone abnormalities became hypotensive with ST depression on induction of anesthesia for congenital cataract repair. Echocardiogram demonstrated decreased left ventricular function (ejection fraction 46%), mild mitral valve regurgitation (MR), and regional wall motion abnormalities. The left coronary artery could not be visualized. Subsequent cardiac catheterization confirmed atresia of the left main coronary artery. The patient underwent cardiac surgery with coronary artery bypass grafting of the left internal mammary artery to the left anterior descending coronary artery. His postoperative course was uncomplicated, his ventricular function normalized, and he was discharged home. Over the next few months, he developed progressive, severe MR refractory to medical management. Repeat cardiac catheterization revealed stenosis of the right proximal coronary artery, raising concern for progressive coronary involvement. In addition to dysmorphic features and failure to thrive, there were profound developmental delays and a finding of vacuolated lymphocytes on blood smear, which led to a diagnosis of mucolipidosis II (Inclusion [I]-cell disease). The patient was referred for mitral valve replacement, which was successful; however, ongoing respiratory issues attributed to the progression of I-cell disease led to a prolonged hospitalization with placement of a tracheostomy. Reports of coronary anomalies in patients with I-cell disease are rare. An association between mucopolysaccharidosis syndromes and coronary artery abnormalities has been established and is supported by this case report, highlighting the importance of considering the potential for coronary artery involvement with I-cell disease and other similar storage diseases.
World Journal for Pediatric and Congenital Heart Surgery | 2017
Heidi B. Schubmehl; Michael F. Swartz; Nader Atallah-Yunes; Carol A. Wittlieb-Weber; Rebecca E. Pratt; George M. Alfieris
Background: The goals following pulmonary valve replacement (PVR) are to optimize right ventricular hemodynamics and minimize the need for subsequent reoperations on the right ventricular outflow tract. We hypothesized PVR using a xenograft valved conduit would result in superior freedom from reoperation with sustained improvement in right ventricular chamber dimensions. Methods: Xenograft valved conduits placed in patients aged >16 years were reviewed from 2000 to 2010 to allow for a 5-year minimum follow-up. Preoperative, one-year, and the most recent echocardiograms quantified right ventricular chamber dimensions, corresponding Z scores, and prosthetic valve function. Magnetic resonance imaging (MRI) studies compared preoperative and follow-up right ventricular volumes. Results: A total of 100 patients underwent PVR at 24 (19-34) years. Freedom from reintervention was 100% at 10 years. At most recent follow-up, only one patient had greater than mild pulmonary insufficiency. The one-year (17.3 ± 7.2 mm Hg; P < .01) and most recent follow-up (18.6 ± 9.8 mm Hg; P < .01) Doppler-derived right ventricular outflow tract gradients remained significantly lower than preoperative measurements (36.7 ± 27.0 mm Hg). Similarly, right ventricular basal diameter, basal longitudinal diameter, and the corresponding Z scores remained lower at one year and follow-up from preoperative measurements. From 34 MRI studies, the right ventricular end-diastolic indexed volume (161.7 ± 58.5 vs 102.9 ± 38.3; P < .01) and pulmonary regurgitant fraction (38.0% ± 15.9% vs 0.8% ± 3.3%; P < .01) were significantly lower at 7.1 ± 3.4 years compared to the preoperative levels. Conclusion: Use of a xenograft valved conduit for PVR results in excellent freedom from reoperation with sustained improvement in right ventricular dimensions at an intermediate-term follow-up.
Pediatric Transplantation | 2017
Carol A. Wittlieb-Weber; Joseph W. Rossano; David R. Weber; Kimberly Y. Lin; Chitra Ravishankar; Christopher E. Mascio; Robert E. Shaddy; Matthew J. O'Connor
We used the NEDS database (2010) to evaluate ED utilization in PED HT recipients compared to other patient populations with focus on characteristics of ED visits, risk factors for admission, and charges. We analyzed 433 ED visits by PED HT recipients (median age 8 [range: 0‐18] years). The most common primary diagnosis category was infectious (n=163, 37.6%), with pneumonia being the most common infectious etiology. When compared to all PED visits, HT visits were more likely to result in hospital admission (32.6% versus 3.9%, P<.001), had greater hospital LOS (median of 3 days [IQR 2‐4] versus 2 days [IQR 1‐4], P=.001), and accumulated greater total hospital charges (median
Heartrhythm Case Reports | 2016
Carol A. Wittlieb-Weber; Katrina M. Haude; Chin-To Fong; Jeffrey M. Vinocur
26 317 [IQR
Journal of the American College of Cardiology | 2014
Carol A. Wittlieb-Weber; Joseph W. Rossano; David R. Lynch; Kimberly Y. Lin
11 438‐
Current Cardiovascular Risk Reports | 2014
Carol A. Wittlieb-Weber
46 407] versus
The Journal of Thoracic and Cardiovascular Surgery | 2014
Carol A. Wittlieb-Weber; Stephen M. Paridon; J. William Gaynor; Thomas L. Spray; David R. Weber
12 332 [IQR
Journal of Cardiac Failure | 2015
Carol A. Wittlieb-Weber; Kimberly Y. Lin; Theoklis E. Zaoutis; Matthew J. O'Connor; Ken Gerald; Stephen M. Paridon; Robert E. Shaddy; Joseph W. Rossano
7092‐
Journal of The American Society of Echocardiography | 2013
Carol A. Wittlieb-Weber; Meryl S. Cohen; Michael G. McBride; Stephen M. Paridon; Robert Morrow; Melissa Wasserman; Yan Wang; Paul Stephens
22 583], P<.001). When compared to visits by other SOT recipients, results varied with similar rates of hospital admission for HT, LUNGT, and KT visits and similar LOS for HT and KT visits but differing total hospital charges. Although PED HT recipients account for a small percentage of overall ED visits, they are more likely to be hospitalized and require greater resource utilization compared to the general PED population, but not when compared to other SOT recipients.