Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Robb L. Romp"'
Autor:
Gregory Von Mering, Shane P. Prejean, Jared Kato, Robb L. Romp, Mark A. Law, Ashley Reed, Thomas E. Watts, Mustafa I. Ahmed, Jacob P. Elrod, Kyle W. Eudailey, Hussein Abu Daya
Publikováno v:
Cardiovascular Revascularization Medicine. 21:39-42
Transcatheter aortic valve replacement (TAVR) offers well established benefit for adults with severe aortic stenosis, although applications in the pediatric population remain limited. We describe a case of a 15-year-old male with complex congenital h
Autor:
Robert J. Dabal, Ashlyn M Alongi, Jozef Pavnica, Robb L. Romp, Luqin Deng, David C. Mauchley, Luz A. Padilla, David C. Cleveland, James K. Kirklin
Publikováno v:
World Journal for Pediatric and Congenital Heart Surgery. 11:166-176
Introduction: Heterotaxy syndrome presents a unique challenge in surgical management, even in the current era. We hypothesized that certain anatomic subsets merit novel strategies. Methods: We analyzed morphologic details, surgeries, comorbidities, s
Publikováno v:
Cardiology in the Young. 27:993-995
Infants of diabetic mothers are at risk for transient hypertrophic cardiomyopathy. These infants are typically asymptomatic, but may develop signs of poor cardiac output from left ventricular outflow tract obstruction. This case illustrates the succe
Autor:
Ayesha S. Bryant, Robb L. Romp, Margaret Tresler, David C. Cleveland, James K. Kirklin, Robert J. Dabal, Kayla D. Isbell, Jozef Pavnica, Manisha Kukreja
Publikováno v:
World journal for pediatriccongenital heart surgery. 7(5)
Background: Consensus is lacking regarding the optimal operation for transposition, ventricular septal defect, and pulmonary stenosis. Methods: Between 1968 and 2012, a total of 76 patients underwent the Rastelli procedure, with 52 mid- or long-term
Publikováno v:
Congenital Heart Disease. 2:327-331
Objective. Neonates with congenital heart disease (CHD) frequently require prompt intervention to improve outcomes and limit morbidities. We sought to determine the time to identification for infants with serious CHD admitted to the State of Alabama'
Autor:
Robb L. Romp, Navin C. Nanda, Oben Baysan, Kurt Duncan, Farhat Mehmood, Anurag Singh, Vinod Patel, Sanjay Rajdev
Publikováno v:
Echocardiography. 23:598-608
We studied nine patients (five newborns and infants, two children, and two adults) with atrioventricular septal defects (four complete, one intermediate, and four partial) utilizing live/real time three-dimensional transthoracic echocardiography (3DT
Novel Technique of Valve-Sparing Aortic Root Replacement in Two Children Younger Than 3 Years of Age
Autor:
James K. Kirklin, Robb L. Romp, William S. McMahon, Walter H. Johnson, Mark A. Law, Edward V. Colvin, Barton B. Cook
Publikováno v:
The Annals of Thoracic Surgery. 94:299-301
A novel technique of valve-sparing aortic root replacement was applied to 2 children younger than 3 years of age with Marfan syndrome and large aortic root aneurysms. Using elements of both the remodeling and reimplantation techniques, circumferentia
Publikováno v:
Journal of the American College of Cardiology. 69:2258
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
Tuberous sclerosis complex (TSC) is a genetic syndrome with a highly variable phenotype that may affect several organ systems. The central nervous system findings were the first to be described, and the classic triad of cognitive impairment, facial a
Autor:
James K. Kirklin, William L. Holman, Robb L. Romp, Yung R. Lau, Cindy S. Barrett, F. Bennett Pearce
Publikováno v:
The Journal of Thoracic and Cardiovascular Surgery. 137(1):e40-e42
exchanged her paracorporeal Levitronix RVAD for a Thoratec intracorporeal VAD (Pleasanton, Calif). Postoperatively, she recovered from MSOF and was discharged from the hospital on postoperative day 53. Repeat RVAD turndown 4 months later showed funct