Zobrazeno 1 - 10
of 30
pro vyhledávání: '"R. Thomas Collins"'
Publikováno v:
The Journal of Thoracic and Cardiovascular Surgery. 163:2175-2181
STRUCTURED ABSTRACT Background Pulmonary atresia with ventricular septal defect and major aortopulmonary collateral arteries (PA/VSD/MAPCAs) is a relatively rare and complex form of congenital heart disease. Unifocalization of MAPCAs has been advocat
Publikováno v:
The Journal of Maternal-Fetal & Neonatal Medicine. 35:9893-9899
To assess the association between hypertrophic cardiomyopathy (HCM) and mortality among infants of diabetic mothers (IDMs).We performed a retrospective cohort study of hospitalized IDMs admitted at ≤14-days-old in the Pediatric Health Information S
Autor:
Justin T. Jack, Kirstie M. Lechich, R. Thomas Collins, Sam Stephens, Paul C. Millett, Dana B. Gal, Joshua A. Daily, Elijah H. Bolin, Hanna K. Jensen, Morten O. Jensen
Publikováno v:
The American Journal of Cardiology. 164:118-122
Supravalvar aortic stenosis (SVAS) severity guides management, including decisions for surgery. Physiologic and technical factors limit the determination of SVAS severity by Doppler echocardiography and cardiac catheterization in Williams syndrome (W
Autor:
Frank L. Hanley, R. Thomas Collins, Richard D. Mainwaring, Elisabeth Martin, William L. Patrick, Kirstie L. MacMillen
Publikováno v:
The Journal of Thoracic and Cardiovascular Surgery. 162:212-219
Objective Patients with Williams and elastin arteriopathy syndromes often have similar cardiac phenotypes characterized by supravalvar aortic stenosis (SVAS), peripheral pulmonary artery stenosis (PPAS), and coronary artery ostial stenosis (CAOS). SV
Autor:
Matthew J. O'Connor, R. Thomas Collins
Publikováno v:
Pediatric Cardiology. 42:875-882
We sought to perform a comprehensive review of reported cases of conjoined thoracopagus twins with cardiovascular conjunction to determine the overall survival after separation and factors that might be associated with survival. We performed a system
Autor:
Kirstie L. MacMillen, Frank L. Hanley, Richard D. Mainwaring, Michal Palmon, R. Thomas Collins
Publikováno v:
The Annals of Thoracic Surgery. 110:949-955
Pulmonary artery stents are widely deployed in patients with stenoses in the branch pulmonary arteries. However, stents do not address more peripheral sites of stenosis and invariably develop in-stent restenosis. The purpose of this study was to revi
Autor:
Rumi Yokota, David M. Kwiatkowski, Chloe Journel, Greg T. Adamson, Evan Zucker, Geovanna Suarez, Kirstie M. Lechich, Abanti Chaudhuri, R. Thomas Collins
Publikováno v:
Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies. 23(3)
Cardiovascular manifestations occur in over 80% of Williams syndrome (WS) patients and are the leading cause of morbidity and mortality. One-third of patients require cardiovascular surgery. Renal artery stenosis (RAS) is common in WS. No studies hav
Autor:
Timothy E, Nissen, Isabella, Zaniletti, R Thomas, Collins, Lawrence E, Greiten, Parthak, Prodhan, Paul M, Seib, Elijah H, Bolin
Publikováno v:
Pediatric cardiology. 43(2)
22q11.2 deletion syndrome (22q11) and trisomy 21 (T21) are frequently associated with tetralogy of Fallot (TOF). We hypothesized that there are differences in postoperative length of stay (LOS) and occurrence of postoperative interventions after comp
Autor:
Nader Z Rabie, R. Thomas Collins, Pearl A. McElfish, Wendy N. Nembhard, Britni L Ayers, Di Chang, James M. Robbins, Xiaoyi Shan
Publikováno v:
Matern Child Health J
Objective Despite heterogeneity among Pacific Islanders, most studies aggregate them regardless of origin. Thus, limited information is available about perinatal outcomes among various subgroups of Pacific Islanders in the United States, including im
Autor:
Marcos Mills, Feifei Quin, Christopher S. Almond, Seth A. Hollander, R. Thomas Collins, Jin Long, David N. Rosenthal
Publikováno v:
Transplantation. 104(6)
Background Despite the routine use of hemodynamic assessment in pediatric heart transplant (HT) patients, expected intracardiac pressure measurements in patients free of significant complications are incompletely described. A better understanding of