*********************************
There is now a CONTENT FREEZE for Mercury while we switch to a new platform. It began on Friday, March 10 at 6pm and will end on Wednesday, March 15 at noon. No new content can be created during this time, but all material in the system as of the beginning of the freeze will be migrated to the new platform, including users and groups. Functionally the new site is identical to the old one. webteam@gatech.edu
*********************************
Phillip Trusty
BioE PhD Proposal Presentation
Date: Thursday, August 3, 2017
Time: 2:00 PM
Location: TEP, 387 Technology Cir NW, Atlanta, GA 30313, RM 104
Advisor:
Ajit Yoganathan, PhD (Georgia Tech, BME)
Committee:
Shriprasad Deshpande, MD (Emory University, Department of Pediatrics)
J. Brandon Dixon, PhD (Georgia Tech, Mechanical Engineering)
Mark Fogel, MD (Children’s Hospital of Philadelphia, Division of Cardiology)
John Oshinski, PhD (Georgia Tech, Biomedical Engineering)
Timothy Slesnick, MD (Emory University, Department of Pediatrics)
Hemodynamic Assessment of Proposed Solutions for Fontan Failure
Congenital heart defects are the most common types of birth defects and are responsible for an estimated 300,000 newborn deaths per year. The most severe of these defects can result in a “single ventricle” physiology. Thankfully, over the last 40 years surgeons have pioneered a set of 3 staged surgeries to palliate single ventricle heart defects, which results in a total cavopulmonary connection. Short term outcomes of these “Fontan” patients are very promising, with a 1 year survival rate around 95%. However, as these patients age, long term complications are inevitable. The central purpose of this thesis is to investigate the effectiveness of current, clinically implemented “solutions” for two of the most common modes of Fontan failure including pulmonary arteriovenous malformations (PAVMs) and liver disease. Specific Aim 1 will test if surgical planning can be used to accurately predict post-operative hepatic flow distribution (a factor in PAVM formation), and if Y-grafts can provide more balanced hepatic flow distribution than traditional Fontan connections. Specific Aim 2 will test if the extent of liver fibrosis in Fontan patients is associated with poor hemodynamics, and if ventricular assist devices can decrease Fontan hepatic congestion by augmenting flow and decreasing inferior vena cava pressure.