Study To Evaluate Endothelial Function of Grafts in Patients Undergoing Coronary Artery Bypass Graft Surgery
MAQUET Cardiovascular LLC, a leading provider of cardiovascular technologies, today announced the initiation of a new prospective trial that is designed to compare the endothelial function of saphenous vein grafts using the MAQUET VASOSHIELD Pressure Controlling Syringe with graft preparation methods using a standard syringe in patients undergoing coronary artery bypass graft (CABG) surgery.
When a vessel is prepared for use as a bypass graft, it is frequently flushed with a standard syringe to check for leaks. If flushing pressure is not controlled, the vessel may be overdistended, potentially damaging the intimal layer. This type of endothelial damage may be prevented by use of a device that controls the pressure exerted on the vessel during preparation. The VASOSHIELD Pressure Controlling Syringe features three
settings that allow the user to control the maximum pressure used during preparation, thereby protecting the conduit from inadvertent damage.
“Accurately assessing and controlling the pressure in conduits using a standard syringe can be difficult,” said Vinod H. Thourani, M.D., Associate Professor of Surgery, Division of Cardiothoracic Surgery, Emory University, and principal investigator of the trial. “We expect this study to demonstrate that a reduced level of
endothelial dysfunction can be induced by using controlled pressure during vessel distension at 150 mm Hg with the use of the MAQUET VASOSHIELD Pressure Controlling Syringe, which regulates the pressure setting during distension.”
The study will enroll 30 patients undergoing elective CABG surgery who require at least two saphenous vein bypass grafts. Obtained using endoscopic vessel harvesting (EVH) techniques, each graft will be randomly assigned to receive vessel distension by either the MAQUET VASOSHIELD device or a standard syringe. The
study endpoints include histological evaluation of vein grafts, assessment of endothelial function and measurement of nitric oxide synthase (NOS) activity, and endothelium-dependent relaxation and contraction.
“This study underscores MAQUET Cardiovascular’s commitment to supporting physicians with tools that optimize graft quality and improve the standard of care,” said Luca Lombardi, M.D., Chief Medical Officer of MAQUET Cardiovascular. “As a leader in the field, MAQUET continues to advance cardiac bypass procedures by investing in technologies and research that help improve patient outcomes and enhance quality of life.”