“…[29][30][31][32] The degree to which SAs increase bleed risk in the CF-LVAD population has been infrequently studied. Three cohort studies have found an increased risk of experiencing GIB for CF-LVAD patients receiving SAs, though these studies have included small sample sizes, 33,34 no HeartMate 3™ devices, 33,35 and lacked analysis of other significant bleeding events including ICH or epistaxis. 33,35 Due to the sparse literature available regarding the association between bleeding and SA use in CF-LVAD patients, we sought to evaluate the impact of SA use on bleeding (GIB, ICH, and epistaxis) in patients supported with CF-LVADs.…”