Jf. Boylan et al., TRANEXAMIC ACID REDUCES BLOOD-LOSS, TRANSFUSION REQUIREMENTS, AND COAGULATION-FACTOR USE IN PRIMARY ORTHOTOPIC LIVER-TRANSPLANTATION, Anesthesiology, 85(5), 1996, pp. 1043-1048
Background: Patients with end-stage liver disease frequently incur lar
ge-volume blood loss during liver transplantation associated with mech
anical factors, preexisting coagulopathy, and intraoperative fibrinoly
sis. Methods: Between April 1992 and May 1994, the authors of this dou
ble-blind, randomized, placebo-controlled study examined the effect of
high-dose tranexamic acid (maximum of 20 g) on blood loss and blood p
roduct requirements in patients undergoing primary isolated orthotopic
liver transplantation. Primary outcome measures were volume of blood
loss (intraoperative blood loss and postoperative drainage) and erythr
ocyte, plasma, platelet, and cryoprecipitate use during surgery and th
e first 24 h of intensive care unit stay. Results: Patients receiving
transexamic acid (n = 25) had less intraoperative blood loss (median,
4.3 l; interquartile range, 2.5 to 7.9; P = 0.006) compared with the p
lacebo group (n = 20; median, 8 l; interquartile range, 5 to 15.8), an
d reduced intraoperative plasma, platelet, and cryoprecipitate require
ments. Median perioperative erythrocyte use was 9 units (interquantile
range, 4 to 14 units) in patients receiving transexamic acid and 13 u
nits (interquantile range, 7.5 to 31 units) in controls (P = 0.03). To
tal perioperative donor exposure was 20.5 units (interquantile range,
16 to 41 units) in patients receiving transexamic acid and 43.5 units
(interquantile range, 29.5 to 79 units) in controls (P = 0.003). Resul
ts for postoperative wound drainage were similar. Hospital stay and ne
ed for retransplantation were comparable in both groups. No patient in
either group showed clinical evidence of hepatic artery or portal ven
ous thrombosis within 1 month of transplantation. Conclusions: High-do
se tranexamic acid significantly reduces intraoperative blood loss and
perioperative donor exposure in patients with end-stage parenchymal l
iver disease who are undergoing orthotopic liver transplantation, with
marked reductions in platelet and cryoprecipitate requirements.