Background/Aims: Terlipressin is used for the treatment of bleeding oesopha
geal varices, We evaluated the effects of terlipressin on hepatic haemodyna
mics, with special focus on the interactions between portal venous flow and
hepatic arterial flow over time. Secondly, we evaluated the estimated hepa
tic blood bow by the ICG clearance method against direct measurements of he
patic blood flow.
Methods: Eight healthy anaesthetised pigs received terlipressin 1 mg or pla
cebo intravenously in a randomised, blind, cross-over design. Hepatic arter
ial flow portal venous flow, systemic haemodynamics, and portal vein diamet
er were recorded simultaneously. Portal venous flow and hepatic arterial fl
ow were measured by transit time ultrasound flowmetry. Estimated hepatic bl
ood flows at baseline and after terlipressin were compared with the sum of
the portal venous flow and hepatic arterial flow.
Results: Portal venous flow decreased significantly 5 min after administrat
ion of terlipressin (p<0.05). At 30 min it had decreased by 34% (p<0.01) an
d the hepatic arterial bow had increased by 81% (p<0.01). The estimated hep
atic blood flow and the hepatic blood flow decreased by 23% (p<0.015). At b
aseline the estimated hepatic blood flow and the hepatic blood flow correla
ted significantly (r=0.85, p<0.01), but this correlation disappeared after
administration of terlipressin (r=0.06, p=ns). The hepatic blood flow was 1
2% higher than the estimated hepatic blood flow before and after terlipress
in.
Conclusions: Terlipressin decreased the portal venous flow hepatic blood fl
ow, and estimated hepatic blood flow significantly and was accompanied by a
substantial increase in hepatic arterial flow The estimated hepatic blood
flow and hepatic blood flow were strongly correlated at baseline, but after
terlipressin the correlation disappeared.