P. Sauer et al., PHENPROCOUMON FOR PREVENTION OF SHUNT OCCLUSION AFTER TRANSJUGULAR INTRAHEPATIC PORTOSYSTEMIC STENT-SHUNT - A RANDOMIZED TRIAL, Hepatology, 24(6), 1996, pp. 1433-1436
Development of stenosis or occlusion of the transjugular intrahepatic
portosystemic stent shunt (TIPSS) is one of the major limiting factors
in the long-term viability of this procedure. The efficacy of anticoa
gulation with heparin which is used in different centers is still uncl
ear. In the present study, we evaluated the effect of phenprocoumon on
shunt patency after TIPSS placement using Palmaz stents; 49 patients
with Child's A and B cirrhosis, who underwent successful TIPSS placeme
nt were randomized into the treatment group (n = 24) who received phen
procoumon and a control group (n = 25). After 11 to 13 weeks, all pati
ents were admitted and had a reevaluation that included control angiog
raphy by transjugular approach. Phenprocoumon treatment was stopped af
ter the first reevaluation and both groups were followed for 1 year af
ter randomization. During the 3-month treatment period 11 of 22 patien
ts of the treatment group and 12 of 23 patients of the control group r
equired reintervention because of an increased portosystemic gradient.
Five of the 12 patients in the control group showed complete occlusio
n of the shunt, whereas no occlusion in the treatment group was observ
ed (P <.05). During the mean follow-up of 8 months after the treatment
was stopped, in both groups stenosis occurred in 50% of patients, but
no further occlusion of the stent was observed. These data indicate t
hat occlusion of the stent is related to thrombosis, whereas stenosis
does not appear to be dependent on blood coagulation. In patients with
preserved liver function occlusion of the shunt may be prevented by p
henprocoumon treatment in the first 3 months after TIPSS placement. Th
ereafter shunt occlusion was not observed and further phenprocoumon tr
eatment seemed unnecessary.