Enoxaparin prevents portal vein thrombosis and liver decompensation in patients with advanced cirrhosis
Articolo
Data di Pubblicazione:
2012
Citazione:
Enoxaparin prevents portal vein thrombosis and liver decompensation in patients
with advanced cirrhosis / Villa, Erica; C., Cammà; M., Marietta; Luongo, Monica; Critelli, Rosina Maria; S., Colopi; C., Tata; Zecchini, Ramona; S., Gitto; S., Petta; B., Lei; Bernabucci, Veronica; Vukotic, Ranka; N., De Maria; Schepis, Filippo; A., Karampatou; C., Caporali; L., Simoni; M., Del Buono; B., Zambotto; Turola, Elena; G., Fornaciari; S., Schianchi; A., Ferrari; D., Valla. - In: GASTROENTEROLOGY. - ISSN 0016-5085. - ELETTRONICO. - 143:5(2012), pp. 1253-1260. [10.1053/j.gastro.2012.07.018]
Abstract:
BACKGROUND & AIMS: We performed a randomized controlled trial to evaluate the safety and efficacy of enoxaparin, a low-molecular-weight heparin, in preventing portal vein thrombosis (PVT) in patients with advanced cirrhosis.
METHODS: In a nonblinded, single-center study, 70 outpatients with cirrhosis (Child-Pugh classes B7-C10) with demonstrated patent portal veins and without hepatocellular carcinoma were assigned randomly to groups that were given enoxaparin (4000 IU/day, subcutaneously for 48 weeks; n = 34) or no treatment
(controls, n = 36). Ultrasonography (every 3 months) and computed tomography
(every 6 months) were performed to check the portal vein axis. The primary
outcome was prevention of PVT. Radiologists and hepatologists that assessed
outcomes were blinded to group assignments. Analysis was by intention to treat.
RESULTS: At 48 weeks, none of the patients in the enoxaparin group had developed
PVT, compared with 6 of 36 (16.6%) controls (P = .025). At 96 weeks, no patient
developed PVT in the enoxaparin group, compared with 10 of 36 (27.7%) controls (P
= .001). At the end of the follow-up period, 8.8% of patients in the enoxaparin
group and 27.7% of controls developed PVT (P = .048). The actuarial probability
of PVT was lower in the enoxaparin group (P = .006). Liver decompensation was
less frequent among patients given enoxaparin (11.7%) than controls (59.4%) (P <
.0001); overall values were 38.2% vs 83.0%, respectively (P < .0001). The
actuarial probability of liver decompensation was lower in the enoxaparin group
(P < .0001). Eight patients in the enoxaparin group and 13 controls died. The
actuarial probability of survival was higher in the enoxaparin group (P = .020).
No relevant side effects or hemorrhagic events were reported.
CONCLUSIONS: In a small randomized controlled trial, a 12-month course of
enoxaparin was safe and effective in preventing PVT in patients with cirrhosis
and a Child-Pugh score of 7-10. Enoxaparin appeared to delay the occurrence of
hepatic decompensation and to improve survival.
Tipologia CRIS:
Articolo su rivista
Keywords:
Portal vein trombosis; Enoxaparin; cirrhosis
Elenco autori:
Villa, Erica; C., Cammà; M., Marietta; Luongo, Monica; Critelli, Rosina Maria; S., Colopi; C., Tata; Zecchini, Ramona; S., Gitto; S., Petta; B., Lei; Bernabucci, Veronica; Vukotic, Ranka; N., De Maria; Schepis, Filippo; A., Karampatou; C., Caporali; L., Simoni; M., Del Buono; B., Zambotto; Turola, Elena; G., Fornaciari; S., Schianchi; A., Ferrari; D., Valla
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