Portal Blood Arterialization with An Extracorporeal Device to Treat Toxic Acute Hepatic Failure in a Swine Model

Author:

Puviani Lorenza1,Cavallari Giuseppe1,Bonaiuto Elisabetta1,Cannistrà Marco1,Zullo Alessandra1,Pariali Milena1,Pisano Alessandro1,Atzeni Francesco1,Nardo Bruno12

Affiliation:

1. Center for Applied Biomedical Research (CRBa), S. Orsola-Malpighi University Hospital, Bologna - Italy

2. Department of Medicine and Surgical Sciences, University of Bologna, Bologna - Italy

Abstract

Purpose This study aimed to determine whether a controlled portal blood arterialization by a liver extracorporeal device (L.E.O2 NARDO) is effective in treating acute hepatic failure (AHF) induced through CCl4 administration in a swine model. Methods 20 swines with AHF induced by intraperitoneal injection of carbon tetrachloride (CCl4) in oil solution, were randomly divided into two groups: animals receiving L.E.O2 NARDO treatment 48 h after the intoxication (study group); animals sham operated 48 h after the intoxication (control group). Blood was withdrawn from the iliac artery and reversed in the portal venous system by an interposed extracorporeal device. Each treatment lasted 6 h. The survival was assessed at 5 days after L.E.O2 NARDO treatment or sham operation. In both groups blood samples were collected for biochemical analysis at different time points and liver biopsies were collected 48 h after intoxication and at sacrifice. Results We observed decreased transaminases levels and a more rapid INR recovery in the study group, as compared to the control group. Eight animals of the study group vs. two animals of the control group survived at five days after surgery with a statistically significant difference (p<0.05). Liver biopsies performed at sacrifice showed a reduction of the damaged hepatic areas in the study group as compared to the control group. Conclusions Arterial blood supply in the portal system through the L.E.O2 NARDO device is easily applicable, efficacious, and safe in a swine model of AHF induced by CCl4 intoxication.

Publisher

SAGE Publications

Subject

Biomedical Engineering,Biomaterials,General Medicine,Medicine (miscellaneous),Bioengineering

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