Abstract

Introduction: Experimentally induced hepatocellular bile salt accumulation impairs liver function and regeneration. Portal Vein Embolisation (PVE) is the current standard to induce FLR hypertrophy. The impact of cholestasis on PVE-induced FLR hypertrophy however remains unclear. We hypothesized that cholestasis impairs PVE induced FLR hypertrophy and compared PVE hypertrophic response between patients with and without cholestasis. Methods: Patients with perihilar cholangiocarcinoma or colorectal liver metasases, who had undergone PVE before a major hemihepatectomy in Uniklinik RWTH Aachen or Maastricht University Medical Center between 2016 and 2019, were enrolled. Clinical and laboratory variables were recorded and volume of segment 2 and 3 on pre- and post-embolization CT-scans were assessed. Diameters of left and right hepatic bile ducts was measured on pre-embolization scans. Bilirubin was used as a clinical marker of cholestasis. The degree of hypertrophy (DH) as a percentage and kinetic growth rate (KGR) as percentage/week were used to assess the increase of the liver volume. Results: In this study,142 patients were enrolled. Sequential pre- and post-CT-scans were available for 53 patients (32 for CRLM, 21 for pCCA). Liver segment II and III volumes increased significantly after PVE in both groups (P < 0.001). pCCA patients with cholangitis (n=4) had an almost blunted DH (P = 0.042). DH and KGR did not differ (P = 0.719 and P = 0.968, respectively) between drained and undrained pCCA patients. Higher initial bilirubin level before biliary drainage was correlated with less PVE-induced DH (ρ=-0.727, P = 0.007). The bilirubin level and bile duct diameter before PVE was not associated with DH and KGR. Conclusion: Initial bilirubin levels before biliary drainage were negatively correlated with PVE-induced liver hypertrophy in patients with pCCA. Biliary duct diameter and bilirubin level right before PVE seems less of influence on PVE induced hypertrophy.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call