Evaluation of potential hepatic recompensation criteria in patients with PBC and decompensated cirrhosis

Author:

Hofer Benedikt Silvester123ORCID,Burghart Lukas34ORCID,Halilbasic Emina13,Simbrunner Benedikt123ORCID,Petrenko Oleksandr13,Mandorfer Mattias123ORCID,Stättermayer Albert Friedrich123,Trauner Michael13,Reiberger Thomas123ORCID

Affiliation:

1. Division of Gastroenterology and Hepatology, Department of Medicine III Medical University of Vienna Vienna Austria

2. Vienna Hepatic Hemodynamic Lab, Division of Gastroenterology and Hepatology, Department of Medicine III Medical University of Vienna Vienna Austria

3. Rare Liver Diseases (RALID) Center of the ERN RARE‐LIVER at the Vienna General Hospital Vienna Austria

4. Klinik Ottakring Wiener Gesundheitsverbund Vienna Austria

Abstract

SummaryBackgroundAetiological therapy improves liver function and may enable hepatic recompensation in decompensated cirrhosis.AimsWe explored the potential for recompensation in patients with decompensated primary biliary cholangitis (PBC) – considering a biochemical response to ursodeoxycholic acid (UDCA) according to Paris‐II criteria as a surrogate for successful aetiological treatment.MethodsPatients with PBC were retrospectively included at the time of first decompensation. Recompensation was defined as (i) resolution of ascites and hepatic encephalopathy (HE) despite discontinuation of diuretic/HE therapy, (ii) absence of variceal bleeding and (iii) sustained liver function improvement.ResultsIn total, 42 patients with PBC with decompensated cirrhosis (age: 63.5 [IQR: 51.9–69.2] years; 88.1% female; MELD‐Na: 13.5 [IQR: 11.0–15.0]) were included and followed for 41.9 (IQR: 11.0–70.9) months after decompensation. Seven patients (16.7%) achieved recompensation. Lower MELD‐Na (subdistribution hazard ratio [SHR]: 0.90; p = 0.047), bilirubin (SHR per mg/dL: 0.44; p = 0.005) and alkaline phosphatase (SHR per 10 U/L: 0.67; p = 0.001) at decompensation, as well as variceal bleeding as decompensating event (SHR: 4.37; p = 0.069), were linked to a higher probability of recompensation. Overall, 33 patients were treated with UDCA for ≥1 year and 12 (36%) achieved Paris‐II response criteria. Recompensation occurred in 5/12 (41.7%) and in 2/21 (9.5%) patients with vs. without UDCA response at 1 year, respectively. Recompensation was linked to a numerically improved transplant‐free survival (HR: 0.46; p = 0.335). Nonetheless, 4/7 recompensated patients presented with liver‐related complications after developing hepatic malignancy and/or portal vein thrombosis and 2 eventually died.ConclusionsPatients with PBC and decompensated cirrhosis may achieve hepatic recompensation under UDCA therapy. However, since liver‐related complications still occur after recompensation, patients should remain under close follow‐up.

Funder

Österreichische Nationalstiftung für Forschung, Technologie und Entwicklung

Christian Doppler Forschungsgesellschaft

Boehringer Ingelheim

Publisher

Wiley

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