Abstract

Ascites represents a critical event in the natural history of liver cirrhosis. From a prognostic perspective, its occurrence marks the transition from the compensated to the decompensated stage of the disease, leading to an abrupt worsening of patients’ life expectancy. Moreover, ascites heralds a turbulent clinical course, characterized by acute events and further complications, frequent hospitalizations, and eventually death. The pathophysiology of ascites classically relies on hemodynamic mechanisms, with effective hypovolemia as the pivotal event. Recent discoveries, however, integrated this hypothesis, proposing systemic inflammation and immune system dysregulation as key mechanisms. The mainstays of ascites treatment are represented by anti-mineralocorticoids and loop diuretics, and large volume paracentesis. When ascites reaches the stage of refractoriness, however, diuretics administration should be cautious due to the high risk of adverse events, and patients should be treated with periodic execution of paracentesis or with the placement of a trans-jugular intra-hepatic portosystemic shunt (TIPS). TIPS reduces portal hypertension, eases ascites control, and potentially modify the clinical course of the disease. Further studies are required to expand its indications and improve the management of complications. Long-term human albumin administration has been studied in two RCTs, with contradictory results, and remains a debated issue worldwide, despite a potential effectiveness both in ascites control and long-term survival. Other treatments (vaptans, vasoconstrictors, or implantable drainage systems) present some promising aspects but cannot be currently recommended outside clinical protocols or a case-by-case evaluation.

Highlights

  • The development of ascites is the most frequent decompensation event in patients with liver cirrhosis

  • Albumin use in patients with cirrhosis is currently recommended for the treatment or prevention of conditions characterized by an acute worsening of effective volemia: its wellestablished indications are the prevention of paracentesis-induced circulatory dysfunction (PICD), of renal dysfunction induced by spontaneous bacterial peritonitis (SBP), and the diagnosis and treatments of HRS

  • This result was further explored in a post hoc analysis [56] that showed two interesting findings: first, the best 18-month survival probability was obtained by patients reaching an on-treatment serum albumin concentration of at least 4 g/dL; second, baseline MELD score and serum albumin value independently predicted the achievement of this threshold

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Summary

Introduction

The development of ascites is the most frequent decompensation event in patients with liver cirrhosis. Five to ten percent of patients with compensated cirrhosis per year develop ascites, an event that represents a cornerstone in the natural history of the disease, so that it has become accustomed considering it the hallmark of the transition to decompensated cirrhosis [1]. It often marks the border between a stable and a turbulent clinical course, burdened with acute events of decompensation, including acute-on-chronic liver failure (ACLF), bacterial infections, and frequent hospitalizations, determining a dramatic worsening in quality of life and prognosis [2]. The present review, after a brief recall of the main pathogenetic mechanisms underlying decompensation and ascites formation in patients with cirrhosis, will discuss the currently available approaches for ascites management, along with some emerging perspectives and areas for future research

Pathophysiology of Ascites and Decompensation
Diagnosis of Ascites
Management of Uncomplicated Ascites
Dietary Salt Restriction
Diuretic Therapy
Therapeutic Paracentesis
Referral for Liver Transplantation
Management of Refractory Ascites
Trans-Jugular Intra-Hepatic Portosystemic Shunt
Long-Term Human Albumin Administration
Study design
Vaptans
Midodrine and Clonidine
Findings
Conclusions
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