Long-term albumin treatment in patients with cirrhosis and ascites

J Hepatol. 2022 Jun;76(6):1306-1317. doi: 10.1016/j.jhep.2022.03.005.

Abstract

Although proposed for the first time several decades ago, the possibility that long-term human albumin could be effective for the treatment of patients with cirrhosis and ascites has become a topic of scientific and clinical discussion in the last decade. Long-term albumin administration represents a completely different treatment perspective compared to acute or short-term uses of albumin. Results from the ANSWER and the MACHT studies indicate that long-term albumin treatment can be effective, safe and able to modify the course of the disease provided that albumin is given at a sufficient dose and for a sufficient time to restore physiological levels and functions of the circulating molecule, which are compromised, at least partially, in patients with decompensated cirrhosis. Further clinical studies and randomised trials are warranted to confirm the clinical benefits of long-term albumin therapy. Important areas for further research include determining the precise target population, the biomarkers of response, the optimal dose and frequency of albumin infusions, the stopping rules, and the cost-effectiveness of treatment in different healthcare systems across the world, particularly in those where the logistical issues and costs related to the periodic intravenous infusions may represent an important limitation to the implementation of this innovative approach in clinical practice. In this review, we will critically analyse the available data on long-term albumin treatment, focusing on the differences that exist between studies, the controversial issues and the future perspectives.

Keywords: ascites; decompensated cirrhosis; disease-modifying intervention; effective albumin concentration; long-term albumin treatment.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Albumins / therapeutic use
  • Ascites* / drug therapy
  • Ascites* / etiology
  • Fibrosis
  • Humans
  • Liver Cirrhosis* / complications
  • Liver Cirrhosis* / drug therapy
  • Serum Albumin, Human

Substances

  • Albumins
  • Serum Albumin, Human