# Personalised Long‐Term Albumin Treatment Based on Three‐Month Ascites Response in Patients With Decompensated Cirrhosis

**Authors:** Enrico Pompili, Giulia Iannone, Salvatore Piano, Pierluigi Toniutto, Antonio Lombardo, Stefania Gioia, Marta Tonon, Roberta Gagliardi, Daniele Carrello, Greta Tedesco, Vito Di Marco, Giacomo Zaccherini, Lorenzo Lani, Maurizio Baldassarre, Silvia Nardelli, Davide Bitetto, Vincenza Calvaruso, Paolo Angeli, Paolo Caraceni

PMC · DOI: 10.1111/liv.70598 · 2026-03-18

## TL;DR

This study shows that how patients with cirrhosis respond to albumin treatment after 3 months can help doctors personalize their long-term care and improve outcomes.

## Contribution

A new method for personalizing long-term albumin treatment based on early ascites response in decompensated cirrhosis patients.

## Key findings

- 36% of patients were responders with better outcomes and higher chances of treatment discontinuation or transplantation.
- Non-responders and partial responders had higher mortality and lower transplantation rates.
- Stratifying patients by 3-month response helps guide individualized treatment and integrate other management options.

## Abstract

Long‐term albumin (LTA) is effective for treating ascites in decompensated cirrhosis. This study aims to analyse the clinical courses of patients receiving LTA and provide a 3 month stratification to personalise management integrating LTA with other options.

Patients receiving LTA included in the multicentre, retrospective, observational Real‐ANSWER study were stratified into three categories according to the response of ascites after 3 months of treatment: ‘responders’ (grade 0–1 ascites), ‘partial responders’ (at least grade 2 ascites not receiving therapeutic paracentesis) and ‘non‐responders’ (at least grade 2 ascites receiving therapeutic paracentesis). Clinical trajectories and outcomes of the different categories were compared.

Of the 252 patients included (median Child‐Pugh 9, MELDNa 18), 36% were responders, 29% partial responders and 35% non‐responders. Responders differed significantly from the other groups, with higher cumulative incidence of LTA discontinuation for clinical improvement (33%) and transplantation (26%), a lower 18 month mortality (13%) and minimal use of TIPS. Partial and non‐responders showed similar trajectories with high mortality (35% and 42%) and low incidence of transplantation (12% and 11%). TIPS was performed predominantly among non‐responders (15%). Both groups had a few patients (12% and 8%) able to stop LTA for clinical improvement frequently related to an effective etiologic treatment.

Using a 3 month stratification according to the ascites response of LTA, patients can be grouped into three categories with different clinical courses and outcomes. This may help to stratify prognosis and inform clinical discussions on the management of ascites by integrating LTA with other available options.

Long‐term albumin should be considered an additional weapon on top of diuretics for treatment of clinically evident grade 2 and 3 ascites in patients with decompensated cirrhosis.The response of ascites after 3 months of long‐term albumin (responders, partial responders and non‐responders) stratifies patients with different trajectories and outcomes.This stratification may help to guide long‐term albumin treatment at the individual level and integrate this approach with the other options available for the management of difficult‐to‐treat ascites.

Long‐term albumin should be considered an additional weapon on top of diuretics for treatment of clinically evident grade 2 and 3 ascites in patients with decompensated cirrhosis.

The response of ascites after 3 months of long‐term albumin (responders, partial responders and non‐responders) stratifies patients with different trajectories and outcomes.

This stratification may help to guide long‐term albumin treatment at the individual level and integrate this approach with the other options available for the management of difficult‐to‐treat ascites.

## Linked entities

- **Diseases:** cirrhosis (MONDO:0005155)

## Full-text entities

- **Genes:** LTA (lymphotoxin alpha) [NCBI Gene 4049] {aka LT, TNFB, TNFSF1, TNLG1E}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}
- **Diseases:** chronic inflammation (MESH:D007249), ACLF (MESH:D065290), liver failure (MESH:D017093), steatotic liver disease (MESH:D008107), Decompensated Cirrhosis (MESH:D006333), HE (MESH:D006501), Cirrhosis (MESH:D005355), CIF (MESH:D012090), metabolic dysfunction (MESH:D008659), circulatory dysfunction (MESH:D012769), Ascites (MESH:D001201), hypersplenism (MESH:D006971), HCC (MESH:D006528), portal hypertension (MESH:D006975), cardiovascular disease (MESH:D002318), alcohol use disorders (MESH:D000437), bacterial infection (MESH:D001424), malnutrition (MESH:D044342), bacterial peritonitis (MESH:D010538), Death (MESH:D003643), extra-hepatic diseases (MESH:D010145), gastrointestinal bleeding (MESH:D006471), End-stage Liver disease (MESH:D058625), cardiac dysfunction (MESH:D006331), infections (MESH:D007239), bleeding (MESH:D006470), anaemia (MESH:D000743), TIPS (MESH:C562830)
- **Chemicals:** bilirubin (MESH:D001663), creatinine (MESH:D003404), Na (MESH:D012964), LVP (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12999546/full.md

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Source: https://tomesphere.com/paper/PMC12999546