# Prolonged Terlipressin Therapy as a Bridge to Curative TIPS for HRS–AKI in a Nontransplant Candidate

**Authors:** Deirdre Reidy, Arun Jesudian, David Salerno, Catherine Lucero

PMC · DOI: 10.1155/crhe/5364905 · Case Reports in Hepatology · 2026-02-27

## TL;DR

The paper presents a case where terlipressin therapy successfully bridged a patient with severe liver disease to a curative treatment without needing a transplant.

## Contribution

It demonstrates the safety and effectiveness of prolonged terlipressin therapy as a bridge to TIPS in a nontransplant candidate with HRS–AKI.

## Key findings

- Terlipressin therapy was safely used to manage HRS–AKI before TIPS placement.
- TIPS provided definitive treatment for HRS–AKI in a nontransplant candidate.
- The combination approach improved outcomes in a patient ineligible for liver transplantation.

## Abstract

Hepatorenal syndrome–acute kidney injury (HRS–AKI) is a severe complication of advanced cirrhosis with high mortality and limited treatment options. Terlipressin is currently the only FDA‐approved therapy for HRS, though recurrence is common upon discontinuation in patients without access to liver transplantation. Transjugular intrahepatic portosystemic shunt (TIPS) may provide definitive treatment for HRS–AKI in nontransplant candidates or in the setting of prolonged waitlists. This case illustrates the safety and success of terlipressin prior to TIPS for definitive treatment of HRS–AKI in a nontransplant candidate.

## Linked entities

- **Chemicals:** terlipressin (PubChem CID 72081)

## Full-text entities

- **Genes:** ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}
- **Diseases:** Infectious (MESH:D003141), pulmonary hypertension (MESH:D006976), Hepatic encephalopathy (MESH:D006501), HRS-AKI (MESH:D058186), nephropathy (MESH:D007674), esophageal varices (MESH:D004932), right heart failure (MESH:D006333), Type 2 diabetes mellitus (MESH:D003924), MASH (MESH:D005234), hydronephrosis (MESH:D006869), HRS (MESH:D020191), pulmonary disease (MESH:D008171), cirrhosis (MESH:D005355), volume overload (MESH:D019190), portal hypertension (MESH:D006975), ascites (MESH:D001201)
- **Chemicals:** Creatinine (MESH:D003404), spironolactone (MESH:D013148), midodrine (MESH:D008879), aldosterone (MESH:D000450), carvedilol (MESH:D000077261), urea (MESH:D014508), Furosemide (MESH:D005665), rifaximin (MESH:D000078262)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12947108/full.md

## References

18 references — full list in the complete paper: https://tomesphere.com/paper/PMC12947108/full.md

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Source: https://tomesphere.com/paper/PMC12947108