# Comparison of the Effects of Sevoflurane and Isoflurane During Liver Transplant Surgery on the Short-Term Cardiac, Hepatic, and Renal Outcome: A Randomized Clinical Trial

**Authors:** Mohammadreza Moshari, Sadaf Tahery, Mastaneh Dahi Taleghani, Shide Dabir, Maryam Vosoughian, Soudeh Tabashi, Mohsen Ariannik, Firoozeh Madadi

PMC · DOI: 10.5812/ijpr-166290 · Iranian Journal of Pharmaceutical Research : IJPR · 2026-02-11

## TL;DR

This study compared isoflurane and sevoflurane during liver transplants and found no significant differences in short-term cardiac, liver, or kidney outcomes.

## Contribution

The study provides new clinical evidence on the comparative effects of two volatile anesthetics in liver transplant surgery.

## Key findings

- No significant differences were found in postoperative liver and kidney function between isoflurane and sevoflurane groups.
- Sevoflurane was associated with higher intraoperative blood product requirements compared to isoflurane.
- Both anesthetics showed similar effects on cardiac biomarkers and hemodynamic parameters.

## Abstract

Liver transplantation is frequently complicated by ischemia-reperfusion injury (IRI), which may impair hepatic, renal, and cardiac function. Volatile anesthetics such as isoflurane and sevoflurane are believed to mitigate this injury.

This study aimed to compare their effects on short-term organ outcomes in deceased donor liver transplant recipients.

In this study, 70 liver transplantation candidates at Taleghani Hospital in Tehran were enrolled after obtaining informed consent, and various variables were assessed before, during, and at two intervals immediately after surgery and one week post-operation. Patients were randomly allocated to receive either isoflurane or sevoflurane for anesthesia maintenance using the sealed opaque envelope technique for allocation concealment. Randomization was performed by a study nurse not involved in patient care using computer-generated random numbers. The primary outcome was defined as the postoperative peak serum alanine aminotransferase (ALT) level. Secondary outcomes included peak aspartate aminotransferase (AST), total bilirubin, creatinine, troponin I, C-reactive protein (CRP), intraoperative blood product requirements (packed red blood cells and fresh frozen plasma), hemodynamic parameters, and urine output.

Baseline characteristics were comparable between groups. No significant differences were found in intraoperative hemodynamics or postoperative laboratory values of liver and renal function (P > 0.05). Postoperative liver enzyme levels increased in both groups following reperfusion, consistent with IRI. However, no statistically significant differences were observed between the isoflurane and sevoflurane groups in peak serum ALT levels, measured 6 hours after reperfusion and on postoperative day 7 (P > 0.05 for all comparisons). Similarly, AST levels did not differ significantly between groups at any postoperative time point. Renal and cardiac biomarkers, including creatinine and troponin I, were also comparable between groups. In contrast, patients receiving sevoflurane required significantly higher volumes of packed red blood cells and fresh frozen plasma intraoperatively compared with the isoflurane group (P < 0.05).

The results obtained in this study showed that the use of isoflurane and sevoflurane did not have a significant difference in the severity of ischemic reperfusion injury caused after liver transplantation surgery on the liver, kidney, and heart; also, in this study, the functional conditions of these organs during and after surgery were evaluated, and by examining at different time intervals, these two inhalation anesthetics did not have a different effect on the short-term outcome of patients after receiving a liver transplant.

## Linked entities

- **Chemicals:** isoflurane (PubChem CID 3763), sevoflurane (PubChem CID 5206), alanine aminotransferase (PubChem CID 251717), creatinine (PubChem CID 588)
- **Diseases:** ischemia-reperfusion injury (MONDO:0005203)

## Full-text entities

- **Genes:** NFE2L2 (NFE2 like bZIP transcription factor 2) [NCBI Gene 4780] {aka IMDDHH, NRF2, Nrf-2}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, HMOX1 (heme oxygenase 1) [NCBI Gene 3162] {aka HMOX1D, HO-1, HSP32, bK286B10}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}
- **Diseases:** graft failure (MESH:D051437), acidosis (MESH:D000138), liver disease (MESH:D008107), inflammation (MESH:D007249), IRI (MESH:D015427), end-stage liver disease (MESH:D058625), death (MESH:D003643), mitochondrial damage (MESH:D028361), ischemia (MESH:D007511), hepatic steatosis (MESH:D005234), multiorgan dysfunction (MESH:D009102), arrhythmias (MESH:D001145), bleeding (MESH:D006470), hepatic injury (MESH:D056486), ischemic reperfusion injury (MESH:D015428), acute kidney injury (MESH:D058186)
- **Chemicals:** bilirubin (MESH:D001663), Cr (MESH:D002857), cisatracurium (MESH:C101584), volatile (-), lidocaine (MESH:D008012), Midazolam (MESH:D008874), Oxygen (MESH:D010100), propofol (MESH:D015742), Sevoflurane (MESH:D000077149), creatinine (MESH:D003404), ROS (MESH:D017382), lipid (MESH:D008055), fentanyl (MESH:D005283), Isoflurane (MESH:D007530), fluoride (MESH:D005459)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

36 references — full list in the complete paper: https://tomesphere.com/paper/PMC12933973/full.md

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Source: https://tomesphere.com/paper/PMC12933973