# Effect of liver transplants with retrograde reperfusion on early postoperative recovery of liver function and its risk factors

**Authors:** Jiajia Shen, Ming Wang, Chengkai Yang, Qiucheng Cai, Yi Jiang, Xiaojin Zhang

PMC · DOI: 10.1186/s12893-024-02467-3 · 2024-06-01

## TL;DR

This study found that liver transplants using retrograde reperfusion improve early liver function recovery compared to initial portal reperfusion.

## Contribution

The study identifies retrograde reperfusion as a better technique for early liver recovery and highlights the MELD score as a risk factor for postoperative dysfunction.

## Key findings

- Retrograde reperfusion resulted in significantly lower ALT and AST levels compared to initial portal reperfusion on postoperative days 3 and 7.
- The MELD score was identified as an independent risk factor for early hepatic allograft dysfunction after liver transplantation.
- Retrograde reperfusion is associated with better early postoperative liver function recovery in transplant patients.

## Abstract

The purpose of this study was to investigate effect of liver Transplants (LT) with retrograde reperfusion on early postoperative recovery of liver function and its risk factors.

We conducted a retrospective analysis of clinical data from 136 liver transplantation (LT) patients at the 900th Hospital of the Chinese People’s Liberation Army Joint Support Army, covering the period from January 2015 to January 2021. All participants provided informed consent, adhering to medical ethics guidelines. Patients were stratified into two groups based on the liver perfusion technique used: retrograde reperfusion (RTR, n = 108) and initial portal reperfusion (IPR, n = 28). Our study focused on a subset of 23 patients from each group to compare postoperative liver function recovery. The final analysis included 86 RTR and 28 IPR cases after excluding 8 RTR patients who underwent initial hepatic artery reperfusion and 14 who received simultaneous hepatic artery and portal vein reperfusion. Further subdivision within the RTR group identified 19 patients with early hepatic allograft dysfunction (EAD) and 67 without, allowing for an assessment of the influence of preoperative and intraoperative parameters, as well as perfusion methods, on EAD incidence post-LT.

Alanine aminotransferase (ALT) was 329 (211 ~ 548) and 176 (98 ~ 282) U/L on the 3rd and 7th day after RTR, respectively, which was significantly lower than 451 (288 ~ 918) and 251 (147 ~ 430) U/L in the IPR group (Z =-1.979, -2.299, P = 0.048, 0.021). Aspartate aminotransferase (AST) on postoperative days 3, 5, and 7 was 252 (193, 522), 105 (79, 163), and 93 (41, 135) U/L in the RTR group, respectively; it was also significantly lower than 328 (251, 724), 179 (129, 306), and 150 (91, 200)U/L in the IPR group (Z=-2.212, -3.221, -2.979; P = 0.027, 0.001, 0.003). Logistic regression analysis showed that MELD score was an independent risk factor for EAD after LT.

RTR LT is more favorable for patients’ early postoperative liver function recovery. For patients undergoing LT for RTR, preoperative MELD score was an independent risk factor for their postoperative development of EAD.

The online version contains supplementary material available at 10.1186/s12893-024-02467-3.

## Full-text entities

- **Genes:** GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}
- **Diseases:** IPR (MESH:D015427), EAD (MESH:D000092122), hepatic allograft dysfunction (MESH:D008107)
- **Species:** Homo sapiens (human, species) [taxon 9606]

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Source: https://tomesphere.com/paper/PMC11143670