Serum Lactate Clearance as a Predictive Biomarker for Optimal Graft Perfusion in Living Donor Liver Transplantation

J Pediatr Surg. 2025 Feb;60(2):161647. doi: 10.1016/j.jpedsurg.2024.07.032. Epub 2024 Jul 26.

Abstract

Background: The optimal balance between the graft volume (GV) and portal venous flow (PVF) in living donor liver transplantation (LDLT) is unclear. As lactate is mainly metabolized in the liver, perioperative lactate levels are reportedly a useful biomarker for early graft dysfunction (EGD). The present study analyzed perioperative lactate levels according to the PVF.

Methods: The PVF/GV (mL/min per 100 g GV) of 97 recipients from 1996 to 2022 was retrospectively classified as low (LPVF; PVF/GV ≤ 100, N = 29), moderate (MPVF; PVF/GV 100-250, N = 40), or high (HPVF; PVF/GV > 250, N = 28). Lactate levels were obtained preoperatively (L0), immediately after graft reperfusion (L1), 4 h after reperfusion (L2), and on postoperative day 3 (L3). The lactate clearances were then calculated.

Results: The lower the PVF/GV ratio, the younger the age at LDLT and the higher the graft-to-recipient weight ratio. The median L2 and L3 in the HPVF group were significantly higher than those in the other groups (p = 0.019 and p = 0.003, respectively). The median ΔL1 in the HPVF group was lower than that in the LPVF and MPVF groups (0.23 vs. 0.50, p < 0.0001 and 0.23 vs. 0.41, p = 0.011, respectively). ΔL1 was negatively correlated with the PVF/GV. Although no patient had EGD, three patients with HPVF with low ΔL1 developed small-for-size syndrome.

Conclusions: Graft hyperperfusion may delay the recovery of the graft function and result in poor lactate clearance. The combination of the PVF/GV and lactate clearance may be useful as a prognostic marker for optimal graft perfusion in LDLT.

Level of evidence: IV.

Keywords: Lactate clearance; Living donor liver transplantation; Portal venous flow.

MeSH terms

  • Adolescent
  • Adult
  • Biomarkers* / blood
  • Biomarkers* / metabolism
  • Child
  • Child, Preschool
  • Female
  • Humans
  • Infant
  • Lactic Acid* / blood
  • Liver / blood supply
  • Liver / metabolism
  • Liver Transplantation*
  • Living Donors*
  • Male
  • Portal Vein
  • Retrospective Studies

Substances

  • Biomarkers
  • Lactic Acid