Abstract

Fluid overload (FO) has been shown to adversely affect multiple organs and survival in critically ill patients. Liver transplantation (LT) carries the risk of massive transfusion, which frequently results in FO. We investigated the association of postoperative weight gain with graft failure, early allograft dysfunction (EAD), and overall mortality in LT. 1833 living donor LT (LDLT) recipients were retrospectively analysed. Patients were divided into 2 groups according to postoperative weight gain (<3% group [n = 1391] and ≥3% group [n = 442]) by using maximally selected log-rank statistics for graft failure. Multivariate Cox and logistic regression analyses were performed. The ≥3% group was associated with graft failure (adjusted HR [aHR], 1.763; 95% CI, 1.248–2.490; P = 0.001). When postoperative weight change was used as a continuous variable, the aHR for each 1% increase in postoperative weight was 1.045 (95% CI, 1.009–1.082; P = 0.015). In addition, the ≥3% group was associated with EAD (adjusted OR [aOR], 1.553; 95% CI, 1.024–2.356; P = 0.038) and overall mortality (aHR, 1.731; 95% CI, 1.182–2.535; P = 0.005). In conclusion, postoperative weight gain may be independently associated with increased risk of graft failure, EAD, and mortality in LDLT recipients.

Highlights

  • Fluid overload (FO) has been shown to adversely affect multiple organs and survival in critically ill patients

  • A total of 1833 adult living donor LT (LDLT) recipients were included in the final analysis (Fig. 1), and the median postoperative follow-up time was 5.1 years (IQR, 3.4–7.0)

  • The mean neutrophil-to-lymphocyte ratio (NLR) values were higher in the ≥3% group than in the

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Summary

Introduction

Fluid overload (FO) has been shown to adversely affect multiple organs and survival in critically ill patients. We investigated the association of postoperative weight gain with graft failure, early allograft dysfunction (EAD), and overall mortality in LT. Postoperative weight gain may be independently associated with increased risk of graft failure, EAD, and mortality in LDLT recipients. Liver transplantation (LT) carries the risk of massive transfusion, which frequently results in fluid overload (FO). Systemic inflammation may provoke hepatic angiogenesis of liver transplants, leading to fibrosis and cirrhotic remodelling that result in decreased graft survival in LT recipients[18,19,20]. We investigated the relationship between early postoperative weight gain and the occurrence of graft failure in living donor LT (LDLT) recipients. We evaluated the occurrence of early allograft dysfunction (EAD), as well as overall mortality

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