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Porcine Liver Transplantation Without Veno-Venous Bypass As an Extended Criteria Donor Model
Published on: August 17, 2022
Risk factors for intraoperative massive transfusion in pediatric liver transplantation: a multivariate analysis
Seok-Joon Jin1, Sun-Key Kim1, Seong-Soo Choi1
1Department of Anesthesiology and Pain Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
Insights
Massive transfusion in pediatric liver transplants is linked to high white blood cell counts, low platelets, and cadaveric donors. This impacts blood transfusion management for these young patients.
Area of Science:
- Hepatology
- Transplantation Surgery
- Hematology
Background:
- Pediatric liver transplantation (LT) frequently involves significant intraoperative blood transfusions.
- High transfusion rates correlate with increased postoperative complications and mortality in pediatric LT recipients.
Purpose of the Study:
- To identify risk factors for massive transfusion during pediatric LT.
- To evaluate the impact of massive transfusion on postoperative outcomes in pediatric LT.
Main Methods:
- Retrospective analysis of pediatric LT cases (December 1994 - June 2015).
- Massive transfusion defined as ≥100% total blood volume replacement.
- Multivariate logistic regression and Kaplan-Meier survival analyses were employed.
Main Results:
- Massive transfusion occurred in 55% of pediatric LT cases.
- High white blood cell count, low platelet count, and use of cadaveric donors predicted massive transfusion.
- A trend towards higher 6-month graft failure in the massive transfusion group (6.6% vs. 1.8%) was observed, though patient mortality did not differ significantly (7.3% vs. 7.1%).
Conclusions:
- High WBC count, low platelet count, and cadaveric donor status are significant predictors of massive transfusion in pediatric LT.
- Understanding these factors aids in optimizing perioperative blood transfusion strategies for pediatric LT.
- This research contributes to improved management of blood transfusions in pediatric liver transplant recipients.
Abstract:
Background: Pediatric liver transplantation (LT) is strongly associated with increased intraoperative blood transfusion requirement and postoperative morbidity and mortality. In the present study, we aimed to assess the risk factors associated with massive transfusion in pediatric LT, and examined the effect of massive transfusion on the postoperative outcomes. Methods: We enrolled pediatric patients who underwent LT between December 1994 and June 2015. Massive transfusion was defined as the administration of red blood cells ≥100% of the total blood volume during LT. The cases of pediatric LT were assigned to the massive transfusion or no-massive transfusion (administration of red blood cells <100% of the total blood volume during LT) group. Univariate and multivariate logistic regression analyses were performed to evaluate the risk factors associated with massive transfusion in pediatric LT. Kaplan-Meier survival analysis, with the log rank test, was used to compare graft and patient survival within 6 months after pediatric LT between the 2 groups. Results: The total number of LT was 112 (45.0%) and 137 (55.0%) in the no-massive transfusion and massive transfusion groups, respectively. Multivariate logistic regression analysis indicated that high white blood cell (WBC) count, low platelet count, and cadaveric donors were significant predictive factors of massive transfusion during pediatric LT. The graft failure rate within 6 months in the massive transfusion group tended to be higher than that in the no-massive transfusion group (6.6% vs. 1.8%, P = 0.068). However, the patient mortality rate within 6 months did not differ significantly between the massive transfusion and no-massive transfusion groups (7.3% vs. 7.1%, P = 0.964). Conclusion: Massive transfusion during pediatric LT is significantly associated with a high WBC count, low platelet count, and cadaveric donor. This finding can provide a better understanding of perioperative blood transfusion management in pediatric LT recipients.
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