Graft Inflow Modulation by Splenic Artery Ligation for Portal Hyperperfusion Does Not Decrease Rates of Early Allograft Dysfunction in Adult Live Donor Liver Transplantation: A Randomized Control Trial.

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Tác giả: Udit Dhingra, Anubhav Kumar, Nihar Mohapatra, Viniyendra Pamecha, Nilesh Sadashiv Patil, Gaurav Sindwani, Shalini Thapar, Gattu Tharun, Anil Yadav

Ngôn ngữ: eng

Ký hiệu phân loại:

Thông tin xuất bản: United States : Annals of surgery , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 688153

 OBJECTIVE: The primary objective was to compare the rates of early allograft dysfunction (EAD) in patients undergoing elective adult live donor liver transplantation (ALDLT) with and without graft portal inflow modulation (GIM) for portal hyperperfusion. The secondary objectives were to compare time to normalization of bilirubin and International Normalized Ratio, day 14 ascitic output more than 1 L, small-for-size syndrome, intensive care unit/high dependency unit and total hospital stay, and 90-day morbidity and mortality. BACKGROUND: GIM can prevent EAD in ALDLT patients with portal hyperperfusion. METHODS: A single-center randomized trial with and without GIM for portal hyperperfusion by splenic artery ligation (SAL) in ALDLT was performed. After reperfusion, patients with portal venous pressure (PVP)>
 15 mm Hg with a gradient (PVP-central venous pressure) of ≥7 mm Hg and/or portal venous flow (PVF) >
 250 mL/min/100 g of liver were randomized into 2 groups: GIM and No GIM. RESULTS: 75 of 209 patients satisfied the inclusion criteria, and 38 underwent GIM. Baseline PVF and PVP were comparable between the GIM and no GIM groups. SAL significantly reduced the PVF and PVP ( P <
 0.001). There were no significant differences in the primary and secondary outcomes between the 2 groups. In the subgroup analysis, with a Graft to Recipient Weight Ratio ≤0.8, there were no significant differences in the primary and secondary outcomes. CONCLUSIONS: SAL significantly decreased PVP and PVF but did not decrease rates of EAD in adult LDLT.
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