American Journal of Transplantation · 2005 · 269 citations · 29 references
MedicineSurgeryHepatologyTransplant SurgeryVascular SurgeryDeceased Donor TransplantationGraft SurvivalHepatic PerfusionLiver Blood FlowLiver TransplantationTransplant OutcomesHepatic Arterial FlowHepatic Blood Flow LimitationLiver Donor SurgeryLiver Graft PerfusionPortosystemic ShuntsRecipient Graft SurvivalSmall-diameter Vascular Grafts
Graft hyperperfusion in small-for-size grafts (SFSG) is considered the main causal factor of small-for-size syndrome (SFSS). We compared SFSG with a graft-to-recipient body ratio ≤0.8, with and without graft inflow modulation (GIM) by means of a hemi-portocaval shunt (HPCS). Thirteen patients underwent adult-to-adult living donor liver transplantation (AALDLT): G1, n = 5 [4 right livers (RL) and 1 left liver (LL)] without GIM, and G2, n = 8 (4 RL and 4 LL) with GIM. In G2 patients, portal vein flow (PVF) was significantly reduced by HPCS: 190 ± 70 mL/min/100 g liver in G2 vs. 401 ± 225 ml/min in G1 (p = 0.002). One- and 6-month post-transplantation graft volume/standard liver volume (GV/SLV) ratio was of 72% and 79.5% in G1; 80% and 101% in G2 (p = ns). SFSS was observed in three G1 recipients (who were retransplanted), but in none of the G2 patients. At 1-year, patient and graft survival was respectively of 40% and 20% in G1,87.5% and 75% in G2 (p = 0.024 and 0.03).It is concluded that drastic reduction of PVF by means of HPCS improves overall patient and graft survival by averting the occurrence of SFSS. Graft inflow modulation through HPCS reduces the risk of complications when transplanting SFSG in adult recipients. Graft hyperperfusion in small-for-size grafts (SFSG) is considered the main causal factor of small-for-size syndrome (SFSS). We compared SFSG with a graft-to-recipient body ratio ≤0.8, with and without graft inflow modulation (GIM) by means of a hemi-portocaval shunt (HPCS). Thirteen patients underwent adult-to-adult living donor liver transplantation (AALDLT): G1, n = 5 [4 right livers (RL) and 1 left liver (LL)] without GIM, and G2, n = 8 (4 RL and 4 LL) with GIM. In G2 patients, portal vein flow (PVF) was significantly reduced by HPCS: 190 ± 70 mL/min/100 g liver in G2 vs. 401 ± 225 ml/min in G1 (p = 0.002). One- and 6-month post-transplantation graft volume/standard liver volume (GV/SLV) ratio was of 72% and 79.5% in G1; 80% and 101% in G2 (p = ns). SFSS was observed in three G1 recipients (who were retransplanted), but in none of the G2 patients. At 1-year, patient and graft survival was respectively of 40% and 20% in G1,87.5% and 75% in G2 (p = 0.024 and 0.03). It is concluded that drastic reduction of PVF by means of HPCS improves overall patient and graft survival by averting the occurrence of SFSS. Graft inflow modulation through HPCS reduces the risk of complications when transplanting SFSG in adult recipients.
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IMPACT OF GRAFT SIZE MISMATCHING ON GRAFT PROGNOSIS IN LIVER TRANSPLANTATION FROM LIVING DONORS1,2
Tetsuya Kiuchi, Mureo Kasahara, Kenji Uryuhara et al. · Transplantation · 1999 · 966 citations
Medicine, Pediatrics, Surgery +16
Calculation of child and adult standard liver volume for liver transplantation
Koichi Urata, Seiji Kawasaki, Hidetoshi Matsunami et al. · Hepatology · 1995 · 961 citations · Full text
Medicine, Pediatrics, Surgery +17
RIGHT LOBE GRAFT IN LIVING DONOR LIVER TRANSPLANTATION 1,2
Yukihiro Inomata, Shinji Üemoto, Katsuhiro Asonuma et al. · Transplantation · 2000 · 375 citations
Medicine, Surgery, Hepatology +12
Functional Analysis of Grafts from Living Donors
Jean C. Emond, John F. Renz, Linda D. Ferrell et al. · Annals of Surgery · 1996 · 374 citations · Full text
Medicine, Pediatrics, Surgery +17