TY - JOUR
T1 - Liver transplantation following the Kasai procedure in treatment of biliary atresia
T2 - A single institution analysis
AU - Sasaki, Hideyuki
AU - Tanaka, Hiromu
AU - Wada, Motoshi
AU - Kazama, Takuro
AU - Nishi, Kotaro
AU - Nakamura, Megumi
AU - Kudo, Hironori
AU - Kawagishi, Naoki
AU - Nio, Masaki
PY - 2014/9
Y1 - 2014/9
N2 - Purpose: This study aimed to assess outcomes of liver transplantation (LTx) in patients with biliary atresia (BA). Methods: The Kasai procedure was performed for 358 patients at Tohoku University Hospital between January 1955 and December 2013; 64 (17.9 %) required LTx. These 64 patients were divided into 4 groups according to their age at the time of transplantation: Group 1, aged <2 years (n = 27); Group 2, aged 2-9 years (n = 16); Group 3, aged 10-19 years (n = 11); and Group 4, aged ≥20 years (n = 10). Clinical parameters were evaluated retrospectively. Results: Both living-donor (n = 57) and deceased-donor (n = 7) LTx were performed. Indications were irreversible jaundice (n = 53), intractable cholangitis (n = 3), hepatopulmonary syndrome (n = 6), portopulmonary hypertension (n = 1), and intestinal bleeding (n = 1). Jaundice occurred more frequently in Groups 1 and 2 than in Groups 3 and 4 (p = 0.031). Survival rates were 81.5, 100, 90.9, and 80 % in Groups 1, 2, 3, and 4, respectively. Conclusion: Although the overall LTx survival rate was satisfactory, some adult recipients experienced LTx-related difficulty. Close follow-up, meticulous assessment of physical and social conditions, presence of a multidisciplinary support system, and appropriate time course for LTx are all essential factors in the treatment of BA.
AB - Purpose: This study aimed to assess outcomes of liver transplantation (LTx) in patients with biliary atresia (BA). Methods: The Kasai procedure was performed for 358 patients at Tohoku University Hospital between January 1955 and December 2013; 64 (17.9 %) required LTx. These 64 patients were divided into 4 groups according to their age at the time of transplantation: Group 1, aged <2 years (n = 27); Group 2, aged 2-9 years (n = 16); Group 3, aged 10-19 years (n = 11); and Group 4, aged ≥20 years (n = 10). Clinical parameters were evaluated retrospectively. Results: Both living-donor (n = 57) and deceased-donor (n = 7) LTx were performed. Indications were irreversible jaundice (n = 53), intractable cholangitis (n = 3), hepatopulmonary syndrome (n = 6), portopulmonary hypertension (n = 1), and intestinal bleeding (n = 1). Jaundice occurred more frequently in Groups 1 and 2 than in Groups 3 and 4 (p = 0.031). Survival rates were 81.5, 100, 90.9, and 80 % in Groups 1, 2, 3, and 4, respectively. Conclusion: Although the overall LTx survival rate was satisfactory, some adult recipients experienced LTx-related difficulty. Close follow-up, meticulous assessment of physical and social conditions, presence of a multidisciplinary support system, and appropriate time course for LTx are all essential factors in the treatment of BA.
KW - Biliary atresia
KW - Donor
KW - Liver transplantation
KW - Long-term follow-up
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U2 - 10.1007/s00383-014-3552-4
DO - 10.1007/s00383-014-3552-4
M3 - Article
C2 - 25064225
AN - SCOPUS:84908355945
SN - 0179-0358
VL - 30
SP - 871
EP - 875
JO - Pediatric Surgery International
JF - Pediatric Surgery International
IS - 9
ER -