TY - JOUR
T1 - The efficacy of kasai operation for biliary atresia
T2 - A single institutional experience
AU - Lin, Jer Nan
AU - Wang, Kuei Liang
AU - Chuang, Jiin Haur
PY - 1992/6
Y1 - 1992/6
N2 - To assess the efficacy of Kasai operation for biliary atresia, 60 cases during a 14-year period (1976 to 1989) at this institution were reviewed. Thirty-four (56.7%) underwent operation within 90 days of life, 11 (18.3%) between 90 and 120 days and 15 (25.0%) beyond 120 days. Fifty-six underwent hepaticoportojejunostomy and 4 underwent hepaticoportocholecystostomy. Follow-up was 1 to 14 years (mean, 7.2 years). The postoperative follow-up of these 60 patients was categorized into five groups: group A (16 patients, 26.7%) was characterized by survival > 3 years and without jaundice; group B (3 patients, 5.0%) was defined as survival > 3 years, but with jaundice; group C (11 patients, 18.3%) was defined by survival but follow-up <3 years, (this group was further divided into C1 [7 patients, 11.7%] if anicteric and C2 [4 patients, 6.7%] if icteric); group D (2 patients, 3.3%) was patients who underwent liver transplantation; and group E (28 patients, 46.7%) was the group of patients who died at time of review. Group A and group C1 were interpreted as success after Kasai operation; hence, the potential success rate in this series was 38.3% (23 patients). They were long-term survivers, and most of them performed normal activities appropriate for their ages. We concluded that approximately one third of patients with biliary atresia would benefit from or be curred by this operation, which should be the first attempt in the treatment of this disease entity.
AB - To assess the efficacy of Kasai operation for biliary atresia, 60 cases during a 14-year period (1976 to 1989) at this institution were reviewed. Thirty-four (56.7%) underwent operation within 90 days of life, 11 (18.3%) between 90 and 120 days and 15 (25.0%) beyond 120 days. Fifty-six underwent hepaticoportojejunostomy and 4 underwent hepaticoportocholecystostomy. Follow-up was 1 to 14 years (mean, 7.2 years). The postoperative follow-up of these 60 patients was categorized into five groups: group A (16 patients, 26.7%) was characterized by survival > 3 years and without jaundice; group B (3 patients, 5.0%) was defined as survival > 3 years, but with jaundice; group C (11 patients, 18.3%) was defined by survival but follow-up <3 years, (this group was further divided into C1 [7 patients, 11.7%] if anicteric and C2 [4 patients, 6.7%] if icteric); group D (2 patients, 3.3%) was patients who underwent liver transplantation; and group E (28 patients, 46.7%) was the group of patients who died at time of review. Group A and group C1 were interpreted as success after Kasai operation; hence, the potential success rate in this series was 38.3% (23 patients). They were long-term survivers, and most of them performed normal activities appropriate for their ages. We concluded that approximately one third of patients with biliary atresia would benefit from or be curred by this operation, which should be the first attempt in the treatment of this disease entity.
KW - Biliary atresia
KW - Kasai operation
KW - hepaticoportoenterostomy
KW - liver transplantation
UR - http://www.scopus.com/inward/record.url?scp=0026623407&partnerID=8YFLogxK
U2 - 10.1016/S0022-3468(05)80095-8
DO - 10.1016/S0022-3468(05)80095-8
M3 - 文章
C2 - 1501027
AN - SCOPUS:0026623407
SN - 0022-3468
VL - 27
SP - 704
EP - 706
JO - Journal of Pediatric Surgery
JF - Journal of Pediatric Surgery
IS - 6
ER -