Medium-term outcomes after laparoscopic revision of laparoscopic Kasai portoenterostomy in patients with biliary atresia

被引:7
作者
Ji, Yi [1 ]
Zhang, Xuepeng [1 ]
Chen, Siyuan [2 ]
Li, Yanan [1 ]
Yang, Kaiying [1 ]
Zhou, Jiangyuan [1 ]
Xu, Zhicheng [1 ]
机构
[1] Sichuan Univ, Dept Pediat Surg, West China Hosp, 37 Guo Xue Xiang, Chengdu 610041, Sichuan, Peoples R China
[2] Sichuan Univ, Pediat Intens Care Unit, West China Hosp, Dept Crit Care Med, Chengdu 610041, Peoples R China
基金
中国国家自然科学基金;
关键词
Biliary atresia; Laparoscopic Kasai portoenterostomy; Revision; Outcomes; LIVER-TRANSPLANTATION; SURGERY; IMPACT;
D O I
10.1186/s13023-021-01835-z
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Objective To determine whether revision laparoscopic Kasai portoenterostomy (RLKPE) is a viable treatment option for patients with biliary atresia (BA) who had undergone initially successful laparoscopic Kasai portoenterostomy (ILKPE). Methods The medical records of 312 patients with nonsyndromic BA who had undergone ILKPE between May 2009 and May 2017 were retrospectively reviewed. The patients were divided into three groups according to their outcomes after ILKPE: group A: 25 patients who had undergone RLKPE; group B: 203 patients who had undergone ILKPE and required no further surgical intervention; group C: 84 patients with failed ILKPE who had either died or required liver transplantation for survival. The 3-year and 5-year survival with native liver (SNL) rates were compared between groups A and B and between groups A and C. Among the 25 patients in group A, the perioperative data of RLKPE were compared with those of ILKPE. Results Of the 312 patients who had undergone ILKPE, 228 reached the normal bilirubin concentration range within 6 months postoperatively. Among them, 25 patients with a sudden cessation of bile flow had undergone RLKPE. Adequate biliary drainage, as evidenced by normalized conjugated bilirubin levels, was achieved in 80% of patients who had undergone RLKPE. The perioperative variables, including the operative time, blood loss, rate of conversion to open surgery and complications of RLKPE, were not significantly different between RLKPE and ILKPE. The 3-year and 5-year SNL rates in patients after RLKPE were 64.0% and 52.0%, respectively, which were not significantly different from the corresponding rates of 86.2% and 73.9%, respectively, in patients after unrevised ILKPE (P > 0.05). Conclusion Our data demonstrated that RPLKE is a viable and effective treatment option in patients with sudden cessation of bile drainage after ILKPE. RPLKE can delay the need for liver transplantation, yielding encouraging medium-term patient outcomes.
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相关论文
共 19 条
[11]   Reappraise the effect of redo-Kasai for recurrent jaundice following Kasai operation for biliary atresia in the era of liver transplantation [J].
Mendoza, Manuel Mikery ;
Chiang, Jiun-Hung ;
Lee, Shin-Yi ;
Kao, Chun-Yu ;
Chuang, Jiin-Haur ;
Tiao, Mao-Meng ;
Hsieh, Chih-Sung .
PEDIATRIC SURGERY INTERNATIONAL, 2012, 28 (09) :861-864
[12]   A New Era of Laparoscopic Revision of Kasai Portoenterostomy for the Treatment of Biliary Atresia [J].
Murase, Naruhiko ;
Uchida, Hiroo ;
Ono, Yasuyuki ;
Tainaka, Takahisa ;
Yokota, Kazuki ;
Tanano, Akihide ;
Shirota, Chiyoe ;
Shirotsuki, Ryo .
BIOMED RESEARCH INTERNATIONAL, 2015, 2015
[13]   Redo surgery for biliary atresia [J].
Nio, Masaki ;
Sasaki, Hideyuki ;
Tanaka, Hiromu ;
Okamura, Atsushi .
PEDIATRIC SURGERY INTERNATIONAL, 2013, 29 (10) :989-993
[14]   Long-term outcomes after revision of Kasai portoenterostomy for biliary atresia [J].
Shirota, Chiyoe ;
Uchida, Hiroo ;
Ono, Yasuyuki ;
Murase, Naruhiko ;
Tainaka, Takahisa ;
Yokota, Kazuki ;
Oshima, Kazuo ;
Shirotsuki, Ryo ;
Hinoki, Akinari ;
Ando, Hisami .
JOURNAL OF HEPATO-BILIARY-PANCREATIC SCIENCES, 2016, 23 (11) :715-720
[15]   A multicenter study of the outcome of biliary atresia in the United States, 1997 to 2000 [J].
Shneider, Benjamin L. ;
Brown, Morton B. ;
Haber, Barbara ;
Whitington, Peter F. ;
Schwarz, Kathleen ;
Squires, Robert ;
Bezerra, Jorge ;
Shepherd, Ross ;
Rosenthal, Philip ;
Hoofnagle, Jay H. ;
Sokol, Ronald J. .
JOURNAL OF PEDIATRICS, 2006, 148 (04) :467-474
[16]  
Sugawara Y, 2004, HEPATO-GASTROENTEROL, V51, P192
[17]   Effect of Repeat Kasai Hepatic Portoenterostomy on Pediatric Live-Donor Liver Graft for Biliary Atresia [J].
Urahashi, Taizen ;
Mara, Yoshiyuki ;
Sanada, Yukihiro ;
Wakiya, Taiichi ;
Yamada, Naoya ;
Okada, Noriki ;
Mizuta, Koichi .
EXPERIMENTAL AND CLINICAL TRANSPLANTATION, 2013, 11 (03) :259-263
[18]   Experience of treating biliary atresia with three types of portoenterostomy at a single institution: extended, modified Kasai, and laparoscopic modified Kasai [J].
Wada, Momoko ;
Nakamura, Hiroki ;
Koga, Hiroyuki ;
Miyano, Go ;
Lane, Geoffrey J. ;
Okazaki, Tadaharu ;
Urao, Masahiko ;
Murakami, Hiroshi ;
Kasahara, Mureo ;
Sakamoto, Seisuke ;
Ishizaki, Yoichi ;
Kawasaki, Seiji ;
Yamataka, Atsuyuki .
PEDIATRIC SURGERY INTERNATIONAL, 2014, 30 (09) :863-870
[19]  
Yamataka A, 2014, SAMJ S AFR MED J, V104, P820, DOI [10.7196/SAMJ.8921, 10.7196/samj.8921]