scholarly journals Bilirubin level 1 week after hepatoportoenterostomy predicts native liver survival in biliary atresia

2019 ◽  
Vol 87 (4) ◽  
pp. 730-734 ◽  
Author(s):  
Cho-Yi Huang ◽  
Mei-Hwei Chang ◽  
Huey-Ling Chen ◽  
Yen-Hsuan Ni ◽  
Hong-Yuan Hsu ◽  
...  
2020 ◽  
Vol 70 (1) ◽  
pp. 87-92
Author(s):  
Catalina Jaramillo ◽  
Stephen L. Guthery ◽  
Amy Lowichik ◽  
Gregory Stoddard ◽  
Taegun Kim ◽  
...  

2019 ◽  
Author(s):  
Quan-yuan Shan ◽  
Bao-xian Liu ◽  
Zhi-hai Zhong ◽  
Hua-dong Chen ◽  
Yu Guo ◽  
...  

Abstract Background Biliary atresia (BA) with a hilar cyst is an uncommon variant of BA that may be misunderstood to have a relatively favorable prognosis. Methods A single-center retrospective review of patients that matched BA with a hilar cyst (n=27) with BA without a cyst (n=27) over a 5-years period was done. All patients were diagnosed as type III BA by histologic examination and cholangiograms. Results There were no significant intergroup differences between baseline characteristics and outcomes after Kasai portoenterostomy surgery in two groups. The Kaplan–Meier survival curves showed no significant difference in cumulative native liver survival rate of the two groups (p = 0.584). Of the 27 BA patients with a hilar cyst, 8 were showed the cyst communicated with the gallbladder on cholangiograms, and Kaplan-Meier survival curves indicated that the cumulative native liver survival rate was significantly shorter (P=0.045) in them than those who the cyst was not communicated with the gallbladder. Conclusions Type III BA with a hilar cyst had no better prognosis compared with Type III BA without a cyst. A cyst communicated with the gallbladder may be associated with a poor eventual outcome for Type III BA with a hilar cyst.


2016 ◽  
Vol 32 (9) ◽  
pp. 839-843 ◽  
Author(s):  
Hideyuki Sasaki ◽  
Hiromu Tanaka ◽  
Motoshi Wada ◽  
Takuro Kazama ◽  
Megumi Nakamura ◽  
...  

2019 ◽  
Vol 29 (1) ◽  
pp. 121-125 ◽  
Author(s):  
Kin Wai Edwin Chan ◽  
Kim Hung Lee ◽  
Hei Yi Vicky Wong ◽  
Siu Yan Bess Tsui ◽  
Jennifer Wai Cheung Mou ◽  
...  

2020 ◽  
Vol 36 (5) ◽  
pp. 597-602
Author(s):  
Panicha Tangtrongchitr ◽  
Sopee Poomsawat ◽  
Voranush Chongsrisawat ◽  
Sittisak Honsawek ◽  
Yong Poovorawan ◽  
...  

Author(s):  
Aitaro Takimoto ◽  
Wataru Sumida ◽  
Hizuru Amano ◽  
Chiyoe Shirota ◽  
Takahisa Tainaka ◽  
...  

Abstract Purpose This study aimed to investigate the negative effects of intestinal obstruction for jaundice-free native liver survival after Kasai portoenterostomy (PE) for biliary atresia (BA). Methods We retrospectively reviewed the records of patients who underwent PE for BA between 2006 and 2019. We evaluated the postoperative morbidity of intestinal obstruction for up to 2 years after PE and the effects of intestinal obstruction on jaundice-free native liver survival. On the basis of their initial operation, patients were divided into open portoenterostomy (Open-PE) and laparoscopic portoenterostomy (Lap-PE) groups, and morbidity was compared. Results Of the 87 patients reviewed, 6 (6.9%) patients developed postoperative intestinal obstruction and underwent surgery to relieve the obstruction. The morbidity of early postoperative intestinal obstruction was 1.68 per 10,000 person days. The jaundice-free native liver survival rate among patients who once achieved jaundice-free status after PE was significantly lower in the patients with intestinal obstruction compared to in those without intestinal obstruction (0% vs. 73.8%; RR = 3.81, p = 0.007). No significant differences were seen in postoperative intestinal obstructions between the Open-PE and Lap-PE groups (p = 0.242). Conclusions Intestinal obstruction negatively impact jaundice-free native liver survival, even in patients who once achieved jaundice-free status after PE for BA.


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