Literature DB >> 33977383

Laparoscopic Kasai portoenterostomy for cystic biliary atresia: midterm follow-up results of 35 patients.

Yi Ji1, Jianyuan Zhou1, Xuepeng Zhang1, Siyuan Chen2, Zhicheng Xu3.   

Abstract

PURPOSE: To investigate the clinical characteristics of cystic biliary atresia (CBA) and evaluate the midterm follow-up outcomes after laparoscopic treatment.
METHODS: We analyzed and compared data retrospectively on CBA patients (group A) and nonsyndromic type III biliary atresia (BA) patients (group B), who underwent laparoscopic Kasai portoenterostomy (LKPE) during the same period.
RESULTS: There were no significant differences in operative time, conversion rate, or the incidence of any postoperative complications between groups A and B (P > 0.05). The mean age at surgery (P < 0.01), rates of clearance of jaundice (CJ), cholangitis (P < 0.05), and 5-year survival with a native liver (SNL) were significantly lower in group A than in group B. Among the 35 patients with CBA, the CJ and 5-year SNL rates were significantly better in those with type I (n = 27) than in those with type IIId (n = 8) (P < 0.05).
CONCLUSIONS: LKPE is a feasible and safe procedure for CBA. The 5-year SNL after LKPE was better in patients with CBA than in those with nonsyndromic type III BA. The 5-year SNL after LKPE for type I CBA was better than that for type IIId CBA.
© 2021. Springer Nature Singapore Pte Ltd.

Entities:  

Keywords:  Biliary atresia; Clearance of jaundice; Laparoscopic Kasai portoenterostomy; Survival with native liver

Mesh:

Year:  2021        PMID: 33977383     DOI: 10.1007/s00595-021-02297-3

Source DB:  PubMed          Journal:  Surg Today        ISSN: 0941-1291            Impact factor:   2.549


  3 in total

1.  Prenatal ultrasonographic appearance of type IIId (uncorrectable type with cystic dilatation) biliary atresia.

Authors:  T Hasegawa; T Sasaki; T Kimura; T Sawai; K Nose; S Kamata; A Okada; K Wada; T Kanzaki
Journal:  Pediatr Surg Int       Date:  2002-05-09       Impact factor: 1.827

2.  Experience in the management of surgically correctable biliary atresia.

Authors:  E Arima; E W Fonkalsrud; R C Neerhout
Journal:  Surgery       Date:  1974-02       Impact factor: 3.982

3.  Differential diagnosis of infantile choledochal cyst with or without biliary atresia.

Authors:  Fu-Chen Huang; Kao-Pin Hwang
Journal:  Acta Paediatr Taiwan       Date:  2006 Jul-Aug
  3 in total

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