Literature DB >> 12149696

Strategy of management for congenital biliary dilatation in early infancy.

Yasuhiro Ohtsuka1, Hideo Yoshida, Tadashi Matsunaga, Katsunori Kouchi, Tadao Okada, Naomi Ohnuma.   

Abstract

PURPOSE: The aim of this study was to establish the optimal management strategy of congenital biliary dilatation (CBD) in early infancy.
METHODS: Over the last 15 years, 14 patients with CBD in early infancy (within 5 months), including 3 antenatally diagnosed patients, were treated in the authors' department. Of the 14 patients, 7 (50%) underwent early definitive surgery (E group), and the other 7 (50%) underwent delayed primary definitive surgery after percutaneous transhepatic cholangiodrainage (PTCD; D group). Both groups were compared retrospectively using clinical data.
RESULTS: Pretreatment status and backgrounds of the patients were clinically homogeneous between the 2 groups. The total length of hospital stay was significantly longer in the D group. As short-term complications, 1 patient in the E group was compromised with hepatolithiasis, and 3 patients in the D group were compromised with catheter-related complications. Other clinical data, such as age at definitive surgery, blood loss, pathologic fibrosis of the liver, jaundice-free day, and long-term complications were not significantly different between the 2 groups.
CONCLUSIONS: The authors propose that the standard of management should be early definitive surgery with wide anastomosis before 2 months of age. However, PTCD might be used under strict consideration of indication and careful management for patients with extremely poor surgical risk. Copyright 2002, Elsevier Science (USA). All rights reserved.

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Year:  2002        PMID: 12149696     DOI: 10.1053/jpsu.2002.34466

Source DB:  PubMed          Journal:  J Pediatr Surg        ISSN: 0022-3468            Impact factor:   2.545


  2 in total

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  2 in total

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