Problems during and after pregnancy in female patients with biliary atresia

被引:22
作者
Sasaki, Hideyuki [1 ]
Nio, Masaki
Hayashi, Yutaka
Ishii, Tomohiro
Sano, Nobuyuki
Ohi, Ryoji
机构
[1] Tohoku Univ, Sch Med, Dept Pediat Surg, Sendai, Miyagi 9808574, Japan
[2] Iwaki Kyoritsu Gen Hosp, Dept Pediat Surg, Iwaki, Fukushima 9738555, Japan
关键词
biliary atresia; pregnancy; complications; liver transplantation;
D O I
10.1016/j.jpedsurg.2007.03.027
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background/Purpose: Advances in the management for biliary atresia (BA) have improved the prognosis and has greatly increased the number of long-term survivors. Even the long-term survivors, however, still face some problems. This retrospective review was performed to assess pregnancy-associated issues in long-term survivors after surgery for BA. Materials and Methods: Of 55 patients with BA surviving for 16 years or more without liver transplantation, 9 patients have experienced pregnancy and delivery. Clinical courses, the outcome of pregnancy and delivery, and current statuses were retrospectively evaluated from their clinical records. Results: The study revealed 14 pregnancies and 11 deliveries. Before pregnancy, no patient showed visible jaundice, but 6 patients had some complications such as episodes of cholangitis and portal hypertension. Two of the patients had both conditions and 2 others developed visible jaundice after pregnancy. One intrauterine fetal death occurred. Conclusions: Our retrospective review suggests that the previously mentioned conditions can be risk factor for cholangitis and gastrointestinal bleeding during or after pregnancy but are not considered to be contraindications for pregnancy and delivery. Complications can occur with pregnancy even during the normal course. Thus, careful observation is recommended. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:1329 / 1332
页数:4
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