Diagnosis of Biliary Atresia Can Not Be Excluded by Declining Trend of Serum Direct Bilirubin

The aim of this paper is to investigate the clinical courses of patients with biliary atresia (BA) during neonatal period. We examined 19 patients with BA, who underwent blood tests including direct bilirubin (D-Bil) within 20 days of age, in 3 tertiary hospitals in Japan. The first blood sample was...

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Published inPediatric reports Vol. 5; no. 4; p. e17
Main Authors Terui, Keita, Higashimoto, Yasuyuki, Saito, Eriko, Saito, Takeshi, Mitsuanga, Tetsuya, Nakata, Mitsuyuki, Iwai, Jun, Yoshida, Hideo
Format Journal Article
LanguageEnglish
Published Italy MDPI AG 01.01.2013
PAGEPress Publications
PAGEPress Publications, Pavia, Italy
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Summary:The aim of this paper is to investigate the clinical courses of patients with biliary atresia (BA) during neonatal period. We examined 19 patients with BA, who underwent blood tests including direct bilirubin (D-Bil) within 20 days of age, in 3 tertiary hospitals in Japan. The first blood sample was collected at 8.4±6.5 days of age. The acholic stool was observed within 2 weeks of age in 16 cases (84.2%). Decrease of T-Bil was observed in all the subjects, with a range of reduction of 6.5±3.3 mg/dL, from 10.4±7.5 to 29.8±9.1 days of age. Decrease of D-Bil was also observed in 17 out of 19 cases (89%), with a range of reduction of 1.1±1.0 mg/dL, from 15.5±8.0 to 24.9±9.6 days of age. A significant decrease of D-Bil was observed in 2 cases of biliary atresia splenic malformation syndrome. We therefore conclude that clinicians treating icteric infants should not exclude a diagnosis of BA even if the level of D-Bil has a declining tendency.
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Conflict of interests: the authors declare no potential conflict of interests.
Contributions: KT performed the statistical analysis and wrote the manuscript; YH and ES collected data; TS, TM, MN and JI provided medical care including surgical procedure; and HY designed the study and reviewed the manuscript. All the authors have read and approved the final manuscript.
ISSN:2036-7503
2036-749X
2036-7503
DOI:10.4081/pr.2013.e17