Japanese Biliary Atresia Registry, 1989 to 1994

Mohamed Ibrahim, Takeshi Miyano, Ryoji Ohi, Morihiro Saeki, Kazuo Shiraki, Koichi Tanaka, Takamichi Kamiyama, Masaki Nio

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42 Citations (Scopus)

Abstract

The Japanese Biliary Atresia Society founded in 1980 for the aim of investigations of all aspects of biliary atresia (BA), started a nationwide registry of BA patients in 1989. A total of 626 cases were registered from 1989 to 1994. The male to female ratio was 0.58. Corrective surgery was performed in 603 patients. Regarding the type of obstruction, 63 cases were Type I, atresia of the common bile duct, 9 were Type II, atresia of the hepatic ducts, and 543 were Type III, atresia of the porta hepatis. As initial corrective procedures, original Roux-en Y, Suruga II and Roux-en Y with intestinal valve were mainly employed. Jaundice cleared in 346 patients (57%) and decreased in 131, while it persisted in 120. The 5-year-follow-up showed that 34 patients, 49% of the patients who were followed up, were alive without jaundice, while 28 (41%) are dead. Thirty five, 33% of the patients who were entered to the Registry, were lost to follow-up.

Original languageEnglish
Pages (from-to)85-95
Number of pages11
JournalTohoku Journal of Experimental Medicine
Volume181
Issue number1
DOIs
Publication statusPublished - 1997 Jan
Externally publishedYes

Keywords

  • Biliary atresia
  • Japan
  • Registry

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)

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