deoxycholic-acid has been researched along with Biliary-Atresia* in 4 studies
4 other study(ies) available for deoxycholic-acid and Biliary-Atresia
Article | Year |
---|---|
Biliary atresia--bile acids and prostaglandin E2 in cell cultures of bile duct epithelia.
In a cell culture model of bile duct epithelial cells, the effect of prostaglandin E2, lithocholic acid and deoxycholic acid was studied. Bile acids and prostaglandin are administered postoperatively in biliary atresia empirically as choleretics. Prostaglandin E2 and the bile acids all had inhibitory effects on bile duct epithelial cells in culture. There is no clinical study proving the efficacy of either bile acids or prostaglandin E2 in biliary atresia. The negative results with these substances in cell cultures warrants reserve in their routine clinical use in biliary atresia. Topics: Adult; Animals; Bile Ducts; Biliary Atresia; Cell Division; Cells, Cultured; Deoxycholic Acid; Dinoprostone; Epithelium; Growth Inhibitors; Humans; Lithocholic Acid; Postoperative Care | 1993 |
Ursodeoxycholic acid therapy in the treatment of biliary atresia.
The prognosis of operated biliary atresia in the cases with bile excretion chiefly depends upon the prevention of ascending cholangitis. An antibiotic is therefore intravenously administered during the early postoperative phase, but cannot be used over a long period. In the cases showing satisfactory bile excretion after operation, ascending cholangitis is rare because of rapid disappearance of jaundice. Regarding this, the authors prescribed ursodeoxycholic acid (UDCA) at 10-15 mg/kg/day to 6 infants with biliary atresia for several weeks after operation, and then determined the effects of UDCA in improving jaundice and bile excretion. As a result, serum bilirubin and serum total bile acid (STBA) levels were decreased in 4 of the 6 infants. In the remaining 2 infants, their STBA levels showed no decrease, but were rather increased; these infants subsequently died of hepatic failure. These results suggested that UDCA is useful in the treatment of cholestasis associated with biliary atresia in the cases attaining postoperative bile excretion. It was also suggested that the treatment with UDCA should be stopped when the STBA levels increased after the beginning of the treatment. Therefore, it was thought that STBA levels measured during UDCA therapy could serve as a good indicator of the choleretic effect of UDCA. Topics: Aging; Alanine Transaminase; Aspartate Aminotransferases; Biliary Atresia; Bilirubin; Birth Weight; Deoxycholic Acid; Female; Gestational Age; Humans; Infant; Infant, Newborn; Male; Ursodeoxycholic Acid | 1989 |
Ursodeoxycholic acid in biliary atresia.
Topics: Bile Acids and Salts; Biliary Atresia; Deoxycholic Acid; Humans; Infant; Infant, Newborn; Postoperative Period; Ursodeoxycholic Acid | 1988 |
Treatment with ursodeoxycholic acid renders children with biliary atresia suitable for liver transplantation.
Topics: Biliary Atresia; Deoxycholic Acid; Humans; Infant; Liver Transplantation; Ursodeoxycholic Acid | 1987 |