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Rev. méd. Chile ; 119(2): 169-71, feb. 1991. tab
Article in Spanish | LILACS | ID: lil-98201

ABSTRACT

In an open, pilot study, the efficancy and safety of ursodeoxycholic acid (UDCA) in the treatment of intrahepatic cholestasis of pregnancy was investigated. four patients received 1 g/ñday of UDCA during 20 days and another 2 patients received identical periods of treatment separated by a 14-day interval free of drug. Pruritus and serum levels of toal bile salts and glutamic-pyruvic transaminase improved significantly during treatment with UDCA. Although pruritus and the laboratory alterations had a relapse in the second week after UDCA was discontinued, they improved again in the patients who received a second treatment with UDCA. No adverse reactions were detected in the mothers or in their babies. All neuborns are thriving normally, in a follow-up lasted 3 to 6 months after delivery. It is concluded that UDCA appears to be safe when administered in late pregnancy; its primising efficacy in the treatment of intrahepatic cholestasis of pregnancy should now be confirmed in controlled clinical trials


Subject(s)
Pregnancy , Humans , Female , Adult , Ursodeoxycholic Acid/therapeutic use , Cholestasis, Intrahepatic/drug therapy , Pregnancy Complications/drug therapy , Bile Acids and Salts/blood , Pilot Projects , Follow-Up Studies , Alanine Transaminase/blood , Ursodeoxycholic Acid/administration & dosage
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