Primary sclerosing cholangitis medical therapy: Difference between revisions
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{{Primary sclerosing cholangitis}} | {{Primary sclerosing cholangitis}}{{CMG}} | ||
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==Overview== | ==Overview== | ||
Standard treatment includes [[ursodiol]], a bile acid naturally produced by the liver, which has been shown to lower elevated liver enzyme numbers in people with PSC, but has not yet been proven effective at prolonging the life of the liver. Treatment also includes medication to relieve itching ([[antipruritic]]s) and bile acid sequesterants (cholestyramine), [[antibiotic]]s to treat infections, and [[vitamin]] supplements, as people with PSC are often deficient in [[vitamin A]], [[vitamin D]], and [[vitamin K]]. | |||
==References== | ==References== | ||
{{reflist|2}} | {{reflist|2}} | ||
Revision as of 22:13, 7 February 2012
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Primary sclerosing cholangitis Microchapters |
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Differentiating Primary sclerosing cholangitis from other Diseases |
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Diagnosis |
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Treatment |
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Case Studies |
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Primary sclerosing cholangitis medical therapy On the Web |
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American Roentgen Ray Society Images of Primary sclerosing cholangitis medical therapy |
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Directions to Hospitals Treating Primary sclerosing cholangitis |
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Risk calculators and risk factors for Primary sclerosing cholangitis medical therapy |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Standard treatment includes ursodiol, a bile acid naturally produced by the liver, which has been shown to lower elevated liver enzyme numbers in people with PSC, but has not yet been proven effective at prolonging the life of the liver. Treatment also includes medication to relieve itching (antipruritics) and bile acid sequesterants (cholestyramine), antibiotics to treat infections, and vitamin supplements, as people with PSC are often deficient in vitamin A, vitamin D, and vitamin K.