QUANTIFYING HEPATIC-FUNCTION IN THE PRESENCE OF LIVER-DISEASE WITH PHENAZONE (ANTIPYRINE) AND ITS METABOLITES

被引:41
作者
STPETER, JV
AWNI, WM
机构
[1] HENNEPIN CTY MED CTR, DRUG EVALUAT UNIT, 701 PK AVE, MINNEAPOLIS, MN 55415 USA
[2] UNIV MINNESOTA, COLL PHARM, MINNEAPOLIS, MN 55455 USA
关键词
D O I
10.2165/00003088-199120010-00004
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The disposition of phenazone (antipyrine), a low extraction compound with low protein binding, is known to be altered in the presence of various types of hepatic dysfunction. As such, its pharmacokinetics may be useful in the objective characterisation of altered liver function. Understanding the known effects of various liver disease states upon the disposition of this probe may provide insight into future applications. This article provides a review of background information about normal plasma phenazone pharmacokinetics, urinary metabolite disposition and tabulations of reported total body clearances of the drug in the presence of cirrhosis, fatty liver, hepatitis and cholestasis in humans. An estimate is made of the sensitivity and specificity of phenazone testing for the verification of the presence of cirrhosis based on this compiled literatue.
引用
收藏
页码:50 / 65
页数:16
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