Antipyrine clearance per unit volume liver: an assessment of hepatic function in chronic liver disease
- PMID: 488757
- PMCID: PMC1412524
- DOI: 10.1136/gut.20.7.596
Antipyrine clearance per unit volume liver: an assessment of hepatic function in chronic liver disease
Abstract
Liver size has been estimated clinically and by a non-invasive ultrasound technique in 16 normal subjects, 16 patients with cirrhosis, 10 patients with chronic biliary obstruction, and three patients with primary hepatoma. Antipyrine disposition was also measured in each subject. Hepatomegaly was not clinically detectable until there was approximately a 20% increase in liver size. Additional increases in size correlated significantly with clinical estimates of hepatomegaly. Antipyrine clearance had a three-fold range in normal subjects. Its mean value was significantly reduced in each subgroup of patients with liver disease. However, 48% of patients with liver disease had values within the normal range. In normal subjects there was a significant correlation between antipyrine clearance and liver volume. Thus, intersubject variation in clearance normalised for liver volume was less than clearance alone. Antipyrine clearance normalised for liver volume in patients with liver disease was significantly lower than in normal subjects and there was no overlap with normal subjects. In conclusion, assessment of drug metabolising efficiency per unit volume of liver increased the discrimination in differentiating subjects with normal from abnormal livers.
Similar articles
-
Saliva and plasma clearance of antipyrine as reflectors of liver function.Eur J Drug Metab Pharmacokinet. 1981;6(4):261-4. doi: 10.1007/BF03189523. Eur J Drug Metab Pharmacokinet. 1981. PMID: 7333326
-
The relationship between liver volume, antipyrine clearance and indocyanine green clearance before and after phenobarbitone administration in man.Br J Clin Pharmacol. 1976 Oct;3(5):907-13. doi: 10.1111/j.1365-2125.1976.tb00646.x. Br J Clin Pharmacol. 1976. PMID: 973986 Free PMC article.
-
Fractional clearance of bromosulfonephthalein and metabolic clearance of antipyrine. Correlative study in liver diseases.Ann Gastroenterol Hepatol (Paris). 1984 Jan-Feb;20(1):1-6. Ann Gastroenterol Hepatol (Paris). 1984. PMID: 6529154 English, French.
-
Quantifying hepatic function in the presence of liver disease with phenazone (antipyrine) and its metabolites.Clin Pharmacokinet. 1991 Jan;20(1):50-65. doi: 10.2165/00003088-199120010-00004. Clin Pharmacokinet. 1991. PMID: 2029802 Review.
-
Noninvasive assessment in vivo of hepatic drug metabolism in health and disease.Ann N Y Acad Sci. 1984;428:293-307. doi: 10.1111/j.1749-6632.1984.tb12305.x. Ann N Y Acad Sci. 1984. PMID: 6378027 Review.
Cited by
-
Assessment of oxidative metabolism in adults with hepatocellular carcinoma in the Sudan.Gut. 1986 Apr;27(4):382-5. doi: 10.1136/gut.27.4.382. Gut. 1986. PMID: 3007307 Free PMC article.
-
Hepatic drug metabolism and aging.Clin Pharmacokinet. 1990 Nov;19(5):359-89. doi: 10.2165/00003088-199019050-00002. Clin Pharmacokinet. 1990. PMID: 2268986 Review.
-
Disposition of antipyrine in patients with extensive metastatic liver disease.Eur J Clin Pharmacol. 1992;42(5):465-9. doi: 10.1007/BF00314851. Eur J Clin Pharmacol. 1992. PMID: 1606991
-
Clinical pharmacokinetic and pharmacodynamic considerations in patients with liver disease. An update.Clin Pharmacokinet. 1995 Nov;29(5):370-91. doi: 10.2165/00003088-199529050-00005. Clin Pharmacokinet. 1995. PMID: 8582120 Review.
-
Cytochrome P450 mediated-drug metabolism is reduced in children with sepsis-induced multiple organ failure.Intensive Care Med. 2003 Jun;29(6):980-984. doi: 10.1007/s00134-003-1758-3. Epub 2003 Apr 16. Intensive Care Med. 2003. PMID: 12698250
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources