Literature DB >> 9820880

Effect of hepatic insufficiency on pharmacokinetics and drug dosing.

R K Verbeeck1, Y Horsmans.   

Abstract

The liver plays a central role in the pharmacokinetics of many drugs. Liver dysfunction may not only reduce the plasma clearance of a number of drugs eliminated by biotransformation and/or biliary excretion, but it can also affect plasma protein binding which in turn could influence the processes of distribution and elimination. In addition, reduced liver blood flow in patients with chronic liver disease will decrease the systemic clearance of flow limited (high extraction) drugs and portal-systemic shunting may substantially reduce their presystemic elimination (first-pass effect) following oral administration. When selecting a drug and its dosage regimen for a patient with liver disease additional considerations such as altered pharmacodynamics and impaired renal excretion (hepatorenal syndrome) of drugs and metabolites should also be taken into account. Consequently, dosage reduction is necessary for many drugs administered to patients with chronic liver disease such as liver cirrhosis.

Entities:  

Mesh:

Year:  1998        PMID: 9820880     DOI: 10.1023/a:1008656930082

Source DB:  PubMed          Journal:  Pharm World Sci        ISSN: 0928-1231


  95 in total

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Journal:  Clin Pharmacol Ther       Date:  1986-08       Impact factor: 6.875

2.  Unpredictability of clinical evaluation of renal function in cirrhosis. Prospective study.

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Journal:  Am J Med       Date:  1987-05       Impact factor: 4.965

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Journal:  Br Med J       Date:  1978-10-14

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Authors:  D G Shand; D M Kornhauser; G R Wilkinson
Journal:  J Pharmacol Exp Ther       Date:  1975-12       Impact factor: 4.030

5.  Caffeine: a model compound for measuring liver function.

Authors:  E Renner; H Wietholtz; P Huguenin; M J Arnaud; R Preisig
Journal:  Hepatology       Date:  1984 Jan-Feb       Impact factor: 17.425

6.  Pharmacokinetics, bioavailability and ECG response of verapamil in patients with liver cirrhosis.

Authors:  A Somogyi; M Albrecht; G Kliems; K Schäfer; M Eichelbaum
Journal:  Br J Clin Pharmacol       Date:  1981-07       Impact factor: 4.335

7.  Assessment of hepatic blood flow in healthy subjects by continuous infusion of indocyanine green.

Authors:  P A Soons; A De Boer; A F Cohen; D D Breimer
Journal:  Br J Clin Pharmacol       Date:  1991-12       Impact factor: 4.335

8.  Dose and serum concentration relationships in cimetidine-associated mental confusion.

Authors:  B J Kimelblatt; F B Cerra; G Calleri; M J Berg; M A McMillen; J J Schentag
Journal:  Gastroenterology       Date:  1980-04       Impact factor: 22.682

9.  Pharmacokinetics of furosemide in patients with hepatic cirrhosis.

Authors:  G González; A Arancibia; M I Rivas; P Caro; C Antezana
Journal:  Eur J Clin Pharmacol       Date:  1982       Impact factor: 2.953

10.  Age, disease, and cimetidine disposition in healthy subjects and chronically ill patients.

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Journal:  Clin Pharmacol Ther       Date:  1981-06       Impact factor: 6.875

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4.  Pharmacokinetics of telbivudine in subjects with various degrees of hepatic impairment.

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Authors:  Matthew E Levison; Julie H Levison
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8.  No influence of mild-to-moderate hepatic impairment on the pharmacokinetics and pharmacodynamics of ximelagatran, an oral direct thrombin inhibitor.

Authors:  Karin Wåhlander; Maria Eriksson-Lepkowska; Lars Frison; Gunnar Fager; Ulf G Eriksson
Journal:  Clin Pharmacokinet       Date:  2003       Impact factor: 6.447

Review 9.  Pharmacokinetic changes of psychotropic drugs in patients with liver disease: implications for dose adaptation.

Authors:  Chantal Schlatter; Sabin S Egger; Lydia Tchambaz; Stephan Krähenbühl
Journal:  Drug Saf       Date:  2009       Impact factor: 5.606

Review 10.  Antiarrhythmics: elimination and dosage considerations in hepatic impairment.

Authors:  Ulrich Klotz
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