Verbeeck R K, Horsmans Y
School of Pharmacy, Brussels, Belgium.
Pharm World Sci. 1998 Oct;20(5):183-92. doi: 10.1023/a:1008656930082.
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.
肝脏在许多药物的药代动力学中起着核心作用。肝功能不全不仅可能降低通过生物转化和/或胆汁排泄消除的多种药物的血浆清除率,还会影响血浆蛋白结合,进而可能影响分布和消除过程。此外,慢性肝病患者肝脏血流减少会降低血流限制性(高摄取)药物的全身清除率,口服给药后门体分流可能会大幅降低其首过消除(首过效应)。为肝病患者选择药物及其给药方案时,还应考虑其他因素,如药物和代谢物的药效学改变以及肾脏排泄受损(肝肾综合征)。因此,对于许多给慢性肝病(如肝硬化)患者使用的药物,有必要减少剂量。