Muscarinic receptor antagonists for overactive bladder treatment: does one fit all?

Curr Opin Urol. 2009 Jan;19(1):13-9. doi: 10.1097/MOU.0b013e32831a6ff3.

Abstract

Purpose of review: To review evidence and regulatory dosing recommendations for muscarinic receptor antagonists used in the treatment of overactive bladder symptom complex (darifenacin, fesoterodine, oxybutynin, propiverine, solifenacin, tolterodine, trospium) in special patient populations.

Recent findings: Growing evidence demonstrates effects of renal impairment, hepatic impairment, genetics and/or comedications on the pharmacokinetics of muscarinic antagonists. They may cause greater exposure in the respective population, which may translate into greater risks for side effects. These possible risks lead to drug-specific regulatory dosing recommendations or even contraindications in certain patient populations.

Summary: Physicians should be aware of pharmacokinetic alterations in special patient populations and possible associated risks. The evidence-based choice of a muscarinic antagonist in such patients should be guided by its specific pharmacokinetic profile.

Publication types

  • Review

MeSH terms

  • Contraindications
  • Cytochrome P-450 CYP2D6 / metabolism
  • Cytochrome P-450 CYP3A / metabolism
  • Dose-Response Relationship, Drug
  • Humans
  • Kidney / physiopathology
  • Liver / physiopathology
  • Muscarinic Antagonists / pharmacokinetics
  • Muscarinic Antagonists / therapeutic use*
  • Urinary Bladder, Overactive / drug therapy*
  • Urinary Bladder, Overactive / physiopathology

Substances

  • Muscarinic Antagonists
  • Cytochrome P-450 CYP2D6
  • Cytochrome P-450 CYP3A
  • CYP3A4 protein, human