Nifedipine gastrointestinal therapeutic system (GITS) as an alternative to slow-release for tocolysis--tolerance and pharmacokinetic profile

Eur J Obstet Gynecol Reprod Biol. 2008 Sep;140(1):27-32. doi: 10.1016/j.ejogrb.2008.02.003. Epub 2008 Apr 3.

Abstract

Objective: To determine nifedipine plasma concentrations after a loading dose of nifedipine 10mg capsules, 40 mg over 1h followed by slow-release tablets (60 mg/d) versus gastrointestinal therapeutic system (GITS) tablets (90 mg/d) for tocolysis.

Study design: Prospective study in 14 pregnant women treated for threatened preterm labor.

Results: Following capsule administration there was a rapid rise in plasma concentration of drug achieving a peak of 97.5 microg/l (median) at 1h, then declined to 59.5 microg/l (median) at 5h. The concentration measured at 7200 min (120 h) was non-significantly higher in the slow-release group (median 25.5, range 6.9-67.2 microg/l) than in the GITS group (median 14.6, range 6.0-20.0 microg/l). Area under the curve (AUC) increased with the applied dose in both groups in a linear regression. Headache was more frequent in the slow-release group than in the GITS group (P=0.001).

Conclusions: GITS tablets 90 mg/d are an alternative dosage regimen to previous used slow-release tablets 60 mg/d for tocolysis with similar pharmacokinetic profile and a good tolerance. However, tocolysis with GITS tablets is simpler than that with slow-release tablets and may be associated with a higher compliance. GITS tablets are therefore also qualified for home monitoring.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Administration, Oral
  • Adult
  • Delayed-Action Preparations / pharmacokinetics
  • Female
  • Humans
  • Nifedipine / administration & dosage
  • Nifedipine / pharmacokinetics*
  • Obstetric Labor, Premature / drug therapy*
  • Pregnancy
  • Tocolytic Agents / administration & dosage
  • Tocolytic Agents / pharmacokinetics*

Substances

  • Delayed-Action Preparations
  • Tocolytic Agents
  • Nifedipine