Raltegravir central nervous system tolerability in clinical practice: results from a multicenter observational study

AIDS. 2012 Nov 28;26(18):2412-5. doi: 10.1097/QAD.0b013e32835aa141.

Abstract

Central nervous system (CNS) symptoms have been reported in clinical trials and case reports in patients receiving raltegravir. We investigated CNS symptoms in 453 HIV-infected patients. Of these 47 (10.4%) developed at least one drug-related CNS symptom. Predictors of CNS symptoms were concomitant therapy with tenofovir or with proton pump inhibitors that can increase raltegravir concentration. Thus, our data suggest a possible correlation between high raltegravir plasma concentrations and CNS symptoms, and therefore their monitoring in clinical practice.

Publication types

  • Multicenter Study

MeSH terms

  • Adenine / adverse effects
  • Adenine / analogs & derivatives
  • Adenine / blood
  • Anti-HIV Agents / administration & dosage
  • Anti-HIV Agents / adverse effects*
  • Anti-HIV Agents / blood*
  • Central Nervous System / drug effects*
  • Central Nervous System / physiopathology
  • Drug Administration Schedule
  • Drug Interactions
  • Female
  • HIV Infections / blood
  • HIV Infections / drug therapy*
  • HIV Infections / physiopathology
  • Humans
  • Male
  • Organophosphonates / adverse effects
  • Organophosphonates / blood
  • Pyrrolidinones / administration & dosage
  • Pyrrolidinones / adverse effects*
  • Pyrrolidinones / blood*
  • Raltegravir Potassium
  • Tenofovir
  • Treatment Outcome
  • Viral Load

Substances

  • Anti-HIV Agents
  • Organophosphonates
  • Pyrrolidinones
  • Raltegravir Potassium
  • Tenofovir
  • Adenine