Impact of the Data Collection on Adverse Events of Anti-HIV Drugs cohort study on abacavir prescription among treatment-naive, HIV-infected patients in Canada

J Int Assoc Provid AIDS Care. 2014 Mar-Apr;13(2):153-9. doi: 10.1177/2325957413495565. Epub 2013 Jul 25.

Abstract

Objective: To evaluate the trends in abacavir (ABC) prescription among antiretroviral (ARV) medication-naive individuals following the presentation of the Data Collection on Adverse Events of Anti-HIV Drugs (DAD) cohort study.

Methods: We conducted a retrospective cohort study of ARV medication-naive individuals in the Canadian Observational Cohort (CANOC).

Results: Between January 1, 2000, and February 28, 2010, a total of 7280 ARV medication-naive patients were included in CANOC. We observed a significant change in the proportion of new ABC prescriptions immediately following the release of DAD (-11%; 95% confidence interval [CI]: -20% to -2.4%) and in the months following the presentation of these data (-0.66% per month; 95% CI: -1.2% to -0.073%). A post-DAD presentation decrease in the odds of being prescribed ABC versus tenofovir (TDF) was observed (adjusted odds ratio, 0.72 per year, 95% CI: 0.54-0.97).

Conclusions: Presentation of the DAD was associated with a significant decrease in ABC use among ARV medication-naive, HIV-positive patients initiating therapy.

Keywords: HIV; abacavir; drug utilization; pharmacoepidemiology.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Anti-HIV Agents / therapeutic use*
  • Canada
  • Cohort Studies
  • Dideoxynucleosides / therapeutic use*
  • Female
  • HIV Infections / drug therapy*
  • Humans
  • Information Dissemination
  • Male
  • Middle Aged
  • Myocardial Infarction / epidemiology
  • Practice Patterns, Physicians' / trends*
  • Retrospective Studies
  • Risk Factors

Substances

  • Anti-HIV Agents
  • Dideoxynucleosides
  • abacavir