AI Article Synopsis

  • A study investigated the effectiveness and durability of dual antiretroviral therapy (DAT) in HIV patients in real clinical settings, comparing it to traditional triple-drug regimens.
  • Of the 51 patients followed for 48 weeks, 83.8% of those with low viral load and 50% with higher viral load achieved virological suppression, with 76.5% maintaining treatment for an average of about 40 weeks.
  • Results showed better adherence and a higher cost for DAT compared to previous regimens, suggesting DAT could be a viable option for patients not responding to triple therapies.

Article Abstract

Background And Objectives: While randomised controlled trials in HIV-infected patients have shown that certain dual antiretroviral therapy (DAT) regimens are non-inferior in terms of efficacy compared with classical triple-drug regimens, few real clinical experiences have been described. The aim of the study was to investigate, in real clinical practice, DAT effectiveness, durability, and risk factors for treatment discontinuation.

Methods: This was a prospective cohort study that included HIV-infected patients treated with DAT (2015-2020). DAT was considered effective when patients achieved or maintained virological suppression and was assessed at 24 and 48 weeks. DAT durability was evaluated using the Kaplan-Meier method. Adherence and treatment cost were compared with patients' previous antiretroviral regimens.

Results: 51 patients were included, 27.5% with HIV-1 RNA ≥50 copies/mL at baseline, treated with a wide range of dual combinations. At 48 weeks follow-up, 83.8% and 50.0% of patients who started DAT with HIV-1 RNA <50 copies/mL and ≥50 copies/mL, respectively, were suppressed. 39 out of 51 patients (76.5%) maintained DAT for a mean treatment duration of 40.5±14.8 weeks. Full adherence was observed in 78.4% of patients compared with 70.2% in the previous regimen. Mean daily cost was €18.6±4.3 compared with €16.1±7.9 in the previous regimen (p=0.008).

Conclusion: DAT effectiveness and durability were higher in patients who were virologically suppressed at baseline. DAT is a possible alternative for virologically non-suppressed patients who cannot be treated with a triple-drug regimen.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10895179PMC
http://dx.doi.org/10.1136/ejhpharm-2022-003277DOI Listing

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