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Relationship between Adherence Level, Type of the Antiretroviral Regimen, and Plasma HIV Type 1 RNA Viral Load: A Prospective Cohort Study
153
Citations
21
References
2008
Year
PharmacotherapyLogistic AnalysisProspective Cohort StudyContraceptionPreventive MedicineHiv/aids CounsellingViral PersistenceHuman RetrovirusClinical EpidemiologyClinical TrialsAntiretroviral-experienced PatientsDrug MonitoringPublic HealthPharmaceutical CareBoosted PiDrug InteractionsNeurovirologyMedicineChronic Viral InfectionHivEpidemiologyAids PathogenesisAdherence LevelTreatment And PreventionPatient SafetyAntiviral TherapyFailure RateRna Viral LoadPharmacoepidemiology
The relationship between adherence, antiretroviral regimen, and viral load (VL) suppression was assessed through a 1 year prospective follow-up study among 1142 HIV-infected patient. Patients on antiretroviral therapy who attended to the pharmacy during a 6-month period were considered eligible. Those included in the final analysis were patients who had been taking the same antiretroviral therapy for >6 months since their inclusion. The cohort included patients taking first line therapy (n = 243) and antiretroviral-experienced patients (n = 899). Naive patients who were included had to have reached undetectable VL at enrollment. Antiretroviral-experienced patients with detectable VL determinations in the previous 6 months were excluded. Adherence was measured by means of announced pill counts and dispensation pharmacy records. Of patients, 58% were taking NNRTI, 31.4% boosted PI, and 10.6% unboosted PI-based regimens. Overall, the relative risk of virologic failure was 9.0 (95% CI 4.0–20.1) in patients with adherence 80–89.9%, 45.6 (95% CI 19.9–104.5) with adherence 70–79.9%, and 77.3 (95% CI 34.2–174.9) with adherence <70%, compared with adherence of ≥90%. The risk of virologic failure in patients with adherence <90% taking unboosted PI was 2.5 times higher than the group taking boosted PI (95% CI 1.2–5.3). There were no statistical differences in patients taking boosted PI and those who were taking NNRTI. Less than 95% of adherence is associated with high virologic success. For patients taking NNRTI- or boosted PI-based regimens with adherence rates of 80%, the failure rate is <10%. These data do not affect the goal of achieving the highest level of adherence possible.
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