The median time to suppression was 4.55 months (IQR 2.99–7.89 months). In multivariate analyses, older age, male sex, treatment in Ontario rather than British Columbia, non-IDU history, and having an AIDS diagnosis at baseline predicted increased likelihood of suppression. Patients with low baseline viral load were more likely to have suppression [4–5 log10 copies/mL, hazard ratio (HR) 1.27, 95% confidence interval (CI) 1.18–1.38; <4 log10 copies/mL, HR 1.49, 95% CI 1.32–1.68] than patients with baseline viral load ≥5 log10 copies/mL; however, this effect ceased after 18 months of follow-up. Suppression was more likely with nonnucleoside reverse transcriptase inhibitors and ritonavir-boosted

HAART. Identification of patients at risk for diminished likelihood of virological suppression will allow focusing of efforts and selleck kinase inhibitor the utilization of resources to maximize the benefits of HAART. It is well documented that highly active antiretroviral therapy (HAART) decreases morbidity and mortality amongst HIV-positive individuals [1–4]. In particular, one of the primary goals of HAART is the obtainment and maintenance of complete HIV RNA suppression [5]. Failure to achieve and maintain suppression can result in the development of drug resistance and also increases the risk of both horizontal and vertical viral transmission [6–8]. When first initiating

antiretroviral therapy, the obtainment of viral load suppression is an important objective that is associated with a variety of socio-demographic and baseline clinical factors [9,10]. Additionally, choice of initial antiretroviral regimen plays selleckchem an important role in the time it takes to achieve a viral load that Sirolimus research buy is undetectable [11,12]. While the long-term clinical benefits of earlier suppression are unclear, achievement of suppression earlier reduces the length of time one

carries detectable virus and may allow more immediate CD4 T-cell reconstitution [13]. Identifying factors that predict time to virological suppression on modern HAART regimens is thus vital to optimizing therapeutic success. Moreover, identifying such factors will provide useful information to improve care and inform therapeutic treatment guidelines for socio-demographic or clinical risk groups across Canada. This study constitutes the first examination of such factors in the Canadian context with patients initiating modern HAART regimens (defined as first initiation after 2000 with a combination of at least three individual antiretroviral agents). Here we investigate the time to virological suppression and factors associated with suppression among a national cohort of individuals on HAART in Canada. The Canadian Observational Cohort (CANOC) Collaboration is a Canadian cohort study of HIV-positive patients with no prior antiretroviral experience initiating HAART on, or after, 1 January 2000.