scholarly journals Changes Over Time in Risk of Initial Virological Failure of Combination Antiretroviral Therapy

2006 ◽  
Vol 166 (5) ◽  
pp. 521 ◽  
Author(s):  
Fiona C. Lampe ◽  
Jose M. Gatell ◽  
Schlomo Staszewski ◽  
Margaret A. Johnson ◽  
Christian Pradier ◽  
...  
AIDS ◽  
2008 ◽  
Vol 22 (1) ◽  
pp. 75-82 ◽  
Author(s):  
Edward M Gardner ◽  
Shweta Sharma ◽  
Grace Peng ◽  
Katherine Huppler Hullsiek ◽  
William J Burman ◽  
...  

Author(s):  
Saira Ajmal ◽  
Zelalem Temesgen

The primary goal of therapy is to prevent HIV-associated morbidity and mortality. In addition to the dramatic decline in HIV-related illness and death that has been observed as a result of the introduction and expansion of combination antiretroviral therapy, evidence is emerging that uncontrolled HIV replication also has a deleterious impact on conditions that are not conventionally associated with immune deficiency. These conditions include cardiovascular disease, kidney disease, liver disease, neurologic complications, and malignancy. Studies have found an independent association between cumulative exposure to replicating virus over time and mortality. Emerging data also increasingly support the earlier use of ART.


2016 ◽  
Vol 3 (2) ◽  
Author(s):  
Gisela Leierer ◽  
Katharina Grabmeier-Pfistershammer ◽  
Andrea Steuer ◽  
Mario Sarcletti ◽  
Maria Geit ◽  
...  

Abstract Background.  Viral loads (VLs) detectable at low levels are not uncommon in patients on combination antiretroviral therapy (cART). We investigated whether a single quantifiable VL predicted virological failure (VF). Methods.  We analyzed patients receiving standard regimens with at least 1 VL measurement below the limit of quantification (BLQ) in their treatment history. The first VL measurement after 6 months of unmodified cART served as baseline VL for the subsequent analyses of the time to reach single VL levels of ≥200, ≥400, and ≥1000 copies/mL. Roche TaqMan 2.0 was used to quantify human immunodeficiency virus-1 ribonucleic acid. Factors associated with VF were determined by Cox proportional hazards models. Results.  Of 1614 patients included in the study, 68, 44, and 34 experienced VF ≥200, ≥400, and ≥1000 copies/mL, respectively. In multivariable analyses, compared with patients who were BLQ, a detectable VL ≤ 50 and VL 51–199 copies/mL predicted VF ≥ 200 copies/mL (hazards ratio [HR] = 2.19, 95% confidence interval [CI] = 1.06–4.55 and HR = 4.21, 95% CI = 2.15–8.22, respectively). In those with VL 51–199 copies/mL, a trend for an increased risk of VF ≥400 and VF ≥1000 copies/mL could be found (HR = 2.13, 95% CI = 0.84–5.39 and HR = 2.52, 95% CI = 0.96–6.60, respectively). Conclusions.  These findings support closer monitoring and adherence counseling for patients with a single measurement of quantifiable VL <200 copies/mL.


2011 ◽  
Vol 16 (5) ◽  
pp. 781-785 ◽  
Author(s):  
Zoe V Fox ◽  
◽  
Alessandro Cozzi-Lepri ◽  
Antonella D’Arminio Monforte ◽  
Anders Karlsson ◽  
...  

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