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      Factors associated with the selection of initial antiretroviral therapy from 2009 to 2012

      research-article
      , MD 1 , , MS 2 , , PhD 3 , , MD, MSPH 4 , , MD 5 , , MD 6 , , MD 1 , , MD, MPH 5 , , PhD 7 , for the CFAR Network of Integrated Clinical Systems (CNICS)
      Journal of acquired immune deficiency syndromes (1999)

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          Abstract

          We examined factors associated with selection of initial antiretroviral regimen in the CNICS cohort. Patients initiating antiretroviral therapy (ART) between July 2009 and Dec 2012 were classified as receiving an NNRTI, boosted-PI, or raltegravir-based regimen. Among 873 patients initiating ART, 488 regimens contained an NNRTI, 319 a boosted-PI, and 66 raltegravir. Patients with depression and women were less likely to receive an NNRTI, while those with underlying cardiovascular disease, liver disease, and those co-infected with hepatitis C were more likely to receive raltegravir. Those with baseline viral load > 100,000 c/ml and those with substance use were more likely to receive a boosted PI. Thus, in the ‘real world’ ARV regimen choices appear to take into account adverse effects and patient baseline characteristics. Factors that impact initial regimen selection will likely become more heterogeneous over time as more choices for HIV therapy become available.

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          Author and article information

          Journal
          100892005
          21821
          J Acquir Immune Defic Syndr
          J. Acquir. Immune Defic. Syndr.
          Journal of acquired immune deficiency syndromes (1999)
          1525-4135
          1944-7884
          23 August 2016
          01 January 2017
          01 January 2018
          : 74
          : 1
          : 60-64
          Affiliations
          [1 ]Division of Infectious Diseases, University of Alabama at Birmingham, Birmingham, AL
          [2 ]Department of Biostatistics, University of Alabama at Birmingham, Birmingham, AL
          [3 ]Department of Epidemiology, University of North Carolina, Chapel Hill, NC
          [4 ]Owen Clinic, University of California, San Diego, San Diego, CA
          [5 ]Division of Allergy & Infectious Diseases, University of Washington, Seattle, WA
          [6 ]Fenway Health Clinic, Harvard Medical School, Boston, MA
          [7 ]Merck Sharp & Dohme Corp., Kenilworth, NJ USA at the time the study was conducted
          Article
          PMC5140679 PMC5140679 5140679 nihpa810278
          10.1097/QAI.0000000000001168
          5140679
          27552153
          5275539c-db9b-46a2-9d57-e45f43a9e153
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