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   <subfield code="a">Antiretroviral therapy initiation in an Australian cohort: implications for increased use of antiretroviral therapy</subfield>
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   <subfield code="c">[I. Stratov, S. Kent]</subfield>
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   <subfield code="a">Human immunodeficiency virus (HIV) management is entering a &quot;universal test and treat” phase, although the benefits from this approach in developed world scenarios are uncertain. We analyzed 79 combination anti-retroviral therapy (cART)-naïve HIV-positive individuals who were intensively prospectively followed from 2004 to 2013. We studied HIV-related illnesses, potential HIV transmissions, impact on sexual behavior, and factors impeding earlier cART initiation. Sixty-eight (86%) subjects commenced cART at a mean of 6.0years after diagnosis: 71% with a CD4 T-cell count &lt;350 cells/μl. A significant minority of subjects (29%) resisted initiation of cART despite physician recommendation for a mean of 18months. Only one HIV-related illness occurred in a patient who had not previously recorded a CD4 T-cell count &lt;500 cell/μl, totaling 195 person-years of observation. A 40% increase in sexually transmitted infections (STIs) occurred after commencing cART. We detected six HIV transmissions in our cohort, all of which were before initiating cART and 5 of them had a prior CD4 T-cell count &lt;500 cells/μl. Illnesses related to cART deferral were rare and most HIV transmissions we detected occurred in people with a prior CD4 T-cell count &lt;500 cells/μl. Our study raises concerns about increasing STI rates after cART initiation. Focusing resources on cART initiation among patients with CD4 T-cell counts &lt;500 cells/μl and enhancing safe sexual practices should remain a priority.</subfield>
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   <subfield code="D">I.</subfield>
   <subfield code="u">Department of Microbiology and Immunology, Peter Doherty Institute, 792 Elizabeth St., 3010, Parkville, VIC, Australia</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
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