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Published byNathan Turner Modified over 6 years ago
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Updated DHHS Adult and Adolescent HIV Treatment Guidelines: Conversation with Dr. Paul Sax
Presentation prepared by: Paul Sax, MD and Brian Wood, MD
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What were the main reasons behind moving tenofovir-emtricitabine-efavirenz (Atripla) from the list of “Recommended” first-line ART options to the list of “Alternative” options?
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Are you still prescribing tenofovir-emtricitabine-efavirenz (Atripla)?
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What is your threshold to offer a change off tenofovir-emtricitabine-efavirenz (Atripla) for a patient who may be experiencing side effects?
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What about the recommendation to avoid efavirenz in a woman of childbearing potential?
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What were the main reasons behind moving the regimen of tenofovir-emtricitabine (Truvada) plus boosted atazanavir (Reyataz with Norvir) from the list of “Recommended” first-line ART options to the list of “Alternative” options?
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What would if a patient is tolerating boosted atazanavir?
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Has it been your experience that atazanavir-induced kidney stones can occur after significant time has passed since atazanavir initiation?
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What are the benefits of boosted atazanavir?
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How do you decide between the 5 different options on the current list of “Recommended” initial ART regimens? And why not give everyone dolutegravir?
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If once-daily dosing of raltegravir were available, would the higher barrier to resistance of dolutegravir still make it more advantageous?
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What do you think of the two NRTI-sparing regimens that are now listed in the guidelines and what do you do if you have a patient who cannot received tenofovir or abacavir?
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Can you comment on potential benefits of tenofovir alafenamide (TAF)?
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Can you give more detail as to your thoughts on the issue of potential cardiovascular risk with abacavir?
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What is your strategy if you have a patient with persistent low-level viremia?
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How much does cost enter into consideration when choosing an initial ART regimen?
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