Antiretroviral pre‐exposure prophylaxis implementation in the United States: a work in progress
Pre-exposure prophylaxis
Underinsured
Emtricitabine
Best practice
DOI:
10.7448/ias.18.4.19980
Publication Date:
2015-07-20T09:32:43Z
AUTHORS (8)
ABSTRACT
After the initial approval of use tenofovir disoproxil fumarate-emtricitabine (TDF/FTC) by US Food and Drug Administration in 2012 for anti-HIV pre-exposure prophylaxis (PrEP), uptake was initially limited, but more recent community surveys expert opinion suggest wider acceptance some key populations.Demonstration projects are underway to determine best practices United States identify at-risk individuals primary care sexually transmitted disease clinics who could benefit from PrEP. Studies PrEP combination with behavioural interventions being evaluated. evaluate HIV-uninfected women HIV-discordant couples interested safe conception also getting underway. The optimal deployment as part a comprehensive national HIV/AIDS strategy has been limited lack knowledge among people medical providers indicating that they do not feel sufficiently knowledgeable comfortable prescribing how assist busy clinicians which their patients Although most federal health insurance programmes will cover costs associated PrEP, underinsured states have enacted reform face additional challenges paying medication appropriate clinical monitoring.PrEP implementation is work progress, increasing awareness populations.
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