4.4 Article

Early Experience Implementing Long-Acting Injectable Cabotegravir/Rilpivirine for Human Immunodeficiency Virus-1 Treatment at a Ryan White-Funded Clinic in the US South

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OPEN FORUM INFECTIOUS DISEASES
卷 9, 期 9, 页码 -

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OXFORD UNIV PRESS INC
DOI: 10.1093/ofid/ofac455

关键词

cabotegravir; rilpivirine; health equity; implementation science; long-acting injectable antiretroviral therapy; people with HIV

资金

  1. Center for AIDS Research, Emory University [P30-AI-050409]
  2. National Center for Advancing Translational Sciences of the National Institutes of Health (NIH) through the Georgia CTSA (Georgia Clinical & Translational Science Alliance) [UL1TR002378, KL2-TL1TR002381]
  3. Program for Retaining, Supporting, and EleVating Early-career Researchers at Emory (PeRSEVERE) from Emory School of Medicine
  4. National Institute of Mental Health of the NIH [R01MH123396]

向作者/读者索取更多资源

Long-acting injectable antiretroviral therapy has the potential to improve medication adherence, reduce HIV stigma, and promote equity in care outcomes among people with HIV. However, implementing this treatment method in the US South faces challenges such as inadequate human resource capital, insurance coverage barriers, and patient ineligibility.
Long-acting injectable antiretroviral therapy may improve adherence, reduce stigma, and promote equity in care outcomes among people with HIV. Implementing a pilot program in the US South was challenged by substantial human resource capital, insurance coverage barriers, and patient ineligibility. Background Long-acting injectable (LAI) antiretroviral therapy (ART) has the potential to improve medication adherence, reduce human immunodeficiency virus (HIV) stigma, and promote equity in care outcomes among people with HIV (PWH). We describe our early experience implementing LAI-cabotegravir/rilpivirine (CAB/RPV) for maintenance HIV-1 treatment. Methods We launched a pilot LAI-ART program at a large Ryan White-funded clinic in the Southeast, which accept provider-initiated referrals from April 14, 2021 to December 1, 2021. Our interdisciplinary program team (Clinician-Pharmacy-Nursing) verified clinical eligibility and pursued medication access for eligible patients. We describe (1) demographic and clinical variables of PWH referred and enrolled and (2) early outcomes among those accessing LAI-CAB/RPV. Results Among 58 referrals, characteristics were median age 39 (Q1-Q3, 30.25-50) years, 74% male, and 81% Black, and payor source distribution was 26% Private, 21% Medicare, 19% Medicaid, and 34% AIDS Drugs Assistance Program. Forty-five patients (78%) met clinical eligibility for LAI-CAB/RPV; ineligibility concerns included evidence of confirmed or possible RPV resistance (n = 8), HIV nonsuppression (n = 3), possible RPV hypersensitivity (n = 1), and pregnancy (n = 1). Among 45 eligible PWH, 39 (87%) enrolled and 15 (38%) initiated LAI-CAB/RPV after a median of 47 (Q1-Q3, 31-95) days since enrollment. Conclusions Implementing LAI-ART at a Southern US Ryan White-funded clinic has been challenged by the following: substantial human resource capital to attain drug, administer injections, and support enrolled patients; delayed therapy initiation due to insurance denials; patient ineligibility primarily due to possible RPV resistance; and inability to provide drug regardless of payor source. These barriers may perpetuate disparities in ART access and outcomes among PWH and should be urgently addressed so that LAI-ART can be offered equitably.

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