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

Author:

Collins Lauren F12ORCID,Corbin-Johnson Della2,Asrat Meron2,Morton Zoey P1,Dance Kaylin1,Condra Alton2,Jenkins Kimberly2,Todd-Turner Marie2,Sumitani Jeri2,Smith Bradley L2,Armstrong Wendy S12,Colasanti Jonathan A123

Affiliation:

1. Department of Medicine, Divison of Infectious Diseases, Emory University School of Medicine , Atlanta , Georgia , USA

2. Grady Healthcare System, Infectious Diseases Program , Atlanta , Georgia , USA

3. Hubert Department of Global Health, Emory University Rollins School of Public Health , Atlanta, Georgia , USA

Abstract

Abstract 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.

Funder

Center for AIDS Research, Emory University

National Center for Advancing Translational Sciences

National Institutes of Health

Georgia CTSA

Program for Retaining, Supporting, and EleVating Early-career Researchers at Emory

Emory School of Medicine

Doris Duke Charitable Foundation

National Institute of Mental Health

NIH

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Oncology

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