Abstract

BackgroundKey populations (KP) are disproportionately infected with HIV and experience barriers to HIV care. KP include men who have sex with men (MSM), female sex workers (FSW), persons who inject drugs (PWID) and transgender people (TG). We implemented three different approaches to the delivery of community-based antiretroviral therapy for KP (KP-CBART) in Benue State Nigeria, including One Stop Shop clinics (OSS), community drop-in-centres (DIC), and outreach venues. OSS are community-based health facilities serving KP only. DIC are small facilities led by lay healthcare providers and supported by an outreach team. Outreach venues are places in the community served by the outreach team. We studied long-term attrition of KP and virological non-suppression.MethodThis is a retrospective cohort study of KP living with HIV (KPLHIV) starting ART between 2016 and 2019 in 3 0SS, 2 DIC and 8 outreach venues. Attrition included lost to follow-up (LTFU) and death. A viral load >1000 copies/mL showed viral non-suppression. Survival analysis was used to assess retention on ART. Cox regression and Firth logistic regression were used to assess risk factors for attrition and virological non-suppression respectively.ResultOf 3495 KPLHIV initiated on ART in KP-CBART, 51.8% (n = 1812) were enrolled in OSS, 28.1% (n = 982) in DIC, and 20.1% (n = 701) through outreach venues. The majority of participants were FSW—54.2% (n = 1896), while 29.8% (n = 1040), 15.8% (n = 551) and 0.2% (n = 8) were MSM, PWID, and TG respectively. The overall retention in the programme was 63.5%, 55.4%, 51.2%, and 46.7% at 1 year, 2 years, 3 years, and 4 years on ART. Of 1650 with attrition, 2.5% (n = 41) died and others were LTFU. Once adjusted for other factors (age, sex, place of residence, year of ART enrollment, WHO clinical stage, type of KP group, and KP-CBART approach), KP-CBART approach did not predict attrition. MSM were at a higher risk of attrition (vs FSW; adjusted hazard ratio (aHR) 1.27; 95%CI: 1.14–1.42). Of 3495 patients, 48.4% (n = 1691) had a viral load test. Of those, 97.8% (n = 1654) were virally suppressed.ConclusionAlthough long-term retention in care is low, the virological suppression was optimal for KP on ART and retained in community-based ART care. However, viral load testing coverage was sub-optimal. Future research should explore the perspectives of clients on reasons for LTFU and how to adapt approach to CBART to meet individual client needs.

Highlights

  • The World Health Organization (WHO) guidelines on HIV prevention, diagnosis, care, and treatment for key populations (KP) identified female sex workers (FSW), men who have sex with men (MSM), prisoners, persons who inject drugs (PWID), and transgender people (TG) as key populations, at substantial risk for becoming infected with HIV and potentially driving HIV transmission [1]

  • Long-term retention in care is low, the virological suppression was optimal for Key populations (KP) on antiretroviral treatment (ART) and retained in community-based ART care

  • We extracted data for 3495 KP living with HIV (KPLHIV) initiated on ART in the CBART programme between 2016 and 2019

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Summary

Introduction

The World Health Organization (WHO) guidelines on HIV prevention, diagnosis, care, and treatment for key populations (KP) identified female sex workers (FSW), men who have sex with men (MSM), prisoners, persons who inject drugs (PWID), and transgender people (TG) as key populations, at substantial risk for becoming infected with HIV and potentially driving HIV transmission [1]. The burden of HIV among KP is disproportionately high compared to that of the general population. Compared to the general population, The risk of HIV acquisition is 25, 35, 26 and 34 times times higher for MSM, PWID, FSW and TG respectively [2]. Despite the high HIV burden among KP in Nigeria, antiretroviral treatment (ART) coverage as of 2020 is still low among FSW (23.7%), PWID (23%), TG (19.5%), and MSM (26.3%) [6]. J Acquir Immune Defic Syndr. 2017 Jan; 74 Suppl 1(Suppl 1):S52–9. https://doi.org/10. 1097/QAI.0000000000001209 PMID: 27930612

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