HIV pre-exposure prophylaxis and early antiretroviral treatment among female sex workers in South Africa: Results from a prospective observational demonstration project
- PMID: 29161256
- PMCID: PMC5697804
- DOI: 10.1371/journal.pmed.1002444
HIV pre-exposure prophylaxis and early antiretroviral treatment among female sex workers in South Africa: Results from a prospective observational demonstration project
Abstract
Background: Operational research is required to design delivery of pre-exposure prophylaxis (PrEP) and early antiretroviral treatment (ART). This paper presents the primary analysis of programmatic data, as well as demographic, behavioural, and clinical data, from the TAPS Demonstration Project, which offered both interventions to female sex workers (FSWs) at 2 urban clinic sites in South Africa.
Methods and findings: The TAPS study was conducted between 30 March 2015 and 30 June 2017, with the enrolment period ending on 31 July 2016. TAPS was a prospective observational cohort study with 2 groups receiving interventions delivered in existing service settings: (1) PrEP as part of combination prevention for HIV-negative FSWs and (2) early ART for HIV-positive FSWs. The main outcome was programme retention at 12 months of follow-up. Of the 947 FSWs initially seen in clinic, 692 were HIV tested. HIV prevalence was 49%. Among those returning to clinic after HIV testing and clinical screening, 93% of the women who were HIV-negative were confirmed as clinically eligible for PrEP (n = 224/241), and 41% (n = 110/270) of the women who were HIV-positive had CD4 counts within National Department of Health ART initiation guidelines at assessment. Of the remaining women who were HIV-positive, 93% were eligible for early ART (n = 148/160). From those eligible, 98% (n = 219/224) and 94% (n = 139/148) took up PrEP and early ART, respectively. At baseline, a substantial fraction of women had a steady partner, worked in brothels, and were born in Zimbabwe. Of those enrolled, 22% on PrEP (n = 49/219) and 60% on early ART (n = 83/139) were seen at 12 months; we observed high rates of loss to follow-up: 71% (n = 156/219) and 30% (n = 42/139) in the PrEP and early ART groups, respectively. Little change over time was reported in consistent condom use or the number of sexual partners in the last 7 days, with high levels of consistent condom use with clients and low use with steady partners in both study groups. There were no seroconversions on PrEP and 7 virological failures on early ART among women remaining in the study. Reported adherence to PrEP varied over time between 70% and 85%, whereas over 90% of participants reported taking pills daily while on early ART. Data on provider-side costs were also collected and analysed. The total cost of service delivery was approximately US$126 for PrEP and US$406 for early ART per person-year. The main limitations of this study include the lack of a control group, which was not included due to ethical considerations; clinical study requirements imposed when PrEP was not approved through the regulatory system, which could have affected uptake; and the timing of the implementation of a national sex worker HIV programme, which could have also affected uptake and retention.
Conclusions: PrEP and early ART services can be implemented within FSW routine services in high prevalence, urban settings. We observed good uptake for both PrEP and early ART; however, retention rates for PrEP were low. Retention rates for early ART were similar to retention rates for the current standard of care. While the cost of the interventions was higher than previously published, there is potential for cost reduction at scale. The TAPS Demonstration Project results provided the basis for the first government PrEP and early ART guidelines and the rollout of the national sex worker HIV programme in South Africa.
Conflict of interest statement
Drug supply for Truvada was donated by Gilead, and Atroiza was donated for HIV treatment by Mylan. In addition to the drug donation associated with this study, WDFV leads a (non-PrEP) study that receives drug donations from Gilead Sciences and ViiV Healthcare, and has received honoraria for participation on PrEP advisory boards and given talks sponsored by Gilead. In addition, he has received honoraria for giving talks and participated in advisory boards for multiple antiretroviral manufacturers, including ViiV, Aspen, Mylan, Abbot, Merk, Adcock-Ingram, all for <$1000, over the last 5 years. Finally, he heads or participates in multiple grants addressing access to PrEP and ART, including from PEPFAR, UNITAID. AIDS Fonds and the Bill and Melinda Gates Foundation. He participates on multiple local and international PrEP and ART treatment guideline committees. Over the last five years, MM has received speaker fees and honoraria from Gilead Sciences, AbbVie, Cipla, Mylan and Janssen, and received conference sponsorship from BD, Gilead, Merck, Cipla and Mylan. In her current role as Senior Research Clinician, her work falls under ART optimisation collaborations which receive funding from South Africa’s MRC, USAID, Unitaid and study drug donations from ViiV Healthcare and Gilead Sciences. The other authors declare no conflicts of interest with regards to this study or publication.
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