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Using routine programmatic data to estimate the population-level impacts of HIV self-testing: The example of the ATLAS program in Cote d’Ivoire

View ORCID ProfileArlette Simo Fotso, View ORCID ProfileCheryl Johnson, View ORCID ProfileAnthony Vautier, Konan Blaise Kouamé, View ORCID ProfilePapa Moussa Diop, View ORCID ProfileRomain Silhol, View ORCID ProfileMathieu Maheu-Giroux, View ORCID ProfileMarie-Claude Boily, View ORCID ProfileNicolas Rouveau, View ORCID ProfileClémence Doumenc-Aïdara, View ORCID ProfileRachel Baggaley, Eboi Ehui, View ORCID ProfileJoseph Larmarange, the ATLAS team
doi: https://doi.org/10.1101/2022.02.08.22270670
This article is a preprint and has not been peer-reviewed [what does this mean?]. It reports new medical research that has yet to be evaluated and so should not be used to guide clinical practice.
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Abstract

Background HIV self-testing (HIVST) is recommended by the World Health Organization as an additional HIV testing approach. Since 2019, it has been implemented in Côte d’Ivoire through the ATLAS project, including primary and secondary distribution channels. While the discreet and flexible nature of HIVST makes it appealing for users, it also makes the monitoring and estimation of the population-level programmatic impact of HIVST programs challenging. We used routinely collected data to estimate the effects of ATLAS’ HIVST distribution on access to testing, conventional testing (self-testing excluded), diagnoses, and antiretroviral treatment (ART) initiations in Côte d’Ivoire.

Methods We used the ATLAS project’s programmatic data between the third quarter (Q) of 2019 (Q3 2019) and Q1 2021, in addition to routine HIV testing services program data obtained from the President’s Emergency Plan for AIDS Relief dashboard. We performed ecological time series regression using linear mixed models.

Findings The results are presented for 1000 HIVST kits distributed through ATLAS. They show a negative but nonsignificant effect of the number of ATLAS HIVST on conventional testing uptake (−190 conventional tests [95% CI: −427 to 37, p=0·10]). We estimated that for 1000 additional HIVST distributed through ATLAS, +590 [95% CI: 357 to 821, p<0·001] additional individuals have accessed HIV testing, assuming an 80% HIVST utilization rate (UR) and +390 [95% CI: 161 to 625, p<0·001] assuming a 60% UR. The statistical relationship between the number of HIVST and HIV diagnoses was significant and positive (+8 diagnosis [95% CI: 0 to 15, p=0·044]). No effect was observed on ART initiation (−2 ART initiations [95% CI: −8 to 5, p=0·66]).

Interpretations Social network-based HIVST distribution had a positive impact on access to HIV testing and diagnoses in Cote d’Ivoire. This approach offers a promising way for countries to assess the impact of HIVST programs.

Funding Unitaid 2018-23-ATLAS

Evidence before this study We searched PubMed between November 9 and 12, 2021, for studies assessing the impact of HIVST on HIV testing, ‘conventional’ testing, HIV diagnoses and ART initiation. We searched published data using the terms “HIV self-testing” and “HIV testing”; “HIV self-testing” and “traditional HIV testing” or “conventional testing”; “HIV self-testing” and “diagnosis” or “positive results”; and “HIV self-testing” and “ART initiation” or “Antiretroviral treatment”. Articles with abstracts were reviewed. No time or language restriction was applied. Most studies were individual-based randomized controlled trials involving data collection and some form of HIVST tracking; no studies were conducted at the population level, none were conducted in western Africa and most focused on subgroups of the population or key populations. While most studies found a positive effect of HIVST on HIV testing, evidence was mixed regarding the effect on conventional testing, diagnoses, and ART initiation.

Added value of this study HIVST can empower individuals by allowing them to choose when, where and whether to test and with whom to share their results and can reach hidden populations who are not accessing existing services. Inherent to HIVST is that there is no automatic tracking of test results and linkages at the individual level. Without systematic and direct feedback to program implementers regarding the use and results of HIVST, it is difficult to estimate the impact of HIVST distribution at the population level. Such estimates are crucial for national AIDS programs. This paper proposed a way to overcome this challenge and used routinely collected programmatic data to indirectly estimate and assess the impacts of HIVST distribution in Côte d’Ivoire.

Implications of all the available evidence Our results showed that HIVST increased the overall HIV testing uptake and diagnoses in Côte d’Ivoire without significantly reducing conventional HIV testing uptake. We demonstrated that routinely collected programmatic data could be used to estimate the effects of HIVST kit distribution outside a trial environment. The methodology used in this paper could be replicated and implemented in different settings and enable more countries to routinely evaluate HIVST programming at the population level.

Competing Interest Statement

CD, AV, JL, PMD, ASF and NR acknowledge funding from UNITAID through the ATLAS project. MCB and RS acknowledge funding from the MRC Centre for Global Infectious Disease Analysis (Reference MR/R015600/1), jointly funded by the UK Medical Research Council (MRC) and the UK Foreign, Commonwealth & Development Office (FCDO), under the MRC/FCDO Concordat agreement and is also part of the EDCTP2 program supported by the European Union. MM-G’s research program is funded by the Tier 2 Canada Research Chair in Population Health Modeling. CJ declares that WHO receives grants to support activities on HIV testing including self-testing from USAID, UNITAID and the Bill and Melinda Gates Foundation All the other authors declare no conflicts of interest.

Clinical Protocols

https://atlas.solthis.org/en/research/

Funding Statement

The ATLAS Project was funded by Unitaid, Grant number 2018-23-ATLAS

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

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I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.

Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

Yes

I have followed all appropriate research reporting guidelines and uploaded the relevant EQUATOR Network research reporting checklist(s) and other pertinent material as supplementary files, if applicable.

Yes

Footnotes

  • ↵g Full composition of the ATLAS Team provided in the Supplementary Materials

  • ORCID & emails:

    Arlette Simo Fotso (PhD): arlette.simofotso{at}ird.fr, CEPED 45 rue des Saint Père, Paris, France

    Cheryl Johnson (MA): johnsonc{at}who.int,WHO Geneva

    Anthony Vautier (MPH): directeurtech.ATLAS{at}solthis.org, Solthis 36, rue OKM 31, Cité Mamelles, Ouakam, Dakar, Sénégal

    Konan Blaise Kouamé (MD): +225 0708047279, kouame.blaise{at}pnls-ci.com, Côte d’Ivoire

    Papa Moussa Diop (DEA): coordinateurm_e.atlas{at}solthis.org, Solthis 36, rue OKM 31, Cité Mamelles Ouakam, Dakar, Sénégal

    Romain Silhol (PhD): r.silhol{at}imperial.ac.uk, MRC Centre for Global Infectious Disease Analysis, Department of Infectious Disease Epidemiology, Imperial College London, St Mary’s Hospital, 2 Norfolk Place, W2 1PG London, United Kingdom

    Mathieu Maheu-Giroux (ScD): mathieu.maheu-giroux{at}mcgill.ca, 2001 Avenue McGill Collège, Suite 1200 Montréal, Québec, H3A, 1G1 Canada

    Marie-Claude Boily (PhD): mc.boily{at}ic.ac.uk, School of Public Health, Medical School Building, St. Mary’s Hospital, Norfolk Place, London W2 1PG, United Kingdom

    Nicolas Rouveau (PharmD): nicolas.rouveau{at}ceped.org, CEPED 45 rue des Saint Père, Paris, France

    Clémence Doumenc-Aïdara (MEcon): directriceprojet.atlas{at}solthis.org, Solthis 36, rue OKM 31, Cité Mamelles Ouakam, Dakar, Sénégal

    Rachel Baggaley (MBBS) : baggaleyr{at}who.int, WHO Geneva

    Eboi Ehui (PhD): ehui.eboi{at}pnls-ci.com

    Joseph Larmarange (PhD): joseph.larmarange{at}ird.fr, CEPED 45 rue des Saint Père, Paris, France

Copyright 
The copyright holder for this preprint is the author/funder, who has granted medRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-ND 4.0 International license.
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Posted February 09, 2022.
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