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      A Novel HIV-1 RNA Testing Intervention to Detect Acute and Prevalent HIV Infection in Young Adults and Reduce HIV Transmission in Kenya: Protocol for a Randomized Controlled Trial

      research-article
      , MD, MPH, PhD 1 , 2 , 3 , , , MBChB, MPH, MSc 4 , , PhD 4 , , MSc, PhD 4 , , BSc 4 , , BPharm, MSc, PhD 4 , , MD, MPH 1 , 2 , 3 , , MBChB, MS, PhD 1 , 5 , , MA, PhD 3 , 6 , , MPH, PhD 7 , , PhD 8 , 9 , 10 , 11 , , MBChB 12 , , MD, MPH 13 , , MD, MPH, PhD 4 , 14
      (Reviewer), (Reviewer)
      JMIR Research Protocols
      JMIR Publications
      diagnostic tests, HIV infection, viral burden, contact tracing, highly active antiretroviral therapy, pre-exposure prophylaxis

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          Abstract

          Background

          Detection and management of acute HIV infection (AHI) is a clinical and public health priority, and HIV infections diagnosed among young adults aged 18 to 39 years are usually recent. Young adults with recent HIV acquisition frequently seek care for symptoms and could potentially be diagnosed through the health care system. Early recognition of HIV infection provides considerable individual and public health benefits, including linkage to treatment as prevention, access to risk reduction counseling and treatment, and notification of partners in need of HIV testing.

          Objective

          The Tambua Mapema Plus study aims to (1) test 1500 young adults (aged 18-39 years) identified by an AHI screening algorithm for acute and prevalent (ie, seropositive) HIV, linking all newly diagnosed HIV-infected patients to care and offering immediate treatment; (2) offer assisted HIV partner notification services to all patients with HIV, testing partners for acute and prevalent HIV infection and identifying local sexual networks; and (3) model the potential impact of these two interventions on the Kenyan HIV epidemic, estimating incremental costs per HIV infection averted, death averted, and disability-adjusted life year averted using data on study outcomes.

          Methods

          A modified stepped-wedge design is evaluating the yield of this HIV testing intervention at 4 public and 2 private health facilities in coastal Kenya before and after intervention delivery. The intervention uses point-of-care HIV-1 RNA testing combined with standard rapid antibody tests to diagnose AHI and prevalent HIV among young adults presenting for care, employs HIV partner notification services to identify linked acute and prevalent infections, and follows all newly diagnosed patients and their partners for 12 months to ascertain clinical outcomes, including linkage to care, antiretroviral therapy (ART) initiation and virologic suppression in HIV-infected patients, and pre-exposure prophylaxis uptake in uninfected individuals in discordant partnerships.

          Results

          Enrollment started in December 2017. As of April 2020, 1374 participants have been enrolled in the observation period and 1500 participants have been enrolled in the intervention period, with 13 new diagnoses (0.95%) in the observation period and 37 new diagnoses (2.47%), including 2 AHI diagnoses, in the intervention period. Analysis is ongoing and will include adjusted comparisons of the odds of the following outcomes in the observation and intervention periods: being tested for HIV infection, newly diagnosed with prevalent or acute HIV infection, linked to care, and starting ART by week 6 following HIV diagnosis. Participants newly diagnosed with acute or prevalent HIV infection in the intervention period are being followed for outcomes, including viral suppression by month 6 and month 12 following ART initiation and partner testing outcomes.

          Conclusions

          The Tambua Mapema Plus study will provide foundational data on the potential of this novel combination HIV prevention intervention to reduce ongoing HIV transmission in Kenya and other high-prevalence African settings.

          Trial Registration

          ClinicalTrials.gov NCT03508908; https://clinicaltrials.gov/ct2/show/NCT03508908

          International Registered Report Identifier (IRRID)

          DERR1-10.2196/16198

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          Most cited references37

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          Dynamics of HIV viremia and antibody seroconversion in plasma donors: implications for diagnosis and staging of primary HIV infection.

          The characterization of primary HIV infection by the analysis of serial plasma samples from newly infected persons using multiple standard viral assays. A retrospective study involving two sets of archived samples from HIV-infected plasma donors. (A) 435 samples from 51 donors detected by anti-HIV enzyme immunoassays donated during 1984-1994; (B) 145 specimens from 44 donors detected by p24 antigen screening donated during 1996-1998. Two US plasma products companies. The timepoints of appearance of HIV-1 markers and viral load concentrations during primary HIV infection. The pattern of sequential emergence of viral markers in the 'A' panels was highly consistent, allowing the definition and estimation of the duration of six sequential stages. From the 'B' panels, the viral load at p24 antigen seroconversion was estimated by regression analysis at 10 000 copies/ml (95% CI 2000-93 000) and the HIV replication rate at 0.35 log copies/ml/day, corresponding to a doubling time in the preseroconversion phase of 20.5 h (95% CI 18.2-23.4 h). Consequently, an RNA test with 50 copies/ml sensitivity would detect HIV infection approximately 7 days before a p24 antigen test, and 12 days before a sensitive anti-HIV test. The sequential emergence of assay reactivity allows the classification of primary HIV-1 infection into distinct laboratory stages, which may facilitate the diagnosis of recent infection and stratification of patients enrolled in clinical trials. Quantitative analysis of preseroconversion replication rates of HIV is useful for projecting the yield and predictive value of assays targeting primary HIV infection.
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            The stepped wedge trial design: a systematic review

            Background Stepped wedge randomised trial designs involve sequential roll-out of an intervention to participants (individuals or clusters) over a number of time periods. By the end of the study, all participants will have received the intervention, although the order in which participants receive the intervention is determined at random. The design is particularly relevant where it is predicted that the intervention will do more good than harm (making a parallel design, in which certain participants do not receive the intervention unethical) and/or where, for logistical, practical or financial reasons, it is impossible to deliver the intervention simultaneously to all participants. Stepped wedge designs offer a number of opportunities for data analysis, particularly for modelling the effect of time on the effectiveness of an intervention. This paper presents a review of 12 studies (or protocols) that use (or plan to use) a stepped wedge design. One aim of the review is to highlight the potential for the stepped wedge design, given its infrequent use to date. Methods Comprehensive literature review of studies or protocols using a stepped wedge design. Data were extracted from the studies in three categories for subsequent consideration: study information (epidemiology, intervention, number of participants), reasons for using a stepped wedge design and methods of data analysis. Results The 12 studies included in this review describe evaluations of a wide range of interventions, across different diseases in different settings. However the stepped wedge design appears to have found a niche for evaluating interventions in developing countries, specifically those concerned with HIV. There were few consistent motivations for employing a stepped wedge design or methods of data analysis across studies. The methodological descriptions of stepped wedge studies, including methods of randomisation, sample size calculations and methods of analysis, are not always complete. Conclusion While the stepped wedge design offers a number of opportunities for use in future evaluations, a more consistent approach to reporting and data analysis is required.
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              Clinical and epidemiologic features of primary HIV infection.

              The acute clinical events surrounding the acquisition of human immunodeficiency virus (HIV) have not been well characterized. To further define the clinical and epidemiologic presentation of primary HIV infection. Descriptive cohort study. University research clinic. 46 adults (43 men and 3 women) with primary HIV infection who enrolled in the study a median of 51 days after HIV seroconversion. Documentation of recent HIV seroconversion. Standardized collection of demographic characteristics and sexual contact history, results of tests for HIV RNA, HIV culture, and T-cell subsets. 41 of 46 patients (89%) developed an acute retroviral syndrome. Primary HIV infection was infrequently diagnosed at the initial medical encounter, even in persons enrolled in routine HIV screening programs. Median numbers of sexual partners 6 months and 1 month before acquisition of HIV were three and one, respectively; 21 patients (46%) reported having had only one partner in the month before seroconversion. Of the 12 patients who could identify the precise date of and activity leading to seroconversion, 4 reported having only oral-genital contact. Primary HIV infection causes a recognizable clinical syndrome that is often underdiagnosed, even in persons enrolled in a program of routine surveillance for HIV infection. Frequency of sexual contact and overall numbers of sexual partners in this group of homosexual men who acquired HIV were markedly lower than those seen a decade ago. Acquisition of HIV does occur, even in persons with relatively few sexual partners. Increased attention to oral-genital contact as a means of acquiring HIV appears to be warranted.
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                Author and article information

                Contributors
                Journal
                JMIR Res Protoc
                JMIR Res Protoc
                ResProt
                JMIR Research Protocols
                JMIR Publications (Toronto, Canada )
                1929-0748
                August 2020
                7 August 2020
                : 9
                : 8
                : e16198
                Affiliations
                [1 ] Department of Global Health University of Washington Seattle, WA United States
                [2 ] Department of Medicine University of Washington Seattle, WA United States
                [3 ] Department of Epidemiology University of Washington Seattle, WA United States
                [4 ] Kenya Medical Research Institute - Wellcome Trust Research Programme Kilifi Kenya
                [5 ] Department of Pharmacy University of Washington Seattle, WA United States
                [6 ] Department of Anthropology University of Washington Seattle, WA United States
                [7 ] Center for Studies in Demography and Ecology University of Washington Seattle, WA United States
                [8 ] Africa Health Research Institute Durban South Africa
                [9 ] HIV Pathogenesis Programme Doris Duke Medical Research Institute University of KwaZulu-Natal Durban South Africa
                [10 ] Max Planck Institute for Infection Biology Berlin Germany
                [11 ] Division of Infection and Immunity University College London London United Kingdom
                [12 ] Department of Health Infrastructure Management Ministry of Health Nairobi Kenya
                [13 ] Division of AIDS National Institute of Allergy and Infectious Diseases National Institutes of Health Rockville, MD United States
                [14 ] University of Oxford Headington United Kingdom
                Author notes
                Corresponding Author: Susan M Graham grahamsm@ 123456uw.edu
                Author information
                https://orcid.org/0000-0001-7847-8686
                https://orcid.org/0000-0003-1053-4463
                https://orcid.org/0000-0001-5106-0466
                https://orcid.org/0000-0001-5296-4264
                https://orcid.org/0000-0003-2372-0310
                https://orcid.org/0000-0002-1808-3292
                https://orcid.org/0000-0001-8575-3439
                https://orcid.org/0000-0003-3834-7141
                https://orcid.org/0000-0003-1009-5763
                https://orcid.org/0000-0003-4334-958X
                https://orcid.org/0000-0003-2962-3992
                https://orcid.org/0000-0002-1523-5879
                https://orcid.org/0000-0003-3859-0977
                https://orcid.org/0000-0002-1062-8921
                Article
                v9i8e16198
                10.2196/16198
                7442943
                32763882
                f809e27c-5cb8-4006-beee-609d41f0eca3
                ©Susan M Graham, Clara Agutu, Elise van der Elst, Amin S Hassan, Evanson Gichuru, Peter M Mugo, Carey Farquhar, Joseph B Babigumira, Steven M Goodreau, Deven T Hamilton, Thumbi Ndung'u, Martin Sirengo, Wairimu Chege, Eduard J Sanders. Originally published in JMIR Research Protocols (http://www.researchprotocols.org), 07.08.2020.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work, first published in JMIR Research Protocols, is properly cited. The complete bibliographic information, a link to the original publication on http://www.researchprotocols.org, as well as this copyright and license information must be included.

                History
                : 9 September 2019
                : 5 March 2020
                : 27 May 2020
                Categories
                Protocol
                Protocol

                diagnostic tests,hiv infection,viral burden,contact tracing,highly active antiretroviral therapy,pre-exposure prophylaxis

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