Modeling the impact of different PrEP targeting strategies combined with a clinic-based HIV-1 nucleic acid testing intervention in Kenya

Background: Up to 69% of adults who acquire HIV in Kenya seek care for acute retroviral symptoms, providing an important opportunity for early diagnosis and HIV care engagement. The Tambua Mapema Plus (TMP) trial tested a combined HIV-1 nucleic acid testing, linkage, treatment, and partner notificat...

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Main Authors: Deven T. Hamilton, Clara Agutu, Martin Sirengo, Wairimu Chege, Steven M. Goodreau, Adam Elder, Eduard J. Sanders, Susan M. Graham
Format: Article
Language:English
Published: Elsevier 2023-09-01
Series:Epidemics
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1755436523000324
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author Deven T. Hamilton
Clara Agutu
Martin Sirengo
Wairimu Chege
Steven M. Goodreau
Adam Elder
Eduard J. Sanders
Susan M. Graham
author_facet Deven T. Hamilton
Clara Agutu
Martin Sirengo
Wairimu Chege
Steven M. Goodreau
Adam Elder
Eduard J. Sanders
Susan M. Graham
author_sort Deven T. Hamilton
collection DOAJ
description Background: Up to 69% of adults who acquire HIV in Kenya seek care for acute retroviral symptoms, providing an important opportunity for early diagnosis and HIV care engagement. The Tambua Mapema Plus (TMP) trial tested a combined HIV-1 nucleic acid testing, linkage, treatment, and partner notification intervention for adults with symptoms of acute HIV infection presenting to health facilities in coastal Kenya. We estimated the potential impact on the Kenyan HIV epidemic of providing PrEP to individuals testing negative in TMP, if scaled up. Methods: We developed an agent-based simulation of HIV-1 transmission using TMP data and current Kenyan statistics. PrEP interventions were layered onto a model of TMP as standard of care, to estimate additional potential population-level impact of enrolling HIV-negative individuals identified through TMP on PrEP over 10 years. Four scenarios were modeled: PrEP for uninfected individuals in disclosed serodiscordant couples; PrEP for individuals with concurrent partnerships; PrEP for all uninfected individuals identified through TMP; and PrEP integrated into the enhanced partner services component of TMP. Findings: Providing PrEP to both individuals with concurrent partnerships and uninfected partners identified through enhanced partner services reduced new HIV infections and was efficient based on numbers needed to treat (NNT). The mean percent of infections averted was 2.79 (95%SI:−10.83, 15.24) and 4.62 (95%SI:−9.5, 16.82) when PrEP uptake was 50% and 100%, respectively, and median NNT was 22.54 (95%SI:not defined, 6.45) and 27.55 (95%SI:not defined, 11.0), respectively. Providing PrEP for all uninfected individuals identified through TMP averted up to 12.68% (95%SI:0.17, 25.19) of new infections but was not efficient based on the NNT: 200.24 (95%SI:523.81, 123.23). Conclusions: Providing PrEP to individuals testing negative for HIV-1 nucleic acid after presenting to a health facility with symptoms compatible with acute HIV adds value to the TMP intervention, provided PrEP is targeted effectively and efficiently. Funding: National Institutes of Health, Sub-Saharan African Network for TB/HIV Research Excellence.
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spelling doaj.art-b85298f86b4e45d997e7285069ff50822023-09-06T04:50:36ZengElsevierEpidemics1755-43652023-09-0144100696Modeling the impact of different PrEP targeting strategies combined with a clinic-based HIV-1 nucleic acid testing intervention in KenyaDeven T. Hamilton0Clara Agutu1Martin Sirengo2Wairimu Chege3Steven M. Goodreau4Adam Elder5Eduard J. Sanders6Susan M. Graham7Center for Studies in Demography & Ecology, University of Washington, Seattle, WA, United States; Correspondence to: UW Seattle, 206 Raitt Hall, P.O. Box 353412, WA 98195-3412, USA.KEMRI - Wellcome Trust Research Programme, Kilifi, KenyaNational AIDS & STI Control Programme, Nairobi, KenyaNational Institutes of Allergy & Infectious Diseases, National Institutes of Health, Rockville, MD, United StatesDepartments of Anthropology and Epidemiology, University of Washington, Seattle, WA, United StatesDepartment of Biostatistics, University of Washington, Seattle, WA, United StatesKEMRI - Wellcome Trust Research Programme, Kilifi, Kenya; University of Oxford, Headington, United KingdomDepartments of Medicine, Global Health, and Epidemiology, University of Washington, Seattle, WA, United StatesBackground: Up to 69% of adults who acquire HIV in Kenya seek care for acute retroviral symptoms, providing an important opportunity for early diagnosis and HIV care engagement. The Tambua Mapema Plus (TMP) trial tested a combined HIV-1 nucleic acid testing, linkage, treatment, and partner notification intervention for adults with symptoms of acute HIV infection presenting to health facilities in coastal Kenya. We estimated the potential impact on the Kenyan HIV epidemic of providing PrEP to individuals testing negative in TMP, if scaled up. Methods: We developed an agent-based simulation of HIV-1 transmission using TMP data and current Kenyan statistics. PrEP interventions were layered onto a model of TMP as standard of care, to estimate additional potential population-level impact of enrolling HIV-negative individuals identified through TMP on PrEP over 10 years. Four scenarios were modeled: PrEP for uninfected individuals in disclosed serodiscordant couples; PrEP for individuals with concurrent partnerships; PrEP for all uninfected individuals identified through TMP; and PrEP integrated into the enhanced partner services component of TMP. Findings: Providing PrEP to both individuals with concurrent partnerships and uninfected partners identified through enhanced partner services reduced new HIV infections and was efficient based on numbers needed to treat (NNT). The mean percent of infections averted was 2.79 (95%SI:−10.83, 15.24) and 4.62 (95%SI:−9.5, 16.82) when PrEP uptake was 50% and 100%, respectively, and median NNT was 22.54 (95%SI:not defined, 6.45) and 27.55 (95%SI:not defined, 11.0), respectively. Providing PrEP for all uninfected individuals identified through TMP averted up to 12.68% (95%SI:0.17, 25.19) of new infections but was not efficient based on the NNT: 200.24 (95%SI:523.81, 123.23). Conclusions: Providing PrEP to individuals testing negative for HIV-1 nucleic acid after presenting to a health facility with symptoms compatible with acute HIV adds value to the TMP intervention, provided PrEP is targeted effectively and efficiently. Funding: National Institutes of Health, Sub-Saharan African Network for TB/HIV Research Excellence.http://www.sciencedirect.com/science/article/pii/S1755436523000324HIV preventionHIV-1 nucleic acid testingPrEPEpidemic modelingKenya
spellingShingle Deven T. Hamilton
Clara Agutu
Martin Sirengo
Wairimu Chege
Steven M. Goodreau
Adam Elder
Eduard J. Sanders
Susan M. Graham
Modeling the impact of different PrEP targeting strategies combined with a clinic-based HIV-1 nucleic acid testing intervention in Kenya
Epidemics
HIV prevention
HIV-1 nucleic acid testing
PrEP
Epidemic modeling
Kenya
title Modeling the impact of different PrEP targeting strategies combined with a clinic-based HIV-1 nucleic acid testing intervention in Kenya
title_full Modeling the impact of different PrEP targeting strategies combined with a clinic-based HIV-1 nucleic acid testing intervention in Kenya
title_fullStr Modeling the impact of different PrEP targeting strategies combined with a clinic-based HIV-1 nucleic acid testing intervention in Kenya
title_full_unstemmed Modeling the impact of different PrEP targeting strategies combined with a clinic-based HIV-1 nucleic acid testing intervention in Kenya
title_short Modeling the impact of different PrEP targeting strategies combined with a clinic-based HIV-1 nucleic acid testing intervention in Kenya
title_sort modeling the impact of different prep targeting strategies combined with a clinic based hiv 1 nucleic acid testing intervention in kenya
topic HIV prevention
HIV-1 nucleic acid testing
PrEP
Epidemic modeling
Kenya
url http://www.sciencedirect.com/science/article/pii/S1755436523000324
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