Evidence map›Paper›PMID 32763152›Full record

ArticleThe lancet. HIV2020

Universal test-and-treat in Zambian and South African correctional facilities: a multisite prospective cohort study.

Michael E Herce, Christopher J Hoffmann, Katherine Fielding, Stephanie M Topp, Harry Hausler, Lucy Chimoyi, Helene J Smith, Candice M Chetty-Makkan, Rachel Mukora, Mpho Tlali and 4 more

Registry-linked trialAbstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in The lancet. HIV, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02946762 (Z 31501 - Treatment as Prevention), which is not on this map. Cited by 17 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 3 pooled it
6.5field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02946762 nacompletednot on this map

Z 31501 - Treatment as Prevention (TasP) in Correctional Facilities in Zambia and South Africa

TypeinterventionalSponsorUniversity of North Carolina, Chapel HillRan2016 to 2018Enrolled419ConditionsHIV, TuberculosisArmsTest and treat
3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 3 syntheses or guidelines pooled it, 30 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 4 institutions in 5 countries.

Michael E HerceCentre for Infectious Disease Research in Zambia (CIDRZ), Lusaka, Zambia; Institute for Global Health and Infectious Diseases, School of Medicine, University of North Carolina, Chapel Hill, NC, USA. Electronic address: michael.herce@cidrz.org.
Christopher J HoffmannSchool of Medicine, Johns Hopkins University, Baltimore, MD, USA; The Aurum Institute, Johannesburg, South Africa.
Katherine FieldingDepartment of Infectious Disease Epidemiology, London School of Hygiene & Tropical Medicine, London, UK; School of Public Health, University of the Witwatersrand, Johannesburg, South Africa.
Stephanie M ToppCollege of Public Health, Medical and Veterinary Sciences, James Cook University, Douglas, QLD, Australia.
Harry HauslerTB HIV Care, Cape Town, South Africa.
Lucy ChimoyiThe Aurum Institute, Johannesburg, South Africa.
Helene J SmithCentre for Infectious Disease Research in Zambia (CIDRZ), Lusaka, Zambia.
Candice M Chetty-MakkanThe Aurum Institute, Johannesburg, South Africa; School of Public Health, University of the Witwatersrand, Johannesburg, South Africa.
Rachel MukoraThe Aurum Institute, Johannesburg, South Africa.
Mpho TlaliThe Aurum Institute, Johannesburg, South Africa.
Abraham J OlivierTB HIV Care, Cape Town, South Africa.
Monde MuyoyetaCentre for Infectious Disease Research in Zambia (CIDRZ), Lusaka, Zambia.
Stewart E ReidCentre for Infectious Disease Research in Zambia (CIDRZ), Lusaka, Zambia; Department of Medicine, Division of Infectious Diseases, School of Medicine, University of Alabama at Birmingham, Birmingham, AL, USA.
Salome CharalambousThe Aurum Institute, Johannesburg, South Africa; School of Public Health, University of the Witwatersrand, Johannesburg, South Africa.
Aurum Institute · ZACentre for Infectious Disease Research in Zambia · ZMJames Cook University · AUUniversity of the Witwatersrand · ZA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDespite the global scale-up of antiretroviral therapy (ART), incarcerated people have not benefited equally from test-and-treat recommendations for HIV. To improve access to ART for incarcerated people with HIV, we introduced a universal test-and-treat (UTT) intervention in correctional facilities in South Africa and Zambia, and aimed to assess UTT feasibility and clinical outcomes.

methodsTreatment as Prevention (TasP) was a multisite, mixed methods, implementation research study done at three correctional complexes in South Africa (Johnannesburg and Breede River) and Zambia (Lusaka). Here, we report the clinical outcomes for a prospective cohort of incarcerated individuals who were offered the TasP UTT intervention. Incarcerated individuals were eligible for inclusion if they were aged 18 years or older, with new or previously diagnosed HIV, not yet on ART, and were expected to remain incarcerated for 30 days or longer. To enable the implementation of UTT at the included correctional facilities, we first strengthened on-site HIV service delivery. All participants were offered same-day ART initiation, and had two study-specific follow-up visits scheduled to coincide with routine clinic visits at 6 and 12 months. The main outcomes were ART uptake, time from cohort enrolment to ART initiation, and retention in care and viral suppression at 6 and 12 months. We estimated the association between baseline demographic characteristics and time to ART initiation using Cox proportional hazard models, and, in a post-hoc analysis, we used logistic regression models to assess the association between demographic and clinical variables, including time to ART initiation, and the proportion of participants with a composite poor outcome (defined as viral load >50 copies per mL, or for participants with a missing viral load, lack of retention in care in the on-site ART programme) at 6 months. This study is registered at ClinicalTrials.gov, NCT02946762.

findingsBetween June 23, 2016, and Dec 31, 2017, we identified 1562 incarcerated people with HIV, of whom 1389 (89%) were screened, 1021 (74%) met eligibility criteria, and 975 (95%) were enrolled and followed up to March 31, 2018. At the end of follow-up, 835 (86%) of 975 participants had started ART. Median time from enrolment to ART initiation was 0 days (IQR 0-8). Of 346 participants who remained incarcerated at 6 months, 327 (95%) were retained in care and 269 (78%) had a documented viral load, of whom 262 (97%) achieved viral suppression (<1000 copies per mL). The mortality rate among the 835 participants who had initiated ART was 1·9 per 100 person-years (95% CI 0·9-3·9). No statistically significant associations were identified between any baseline characteristics and time to ART initiation or composite poor outcome.

interpretationUTT implementation is feasible in correctional settings, and can achieve levels of same-day ART uptake, retention in care, and viral suppression among incarcerated people with HIV that are comparable to those observed in community settings.

fundingUK Department for International Development, Swedish International Development Cooperation Agency, Norwegian Agency for Development Cooperation.

Indexed as

Correctional FacilitiesAdultAntiretroviral Therapy, Highly ActiveDisease ManagementFemaleHIV InfectionsHIV TestingHumansMaleMass ScreeningMiddle AgedOutcome Assessment, Health CareProspective StudiesSouth AfricaTime-to-TreatmentViral Load

Identifiers

PMID32763152
OpenAlexW3046995018

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.