Evidence map›Paper›PMID 38923981›Full record

ArticlePloS one2024

High viral suppression rates among PLHIV on dolutegravir who had an initial episode of viral non-suppression in Uganda September 2020-July 2021.

Grace A Namayanja, Juliana de Fatima Da Silva, Bill Elur, Pamela M Nasirumbi, Elliot Raizes, Julius Ssempiira, Esther Nazziwa, Miriam Nabukenya, Isaac Sewanyana, Jennifer Balaba and 11 more

Abstract read
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors.

Grace A NamayanjaDivision of Global HIV and TB, US Centers for Disease Control and Prevention, Kampala, Uganda.ORCID 0000-0003-0154-6788
Juliana de Fatima Da SilvaDivision of Global HIV and TB, US Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Bill ElurDivision of Global HIV and TB, US Centers for Disease Control and Prevention, Kampala, Uganda.
Pamela M NasirumbiDivision of Global HIV and TB, US Centers for Disease Control and Prevention, Kampala, Uganda.
Elliot RaizesDivision of Global HIV and TB, US Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Julius SsempiiraDivision of Global HIV and TB, US Centers for Disease Control and Prevention, Kampala, Uganda.
Esther NazziwaDivision of Global HIV and TB, US Centers for Disease Control and Prevention, Kampala, Uganda.
Miriam NabukenyaCentral Public Health Laboratories, Ministry of Health, Kampala, Uganda.
Isaac SewanyanaCentral Public Health Laboratories, Ministry of Health, Kampala, Uganda.
Jennifer BalabaMonitoring and Evaluation Technical Support, Makerere University School of Public Health, Kampala, Uganda.
Jonathan NtaleDivision of Global HIV and TB, US Centers for Disease Control and Prevention, Kampala, Uganda.
Jackie CalnanOffice of Health and HIV, United States Agency for International Development, Kampala, Uganda.
Estella BirabwaWalter Reed Army Institute of Research, US Mission, Kampala, Uganda.ORCID 0009-0001-4802-7398
Juliet AkaoUnited States Department of Defense, US Mission, Kampala, Uganda.
Christina MwangiDivision of Global HIV and TB, US Centers for Disease Control and Prevention, Kampala, Uganda.
Mary NaluguzaDivision of Global HIV and TB, US Centers for Disease Control and Prevention, Kampala, Uganda.
Arthur AhimbisibweAIDS Control Program, Ministry of Health, Kampala, Uganda.
Cordelia KatureebeAIDS Control Program, Ministry of Health, Kampala, Uganda.
Susan NabaddaCentral Public Health Laboratories, Ministry of Health, Kampala, Uganda.
Lisa NelsonDivision of Global HIV and TB, US Centers for Disease Control and Prevention, Kampala, Uganda.
Emilio DirlikovDivision of Global HIV and TB, US Centers for Disease Control and Prevention, Kampala, Uganda.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn 2019, WHO recommended dolutegravir (DTG) as a backbone for first- and second-line antiretroviral therapy (ART) regimens for people living with HIV (PLHIV). According to the 2018 Uganda's HIV treatment guidelines, patients with viral non-suppression (≥1,000 copies/mL) should receive intensive adherence counseling (IAC) with repeat viral load (VL) within 6 months. This analysis focused on the prevalence and factors associated with viral suppression following IAC among PLHIV on DTG-based regimens (DBRs) with an initial episode of viral non-suppression (VNS) in Uganda.

methodsWe conducted a retrospective analysis for PLHIV on DBRs with an initial episode of VNS (≥1,000 copies/mL) in Uganda during October 2019-September 2020 who had a follow up VL test result during September 2020-July 2021. Data were abstracted from the Central Public Health Laboratory (CPHL) database, including patient demographics and VL results. Viral non-suppression (VNS) was defined as a VL test result of ≥1,000 copies/mL. We characterized PLHIV on DBRs and used logistic regression models to determine factors associated with VL suppression after an initial episode of VNS.

resultsA total of 564 PLHIV on DBRs with an initial episode of VNS were followed up and 43 were excluded due to missing data. Of the 521, 220 (42.2%) were children (<15 years) and 231 (44.3%) were female. Median age was 28 years (interquartile range [IQR]: 12-43 years), and median duration on DBRs was 12 months (IQR: 6-15 months). Overall, 80.8% (421/521) PLHIV had a suppressed viral load at first follow up testing (children = 74.5% [164/220]; adults = 85.4% [257/301]). Children with initial VL results ≥5,000 copies/mL were less likely to achieve viral suppression at follow up testing compared to those with <5,000 copies/mL (AOR: 0.38; 95% CI: 0.20-0.71; p = 0.002).

conclusionsIn a programmatic setting, most adults and children suppressed following an initial episode of VNS on DBRs. High rates of suppression after VNS suggest adherence challenges, rather than drug resistance. Continuation of DBRs should be considered before regimen switch.

Indexed as

Heterocyclic Compounds, 3-RingHIV InfectionsOxazinesPiperazinesPyridonesViral LoadAdolescentAdultAnti-HIV AgentsChildDolutegravirFemaleHIV-1HIV Integrase InhibitorsHumansMaleAnti-HIV AgentsDolutegravirHeterocyclic Compounds, 3-RingHIV Integrase InhibitorsOxazinesPiperazinesPyridones

Identifiers

PMID38923981
PMCPMC11206940

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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.