Evidence map›Paper›PMID 33882938›Full record

ArticleAIDS research and therapy2021

Predictors of failure on second-line antiretroviral therapy with protease inhibitor mutations in Uganda.

Hellen Musana, Jude Thaddeus Ssensamba, Mary Nakafeero, Henry Mugerwa, Flavia Matovu Kiweewa, David Serwadda, Francis Ssali

Open access · goldAbstract read
In one paragraph

Article in AIDS research and therapy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.6field-weighted citation impact, top 30% 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.

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

15 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
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

7 authors at 5 institutions in 2 countries.

Hellen MusanaCollege of Health Sciences, School of Public Health, Makerere University, Kampala, Uganda. wambohellen@gmail.com.ORCID 0000-0003-0575-754X
Jude Thaddeus SsensambaCollege of Health Sciences, School of Public Health, Makerere University, Kampala, Uganda.ORCID 0000-0003-3939-4951
Mary NakafeeroCenter for Innovations in Health Africa (CIHA Uganda), Kampala, Uganda.ORCID 0000-0003-2943-0744
Henry MugerwaJoint Clinical Research Centre, Kampala, Uganda.
Flavia Matovu KiweewaCollege of Health Sciences, School of Public Health, Makerere University, Kampala, Uganda.ORCID 0000-0002-0046-4353
David SerwaddaCollege of Health Sciences, School of Public Health, Makerere University, Kampala, Uganda.ORCID 0000-0001-6532-6587
Francis SsaliJoint Clinical Research Centre, Kampala, Uganda.
Joint Clinical Research Centre · UGMUJHU Research Collaboration · UGInnovations for Poverty Action · UGKatholieke Hogeschool Vives · BEMakerere University · UG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionFailure on second-line antiretroviral therapy (ART) with protease inhibitor (PI) mutations (VF-M) is on the rise. However, there is a paucity of information on the factors associated with this observation in low-income countries. Knowledge of underlying factors is critical if we are to minimize the number of PLHIV switched to costly third-line ART. Our study investigated the factors associated with VF-M.

methodsWe conducted a matched case-control analysis of patients' records kept at the Joint Clinical Research Center, starting from January 2008 to May 2018. We matched records of patients who failed the second-line ART with major PI mutations (cases) with records of patients who were virologically suppressed (controls) by a ratio of 1:3. Data analysis was conducted using STATA Version 14. Categorical variables were compared with the outcomes failure on second-line ART with PI mutations using the Chi-square and Fisher's exact tests where appropriate. Conditional logistic regression for paired data was used to assess the association between the outcome and exposure variables, employing the backward model building procedure.

resultsOf the 340 reviewed patients' records, 53% were women, and 6.2% had previous tuberculosis treatment. Males (aOR = 2.58, [CI 1.42-4.69]), and patients concurrently on tuberculosis treatment while on second-line ART (aOR = 5.65, [CI 1.76-18.09]) had higher odds of VF-M. ART initiation between 2001 and 2015 had lower odds of VF-M relative to initiation before the year 2001.

conclusionMales and patients concomitantly on tuberculosis treatment while on second-line ART are at a higher risk of VF-M. HIV/AIDS response programs should give special attention to this group of people if we are to minimize the need for expensive third-line ART. We recommend more extensive, explorative studies to ascertain underlying factors.

Indexed as

Anti-HIV AgentsHIV InfectionsFemaleHumansMaleMutationProtease InhibitorsTreatment FailureUgandaViral LoadAnti-HIV AgentsProtease InhibitorsPredictorsProtease inhibitor mutationsSecond-line ART failureUganda

Identifiers

PMID33882938
PMCPMC8059285
OpenAlexW3154841276

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.