Evidence map›Paper›PMID 37459349›Full record

Observational studyPloS one2023

Optimizing antiretroviral therapy for children living with HIV: Experience from an observational cohort in Lesotho.

Vincent J Tukei, Nicole Herrera, Matseliso Masitha, Lieketseng Masenyetse, Majoalane Mokone, Mafusi Mokone, Limpho Maile, Michelle M Gill

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
0.8field-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

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 4 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. 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

8 authors at 3 institutions in 2 countries.

Vincent J TukeiElizabeth Glaser Pediatric AIDS Foundation, Maseru, Lesotho.ORCID 0000-0002-9525-2600
Nicole HerreraElizabeth Glaser Pediatric AIDS Foundation, Washington, D.C., United States of America.
Matseliso MasithaElizabeth Glaser Pediatric AIDS Foundation, Maseru, Lesotho.
Lieketseng MasenyetseElizabeth Glaser Pediatric AIDS Foundation, Maseru, Lesotho.
Majoalane MokoneElizabeth Glaser Pediatric AIDS Foundation, Maseru, Lesotho.
Mafusi MokoneElizabeth Glaser Pediatric AIDS Foundation, Maseru, Lesotho.
Limpho MaileMinistry of Health, Maseru, Lesotho.
Michelle M GillElizabeth Glaser Pediatric AIDS Foundation, Washington, D.C., United States of America.
Lesotho Planned Parenthood Association · LSElizabeth Glaser Pediatric AIDS Foundation · USMinistry of Health · LS

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionWe describe transition of HIV-positive children from efavirenz- or nevirapine-based antiretroviral therapy (ART) to optimal dolutegravir (DTG) or lopinavir/ritonavir (LPV/r) (solid formulation)-based ART in Lesotho.

methodsWe followed a cohort of children less than 15 years of age who were initiated on ART on or after January 1, 2018 from 21 selected health facilities in Lesotho. From March 2020 to May 2022, we collected data retrospectively through chart abstraction and prospectively through caregiver interviews to cover a period of 24 months following treatment initiation. We used a structured questionnaire to collect data on demographics, ART regimen, drug formulations and switches, viral suppression, retention, and drug administration challenges. Data were summarized as frequencies and percentages, using SAS ver.9.4.

resultsOf 310 children enrolled in the study, 169 (54.5%) were female, and median age at ART initiation was 5.9 years (IQR 1.1-11.1). During follow-up, 19 (6.1%) children died, 41 (13.2%) were lost to follow-up and 74 (23.9%) transferred to non-study sites. At baseline, 144 (46.4%) children were receiving efavirenz-based ART regimen, 133 (42.9%) LPV/r, 27 (8.7%) DTG, 5 (1.6%) nevirapine; 1 child had incomplete records. By study end, 143 (46.1%) children were receiving LPV/r-based ART regimen, 109 (35.2%) DTG, and 58 (18.7%) were on efavirenz or nevirapine-based regimen. Of 116 children with viral load results after six months or more on a consistent regimen, viral suppression was seen in 35/53 (66.0%) children on LPV/r, 36/38 (94.7%) children on DTG and 19/24 (79.2%) children on efavirenz.

conclusionFollowing optimal ART introduction in Lesotho, most children in the cohort were transitioned and many attained or maintained viral suppression after transition; however, we recommend more robust viral load monitoring and patient tracking to reduce losses and improve outcomes after ART transition.

Indexed as

Anti-HIV AgentsHIV InfectionsAlkynesBenzoxazinesChildChild, PreschoolCyclopropanesFemaleHumansInfantLesothoLopinavirMaleNevirapineRetrospective StudiesRitonavirAlkynesAnti-HIV AgentsBenzoxazinesCyclopropanesefavirenzLopinavirNevirapineRitonavir

Identifiers

PMID37459349
PMCPMC10351696
OpenAlexW4384521669

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.