Evidence map›Paper›PMID 30373620›Full record

SynthesisAIDS research and therapy2018

A meta-analysis comparing 48-week treatment outcomes of single and multi-tablet antiretroviral regimens for the treatment of people living with HIV.

Patrick G Clay, Wei C Yuet, Christiane H Moecklinghoff, Inge Duchesne, Krzysztof L Tronczyński, Sandip Shah, Dong Shao

Open access · goldAbstract readMeta-Analysis
In one paragraph

Synthesis in AIDS research and therapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
3.5field-weighted citation impact, top 6% 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

35 citing papers in PubMed, 1 synthesis or guideline pooled it, 61 citations in OpenAlex.

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  16. HIV infection.Nature reviews. Disease primers · 2023
    Review
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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

7 authors at 3 institutions in 3 countries.

Patrick G ClayUniversity of North Texas System College of Pharmacy, 3500 Camp Bowie Blvd, Fort Worth, TX, 76107, USA. Patrick.Clay@unthsc.edu.
Wei C YuetUniversity of North Texas System College of Pharmacy, 3500 Camp Bowie Blvd, Fort Worth, TX, 76107, USA.
Christiane H MoecklinghoffJannsen-Cilag GmbH, Johnson & Johnson Platz 1, 41470, Neuss, Germany.
Inge DuchesneJanssen EMEA, Turnhoutseweg 30, 2340, Beerse, Belgium.
Krzysztof L TronczyńskiJanssen-Cilag Polska Sp. Z o.o, Iłżecka 24, 02-135, Warsaw, Poland.
Sandip ShahMarket Access Solutions, LLC, 575 NJ-28, Raritan, NJ, 08869, USA.
Dong ShaoMarket Access Solutions, LLC, 575 NJ-28, Raritan, NJ, 08869, USA.
University of North Texas Health Science Center · USJanssen (Belgium) · BEJohnson & Johnson (Germany) · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo compare outcomes with single tablet regimens (STR) versus multi-tablet regimens (MTR) for human immunodeficiency virus (HIV) treatment using published data.

designSystematic review and random-effects meta-analysis of literature on approved and investigational HIV regimens.

methodsThe research followed the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines. Single or un-blinded studies reporting a direct comparison between STR and MTR were eligible for the meta-analysis. Double-blinded studies were excluded due to lack of difference in pill burden between cohorts. The key outcomes of interest included: adherence rates/proportion meeting target, efficacy, safety/tolerability, non-clinical and economic outcomes.

resultsAfter screening 63 full-text articles and posters, 14 studies were eligible for the meta-analysis. The analysis showed that patients taking STR had improved outcomes over those taking MTR. Patients were significantly more adherent regardless of daily dosing frequency (odds ratio [OR]: 1.96, p < 0.001) and were more likely to achieve virological suppression (relative risk [RR]: 1.05, p = 0.002). There was a trend toward a lower discontinuation risk in the STR cohort, together with reported higher therapy satisfaction, better symptom control, improved health status, reduced healthcare resource utilization and demonstrated cost-effectiveness compared to MTR. There were no differences in CD4 cell count increase (at 48 weeks) or safety outcomes.

conclusionsThe findings of this study confirm previously reported preliminary findings of the advantages of STR over MTR for HIV treatment in adherence, therapy continuation, viral suppression, tolerability, quality of life improvement, cost-effectiveness and healthcare resource utilization.

Indexed as

Anti-HIV AgentsAntiretroviral Therapy, Highly ActiveCD4 Lymphocyte CountHIV InfectionsHumansOdds RatioPatient Reported Outcome MeasuresTabletsTime FactorsTreatment OutcomeViral LoadAnti-HIV AgentsTabletsEconomics pharmaceuticalHuman immunodeficiency virusQuality of lifeTreatment adherence and complianceTreatment outcome

Identifiers

PMID30373620
PMCPMC6206661
OpenAlexW2898665378

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.