Evidence map›Paper›PMID 20235836›Full record

Trial reportThe Journal of infectious diseases2010

Long-term impact of acyclovir suppressive therapy on genital and plasma HIV RNA in Tanzanian women: a randomized controlled trial.

Clare Tanton, Helen A Weiss, Mary Rusizoka, Jerome Legoff, John Changalucha, Kathy Baisley, Kokugonza Mugeye, Dean Everett, Laurent Belec, Tim C Clayton and 3 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in The Journal of infectious diseases, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 3 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

22 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
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  4. Trial
  5. Valacyclovir Decreases Plasma HIV-1 RNA in HSV-2 Seronegative Individuals: A Randomized Placebo-Controlled Crossover Trial.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2015
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  12. Does suppressive antiviral therapy for herpes simplex virus prevent transmission in an HIV-positive population? A systematic review.Canada communicable disease report = Releve des maladies transmissibles au Canada · 2016
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  14. Review
  15. Article
  16. Review
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  18. Time to refocus on HSV interventions for HIV prevention?The Journal of infectious diseases · 2011
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Clare TantonLondon School of Hygiene and Tropical Medicine, London, United Kingdom. ctanton@gum.ucl.ac.uk
Helen A Weiss
Mary Rusizoka
Jerome Legoff
John Changalucha
Kathy Baisley
Kokugonza Mugeye
Dean Everett
Laurent Belec
Tim C Clayton
David A Ross
Richard J Hayes
Deborah Watson-Jones

Funding

Medical Research Council G0400456Medical Research Council G0501954Medical Research Council G0700837Wellcome Trust 066688
6 · The paper itself

Abstract

backgroundHerpes simplex virus (HSV) suppressive therapy reduces genital and plasma human immunodeficiency virus type 1 (HIV-1) RNA over periods up to 3 months, but the long-term effect is unknown.

methodsA total of 484 HIV-1 and HSV type 2 seropositive Tanzanian women aged 16-35 years were enrolled in a randomized placebo-controlled trial of acyclovir administered at a dosage of 400 mg twice daily. Cervico-vaginal lavage and blood samples were collected at 6 months, 12 months, and 24 months for quantification of genital and plasma HIV-1 RNA and genital HSV DNA. Primary outcomes were detection and quantity of cervico-vaginal HIV-1 RNA at 6 months.

resultsAt 6 months, there was little difference between the acyclovir and placebo arms for cervico-vaginal HIV-1 RNA detection (88 [ 41 .3%] of 213 vs 84 [ 44 .0%] of 191; odds ratio [OR], 0.90; 95% confidence interval [CI], 0.60-1.33), HSV DNA detection (20 [ 9 .4%] of 213 vs 22 [ 11 .5%] of 191; OR, 0.80; 95% CI, 0.42-1.51), genital HIV or HSV loads, or plasma HIV-1 RNA load. Estimated median adherence was 91%. There was a suggestion of an impact on cervico-vaginal HIV-1 RNA detection among women with estimated adherence 90% (OR, 0.74; 95% CI, 0.50-1.09) when data from all 3 visits were included.

conclusionsAcyclovir administered at a dosage of 400 mg twice daily is unlikely to be a useful long-term intervention to reduce HIV transmission. The lack of effect on HIV may be attributable to suboptimal adherence or treatment regimen.

Indexed as

AcyclovirAdolescentAdultAnti-HIV AgentsAntiviral AgentsDNA, ViralFemaleHerpes GenitalisHerpesvirus 2, HumanHIV-1HIV InfectionsHumansPatient ComplianceRNA, ViralTanzaniaTime FactorsAcyclovirAnti-HIV AgentsAntiviral AgentsDNA, ViralRNA, Viral

Identifiers

PMID20235836
PMCPMC2948536

What OpenQuestion holds

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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.