Evidence map›Paper›PMID 29112073›Full record

ArticleAIDS (London, England)2018

Benefits and risks of rapid initiation of antiretroviral therapy.

Nathan Ford, Chantal Migone, Alexandra Calmy, Bernhard Kerschberger, Steve Kanters, Sabin Nsanzimana, Edward J Mills, Graeme Meintjes, Marco Vitoria, Meg Doherty and 1 more

Abstract read
In one paragraph

Article in AIDS (London, England), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 171 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
171citing papers in PubMed, 7 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

171 citing papers in PubMed, 7 syntheses or guidelines pooled it.

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  6. Rapid initiation of antiretroviral therapy for people living with HIV.The Cochrane database of systematic reviews · 2019
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111 more citing papers are in PubMed but not listed here.

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

11 authors.

Nathan FordDepartment of HIV, World Health Organization, Geneva, Switzerland.
Chantal MigoneDepartment of HIV, World Health Organization, Geneva, Switzerland.
Alexandra CalmyHIV Unit, Division of Infectious Diseases, Geneva University Hospital, Geneva, Switzerland.
Bernhard KerschbergerMédecins sans Frontières, Mbabane, Swaziland.
Steve KantersSchool of Population and Public Health, University of British Columbia, Vancouver, British Columbia, Canada.
Sabin NsanzimanaHIV/AIDS and STIs Diseases Division, Rwanda Biomedical Centre, Kigali, Rwanda.
Edward J MillsUniversity of Rwanda, Kigali, Rwanda.
Graeme MeintjesDepartment of Medicine, University of Cape Town Health Sciences Faculty, Cape Town, South Africa.
Marco VitoriaDepartment of HIV, World Health Organization, Geneva, Switzerland.
Meg DohertyDepartment of HIV, World Health Organization, Geneva, Switzerland.
Zara ShubberDepartment of Infectious Disease Epidemiology, Imperial College London, London, UK.

Funding

World Health Organization 001
6 · The paper itself

Abstract

backgroundRecent attention has focused on the question of how quickly antiretroviral therapy (ART) should be started once HIV diagnosis is confirmed. We assessed whether rapid ART initiation improves patient outcomes.

methodsWe searched five databases from inception up to August 2017. Rapid ART initiation was defined as initiation within 14 days of HIV diagnosis. Data were pooled using random effects meta-analysis.

resultsAcross the randomized trials, ART start on the same day increased viral suppression at 12 months [three trials: relative risk (RR) 1.17, 95% confidence interval (CI) 1.07-1.27], retention in care at 12 months (RR 1.11, 95% CI 0.99-1.26), and the likelihood of starting ART within 90 days (four trials: RR 1.35, 95% CI 1.13-1.62) and 12 months after eligibility was established (three trials: RR 1.17, 95% CI 1.07-1.27). There was a nonsignificant trend toward reduced mortality (three trials: RR 0.53, 95% CI 0.24-1.08), as well as reduced loss to follow-up at 12 months (2 trials: RR 0.66, 95% CI 0.42-1.04). In the observational studies, offering accelerated ART initiation resulted in a greater likelihood of having started ART within 3 months (two studies: RR 1.53, 95% CI 1.11-2.10). There was a trend toward an increased risk of being lost to follow-up at 6 months (three studies: RR 1.85, 95% CI 0.96-3.55).

conclusionAccelerated ART initiation can lead to improved clinical outcomes and is likely to be of particular benefit in those settings where extensive patient preparation prior to starting ART results in long delays. These findings informed a WHO recommendation supporting accelerated ART initiation, including same day ART start.

Indexed as

Secondary PreventionAnti-Retroviral AgentsAntiretroviral Therapy, Highly ActiveHIV InfectionsHumansRisk AssessmentTime FactorsTreatment OutcomeAnti-Retroviral Agents

Identifiers

PMID29112073
PMCPMC5732637

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.