Evidence map›Paper›PMID 27029828›Full record

ArticleJournal of the International AIDS Society2016

Survival benefits of antiretroviral therapy in Brazil: a model-based analysis.

Paula M Luz, Michael P Girouard, Beatriz Grinsztejn, Kenneth A Freedberg, Valdilea G Veloso, Elena Losina, Claudio J Struchiner, Rachel L MacLean, Robert A Parker, A David Paltiel and 1 more

Abstract read
In one paragraph

Article in Journal of the International AIDS Society, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Observational
  5. Article
  6. Observational
  7. Article
  8. Article
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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

11 authors.

Paula M LuzThe Instituto Nacional de Infectologia Evandro Chagas, Fundação Oswaldo Cruz, Rio de Janeiro, Brasil; paula.luz@ipec.fiocruz.br.
Michael P GirouardMedical Practice Evaluation Center, Massachusetts General Hospital Boston, MA, USA.
Beatriz GrinsztejnThe Instituto Nacional de Infectologia Evandro Chagas, Fundação Oswaldo Cruz, Rio de Janeiro, Brasil.
Kenneth A FreedbergMedical Practice Evaluation Center, Massachusetts General Hospital Boston, MA, USA.
Valdilea G VelosoThe Instituto Nacional de Infectologia Evandro Chagas, Fundação Oswaldo Cruz, Rio de Janeiro, Brasil.
Elena LosinaMedical Practice Evaluation Center, Massachusetts General Hospital Boston, MA, USA.
Claudio J StruchinerThe Instituto Nacional de Infectologia Evandro Chagas, Fundação Oswaldo Cruz, Rio de Janeiro, Brasil.
Rachel L MacLeanMedical Practice Evaluation Center, Massachusetts General Hospital Boston, MA, USA.
Robert A ParkerMedical Practice Evaluation Center, Massachusetts General Hospital Boston, MA, USA.
A David PaltielDepartment of Health Policy and Management, Yale School of Public Health, New Haven, CT, USA.
Rochelle P WalenskyMedical Practice Evaluation Center, Massachusetts General Hospital Boston, MA, USA.

Funding

The FIOCRUZ Therapeutic and Prevention HIV/AIDS Clinical Trials Unit (FioTrials)UM1AI069476 · NIAID · FUNDACAO OSWALDO CRUZ · PI BEATRIZ GRINSZTEJN · 2012 to 2026
$26.3M
Optimizing HIV Care in Less Developed CountriesR01AI058736 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI Kenneth Alan Freedberg, Emily Parker Hyle · 2004 to 2026
$21.5M
NIAID NIH HHS R01 AI058736NIAID NIH HHS UM1 AI069476
6 · The paper itself

Abstract

objectiveIn Brazil, universal provision of antiretroviral therapy (ART) has been guaranteed free of charge to eligible HIV-positive patients since December 1996. We sought to quantify the survival benefits of ART attributable to this programme.

methodsWe used a previously published microsimulation model of HIV disease and treatment (CEPAC-International) and data from Brazil to estimate life expectancy increase for HIV-positive patients initiating ART in Brazil. We divided the period of 1997 to 2014 into six eras reflecting increased drug regimen efficacy, regimen availability and era-specific mean CD4 count at ART initiation. Patients were simulated first without ART and then with ART. The 2014-censored and lifetime survival benefits attributable to ART in each era were calculated as the product of the number of patients initiating ART in a given era and the increase in life expectancy attributable to ART in that era.

resultsIn total, we estimated that 598,741 individuals initiated ART. Projected life expectancy increased from 2.7, 3.3, 4.1, 4.9, 5.5 and 7.1 years without ART to 11.0, 17.5, 20.7, 23.0, 25.3, and 27.0 years with ART in Eras 1 through 6, respectively. Of the total projected lifetime survival benefit of 9.3 million life-years, 16% (or 1.5 million life-years) has been realized as of December 2014.

conclusionsProvision of ART through a national programme has led to dramatic survival benefits in Brazil, the majority of which are still to be realized. Improvements in initial and subsequent ART regimens and higher CD4 counts at ART initiation have contributed to these increasing benefits.

Indexed as

Life ExpectancyAdultAnti-HIV AgentsBrazilCD4 Lymphocyte CountHIV InfectionsHumansModels, TheoreticalAnti-HIV AgentsBrazilhighly active antiretroviral therapyHIVLatin Americamodellingsurvival

Identifiers

PMID27029828
PMCPMC4814587

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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.