Evidence map›Paper›PMID 22546987›Full record

ArticleAIDS (London, England)2012

The effect of efavirenz versus nevirapine-containing regimens on immunologic, virologic and clinical outcomes in a prospective observational study.

Lauren E Cain, Andrew Phillips, Sara Lodi, Caroline Sabin, Loveleen Bansi, Amy Justice, Janet Tate, Roger Logan, James M Robins, Jonathan A C Sterne and 18 more

Abstract readComparative Study
In one paragraph

Article in AIDS (London, England), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 3 pooled it
3.0field-weighted citation impact, top 9% 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

20 citing papers in PubMed, 3 syntheses or guidelines pooled it, 41 citations in OpenAlex.

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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

28 authors at 1 institution in 1 country.

Lauren E Cain
Andrew Phillips
Sara Lodi
Caroline Sabin
Loveleen Bansi
Amy Justice
Janet Tate
Roger Logan
James M Robins
Jonathan A C Sterne
Ard van Sighem
Frank de Wolf
Heiner C Bucher
Luigia Elzi
Giota Touloumi
Georgia Vourli
Anna Esteve
Jordi Casabona
Julia del Amo
Santiago Moreno
Rémonie Seng
Laurence Meyer
Santiago Pérez-Hoyos
Roberto Muga
Sophie Abgrall
Dominique Costagliola
Miguel A Hernán
HIV-CAUSAL Collaboration
Harvard University · US

Funding

Using Coincidence Analysis to Investigate Factors Affecting PrEP Initiation and Continuation in Southern ending the Epidemic CountiesP30MH062294 · NIMH · YALE UNIVERSITY · PI E. Jennifer Edelman · 2001 to 2026
$48.5M
Alcohol Associated Outcomes Among HIV+/- Aging VeteransU10AA013566 · NIAAA · YALE UNIVERSITY · PI JUSTICE, AMY CAROLINE · 2006 to 2010
$12.7M
Alcohol and Multisubstance Use in the Veterans Aging Cohort StudyU01AA020790 · NIAAA · YALE UNIVERSITY · PI JUSTICE, AMY CAROLINE · 2011 to 2020
$7.7M
Analytic Methods for HIV Treatment and Co-Factor EffectsR37AI032475 · NIAID · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI ROBINS, JAMES M · 2005 to 2014
$6.0M
Cardiovascular Disease Mechanisms in HIV Infected and Uninfected VeteransR01HL095136 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI FREIBERG, MATTHEW S, JUSTICE, AMY CAROLINE · 2008 to 2012
$5.6M
Sex Disparities in Overall Response to ART Among HIV Infected IndividualsU24AA020794 · NIAAA · YALE UNIVERSITY · PI JUSTICE, AMY CAROLINE · 2011 to 2020
$5.5M
Longitudinal Studies of HIV-Associated Lung Infections and ComplicationsR01HL090342 · NHLBI · YALE UNIVERSITY · PI CROTHERS, KRISTINA ANNE · 2007 to 2011
$4.0M
Clinical Prediction of Hepatotoxicity & Comparative Hepatic Safety of MedicationsR01HS018372 · AHRQ · UNIVERSITY OF PENNSYLVANIA · PI LO RE, VINCENT · 2010 to 2014
$2.5M
Pooling HIV Cohorts to Inform Clinical DecisionR01AI073127 · NIAID · HARVARD SCHOOL OF PUBLIC HEALTH · PI HERNAN, MIGUEL · 2007 to 2010
$1.5M
Risk, Severity and Outcome of Bacterial Pneumonia in an HIV +/- Veteran CohortRC1HL100347 · NHLBI · UNIVERSITY OF WASHINGTON · PI CROTHERS, KRISTINA ANNE · 2009 to 2010
$998k
AHRQ HHS R01 HS018372AHRQ HHS R01-HS018372Medical Research Council G0700820Medical Research Council G0900274NHLBI NIH HHS R01 HL090342NHLBI NIH HHS R01-HL090342NHLBI NIH HHS R01 HL095136NHLBI NIH HHS R01-HL095136NHLBI NIH HHS RC1 HL100347NHLBI NIH HHS RCI-HL100347NIAAA NIH HHS U01 AA020790NIAAA NIH HHS U01-AA020790NIAAA NIH HHS U10 AA013566NIAAA NIH HHS U10-AA013566NIAAA NIH HHS U24 AA020794NIAAA NIH HHS U24-AA020794NIAID NIH HHS R01 AI073127NIAID NIH HHS R01-AI073127NIAID NIH HHS R37 AI032475NIMH NIH HHS P30 MH062294NIMH NIH HHS P30-MH062294PHS HHS U01-A1069918
6 · The paper itself

Abstract

objectiveTo compare regimens consisting of either efavirenz or nevirapine and two or more nucleoside reverse transcriptase inhibitors (NRTIs) among HIV-infected, antiretroviral-naive, and AIDS-free individuals with respect to clinical, immunologic, and virologic outcomes.

designProspective studies of HIV-infected individuals in Europe and the US included in the HIV-CAUSAL Collaboration.

methodsAntiretroviral therapy-naive and AIDS-free individuals were followed from the time they started an NRTI, efavirenz or nevirapine, classified as following one or both types of regimens at baseline, and censored when they started an ineligible drug or at 6 months if their regimen was not yet complete. We estimated the 'intention-to-treat' effect for nevirapine versus efavirenz regimens on clinical, immunologic, and virologic outcomes. Our models included baseline covariates and adjusted for potential bias introduced by censoring via inverse probability weighting.

resultsA total of 15 336 individuals initiated an efavirenz regimen (274 deaths, 774 AIDS-defining illnesses) and 8129 individuals initiated a nevirapine regimen (203 deaths, 441 AIDS-defining illnesses). The intention-to-treat hazard ratios [95% confidence interval (CI)] for nevirapine versus efavirenz regimens were 1.59 (1.27, 1.98) for death and 1.28 (1.09, 1.50) for AIDS-defining illness. Individuals on nevirapine regimens experienced a smaller 12-month increase in CD4 cell count by 11.49 cells/μl and were 52% more likely to have virologic failure at 12 months as those on efavirenz regimens.

conclusionsOur intention-to-treat estimates are consistent with a lower mortality, a lower incidence of AIDS-defining illness, a larger 12-month increase in CD4 cell count, and a smaller risk of virologic failure at 12 months for efavirenz compared with nevirapine.

Indexed as

AdultAlkynesAnti-HIV AgentsBenzoxazinesCD4 Lymphocyte CountCyclopropanesDrug Administration ScheduleFemaleFollow-Up StudiesHIV-1HIV Reverse TranscriptaseHIV SeropositivityHumansMaleNevirapineProspective StudiesAlkynesAnti-HIV AgentsBenzoxazinesCyclopropanesefavirenzHIV Reverse TranscriptaseNevirapineReverse Transcriptase Inhibitors

Identifiers

PMID22546987
PMCPMC3647467
OpenAlexW1607406129

What OpenQuestion holds

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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.