Evidence map›Paper›PMID 38838873›Full record

ArticleAnnals of epidemiology2024

Semiparametric g-computation for survival outcomes with time-fixed exposures: An illustration.

Jessie K Edwards, Stephen R Cole, Paul N Zivich, Michael G Hudgens, Tiffany L Breger, Bonnie E Shook-Sa

Abstract read
In one paragraph

Article in Annals of epidemiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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

3 citing papers in PubMed.

  1. Article
  2. An Improved Pooled Logistic Regression Implementation.Epidemiology (Cambridge, Mass.) · 2026
    Article
  3. Article
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

6 authors.

Jessie K EdwardsDepartment of Epidemiology, University of North Carolina at Chapel Hill, USA; Carolina Population Center, University of North Carolina at Chapel Hill, USA. Electronic address: jessedwards@unc.edu.
Stephen R ColeDepartment of Epidemiology, University of North Carolina at Chapel Hill, USA.
Paul N ZivichSchool of Medicine, University of North Carolina at Chapel Hill, USA.
Michael G HudgensDepartment of Biostatistics, University of North Carolina at Chapel Hill, USA.
Tiffany L BregerSchool of Medicine, University of North Carolina at Chapel Hill, USA.
Bonnie E Shook-SaDepartment of Biostatistics, University of North Carolina at Chapel Hill, USA.

Funding

Virology, Immunology, and Microbiology CoreP30AI050410 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DAVID M. MARGOLIS · 2001 to 2026
$76.9M
UNC MACS/WIHS Combined Cohort Study Clinical Research SiteU01HL146194 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Michael Bradley Drummond, Michelle Floris-Moore · 2019 to 2026
$23.2M
Improved analysis of experiments and observational studies in HIVR01AI157758 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Stephen R Cole, Jessie Edwards · 2020 to 2026
$5.0M
NHLBI NIH HHS U01 HL146194NIAID NIH HHS P30 AI050410NIAID NIH HHS R01 AI157758
6 · The paper itself

Abstract

purposeGeneralized (g-) computation is a useful tool for causal inference in epidemiology. However, in settings when the outcome is a survival time subject to right censoring, the standard pooled logistic regression approach to g-computation requires arbitrary discretization of time, parametric modeling of the baseline hazard function, and the need to expand one's dataset. We illustrate a semiparametric Breslow estimator for g-computation with time-fixed treatments and survival outcomes that is not subject to these limitations.

methodsWe compare performance of the Breslow g-computation estimator to the pooled logistic g-computation estimator in simulations and illustrate both approaches to estimate the effect of a 3-drug vs 2-drug antiretroviral therapy regimen among people with HIV.

resultsIn simulations, both approaches performed well at the end of follow-up. The pooled logistic approach was biased at times between the endpoints of the discrete time intervals used, while the Breslow approach was not. In the example, both approaches estimated a 1-year risk difference of about 6 % in favor of the 3-drug regimen, but the shape of the survival curves differed.

conclusionsThe Breslow g-computation estimator of counterfactual risk functions does not rely on strong parametric assumptions about the time-to-event distribution or onerous dataset expansions.

Indexed as

HIV InfectionsAnti-HIV AgentsComputer SimulationHumansLogistic ModelsModels, StatisticalSurvival AnalysisTime FactorsAnti-HIV AgentsAntiretroviral therapyCausationG-computationHIVPharmacoepidemiologySurvival Analysis

Identifiers

PMID38838873
PMCPMC11283356

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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.