Evidence map›Paper›PMID 40276874›Full record

ArticlePaediatric and perinatal epidemiology2026

Selection Biases in Perinatal Research: A Comparison of Inverse Probability Weighting, Instrumental Variable and Sibling-Comparison Design.

Basma N Dib, Ellen C Caniglia, Sean Brummel, Roger Shapiro, Sonja A Swanson

Abstract readComparative Study
In one paragraph

Article in Paediatric and perinatal epidemiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

5 authors.

Basma N DibDepartment of Epidemiology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.ORCID https://orcid.org/0009-0000-3359-398X
Ellen C CanigliaPerelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Sean BrummelThe Center for Biostatistics in AIDS Research, Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA.
Roger ShapiroDepartment of Immunology and Infectious Diseases, Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA.
Sonja A SwansonDepartment of Epidemiology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.

Funding

Tsepamo Plus: Expanded Congenital Abnormalities Surveillance with an Emulated Clinical Trial to Evaluate Weight Impact on Birth Outcomes for Newer ART RegimensP01HD107670 · NICHD · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI SHAPIRO, ROGER L · 2021 to 2025
$6.1M
Botswana Birth Outcomes Surveillance ExtensionR01HD095766 · NICHD · HARVARD SCHOOL OF PUBLIC HEALTH · PI SHAPIRO, ROGER L · 2018 to 2022
$3.3M
Iron and folic acid supplementation strategies during pregnancy and adverse pregnancy outcomes in Botswana - Resubmission - 1K01HD100222 · NICHD · UNIVERSITY OF PENNSYLVANIA · PI CANIGLIA, ELLEN CHRISTINA · 2020 to 2024
$632k
National Institute of Child Health and Human DevelopmentNICHD NIH HHS K01 HD100222NICHD NIH HHS P01 HD107670NICHD NIH HHS R01 HD095766
6 · The paper itself

Abstract

backgroundLongitudinal perinatal studies that study the effects of preconception or prenatal treatments on pregnancy outcomes can have inherent forms of selection bias. For example, these studies often restrict analyses to those who had a livebirth, those with a specified gestation duration or those with complete follow-up. These selection factors are often associated with the treatment and have shared causes with the outcome, which may induce bias in estimating causal effects. Though such selection bias can affect all causal inference approaches, what is unknown is how this bias compares in direction and magnitude across different approaches.

objectivesWe conducted a simulation study to assess and compare the direction and magnitude of bias due to censoring across three common analytic approaches: inverse probability weighting (IPW), instrumental variable (IV) and sibling-comparison design.

methodsWe simulated data for various scenarios under two censoring mechanisms (loss to follow-up; and competing events) with a null true causal treatment effect. The simulated scenarios varied in the probability of the censoring mechanism or its strength of association with treatment or outcome. For each scenario, we generated 500 datasets (sample size = 10,000) and calculated the mean bias in risk difference estimates obtained from the three analytic approaches.

resultsAcross all approaches, the proportion of censoring had no specific effect on mean bias. However, increasing the association of censoring with treatment or outcome increased the mean bias. The mean bias in all approaches was generally away from the null in the same direction and often to a similar extent (e.g., 0.5 percentage points away from the null in simulated scenarios with moderate association between treatment and censoring). However, in simulated scenarios with strong association between treatment and censoring, IV analyses were meaningfully more biased than IPW and sibling-comparison design analyses, with mean bias reaching two percentage points.

conclusionsAcross the simulated scenarios, the mean bias in all three approaches was generally away from the null in the same direction and often to a similar extent. Thus, triangulating effect estimates from different analytic approaches in perinatal studies is challenging and may lead to invalid interpretations in the presence of selection processes.

Indexed as

Research DesignComputer SimulationFemaleHumansLongitudinal StudiesPregnancyPregnancy OutcomeProbabilitySelection BiasSiblingscausal inferenceinstrumental variableperinatalselection biassibling‐comparison designtriangulation

Identifiers

PMID40276874
PMCPMC12353985

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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.