Evidence map›Paper›PMID 41263314›Full record

ArticleAmerican journal of epidemiology2026

Pregnancy identification method as a source of bias in studies of prenatal exposures using real-world data.

Chase D Latour, Jessie K Edwards, Michele Jonsson Funk, Elizabeth A Suarez, Kim Boggess, Mollie E Wood

Abstract read
In one paragraph

Article in American journal of epidemiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Chase D LatourDepartment of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States.ORCID 0000-0002-9362-2516
Jessie K EdwardsDepartment of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States.ORCID 0000-0002-1741-335X
Michele Jonsson FunkDepartment of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States.ORCID 0000-0002-3756-7540
Elizabeth A SuarezCenter for Pharmacoepidemiology and Treatment Science, Rutgers Institute for Health, Health Care Policy and Aging Research, New Brunswick, NJ, United States.ORCID 0000-0001-8989-7878
Kim BoggessDepartment of Obstetrics and Gynecology, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States.ORCID 0000-0003-0527-5743
Mollie E WoodDepartment of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States.ORCID 0000-0002-9302-2641

Funding

Training Program in Reproductive, Perinatal, and Pediatric EpidemiologyT32HD052468 · NICHD · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Julie L Daniels · 2008 to 2026
$3.8M
AHRQ HHS T32 HS000032National Research Service Award Pre-Doctoral/Post-Doctoral Traineeship from the Agency for Healthcare Research and Quality sponsored by The Cecil G. Sheps Center for Health Services Research, The University of North Carolina at Chapel Hill T32-HS000032NICHD NIH HHS T32 HD052468
6 · The paper itself

Abstract

Researchers typically identify pregnancies in healthcare data based on observed outcomes. This approach misses pregnancies that received prenatal care but whose outcomes were not recorded, potentially inducing selection bias in prenatal effect estimates. Alternatively, prenatal encounters can be used to identify pregnancies with unobserved outcomes, but this requires addressing loss to follow-up (LTFU). We simulated 10 000 000 pregnancies and estimated the total effect of treatment on preeclampsia. Across 36 scenarios, we varied the treatment effect on miscarriage and/or preeclampsia; percent LTFU (5% or 20%); and cause of LTFU: (1) measured covariates, (2) unobserved miscarriage, and (3) both. We created analytic samples to address LTFU-observed deliveries, observed deliveries and miscarriages, and all pregnancies-and estimated treatment effects using nonparametric direct standardization. Risk differences (RDs) and risk ratios (RRs) from the samples were similarly biased when LTFU was due to miscarriage (log-transformed RR bias: -0.12 to 0.33 among observed deliveries, -0.11 to 0.32 among observed deliveries and miscarriages, and -0.11 to 0.32 among all pregnancies). When predictors of LTFU were measured, only estimates among all pregnancies were unbiased (-0.27 to 0.33, -0.29 to 0.03, and -0.02 to 0.01, respectively). While including all pregnancies does not prevent bias, it quantifies the extent of selection, enabling direct assessment of its potential impact on findings.

Indexed as

Lost to Follow-UpPrenatal CareAbortion, SpontaneousBiasFemaleHumansPre-EclampsiaPregnancyPregnancy OutcomeSelection Biasmiscarriagemissing dataperinatal epidemiologypharmacoepidemiologypregnancyprenatal exposureselection bias

Identifiers

PMID41263314
PMCPMC12666898

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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.