ArticleActa obstetricia et gynecologica Scandinavica2026
First-trimester aspirin allocation strategies and preterm preeclampsia in women with pregestational diabetes: A national multicenter observational cohort study.
Article in Acta obstetricia et gynecologica Scandinavica, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
11 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
introductionWomen with pregestational diabetes mellitus (PGDM) are at increased risk of preeclampsia (PE) and are commonly prescribed aspirin prophylaxis based on clinical risk factors alone. First-trimester screening algorithms may allow a more individualized allocation of aspirin. We aimed to compare the association between three first-trimester aspirin allocation strategies and the incidence of preterm PE in women with PGDM in routine clinical practice. MATERIAL AND
methodsThis retrospective multicenter observational cohort study included 519 singleton pregnancies with PGDM managed at six tertiary hospitals in Spain between January 2017 and December 2022. Women were classified according to the strategy used to allocate aspirin prophylaxis: clinical risk factor-based prophylaxis, first-trimester algorithm-based screening without placental growth factor (PlGF), or algorithm-based screening including PlGF. The primary outcome was preterm PE (<37 weeks). Secondary outcomes included overall and severe PE, gestational age at delivery, spontaneous preterm birth, birthweight, small-for-gestational-age infants, and neonatal intensive care unit admission. Multivariable regression models were adjusted for prespecified maternal characteristics.
resultsAmong 519 pregnancies, 255 were managed using clinical risk factor-based prophylaxis, 119 using the algorithm without PlGF, and 145 using the algorithm with PlGF. Aspirin was prescribed to 100%, 16.8%, and 28.3% of women, respectively. Preterm PE rates were 4.7%, 5.9%, and 4.2%, respectively. After multivariable adjustment, no statistically significant differences in preterm PE were observed for the algorithm without PlGF (adjusted odds ratio [aOR] 1.89, 95% confidence interval [CI] 0.62-5.45) or with PlGF (aOR 1.33, 95% CI 0.41-3.91) compared with clinical risk factor-based prophylaxis. Secondary maternal and perinatal outcomes were also comparable across groups.
conclusionsIn women with PGDM, algorithm-based aspirin allocation strategies were associated with substantially lower aspirin exposure without evidence of increased preterm PE or adverse perinatal outcomes compared with clinical risk factor-based prophylaxis. However, given the observational design, baseline differences, and limited number of events, the study was not powered to demonstrate equivalence or exclude smaller clinically relevant differences. These findings should therefore be considered exploratory and require confirmation in adequately powered prospective studies.
Indexed as
Identifiers
What Socratic holds
Registered trials
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 Socratic graph.