Evidence map›Paper›PMID 41545956›Full record

ArticleBMC pregnancy and childbirth2026

Impact of doppler reference chart selection on risk stratification in fetal growth restriction.

Misgav Rottenstreich, Dahlia Klein, Bryon DeFrance, Jon Fr Barrett, Eran Ashwal

Abstract read
In one paragraph

Article in BMC pregnancy and childbirth, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Misgav RottenstreichDepartment of Obstetrics & Gynecology, Shaare Zedek Medical Center, affiliated with the Hebrew University School of Medicine, 12 Bayit Street, Jerusalem, 91031, Israel. misgavr@gmail.com.
Dahlia KleinFaculty of Medicine, Université de Montréal, Québec, Canada.
Bryon DeFranceDivision of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, McMaster University, Hamilton, Ontario, Canada.
Jon Fr BarrettDivision of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, McMaster University, Hamilton, Ontario, Canada.
Eran AshwalDivision of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, McMaster University, Hamilton, Ontario, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDoppler studies play a crucial role in evaluating fetuses with impaired fetal growth.

objectiveWe aimed to assess the clinical variability of various published Doppler reference ranges for umbilical artery (UA) pulsatility index (PI), middle cerebral artery (MCA) PI, and cerebroplacental ratio (CPR) in pregnancies complicated by impaired fetal growth, and their association with adverse perinatal outcomes. STUDY

designThis retrospective cohort study included all singleton pregnancies with estimated fetal weight (EFW) and/or abdominal circumference (AC) below the 10th percentile for gestational age (2017-2022). Eligible cases had a concurrent sampling of UA-PI, MCA-PI, and CPR within 14 days of birth. Abnormal fetal Doppler was defined using clinically relevant cut-offs for gestational age: UA-PI > 95th percentile, MCA-PI < 5th percentile, and CPR < 5th percentile. The primary outcome was a composite of adverse perinatal outcomes The association between published Doppler thresholds and adverse perinatal was assessed using univariate and multivariable logistic regression analyses.

resultsThe cohort included 947 patients, of whom 438 (46.3%) experienced adverse perinatal outcomes, while 509 (53.7%) had normal outcomes. The predictive performance for adverse perinatal outcomes of various published Doppler reference values showed variability. Sensitivity ranged from 58.5% to 67.4% for UA-PI, 55.4% to 61.4% for MCA-PI, and 52.1% to 58.8% for CPR. Corresponding specificities ranged from 56.0% to 60.0%, 58.0% to 60.7%, and 61.4% to 61.9%, respectively. After multivariate analysis, which controlled for relevant covariates, strong associations were demonstrated between abnormal UA-PI, MCA-PI, and CPR Dopplers and adverse perinatal outcomes in preterm deliveries. Baschat’s reference chart for CPR was the only one that was found to have an association with adverse perinatal outcomes in term pregnancies.

conclusionChoosing a Doppler reference chart may result in significant variation in the clinical management of pregnancies complicated by impaired fetal growth.

Indexed as

Fetal Growth RetardationUltrasonography, DopplerUltrasonography, PrenatalUmbilical ArteriesAdultFemaleGestational AgeHumansInfant, NewbornMiddle Cerebral ArteryPregnancyPregnancy OutcomePulsatile FlowReference ValuesRetrospective StudiesRisk AssessmentDoppler measurementDoppler ultrasoundFetal growth restriction (FGR)Middle cerebral artery pulsatility index (MCA-PI), cerebroplacental ratio (CPR) small-for-gestational-age (SGA)Perinatal outcomesUmbilical artery pulsatility index (UA-PI)

Identifiers

PMID41545956
PMCPMC12934067

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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.