Evidence map›Paper›PMID 34167497›Full record

ArticleBMC pregnancy and childbirth2021

Do maternal demographics and prenatal history impact the efficacy of betamethasone therapy for threatened preterm labor?

Mary T Kinney, Sara K Quinney, Hayley K Trussell, Larissa L Silva, Sherrine A Ibrahim, David M Haas

Open access · goldAbstract read
In one paragraph

Article in BMC pregnancy and childbirth, 2021. 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
0.3field-weighted citation impact, top 41% of its field
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, 2 citations in OpenAlex.

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 at 2 institutions in 1 country.

Mary T KinneyDivision of Clinical Pharmacology, Indiana University School of Medicine, Indianapolis, USA.
Sara K QuinneyDivision of Clinical Pharmacology, Indiana University School of Medicine, Indianapolis, USA.
Hayley K TrussellDepartment of Obstetrics and Gynecology, Indiana University School of Medicine, 550 N. University Blvd, UH 2440, IN, 46202, Indianapolis, USA.
Larissa L SilvaDivision of Clinical Pharmacology, Indiana University School of Medicine, Indianapolis, USA.
Sherrine A IbrahimDepartment of Obstetrics and Gynecology, Indiana University School of Medicine, 550 N. University Blvd, UH 2440, IN, 46202, Indianapolis, USA.
David M HaasDivision of Clinical Pharmacology, Indiana University School of Medicine, Indianapolis, USA. dahaas@iupui.edu.
Indiana University – Purdue University Indianapolis · USIndiana University School of Medicine

Funding

Quality Assurance and Quality Control Project Management: Improving Submissions and Study Conduct in the Human Subjects Research Prior Approval ProcessUL1TR002529 · NCATS · INDIANA UNIVERSITY INDIANAPOLIS · PI MOE, SHARON M, WIEHE, SARAH ELIZABETH · 2018 to 2022
$27.2M
Pharmacokinetics and modeling of betamethasone therapy in threatened preterm birthR01HD088014 · NICHD · INDIANA UNIVERSITY INDIANAPOLIS · PI HAAS, DAVID M. · 2016 to 2020
$2.6M
Eunice Kennedy Shriver National Institute of Child Health and Human Development R01HD088014NIH HHS UL1TR002529
6 · The paper itself

Abstract

backgroundBetamethasone (BMZ) is used to accelerate fetal lung maturation in women with threatened preterm birth, but its efficacy is variable and limited by the lack of patient individualization in its dosing and administration. To determine sources of variability and potential opportunities for individualization of therapy, the objective of this study was to evaluate maternal factors associated with development of neonatal respiratory distress syndrome (RDS) in a cohort of women who received betamethasone.

methodsThis study prospectively enrolled women, gestational ages 23-34 weeks, who received betamethasone for threatened preterm birth. Maternal demographics, prenatal history, and neonatal outcomes were abstracted from hospital records. RDS was the primary outcome. Associations between RDS diagnosis and maternal demographics, prenatal history, and betamethasone dosing were evaluated in a case-control analysis and multivariable regression adjusted for gestational age at delivery. Secondary analyses limited the cohort to women who delivered within 1 or 2 weeks of betamethasone dosing.

resultsOf 209 deliveries, 90 (43 %) resulted in neonatal RDS. Within the overall cohort and controlling for gestational age at birth, RDS was only associated with cesarean births compared to vaginal births (adjusted OR 1.17 [1.06-1.29]). Route of delivery was also the only significant factor related to RDS in the 83 neonates delivered within 7 days of BMZ dosing. However, among 101 deliveries within 14 days of betamethasone dosing and controlling for gestational age at birth, women who experienced preterm premature rupture of membranes (PPROM) had lower RDS rates than those without PPROM (57.9 % vs. 80.2 %, adjusted OR 0.81 [0.67-0.99]). Maternal age, BMI, race, and ethnicity were not associated with RDS in the regression models.

conclusionsOf maternal characteristics analyzed, only delivery by cesarean was associated with neonatal RDS after antenatal betamethasone use.

Indexed as

AdultBetamethasoneCase-Control StudiesDelivery, ObstetricDemographyFemaleGestational AgeHumansInfant, NewbornObstetric Labor, PrematurePregnancyPremature BirthPremature Rupture of Fetal MembranesPrenatal CareProspective StudiesRegression AnalysisBetamethasoneAntenatal corticosteroidsBetamethasoneCesareanPreterm birthRespiratory distress syndrome (RDS)

Identifiers

PMID34167497
PMCPMC8228510
OpenAlexW3175667778

What OpenQuestion holds

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LicenceCC BY
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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.