Evidence map›Paper›PMID 30579586›Full record

ArticleThe Journal of pediatrics2019

Furosemide Exposure and Prevention of Bronchopulmonary Dysplasia in Premature Infants.

Rachel G Greenberg, Sreepriya Gayam, Destiny Savage, Andrew Tong, Daniel Gorham, Ari Sholomon, Reese H Clark, Daniel K Benjamin, Matthew Laughon, P Brian Smith and 1 more

Registry-linked trialOpen access · greenAbstract readMulticenter Study
In one paragraph

Article in The Journal of pediatrics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04971694 (A Retrospective Chart Review Evaluating the Impact of Steroid, Diuretic, and Fluid Use Practice Trends in Extreme Premature Infants At Risk for Bronchopulmonary Dysplasia), which is not on this map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
4.9field-weighted citation impact, top 4% 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.

NCT04971694 completednot on this mapstarted 2021, after this paper: background citation

A Retrospective Chart Review Evaluating the Impact of Steroid, Diuretic, and Fluid Use Practice Trends in Extreme Premature Infants At Risk for Bronchopulmonary Dysplasia (BPD) At a Single Center Neonatal Intensive Care Unit

TypeobservationalSponsorPediatrixRan2021 to 2024Enrolled175ConditionsBPD - Bronchopulmonary DysplasiaArmsNo interventions or procedures
3 · Its place in the literature

Who cites it

26 citing papers in PubMed, 53 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Predicting pulmonary hypertension in infants with bronchopulmonary dysplasia.Journal of perinatology : official journal of the California Perinatal Association · 2026
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Clinical characteristics of bronchopulmonary dysplasia in very preterm infants.Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2023
    Article
  10. Cardiopulmonary physiological effects of diuretic therapy in preterm infants with chronic pulmonary hypertension.Journal of perinatology : official journal of the California Perinatal Association · 2023
    Article
  11. Article
  12. Online clinical tool to estimate risk of bronchopulmonary dysplasia in extremely preterm infants.Archives of disease in childhood. Fetal and neonatal edition · 2022
    Article
  13. Association between postmenstrual age and furosemide dosing practices in very preterm infants.Journal of perinatology : official journal of the California Perinatal Association · 2022
    Observational
  14. Review
  15. Review
  16. Article
  17. Optimizing respiratory management in preterm infants: a review of adjuvant pharmacotherapies.Journal of perinatology : official journal of the California Perinatal Association · 2021
    Review
  18. Use of diuretics in the neonatal period.Pediatric nephrology (Berlin, Germany) · 2021
    Review
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 1 country.

Rachel G GreenbergDepartment of Pediatrics, Duke University School of Medicine, Durham, NC; Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC. Electronic address: rachel.greenberg@duke.edu.
Sreepriya GayamDuke Clinical Research Institute, Duke University School of Medicine, Durham, NC.
Destiny SavageDuke Clinical Research Institute, Duke University School of Medicine, Durham, NC.
Andrew TongDuke Clinical Research Institute, Duke University School of Medicine, Durham, NC.
Daniel GorhamDuke Clinical Research Institute, Duke University School of Medicine, Durham, NC.
Ari SholomonDuke Clinical Research Institute, Duke University School of Medicine, Durham, NC.
Reese H ClarkPediatrix-Obstetrix Center for Research and Education, Sunrise, FL.
Daniel K BenjaminClemson University, Clemson, SC.
Matthew LaughonDepartment of Pediatrics, The University of North Carolina-Chapel Hill, Chapel Hill, NC.
P Brian SmithDepartment of Pediatrics, Duke University School of Medicine, Durham, NC; Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC.
Best Pharmaceuticals for Children Act—Pediatric Trials Network Steering Committee
Duke University · USClemson University · USUniversity of North Carolina at Chapel Hill · US

Funding

Physiologically-Based Pharmacokinetic Models for Optimal Drug Dosing in ChildrenR01HD076676 · NICHD · DUKE UNIVERSITY · PI COHEN-WOLKOWIEZ, MICHAEL · 2014 to 2017
$2.6M
PATIENT SAFETY RESEARCH DURING NEONATAL CARE (R21)R21HD080606 · NICHD · DUKE UNIVERSITY · PI SMITH, PHILLIP BRIAN · 2015 to 2016
$457k
NIAAA NIH HHS HHSN275201000003CNIAID NIH HHS HHSN272201300017CNIAID NIH HHS HHSN272201300017INIAID NIH HHS HHSN272201500006CNICHD NIH HHS HHSN275201000003INICHD NIH HHS R01 HD076676NICHD NIH HHS R21 HD080606
6 · The paper itself

Abstract

objectiveTo evaluate the association between furosemide exposure and risk of bronchopulmonary dysplasia (BPD). STUDY

designThis retrospective cohort study included infants (2004-2015) born at 23-29 weeks gestational age and 501-1249 g birth weight. We compared the demographic and clinical characteristics of infants exposed and not exposed to furosemide between postnatal day 7 and 36 weeks postmenstrual age. We examined the association between furosemide exposure and 2 outcomes: BPD and BPD or death. We performed multivariable probit regression models that included demographic and clinical variables in addition to 2 instrumental variables: furosemide exposure by discharge year, and furosemide exposure by site.

resultsOf 37 693 included infants, 19 235 (51%) were exposed to furosemide; these infants were more premature and had higher respiratory support. Of 33 760 infants who survived to BPD evaluation, 15 954 (47%) had BPD. An increase in the proportion of furosemide exposure days by 10 percentage points was associated with a decrease in both the incidence of BPD (4.6 percentage points; P = .001), and BPD or death (3.7 percentage points; P = .01).

conclusionsMore days of furosemide exposure between postnatal day 7 and 36 weeks was associated with decreased risk of BPD and a combined outcome of BPD or death.

Indexed as

Birth WeightBronchopulmonary DysplasiaDrug Administration ScheduleFemaleFurosemideGestational AgeHumansInfant, NewbornInfant, PrematureInfant, Premature, DiseasesInfant, Very Low Birth WeightMaleMultivariate AnalysisRetrospective StudiesSodium Potassium Chloride Symporter InhibitorsTreatment OutcomeFurosemideSodium Potassium Chloride Symporter InhibitorsBPDchronic lung diseasediureticneonatepreterm

Identifiers

PMID30579586
PMCPMC6486845
OpenAlexW2905830488

What OpenQuestion holds

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Read underepoch 390

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 OpenQuestion graph.