Evidence map›Paper›PMID 37430233›Full record

ArticleBMC pediatrics2023

Effect of reduced versus usual lipid emulsion dosing on bilirubin neurotoxicity and neurodevelopmental impairment in extremely preterm infants: study protocol for a randomized controlled trial.

Lindsay F Holzapfel, Cody Arnold, Jon E Tyson, Steven M Shapiro, Eric W Reynolds, Claudia Pedroza, Emily K Stephens, Alan Kleinfeld, Andrew H Huber, Matthew A Rysavy and 2 more

Registry-linked trialOpen access · goldAbstract readClinical Trial Protocol
In one paragraph

Article in BMC pediatrics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04584983 (Bilirubin Neurotoxicity), which is not on this map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.2field-weighted citation impact, top 19% 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.

NCT04584983 phase2active not recruitingnot on this map

Bilirubin Neurotoxicity (BN) and Neurodevelopmental Impairment (NDI) in Extremely Preterm (EP) Infants: Avoidable by Reducing the Usual Intravenous Lipid (UL) Administration

TypeinterventionalSponsorThe University of Texas Health Science Center, HoustonRan2021 to 2026Enrolled134ConditionsBilirubin EncephalopathyArmsusual prescribed intralipid (UL) regimen, restricted prescribed intralipid (RL) regimen
3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Trial
  2. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 5 institutions in 1 country.

Lindsay F HolzapfelDivision of Neonatology, McGovern Medical School at the University of Texas Health Science Center at Houston, 6431 Fannin, MSB 3.236, Houston, TX, 77030, US. lindsay.n.fleig@uth.tmc.edu.
Cody ArnoldDepartment of Pediatrics, Division of Neonatal and Developmental Medicine, Stanford University, Palo Alta, CA, US.
Jon E TysonDivision of Neonatology, McGovern Medical School at the University of Texas Health Science Center at Houston, 6431 Fannin,MSB 2.106, Houston, TX, 77030, US.
Steven M ShapiroDepartment of Neurology, University of Kansas Medical Center, 3901 Rainbow Blvd, MS 2012-SSB, Kansas City, KS, 66160, US.
Eric W ReynoldsDivision of Neonatology, McGovern Medical School at the University of Texas Health Science Center at Houston, 6431 Fannin,MSB 3.254, Houston, TX, 77030, US.
Claudia PedrozaCenter for Evidence Based Medicine, McGovern Medical School at the University of Texas Health Science Center at Houston, 6431 Fannin, MSB 2.106, Houston, TX, 77030, US.
Emily K StephensNeonatal Research Network, McGovern Medical School at the University of Texas Health Science Center at Houston, 6431 Fannin, MSB 3.252, Houston, TX, 77030, US.
Alan KleinfeldFluoresprobe Sciences, 3550 General Atomics Ct, B-2-118, San Diego, CA, 92121, US.
Andrew H HuberFluoresprobe Sciences, 3550 General Atomics Ct, B-2-118, San Diego, CA, 92121, US.
Matthew A RysavyDivision of Neonatology, McGovern Medical School at the University of Texas Health Science Center at Houston, 6431 Fannin,MSB 2.106, Houston, TX, 77030, US.
Maria Del Mar Romero LopezDivision of Neonatology, McGovern Medical School at the University of Texas Health Science Center at Houston, 6431 Fannin, MSB 3.236, Houston, TX, 77030, US.
Amir M KhanDivision of Neonatology, McGovern Medical School at the University of Texas Health Science Center at Houston, 6431 Fannin, MSB 3.236, Houston, TX, 77030, US.
The University of Texas Health Science Center at Houston · USGeneral Atomics (United States) · USResearch Network (United States) · USStanford University · USUniversity of Kansas Medical Center · US

Funding

Institutional Career Development CoreKL2TR003168 · NCATS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MILLER, CHARLES C · 2019 to 2023
$4.9M
NCATS NIH HHS KL2 TR003168NICHD NIH HHS L40 HD109887
6 · The paper itself

Abstract

backgroundBilirubin neurotoxicity (BN) occurs in premature infants at lower total serum bilirubin levels than term infants and causes neurodevelopmental impairment. Usual dose lipid infusions in preterm infants may increase free fatty acids sufficiently to cause bilirubin displacement from albumin, increasing passage of unbound bilirubin (UB) into the brain leading to BN and neurodevelopmental impairment not reliably identifiable in infancy. These risks may be influenced by whether cycled or continuous phototherapy is used to control bilirubin levels.

objectiveTo assess differences in wave V latency measured by brainstem auditory evoked responses (BAER) at 34-36 weeks gestational age in infants born ≤ 750 g or < 27 weeks' gestational age randomized to receive usual or reduced dose lipid emulsion (half of the usual dose) irrespective of whether cycled or continuous phototherapy is administered.

methodsPilot factorial randomized controlled trial (RCT) of lipid dosing (usual and reduced) with treatment groups balanced between cycled or continuous phototherapy assignment. Eligible infants are born at ≤ 750 g or < 27 weeks' gestational age enrolled in the NICHD Neonatal Research Network RCT of cycled or continuous phototherapy. Infants will randomize 1:1 to reduced or usual dose lipid assignment during the first 2 weeks after birth and stratified by phototherapy assignment. Free fatty acids and UB will be measured daily using a novel probe. BAER testing will be performed at 34-36 weeks postmenstrual age or prior to discharge. Blinded neurodevelopmental assessments will be performed at 22-26 months. Intention-to-treat analyses will be performed with generalized linear mixed models with lipid dose and phototherapy assignments as random effects covariates, and assessment for interactions. Bayesian analyses will be performed as a secondary analysis. DISCUSSION: Pragmatic trials are needed to evaluate whether lipid emulsion dosing modifies the effect of phototherapy on BN. This factorial design presents a unique opportunity to evaluate both therapies and their interaction. This study aims to address basic controversial questions about the relationships between lipid administration, free fatty acids, UB, and BN. Findings suggesting a reduced lipid dose can diminish the risk of BN would support the need for a large multicenter RCT of reduced versus usual lipid dosing.

trial registrationClinical Trials.gov, NCT04584983, Registered 14 October 2020, https://clinicaltrials.gov/ct2/show/NCT04584983 Protocol version: Version 3.2 (10/5/2022).

Indexed as

BilirubinInfant, Extremely PrematureEmulsionsFatty Acids, NonesterifiedHumansInfantInfant, NewbornMulticenter Studies as TopicPhototherapyRandomized Controlled Trials as TopicBilirubinEmulsionsFatty Acids, NonesterifiedBilirubin neurotoxicityBrainstem auditory evoked responsesExtremely preterm infantsLipid emulsionsNeurodevelopmental impairmentPhototherapyRandomized controlled trial

Identifiers

PMID37430233
PMCPMC10332033
OpenAlexW4383737602

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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.