Evidence map›Paper›PMID 41570998›Full record

Observational studyPediatrics2026

Sleep-Disordered Breathing in Newborns After Myelomeningocele Repair.

Renée A Shellhaas, Fauziya Hassan, Thornton A Mason, Jagruti Anadkat, Ellen Bendel-Stenzel, Stephanie Eyerly-Webb, Cindy K Jon, Robin M Lloyd, Julie S Moldenhauer, Ramesha Papanna and 15 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Pediatrics, 2026. 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
–field-weighted citation impact
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.

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

25 authors.

Renée A ShellhaasDepartment of Neurology, Washington University in St Louis School of Medicine, St Louis, Missouri.
Fauziya HassanDepartment of Pediatrics, University of Michigan, Ann Arbor, Michigan.
Thornton A MasonDivision of Pediatric Neurology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Jagruti AnadkatDivision of Neonatology, Department of Pediatrics, Washington University in St Louis School of Medicine, St Louis, Missouri.
Ellen Bendel-StenzelMayo Clinic Children's Center, Rochester, Minnesota.
Stephanie Eyerly-WebbMidwest Fetal Care Center, Children's Minnesota, Minneapolis, Minnesota.
Cindy K JonDivision of Pulmonary and Sleep Medicine, Department of Pediatrics, UT Health Houston, Houston, Texas.
Robin M LloydMayo Clinic Center for Sleep Medicine, Rochester, Minnesota.
Julie S MoldenhauerNemours Institute for Maternal Fetal Health, Nemours Children's Health, Orlando, Florida.
Ramesha PapannaUTHealth Houston Fetal Institute, UTHealth Houston Fetal Center, Department of Obstetrics and Gynecology, McGovern Medical School at Houston, Texas.
John E PascoeDivision of Pulmonary and Sleep Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio.
Stefanie RiddleDivision of Neonatology, Cincinnati Children's Hospital Medical Center and the Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio.
Regina ReynoldsSection of Neonatology, Department of Pediatrics, University of Colorado School of Medicine, Aurora, Colorado.
Brandon G RocqueDepartment of Neurosurgery, University of Alabama at Birmingham, Children's of Alabama, Birmingham, Alabama.
Narong SimakajornboonDivision of Pulmonary and Sleep Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio.
Marjorie C TreadwellDepartment of Obstetrics & Gynecology, University of Michigan, Ann Arbor, Michigan.
R Bradley TroxlerDivision of Pediatric Pulmonary and Sleep Medicine, University of Alabama at Birmingham, Birmingham, Alabama.
Lydia S YoumansDivision of Neonatology, Department of Pediatrics, McGovern Medical School at UTHealth Houston, Houston, Texas.
Niko A KacirotiDepartment of Pediatrics, University of Michigan, Ann Arbor, Michigan.
Harlan McCafferyDepartment of Pediatrics, University of Michigan, Ann Arbor, Michigan.
Hemant A ParmarDepartment of Radiology, University of Michigan, Ann Arbor, Michigan.
Lora MerleySleep Disorders Center, University of Michigan, Ann Arbor, Michigan.
Stephanie Md RauDepartment of Pediatrics, University of Michigan, Ann Arbor, Michigan.
Ronald D ChervinSleep Disorders Center, University of Michigan, Ann Arbor, Michigan.
John D E BarksDepartment of Pediatrics, University of Michigan, Ann Arbor, Michigan.

Funding

Sleep-disordered breathing in infants with myelomeningoceleR01HL147261 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BARKS, JOHN D, CHERVIN, RONALD D · 2020 to 2024
$3.6M
NHLBI NIH HHS R01 HL147261
6 · The paper itself

Abstract

BACKGROUND &

objectiveSleep-disordered breathing (SDB) may be a remediable contributor to abnormal cognitive outcomes for children with myelomeningocele. We investigated the frequency of SDB among neonates with fetal vs postnatal myelomeningocele repair.

methodsIn this nine-center, prospective, observational study, neonates with myelomeningocele born at more than 30 weeks gestational age underwent a 10-hour bedside polysomnogram at at least 35 weeks postmenstrual age, before hospital discharge. The primary outcome was SDB severity, reflected by the apnea-hypopnea index (AHI; number of respiratory events per hour of sleep). Decisions regarding surgical timing (fetal vs postnatal), technique (open fetal vs fetoscopic approach), and SDB treatment were made by the clinical teams.

resultsAmong 173 infants, 92/173 (53%) had SDB (median AHI 22.5, IQR 12.2-44.2). In unadjusted analysis, AHI was higher among the 90 neonates with fetal repair vs 83 with postnatal surgery (median 29, IQR 14-49, vs 19, IQR 10-36, P = .008). In propensity-adjusted multivariable models, prematurity was independently associated with AHI, whereas surgical timing (fetal vs postnatal) was not. Hindbrain herniation, myelomeningocele level, and clinical need for ventriculoperitoneal shunt did not predict AHI in adjusted models. Supplemental oxygen was commonly prescribed, for 44% of fetal vs 39% of postnatal myelomeningocele repair infants (P = .5).

conclusionsSDB affects more than half of neonates with myelomeningocele. The higher AHI after fetal surgery could stem from the elevated incidence of prematurity in this group. As SDB is treatable and has a potential impact on neurodevelopment, routine screening could become an integral part of a strategy to optimize long-term medical and neurodevelopmental outcomes.

Indexed as

MeningomyelocelePostoperative ComplicationsSleep Apnea SyndromesFemaleHumansInfant, NewbornMalePolysomnographyProspective Studies

Identifiers

PMID41570998
PMCPMC13032742

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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.