Evidence map›Paper›PMID 27203134›Full record

ArticleJournal of neurosurgery. Pediatrics2016

Diffusion tensor imaging study of pediatric patients with congenital hydrocephalus: 1-year postsurgical outcomes.

Francesco T Mangano, Mekibib Altaye, Robert C McKinstry, Joshua S Shimony, Stephanie K Powell, Jannel M Phillips, Holly Barnard, David D Limbrick, Scott K Holland, Blaise V Jones and 6 more

Open access · bronzeAbstract readMulticenter Study
In one paragraph

Article in Journal of neurosurgery. Pediatrics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
5.1field-weighted citation impact, top 5% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

  1. Neurodevelopmental outcomes after ventriculoperitoneal shunt placement in children with non-infectious hydrocephalus: a meta-analysis.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2021
    Pooled it
  2. Article
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  10. Not all ventriculomegaly is created equal: diagnostic overview of fetal, neonatal and pediatric ventriculomegaly.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2020
    Review
  11. Abnormal anisotropic diffusion properties in pediatric myelomeningocele patients treated with fetal surgery: an initial DTI study.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2020
    Article
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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

16 authors at 7 institutions in 2 countries.

Francesco T ManganoDivision of Pediatric Neurosurgery.
Mekibib AltayeDivision of Biostatistics and Epidemiology.
Robert C McKinstryMallinckrodt Institute of Radiology.
Joshua S ShimonyMallinckrodt Institute of Radiology.
Stephanie K PowellDepartment of Neurology, and.
Jannel M PhillipsDivision of Developmental and Behavioral Pediatrics-Psychology, Cincinnati Children's Hospital Medical Center, Cincinnati;
Holly BarnardDivision of Developmental and Behavioral Pediatrics-Psychology, Cincinnati Children's Hospital Medical Center, Cincinnati;
David D LimbrickDepartment of Neurological Surgery.
Scott K HollandDepartment of Radiology, and.
Blaise V JonesDepartment of Radiology, and.
Jonathan DoddDepartment of Neurology, and.
Sarah SimpsonDepartment of Radiology, and.
Deanna MercerDepartment of Neurological Surgery.
Akila RajagopalDepartment of Radiology, and.
Sarah BidwellDepartment of Radiology, and.
Weihong YuanDepartment of Radiology, and.
University of Cincinnati Medical Center · USSt. Louis Children's Hospital · USWashington University in St. Louis · USCancer Research And Biostatistics · USCincinnati Children's Hospital Medical Center · USMallinckrodt (United States) · USNeurological Surgery · US

Funding

Washington University Intellectual and Developmental Disabilities Research Center-Administrative Down Syndrome SupplementU54HD087011 · NICHD · WASHINGTON UNIVERSITY · PI CONSTANTINO, JOHN N. · 2015 to 2019
$7.1M
Longitudinal DTI study in Children Treated for Congenital HydrocephalusR01NS066932 · NINDS · CINCINNATI CHILDRENS HOSP MED CTR · PI MANGANO, FRANCESCO, YUAN, WEIHONG · 2009 to 2012
$1.8M
NICHD NIH HHS U54 HD087011NINDS NIH HHS R01 NS066932
6 · The paper itself

Abstract

OBJECTIVE The purpose of this study was to investigate white matter (WM) structural abnormalities using diffusion tensor imaging (DTI) in children with hydrocephalus before CSF diversionary surgery (including ventriculoperitoneal shunt insertion and endoscopic third ventriculostomy) and during the course of recovery after surgery in association with neuropsychological and behavioral outcome. METHODS This prospective study included 54 pediatric patients with congenital hydrocephalus (21 female, 33 male; age range 0.03-194.5 months) who underwent surgery and 64 normal controls (30 female, 34 male; age range 0.30-197.75 months). DTI and neurodevelopmental outcome data were collected once in the control group and 3 times (preoperatively and at 3 and 12 months postoperatively) in the patients with hydrocephalus. DTI measures, including fractional anisotropy (FA), mean diffusivity (MD), axial diffusivity (AD), and radial diffusivity (RD) values were extracted from the genu of the corpus callosum (gCC) and the posterior limb of internal capsule (PLIC). Group analysis was performed first cross-sectionally to quantify DTI abnormalities at 3 time points by comparing the data obtained in the hydrocephalus group for each of the 3 time points to data obtained in the controls. Longitudinal comparisons were conducted pairwise between different time points in patients whose data were acquired at multiple time points. Neurodevelopmental data were collected and analyzed using the Adaptive Behavior Assessment System, Second Edition, and the Bayley Scales of Infant Development, Third Edition. Correlation analyses were performed between DTI and behavioral measures. RESULTS Significant DTI abnormalities were found in the hydrocephalus patients in both the gCC (lower FA and higher MD, AD, and RD) and the PLIC (higher FA, lower AD and RD) before surgery. The DTI measures in the gCC remained mostly abnormal at 3 and 12 months after surgery. The DTI abnormalities in the PLIC were significant in FA and AD at 3 months after surgery but did not persist when tested at 12 months after surgery. Significant longitudinal DTI changes in the patients with hydrocephalus were found in the gCC when findings at 3 and 12 months after surgery were compared. In the PLIC, trend-level longitudinal changes were observed between preoperative findings and 3-month postoperative findings, as well as between 3- and 12-month postoperative findings. Significant correlation between DTI and developmental outcome was found at all 3 time points. Notably, a significant correlation was found between DTI in the PLIC at 3 months after surgery and developmental outcome at 12 months after surgery. CONCLUSIONS The data showed significant WM abnormality based on DTI in both the gCC and the PLIC in patients with congenital hydrocephalus before surgery, and the abnormalities persisted in both the gCC and the PLIC at 3 months after surgery. The DTI values remained significantly abnormal in the gCC at 12 months after surgery. Longitudinal analysis showed signs of recovery in both WM structures between different time points. Combined with the significant correlation found between DTI and neuropsychological measures, the findings of this study suggest that DTI can serve as a sensitive imaging biomarker for underlying neuroanatomical changes and postsurgical developmental outcome and even as a predictor for future outcomes.

Indexed as

Diffusion Magnetic Resonance ImagingDiffusion Tensor ImagingAdolescentBrainChildChild, PreschoolCross-Sectional StudiesFemaleFollow-Up StudiesHumansHydrocephalusInfantInfant, NewbornLongitudinal StudiesMaleNeuroendoscopyABAS-II = Adaptive Behavior Assessment System, Second EditionAD = axial diffusivityBayley III = Bayley Scale of Infant Development, Third EditionCCHMC = Cincinnati Children's Hospital Medical CenterDTIDTI = diffusion tensor imagingFA = fractional anisotropyFDR = false discovery rateFOHR = frontal and occipital horn ratioGAC = general adaptive compositegCC = genu of corpus callosumhydrocephalusICP = intracranial pressureMD = mean diffusivityoutcomePLIC = posterior limb of internal capsulepostsurgeryRD = radial diffusivityROI = region of interestSLCH/WashU = St. Louis Children's Hospital and Washington Universitywhite matter injuryWM = white matter

Identifiers

PMID27203134
PMCPMC5035704
OpenAlexW2403187282

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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.