Evidence map›Paper›PMID 33404719›Full record

ArticleChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2021

Neurodevelopmental outcome of children born with an isolated atretic cephalocele.

Itay Tokatly Latzer, Jonathan Roth, Shlomi Constantini, Gustavo Malinger, Alina Weissmann-Brenner, Liat Ben-Sira, Aviva Fattal-Valevski, Hadas Meirson

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Article in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
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

8 authors at 1 institution in 1 country.

Itay Tokatly LatzerPediatric Neurology Institute, The Dana-Dwek Children's Hospital, Tel Aviv Sourasky Medical Center, 6423906, Tel Aviv, Israel. itaylatzer@gmail.com.ORCID 0000-0003-3132-1379
Jonathan RothSackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Shlomi ConstantiniSackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Gustavo MalingerSackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Alina Weissmann-BrennerSackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Liat Ben-SiraSackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Aviva Fattal-ValevskiPediatric Neurology Institute, The Dana-Dwek Children's Hospital, Tel Aviv Sourasky Medical Center, 6423906, Tel Aviv, Israel.
Hadas MeirsonPediatric Neurology Institute, The Dana-Dwek Children's Hospital, Tel Aviv Sourasky Medical Center, 6423906, Tel Aviv, Israel.
Tel Aviv University · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe existing data on the neurodevelopmental outcome of children born with an isolated atretic cephalocele (IAC) are scant. We aimed to expand upon these data by describing our experience with affected children, as well as assist parents and clinicians in deciding how to proceed when an IAC is diagnosed prenatally.

methodsA follow-up study was conducted on nine children who were born with an IAC. Evaluations were performed by pediatric neurologists and child development specialists. Developmental outcomes were based on a global development evaluation that assessed gross and fine motor skills, receptive and expressive language levels, activities of daily living, communication skills, and social domains. Adaptive skills were estimated by the Adaptive Behavior Assessment System, Second Edition.

resultsNone of the nine children (median age 4 years and 6 months) had abnormal findings on neurological examination. Six children had age-appropriate developmental milestones, two had a mild motor delay, and one had mild expressive language delay (catchup was achieved by all of the latter three by ~ 3.5 years of age). The mean general adaptive composite score was 105 ± 11.7 (normal = 100). None of the children had behavioral, social, or communication problems.

conclusionsChildren diagnosed with an IAC with/without a falcine sinus and devoid of coexisting intracranial abnormalities seem to have a normal neurodevelopmental outcome. Continuation of pregnancy may be recommended when an IAC is detected prenatally, and reassurance if detected postnatally.

Indexed as

Activities of Daily LivingEncephaloceleChildChild DevelopmentChild, PreschoolFemaleFollow-Up StudiesHumansNeurologic ExaminationPregnancyAtretic cephaloceleChildrenDevelopmentPrenatalPrognosis

Identifiers

PMID33404719
OpenAlexW3118635209

What OpenQuestion holds

Textmetadata
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Registered trials

None linked

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.